Mercury Caused Disorders: Alzheimers, Autism, Depression, Homosexuality, Parkinsons, Prion, Schizophrenia// Medical Science series, book 1 by Archimedes Plutonium This is AP's 36th published book of science published on Internet, Plutonium-Atom-
109 views
Skip to first unread message
Archimedes Plutonium
Sep 7, 2024, 6:47:29 PM9/7/24
to Plutonium Atom Universe
*Mercury Caused Disorders: Alzheimers, Autism, Depression, Homosexuality,
Parkinsons, Prion, Schizophrenia// Medical Science series, book 1*
by Archimedes Plutonium
This is AP's 36th published book of science published on Internet,
Plutonium-Atom-Universe,
PAU newsgroup is this.
https://groups.google.com/forum/?hl=en#!forum/plutonium-atom-universe
Preface: This book reads like a research notebook, not a textbook, a
research notebook from 1996-2007. This was my research notebook from 1996
to 2007 detailing the notes I took on various diseases and disorders mainly
due to compounds of mercury found in air, food, water. Back in 1996, I
started a conjecture starting off first with prion disorder, then moving
into other disorders which would end up saying that the common widespread
industrial pollution of mercury (mostly from fossil fuel burning) was going
to be the underlying cause of _several_ major disorders. At the time of
1996 and thereafter, I was living in New Hampshire where a college
professor accidentally spilled a tiny drop of a mercury compound on a
gloved hand. She was wearing gloves, but the mercury seeped straight
through the gloves and killed her. The lethal potency of mercury and the
pollution exposure of mercury in modern industrial society, makes any good
scientist want to stand up, and research and study to what extent are new
disorders linked to mercury. For if so very little mercury can cause quick
death and since so much modern day pollution is containing mercury, then
one has to wonder how much of our disorders have a mercury origin, or
mercury disorder acceleration, or mercury link. Note of caution: I argue
mercury is dangerous, yet also, being not vaccinated is dangerous, but some
vaccines have mercury used in the vaccine. So I see faults in both, and
that I request those who advocate vaccines to find a alternative to using
mercury in vaccines. Yes-- have vaccinations, by all means have
vaccinations, but please, do not use mercury in vaccines.
Cover Picture: a picture of several coal fired power station that sends a
lot of mercury into the air we breathe. The intake of mercury in large
amounts is a modern industrial phenomenon, and easy to see that some
disorders are rooted in this mercury.
---------------------------
Table of Contents
---------------------------
1) History of this notebook.
2) Earlier metal disorders: lead then mercury then asbestos and now mostly
mercury.
3) Asbestos disorders, a semi-metal disorders.
4) Prion
5) Autism
6) Alzheimers
7) Parkinsons
8) Schizophrenia
9) Depression
10) Homosexuality
11) Future commentary.
----------------------
Notebook Text
----------------------
*1) History of this notebook.*
I had come to the Usenet in Autumn of 1993 and carrying much much science,
especially the Atom Totality theory which is my major discovery of 1990. So
I wanted to broadcast and make public this theory. Also I had some
mathematics proofs to post and Usenet was a new forum, with world wide
publicity, just ideal for posting ideas of science.
By 1996, prion disease was a major topic in biology and medicine and so I
wanted to investigate this disorder, for we were hearing of mad cow disease.
And I had always been watchful of air pollution, the dirt and grime and
mercury in the air we breathe. I knew mercury compounds were plentiful in
coal burning as it released those mercury compounds into the air. I knew
mercury was extremely dangerous and in just a small quantity. So it was not
long before I linked up mercury with many disorders and diseases.
Metal causing disorders -- Homosexual, Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion to list a few.
Mercury compounds are highly toxic, and just a small amount will kill you.
And like lead poisoning, mercury is like lead in the body-- it accumulates
and accumulates and cannot get out of the body, but just builds up until it
causes disease or death. So if every day we breathe in small amounts,
micrograms of mercury, it continues to build up in our bodies and then
causes disorder, disease, even death.
So from 1996 through 2007 I kept posting about mercury caused disorder and
disease in sci.med, sci.chem, sci.bio.misc. And then in April 2007, I
assimilated these posts into a book.
*2) Earlier metal disorders: lead then mercury then asbestos and now mostly
mercury.*
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: "a_plutonium" <a_pluton...@hotmail.com>
Date: 8 Apr 2007 14:31:23 -0700
Subject: Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Autism, Alzheimers, Parkinsons, Schizophrenia, Prion)
a_plutonium wrote:
"Metal Causation coupled with Weak-Protein-Point Theory of
Medicine (Autism, Alzheimers, Parkinsons, Schizophrenia, Prion)",
Archimedes Plutonium, Internet book published 1996-2007 (assimilated
in April 2007 in sci.med,sci.chem,sci.bio.misc)
Well this is kind of what I love about science, is that it is so
compelling as to wanting to know
that it takes precedence over wanting to organize. This book is about
organizing my thoughts
and research on this subject since 1996, but the opening pages catch
me in leaping forward
to the chapter on Prion diseases and the chapter on Autism. So I will
try to stick to my goal
of organizing and well-ordering of this book, but I seem to lapse into
those occasions where
my curiosity bolts me forward and out of place.
Question: have researchers of Prion disease ever found a mercury atom
as the center of the prion
protein molecule? I know they find copper atoms as the center of the
prion protein molecule, but
have they ever found mercury? This is similar to the idea that a
hemoglobin molecule has iron as
its center. And, has any researcher placed mercury compounds in a
solution of prion protein
molecules and observed what happened, and not forgetting to add a
current to the solution to
simulate the brain currents.
One must keep in mind that all the above diseases are brain diseases
and the brain is the part
of the body that is Electrical. This electricity of the brain is the
major factor why these diseases
occur in the first place.
Autism: as to autism the Japanese mercury tragedy of Minamata involved
methylmercury. The Thimerosal
preservative for vaccines to babies is almost 50% ethylmercury. The
symptoms of Autism through its
broad spectrum of symptoms closely matches the symptoms of mercury
poisoning.
Question: has anyone conducted a survey of families where an autistic
child is born and whether the mother
had a lot of Tuna fish or other seafood in her diet up to the pregnancy
and up to the birth of her child?
Anyway, I was avidly looking for research on the myelin sheaths of
brain nerves for it is the Myelin Sheaths
that is attacked by mercury poisoning. And looking for the location of
the brain of babies where autism would
take hold by not forming adequate Myelin Sheaths of Brain cells. I am
trying to locate the part of the brain that
is so to speak "dissolved by mercury presence" so that brain sheaths
cannot form. And this region of the brain
would cause the Autistic antisocial behavior.
I could not find anything in the Autism research as to a location of
damaged brain cells for autism.
What I am trying to link is the known fact that mercury prevents the
formation of nerve sheaths. If I can show
that autism is the lack of development of a mass of nerve sheaths,
then I have linked Autism to Mercury
poisoning.
So, I know as a solid fact that mercury prevents the formation of
Nerve Sheaths. So all I have to show now, is that
Autism is the lack of development of some specific nerve sheaths. If I
can do that, then I will have shown
that Autism is in fact mercury poisoning.
Now there is a huge range or spectrum of Autism, and to me that means
there is a huge range of what kind
of mercury compound and the dosage of the mercury compound and when
the infant had contact with that
mercury compound.
Now there was a very silly report out of Israel about Autism connected
to older men. This is silly because
it is statistical and the explanation could well be something as
simple as the fact that older men were
able to get free medical care and required to get Thimerosal shots for
their infants. Or it could be the case that families with
older men ate twice as much tuna fish. So this older men hypothesis is
really bad science for it is easily
explained away.
*3) Asbestos disorders, a semi-metal disorders.*
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: "a_plutonium" <a_pluton...@hotmail.com>
Date: 8 Apr 2007 22:26:08 -0700
Subject: Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Autism, Alzheimers, Parkinsons, Schizophrenia, Prion)
"Metal Causation coupled with Weak-Protein-Point Theory of
Medicine (Autism, Alzheimers, Parkinsons, Schizophrenia, Prion)",
Archimedes Plutonium, Internet book published 1996-2007 (assimilated
in April 2007 in sci.med,sci.chem,sci.bio.misc)
This is a beautiful book and a change of pace for me as my last
several books have been
monograph-books. Monographs are shortened books and focused on a
specific topic and of
100 pages or less. A full book is long and expansive and tends to be
general and not so
specific. In this book I will cover 5 well known diseases that are
afflicting modern society
and this book gives a new theory about all these five diseases. It is
a new theory because
a disease was never considered to be a overdose of some natural
material. In the case of the
5 diseases, the most common culprit is mercury, but in the case of say
schizophrenia it
maybe a combination of silver and mercury or in the case of prion
disease a combination of
copper and mercury or even cesium and rubidium, or in the case of
Parkinsons, a combination
of mercury and some other element.
The fundamental idea is that the brain is an electrical environment
which does something to
mercury and other elements that are foreign to the brain and wrecks
havoc on the brain.
And because these foreign elements are in the brain which should not
be, that at a high
enough dosage, there is a breakdown of a weakpoint in the brain to
these foreign metals.
For Autism it is the lack of nerve sheaths; for Parkinsons the weak
point is alpha synuclein;
for Alzheimers the weak point is beta amyloids; for Prion it is prion
proteins.
So the basic idea is that when the brain has too much of a metal,
there is a weakpoint that
is damaged. Once damaged the disease has started.
Now some consider the above 5 diseases as genetic or partly genetic.
That is not true for
these diseases are all environmental. Because mercury overdose is an
environment issue.
And the very best way to talk about these 5 diseases is to make the
analogy to a another
environment disease that is well known-- Asbestosis. So Autism, and
Alzheimers and Parkinsons
and Schizophrenia, and Prion are diseases very much like Asbestosis
only the toxic agent is
not a asbestos fiber but a overdose of mercury and other metals that
reach the brain.
Once these toxic metals reach the brain and are in an overdose
capacity, they wreck havoc on
a weak-point of the brain and thus start the individual disease. In
the case of Alzheimers and Parkinsons
and Prion CJD are most often old age diseases and this is because at a
certain age our body can no
longer dismiss the mercury buildup of all those years. Remember that
the young body removes metals,
but that the older and aging body loses its ability to remove foreign
metals from the brain. So the onset
of Alzheimers is most often in old age.
And one could say that Alzheimers is the Autism of old age or the
other way of saying that Autism is a
infant that has caught Alzheimers. Both involve mercury destruction of
part of the brain.
And I would like to challenge the science medical community to
statistically research the numbers of Autism
and Alzheimers as per geography with coal fired power stations and the
eating of Tuna fish and other fish.
In other words the geography where there is a lot of mercury in the
environment is the place where the highest
rates of both Autism and Alzheimers occurs.
It is nice getting back to writing a full length book, but I am going
to make it easy on myself because I am
going to refer to the thousands and thousands of past posts to the
science newsgroups on these 5 diseases
that I have been discussing with many other scientists since 1996.
There were many dead-ends in the discussion
and many time wasting excursions, such as for example when I started
this discussion in 1996 I thought
prion disease was really caused by fungus, analogy to the ant that is
killed and brain parasitized by fungus.
But that massive discussion starting in 1996 was all fruitful since it
culminated in this theory that includes
5-7 major diseases.
The key to this book and theory is that I picked a beautiful analogy
of Asbestosis, which I will compare with
each of these 5-7 diseases.
In the future of humanity will arise new diseases, here to for
unknown, because these new diseases will be
an overdose of some metal which we do not have now. Perhaps some
element which we have little use now
will be prevalent in the environment and this will lead to a new
disease when in overdose in our body.
So the key to this book is the analogy to Asbestosis. And the idea of
this book is that the brain is a special
environment of electrical pulses and for which too much mercury or
other foreign metals will attack a weak point
of the brain and cause to arise one of the 5 diseases listed.
*4) Prion *
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: plutonium.archime...@gmail.com
Date: Mon, 31 Mar 2008 12:33:25 -0700 (PDT)
Subject: the evidence is mounting against Prusiner .. about Prion disease
and that mercury or chemical is the cause (not biology cause): Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
Every good scientist has to love
organization and order. If not, then you cannot
become a good scientist. The ability and desire to "order things" is
tantamount to being a scientist.
I did a Google search with these terms:
"mercury heat prion".
The energy it takes to destroy Prion disease provides us the
clue ... Group: sci.med
To destroy the prion disease is clear. You incinerate at 700 degrees
C. To inactivate,
does that mean when transplanted into an animal, it procures the
disease. So what
is this reference doing in this discussion anyway? Did you make a
mistake here
Bob by posting it? And there is a big difference between dry heat ...
Aug 29 2006 by a_plutonium - 156 messages - 12 authors
whether Cs or Rb or Hg is the metal cause of Prion disease Re:
the ... Group: sci.med
When the thread is about sterilizing, and Bob enters with something
other than
sterilizing such as inactivation (whatever that means regards prion
disease) ...
If you're going to assume what he has posted accurately, then logic
says that
you have to believe it when he says that 140 C of wet heat without
caustic and ...
Aug 29 2006 by a_plutonium - 156 messages - 12 authors
tell us precisely what metals are inside a good prion versus a
bad ... Group: sci.med
If that were true then it would work without heat (or without much
heat).
But that is not so. It would be interesting to see if the autoclave
fluids would
... That is simply FALSE. bob Since the mercury and cesium/rubidium
would be
ions, I see no harm and no waste of time in performing experiments
where the water ...
Sep 8 2006 by a_plutonium - 156 messages - 12 authors
burning prions may make them more infectious Re: destruction
of ... Group: sci.med
a_plutonium a_pluton...@hotmail.com sci med sci chem sci bio
technology Bob wrote:
On Fri, 25 Aug 2006 01:58:12 GMT, <luca...@sbcglobal.net> wrote: "Bob"
<bbx107.
.... It maybe the case that mercury attaches to the copper atoms in
prion molecules
and is the mechanism of changing the shape of other prion
molecules. ...
Aug 25 2006 by a_plutonium - 156 messages - 12 authors
how do they check to see if samples are sterile Re: focus only
on ... Group: sci.med
Thus overall the big message is that heat -- wet or dry -- inactivates
prion
infectivity with kinetics consistent with a moderately heat stable
protein.
It does have a tendency to stabilize itself ... So it was 1000 degrees
C for 15
minutes and not 600 degrees C. Bob, what happens when you put cesium
with mercury. ...
Sep 7 2006 by a_plutonium - 156 messages - 12 authors
The evidence is mounting against Prusiner and his proxy advocate of
Bob. The Prusiner Model (hate
to call it a theory since it is a fake) posits that CJD and Mad Cow
Disease and these other brain related
diseases commonly called spongiform or Prion disease, posits that the
cause is a protein molecule
that self reproduces.
The last time I discussed this with Bob, I put Bob back and up against
a wall of evidence that Prion
disease is not caused by a protein molecule but caused by a chemistry
poison of mercury or
mercury compound such as Mercuric Cesium or Mercury Fluoride or
perhaps Mercuric Rubidium.
I had argued Bob into a corner because the Evidence shows that Prion
disease needs to be
burned at high temperatures to become sterile. This evidence implies
that the cause is no longer
biological molecules but some chemical poison inside the brain that is
causing Prion disease.
And when cattle are fed the brain remains of dead cattle who have the
disease will contract Prion
disease because the chemical molecule of Mercury Cesium was ingested.
Bob thinks he squeaked out of the discussion with a victorious answer
that sterilization can be
a biological protein. But I have news for him and Prusiner, in that
the high heat of sterilization
destroys their Prion Protein Model.
I did not introduce another great line of Evidence back in October of
2007, as the evidence mounts
against the Prusiner Model. Another evidence that destroys both
Prusiner and proxy Bob adherence
to that protein model.
Remember the evidence in England of around early 1990s or even 1980s,
sometime in that time period,
where a cluster or small group of people in a small town of England
who were all young people and all
of them contracted a rapid form of CJD. There have been other clusters
of CJD but this England one
really sticks out as evidence that the Prusiner Model is a fakery of
science. In the England cluster were
all very young people who contracted a rapid motion CJD in that they
died in a few years. Up until that time
it was unheard of that CJD can have a rapid motion disease and can
affect very young people.
What does the England CJD Cluster remind one of as a disease agent?
Well, a commonsense person
would say they had been poisoned. To be poisoned does not mean
catching a protein molecule that
reproduces. To be poisoned means that some chemical in the environment
such as Mercury Cesium, or
Mercury Rubidium, or Mercury Fluoride was eaten or drunk by these
England Cluster.
So to people, who can teach Chemistry and do chemistry
experiments, but when it comes to
assessment or evaluation of a Model such as Prusiner's Model of Prion
Disease, ..
who do more damage and harm to science because they lack the ability
to apply commonsense to
the evidence.
We can all understand why Prusiner would back his Model regardless of
the mounting evidence against him
in that 99% of scientists seek fame more than they ever seek the
truth. And where Prusiner can never
reconcile that the Heat of Sterilization and the evidence of rapid
disease mechanism of the England Cluster
point to a chemical poison in the environment and not a biological
protein that does miracle-reproduction.
Also, I should touch on the social background or social environment of
the 1990s that allowed a Fake theory
or fake Model of Prusiner to become accepted. If you look at those
social times throughout the world, the
poison of mercury was very much litigious, that is, mercury poisoning
was very much in lawsuits around the
world. Where even in the USA, the government bureaus of Health and
Medicine denied that teeth fillings of
mercury are dangerous and could lead to Alzheimers, or that
preservative of mercury in immunity shots given to infants was
dangerous and
could cause Autism in children.
So we had a social environment of the 1990s where the entire Health
community and Chemists were
covering up the dangers of mercury and mercury compounds. In an
environment such as this, persons like
Prusiner would fare well with fake theory of Prion disease
caused by some rogue protein, because
then the real culprit of Prion disease such as a Mercury compound
would not be so big and alarming
to the already worried.
But I am happy to announce that the Truth is breaking loose and
breaking free, in that recently a court
case awarded a family of their autistic child which was pointed at the
mercury laden immune shot.
The huge mounting evidence such as the Heat of Sterilizing Mad Cow
disease implies a mercury compound poison.
The huge mounting evidence of clusters of young people who quickly die
from CJD implies a mercury
compound poison.
The huge mounting evidence that elk species and deer species around
the Colorado region have a high
density of brain spongiform is not indicative of a Protein Only Cause
but is indicative that a Mercury
Compound is a poison and is concentrated in that Colorado environment.
I must say something good about Bob, since I said so much bad about
him, and the good thing he
brings to the conversation is that he does discuss the topics. The
worst enemy of a scientist is not
those who oppose in discussion, but those who ignore and do not
participate.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 12 Jun 2007 03:38:14 -0700
Subject: news of thimerosal and beta amyloid: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
Now I am beginning to realize that I should have a last chapter in all
of these books as a "news follow-up chapter".
This is something the old way of publishing books could never do where
the latest news can be included in
the book itself.
On the late night news of June 11, 2007 was two pieces of information
that directly applies to the theory of this book. That a
metal such as mercury can cause these 5 diseases. In the news was word
that about 5,000 cases of
autism are seeking litigation over thimerosal (mercury preservative)
vaccine. What appears to be the
case for the autistic families is the sudden appearance of autism in
their child shortly after the vaccine
was administered. So that what appears as the logic of their case is
that their child quickly displayed
autistic symptoms shortly after administered the vaccine.
Whether the defense in the thimerosal cases can show that autistic
children displayed autism before their
thimerosal injection remains to be seen.
But it would certainly be a strong case if these parents of autistic
children provide documentary evidence that
their child displayed autism shortly after the thimerosal injection.
And the other news was that there are 3 new alleged treatments for
Alzheimers in which one is alleged a
cure for the disease. And is based on the idea that beta amyloid is
the cause of the disease. The idea that
beta amyloid causes Alzheimers in the analogy that hepatitis is caused
by a virus. Before, it was thought
beta amyloid was a symptom of the disease but these drugs allege that
beta amyloid actually causes the
disease.
What I want to focus on in that beta amyloid report is the similarity
between Prion disease and Alzheimers
in that the prion protein is the cause of Prion disease and now this
beta amyloid is implicated as the
cause of the Alzheimer disease. So this news further confirms and
supports the theory of this book. That
these 5 diseases are all related and all have a causation mechanism
that leads back to some metal
poison such as mercury or cesium or rubidium whether alone or metals
in combinations.
And it is not the Prion protein or beta amyloid that goes around
changing other proteins to become a rogue
protein but rather what has happened is that the mercury or metal
poisons have altered the synthesis of
proteins in the brain so that some site in the brain spews out more
unwanted rogue proteins.
In the 1990s the science medical community accepted this really silly
and stupid theory that prion proteins
go around and change other proteins to be a like-copy of themselves.
And so what Alzheimers and beta
amyloid now tell us is that some site of protein synthesis has gone
amok and spewing out more unwanted
beta amyloid. But if the prion model were correct then beta amyloid
would be of that model also. It is not.
Beta amyloid does not run around in the brain converting other
proteins to be more beta amyloid. It is the
metals such as mercury that causes some site in the brain to spew more
beta amyloid and thus the disease.
*5) Autism*
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 12 Jun 2007 23:46:01 -0700
Subject: news of thimerosal and beta amyloid: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
a_plutonium wrote:
> Whether the defense in the thimerosal cases can show that autistic
> children displayed autism before their
> thimerosal injection remains to be seen.
> But it would certainly be a strong case if these parents of autistic
> children provide documentary evidence that
> their child displayed autism shortly after the thimerosal injection.
I am thinking there is a good science study of these 5,000 litigants
of thimerosal. To find out
when each of the 5,000 children were administered thimerosal. Next, to
find out as accurately
as possible when the parents first realized their child was autistic.
Finally, to measure to what
degree each of those children is stricken with autism, for I realize
autism varies in the degree of
severity.
What I am saying is that these 5,000 offer up more clues of
understanding this disease of autism.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 09:34:37 -0700
Subject: excess fluorine accounting for the rise of Alzheimer: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
I have talked a lot about mercury in this book with the modern day
common prevalence of mercury in the environment
especially the air we breathe and coal fired electric power stations.
And the fact that mercury in very tiny doses
is a huge damage especially to babies and infants.
I also talked about cesium and rubidium in the environment especially
with Prion diseases.
I talked about silver in the environment especially with
Schizophrenia.
I mentioned aluminum and manganese and copper.
What I did not mention was fluorine in excess. When was fluorine
recognized to prevent tooth decay? A
little bit of fluorine in the water is okay but we can easily overdose
on fluorine if it is in the water and where
officials who add the fluorine could easily make mistakes. But also
when tooth products add flourine to the
"dental floss" or toothbrush so that combinations of water, tooth
brushing and we easily get overdoses of
fluorine.
When was Schizophrenia recognized to be on the rise as a disease? Was
it when fluorine was added to
the water? When was Alzheimers seen rising? Was it when fluorine was
routine treatment? When was
Parkinson on the rise? Was it around the time that fluorine was added
to the water supply?
This is why it is important to keep records of date and time of these
diseases because something like
routine fluorine additive just maybe the cause of a major disease such
as Alzheimers.
We do not know what happens when you have mercury with fluorine
present in the brain in excess doses.
MY GUESS: I am guessing that excess fluorine in the human body is
easily recognized by this symptom.
That the skin in the mouth sheds more rapidly due to excess fluorine
to the body. I know the skin that lines
the mouth sheds periodically, but I think that with excess fluorine in
the body, that the white skin of the
mouth sheds too much. But I would need a medical study to confirm this
speculation.
One thing is certain, that excess fluorine acts as a poison. The old
adage that too much of anything begins to
act as a poison is true.
All 5 of these diseases involve proteins. Mercury affects protein
synthesis and protein sequencing. Fluorine
would do harm to proteins.
It is thought that well-water has something to do with the large
numbers of Parkinson cases in the Midwest
USA of the farm community. Could it be that treatment of well-water
was a fluorine additive and that it is
easy to make the mistake of fluorine overdoses.
The rise of Alzheimer disease in the past decades is usually
attributed to the fact that people live longer, but
that may be a convenient scapegoat. Perhaps the rise of Alzheimers,
and especially women more than men
is due to the proclivity of the tap water being overdosed with
fluorine. So that a brain that receives too much
mercury along with fluorine is going to be set on a course of acquired
Alzheimer disease.
I challenge anyone in the Medical Community to explain where excess
fluorine in a diet goes? Does it end
up in the brain and does it affect beta amyloid formation?
If we set up an experiment of the representative proteins of these 5
diseases such as the Prion Protein, Beta
Amyloid protein, Alpha Synuclein protein and placed excess fluorine in
that cell culture environment then
do we start to see the formation of those diseases?
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 09:47:28 -0700
Subject: excess fluorine accounting for the rise of Alzheimer: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
a_plutonium wrote:
> MY GUESS: I am guessing that excess fluorine in the human body is
> easily recognized by this symptom.
> That the skin in the mouth sheds more rapidly due to excess fluorine
> to the body. I know the skin that lines
> the mouth sheds periodically, but I think that with excess fluorine in
> the body, that the white skin of the
> mouth sheds too much. But I would need a medical study to confirm this
> speculation.
So the easy analogy above of mouth skin shedding due to excess
fluorine is
to think of the brain with its beta amyloid protein that it sheds the
beta amyloid
as a waste product because of the excess fluorine inside the brain.
The skin lining of the mouth keeps shedding the white skin because of
excess
fluorine and the mouth continues to replace the shed white skin.
Likewise the
analogy inside the brain where the excess fluorine starts to shed the
beta
amyloid of Alzheimers and the brain keeps wanting to replace this beta
amyloid
so produces even more beta amyloid. So the excess fluorine causes this
vicious cycle of protein replacement and thus the disease.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 10:03:52 -0700
Subject: excess fluorine symptoms-shedding of mouth lining and eyes with
blurred vision: Metal Causation coupled with Weak-Protein-Point Theory of
Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
a_plutonium wrote:
> > MY GUESS: I am guessing that excess fluorine in the human body is
> > easily recognized by this symptom.
> > That the skin in the mouth sheds more rapidly due to excess fluorine
> > to the body. I know the skin that lines
> > the mouth sheds periodically, but I think that with excess fluorine in
> > the body, that the white skin of the
> > mouth sheds too much. But I would need a medical study to confirm this
> > speculation.
> So the easy analogy above of mouth skin shedding due to excess
> fluorine is
> to think of the brain with its beta amyloid protein that it sheds the
> beta amyloid
> as a waste product because of the excess fluorine inside the brain.
> The skin lining of the mouth keeps shedding the white skin because of
> excess
> fluorine and the mouth continues to replace the shed white skin.
> Likewise the
> analogy inside the brain where the excess fluorine starts to shed the
> beta
> amyloid of Alzheimers and the brain keeps wanting to replace this beta
> amyloid
> so produces even more beta amyloid. So the excess fluorine causes this
> vicious cycle of protein replacement and thus the disease.
I think there is another symptom of excess fluorine in the diet
involving the eyes and
vision. I believe with excess fluorine that we tend to see flashing
lights especially in
the morning from waking up that our peripheral vision is dotted with
flashing lights
which goes away as the day carries on. I am going to call it simply
blurred vision.
Now if fluorine is a major contributor to the disease of Alzheimers
and since
Alzheimers cases have been on the rise for the past 3 decades, then
one would
suspect that some eye diseases have been on a concurrent rise as with
Alzheimers.
Because if excess fluorine is the contributing cause, then a disease
of eyesight
would parallel Alzheimers.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 10:52:27 -0700
Subject: excess fluorine; New Jersey the highest rate of Austism?: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
If my memory is correct when I was doing this book I looked up where
the highest rates of Autism occurred in
the USA and my memory says it was New Jersey.
So indulge with me for a moment about excess fluorine as a major
factor of these 5 diseases and Autism
in particular. Now New Jersey is one of the most technology advanced
states of our union and home of the
prestigious university of Princeton. So it is not a backward nor
backwash place of the USA. And if it is known
that fluorine prevents tooth decay it is easy to imagine that New
Jersey would be amply following a fluorine
additive to drinking water and easy to see of excess additive.
So what I am wondering is whether anyone has records of the highest
incidents of Autism. Can we break
those statistics down into whether one city has fluorine additive and
another does not and whether the
highest rates of Autism match the practice of adding fluorine to
drinking water.
Do we have a case where a county is supplied with drinking water that
has no fluorine added and where
there was never any case of Autism? And yet another county whose water
supply has always added fluorine
and where there are many cases of Autism?
Ditto for the disease of Alzheimers. Do we find some pattern as to
disease and drinking water with fluorine.
So these are questions that have to be looked into and answered.
P.S. if any of the above is true in part or whole, it is kind of funny
in a devilish way that we have such zeal
to prevent tooth decay by adding fluorine to the water and end up with
contracting a brain disease of
either Autism or Alzheimers because of that fluorine.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 26 Jun 2007 23:50:47 -0700
Subject: comment on mercury causing Autism and lawsuit of CDC; (Nightline
report): Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
On the TV tonight was Nightline with a story on Autism and a group
suing the CDC for the mercury in
vaccines administered to babies. Nightline did a rather poor job of
reporting in that it kept attacking Dr. & Dr.
Geier (hope I spelled that correctly) of a father son doctors who
support the theory of mercury causation for
autism.
In courts and in litigation, often it is science itself that gets
degraded.
For example, the CDC last year and previous years has advocated and
supported the issue of warding off
people from eating too much fish such as tuna because of mercury. And
their warning is particularly directed
at pregnant women. I forget what they specifically recommended such as
only one serving per month. And
these warnings are because of the high content of mercury. So the CDC
is very much hypocrites for on the one
hand they tell how dangerous fish are for pregnant women and on the
other hand they want to enter the
courtroom by saying that Dr Geier & Dr. Geier have no scientific
evidence that mercury in the vaccines harms
and causes autism.
So why attack Dr. Geier when it is obvious commonsense that no babies
should be exposed to mercury
especially at such a young age.
Why should the CDC bother about warning pregnant women over fish, when
they act as hypocrites trying to
defeat a lawsuit on mercury administered to babies.
What bothers me most in this case of a lawsuit is that the CDC
abandons science. They seem to bend over
backwards in attacking Dr. Geier and they label mercury research as
"junk science", yet they are two-faced
in warding off pregnant women from eating fish.
Let the facts speak in the lawsuit. It is obvious mercury is
dangerous. It is obvious mercury is more dangerous
to babies than to older people. So why was mercury allowed to be
administered to babies and the answer
is obvious that the CDC cares more about making money for drug
companies and winning lawsuits
than about applying commonsense. For science is commonsense.
The CDC really should not even be in the courtroom since it is
indefensible to be in the witness chair and
say that mercury is dangerous for pregnant women by eating too much
fish, and then say that mercury
as a component of vaccines for babies has no role in Autism.
What the Nightline report brings into focus is that the CDC acts more
like a puppet to drug companies
defending drug companies, then it spends on science. And the CDC in
this lawsuit will likely end up
degrading science.
Granted, the precise steps of interaction of mercury in a baby and how
that mercury leads to autism
is not yet known, and it is not known whether mercury even causes
Autism. But it is known for certain
that mercury in the brains of human adults is dangerous and thus it is
even more dangerous to babies.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 27 Jun 2007 02:37:58 -0700
Subject: mercury laden vaccines and Autism and lawsuit over: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
In that TV Nightline report the CDC was mentioned, but I do not know
for sure whether the lawsuit is with the CDC
for it maybe the dept. of Health of the government. A group of
families with autistic children are suing the
government for the administering of mercury laden vaccine to their
infants. Mercury was used as a preservative
in vaccines in the 20th century.
My gripe is that the lawsuit will degrade the science. That the
government will say there is no proof that
mercury causes autism. But there is no proof that mercury can cause
autism. In other words there is
"no proof" either way. And that is because we simply do not know
enough about Autism at this time.
So I hope the court battle does not end up as a degradation of
science, because there is no science
evidence either way about Autism. Some future research may finally
uncover the workings of Autism
and how much was a factor of mercury remains to be seen.
So, in my opinion, the way the court case of this should go is to
prove that the government was reckless
and negligent in keeping the use of mercury as a preservative of
vaccines and the potential harm and
danger that creates for babies and infants. It is my opinion that the
trial over mercury laden vaccines
is not one of proving cause of Autism but rather the proving of
Government negligence in allowing
a mercury laden product that exposed thousands of infants to a toxic
substance of mercury.
That the case should dwell on the fact that mercury is a known toxic
substance, especially young
people. And that the government should have insisted the mercury be
banned.
From my viewpoint the government was reckless and negligent by
insisting that mercury laden vaccine was not
dangerous. The government should have pulled all mercury laden
products from the market. And the government
failed in informing parents in the 1900s that the vaccine contained a
toxic substance. If parents knew that
drugs and vaccines were labeled as to contents and read "contains
mercury", then many of those
parents may have opted out. But instead, ingredients were never
labeled. So in this regard of a known
toxic substance is used but not labeled and the unquestionable danger
of mercury, that the government
should be found guilty.
The trial is not over whether mercury causes autism. The trial is over
the fact that mercury is a toxic
substance and the government did not ban its use from the start.
An analogy would be to use trans-fat or hydrogenated fat in all your
cooking and feed it to guests without
telling them of the content. Or another analogy would be to make
respirators out of asbestos, and claiming
that the asbestos is harmless.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Fri, 29 Jun 2007 10:42:57 -0700
Subject: Lawsuit of parents of Autism versus USA govt over mercury laden
vaccines: Metal Causation coupled with Weak-Protein-Point Theory of
Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
The use of mercury as a preservative in vaccines such as Thimerosal is
being challenged in the court system
by angry parents of Autistic children. Normally I would avoid such
issues since they are more social
than they are scientific. But here I am giving my opinion because the
government and its science health
department is abandoning science itself and degrading science and
acting more as a "lets save money"
than acting as "lets pursue the truth".
The govt-health-science is claiming in the lawsuit that "mercury has
not been proven to cause Autism". This
is a true statement. Since there exists only some hints and some
indications but not proof. What the
govt-health-science neglects to say is "there is no proof the other
direction that mercury plays a major
role in causing Autism." So, yes, there is no proof that mercury
causes Autism, but there is no proof in
the other direction that mercury is the major factor in causing
Autism. However, THERE IS PROOF THAT
MERCURY IS A TOXIC POISON ESPECIALLY TO YOUNG CHILDREN AND BABIES.
There is that proof
and this is what the govt-health-department should be on trial for.
That the govt should be found guilty
in this Autism case because it allowed a known toxic poison to enter
the bodies of babies and infants.
When science knows of a toxic poison, then no health department should
ever allow that poison to be
used in some way shape or form. So this is what the legal case, in my
opinion, is all about.
Analogy, suppose some company wanted to make money from making
respirators that used asbestos fibers
and because they could make money from it, the govt health department,
knowing that asbestos near lungs
of humans is a dangerous substance, but because of the money profit
involved, the govt health department
allowed it. Same thing with Thimerosal.
This lawsuit is not a legal battle to prove whether mercury causes or
does not cause Autism. This lawsuit
is about whether the govt health department knowing mercury is a acute
toxic poison and yet allowed it
to be widely used.
It will take some years or months longer before science has the
definitive answer as to what role mercury
plays in causing Autism, whether it plays a major role or a minor role
or no role. Future science will prove
it. But this lawsuit is not about that "proof" which will come in the
future. This lawsuit is about a Government
Health Department that knows and knew full well in the last century
that mercury is a very toxic poison
and that mercury had no business and no reason for ever being allowed
in the bodies of young children.
One thing good about this lawsuit is that it will speed up this
science research topic of finding out just exactly
how much involvement mercury has with causing Autism. In my
estimation, mercury is key in causing
Autism and it maybe that mercury in conjunction with some other
element such as FLUORIDE maybe the
cause of this horrible disease of Autism. It maybe the case that
mercury-fluoride is the transport of fluoride
to the brain area that destroys the part of the brain which results in
Autism. So this trial may thus speed
up this research.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Fri, 29 Jun 2007 10:57:47 -0700
Subject: no proof that mercury is not the major factor in Autism
(correcting my mistake): Metal Causation coupled with Weak-Protein-Point
Theory of Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
Correction of my writing mistake:
> The govt-health-science is claiming in the lawsuit that "mercury has
> not been proven to cause Autism". This
> is a true statement. Since there exists only some hints and some
> indications but not proof. What the
> govt-health-science neglects to say is "there is no proof the other
> direction that mercury plays a major
> role in causing Autism." So, yes, there is no proof that mercury
> causes Autism, but there is no proof in
> the other direction that mercury is the major factor in causing
> Autism. However, THERE IS PROOF THAT
> MERCURY IS A TOXIC POISON ESPECIALLY TO YOUNG CHILDREN AND BABIES.
> There is that proof
> and this is what the govt-health-department should be on trial for.
> That the govt should be found guilty
> in this Autism case because it allowed a known toxic poison to enter
> the bodies of babies and infants.
I think I made those writing mistakes because of my aversion to
"double negatives".
Maybe I made the mistake in writing so as to emphasize this post.
The above should have read:
(1) "there is no proof the other direction that mercury does not play
a major role in causing Autism."
(2) there is no proof in the other direction that mercury is not the
major factor in causing Autism
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Sat, 30 Jun 2007 10:55:32 -0700
Subject: can the CDC provide proof that mercury does not cause Autism??:
Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
From the TV, it sounds as though the CDC is trying to squeak out of
this lawsuit by angry parents of Autistic
children with a mantra of "there is no proof that mercury causes
Autism".
What I am saying is that the CDC cannot cling to that mantra because
of the reverse statement "
there is no proof that mercury does not cause Autism".
So if the CDC scientists try to cling to the excuse of proof or no
proof, they cannot cling because science
has not proven either way of what mercury does.
It is my opinion that the CDC and the entire USA Health dept is on
trial because it allowed a known
and proven toxic poison of mercury to be used as a preservative for
vaccines called Thimerosal. It is
my opinion they are obviously guilty. To me, it is like allowing
manufactures to make respirators out
of asbestos fibers. Or like allowed to add hydrofluoric acid to soft
drink to give it fizzle.
Perhaps the CDC and USA govt health dept allowed Thimerosal from the
bad judgement that mercury was
used in dental fillings with no apparent harm. But it is time now to
also remove mercury from dentistry
since we have great substitutes of plastic fillings and do not need
mercury ever to be used as fillings.
I searched for Minamata mercury Autism and found this website:
quoting from:
http://www.ewg.org/reports/autism/part4.php
The indisputable toxicity of mercury to the brain, particularly the
developing brain (Limke 2004, Clarkson 2002, Mahaffey 1999).
Peer-reviewed reports showing that autistic children are extremely
poor at ridding their bodies of mercury as measured by mercury hair
levels (Holmes 2003).
The recent finding that autism-like symptoms are triggered by
thimerosal in mice with a predisposition to autoimmunity (Hornig
2004).
The fact that the prevalence of autism in boys is four times that in
girls, and that boys have elevated incidence of damage from mercury
exposure in epidemiologic studies (Vahter 2002).
--- end quoting ---
As I said before, there is no proof that mercury causes Autism, but
then again, there is no proof that
mercury does not cause Autism. This is because the Science has not
found the answers yet. The
science is premature, but give it some time, perhaps 5 or 10 years and
we should know a lot of the
answers about mercury involvement with Autism.
The world in the past year has witnessed the terrific toxicity of
Polonium 210 and how it killed a Russian
living in England. The world has witnessed the accidental poisoning of
a small minute
amount of methylmercury which can penetrate through latex gloves and
kill. Mercury is one of the most
deadly poisons and yet ironically for decades the USA government
Health authorities said that mercury
in vaccines for babies and infants is okay.
If the families of these autistic children win the lawsuit, and I
believe they should win, then it is a victory
for commonsense, that when a government lists Toxic Poisons, then do
not use them, ever, no matter
what the excuse is (such as the silly excuse of preservative).
And let us get mercury use out of dentistry completely. When you know
something is a toxic poison then
find a safe substitute and use that substitute.
*6) Alzheimers*
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 23:03:01 -0700
Subject: excess fluoride accounting for the rise of Alzheimer: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
Sassman wrote:
> Uh, I think they add fluoride to water supplies not fluorine.
> ---
> www.analyticalchem.com
Fluoride ion begot from NaF or Na2SiF6 to be 1 ppm in drinking water.
But who can trust all municipalities
to have 1 ppm. Perhaps a employee dumps in 1,000 ppm.
And what of the compound Hg2F2, mercury fluoride. Does it transport
fluoride into the brain?
I am not sure that fluoride causes the mouth lining to shed. The skin
inside the mouth that periodically sheds and
we feel it and notice it as white globules. But when you have too much
fluoride, does it increase the shedding
of the mouth lining? I know too much fluoride causes teeth mottling
where there are white circles on the teeth.
But what about the skin lining of the mouth?
So, if too much fluoride causes excess shedding of skin cells, then
perhaps too much fluoride inside the
brain causes too much production of beta amyloid. Because as soon as
the mouth sheds its lining, more
new cells are created to replace those. Likewise in the brain for
Alzheimers, if fluoride causes beta amyloid
to shed, then more beta amyloid is manufactured.
I admit there is a lot of speculation in those sentences above, but a
logical pattern has been elucidated.
So I would need to confirm that if excess fluoride causes the mouth
lining to shed more frequently than normal
and thus increases the production of new mouth lining would be
analogous to excess fluoride in the brain
causing beta amyloid to shed and thus the brain producing more
unwanted beta amyloid. So this picture is
rather logical and clear and can be the mechanism of Alzheimers. But
it needs confirmation.
And there is very little information as to mercury fluoride molecule.
How would it be formed in the body? Perhaps
from dental amalgams? And would this molecule become a transport
system of excess fluoride ions ending
up inside the brain.
And we need to know how fluoride interacts with beta amyloid? Is the
mouth lining chemistry similar to
beta amyloid and is the mouth lining when it sheds and we spit out or
pull out those white globules, have
similar chemistry to the beta amyloid plaques in Alzheimers? Also
there are the tau tangles in Alzheimers
and they maybe accounted for by these excess fluoride in the brain in
that fluoride would shed both of these
proteins and cause more unwanted of these two proteins to be formed.
In the mouth when the lining is shed
we simply spit it out or sequester it with our fingers or tongue. But
in the brain, we cannot sequester it out
and thus we have this major disease of waste piling up.
A lot of questions above need answers, but the point I am making is
that there is a clear and logical mechanism
pointed out as to how Alzheimers all takes place with the mouth lining
analogy.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 13 Jun 2007 23:27:04 -0700
Subject: cesium, rubidium causing Prion disease with mercury as transport
agent: Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
I wrote a few minutes ago:
> I am not sure that fluoride causes the mouth lining to shed. The skin
> inside the mouth that periodically sheds and
> we feel it and notice it as white globules. But when you have too much
> fluoride, does it increase the shedding
> of the mouth lining? I know too much fluoride causes teeth mottling
> where there are white circles on the teeth.
> But what about the skin lining of the mouth?
> So, if too much fluoride causes excess shedding of skin cells, then
> perhaps too much fluoride inside the
> brain causes too much production of beta amyloid. Because as soon as
> the mouth sheds its lining, more
> new cells are created to replace those. Likewise in the brain for
> Alzheimers, if fluoride causes beta amyloid
> to shed, then more beta amyloid is manufactured.
> I admit there is a lot of speculation in those sentences above, but a
> logical pattern has been elucidated.
> So I would need to confirm that if excess fluoride causes the mouth
> lining to shed more frequently than normal
> and thus increases the production of new mouth lining would be
> analogous to excess fluoride in the brain
> causing beta amyloid to shed and thus the brain producing more
> unwanted beta amyloid. So this picture is
> rather logical and clear and can be the mechanism of Alzheimers. But
> it needs confirmation.
> And there is very little information as to mercury fluoride molecule.
> How would it be formed in the body? Perhaps
> from dental amalgams? And would this molecule become a transport
> system of excess fluoride ions ending
> up inside the brain.
> And we need to know how fluoride interacts with beta amyloid? Is the
> mouth lining chemistry similar to
> beta amyloid and is the mouth lining when it sheds and we spit out or
> pull out those white globules, have
> similar chemistry to the beta amyloid plaques in Alzheimers? Also
> there are the tau tangles in Alzheimers
> and they maybe accounted for by these excess fluoride in the brain in
> that fluoride would shed both of these
> proteins and cause more unwanted of these two proteins to be formed.
> In the mouth when the lining is shed
> we simply spit it out or sequester it with our fingers or tongue. But
> in the brain, we cannot sequester it out
> and thus we have this major disease of waste piling up.
> A lot of questions above need answers, but the point I am making is
> that there is a clear and logical mechanism
> pointed out as to how Alzheimers all takes place with the mouth lining
> analogy.
There are two of these five diseases that are a buildup of a waste
protein that cannot be easily
removed from the brain. So death is caused by a garbage dump forming
in the brain. The analogy
of the skin shedding inside the mouth and accelerated by excess
fluoride would serve not only
for Alzheimers but for Prion Disease. Instead of fluoride, for Prion
disease is likely caused by
cesium and rubidium that gets inside the body. I say cesium and
rubidium because the deer and
antelope populations out in Colorado are highly inflicted with prion
disease and there are cesium
and rubidium found in those animals.
So here the question is whether the animals that catch prion disease
have eaten cesium and rubidium
which then gets transported into the brain via mercury compounding
with cesium or rubidium and this
ending up inside the brain. Once in the brain the cesium and rubidium
seem to attach to prion molecules
and force them to shed, much like our mouth lining sheds those white
globules. And when the prion
molecule is shed, that forces the cells to produce more prion
molecules. And thus a gradual buildup of
unwanted protein molecules that leads to death.
Now I am unaware of a buildup of a unwanted protein in Autism, in
Parkinson and in Schizophrenia. So
the above scenario may apply only to Alzheimers and Prion disease. And
that a different mechanism applies
to Autism Parkinson and Schizophrenia, but, however all five involve a
metal poisoning of the brain.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Thu, 14 Jun 2007 12:25:45 -0700
Subject: "peeling of mouth mucous membrane" and lactoferrin: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
Funny how I am not able to find a medical or health website for the
normal peeling of the mouth mucous membrane.
Maybe I do not have the correct combination of words for a Google
Search to find what I am looking for.
I think it was in my teens or maybe in my 20s when I first noticed
that the body naturally replaces the
mouth lining and that these white stringy things shed from inside the
mouth. And I looked it up is some
book which said it was a natural occurrence of the body. Just like it
is natural for the skin to replace itself
all over the body. But doing a Google search just never seems to find
a website that tells us that replacement
of the mucous membrane that lines the mouth is natural.
And I made a Google search for the composition of the Mouth Mucous
Membrane, hoping to find that it is a
protein molecule. Those white stringy pieces. I only found
lactoferrin.
So this topic is not easy to find in a Google search because it brings
up mostly rare diseases rather than
what is normal for the mucous membrane.
Why this is important. Well, I feel it is important because the mouth
mucous membrane is almost a perfect
analogy to the diseases of Alzheimers and Prion. That I speculate
excess fluoride in the mouth will cause
increasing mucous membrane peeling and thus increasing replacement of
that shedded membrane. Because it
is in the mouth we can get rid of the shedded white stringy protein.
But when the shedding of a protein
occurs in the brain, it cannot be removed such as beta amyloid or tau
protein or prion protein. So that
if excess fluoride causes shedding of the mucous mouth membrane then
some chemical causes the buildup
of unwanted brain proteins. Perhaps it is fluoride also in the brain
that is transported to the brain via mercury.
Perhaps it is mercury-fluoride. So that people over a lifetime of
drinking excess fluoride water and too much
fluoride in toothbrushing end up with almost assured Alzheimers by the
80s.
Almost a perfect analogy as to how Alzheimers and Prion disease work.
That the mucous membrane of the
mouth can be made to peel or shed faster than normal by the presence
of excess fluoride in the mouth. So
the presence of some excess chemical in the brain such as perhaps
mercury and fluoride causes the
diseases of Alzheimers and Prion.
Now I do not know why it was so easy for me to find in a medical book
in my teens or 20s (1960s through
1970s) that stated the peeling of white stringy masses inside the
mouth lining was a normal and periodic
occurrence for the mouth lining and why here in 2007 it is almost
impossible to find on a Google search.
Perhaps I am not searching the proper words. Or perhaps the way Google
is set up that "normal" things
are too difficult to find but that only abnormal and rare things make
it to the top of a Google search in science.
So that if you want to know what is normal and the basics of the mouth
mucous membrane that it is almost
impossible to find from Google. But that all the rare and
irrelevancies of mouth mucous membrane appear in
a search.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Fri, 15 Jun 2007 00:36:53 -0700
Subject: Histochemistry of Oral Mucous Membrane: Metal Causation coupled
with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
J Dent Res 40(3): 436-445, 1961
International and American Associations for Dental Research
Histochemistry of Oral Mucous Membrane: Total Protein, Sulfhydryls,
Disulfides, Ribonucleic Acid, and Desoxyribonucleic Acid
LOUIS A. CANCELLARO, JULES KLINGSBERG, and EARL O. BUTCHER
The above is somewhat the information I want, but for some reason it
would not download. So it leaves
me with only the title. I was wanting to know how much of a percentage
is the mucous membrane
proteins? And what type of proteins. Are these proteins like that of
beta amyloid and tau proteins in
Alzheimer? Are they like the prion protein molecule? And I wanted to
know if fluoride affects these
proteins. Affects them to the point where they peel or shed from the
mouth and so starting a new
round of growing back mucous membrane to that of the lost mucous
membrane.
Then I want some science journal that specifically tells me when and
how the mucous membrane
naturally and of its own accord replaces itself? And details of the
nature of its shedding or peeling? What
is the average lifespan of mucous membrane?
And I suppose someone has researched Alzheimers plaque buildup, and
whether it follows a similar
pattern as to the shedding or peeling of the mucous membrane.
Of course, if there is a chemical involved such as mercury and or
fluoride then the cure would be removal
of the mercury and fluoride but as long as they are present in the
brain, more plaques accrue.
Now there are new drugs on the market that supposedly treat Alzheimers
or halt its progression. So I wonder
if these drugs work, whether they have something to do with removal of
fluoride ions in the brain?
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Mon, 18 Jun 2007 10:48:51 -0700
Subject: AUTISM, whether fluoride or mercury or both: Metal Causation
coupled with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia)
Below is what I wrote in April, since I did not think fluoride was a
leading cause of these 5 diseases. However
now I believe that fluoride is a major contributing factor of both
Autism and Alzheimers, and perhaps involved with
Prion disease.
I have read several websites after searching for "fluoride autism" in
Google. And these are the proteins
and concepts of that search:
G-alpha proteins
Retinoid Receptors
Hippocampus
Night Blindness
So I am going to have to revise the April entries on Autism and
Alzheimer, because suspect that fluoride
is a major contributing factor. Whether mercury is involved at all in
Autism or Alzheimer, I am not sure. Maybe
the mercury is the transportation means for fluoride to get into the
brain which it otherwise would not. If
mercury is the transport, then mercury is a major contributor of
these diseases. I am not sure how easy
or difficult it is for fluoride in water to get by the blood brain
barrier and whether it needs mercury transport.
One thing I find rather ominous is the fact that Autism really never
gets widespread attention until starting
around 1940s or 1950s when fluoridation of drinking water becomes
common practice. And Alzheimers never
really becomes widespread until after the 1950s. Most would say this
is because we are living longer, but
I would say there is more to it than that.
Now I wonder about the German doctor Dr. Alzheimer who analyzed the
first known victim in the 1890s and
announced the plaques in the brain of that first victim. What I wonder
is whether that first victim had a lot
of fluoridated drinking water? Some parts of the world have natural
fluoridation of their drinking water.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 18 Apr 2007 09:15:32 -0700
Subject: Autism: Metal Causation coupled with Weak-
Protein-Point Theory of Medicine (Autism, Alzheimers, Parkinsons,
Schizophrenia, Prion)
a_plutonium wrote:
> "Metal Causation coupled with Weak-Protein-Point Theory of
> Medicine (Autism, Alzheimers, Parkinsons, Schizophrenia, Prion)",
> Archimedes Plutonium, Internet book published 1996-2007 (assimilated
> in April 2007 in sci.med,sci.chem,sci.bio.misc)
> Chapters of this new book:
> (1) Preface & Introduction
> (2) Analogy disease of Asbestosis
> (3) Autism
> (4) Alzheimers
> (5) Parkinsons
> (6) Schizophrenia
> (7) Prion
> (8) how to medically prove the assertions of this book-- mass
> spectroscopy of brain tissue
With each of these 5 diseases, I would like to list a protein molecule
for which the synthesis of
that molecule has gone awry in the brain. Where the electrical
environment of the brain facilitates
the gone awry synthesis and where mercury and other toxic metals
causes this gone awry
pathology. In the case of Autism I am sorry I cannot point to a
protein or even point to a very specific
region of the brain which can be called the site or location of
Autism.
Perhaps one of the reasons I cannot point to a location is because
Autism is the missing of part of
a normal brain. The nerve sheaths of the brain that makeup a normal
person was destroyed by
mercury and other toxic metals. So we have a disease where we have
missing nerve sheaths and those
sheaths have not be enumerated and cataloged.
Where is the likely source of the mercury poisoning? A real good
candidate is Thimerosal which is a
mercury compound used in vaccines to preserve the vaccine and
administered to young infants during
much of the second half of the 20th century. But mercury is prevalent
in the air we breathe due to coal
fired electric power stations and prevalent in the food we eat such as
tuna fish and other fish.
Geography supports the assertion that mercury is involved in Autism by
the fact that many cases of
Autism are near coal fired power stations.
Researchers of Autism need to find out what nerve sheaths are missing
in Autism.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Mon, 18 Jun 2007 23:42:40 -0700
Subject: AUTISM, ALZHEIMER G-alpha proteins versus beta-amyloid: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
I really should include the oral mucous membrane along with G-alpha
proteins and beta-amyloid.
Years back the PBS TV documented Alzheimer and there they graphically
showed that the scissors that
cuts beta-amyloid is a corrupted scissors in that it leaves this stubb
behind which is the beta-amyloid and
which would then accumulate and cause death. So if that is the entire
mechanism in Alzheimer, then
what corrupts the cutting scissors? Is the corruption of the scissors
caused by fluoride or by mercury?
In Autism, it is alleged that the mechanism is a separation of the G-
alpha protein from retinoid receptors. Perhaps
this is another one of those enzymatic scissors gone awry as the
Alzheimer scissors gone awry. Here again
we ask the same question. What causes the separation of the G-alpha
protein from retinoid receptors? Is it
fluoride ions or is it mercury?
In the Oral Mucous Membrane, when it naturally and periodically peels
those white stringy proteins. This is
normal peeling and replacement by new Mucous Membrane. But when we
have too much fluoride ions present
in the mouth and body then this peeling becomes more frequent and more
abundant. So what does fluoride ions
do to the mucous membrane that causes it to peel excessively?
I tried looking for details of the proteins G-alpha and beta-amyloid
and Mucous Membrane. There is little
literature of these proteins on the Internet. So these three proteins
must be in journals which are more
difficult to access.
What I think is true is that fluoride ions make their way into the
brain via mercury-fluoride, hitching a ride with
mercury to enter the brain. Once in the brain, the electrical energy
of the brain can easily separate mercury
from fluoride ions. The fluoride ions cause the corruption of the
Alzheimer scissors that leaves the stubs
of beta amyloid. And as the years go by with more and more fluoride in
the brain, more and more beta amyloid
plaques build up.
What I think happens for Autism is that just a tiny dose of mercury
fluoride makes its way into the brain
of a infant and the fluoride ions disconnect the retinoid receptors or
possibly damage them for life.
Now I may as well surmise what happens in Prion diseases. Since prion
is a accumulation of unwanted proteins.
And the prion protein is very much similar to the function of the
protein of the Mucous Membrane as a cell
wall acting protein. So that too much fluoride in the mouth leads to a
peeling or shedding of the mucous
membrane that too much fluoride ions in conjunction with mercury leads
to a disfiguring of normal prion proteins
into misshaped prion proteins which accumulate and cause death. So
what the Kuru and cattle in mad cow
disease were eating that was fatal is the mercury and fluoride found
in those diseased brains.
A nice check on Prion disease is to explain sheep scrapie. Do the
sheep in England get more fluoride in their
diet than normal?
And history seems to support the above scenarios, since the rise of
these three named above diseases
coincides with the ever prevalence of fluoride drinking water and the
rise of mercury in the air we breathe.
Back in the 1800s few people in their 70s and 80s and 90s showed signs
of Alzheimer and few infants
showed signs of Autism. That is probably because fluoride in the
drinking water was uncommon. But by
the last decades of the 1900s each person in the USA is in contact
with large doses of both fluoride
and mercury.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 19 Jun 2007 00:19:17 -0700
Subject: telling incident about Prion disease in England in 1990s
supporting mercury-fluoride: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
I wrote a few minutes ago:
> Now I may as well surmise what happens in Prion diseases. Since prion
> is a accumulation of unwanted proteins.
> And the prion protein is very much similar to the function of the
> protein of the Mucous Membrane as a cell
> wall acting protein. So that too much fluoride in the mouth leads to a
> peeling or shedding of the mucous
> membrane that too much fluoride ions in conjunction with mercury leads
> to a disfiguring of normal prion proteins
> into misshaped prion proteins which accumulate and cause death. So
> what the Kuru and cattle in mad cow
> disease were eating that was fatal is the mercury and fluoride found
> in those diseased brains.
> A nice check on Prion disease is to explain sheep scrapie. Do the
> sheep in England get more fluoride in their
> diet than normal?
There was a telling incident that happened in the history of Prion
disease in the 1990s (if
memory serves me). There was a case of where about 4 or 5 or 6 young
people all died
of Prion disease, and they called it something like variant-CJD. What
was odd about it
was that they were very young people, I believe some in their 20s. And
CJD just never
was seen before in such young people. They checked what they had in
common and it
was narrowed down to a restaurant where all had eaten. So it was
supposed that some
cattle meat was contaminated (as best my memory can serve), but
nothing really was
found.
But this whole story makes a lot more sense if the disease were caused
by excess fluoride
and mercury in the brain. That at the restaurant they had eaten
something which had a
mega dose of fluoride and/or mercury. So that it does not matter what
age one is, but how much
fluoride and mercury gets into the body. Both Alzheimer and Prion
disease are slow time
progressive diseases which makes sense as to fluoride poisoning is a
slow and gradual
process. But if you get a mega dosage of fluoride and there is mercury
in the mouth such as
dental amalgam, then the risk is high that this mercury-fluoride
compound makes its way into
the brain.
Now the first cases studied of Prion disease if memory serves me was
in New Guinea with
the ritual practice of cannibalism, eating the brains of the departed.
Now there is mercury
mining activity in Papua New Guinea so there is mercury in the
environment. Could there also
have been fluoride treatment of the water in New Guinea? Or fluoride
found abundantly in the natural
environment in New Guinea? So that what the Kuru victims ate that was
fatal to them was not a
protein molecule but rather the mercury-fluoride compound that still
remained in the brains of the
deceased.
Perhaps Medical Science can reopen these two incidents of the England
fatalities and the Kuru
fatalities and do a autopsy and check for levels of fluoride and
mercury in the brain.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 19 Jun 2007 10:00:12 -0700
Subject: "natural fluoridation" geographically traces out the highest rates
of Autism, Alzheimer, and Prion: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
I made a Google search for "natural fluoridation" and came up with
these three sites:
http://www.york.ac.uk/inst/crd/pdf/appc3.pdf
http://www.nature.com/bdj/journal/v186/n8/full/4800122a.html
http://www.quackwatch.org/03HealthPromotion/fluoride.html
The third one although it is poorly named is one of the best
historical sites on the subject of
natural fluoridation for it tells of the history of discovery that
fluoride saves the teeth from decay discovered
by a Colorado dentist in the early 1900s and was called also "Texas
teeth".
The first two sites speak of Hartlepool England having about 1.2 ppm
natural fluoridation. I do not know
where Hartlepool is located, whether in the agriculture districts of
England where there is a lot of sheep
scrapie and Mad cow disease?
Anyway, it appears to me as a speculation that the geography of
natural fluoridation traces roughly where
the most incidents of Autism, Alzheimer and Prion diseases occur.
I have often said that England has the highest cases of Prion disease
in the world. Now if England has one
of the highest concentrations of "natural fluoridation" then those two
should be more than a coincidence.
And Texas is known as one of the highest Autism rates in the USA if
not the very highest. And Colorado
is known for one of the highest Prion disease rates for deer and
antelope type species, the genus that the
deer is in.
Now I do not know as of yet, whether the rates of Alzheimer disease is
highest in these places of England
and USA where natural fluoridation is high. If Alzheimer rates are
very high in Texas and Colorada regions
then that would not be coincidence.
So what I am speculating is that many towns and municipal water across
England and USA and Canada
do not check what their water has in terms of Natural Fluoridation and
add 1 ppm regardless if the water
already has over 1 ppm naturally. So they end up with 2 ppm fluoride
water.
Now I have not seen a website that tells me how high "Natural
Fluoridation" can be. Can you have some
regions of the world where fluoride in the water is say 100 ppm? Are
there regions of Colorado, Texas, and
Hartlepool England that have huge doses of natural fluoridation?
Fluoride is a strong chemical that easily prevents tooth decay. But
fluoride is so strong of a chemical that
it easily attacks many proteins of the body when in a steady dosage
such as drinking water. And where
modern civilization can easily make errors in excess adding of
fluoride. We see this excess in the toothpaste
as well as dental floss so that a average person is now saturated with
daily contact of fluoride.
And so the rise of these 3 diseases of Autism, Alzheimer and Prion
closely match the rise of fluoridation
additive since about 1950 onwards.
One of the things I recently noticed for myself is the excessive
peeling or shedding of my mucous membrane
in my mouth when I drank and used the fluoride water of the city and
used the fluoride toothpaste and fluoride
dental floss. It is natural for the Mucous Membrane to shed
periodically but not natural for it to shed almost
all at once in a few days and frequent shedding. I think this is
because I just had too much fluoride all at once.
And have reverted to my old habit of drinking distilled water and
cutting back on products with fluoride. We
tend to overdo good things like preventing dental decay and by
overdoing when run the reverse risk of catching
a major disease like Autism, Alzheimer and Prion. It certainly is good
to have no tooth decay but then we
must be careful that we then do not cause a major disease.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 20 Jun 2007 08:42:08 -0700
Subject: best way to get rid of "fluoridated drinking water" is to show it
causes Alzheimer or Autism: Metal Causation coupled with Weak-Protein-Point
Theory of Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
nyscof wrote:
> Areas with very high natural fluoride concentrations in drinking water
> and its consequences:
> http://fluoridealert.org/fluorosis-india.htm
> pictures:
> http://www.nalgonda.org/fluorosis/flourosis_victim_pics.htm
> UNICEF: Overexposure to fluoride is poisonous
> http://yementimes.com/article.shtml?i=1060&p=health&a=1
> Fluoridation 101
> http://www.orgsites.com/ny/nyscof
> Fluoridation News Releases
> http://tinyurl.com/6kqtu
> Tooth Decay Crises in Fluoridated Areas
> http://www.fluoridenews.blogspot.com/
> Fluoride Action Network http://www.FluorideAction.Net
> Fluoride Journal http://www.FluorideResearch.Org
Thanks for the above sources. It told me that 4 ppm was the toxic
level and that 1 ppm is routinely
added to the drinking water. But I can believe that so many cities and
towns across the USA could
easily and routinely make mistakes and errors and dump more than 1 ppm
and easily dump say
10 ppm into that drinking water. So has anyone reported the mistakes
that communities make as
far as adding fluoride?
I do not like the idea that 1 ppm is only a small step away from 4
ppm.
Another item of the above reports is that Scandinavian countries of
Finland, Sweden, Denmark are
nonfluoridated water and yet there cavity rate is 2% whereas
fluoridated USA is 50%.
The above reports also tells me that 1.5 milligrams per liter is the
alleged safe upper limit and that
places like Yemen routinely have "natural fluoride" as high as 3 to
6.5 milligrams per liter. I wonder
how high the natural fluoride was for Colorado and Texas?
But the above did not really touch on the idea that if a chemical such
as fluoride can damage the
bones so easily, then such a potent chemical must also harm the
synthesis of many proteins.
I believe that fluoride first signs of damage are not the teeth or
bones but the Oral Mucous Membrane
and that those stringy white substance is peeled or shed from the
Mucous Membrane. So that if one
fears too much fluoride and if one has a peeling of white stringy
substance in their mouths then that is
the first indication that their bodies has too much fluoride.
I suspect that Alzheimer disease, if not caused by fluoride in the
brain, is accelerated by fluoride in the
brain. I suspect that Autism is connected with too much fluoride for
babies. Whether mercury compounded
with fluoride is the transport system of getting fluoride into the
brain is unknown to me. Whether it is both
mercury and fluoride together or alone that causes or accelerates
Autism and Alzheimers.
Anyway, if it can be shown that Autism and Alzheimer are linked with
too much fluoride in the body, then
I believe that is the easiest and most simple way of turning back the
clock and getting fluoride out of our
drinking water. I believe that people who want fluoride should be able
to buy it in a toothpaste form and that
outlaw fluoride from the drinking water. In other words, if you want
fluoride then buy toothpaste, but do not
force it on everyone who wants to drink water.
So the moment a science research shows us that Autism and Alzheimer
are connected to excess fluoride
is the moment where drinking water can become nonfluoridated.
Does anyone know if the Scandinavian countries of Denmark, Sweden,
Finland have less Autism and
less Alzheimer?
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 20 Jun 2007 23:15:27 -0700
Subject: found that AlF3 in 0.5ppm causes more death than 5ppm or 50ppm:
Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
http://www.fluoridealert.org/health/brain/varner-1998.pdf
The above is a really good website about transport of Fluoride ion to
the brain and that AlF3 crosses
the Blood Brain Barrier BBB much easier than does the ions separately.
I wonder if anyone has researched whether HgF crosses the BBB better
than AlF3?
But there was a peculiar paragraph in the above that said AlF3 in
dosage of 0.5ppm caused
more illness and death than doses of 5ppm and 50ppm. No explanation is
known, but that was 1997-8.
Perhaps ten years later someone has explained it?
Perhaps the explanation involves the idea that if in large doses, the
complex does not separate but
reforms with a nearby AlF3. Whereas in the low dose of 0.5ppm when the
AlF3 complex separates
it stays separate and the damage and harm is caused by the separate F
ions. Another explanation
maybe that in large doses the body just sends it into the waste tract
of excrement or urination, or
throwup.
Read another website which discussed the toxicity of concentrated
hydrofluoric acid and how a tiny
accidental spill is quickly uptaked into deep internal organs leading
to quick death.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Wed, 20 Jun 2007 23:41:24 -0700
Subject: found that AlF3 in 0.5ppm causes more death than 5ppm or 50ppm:
Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
a_plutonium wrote:
> http://www.fluoridealert.org/health/brain/varner-1998.pdf
> The above is a really good website about transport of Fluoride ion to
> the brain and that AlF3 crosses
> the Blood Brain Barrier BBB much easier than does the ions separately.
> I wonder if anyone has researched whether HgF crosses the BBB better
> than AlF3?
> But there was a peculiar paragraph in the above that said AlF3 in
> dosage of 0.5ppm caused
> more illness and death than doses of 5ppm and 50ppm. No explanation is
> known, but that was 1997-8.
> Perhaps ten years later someone has explained it?
> Perhaps the explanation involves the idea that if in large doses, the
> complex does not separate but
> reforms with a nearby AlF3. Whereas in the low dose of 0.5ppm when the
> AlF3 complex separates
> it stays separate and the damage and harm is caused by the separate F
> ions. Another explanation
> maybe that in large doses the body just sends it into the waste tract
> of excrement or urination, or
> throwup.
> Read another website which discussed the toxicity of concentrated
> hydrofluoric acid and how a tiny
> accidental spill is quickly uptaked into deep internal organs leading
> to quick death.
Perhaps the explanation is that 0.5ppm can easily form into
hydrofluoric acid whereas
5ppm or 50ppm cannot.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: Thu, 21 Jun 2007 13:11:35 -0700
Subject: explaining why AlF3 is more dangerous at 0.5ppm than at 5ppm or
50ppm-- does there exist any chemistry analogy??: Metal Causation coupled
with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
Last night I wrote:
> Perhaps the explanation is that 0.5ppm can easily form into
> hydrofluoric acid whereas
> 5ppm or 50ppm cannot.
The above concerns this website:
http://www.fluoridealert.org/health/brain/varner-1998.pdf
And I was wondering if in chemistry there ever was a example of where
a substance in small
doses was a health risk but in larger doses was not? And I cannot
think of a single example of
where that is true. That in all cases of a substance being a health
risk that it is even more of a
risk in large doses.
But I do not know of all of chemistry. So maybe some chemist who daily
works in a chemistry
laboratory knows of a chemical substance that is a health risk in
small doses but not in larger
doses.
Since I cannot think or know of a substance that is more dangerous in
small doses then I have to,
by logic, say that the research of the above website needs to be
duplicated and checked out. If
the experiment is repeated and the results confirm the above "varner
report" then this maybe a
chemistry first discovery
of where a small dose is more dangerous than a larger dose.
Could it be that in a small dose of 0.5ppm that the AlF3 molecule can
form the dangerous
hydrofluoric acid but in large dose of 5ppm or 50ppm that hydrofluoric
acid cannot form??
That certainly would explain the bizarre Varner Report above. And I
think there are many analogies
or examples in chemistry where a reaction does not take place except
for in a specified concentration.
An easy example is that too much salt simply precipitates out
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Fri, 20 Jul 2007 02:10:51 -0700
Subject: brain makes minute hydrofluoric acid which creates Alzheimer:
Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
I found a good website that surveyed aluminum and fluoridation intake
as to prevalence of Alzheimer
disease. I was looking to see if the frequency of Alzheimer was
greater in fluoridated countries like
USA, Australia, Ireland, New Zealand than in nonfluoridated countries
like Norway, Finland, Japan,
Switzerland, France, Germany.
According to one survey, high aluminum concentrations in the water and
low fluoridation have a
highest frequency of Alzheimer. With the idea that high fluoridation
scavenges aluminum. But the
survey inconclusive.
What I suspect is that aluminum is not the culprit. I suspect it is
fluoridation coupled with mercury.
What I suspect is happening is that the APP scissors that makes the
beta amyloid plaques
by wrongly cutting the protein and leaving the beta amyloid stub which
then accumulates is caused
by hydrofluoric acid. The hydrofluoric acid corrupts the APP scissors.
So I need to find out if hydrofluoric acid can be created in the brain
of minute amounts? I need
to find out if mercury is involved in that process?
So what I suspect is the culprit of Alzheimer disease is mercury
coupled with fluoride. In all
industrialized countries, Alzheimers is prevalent and so is mercury
and fluoride in the
environment.
I suspect the combination of mercury and fluoride over years of
exposure develops tiny amounts of
hydrofluoric acid in the brain. That acid when in contact with the APP
scissors corrupts that scissors
and consequently spews out beta amyloid.
So I need to look up as to whether anyone has reported that tiny
amounts of hydrofluoric acid can
be created inside the body and specifically the brain. And whether
mercury plays some role in
creating hydrofluoric acid.
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: 20 Jul 2007 10:39:34 -0700
Subject: brain makes minute hydrofluoric acid (mercury-fluoride) which
creates Alzheimer Autism Parkinson: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
a_plutonium wrote:
> What I suspect is happening is that the APP scissors that makes the
> beta amyloid plaques
> by wrongly cutting the protein and leaving the beta amyloid stub which
> then accumulates is caused
> by hydrofluoric acid. The hydrofluoric acid corrupts the APP scissors.
> So I need to find out if hydrofluoric acid can be created in the brain
> of minute amounts? I need
> to find out if mercury is involved in that process?
Made a Google search of "hydrofluoric acid brain" and this is what
spit out:
Effect of hydrofluoric acid on glucose metabolism of the mouse ...
On the other hand, after hydrofluoric acid poisoning, it was found
that (1) the radioactivity of brain was unchanged throughout all the
poisoning; ...
www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_ui...
- Similar pages - Note this
Hydrolysis of sphingomyelin to ceramide with hydrofluoric acid.
Reddy PV, Natarajan V, Sastry PS.MeSH Terms Animals Brain Chemistry
Ceramides* Chemistry Chromatography, Thin Layer Fatty Acids/analysis
Hydrofluoric Acid ...
www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_ui...
- Similar pages - Note this
Hydrofluoric acid effects on health and the environment
Hydrofluoric acid and HF vapor can cause severe burns to the eyes,
which may lead to ... Excessive exposure to sulfur hexafluoride may
affect the brain. ...
www.corrosion-doctors.org/Acids/Hydrofluoric.htm - 12k - Cached -
Similar pages - Note this
Sodium bifluoride (1333-83-1). Adverse Effects. Fluoride Action ...
Symptoms of the chronic effects of hydrofluoric acid include weight
loss, malaise, anemia, ... The more critical dysfunctions are those of
the brain. ...
www.fluoridealert.org/pesticides/epage.sodium.bifluoride.htm - 40k -
Cached - Similar pages - Note this
Hydrofluoric acid-treated tau PHF proteins display the same ...
Following hydrofluoric acid (HF) treatment, tau PHF proteins are heat-
and .... Glycogen Synthase Kinase-3beta Is Complexed with Tau Protein
in Brain ...
www.jbc.org/cgi/content/abstract/267/1/564 - Similar pages - Note this
What I am looking for is whether the brain is a environment where
fluoride can be turned into dangerous
fluoride such as HYDROFLUORIC ACID and other fluoric compounds such as
MERCURY FLUORIDE.
We all know that the brain has distinct diseases such as Autism
Alzheimer Parkinson Prion and
Schizophrenia. But can the brain serve as a cavity or chamber in which
innocuous fluoride turns into
dangerous poisonous fluoride such as hydrofluoric acid? Such that a
disease of Alzheimers is really the
creation of hydrofluoric acid in minute quantities over time in which
the APP scissors is corrupted and
thus accumulation of beta amyloid.
Is the Autism disease the conversion of fluoride plus mercury into
some minute quantity of a dangerous
fluoride such as Mercury-Fluoride which then causes the brain to have
missing parts.
Is the active agent in Prion diseases really a tiny minute quantity of
a mercury-fluoride compound?
One of the Google hits above talks at length about pesticides as
fluoride compounds and it is well
known that the MidWest farm belt of the USA has the highest Parkinson
rates. So it is very easy to see
that exposure to fluoride by farmers.
Apparently, Alzheimers is a lifetime of exposure to a dangerous poison
that corrupts the APP scissors and
this slow and gradual corruption accumulates beta amyloid. This sounds
like something in the drinking
water such as fluoride. So that the constant exposure coupled with a
brain environment where much
electricity in the brain can turn fluoride and mercury into dangerous
poisons such as Hydrofluoric acid
or Mercury Fluoride.
One of the websites above speaks of tau protein, and it is long been
known that Alzheimers has two
proteins involved of beta amyloid and tau protein but it is a mystery
as to how both are involved. But is it
a mystery if the culprit is a form of fluoride?
Is it a mystery for Prion disease if we consider the culprit as a
fluoride poison that alters the geometry
of a prion protein, rather than the old-goofy-theory of protein-only?
Long time ago I asked whether any person ever caught two or more of
these diseases? Whether one
can catch Parkinsons and then later die of Alzheimers or vice versa.
Or whether one can catch CJD
and later catch Alzheimers. Seems as though this never happens, but it
should happen if these
diseases are various forms of mercury and fluoride and other chemical
poisons.
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Fri, 20 Jul 2007 23:09:08 -0700
Subject: Cesium Fluoride CsF may give 15 different strains of scrapie:
Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
Tonight I was looking for information as to whether the CsF ion can
conformation change the scrapie prion
molecule. That if a beaker of normal prion molecules and a CsF ion
were added, would there appear after some
time, various different prion conformations?
According to this website:
http://www.tulane.edu/~dmsander/WWW/335/Prions.html
Scrapie has at least 15 strains.
Now maybe it is not CsF that is doing the conformation changes in
prion diseases. Maybe it is CsHg
or maybe HgF.
My basic point is this-- these 5 diseases in the title are all caused
by foreign metals in the brain.
So what I am looking for is experiments wherein you have normal prion
molecules, add some metal
ions such as CsF, and look for conformation changes.
The old theory of "protein only causing agent" is fake science for it
cannot explain 15 strains of
scrapie. What can explain 15 strains is some foreign metal that has
a lot of disruptive interaction
with normal prion molecules and where the number of strains are a huge
number.
Whether it is the cesium or fluorine or mercury atom or ion which when
in contact with a normal prion
molecule will alter the shape. As a analogy, picture iron filings
spread randomly and pass a weak
magnet over them. There will be conformation changes.
Which metal is the cause of Prion Disease? I would guess it is cesium
because of the temperature
needed to sterilize an infectious sample.
Newsgroups: sci.chem
Date: Tue, 23 Jul 2013 17:26:10 -0700 (PDT)
Subject: corrected copy Re: News that cancer thwarts Alzheimers and
Alzheimers thwarts cancer and the reason why: Metal Causation Diseases
From: plutonium....@gmail.com
Re: News that cancer thwarts Alzheimers and Alzheimers thwarts cancer and
the reason why: Metal Causation Diseases.
On Tuesday, July 23, 2013 7:19:36 PM UTC-5, plutonium....@gmail.com wrote:
> Alright, recently in the news is a statistics report that if you have
cancer, you are less prone to
acquire Alzheimers and if you have Alzheimers, you are not likely to
acquire cancer. > > > > So does that recent report fit the facts of
Alzheimers disease being too much mercury in the body? > > > >
Why, yes of course. if a body A, has more mercury than body B, the mercury
tends to kill cancer cells from ever forming in the first place.
Now I was searching for research reports that mercury decreases cancer. > >
> > Now the reverse, if body A has cancer and body B has no cancer, and
both bodies have a bit more mercury in their bodies than normally they
should have, then the cancer cells act to chelate the mercury. And so a
body without cancer and a buildup of mercury would end up catching
Alzheimers disease. > >
So here, I was looking for research reports that cancer cells act to
chelate a body, that is, excess mercury tends to be attracted to cancer
cells. When the two meet up, they destroy one another.
Newsgroups: sci.chem
Date: Tue, 23 Jul 2013 22:35:42 -0700 (PDT)
Subject: Re: corrected copy Re: News that cancer thwarts Alzheimers and
Alzheimers thwarts cancer and the reason why: Metal Causation Diseases
From: plutonium....@gmail.com
Injection-Date: Wed, 24 Jul 2013 05:35:43 +0000
Re: News that cancer thwarts Alzheimers and Alzheimers thwarts cancer and
the reason why: Metal Causation Diseases.
Alright there is some statistical data that implies cancer protects against
Alzheimers disease and vice versa that Alzheimers protects against cancer
formation.
Here are those numbers reported reading from Science News: Source:
Neurology, 10July2013:
204,468 people 60 years or older in northern Italy, during 6 year period,
21,451 got cancer and 2,832 got Alzheimers. A total of 161 got both,
whereas the expected number was 281 for cancer and 246 for Alzheimers. Thus
the risk of cancer was cut to 50% for people with Alzheimers and the risk
of Alzheimers was cut to 35% for people with cancer.
As I stated earlier, my take on this report is that Alzheimers has excess
mercury in the body and mercury inhibits cancer formation. While cancer
acts to chelate excess mercury and thus people with cancer are less prone
of getting Alzheimers.
Newsgroups: sci.physics
Date: Fri, 10 Jun 2016 22:14:42 -0700 (PDT)
Subject: geothermal & Alzheimers / Stefan Boltzmann law: Geothermal, is it
4 to 1 superior to Solar or 5000 to 1
From: Archimedes Plutonium <plutonium....@gmail.com>
Injection-Date: Sat, 11 Jun 2016 05:14:43 +0000
Geothermal & Alzheimers / Stefan Boltzmann law: Geothermal, is it 4 to 1
superior to Solar or 5000 to 1.
Alzheimer
Was looking through the recent New Scientist magazine, June 4-10 in hopes
of some article on geothermal. None to be found and why I deem all science
magazines doing a pitiful job overall.
This magazine did discuss a mechanism of Alzheimers on page 10 discussing
how it was found that some bacteria or virus was captured by beta amyloid
which causes then, inflammation bringing forth tau proteins and full blown
Alzheimers disease.
Now a decade or more back, I proposed the theory of mercury causing
Alzheimers.
It maybe the case that both mercury and pathogens like pneumonia are
trapped in the beta amyloids to ward them off.
I remember reading a decade or more ago where these proteins of beta and
tau had heavy metals as a component of their molecular structure.
Newsgroups: sci.math
Date: Tue, 20 Dec 2016 21:43:21 -0800 (PST)
Subject: Advancements in Alzheimer and Parkinson disease related to Metal
Causation theory
From: Archimedes Plutonium <plutonium....@gmail.com>
Injection-Date: Wed, 21 Dec 2016 05:43:22 +0000
Advancements in Alzheimer and Parkinson disease related to Metal Causation
theory.
Back in 2007, I started a book: Metal Causation diseases of Autism,
Alzheimers, Parkinsons, Schizophrenia, Prion, Homosexuality. Arguing that
mercury causes all these diseases.
That was 2007, and now is 2016 and there have been many advances. Some have
bolstered this Metal Causation theory, some have rather averted the many
theme of these diseases, denying that metals, especially mercury causes the
disease.
Let me list a few of the latest news reports.
In SCIENCE NEWS, 25JUN2016, page 7 talks about how Alzheimer disease is
where proteins surround a invader-- bacteria, virus and cause plaque
buildup and hence the disease. But the invader could just as easily be
mercury metal.
In NEW SCIENTIST 3DEC2016 on page 8 is talk of how Parkinson's disease
starts in the stomach with synuclein buildup that migrates to the brain and
initiates Parkinson. It failed to say what causes the synuclein in the
stomach to fibre up, so here it can be mercury that starts the synuclein
and then moves into the brain.
Trouble with all these reports on Alzheimers, Parkinsons, Autism, is for
researchers time and time again failing to run an exhaustive research on
whether people with these diseases have abnormal mercury levels. Whether
these plaques or entangled proteins are caused by mercury doing the
entangling.
There is one well known research effort that has already linked mercury to
Homosexuality. Frogs and reptiles with mercury nearly all become
homosexual. Research that clearly links mercury to homosexuality.
Trouble with research on mercury, is that nearly every pharma company and
the medical and hospital industry have vested money interests in stopping
all research that has mercury as the culprit. This hatred of mercury
research is far worse than the hatred of finding out that ulcers were
caused by bacteria, but most people wanted to make money off of ulcers, not
find the truth behind ulcers.
I need to update this Medical book of 2007, when I get some free time.
Newsgroups: sci.physics
Date: Mon, 11 Feb 2019 21:52:39 -0800 (PST)
Subject: Bacteria in gut causing Autism// now we have gum disease bacteria
causing Alzheimers
From:Archimedes Plutonium <plutonium....@gmail.com>
Injection-Date: Tue, 12 Feb 2019 05:52:39 +0000
Bacteria in gut causing Autism// now we have gum disease bacteria causing
Alzheimers.
See the recent New Scientist, Feb2-8 special report on a possible link
between gum disease and Alzheimers.
I record this especially because back in the 1990s i proposed a theory that
mercury was the root cause of Alzheimers and Autism, not bacteria. And so,
being a good scientist, i must admit that it is tentatively looking as
though my conjectures were wrong for Autism and Alzheimers, unless of
course elemental mercury is involved in bacteria of the mouth and gut. Even
then— it appears for Alzheimers there is a increase in proteins to tackle
the gingivitis bacteria, not a increase in protein to tackle mercury.
So it looks like my 1990s theory on Alzheimers is looking to be false. But
for Autism my theory is still relevant where gut bacteria could be a
delivery system for mercury to the brain.
And then again we have to rule out whether gum bacteria carry mercury into
the brain for Alzheimers and the mercury somehow allowing those bacteria
immunity and multiply.
Newsgroups: sci.physics
Date: Fri, 5 Apr 2019 12:23:04 -0700 (PDT)
Subject: the old AP hypothesis of mercury caused diseases Re: Bacteria in
gut
causing Autism// now we have gum disease bacteria causing Alzheimers
From: Archimedes Plutonium <plutonium...@gmail.com>
Injection-Date: Fri, 05 Apr 2019 19:23:05 +0000
The old AP hypothesis of mercury caused diseases Re: Bacteria in gut
causing Autism// now we have gum disease bacteria causing Alzheimers. On
Monday, February 11, 2019 at 11:52:43 PM UTC-6, Archimedes Plutonium
wrote: > See the recent New Scientist, Feb2-8 special report on a possible
link between gum disease and Alzheimers. > > I record this especially
because back in the 1990s i proposed a theory that mercury was the root
cause of Alzheimers and Autism, not bacteria. And so , being a good
scientist, i must admit that it is tentatively looking as though my
conjectures were wrong for Autism and Alzheimers, unless of course
elemental mercury is involved in bacteria of the mouth and gut. Even then—
it appears for Alzheimers there is a increase in proteins to tackle the
gingivitis bacteria, not a increase in protein to tackle mercury. > My
old hypothesis is not out of the picture yet, not to be dismissed yet, for
it could be the case that mercury starts the mouth and gut bacteria to
become disease bacteria. > So it looks like my 1990s theory on Alzheimers
is looking to be false. But for Autism my theory is still relevant where
gut bacteria could be a delivery system for mercury to the brain. > No,
I wrote that too hastily. My Mercury Hypothesis is still in the game and
that it maybe the ultimate cause of many of the listed diseases. > And
then again we have to rule out whether gum bacteria carry mercury into the
brain for Alzheimers and the mercury somehow allowing those bacteria
immunity and multiply. > Some things are certain-- just a little mercury
is lethal. Much of modern industrial world air is full of mercury from
fossil fuel burning. So many modern diseases are common only in modern
times. Only a fool would say-- there is no link up.
Newsgroups: sci.physics
Date: Fri, 5 Apr 2019 17:44:49 -0700 (PDT)
Subject: bacteria implicated in Autism and Alzheimers supports the Mercury
Hypothesis Re: Bacteria in gut causing Autism// now we have gum disease
bacteria causing Alzheimers
From: Archimedes Plutonium <plutonium...@gmail.com>
Injection-Date: Sat, 06 Apr 2019 00:44:50 +0000
Bacteria implicated in Autism and Alzheimers supports the Mercury
Hypothesis Re: Bacteria in gut causing Autism// now we have gum disease
bacteria causing Alzheimers.
What I am saying, is the AP's Mercury Hypothesis as a cause of several
major modern day diseases is still active and ongoing as a valid science
hypothesis that needs to be proven true or false. Just because bacteria in
the gut and bacteria in the mouth are implicated in Autism and Alzheimers,
does not absolve the mercury hypothesis of Autism or Alzheimer. To the
contrary, that bacteria associated with Autism and Alzheimers is likely to
support the Mercury Hypothesis. For the entry of mercury into the body, is
not only the air we breathe but the food we consume.
Newsgroups: sci.physics
Date: Fri, 7 Jun 2019 13:50:01 -0700 (PDT)
Subject: news from The Economist on autism--June 1st, 2019, pages 67&68//
DNA
sequenced gut bacteria
From: Archimedes Plutonium <plutonium...@gmail.com>
News from The Economist on autism--June 1st, 2019, pages 67&68// DNA
sequenced gut bacteria.
--- Quoting from The Economist ---
Rosa Krajmalnik-Brown of Arizona State University, .. and James Adams,..
sequenced the DNA of gut bacteria from 20 autistic children to discover
which species were present. They found that the children in their sample
were missing hundreds of the thousand-plus bacterial species that colonize
a "neurotypical" person's intestine. One notable absence was Prevotella.
This bug, which makes its living by fermenting otherwise-indigestible
carbohydrate polymers in dietary fiber,...
--- end quoting ---
Now, my hypothesis started way back in 1996, saying basically that the
modern day environment with so much air pollution containing especially,
mercury, that it would be the main cause of so much diseases, the driving
force behind the disease.
One of those diseases I listed was Autism caused by mercury. Never in my
wildest imagination would I think that by 2019, it looks like the intestine
microbes have a major role in autism.
But my hypothesis that mercury is the main cause of Autism, is not ruled
out by this gut bacteria findings.
In order to rule out that mercury has no role in autism, we must show or
prove that it was **not mercury** that killed or destroyed the gut bacteria
of the autistic child. The Gut seems to be the highway for autism. But when
a young child contracts autism. Could it be that the child ingested or
breathed in mercury, and that mercury found its way to the intestine where
that mercury destroyed the bacteria culture of the gut.
Which sets up an interesting research. For we can take gut microbes and
subject them to mercury and find out if say, Prevotella is acutely affected
by mercury while other bacteria not so.
So the mercury caused Autism is not ruled out as yet, and in fact, maybe
enhanced, for when mercury enters the gut, it destroys microbes since they
are so much more vulnerable, and mercury is a sulfur magnet and wants to
get into the brain for the brain is sulfur rich for mercury. So the pathway
from gut bacteria to brain, is a natural pathway of mercury.
And one item in passing, The Economist shows a picture of a young child
with a telephone in the gut and the cord and mouthpiece in the brain. Which
much reminds me of my picture of a head with a radio replacing the brain in
my theory of How the Brain/Mind Works. So I wonder, just wonder if the
artists at The Economists had seen or read my book before making their
autism drawing.
Brain=Mind=Radio-Receiver=Superdeterminism
by Archimedes Plutonium (Author)
Psychologists no longer need to find out how the brain and mind works, for
this theory explains it.
This is undoubtedly one of my prettiest theories and one of my
prettiest books. The reason I say pretty is
because it comes totally out of the blue and 180 degrees opposite of
where all the scientists figuring out how
the mind works. All the scientists working on "the mind" think that
the mind comes from chemistry sloshing
around in the brain, inside the head. I say 180 degrees opposite, that
the mind comes from "out of the body".
The Brain Locus theory says every thought, and every action comes from
the Nucleus of the Atom Totality
via photons or neutrinos shot into every brain and ordering up that
"thought". In the Brain Locus theory
the mind is like a radio receiver that picks up radio messages. The
chemistry of the brain and head then
respond to the thought of the mind.
All thoughts and thus all actions were ordered up by the Protons and
Neutrons inside the Plutonium Atom Totality
Nucleus which then assembles that "thought" into a photon or neutrino
which is shot into the brain of the
recipient and thus committed to fulfill that "thought".
Newsgroups: sci.physics
Date: Fri, 7 Jun 2019 22:18:52 -0700 (PDT)
Subject: news from The Economist on autism--June 1st, 2019, pages 67&68//
DNA
sequenced gut bacteria
From: Archimedes Plutonium <plutonium...@gmail.com>
News from The Economist on autism--June 1st, 2019, pages 67&68// DNA
sequenced gut bacteria.
Also, recently it was reported a link between the bacteria in the mouth and
Alzheimers. So here again I wonder if the bacteria is a sort of pathway for
mercury to connect or reach up to the brain. So that these diseases— autism
is a gut pathway for mercury to brain. Alzheimers is a dental pathway for
mercury to brain.
News Update:: In December of 2019 and January 2020, I had so much
information and research as to the actual mechanics of some of these
diseases by mercury chemical as to pinpoint the disorder of the electrical
system of the human body that the mercury causes. With that in mind I need
a whole new textbook that incorporates the electrical disorder and
disturbance of the cells of the body, the nervous system and brain in
particular due to the presence of mercury in the body. With that in mind I
keep this old textbook, much as is for a reference and history, and apply
all my new research in these newer books of the series on medicine.
Archimedes Plutonium Apr 16, 2024, 12:46:31 AM to Plutonium Atom Universe
newsgroup.
The Economist's "Can Alzheimer's be transmitted?" New evidence suggests it
can, in very rare circumstances// The folly of Prusiner's prion
conjecture// ADD to my 36th published book
Dr. Prusiner in medical science reminds me a lot about Dr. Wiles in
mathematics. Both seeking fame and fortune in science, but not seeking the
truth of science. Prusiner claims proteins fold similar proteins but had
Prusiner ever studied chemistry or physics to understand a molecule similar
to another molecule cannot change that molecule for it lacks sufficient
energy to do so. What AP says is that it is the element mercury that causes
proteins to fold, and this mercury can lie in molecules of protein and thus
when the mercury laden protein molecule meets another similar protein
molecule, it is actually the mercury that misshapens the protein. But try
telling that to Prusiner who does not care for the truth of science, only
the glory and money. With Wiles and his monsterous so called proof of
Fermat's Last Theorem FLT, why Dr. Wiles is so dumb about FLT that he never
spotted that Euler had a fake proof of FLT for exponent 3, yet Dr. Wiles
being so dumb about math proofs uses Euler's fake proof to further his own
fake FLT. AP wrote several books on a true proof of FLT. So many
scientists, I should say-- so called scientists are in this business not
for truth but for fame and fortune and it is sad because it wastes the time
of journals and magazines covering these stories. In the Economist Feb 3,
2024 is an article describing where young people had HGH, human growth
hormone injections when they were children. Sadly, some of these injections
had CJD disease and also amyloid beta from Alzheimers because the HGH was
collected from the brains of cadavers. As a consequence early death for
many of these children. You see, as the world still continues to believe
the error filled Prusiner idea of prions when in truth it is the mercury
atoms in the CJD and in the beta-amyloid Alzheimers that is the real
culprit of these diseases. But what AP is hopeful for, in this article
mentions two researchers John Collinge of University College London and Dr.
Banerjee also at UCL working from these sets of cadavers, that AP is
hopeful either Collinge or Banerjee or both pith in and see if there is
large amounts of mercury atoms present in the proteins from these sets of
cadavers. I know Dr. Prusiner would not research into whether he had his
science all wrong-- similar proteins altering similar other proteins. But
like what AP says-- some catalyst like mercury atoms in amongst the
proteins that alters the shape of other proteins. For if Prusiner engaged
in real true science, he may have to return his Nobel Prize.
*7) Parkinsons.*
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Sun, 22 Jul 2007 11:03:12 -0700
Subject: Welders get a lot of Parkinsons; manganese. Mercury not the only
cause: Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
Ran across several websites that spoke of welders as a group at large
risk of contracting Parkinson's disease.
It is blamed on the manganese fumes in welding.
This book is about a lot of metals that cause diseases of the brain,
and even some non-metals such as
fluorine. This book is about chemicals that cause these major diseases
of the brain. The major culprit
is mercury and then the second major culprit is mercury compounds.
Then we arrive at other metals
or chemicals that cause these diseases. Cesium by itself, just may
cause Prion disease. Manganese
by itself, or Magnetic Manganese by itself may just cause Parkinsons.
But the central idea behind this book is that some protein of the body
is under attack whenever the body
has too much of a metal present and that the protein goes into
abnormal interaction. In Alzheimers, the
APP scissors is corrupted and cuts stubs for proteins which then
accumulate. In Prion disease, the metal
present that causes CJD bends and misshapen normal prion proteins
into a bent shape that then
accumulates because protease can no longer remove these bent shaped
proteins. In Autism, the metal
or chemical (probably a mercury compound) prevents the formation of
some connective brain sheaths
from developing.
So in all these 5 diseases of the brain that I have written about in
this book may have one or two or several
metals or metal compounds or chemicals that cause the disease. As an
analogy, insecticides of chemicals
are not just one chemical that kills insects, but that you have a
broad choice of chemicals that can form
insecticides and kill insects. Likewise for the brain in humans, in
that mercury is not the only toxic poison
that damages proteins and protein synthesis. If you have too much
cesium or rubidium or fluorine or
manganese or silver in the brain, then expect some proteins to go awry
and cause death.
The world health organizations have made a broad coverup of data and
knowledge of these above 5 diseases.
I have spent a good deal of time in hunting down the surveys of where
Alzheimer, Autism, Parkinson, Prion
and Schizophrenia are most frequent. Some surveys are accurate such as
Nebraska being the world's
highest rate of Parkinsons disease and thus believed to be some farm
chemical.
But surveys on Alzheimer, Autism, Prion have been so much kept under
governmental wraps that I suspect
some overall coverup. That the health bureaus of governments do not
want people to know the details. Details
of communities living close and downwind of a coal fired electric
plant or a oil refinery. Governments like
the USA keeping a tight lid wrap over mercury in thimerosal vaccines,
and for which the USA is being now
lawsuited. People should be able to easily find where the vast
majority of cases of Alzheimer, Autism, Parkinson
Prion and Schizophrenia are reported, just as easy as to find out each
case of H5N1 birdflu that is
reported. We easily can find out every birdflu case. But when it comes
to finding out the cases of Autism
or Alzheimer, downwind of airpolluters, then we run into what I
suspect is a coverup of science data.
And as I wanted data and surveys of fluoridation uses in the world we
come upon another suppression of
data and survey information. I say much of this because it should be
very, very easy for me to search for
a world map of the frequency of cases of Autism in the world and for a
map showing the frequency of
cases of Alzheimers and of Prion and Parkinson and Schizophrenia. For
we have lived with these diseases
for almost 1/2 a century now and yet no such maps exist, or I have not
found any. So this suggests to
me that there is some government suppression of this information,
especially on Autism and Alzheimers.
Suppression because governments fear having to be held accountable to
mercury in vaccines and governments
fear having to intervene in coal fired electric plants, forcing them
to become cleaner.
If such maps were available and as informative as are maps of birdflu,
H5N1, then it is my guess that such
maps would show that Autism and Alzheimers are connected with the
amount of mercury in the air we
breathe.
If maps and surveys were available for lung cancer, they would show a
connection to big cities and the
amount of asbestos still in the air due to brakes made of asbestos.
If such maps were available, it is my guess that states like Utah
would show some of the highest number
of cases of Autism, Alzheimers, Prion and Parkinson because of the
amount of mercury in the air of Utah.
Because of mercury mining in Nevada which is downwind of Utah, and
coupled with the fact of a lot of coal
fired plants in Utah that the air of Utah is especially a health
hazard, and which suppression of this knowledge
would be wanted by the government of the USA and even the government
of the state of Utah. Nebraska is
known as the highest Parkinson disease rate. So if not Utah as the
most mercury filled air state, then what
state is the most mercury filled air state? If not Utah, is it Texas?
So until the government of the USA and its 50 State governments comes
clean on the surveys and data
and information, instead of roadblocking and stifling and suppressing
the data, can we really come to tackling
these 5 diseases.
It is supremely and obnoxiously funny that the USA health departments
have for decades run alerts and
alarms to pregnant women about eating tuna fish and other fish because
of too much mercury, and then,
ironically, in 2007, that same USA department of health arguing that
Thimerosal mercury in vaccines
for babies and infants was safe. How any government scientist of the
USA could take a stance where they
have been ringing the alarm for 30 years that tuna fish is bad for
pregnant women and yet are more than
happy to inject mercury into a infant for a vaccine.
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Mon, 23 Jul 2007 01:24:32 -0700
Subject: Mercury as a Conformational Changer of proteins as in Prion
disease: Metal Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
So in my researches I have reached a point where I am looking for a
mercury molecule that would change
a normal prion protein into the diseased prion protein.
I am not sure of chemists call such molecules or ions as "denaturation
agents". The term for an agent that
causes a conformation change of the geometry of a protein molecule. In
other words, in prion disease, it is not
a protein molecule that changes the shape of other protein molecules,
but rather, it is a chemical agent such
as mercury or a mercury compound of perhaps CsHg or HgF or MnHg or
many other mercury compounds. Perhaps
the disease agent in prion disease is hydrofluoric acid.
Anyway, what I am looking for is a chemical agent that changes the
shape of prion proteins. For approximately
ten years now I have argued that the Prusiner model is a fake, because
it is not caused by proteins but rather
caused by a toxic chemical poison. Because of the large number of deer
and elk animals around
Colorado USA have high levels of cesium and mercury in their bodies, I
suspect the culprit that alters the
prion proteins is CsHg. England also has a large amount of cesium and
mercury in the environment.
So why would eating the brains of infected animals spread the disease?
Not because of eating the altered
prion proteins but because the chemical that caused the alterations is
still present in those brains. Perhaps
all it takes is three molecules of CsHg ingested that will start the
onset of the prion disease.
And the reason for the plethora of strains is that RbHg would also
cause the disease as well as many other
alkali metal ions with mercury.
Which brings us the interesting question of whether Alzheimers is a
conformational change of the APP scissors
that starts the onslaught of Alzheimer's disease. So is the corruption
of the APP scissors due to a mercury
ion which interacts with a normal APP scissors and leaves it abnormal
so that it creates the beta
amyloid.
Parkinson's disease is a corruption of alpha synuclein protein. Is
this disease another example of a conformational
change caused by some toxic chemical such as perhaps magnetic-
manganese?
Autism is the missing development of sheaths in several parts of the
brain. Missing tissue giving rise to
autism. Is that another conformation change in the proteins of the
brain? I doubt it because there is no
accumulation of a protein that cannot be removed as in the cases of
Prion and Alzheimers. In Autism, the
picture seems to be that of a missing tissue. So how would mercury
stop the development of tissue? To
answer that question, I would need to find out if mercury ever causes
the interruption or omission of the
protein development. And in this sense, Autism is much more alike that
of Parkinson's where connections
of the brain are destroyed. So in that sense, Autism is Parkinsons of
the young and Parkinson's is Autism
of the old age people, where toxic chemicals destroy a tissue of the
brain. In Alzheimers and Prion, the
chemical poison alters proteins that collect as garbage and unable to
be removed in time to cause death.
Now what would be very interesting to observe, since I suspect mercury
is one of those chemical poisons,
is whether a Autistic child grows up and later catches Alzheimers, and
where the same mercury poison caused
the Autism and caused the Alzheimers.
Or to see a case in which the same mercury poison causes both
Alzheimer's and CJD all in one brain. Such
a case would not prove the Metal Causation theory but it would cast
grave doubt of the correctness of the Prusiner
Model.
Now there is another disease in this book which I know less of than
these other four. I am talking of
Schizophrenia which seems to involve a protein gone awry. I think
mercury and silver are involved with
Schizophrenia and since our modern times have replaced silverware with
mostly stainless steel, I would
hazard to guess that Schizophrenia rates have gone steadily down since
about 1950 onwards. But then
the frequency of contact with mercury has steadily gone up since 1950
so that Schizophrenia may not be
on the decline but on the rise. And which is Schizophrenia more like?
Is it more like Alzheimers and Prion
with accumulation of garbage proteins not removable or is it like
Autism and Parkinsons where the brain
has missing tissue? I suspect Schizophrenia is more like Autism and
Parkinsons and thus has missing
tissue as the disease progresses.
*8) Schizophrenia*
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Mon, 23 Jul 2007 09:40:58 -0700
Subject: Schizophrenia disease table: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
a_plutonium wrote:
> And which is Schizophrenia more like?
> Is it more like Alzheimers and Prion
> with accumulation of garbage proteins not removable or is it like
> Autism and Parkinsons where the brain
> has missing tissue? I suspect Schizophrenia is more like Autism and
> Parkinsons and thus has missing
> tissue as the disease progresses.
Back in April of 2007 I began a table on each one of these five
diseases, and I should have
reread that table because zinc, not silver is implicated as the metal
that drives this disease.
It is found that zinc replaces dopamine.
> (1) Proteins gone awry involved --
> dopamine
Technically, dopamine is not a protein.
But like Parkinson's disease, dopamine is affected.
> --------------------------------------------------------------------
> (2) Function of proteins gone awry --
> neurotransmitter, sort of like the wires in electricity as an analogy
> --------------------------------------------------------------------
> (3) Metals found in those proteins gone awry --
> Not in those proteins, but it was found that zinc ions behave similar
> to the neurotransmitter of dopamine
> --------------------------------------------------------------------
> (4) Site or Location of brain where this disease unfolds --
> striatum, frontal lobes, hippocampus, and temporal lobes
> --------------------------------------------------------------------
> (5) Pathology of disease --
> affects the amount of dopamine and a blocking of dopamine pathways
> ---------------------------------------------------------------------
> (6) When was the first reliably known case --
> 1893 by Kraepelin
> ---------------------------------------------------------------------
> (7) Statistical incidences of Schizophrenia in the general population --
> 7.5 and 16.3 cases per year per 100,000 population
> ---------------------------------------------------------------------
> (8) Age of its victims --
> Usually starts in the teenager years for males and in the 20s for
> females
> ---------------------------------------------------------------------
> (9) Geography of disease prevalence --
> worldwide, but I suspect a concentration by geography where there is
> a lot
> of mercury in the environment
> ----------------------------------------------------------------------
> (10) Any mass spectroscopy of brain tissue of disease or of the hair
> of diseased victims and what metals were found --
> -----------------------------------------------------------------------
> (11) Any chemicals that may relieve the disease pathology --
> phenothiazines
> -----------------------------------------------------------------------
> (12) Toxic metals that are hypothesized by AP as the root cause:
> Organic mercury in conjunction with possibly zinc.
Also, I suspect fluoride in conjunction with mercury has something to
do
with Schizophrenia in that in modern times our environment is daily
overflooded
with the intake of unnecessary fluoride in our drinking water.
Fluoride in the
form of HgF ions may play a key role in whether Schizophrenia starts.
> -----------------------------------------------------------------------
So from reading the above, it sounds as though blockage of the
dopamine passages is
an accumulation of some unwanted material which sounds like the
mechanism of disease
progression in Alzheimer and Prion where accumulated waste occurs. Is
it zinc that causes the
blockage of dopamine? Is Schizophrenia the accumulation of zinc and
perhaps copper
or some other metal compound which builds up, similar to the buildup
of beta amyloid
plaques in Alzheimer disease? I somehow envision a picture similar to
the clotting of
arteries to the heart as Schizophrenia a clotting of the dopamine
passages.
I should make some new categories for the above table.
(13) Is the disease one of missing tissue or is the disease that of
the accumulated garbage waste
of a protein or other material?
For Alzheimer and Prion and Schizophrenia, it is accumulation of
garbage in the brain. For Autism, Parkinson
it appears as though there is missing tissue.
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Mon, 06 Aug 2007 10:26:47 -0700
Subject: Geography correlations as to incidence and prevalence of Alzheimer
& Autism where Norway is lowest, Utah & England highest: Metal Causation
coupled with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia)
In this theory of metal as the primary cause of these five diseases
would entail geography. That these
five diseases would be significantly higher in incidence and in
prevalence where on the globe the metal
contact with humans is the highest or lowest. It is like asbestos
disease where if you are in an environment
of frequent contact with asbestos, the incidence and prevalence
matches the contact.
Mercury is very much worldwide but some places have much more than the
usual amount. Utah in the USA
and much of the UK has more than normal amounts of mercury in the air
we breathe due to coal fired
electricity stations.
The mercury in thimerosal vaccine preservative was administered to
infants around the world.
The mercury in fish that humans eat is widespread.
The mercury in instruments such as thermometers was around the world.
However Fluoridation of water was not prevalent around the world.
There were many countries that never
added fluoride to its water supply. And some places have natural
occurring fluoridation.
Utah and UK rank as some of the highest incidents and prevalence of
both Alzheimer and Autism. (Also
they rank high in Prion diseases.) Both Utah and UK have more than
normal amounts of mercury in the
environment and more than normal amounts of fluoride.
Scandinavian countries such as Norway, Denmark, Sweden, Finland have
some of the lowest
incidents and prevalence of Alzheimers and Autism. These countries do
not have fluoridation of
water supply and these countries have relatively less mercury in the
air they breathe due to coal
fired electricity stations.
There is the correlation of geography and incidence and prevalence of
these diseases, but a lot of
health organizations due to lawsuits are masking the statistics.
A lot of health organizations and entire government bureaucracies are
doing "cover up" as to mercury
such as in vaccines and they are doing "cover up" as to fluoride in
drinking water.
The rise of Autism and Alzheimers matches the rise of mercury and
fluoride in the daily contact in
people's lives. There is now such silly and stupid things like
fluoride floss and fluoride toothpaste
in addition to the water being fluoridated. So the amount of fluoride
that people ingest every day is
wickedly enormous. No wonder that 90% of the people in the USA who
reach the age of 80 have
Alzheimers. No human brain can withstand that much fluoride without
burning out the brain itself.
It takes how much Hydrofluoric Acid to kill a human? Very little is
the answer. Does any chemist
or biologist know of how all that fluoride that is ingested every day
can avoid becoming some minute-
amounts of Hydrofluoric Acid? And how much hydrofluoric acid would it
take to say cause Autism
in a infant or cause Alzheimers?
So the widespread presence of both mercury and fluoride in the modern
day environment, is it any
wonder that in Utah 1 in 160 children contract Autism whereas in
Norway 1 in 750 (as far as I know).
Evidently Utah has that much more mercury and fluoride present.
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: a_plutonium <a_pluton...@hotmail.com>
Date: Tue, 16 Oct 2007 20:19:33 -0700
Subject: NOVA program on Epigenomics: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
Really excellent program on TV tonight about Epigenome which regulates
the genome of a human.
So the Epigenome is just as important and perhaps even more important
about a human life
than is the genome.
What the Epigenome is mostly like switches that turn on or turn off
our genome and it was
amazing that what my parents did in life or grandparents did could
affect me. As a study
on Sweden region showed how famine in past history affected the recent
generation. Or
the study in Washington State where pesticide caused a disease in rats
which was
transmitted to the offspring who never had contact with the pesticide.
What I was listening to carefully was the story on Autism shown by a
twin of identical
twins who kept rubbing a computer screen monitor for hours on end
(this connects with
my Brain Locus theory as interpretation in that the mind is reverted
to a past-life). In the
Brain Locus theory, if our minds are injured in this life, we easily
revert to instincts of a
previous incarnated life.
Anyway getting back to the Autism as reported in this NOVA tv show as
reported
by Feinberg & Kaufmann. What they noticed is that the Hippocampus was
far smaller
in the autistic case and where they methyl markers of epigenomics.
My theory is that mercury is the likely cause and this report really
does not threaten my
theory, and in fact probably supports the metal causation theory in
that mercury would act
like a epigenomic-determinant.
But it appears that the biggest issue would be that the Hippocampus of
autism is very much
smaller in size. So can mercury poisoning cause a smaller Hippocampus?
Could mercury or a combination of metal elements or compounds cause
the Hippocampus
to diminish in size, to thwart to growth of the Hippocampus?
Newsgroups: sci.chem, sci.med, sci.bio.technology
From: Archimedes Plutonium <a_pluton...@hotmail.com>
Date: Wed, 17 Oct 2007 01:03:17 -0500
Subject: can mercury exposure shrink the Hippocampus research: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
Archimedes Plutonium wrote:
> Really excellent program on TV tonight about Epigenome which regulates
> the genome of a human.
> So the Epigenome is just as important and perhaps even more important
> about a human life
> than is the genome.
I did some searching around on the Internet to see if any evidence
in research whether the exposure to mercury can shrink the Hippocampus.
I found a website that said in Alzheimers disease the brain shrinks by
as much as 25%. But I reckon this shrinkage is not directly from the
exposure to mercury but the slow pathology set in motion by the mercury.
So I wonder if anyone has done a in depth research as to the possible
link between the shrinkage in Alzheimers versus the shrinkage in just
the Hippocampus in Autism. So that if there is a common cause of both
Alzheimers and Autism due to mercury, then the shrinkage should fit into
some linked pattern. So that Alzheimers is the entire brain whereas
Autism is a localized in the Hippocampus region.
One website said that some of those 1990's vaccines for children
contained as much as 250 micrograms of mercury, which is far far
too much for a infant brain trying to grow. And it said that the
Hippocampus is the first region of the brain as mercury would enter
the brain so it is the first region to be damaged. And that the
mercury source for older people who contract Alzheimers is likely to
be teeth amalgam fillings which can emit as much as 10 micrograms of
mercury per day. So if a infant gets 250 micrograms in one fell swoop
leading to Autism whereas an adult gets 10 micrograms each and every
day with tooth fillings should be able to make some mathematical sketch
correlations. So if a person gets say four tooth fillings at age 20
and develops Alzheimers at age 70 is 50 years. And at 40 micrograms per
day is 730,000 micrograms of mercury leading up to Alzheimers.
So would the math be in some agreement between these two diseases of
Alzheimers and Autism? That if you are an infant receiving 250
micrograms of mercury, would your Hippocampus be damaged and if you are
a 20 year old with four amalgam teeth receiving 730,000 by age 70 damage
the entire brain?
Now I am aware that the body has some proteins that clean out the brain
of mercury called APO. So we have to consider whether this APO can clean
out 40 micrograms per day from teeth fillings?
Now I was looking for a website that collected the statistics of
Alzheimers victims and whether they had teeth fillings. I found none.
Also, it must be noted that another huge source of mercury is coal fired
electric power plants and the states in the USA where Autism is the
largest are places like Utah and Texas where these coal fired power
plants are abundant.
So it seems to me, that a research should be conducted that correlates
the shrinkage process in Autism versus Alzheimers due to mercury.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: plutonium.archime...@gmail.com
Date: Sat, 28 Jun 2008 01:05:49 -0700 (PDT)
Subject: instructive to group these 5 diseases as to age of attack and as
to metal in rogue protein: Metal Causation coupled with Weak-Protein-Point
Theory of Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
I notice there is a nice grouping of these 5 diseases as per age of
attack:
Autism in infants before age 10
Schizophrenia in boys as teenagers and girls in 20s
Alzheimers Parkinsons Prion in old age
So we have almost every age group represented except for maybe 30s to
50s.
So does the age grouping match the idea of mercury poisoning? I would
say so, because
mercury can be an accumulative affect and so most are old age
diseases. And as for
Autism, a large dosage of mercury can damage brain sheaths from
developing.
Now I spent a long time considering different compounds of mercury to
explain the different
5 diseases, so that say prion was mercury cesium whereas Alzheimers
was mercury fluoride.
That may have been the wrong approach. Perhaps a better approach would
have been to
focus on the metal ions in the proteins under attack in the disease,
or to focus on what
metals the proteins bind. In Alzheimers, instead of wondering what the
mercury compound
is such as mercury rubidium, instead, focus on what metal ions
constitute the APP scissors
and the protein that is cut. If zinc ions are involved in Parkinsons
alpha synuclein and zinc and
copper in amyloids of Alzheimers and copper and manganese for Prion
proteins. Then I should
not worry so much as what form of mercury is involved, for the concern
is that mercury acts
differently on zinc ions than on copper ions.
So if the reaction of mercury to copper ions is different than the
reaction of mercury on zinc ions
then we can explain why prion disease is different than Alzheimers
disease, for the one is mercury
attacking the zinc ions in Alzheimers and mercury attacking the copper
ions in Prion. Whereas before
I was focused on mercury-cesium versus mercury-fluoride as the
difference between prion and
Alzheimers. In the end, it may well be both the type of mercury and
the type of metal ion in the
protein.
One other note is that there has never been a case where a person
contracted any two or three
of the three old age diseases of Parkinsons, Prion and Alzheimers. I
know of no case where a person had say Parkinsons and then
also had Alzheimers. Now this may or may not support this theory of
mercury as the cause, because
one would think that if mercury is the poison cause that in some
people the mercury would set up two
or more of these diseases simultaneously. And perhaps even see cases
of Autistic children starting to
have Alzheimers or Parkinsons. Now maybe there are such cases but have
not been reported. And
maybe there are many such cases but one of the diseases takes over and
masks the presence of
the other disease and noone bothered to autopsy for 2 or more diseases
simultaneously.
Now in the case of Schizophrenia we have dopamine blockage and perhaps
zinc ions as substitute
for dopamine. So Schizophrenia is much similar to Parkinsons in that
dopamine is reduced. And where
Prion and Alzheimers are very much alike in the fact that a protein
garbage dump is set up in the
brain which kills. So in Autism, Schizophrenia and Parkinsons we have
things "missing in the brain"
whereas in Prion and Alzheimers we have garbage accumulation
strangulation.
So the mercury maybe all the same in all these 5 diseases where it
could be ethyl mercury. But
I rather suspect it is mercury compounds that facilitates the onslaught
of these 5 different diseases.
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: plutonium.archime...@gmail.com
Date: Thu, 12 Feb 2009 23:43:57 -0800 (PST)
Subject: more information on Parkinson's: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
On TV a few days back was a program of a news reporter who contracted
Parkinson's and he
provided much good information. Information that I did not cover when I
wrote
this edition of the
book. For those reading this for the first time, my theory posits that
mercury and
several mercury compounds cause a wide spectrum of diseases and
Parkinson's
happens to be one of them. That these five listed diseases in the
title can be
consequences of too much mercury in the body which attacks some brain
and
neurological centers. Now my theory is not that only mercury can cause
these
diseases but that other chemicals can also act like mercury and cause
them.
In the TV show it spoke of a researcher named Langston who pointed out
that
a heroin brain elicited the same condition as Parkinson's with the
chemical
MPTP as a toxin that creates a "state of Parkinson's". Also it was
pointed out
that paraquat a herbicide is implicated as causing Parkinson's. But I
wonder
if the herbicide is bathed in some mercury type solution to act as a
fungicide
also. I think some agro products such as seeds are bathed in a mercury
solution
for fungicidal action.
And I do know that the farm regions of the USA such as Iowa have the
highest
rates of Parkinson's. And that there also was a study on well-water in
agro states
thinking that mercury is commonly found in well-water.
The TV program did cite that the first historical record of
Parkinson's starts 1817.
But mercury and its compounds goes back to ancient times. Whether it
was
called tremors and dementia in ancient times or whether Parkinson's
disease was
present only since 1817 is hard to know.
AP
sci.med,sci.chem,sci.bio.misc
from: plutonium....@gmail.com
subject: more information on Autism: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
2009, Sep 25, 1:34 pm
A few nights ago PBS had more information on Autism from a NOVA show
on twins. Talking about
methyl tags in the epigenome.
I need to keep the tables started below in 2007 up to date.
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/286caf9a10038208%3Fhl%3Den&msg=165592ba8102d65f>
@gmail.com
Date: Thu, 12 Feb 2009 23:43:57 -0800 (PST)
Subject: more information on Parkinson's: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/286caf9a10038208%3Fhl%3Den&msg=165592ba8102d65f>
@hotmail.com>
Date: 22 Apr 2007 20:35:00 -0700
Subject: Table for AUTISM: Metal Causation coupled
with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia)
AUTISM DISEASE
----------
(1) Proteins gone awry involved --
Missing nerves and nerve sheaths.
----------
(2) Function of proteins gone awry --
Allows electrical communication which allows for normal socialization
of a human being.
----------
(3) Metals found in those proteins gone awry --
----------
(4) Site or Location of brain where this disease unfolds --
Lack of neurons and neuron sheaths in amygdala.
----------
(5) Pathology of disease --
Mercury poisoning prevents nerves and nerve sheaths from forming. So
in Autism, there
are nerves and nerve sheaths missing.
----------
(6) When was the first reliably known case --
----------
(7) Statistical incidences of Autism in the general USA population --
About 40 cases per 6,000 population.
----------
(8) Age of its victims --
>From birth to around 7 years old, depending on the dose
of mercury contact.
----------
(9) Geography of disease prevalence --
A study done in Texas gives this information.
Quoting from this website:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&...
AbstractPlus&list_uids=16338635
"There was a significant increase in the rates of special education
students and
autism rates associated with increases in environmentally released
mercury. On
average, for each 1,000 lb of environmentally released mercury, there
was a 43%
increase in the rate of special education services and a 61% increase
in the rate
of autism."
----------
(10) Any mass spectroscopy of brain tissue of disease and what metals
were found --
----------
(11) Any chemicals that may relieve the disease pathology --
----------
(12) Toxic metals that are hypothesized by AP as the root cause:
I believe it is mercury, some organic mercury compound. I
believe mercury for old people is the reverse of mercury for babies in
that mercury in babies leads to Autism and mercury in old people
leads to Alzheimers.
AP
sci.med,sci.environment,sci.bio.misc
from: plutonium....@gmail.com
subject: mercury spills from fluorescent lamps related
to autism Metal Causation diseases
2009, Sep 25, 2:18 pm
Based on the recent NOVA program on "twins"
it was revealed that the Epigenetic influence on
human growth is very much significant. The show
spotlighted a set of twins which one had autism
and the other did not. In our modern society where
mercury metal is so often used and prevalent such
as for example in light bulbs of fluorescent lamps,
which are easily broken in hospitals or homes, that
there is a concentration buildup of mercury, so that
contact with mercury in our everyday life is commonplace.
I have asked the USA government, the EPA, to
ban mercury light bulb lamps before it becomes
a huge cleanup problem of every home in the USA
just as asbestos cleanup was a problem of past
decades.
AUTISM DISEASE
----------
(1) Proteins gone awry involved --
Missing nerves and nerve sheaths.
----------
(2) Function of proteins gone awry --
Allows electrical communication which allows for normal socialization
of a human being.
----------
(3) Metals found in those proteins gone awry --
----------
(4) Site or Location of brain where this disease unfolds --
Lack of neurons and neuron sheaths in amygdala.
More than likely the hippocampus since the
hippocampus is smaller in those who have
autism.
----------
(5) Pathology of disease --
Mercury poisoning prevents nerves and nerve sheaths from forming. So
in Autism, there
are nerves and nerve sheaths missing.
----------
(6) When was the first reliably known case --
----------
(7) Statistical incidences of Autism in the general USA population
--
About 40 cases per 6,000 population.
----------
(8) Age of its victims --
>From birth to around 7 years old, depending on the dose of mercury
contact.
----------
(9) Geography of disease prevalence --
A study done in Texas gives this information.
Quoting from this website:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&...
AbstractPlus&list_uids=16338635
"There was a significant increase in the rates of special education
students and
autism rates associated with increases in environmentally released
mercury. On
average, for each 1,000 lb of environmentally released mercury,
there
was a 43%
increase in the rate of special education services and a 61%
increase
in the rate
of autism."
----------
(10) Any mass spectroscopy of brain tissue of disease and what metals
were found --
In the NOVA show on "Twins" recently was information on methyl tags
that affect the reading
of the genetic DNA by the epigenome. So that
methyl markers can disturb or ruin the reading
of DNA
----------
(11) Any chemicals that may relieve the disease pathology --
----------
(12) Toxic metals that are hypothesized by AP as the root cause:
I believe it is mercury, some organic mercury compound. I
believe mercury for old people is the reverse of mercury for babies
in
that mercury in babies leads to Autism and mercury in old people
leads to Alzheimers.
As modern society uses more and more mercury,
especially with the use of mercury in "light bulbs"
of fluorescent lamps and how easy they are to break and release the
mercury so that in hospitals
and homes where spills occur that just one encounter by young persons
and babies would
cause autism.
----------
AP
sci.med,sci.environment,sci.bio.misc
plutonium....@gmail.com
How much mercury from broken Fluorescent
lamps in our hospitals, schools and homes?
Sep 26, 2:48 pm
Have you ever read the government instructions on
how to clean up a broken lamp that contained mercury? Well, you would
think it was a surrealistic
haz-mat project akin to say having nuclear waste
material in your home, office, hospital or school.
It is said that when mercury spills onto the floor,
it remains there as long as the floor is there. In
other words, almost impossible to remove.
And the government environment protection of EPA
has never really been very good at protecting homes and buildings in
the past centuries for witness the allowance of asbestos into homes
during the 20th century.
Apparently, "making money" is more important than
the judgement of having safe and healthy homes
and buildings.
Mercury is one of the most toxic chemicals to humans, yet the EPA
allows the sales of lamps
that contain dangerous mercury. And every time
a lamp is broken in a home, that mercury is an
invisible health risk.
I would hazard to guess, that if a mercury measuring devise were
readily available and easy to
use and that schools, hospitals, homes, stores were measured for
mercury, that we would all be
surprized of how much mercury they contain.
No wonder the Autism rate climbs higher and higher
each decade.
No wonder the Alzheimers rate climbs higher and
higher.
We used to have mercury-silver tooth fillings, but
have veered away by replacing them with composites that are just as
good.
But why is the EPA asleep at the switch when it comes to filling up
homes with lamps that are easily broken and easily leaking of mercury?
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 22 Apr 2007 11:41:28 -0700
Subject: Table for Alzheimers: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
a_plutonium wrote:
> "Metal Causation coupled with Weak-Protein-Point Theory of
> Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)",
> Archimedes Plutonium, Internet book published 1996-2007 (assimilated
> in April 2007 in sci.med,sci.chem,sci.bio.misc)
> Chapters of this new book:
> (1) Preface & Introduction
> (2) Analogy disease of Asbestosis
> (3) Alzheimers
> (4) Autism
> (5) Parkinsons
> (6) Prion
> (7) Schizophrenia
> (8) how to medically prove the assertions of this book-- mass
> spectroscopy of brain tissue
Now I would like to get these diseases into a table-like format where
it
is easy to edit, and it focuses on what is important and the table-
format
is predictive of other diseases in that if we have similarities in one
disease
to the table of another disease implies these two diseases have common
causality. I believe when these tables are completed that the five
diseases
listed have more in common than disparate.
Perhaps if I put lines through each concept will enhance the tabular
format.
> ALZHEIMER DISEASE
----------
> Proteins gone awry involved -- beta amyloid
tau protein
----------
> Function of proteins gone awry --
----------
> Metals found in those proteins gone awry --
----------
> Site or Location of brain where this disease unfolds --
Temporoparietal Cortex
----------
> Pathology of disease --
buildup accumulation of those two proteins listed and no way of
getting rid of them; a garbage
dump effect
----------
When was the first reliably known case -- 1901
----------
> Age of its victims --
most commonly starts in 70s and estimated that 80% of those over 85
contract the
disease
----------
> Geography of disease prevalence --
industrialized and affluent countries, keeping age constant, have
higher incidence
----------
> Any mass spectroscopy of brain tissue of disease and what metals were
> found --
----------
> Any chemicals that may relieve the disease pathology --
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 22 Apr 2007 19:53:25 -0700
Subject: Table for Alzheimers: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
> ALZHEIMER DISEASE
----------
> Proteins gone awry involved --
beta amyloid and
tau protein
----------
> Function of proteins gone awry --
----------
> Metals found in those proteins gone awry --
----------
> Site or Location of brain where this disease unfolds --
Temporoparietal Cortex
----------
> Pathology of disease --
Buildup accumulation of those two proteins listed and no way of
getting rid of them; a garbage dump effect.
This is what I wrote in January of 2004
---
Newsgroups: sci.med, sci.chem, sci.bio.technology
From: a_pluton...@hotmail.com (Archimedes Plutonium)
Date: 26 Jan 2004 22:56:23 -0800
Subject: how the APP Scissors becomes rogue and whether magnetic-
manganese or fluorine is to blame??
I am still pondering how the APP scissors in Alzheimers makes two cuts
of above and a tinier fragment below in which this tiny fragment is
beta amyloid and wanders off to congregate into plaque. I am wondering
if the MagneticManganese is the cause of this normal Scissors turning
into a rogue scissors and thus the fundamental cause of Alzheimers
disease? So does the MagneticManganese get into the Chromosome #21
where Downs Syndrome starts and where fast-acting hereditary
Alzheimers starts? Does the MagneticManganese enter into the
Chromosome 21 and thus cause the creation of faulty rogue scissors? Or
does the MagneticManganese alter the scissors after Chromosome #21 has
created partially rogue scissors.
---
----------
When was the first reliably known case -- 1901
----------
> Age of its victims --
most commonly starts in 70s and estimated that 80% of those over 85
contract the disease
----------
> Geography of disease prevalence --
quoting from this website:
http://www.cdc.gov/mmwr/preview/mmwrhtml/00001820.htm
"In 1987, age-adjusted death rates were highest in the Rocky Mountain
states and in New England
(Table 2). Montana and Utah had the highest rates in 1987 and the
greatest differences in rates
between 1979 and 1987. New York and Alaska had the lowest rates in
1987 and the smallest
differences in rates between 1979 and 1987."
The state of Utah, sorry to say, has one of the highest exposure to
mercury from the mining and
wind blown over Nevada mercury mining. Sorry to say that Utah fares
badly in concentration of these
five diseases and the thesis of this book is that mercury is the main
causation.
----------
> Any mass spectroscopy of brain tissue of disease and what metals were
> found --
----------
> Any chemicals that may relieve the disease pathology --
----------
Toxic metals that are hypothesized by AP as the root cause:
I believe it is mercury in combination with perhaps other toxic
metals. I
believe mercury for old people is the reverse of mercury for babies in
that mercury in babies leads to Autism and mercury in old people
leads to Alzheimers.
----------
Newsgroups: sci.med, sci.bio.misc, sci.chem
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?_done=/group/sci.bio.misc/browse_thread/thread/d4ab231bdaf64975&msg=21fb1cf3ef5be3fc>
@gmail.com>
Date: Sun, 17 Apr 2011 01:40:33 -0700 (PDT)
Subject: McNeil & Lehrer Newshour: Table for AUTISM; book: Metal Causation
coupled with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia)
On the PBS Newshour last week was reported that
McNeil of McNeil-Lehrer Newshour had filmed a documentary of his
grandson's case of autism, which
airs this coming week.
Lehrer asked some important questions to McNeil, one being whether a
cause is known? And McNeil gave a satisfactory response, which I had
not expected he would. He responded by saying the scientists believe
it is a mix of environmental toxins and of genetics, words to that
effect.
I should resume this book of mine and get it up to date.
If I were asking McNeil some questions, I would first ask what state
their grandson lived in and whether they were close or nearby to a
coal electric plant with its mercury in the air pollution. States like
Texas and Utah and Wyoming and Colorado which have a lot of
coal electric power plants have a lot of mercury emitted into the air.
Secondly, I would ask if a lot of babies borne at particular hospitals
get a inordinate number of cases
of autism over other hospitals? The widespread use of mercury in
fluorescent lamp lighting is a hazard in the making, where breakage of
these lamps is commonplace and the mercury that leaks out is almost
permanently in those hospital rooms.
I would also check school buildings that use a lot of fluorescent lamps
and check for mercury presence.
Also, a lot of switches in houses have mercury in them and nowadays, it
is sad that the EPA has not banned mercury in lamps and that we have
widespread mercury lamps in many houses across the world. Whenever
those lamps get broken, the mercury just sits there as a poison,
invisible and almost impossible to remove.
A disease that is easily linked to a environmental poison is asbestos
of a special kind of lung cancer.
Before asbestos was rare to be in contact with large numbers of
people, by the 20th century, asbestos was commonplace in many if not
most houses in the USA, where various products containing asbestos
were installed into the house of many people. Until people wised up
and realized that asbestos is too dangerous to have so widespread and
common.
But people have not become wise about mercury as of yet. The five
diseases listed in this book and the ever increasing cases of these
five diseases, as McNeil, wisely reported that about 1 in 110 infants
are now diagnosed with autism.
I do know the first case of Alzheimers was reported in Germany by
Doctor Alzheimer, and it was believed that Alzheimers goes back in
history to Ancient Rome, but it is not true that Alzheimers was
prevalent, and only prevalent until recent times. Same thing for
Autism, in that it is mostly a recent phenomenon. Sure, there was
mercury in Ancient Rome, but on the scale of where humans, daily, come
in contact with mercury in the air they breathe, in the home
environment and in the daily visits to other buildings.
And the form of mercury when it seeps out of a fluorescent lamp or
floats in the air from being in a electric power furnace, the form of
that mercury is probably far more dangerous than the form found in
cinnabar in Nature.
The talk of genetics as forming 1/2 the cause is overblown and
illogical. We can say that if a person drinks a poison and dies from
it that his genetics could not handle it, but that is not the truth,
for the truth is that if you come in contact with a poison, it is the
poison itself that does the damage. Some people can process a small
amount of mercury out of their bodies, but we should not thence call
it a genetic disease of autism when a few people can process it out,
whilst the majority of infants succumbs to autism by the mercury
exposure.
Mercury is a very toxic, lethal chemical, and we should not be
surprized at all that a tiny amount of mercury exposure can damage an
infant with autism.
When one maps the prevalence of autism and the other diseases listed,
one quickly sees a correlation between the presence of mercury in the
environment.
China is supposedly firing a new coal electric plant every week. But
does China report the alarming increases in autism in China?
I used to think the large number of cases of prion disease in England
was due to the cool damp climate
and the abundant fungi in the country, and that desert climate has
rarely prion disease. But now that I look at the situation, England
was a heavily industrial nation burning a lot of coal and emitting a lot
of mercury.
When we compare industrial nations of their coal burning and mercury
in the environment with countries of little mercury presence we find
the statistics that the five diseases correlate.
And I should mention the mercury laced vaccinations given to infants
and toddlers in the past century.
So it is good that McNeil throws light on autism. And hopefully what
comes out of that reporting is more
people wanted the facts and data of mercury in the
environment.
Not until people recognized that asbestos is a horrible cancer causing
material, do we save our health from
removing asbestos in our daily lives. And not until
society in whole really grasps how dangerous mercury is and that we
should stop spreading it in the air and water and food and homes and
buildings.
--- old post ---
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...
<http://groups.google.com/groups/unlock?_done=/group/sci.bio.misc/browse_thread/thread/d4ab231bdaf64975&msg=21fb1cf3ef5be3fc>@hotmail.com>
Date: 23 Apr 2007 23:02:54 -0700
Subject: ... Table for AUTISM: Metal Causation coupled
with Weak-Protein-Point Theory of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia)
Another study:
http://www.environmentalintegrity.org/pubs/EIP%2050%20dirtiest%20news
<http://www.google.com/url?sa=D&q=http://www.environmentalintegrity.org/pubs/EIP%252050%2520dirtiest%2520news>
...
Which says:
Plants in Texas, Pennsylvania, Alabama and Georgia ranked in top 50
plants, emitting 15 tons of
mercury into the air, or 30% of all power plant mercury pollution.
Which nicely explains why New Jersey, Georgia, Utah have the three
highest rates when you
consider the direction of wind. And for Utah which burns a lot of coal
and Nevada has a lot of
mercury mining.
It would be interesting to see if Europe also has highest rates of
autism linked with nearby
coal-fired power stations.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 24 Apr 2007 10:14:15 -0700
Subject: Table for PARKINSON's Disease: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
PARKINSON DISEASE
----------
(1) Proteins gone awry involved --
Alpha-synuclein
Ubiquitin
----------
(2) Function of proteins gone awry --
----------
(3) Metals found in those proteins gone awry --
----------
(4) Site or Location of brain where this disease unfolds --
Quoting Wikipedia on Parkinson:
"decreased stimulation of the motor cortex by the basal ganglia,
normally caused
by the insufficient formation and action of dopamine"
----------
(5) Pathology of disease --
Quoting Wikipedia on Parkinson:
"The mechanism by which the brain cells in Parkinson's are lost
may consist of an abnormal accumulation of the protein alpha-
synuclein
bound to ubiquitin in the damaged cells. The alpha-synuclein-
ubiquitin
complex cannot be directed to the proteosome. This protein
accumulation
forms proteinaceous cytoplasmic inclusions called Lewy bodies. Latest
research on pathogenesis of disease has shown that the death of
dopaminergic
neurons by alpha-synuclein is due to a defect in the machinery that
transports
proteins between two major cellular organelles - the endoplasmic
reticulum (ER)
and the Golgi apparatus."
----------
(6) When was the first reliably known case -- 1817
----------
(7) Statistical incidences of Parkinson's in the general population --
Approximately 20 per 100,000 in parts of USA. And as high as 1 in 100
aged over 65 in parts of China.
----------
(8) Age of its victims --
Usually starts at age 57 - 60
----------
(9) Geography of disease prevalence --
Linked to farming and agriculture environment of mercury containing
pesticides and fungicides.
Linked also to well-water of mercury-eating-bacteria.
Quoting from this site about bacteria involving mercury:
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=187012
"The fate and impact of elemental mercury in closed bacterial cultures
were examined.
The quantity of elemental mercury oxidized by bacteria ranged from
small amounts for
Pseudomonas aeruginosa, P. fluorescens, Escherichia coli, and
Citrobacter to
essentially all of the added elemental mercury for Bacillus subtilis
and B. megaterium."
----------
(10) Any mass spectroscopy of brain tissue of disease or of the hair
of
diseased victims and what metals were found --
----------
(11) Any chemicals that may relieve the disease pathology --
----------
(12) Toxic metals that are hypothesized by AP as the root cause:
Organic mercury and possibly in conjunction with cadmium and lead
----------
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@dtgnet.com>
Date: Wed, 25 Apr 2007 00:01:29 -0500
Subject: pattern emerging from Alzheimer, Autism, Parkinson: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
The pattern was not obvious with just Alzheimer and Autism, but quite
obvious now with a third disease of Parkinson. The pattern I speak of
is that a toxic heavy metal such as mercury gets into the body and
easily enters the brain where it destroys or alters the protein
synthesis. This altered protein synthesis produces an unwanted protein
such as beta amyloid in Alzheimer or alpha synuclein in Parkinson where
it accumulates like a garbage dump leading to death. In Autism, the
mercury prevents some nerves or nerve sheaths from forming to make a
normal person. In Alzheimer and Parkinson, the mercury corrupts the
protein synthesis creating roque proteins that kill the person.
Mercury, like asbestos, is toxic to humans. And if you get enough
mercury or asbestos in the body, it could easily lead to death.
Now there are many forms of mercury, to mention just three--
methylmercury and ethylmercury and dimethylmercury. Each of which
could lead to different diseases in different parts of the brain.
And depending on what age of the person and depending on the dosage.
But not only are there many types of organic and inorganic mercury,
but there are also combinations of toxic metals that may cause different
types of diseases and varieties of those specific diseases. There are
many types of Parkinson disease.
So the main thesis of this book is that mercury is a toxic metal and a
small dose can bring on a brain disease which causes unwanted proteins
to accumulate and lead to death.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 27 Apr 2007 10:59:02 -0700
Subject: PRION DISEASE: Metal Causation coupled with Weak-Protein-Point
Theory of Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
PRION DISEASE
----------
(1) Proteins gone awry involved --
Prion protein PrP
----------
(2) Function of proteins gone awry --
transport copper out of brain or body
----------
(3) Metals found in those proteins gone awry --
copper, zinc
manganese?
----------
(4) Site or Location of brain where this disease unfolds --
----------
(5) Pathology of disease --
Similar to Alzheimers in a garbage dump buildup
of the PrP protein that strangles or suffocates the
brain
----------
(6) When was the first reliably known case --
mid 1900s in New Guinea with Kuru
----------
(7) Statistical incidences of Prion in the general population --
Rare
----------
(8) Age of its victims --
Usually starts after 60
----------
(9) Geography of disease prevalence --
England in Europe has the highest density
Canada in North America and the Rocky Mtn region of USA has highest
density in North America
----------
(10) Any mass spectroscopy of brain tissue of disease or of the hair
of diseased victims and what metals were found --
----------
(11) Any chemicals that may relieve the disease pathology --
----------
(12) Toxic metals that are hypothesized by AP as the root cause:
Organic mercury in conjunction with cesium and rubidium
----------
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 27 Apr 2007 23:15:33 -0700
Subject: SCHIZOPHRENIA DISEASE: Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
SCHIZOPHRENIA DISEASE
(note, I used Wikipedia as a main source for much of the below table)
----------
(1) Proteins gone awry involved --
dopamine
----------
(2) Function of proteins gone awry --
neurotransmitter, sort of like the wires in electricity as an analogy
----------
(3) Metals found in those proteins gone awry --
Not in those proteins, but it was found that zinc ions behave similar
to the neurotransmitter of dopamine
----------
(4) Site or Location of brain where this disease unfolds --
striatum, frontal lobes, hippocampus, and temporal lobes
----------
(5) Pathology of disease --
affects the amount of dopamine and a blocking of dopamine pathways
----------
(6) When was the first reliably known case --
1893 by Kraepelin
----------
(7) Statistical incidences of Prion in the general population --
7.5 and 16.3 cases per year per 100,000 population
----------
(8) Age of its victims --
Usually starts in the teenager years for males and in the 20s for
females
----------
(9) Geography of disease prevalence --
worldwide, but I suspect a concentration by geography where there is
a lot
of mercury in the environment
----------
(10) Any mass spectroscopy of brain tissue of disease or of the hair
of diseased victims and what metals were found --
----------
(11) Any chemicals that may relieve the disease pathology --
phenothiazines
----------
(12) Toxic metals that are hypothesized by AP as the root cause:
Organic mercury in conjunction with possibly silver
----------
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...@hotmail.com>
Date: 27 Apr 2007 23:44:11 -0700
Subject: SCHIZOPHRENIA DISEASE and dopamine link between Parkinson: Metal
Causation coupled with Weak-Protein-Point Theory of Medicine (Alzheimers,
Autism, Parkinsons, Prion, Schizophrenia)
a_plutonium wrote:
> SCHIZOPHRENIA DISEASE
> (note, I used Wikipedia as a main source for much of the below table)
> (1) Proteins gone awry involved --
> dopamine
I guess technically, dopamine is not a protein.
> (2) Function of proteins gone awry --
> neurotransmitter, sort of like the wires in electricity as an analogy
> (3) Metals found in those proteins gone awry --
> Not in those proteins, but it was found that zinc ions behave similar
> to the neurotransmitter of dopamine
> (4) Site or Location of brain where this disease unfolds --
> striatum, frontal lobes, hippocampus, and temporal lobes
> (5) Pathology of disease --
> affects the amount of dopamine and a blocking of dopamine pathways
> (6) When was the first reliably known case --
> 1893 by Kraepelin
> (7) Statistical incidences of Prion in the general population --
> 7.5 and 16.3 cases per year per 100,000 population
> (8) Age of its victims --
> Usually starts in the teenager years for males and in the 20s for
> females
> (9) Geography of disease prevalence --
> worldwide, but I suspect a concentration by geography where there is
> a lot
> of mercury in the environment
> (10) Any mass spectroscopy of brain tissue of disease or of the hair
> of diseased victims and what metals were found --
> (11) Any chemicals that may relieve the disease pathology --
> phenothiazines
> (12) Toxic metals that are hypothesized by AP as the root cause:
> Organic mercury in conjunction with possibly zinc
For some years I thought Schizophrenia had a high rate in
wealthy families and so I suspected silver. But making some
searches I find that had no evidence. But it is known that zinc
ions act like dopamine. So I wonder if zinc is connected to
mercury as a cause of Schizophrenia.
And I cannot escape the links of Autism as a infant's form of
Alzheimers, and Schizophrenia as a teenagers form of Parkinson,
where mercury is the culprit in all four diseases.
For it is known that in Parkinson there is damage to the dopamine
pathways, likewise for Schizophrenia.
So the overall picture is that if you get mercury into the brain when
a
baby, you may end up with Autism, and this same mercury over a
lifetime ends up as Alzheimers. And a different mercury in teenagers
may end up with Schizophrenia, and that same mercury over a lifetime
ends up as Parkinson.
Now all of the above would be easily and simply proven true if medical
science did mass spectroscopy on diseased patients for mercury
analysis.
And also, an interesting supporting evidence would be the geography
data.
If it turns out that some state such as Utah has the highest rates of
a number
of these diseases, then that would strongly indicate the environment
and the
presence of mercury as a cause.
Newsgroups: sci.med, sci.bio.misc, sci.chem
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?_done=/group/sci.med/browse_thread/thread/d4ab231bdaf64975/3ec2124fcaf599ef%3Flnk%3Draot&msg=3ec2124fcaf599ef>
@gmail.com>
Date: Sat, 23 Apr 2011 23:50:15 -0700 (PDT)
Subject: poor reporting by McNeil on Autism; Metal Causation coupled with
Weak-Protein-Point Theory of Medicine (Alzheimers, Autism, Parkinsons,
Prion, Schizophrenia)
I feel this is poor reporting by Robert McNeil on Autism.
Unfortunately I missed seeing the 3rd program that bespeaks of causes,
but the prelude
never mentions the chemical "mercury" only mentions "vaccines".
So I feel the medical community is being bought up and bought out by a
consortium of pharmaceuticals
and electric companies who have the most to lose in a legal court
fight over mercury. That just like the
oil companies buying out scientists to say the opposite of Global
Warming.
What McNeil showed and interviewed were scientists who only screamed
of "genetics, genetics, genetics".
So overall McNeil did a disservice to Autism in its "causes".
It would have been like reporting on smoking in the 1970s where
scientists bought out by the cigarette companies and saying there is
no link of smoking to cancer.
Or like the asbestos companies buying up scientists to say that there
is no link of asbestos with cancer.
There is a fascinating analogy of asbestos and diseases of asbestos
with that of mercury and autism, alzheimers,
schizophrenia and parkinsons and prion disease.
So many off-track scientists who are enamored with genetics as the
source of disease, would have in the 1970s said if McNeil had
interviewed them in 1970s about mesol--- cancer that it was a genetic
cancer because families
were coming in with that disease. And the scientists back then would
have never mentioned the toxic substance
asbestos to McNeil, just as those culled for the autism program
yakkity yak about genetics and not mercury.
So that in 1970 as houses were insulated with asbestos and asbestos
products in numerous items in the home,
and where a family comes in constant contact with the asbestos leaking
from the ceilings into the lungs of the family occupants. Yet the
scientists interviewed by McNeil would bandy on and on about genes and
genetics and
whole families coming in with asbestos cancers.
Nowadays, with coal electric plants spewing out mercury into the air
and where many buildings have broken
fluorescent lamps and hospitals floors soaked from mercury from broken
lamps and where dentists still put
mercury fillings and where toothbrushes used to be sterilized in
mercury and with vaccines coated in mercury.
So our modern day human society is awash in mercury in the
environment. There are fish eating warnings in most
countries and where women today that are pregnant, a study found that
1 in 8 pregnant woman have so much mercury in their bodies that will
cause a damage to the new born.
Think of all that mercury going into land fills and garbage dumps that
leaks into the groundwater and eventually turning into the dangerous
ethyl and methyl mercury compounds.
So that McNeil properly voices that 1 in 110 infants now have autism.
What McNeil should then have done was research that the presence of
mercury throughout modern day human society has increased by 1000
times more
than what that mercury exposure was in year 1890.
It was sad when reporters cowed to the cigarette companies for lung
cancer
It was sad that the reporters and scientists cowed to the asbestos
industry and cancer
Now it is truly sad that the reporters and scientists are cowed and
act cowardly to the widespread increase of mercury in the environment
and to pretend that such a vast exposure is not going to cause health
problems.
I vote that Mr. McNeil re-do that program on Autism and get someone to
talk for some length on the fact that
Autism is increasing to 1 in 110 afflicted and so has the exposure to
mercury increased in the same time interval.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/ffbfa5d287399d33%3Fhl%3Den&msg=30d0f87ed80059fe>
@gmail.com>
Date: Sat, 16 Jun 2012 00:10:01 -0700 (PDT)
Subject: book: MERCURY Metal Diseases of Medicine (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia, Huntington)
Tonight I saw Charlie Rose "brain series" on Parkinson's and
Huntington disease. So I felt compelled to retort to that program
since I wrote a book in the 1990-2000s with the
theme that modern society is awash in toxic mercury which leads to the
plethora or rainbow spectrum of brain diseases.
In Ancient Rome, there was a abundance of lead in the environment and
lead to many lead caused diseases of brain damage. It even caused
disease to explorers on ships who ate food from lead containers.
Another toxic element in the environment was asbestos which leads to a
lung cancer.
There was little mistaking the lung cancer to asbestos, but there were
argumentative people who had money at stake.
But as for mercury, humanity has not yet fully accepted the idea that
this very toxic
chemical can accumulate and can increase in exposure as humanity
becomes more
industrial and commercial, and there will be the "deniers" such as the
deniers of global
warming since deniers have money at stake, such as the drug companies
using mercury in vaccines. But the largest spreading of mercury is the
burning of fossil fuels like coal.
Ever wonder why Prion disease is so frequent in England? Ever notice
that coal burning
occurred in England for many centuries.
It is not proteins that bend the shape of other proteins that causes
prion disease, but rather it is the mercury in the body that attacks
other metals such as copper in proteins
or the metals that compose those proteins are susceptible to mercury.
Ever wonder why when a prion disease cow is killed that the disease
needs to be burned at a high temperature? It is not because the
protein is dangerous, but because
the proteins have mercury inside them.
In modern society, the amount of mercury in the air, in the water, in
the food even in our houses with those light fixtures that contain
mercury and when broken fill the floor boards and cabinets with loose
mercury. Even dental fillings were mercury.
So our air is full of mercury from all the coal burning power plants.
Does anyone wonder why Autism now is that 1 in every 90 children has
autism. And the USA has the highest frequency of autism and no wonder
since the air that we breathe in the USA has one of the world's
highest mercury level. Autism is especially high in Texas, and Texas
has a lot of coal burning and oil refining and so it has a lot of
mercury.
Of course, all those people who have money riding on vaccines or drugs
with mercury are going to say no, no, no and deny. But that is what
anyone who stands to make money would do, deny.
Charlie Rose show 15JUN2012 Eric Kindle, Stanley Prusiner trying to
feed the line that prions are the common denominator when in fact
mercury is the common denominator. An interesting fact was noted about
Huntington disease by Ann of Harvard that you need 39 cgt changes to
get the disease if you stop at 35 cgt changes
the disease has no onset (sorry if I got some of that data wrong for I
was leisurely watching and tried to remember). What this suggests or
may indicate is some minimum amount of mercury is necessary.
Now Huntington is a genetic disease, but more important, it needs the
environment for the toxic mercury to initiate. We could just as well
say Autism, prion disease, Parkinsons are genetic diseases only
because some genes are better able to stave off
mercury, but when mercury is so abundant that entire families in their
environment are struck by the disease, that it appears genetic. An
entire family exposed to mercury would have a high chance of all
ending up sick with disease, and then misleadingly
called a pure genetic disease.
Funny how Prusiner cannot even admit that these proteins have metals
involved, such as copper and that mercury changes those metals. So
that in prion disease, it is not a protein that is the source of the
disease but something smaller than the protein-- a toxic chemical of
the environment that causes prion disease and all the other diseases
listed.
Funny how I would consolidate all these diseases in the 1990s through
2000s, saying that the common factor is increase of mercury in the
environment and then come
2012, Prusiner trying to consolidate these diseases into his erroneous
"prion concept".
Bad, bad show, Mr. Charlie Rose.
After I write this Physics book which I am on page 754 and aim for
about 1200 pages, after I get that done, I intend to write the Geology
book, New Geology that uses electricity magnetism to explain plate
tectonics, and coincident, I intend to make a new edition on this
Metal Diseases for 2007 was a long time back and that book needs
revision.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/ffbfa5d287399d33%3Fhl%3Den&msg=30d0f87ed80059fe>@hotmail.com>
Date: 27 Apr 2007 23:44:11 -0700
Subject: SCHIZOPHRENIA DISEASE and dopamine link between Parkinson: Metal
Causation coupled with Weak-Protein-Point Theory
of Medicine (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia)
a_plutonium wrote:
> SCHIZOPHRENIA DISEASE
> (note, I used Wikipedia as a main source for much of the below table)
> (1) Proteins gone awry involved --
> dopamine
I guess technically, dopamine is not a protein.
For some years I thought Schizophrenia had a high rate in
wealthy families and so I suspected silver. But making some
searches I find that had no evidence. But it is known that zinc
ions act like dopamine. So I wonder if zinc is connected to
mercury as a cause of Schizophrenia.
And I cannot escape the links of Autism as a infant's form of
Alzheimers, and Schizophrenia as a teenagers form of Parkinson,
where mercury is the culprit in all four diseases.
For it is known that in Parkinson there is damage to the dopamine
pathways, likewise for Schizophrenia.
So the overall picture is that if you get mercury into the brain when
a
baby, you may end up with Autism, and this same mercury over a
lifetime ends up as Alzheimers. And a different mercury in teenagers
may end up with Schizophrenia, and that same mercury over a lifetime
ends up as Parkinson.
Now all of the above would be easily and simply proven true if medical
science did mass spectroscopy on diseased patients for mercury
analysis.
And also, an interesting supporting evidence would be the geography
data.
If it turns out that some state such as Utah has the highest rates of
a number
of these diseases, then that would strongly indicate the environment
and the
presence of mercury as a cause.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/ae85056de5817751%3Fhl%3Den&msg=d5e90aaefa0e9ac5>
@gmail.com>
Date: Sat, 16 Jun 2012 12:34:41 -0700 (PDT)
Subject: MERCURY Diseases (Alzheimers, Autism, Parkinsons, Prion,
Schizophrenia, Huntington)
Now I started this book sometime in 1990s, and the Usenet would be
proof of this book, and only in the 2000s did I collect the
information to consolidate into a book form. I titled it, as can be
seen from this post:
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: a_plutonium <a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/ae85056de5817751%3Fhl%3Den&msg=d5e90aaefa0e9ac5>@hotmail.com>
Date: 27 Apr 2007 23:44:11 -0700
Subject: SCHIZOPHRENIA DISEASE and dopamine link between
Parkinson: Metal Causation coupled with Weak-Protein-
Point Theory
of Medicine (Alzheimers, Autism, Parkinsons, Prion,
Schizophrenia)
But let me title it as simply MERCURY Diseases for it is the metal
mercury that is
the underlying cause of a spectrum of brain diseases. When a person
gets too much mercury in them, it accumulates and affects each person
in a spectrum of disorder, for
we notice that in Autism especially which indicates it is mercury as
the root cause.
Now I need to renew this book because last night on the Charlie Rose
show of his Brain Series with Eric Kandel and Stanley Prusiner are
"pulling the wool over the science and public eyes" so to speak.
The biology community really does not have solid evidence that
proteins of prions can bend the shape of other proteins for it is not
proven that the mercury inside those proteins are doing the bending.
In other words, prion disease is not a protein disease, but simply a
toxic mercury disease.
So, scientifically, it is wrong and bad for Kandel and Prusiner to get
on a TV show and
proclaim that prions are some broad connecting link for many brain
diseases when in fact that mercury is the real culprit, and that prion
disease is not even a valid true disease save for the mercury
involved. That mercury causes prion disease. So to use Charlie Rose
show as a stage platform to broadcast bogus science claims by Prusiner
and Kandel is very much in bad taste.
Now let us suppose that humanity, all 7 billion humans of Earth ate
food and breathed air and drank water that was contaminated with
asbestos, just little tiny amounts, on the scale of the prevalence of
mercury in modern day human society. Can you imagine
what the hospitals across the world would be dealing with? Well,
pretty much the same as with Autism, Alzheimers, Prion, Schizophrenia,
Parkinsons and Huntington diseases collectively. Only instead of brain
disease filling the hospitals, you have cancer disease
of stomach, lung. You would have 1 in 90 infants diagnosed with
stomach or lung cancer instead of Autism. The older folks, after a
lifetime of accumulating asbestos in their bodies would all surely
come down with either stomach cancer or lung cancer.
You see, if we built electronic devises that could test the air or
water or food we intake for presence of mercury, a device the size of
a cell phone that can detect the presence of mercury, we would all be
screaming in fear, like the famous picture The Scream, at realizing
how much mercury is in the air we breathe, the food we eat and the
water we drink.
The major culprit is mercury and the major means of making mercury
everywhere is the burning of fossil fuels such as coal. But we even
use it in dental fillings and now, our
houses and homes are slowly collecting mercury whenever a lamp
containing mercury is broken. Mercury is so high in fish food, that
pregnant woman are warned not to eat any fish during pregnancy.
If we had a geiger type cell phone that can measure mercury presence,
we would be horrified.
Mercury, when it gets into a human body, goes directly to where the
body best accommodates mercury-- the brain. Since the environment is
full of mercury, it is no wonder that our brains have too much mercury
present.
It is said that as you reach age 70, you have a 50 to 50 chance of
having Alzheimers
and at age 90 the chances are 90% you have Alzheimers. But as we
increase the
mercury in the environment by 2050, those numbers should be coming in
that by age
50 nearly 90% of those alive have Alzheimers, all because mercury is
so widespread.
The numbers for Autism keep increasing also. A decade or two ago the
cases of Autism were something like 1 in 500, then it was 1 in 200,
and now it is 1 in 90, matching the increase in mercury in the
environment.
Some have made the silly and stupid remark that old men with their
semen has a role in Autism. When you are an old man, your body has
more mercury in it than a young man and your habits are such that you
are exposed to more mercury. Has anyone ever
scientifically looked at the semen of old men for mercury presence
compared to young men?
In the Roman times the element lead was a major health problem. Then
came asbestos. And ever since the industrial age where mercury is
vital to industry, are we
slowly coming to recognize that a vast swathe of health problems are
all due to the failure to recognize how toxic mercury is, and how we
have filled the environment for
easy intake of mercury to the human body.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/ae85056de5817751/2e315c026325624f%3Fhl%3Den&msg=2e315c026325624f>
@gmail.com>
Date: Sun, 17 Jun 2012 01:26:17 -0700 (PDT)
Subject: book MERCURY Diseases (Alzheimers, Autism, Parkinsons, Prion,
Schizophrenia, Huntington)
These are some old notes I need to take care of when I write the next
edition of this book.
For Parkinson's where is the disease? answer; substanta nigra.
Alzheimers starts in the hippocampus region and then spreads to two
other regions.
Alzheimers is the clumping of the beta amyloid plaques and the tau
tangles. I realize the clumping is the key logical item and that
perhaps mercury molecules are involved in that clumping. Although I
think that mercury
is chiefly involved with other metals in cells. Mercury as a catalyst
is a subject not well known.
In Alzheimers, the snipping or cutting of the peptide and then the
debris, but the debris is not toxic until it begins to clump of the
beta amyloid outside the cell and the tau tangles clump on the inside
of the cell.
This reminds me a lot about prion disease in that it is cell walls of
the prion protein and that it clumps also. However in the cutting of
the prion protein, it maybe the cutting of defective proteins.
In the long history of humanity with toxic substances such as lead in
Ancient Rome, one wonders when if
ever the Romans actually became aware that lead was a dangerous
substance? One would think they
never realized because some explorers took lead cans on their ships
and were lead poisoned in their voyages. Substances like tobacco,
although it looked as though it was not life threatening, that it took
a long
time to realize by society that the lung cancers were directly linked
to tobacco.
Then there was the time period of 1900 to about 1980 when it was not
realized that this asbestos use
was dangerous and a toxic substance.
Now fast forward to 1980 to 2012, and would anyone of any commonsense
think that the world is free of toxic
substances? You would have to be a fool to think the world was free of
toxic substances.
Even on a recent MI5 TV show was posed a threat on London of releasing
dimethyl mercury (although a fiction TV series) the truth of it is
that most people know mercury is extremely dangerous and just a tiny
bit of dimethyl mercury will kill you. Yet modern society is spewing
mercury into the air we breathe, the food we eat and the water we
drink.
And to think that with the increasing amount of mercury, would entail
increasing amounts of brain diseases
among infants, teenagers, adults and old people. All age groups
affected by mercury increase in society.
Of course we all will hear the siren and harpie calls by those who
make money from mercury usage
in commerce. Of course we expect drug companies and doctors to hush
hush about mercury and not tip the
apple cart.
But what we really need is some common easy way of measuring mercury.
So that anyone can flip open
a tiny gadget that measures the presence of mercury.
Recently in Sioux City Iowa, some store dropped its fluorescent lamps
and broke them on the floor and they
knew it had mercury in them. So they called a HAZMAT team wearing
space suit gear and with special
cleaning material trying to remove the mercury contamination which was
invisible. But that sort of situation is
playing out all across the USA now a days since stores sell
fluorescent lamps and people breaking them, but
not calling for a HAZMAT clean up. And most of those lamps end up in
municipal dumps where the mercury
leaks out and ends up in the water supply.
Nowadays, most everyone in the USA lives about 100 or 200 miles from a
coal fired electricity plant and breathes the air. Coal concentrates
mercury and when it is burned, releases that mercury into the air and
many of us end up breathing it. Mercury accumulates in the body and is
very tough to get it out of the body.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/ae85056de5817751/2e315c026325624f%3Fhl%3Den&msg=599d801d3bd3d711>
@gmail.com>
Date: Sun, 17 Jun 2012 10:01:03 -0700 (PDT)
Subject: Huntington disease is mercury caused book MERCURY Diseases
(Alzheimers, Autism, Parkinsons, Prion, Schizophrenia, Huntington)
Now the reason I have made this spot-renewal of this book from it
previous edition of
year 2007 is because on the Charlie Rose show of 15JUN2012 appeared
another episode
of the Brain Series with Eric Kandel and Stanley Prusiner and others
talking about
Huntington and Parkinson disease with the silly notion of Prusiner and
Kandel in thinking
that several brain diseases are prion diseases. Where prions are a
common denominator.
And where Prusiner on the show said in all his years of researching
prion disease, he
never found a virus as causative agent. But Prusiner is not a logical
scientist, for he
has never thought that the underlying cause and agent of prion disease
is a toxic substance
like mercury, for which many proteins of the body contain metals in
their composition and
where mercury would wreck havoc on those metals bonded in proteins.
Sure, Prusiner never found any viruses with prion disease, but did he
ever stop to think
that the disease is not a protein but a toxic element such as mercury
or mercury compounds?
No, so he does not have a logical foundation to even suggest that
other diseases are
prion caused, and to offer such a silly idea, when he never eliminated
mercury or other
inorganic substances.
Prion disease is most likely to be found to be caused by some mercury
compounds. The highest
rates of prion disease are from England going back in history. Perhaps
it was first witnessed in
England. And England has a lot of coal which has been used for long
periods of times in English history and the burning of coal releases
the concentrated mercury. This makes sense also, in the fact that
to get rid of Mad Cow Disease, the cattle were often burned in
excessive heat. But a protein, if the cause
does not need high heat temperature, but mercury if the cause does
need high heat. As for the New Guinea
incidents of prion disease, here again, mercury is concentrated in the
brains of a animal or human
and if eaten, it is not the proteins that are dangerous, but that the
mercury inside the proteins and brain tissue that are dangerous.
Now the TV program was not a total waste and false science, but that
there was a guest named Ann from
Harvard (pardon me if I have the name and such wrong for I did not jot
down details) talking about Huntington.
In the older edition of this book, 2007, I had not included Huntington
because I deemed it as purely
genetic disease, not knowing its pathology. But after listening to
what Ann was discussing on the disease,
I come to realize it is not a genetic disease after all. And I look in
Wikipedia and see that the "Hereditary
Disease Foundation" funded the research and so that tells me,
Huntington was given its connotation of
"hereditary disease" even though it is not such. What Ann said, and my
memory is vague on this, so correct
me if wrong, that is so very important is that if 34 of the 39 of the
ctg are changed but not 35 changed then you will not get Huntington
disease, but if 35 are changed then you have Huntington's disease.
What that means is that the disease is not hereditary because it
depends on the environment to get that minimum dosage of 35 changes.
It is, metaphorically, like a calibrated test tube with 39 markings
and if 35 of those marks are filled by mercury to make those 35
changes, then you have Huntington's disease. So in the 2007 book I
opined that Huntington's disease was genetic, but after hearing Ann
explain it, I realized the disease
relies on the environment to boost it into the minimum changes to
start the onset.
And speaking of onset, can anyone tell me if there ever was a person
who upon birth, was recognized to have Autism at the moment of birth?
I believe that all infants with Autism have about a 2 year reprieve
before it is recognized "something is wrong". I know of no case of
Autism, that the newborn shows signs of Autism and that all autism
cases had a time period of "being normal". So here again, if Autism is
mercury caused, then the exposure has to build up to a minimum load
before the disease is manifest.
Also, reading Wikipedia on Huntington, it says: "It is much more
common in people of Western European
descent than in those of Asian or African ancestry." That would make
sense in that Europe burned a lot
of coal releasing a lot of mercury and was industrialized, so the
exposure to mercury was mostly a European
phenomenon. Also, it is noted that Parkinson's disease is often called
"welder's disease" because the
occupation of welding is around more mercury vapor than normal.
Now many people would say that Asia now a days is showing more signs
of these brain diseases than in the past. And that would be true for a
mercury based cause of these diseases, for it is said that China is
opening up a new coal fired power station about every month now, or
was it every week now? And people must realize that the coal burned in
China releasing mercury into the air stays in the air and transits the
globe so that people in the USA are breathing not only the mercury
from USA power plants but the mercury from the coal burned in China
power plants. The mercury in the air we breath no longer stays put in
one geography but makes the air a ocean of toxic mercury that all
humans are now exposed to.
In Wikipedia on Autism, says that worldwide the disease affects 1-2
per 1000, but that for the USA in particular, it affects 11 per 1000.
That statistic matches the fact that the mercury in the environment of
the USA is about 10 times worse than worldwide. And as for China,
autism was not a problem for China by 1950
but ever since China became industrial nation in the 1990s, these
mercury caused diseases of
Alzheimers, Autism, Prion, Schizophrenia, Parkinsons and Huntingtons
have sharply risen in China.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/7c020609988611b3%3Fhl%3Den&msg=da9a2b73d465342d>
@gmail.com>
Date: Sun, 17 Jun 2012 14:01:16 -0700 (PDT)
Subject: insects affected by prevalence of mercury; Bee Colony Collapse;
book : MERCURY Diseases (Alzheimers, Autism, Parkinsons, Prion,
Schizophrenia, Huntington)
Mercury is pretty much a toxic substance to most life, especially
animals. Now since insects are so much smaller, one would think the
rise in mercury levels should see
noticeable declines in some insect species. If mercury can cause so
much harm
to the human brain, one would think that the brains of insects would
be harmed.
So let us ask a question, do we notice any insect species that is
disoriented as are
humans with Alzheimers, Autism etc etc? And the first candidate that
popps to mind
is the honey bee Colony Collapse Disorder.
Now I am reading in Wikipedia that by 2010, US researchers found a co-
infection of
invertebrate iridescent virus type 6 and Nosema ceranae were found in
all CCD colonies
tested.
What I am suggesting is that researches begin to analyze the brains of
bees, looking for
mercury content. A person with Alzheimers would be a bee that cannot
find its way back home to the colony.
Honey bee CCD is worst in the USA and the USA has the worst mercury
pollution, with
China probably second place. So, is the CCD in China becoming
prevalent? I remember a TV program that showed a village in China that
had no more bees to pollinate the pear trees and that the villagers
were hand pollinating the pear trees.
So maybe, the bees are a casualty of mercury in the environment.
But I bet there are many smaller species that have been affected worst
than humans with mercury, but they are not reported so heavily as
honey bees. I bet there are insect species that are going extinct
because of the rise of mercury in the environment.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/8bf6bec428555809%3Fhl%3Den&msg=921e0e2e9d7f6c94>
@gmail.com>
Date: Tue, 19 Jun 2012 11:32:18 -0700 (PDT)
Subject: whales and fish affected by prevalence of mercury : MERCURY
Diseases (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia, Huntington)
In my last post, I spoke of the fact that ever since the Industrial
Revolution with the burning of coal and fossil fuels that the globe is
being increased of its mercury exposure.
That mercury is so widespread and in contact with living species that
it is impossible
to not have a health risk for this toxic substance. And the way it
shows up in humans
is the brain disorders and the rise and increase in brain disease.
I spoke of how likely it is showing up in bees and insects such as
Colony Collapse Disorder, even though many suspect it is a chemical
insecticide or viruses to blame.
However, no research has been given to the mercury content inside of
affected bees
and until that research is done, we cannot rule out that CCD is a
mercury caused
disease of bees.
Now let me add another possible case of mercury poisoning in species.
The oceans have fish and mercury concentrates in large fish, for we
even have warnings to pregnant women to not eat any fish before birth.
So do we ever see mental or brain dysfunction in fish or mammals of
the oceans? Well, whales are known to be beached from ships that are
practicing on sonar and these whales are disoriented. But some whales
are beached without sonar drills by ships. So has anyone actually
tested the brains of a dead whale that is beached for mercury content?
I suspect not.
In our modern day world where our activity is industrial and
commercial, we tend to spread mercury all over the globe, in the air,
food, water. And this increase in mercury
exposure would cause diseases in living organisms because it takes
just a little bit of
mercury to affect a living creature.
In the 1990s, the chemist Karen Wetterhahn was studying mercury and
accidentally spilled dimethylmercury, a drop is all it takes, of this
extremely dangerous form of
mercury and died of the accident. Now can one molecule of
dimethylmercury kill a
human? Probably not, but perhaps one molecule of dimethylmercury could
cause
autism or prion disease in a human. Perhaps 3 molecules in the brain
of a adult
human can start Alzheimers or Parkinsons disease. Perhaps a beached
whale
has 3 molecules of dimethylmercury in its brain and the cause of its
beached state.
The trouble with modern society is the ever increasing push and pull
for commercial making a dollar, even if it means making mercury so
prevalent, and thus is opened the door for a large health risk to all
life on Earth.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/8bf6bec428555809%3Fhl%3Den&msg=77cf8ca19a8cb711>
@gmail.com>
Date: Tue, 19 Jun 2012 23:51:12 -0700 (PDT)
Subject: Re: whales and fish affected by prevalence of mercury: MERCURY
Diseases (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia, Huntington)
On Jun 19, 3:23 pm, Dean <damark...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/8bf6bec428555809%3Fhl%3Den&msg=77cf8ca19a8cb711>@gmail.com>
wrote:
> There is this wonderful search engine called Google. If you had tried
it, you'd know that such work has been done.
> http://www.ncbi.nlm.nih.gov/pubmed/1413402
<http://www.google.com/url?sa=D&q=http://www.ncbi.nlm.nih.gov/pubmed/1413402&usg=AFQjCNGSCFsHnxACPjNKK4i89G5U-KeJQw>
Thanks.
--- quoting from this website, some mercury data ---
Vet Med (Praha). 1992 Jul;37(7):405-12.
[Levels of mercury in samples of bees and honey from areas with and
without industrial contamination].
[Article in Slovak]
Toporcák J, Legáth J, Kul'ková J.
Source
Univerzita veterinárskeho lekárstva, Kosice.
The following mercury levels were found in bees from the contaminated
area: heads 0.029-0.385 mg/kg, thorax 0.028-0.595 mg/kg and abdomen
0.083-2.255 mg/kg. Mercury levels in samples from uncontaminated areas
ranged from 0.004 to 0.024 mg/kg in the heads, from 0.004 to 0.008 mg/
kg in the thorax and from 0.008 to 0.020 mg/kg in the abdomen.
--- end quote ---
Those are alarmingly high levels of mercury, and I am guessing from
bees in Europe. Now I realize that bee
CCD is worse in the USA than in France. And I realize that USA does
far more coal burning than does Europe and France with their nuclear
power.
So I wonder if someone did the same study of bees in the USA would get
a far worse data of mercury levels
in bees than the above.
As for humans with brain disease, I believe we should begin to analyze
mercury levels in cases of Autism,
Alzheimers, Prion, Parkinsons, Huntington's, and Schizophrenia. We
probably know more about how much
mercury in those bees than we know about mercury levels in humans.
This is probably because no one really
cares how lousy our environment is, so long as others are making money
and a living.
I do remember the first case of Alzheimers was in Germany, and likely
the coal burning Ruhr region. Parkinsons is the welders disease and
likely because of the minute mercury fumes.
So if we can get a study of France's bee mercury levels compared to
USA CCD bees mercury levels
we can likely find a connection. That France has far less mercury for
bees to intake whereas in the USA,
with all its coal plants the bees have little chance.
Now with all the mercury in the oceans, I would not be surprised that
all those animals have too much mercury in them and that they show
signs of behavior that is abnormal. Behavior such as whales beaching.
Or schools of fish wandering off their normal routes of swimming.
We are always frightened by virus plagues, contagious and harmful and
invisible. Yet we should now be afraid
of a elemental poison that is invisible, that stays around for a long
time when spilled, that accumulates in the body once inside the body,
and where a tiny bit of it can lead to disease or death.
We are so scared of mercury, that few of us want to admit that mercury
is a poison and that we are not
measuring for mercury in the USA medical profession. It is like
asbestos from 1900 to 1990. Only until
1980 was the news released that this stuff is toxic and deadly and
that we should stop using it, and stop
filling our houses with it. As for Autism, Alzheimers, Prion,
Parkinson, Huntington, Schizophrenia, no one
in the medical profession wants to research mercury or collect the
data, because everyone in the medical
profession is making good money on the status quo. Even when mercury
is used for vaccines, hush little
baby, do not cry, for the status quo and money making is more
important.
I bet if an instrument was built that was the size of a cell phone
that can measure the amount of mercury
present in a floor, that half of the big chain stores and nearly most
old hospitals across the USA would have
to hire a HAZMAT team to clean the place up. I bet in 50 years from
now, buying and selling homes in the USA would require a mercury
testing in upscale homes, just as no-one in their right mind would
want to buy
a home that has asbestos insulation, or lead water pipes.
We should build a device that can measure the presence of mercury, and
when we have such a device, then
we can start to clean up this awful environment of too much mercury.
P.S. I recently heard a report that China has alarmingly high Autism
cases, a record high rate that was never there before. But if you
correlate the coal burning increase in China, then it is
understandable that China and USA will rival one another in the
highest rates of these 6 diseases listed.
Newsgroups: sci.bio.misc, sci.med, sci.chem
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/c97e9de11a9fe33e%3Fhl%3Den&msg=e68d66f35cce319a>
@gmail.com>
Date: Thu, 15 Nov 2012 23:06:46 -0800 (PST)
Subject: fevers increase autism rates and Autism in animals-- bonobos,
cats, horses book: MERCURY Diseases (Alzheimers, Autism, Parkinsons, Prion,
Schizophrenia, Huntington)
Last time I wrote on this book was June 2012. Not much news in the way
of these diseases. Although the rates of autism seem to increase every
year. Last I remember is that 1 in 88 children have autism whereas the
last time I recall it was 1 in 110.
Now most scientists think autism is genetic, but I believe it is due
almost entirely to the environment and the contact of mercury in the
environment.
Ever since the 1900s was ushered in the industry and commerce of the
world has increasingly used mercury in all sorts of items. And mercury
has increasingly been a major pollution concern in the burning of
fossil fuel.
To me, the reason that autism was something like 1 in 1000 diagnosed
in 1800 is because mercury was not so common in the environment as it
is in 2012. In the 1800, you could get a breath of fresh air without
pollution in it and without mercury. By 2012, with coal fired power
stations and with mercury in the medicines and vaccines and with
mercury from incandescent lamps in the homes and with mercury in teeth
fillings and with mercury in the fish we eat, it is terribly difficult
to avoid mercury entering your body each and every day. It is coming
at us from every angle, every day of our modern technology lives.
So to hear that a study in Europe showing that a mother has increased
chances of an autistic child if she has a fever during pregnancy raises
some questions. It is likely not a virus that causes autism but
rather, that the mother took some medicine to relieve the fever and
that medicine had residual mercury such as the mercury that is
antifungal for vaccines.
Another report says that couples with older men increase the chances
of autism. Here again, it is likely that older men visit the hospital
with their wives and administered medicine or hospital conditions
where there is a lot of mercury in the environment. I suspect that if
we had a mercury geiger counter and visited hospitals to see what
levels of mercury are found, we would be aghast of how large the
readings would be.
But anyway, I saw a NATURE TV show about odd couple friendships in the
animal kingdom showing a gibbon monkey that did not want to live with
its own species but rather lived with capuchins. I forgotten his name
but he was a white gibbon. And I thought to myself, that is really odd
behavior, is it a form of autism?
Then a few days later that gibbon thought reminded me of one of my
cats, who is much like a autistic person only he is a cat. And I have
a horse that is behaving like a autistic person.
So tonight I checked the Internet to see if any reports of animals
with autism like behavior and one hit is this bonobo named Teco in
the Discovery News of Sept 2011.
So, what I am driving at in reasoning, is that if Autism is really a
genetics disease, then it should not appear in a broad list of diverse
animal species. If Autism is mercury caused, then animals and humans,
who come in contact with mercury will be affected adversely.
A huge problem of our modern day times, as seen in Global Warming and
seen in Autism is that there are deep pocketed money interests
blocking the science. In the case of Global Warming the money
interests are obvious, but in the case of Autism and other mercury
diseases, there will be an intense effort to downplay mercury, when it
is mercury that is the culprit.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/59e395049c394bbf%3Fhl%3Den&msg=a24c9f5d6830e7be>
@gmail.com>
Date: Thu, 21 Feb 2013 23:54:01 -0800 (PST)
Subject: folic acid reduces autism, perhaps by chelation of mercury:
MERCURY Diseases (Alzheimers, Autism, Parkinsons, Prion, Schizophrenia,
Huntington)
Last time I reported to this book was Nov 2012 as seen
here:
Newsgroups: sci.bio.misc, sci.med, sci.chem
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/59e395049c394bbf%3Fhl%3Den&msg=a24c9f5d6830e7be>@gmail.com>
Date: Thu, 15 Nov 2012 23:06:46 -0800 (PST)
Subject: fevers increase autism rates and Autism in animals-- bonobos,
cats, horses: MERCURY Diseases (Alzheimers, Autism,
Parkinsons, Prion, Schizophrenia, Huntington)
But recently there was news that folic acid as a vitamin supplement
reduced the risk of autism born child by over 1/2 as reported in a
Norwegian study of about 85,000 births.
This is good news for the mercury basis of these diseases, for the
folic acid would act (in my opinion) like a chelation on mercury
present in the mother's body and chelate that mercury out of the body
and prevent the mercury entering into the child.
If a disease is caused by the environment and chemicals in the
environment, then, other chemicals should lessen the disease itself,
that is, combat the toxic chemical. If the disease is a genetic based
disease, then a chemical should not lessen the disease such as folic
acid.
Chelation is like a cleaning activity.
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/b9bbcdd86346bc78%3Fhl%3Den&msg=e1ed091efe6cf278>
@gmail.com>
Date: Sun, 17 Mar 2013 15:54:41 -0700 (PDT)
Subject: Need to add to my book of 1996 Metal Causation Diseases Re: Metals
In Autism
Found an interesting alleged research report, and have to check to see
if any of it is true.
But regardless, need to add the below to my book of 1996 that argues
many diseases of common affliction are the metals in the environment.
The world had never known of a asbestos disease
until asbestos was widespread in human contact and mining. Coal
disease was never known until humans
mined and used it. By the 20th century, human society needs many
metals such as mercury, lead, chromium (report on PBS of Chromium-6
and how dangerous). So as human society puts more dangerous metals
easily in reach of large numbers of people, that we end up with
diseases like autism, parkinsons, alzheimers, schizophrenia and prion
disease.
Of course the chemical companies and companies profiting from these
dangerous metals are going to pooh pooh any report linking these
metals to health issues.
Also on PBS of their pledge week, they sponsored several brain
doctors, and one said that the increase in iron and the increase in
copper and aluminum in the food we eat and the cookware we use,
increases the
chances of the plaques forming in Alzheimers.
Any rational, any common sense reasoning person can see or witness
that Autism has grown from 1 in a 1000 to now where it is 1 in 110.
And likewise anyone can see that the presence of toxic metals in our
homes and environment has increased from 1 in 1000 to 1 in 110.
Every time you eat fish, you fill up on mercury poison. Every time you
breathe the air from nearby coal fired plants you fill up on mercury.
Every time you buy and break a incandescent light bulb, you fill up on
mercury in your body. Every time you get a vaccine immersed with
mercury, you fill up on mercury.
Many human diseases are due to the prevalence of toxic metals in our
environment.
Just listen to that chromium 6, hexavalent chromium of PBS last friday
where the reporter commented that the EPA would rather give a toxic
chemical the benefit of doubt rather than giving the benefit of doubt
to the human health and safety.
On Feb 25, 6:25 pm, ironjustice <ironjust...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/b9bbcdd86346bc78%3Fhl%3Den&msg=e1ed091efe6cf278>@rock.com>
wrote:
> Study finds higher levels of several toxic metals in children with
> autism
> Posted in: Faculty, Research
> James Adams, a professor of materials science and engineering, has
> done extensive research into autism. He directs the ASU Autism/
> Asperger’s Research Program.
> Posted February 25, 2013
> In a recently published study in the journal Biological Trace Element
> Research, Arizona State University researchers report that children
> with autism had higher levels of several toxic metals in their blood
> and urine compared to typical children. The study involved 55 children
> with autism ages 5–16 years compared to 44 controls of similar age and
> gender.
> The autism group had significantly higher levels of lead in their red
> blood cells (+41 percent) and significantly higher urinary levels of
> lead (+74 percent), thallium (+77 percent), tin (+115 percent), and
> tungsten (+44 percent). Lead, thallium, tin, and tungsten are toxic
> metals that can impair brain development and function, and also
> interfere with the normal functioning of other body organs and
> systems.
> A statistical analysis was conducted to determine if the levels of
> toxic metals were associated with autism severity, using three
> different scales of autism severity. It was found that 38-47 percent
> of the variation of autism severity was associated with the level of
> several toxic metals, with cadmium and mercury being the most strongly
> associated.
> In the paper about the study, the authors state “We hypothesize that
> reducing early exposure to toxic metals may help ameliorate symptoms
> of autism, and treatment to remove toxic metals may reduce symptoms of
> autism; these hypotheses need further exploration, as there is a
> growing body of research to support it.”
> The study was led by James Adams, a President’s Professor in the
> School for Engineering of Matter, Transport and Energy, one of ASU’s
> Ira A. Fulton Schools of Engineering. He directs the ASU Autism/
> Asperger’s Research Program.
> Adams previously published a study on the use of DMSA, an FDA-approved
> medication for removing toxic metals. The open-label study found that
> DMSA was generally safe and effective at removing some toxic metals.
> It also found that DMSA therapy improved some symptoms of autism. The
> biggest improvement was for children with the highest levels of toxic
> metals in their urine.
> Overall, children with autism have higher average levels of several
> toxic metals, and levels of several toxic metals are strongly
> associated with variations in the severity of autism for all three of
> the autism severity scales investigated.
> The study was funded by the Autism Research Institute and the Legacy
> Foundation.
> Media Contact:
> Joe Kullman, joe.kull...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/b9bbcdd86346bc78%3Fhl%3Den&msg=e1ed091efe6cf278>@asu.edu
> Ira A. Fulton Schools of Engineering
Newsgroups: sci.med, sci.chem, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/b9bbcdd86346bc78%3Fhl%3Den&msg=726a6b2ab48c0e41>
@gmail.com>
Date: Sun, 17 Mar 2013 20:44:57 -0700 (PDT)
Subject: PBS NEWSHOUR on chromium-6 Re: Need to add to my book of 1996
Metal Causation Diseases Re: Metals In Autism
On Mar 17, 5:54 pm, Archimedes Plutonium
Now in the PBS Newshour of Friday, March 15, Miles OBrien went to the
Wise Laboratory of Univ Southern Maine to see how dangerous Chromium 6
was to health and he shows a slide of a cell in replication of
mitosis, only instead of there being 2 centrosomes, there were 4
centrosomes-- very very dangerous.
Now we can take a clue or link to Alzheimers and Prion disease where
we have a waste build-up of plaques in the brain. Plaque build-up is
where protein filaments stick together in clusters and thus unable to
be removed.
So now, if Chromium 6 can mess up centrosomes so that there are 4
centrosomes when there should be only 2, means that metals can cause a
clumping of proteins when no clumping is wanted. In other words, the
metal caused two more clumps of genes. So if chromium 6 can cause
centers of clumping when none should clump, then metals can be the
same mechanism that causes plaques in Alzheimers or Prion.
Here we can see a mechanism in action. If the brain has toxic metals,
be they chromium-6 or the various compounds of mercury, as they get
into the brain, they cause clumping of proteins and thus, Alzheimers
or Prion.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/26a7911d1ae95eab%3Fhl%3Den&msg=5ec5252dd7e3850e>
@gmail.com>
Date: Mon, 18 Mar 2013 23:50:07 -0700 (PDT)
Subject: levels of mercury in children matches severity of Autism report:
Book:Metal Causation Diseases
Alright, I went to see if this research news was valid, and it turns
out to be very very valid. It was done by researchers at Arizona State
University and published in the journal Biological Trace Element
Research.
--- quoting ---
http://www.naturalnews.com/039492_autism_children_heavy_metals.html
<http://www.google.com/url?sa=D&q=http://www.naturalnews.com/039492_autism_children_heavy_metals.html&usg=AFQjCNFqIyeWKDgdTMqNB4_25-zfRc8ygA>
Based on three separate scales of autism severity, the researchers
also found that higher blood levels of toxic metals were associated
with more severe cases of autism. In fact, between 38 and 47 percent
of all variation in autism severity could be explained by varying
heavy metal levels, particularly cadmium and mercury. This made toxic
metal burden the single "strongest factor" predicting severity, the
researchers said.
--- end quoting ---
After 1996, I wrote this book whose underlying principle is that as
human society moves into the future, that we encounter more and more
chemicals that are not safe. And we encounter these chemicals
insidiously in the environment as more and more chemicals are offered
to us to make life more comfortable. Unfortunately many new chemicals
are very dangerous and lead to diseases. So if we go back in time to
Ancient Rome, we see the first dangerous chemical of lead in lead
pipes and containers to hold water and wine. Many ancient Romans were
poisoned by the lead or made mentally unstable. Moving on in history
we encounter mercury poisoning "mad as a hatter" but mercury was not
widespread in society until about the end of the 1800s
when coal was burned. So in the 1800s we had a new disease of "coal
black lung" but it was not widespread, only the miners affected. But
the mercury inside of the coal was released and the mercury since
1890s to 1970s became so very much widespread, that it caused the
diseases of Autism, Prion, Alzheimers, Parkinsons, and Schizophrenia.
In the interim of about 1960s to 1980s we had the Asbestos disease
where asbestos causes cancer and society paid a heavy price of cancer
and had to remove asbestos in all the buildings that could afford to
be removed. The people removing asbestos wore space suits to keep from
contaminating themselves.
Health and Medicine have a difficult time of realizing that diseases
are often caused by toxic substances, and whenever a disease comes
along that appears to be new or increasing in frequency, the obtuse
scientists look for a genetic cause, before they ever get the smarts
to think that increasing contact of toxic chemicals is the cause.
The average person in the world today is likely to encounter mercury
getting into their bodies on a daily frequency. All one has to do is
go outside and breathe in air for which all the coal fired plants
around the world, especially China and USA, coal fired plants put
enough mercury in the air that everyone in the world has a hard time
of avoiding the chemical mercury. And if you eat fish, you likely will
go to bed with as much mercury in you of a comparable level as the Mad
Hatters of past history.
Now in 1996 and thereafter, I was on these newsgroups begging and
pleading for scientists to run research on how much mercury in the
bodies of autism, parkinsons, alzheimers, prion and schizophrenia. It
looks like that data is finally coming in, even though rather late.
Now there was a very very silly report in the last decades pinning
autism to old men having babies and that their semen was the cause of
autism. A very silly and pathetic idea. It is that people do not want
to believe chemicals are toxic such as mercury, and look for any
excuse to blame something other than the true cause. If you think
about it, old men and their wifes with babies are more likely to go to
a hospital that is contaminated with mercury from broken incandescent
light fixtures and the babies injected with mercury laden vaccines.
Parkinsons disease is welders disease. If you want Parkinsons, just do
a lot of welding where you constantly are in contact with toxic
metals.
Prion disease is where the cause cannot even succumb to burning and
where you have to have deep burial-- sounds like what? Sounds like a
chemical, not a biological entity.
Alzheimers is the constant accumulation of toxic metals over the years
which forms plaques, just like what PBS's Miles OBrien showed on 15
March of 4 centrosomes when proper mitosis needs just 2 centrosomes.
If chromium 6 can cause a "plaque of genes", then mercury can cause a
plaque of proteins.
The rise in Autism from 1950 to 1 in 1000 and now it is 1 in 80, is
not because of under-reporting as the hazy and obtuse scientists would
believe, but the rise parallels the rise in the amount of mercury in
daily contact with virtually every person on Earth.
Mercury is a very very dangerous metal as Dr. Wetterhahn of Dartmouth
College who died of mercury after spilling one drop on her hand. One
drop is all it takes, so just imagine all the mercury we breathe in
and eat on a daily basis, and then realize the increasing rise of
Alzheimers, Prion, Parkinsons, Schizophrenia, Autism. Not hard to
imagine at all.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/78f76b92e575a201%3Fhl%3Den&msg=5255b0c19c69f389>
@gmail.com>
Date: Tue, 19 Mar 2013 15:49:31 -0700 (PDT)
Subject: researchers measuring mercury inside body; geiger-counter style
device to measure elsewhere Book:Metal Causation Diseases
Sorry, I was typing too fast and should have typed fluorescent lamp
and not incandescent. Somehow I am mixing up the two when I fully know
that the fluorescent lamp contains mercury and the incandescent does
not. But perhaps that is good of me to keep informing people there is
a huge difference in that the one lamp when broken is exceedingly
dangerous to health, for once mercury is free and loose in a building,
it seems to stay around a long time and getting inside of human
bodies.
If it had been up to me, I would have outlawed the making and selling
of fluorescent lamps for all-time, because they simply are too
dangerous with mercury.
Now it is nice that humanity is beginning to measure how much toxic
metals in human bodies as seen recently from researchers at Arizona
State
University and published in the journal Biological Trace Element
Research. This report shows that infants with autism have more
mercury than those without autism.
But now, what we need also is a Geiger Counter type of instrument that
lets anyone measure the levels of mercury in the environment
especially buildings of homes, work or even hospitals.
Since mercury is pervasive in home products such as fluorescent lamps,
that we maybe stunned to find out that some places we frequent that
the building is so full of mercury on the floors and surfaces that it
is a health hazard.
So as we increase the measuring of mercury inside human bodies. Let us
also increase the measuring of mercury in our environment, especially
buildings. Let us invent a Geiger Counter type of machine that can
measure mercury.
And I would not be surprised at all, that many infant wards in
hospitals are unsafe to care for infants. I remember a recent accident
that happened in Sioux City Iowa where a bunch of fluorescent lamps
were accidentally broken and they had to call in a special clean up crew
wearing space-suits to remove the mercury. But think of all the times
fluorescent lamps are broken and no-one cared to clean up.
You see, that is the extra danger of mercury, you cannot see it.
Unlike asbestos or coal or lead-- you usually see something, the
dangerous chemical, but mercury is so invisible yet so dangerous.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/32d9853c6fc665fb%3Fhl%3Den&msg=62159bc8578d4ea2>
@gmail.com>
Date: Thu, 21 Mar 2013 00:33:44 -0700 (PDT)
Subject: update on Autism frequency to 1 in 50 infants Book:Metal Causation
Diseases
PBS Newshour tonight updated the prevalence of Autism disease. It used
to be 1 in 110, then it dropped to 1 in 88, but tonight a revision has
been proclaimed that the latest data of science gives the figure of 1
in 50 infants of the same age has autism.
Now this book places the cause of Autism, along with Parkinsons,
Alzheimers, Prion and Schizophrenia, the cause being a metal in the
body that makes cells go corrupt. Usually the metal is mercury, but
other metals can do the harm.
When I wrote this book in 1996, the prevalent view of these diseases
was a hereditary or genetic cause. And still today with clear evidence
from researchers at Arizona State University and published in the
journal Biological Trace Element Research. What they found is that the
levels of severity of Autism matches the amount of mercury and other
metals found in autistic children and not found in normal children.
Now years back, some people tried to lawsuit the drug companies for
vaccines laced with mercury as the cause of their child's autism but
the court system was far far too
obtuse, and in the woods about metal causing diseases. Obtusity of
metal disease reflects obtusity in general areas of life-- for many
people still cannot believe in global warming when even after the ice
caps are melted away. If they put someone on trial for global warming
the same results would have likely happened.
So the Arizona State University research linked mercury to Autism.
What I would like to see now is a link up of the frequency rate of
Autism reported through the years to the susceptibility of getting
mercury inside of infants bodies in that same time period.
So we have this historical data:
1970s to 1990 the Autism frequency was 1 in 110
1990s to 2010 the Autism frequency was 1 in 88
2010 to present the Autism frequency was 1 in 50
Now I would like to see researchers filling in this table:
1970s to 1990 the susceptibility of getting mercury inside a human
body in that time period was 1 in 110 of getting a specific quantity.
In that time period, China did not spew mercury in the air in coal
fired plants and fluorescent lamps were not widespread and the mercury
in fish in oceans was not that horribly bad
1990s to 2010 the susceptibility of getting mercury inside a human
body in that time period was 1 in 88 because China along with the USA
filled the atmosphere, the air we breathe with so much mercury that
the figures went from 1 in 110 to 1 in 88
2010 to present, the mercury in fish food because of the mercury in
the air goes into the oceans, that the frequency of catching Autism of
1 in 50 matches the overall prevalence of mercury in our daily life.
It is extremely difficult in modern life to go through a day without
breathing, eating or drinking some mercury atoms.
Now, Autism is mercury and metal poisoning of the young people, and
Alzheimers is the accumulation of that mercury for all those years. So
that if mercury does not give you Autism while you are a youngster,
then the lifelong intake of mercury will finally catchup with you with
Alzheimers disease.
Bleak, bleak, bleak it is. But look on the good side-- we cannot live
forever. Also, there are some foods that combats the mercury build up
in the body, and so I overdose on those foods. Whether it is working
well, I cannot be sure, but I am now 63 in a few months and at the
peek-prime of doing physics, so something seems to be working.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/d841852396479f92%3Fhl%3Den&msg=aec47d3457e0c410>
@gmail.com>
Date: Thu, 21 Mar 2013 13:32:33 -0700 (PDT)
Subject: Math-Statistical proof that these diseases are caused by metals:
book Metal Causation Diseases
I am going to open up a topic of huge importance to biology. How much
of a proof is mathematical statistics in biology-- is the main
question. And I devote an entire chapter in this book to that
question.
Is statistical evidence a proof in science that metals cause the
diseases of Autism, Alzheimers, Parkinsons, Schizophrenia, Prion?
Back in 1996 when this book of mine began with posts to the Internet
science newsgroups, I was wanting researchers to measure how much
mercury was in the bodies of normal people compared to autistic
people. Well, I had to wait a long time until 2013 with this Arizona
State University report:
--- posted in sci.med ---
> Study finds higher levels of several toxic metals in children with
> autism
> Posted in: Faculty, Research
> James Adams, a professor of materials science and engineering, has
> done extensive research into autism. He directs the ASU Autism/
> Asperger’s Research Program.
> Posted February 25, 2013
> In a recently published study in the journal Biological Trace Element
> Research, Arizona State University researchers report that children
> with autism had higher levels of several toxic metals in their blood
> and urine compared to typical children. The study involved 55 children
> with autism ages 5–16 years compared to 44 controls of similar age and
> gender.
--- end quote ---
I need to track down that full report in that journal.
But the question looms large-- if we see spectrum levels of autism
matching the amount of mercury in the bodies of autistic children,
then to me, that is math-statistical proof that mercury is the cause
of autism.
Now I would like to further that Statistical research to the history
of autism and its frequency during the past 150 years.
So we have this historical data:
1970s to 1990 the Autism frequency was 1 in 110
1990s to 2010 the Autism frequency was 1 in 88
2010 to present the Autism frequency was 1 in 50
Now I would like to see researchers filling in this table:
1970s to 1990 the susceptibility of getting mercury inside a human
body in that time period was 1 in 110 of getting a specific quantity.
In that time period, China did not spew mercury in the air in coal
fired plants and fluorescent lamps were not widespread and the mercury
in fish in oceans was not that horribly bad.
1990s to 2010 the susceptibility of getting mercury inside a human
body in that time period was 1 in 88 because China along with the USA
filled the atmosphere, the air we breathe with so much mercury that
the figures went from 1 in 110 to 1 in 88
2010 to present, the mercury in fish food because of the mercury in
the air goes into the oceans, that the frequency of catching Autism of
1 in 50 matches the overall prevalence of mercury in our daily life.
It is extremely difficult in modern life to go through a day without
breathing, eating or drinking some mercury atoms.
Last night, before going to bed I was wondering how Schizophrenia
statistics would come out with mercury as the culprit. My memory is
hazy at the moment, but I believe I read somewhere that in the 1800s
or early 1900s that schizophrenia was a rich man's or rich women
disease. So I was thinking of possibly silver in silverware.
But then it dawned on me that rich people often smoke and come to find
out that cigarettes and cigars have quite a bit of mercury in them.
But it is not the quantity of mercury in smoking but rather the
intense high heat involved in smoking that transforms the mercury into
especially dangerous form of mercury.
So I went to look for frequency of schizophrenia disease and
pleasantly found that countries that heavily smoke such as China and
Asia are the highest rates of Schizophrenia. And that the USA is far
lower in this disease, probably because the USA is anti-smoking. So
here is another statistical research opportunity.
*9) Depression*
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/d841852396479f92%3Fhl%3Den&msg=e9a93022d67b5494>
@gmail.com>
Date: Fri, 22 Mar 2013 01:15:16 -0700 (PDT)
Subject: logically need to include Depression as caused by too much
mercury: Metal Causation Diseases
On Mar 21, 3:32 pm, Archimedes Plutonium
<plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/d841852396479f92%3Fhl%3Den&msg=e9a93022d67b5494>@gmail.com>
wrote:
> So I went to look for frequency of schizophrenia disease and
> pleasantly found that countries that heavily smoke such as China and
> Asia are the highest rates of Schizophrenia. And that the USA is far
> lower in this disease, probably because the USA is anti-smoking. So
> here is another statistical research opportunity.
Major logical problem: Metal Causation Diseases of Autism,
Depression, Alzheimers, Parkinsons, Schizophrenia, Prion
Alright I have run into a major logical problem. I claim many metals
cause major diseases but mostly mercury is the main disease causing
metal. Chromium-6 is dangerous also, but I am focused on the brain
diseases and metals. I do not know if Chromium-6 can get past the
brain barrier, so I have to hunt that data down first.
But my major problem is this with mercury. At a baby to infant age
mercury causes Autism and mercury causes Schizophrenia
for teenagers in boys and 20s in girls and then there is a huge gap in
age of any major mercury causing disease until we reach the ages of 60
and beyond for Alzheimers and Parkinsons and Prion.
So there seems to be a gap of ages 30 to 40 to 50 to 60 for any major
mercury disease.
Now we would logically think that it is highly unreasonable to think
that the age of humans from 30 to 60 years of age is some sort of
protection or immunity from mercury intake into the body.
Nay, a logical person would reason that I missed a major mercury
causing disease category. So what disease is commonplace in humans and
is of ages 30 to 60. The answer is simple, Depression. It is a major
disease.
And one of the most successful cures for Depression is electrotherapy.
That is telling because mercury would be affected by electric
currents.
I had a look in Wikipedia for what modern medicine attributes the
cause and as usual the nattering nutter crowd of heredity and genes is
nattering away.
Now there are some good drug medications, but I think these only
alleviate the symptoms, not remove the mercury inside the head that is
the cause of depression. So it would be nice to analyze how these
medicines would affect cells that contain atoms of mercury.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/f5b8147ce2af761a%3Fhl%3Den&msg=aff429d283293e5b>
@gmail.com>
Date: Fri, 22 Mar 2013 14:58:04 -0700 (PDT)
Subject: statistics of Schizophrenia worldwide Chapt3 Math-Statistics
proving: Metal Causation Diseases
Now the importance of the Arizona State University research that
Autistic people have more mercury in their bodies than do normal
people is that we an actually begin to **measure the amount of
mercury** in bodies of afflicted people. And if the mercury load is
greater in diseased people than normal people, one can say it is
**Statistically proven via math that mercury is the cause**.
Now a better proving force is shown on the PBS Newshour where
hexavalent chromium, Chromium 6 is shown on Friday, March 15, Miles
OBrien went to the
Wise Laboratory of Univ Southern Maine to see how dangerous Chromium
6
was to health and he shows a slide of a cell in replication of
mitosis, only instead of there being 2 centrosomes there are 4
centrosomes.
So chromium 6 and cancer forming agent is proven to cause cancer.
Unfortunately we do not yet have a slide showing where mercury causes
plaques in cells to form Alzheimers or Prion disease.
In Chromium 6 we have direct eyewitness proof that it causes cancer.
In mercury as agent of the diseases Depression, Autism, Alzheimers,
Parkinsons, Prion, Schizophrenia we have no eye witness proof as yet,
but instead we have Mathematical Statistical proof that Autism is
caused by mercury, for we have that Arizona State University evidence
of a direct link and correlation between the severity of Autism and
the amount of mercury inside the body.
I looked it up and Chromium 6 is not able to cross the blood-brain-
barrier so chromium 6 does not cause these brain diseases I listed.
But today I want to focus on Schizophrenia and a Math-Statistical
proving it is caused by mercury, too much mercury intake into the
body. Of course, we need another Arizona State University type of
research on the mercury in the bodies of Schizophrenia patients
compared to normal patients. But have a look at this mapping in
Wikipedia under Schizophrenia Epidemiology:
That map shows Asia as the highest frequency of Schizophrenia with as
much as 295 cases per 100,000 inhabitants in 2004 and the USA is shown
to have around
197 cases while Mexico is shown to have 251 ( if I am reading the
colors correctly?). How does that map correlate with mercury in the
environment to Schizophrenia? Well, a lot of mercury is intaken into
the body from cigarette and cigar smoking and in Asia and Mexico,
smoking is commonplace. Also, China is the world's largest mercury
polluter due to its coal fired electric stations.
So, although we do not have direct eye witness evidence that
Schizophrenia is a mercury poisoning as we have that chromium 6 is a
cancer causing agent, we can test mercury in Schizophrenia patients
and make the correlations.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/85fbe2db0e58776c%3Fhl%3Den&msg=037dd7d4d33dcebc>
@gmail.com>
Date: Fri, 22 Mar 2013 23:57:21 -0700 (PDT)
Subject: Chapt3 Math-Statistics proving method: Metal Causation Diseases
Now let us examine the difference in scientific proving via a visual
demonstration versus a statistical matching of rates. What I mean is
that the chromium-6 was proven to cause cancer on PBS Newshour on
Friday, March 15, Miles OBrien went to the Wise Laboratory of Univ
Southern Maine to see how dangerous Chromium-6 was to health and he
shows a slide of a cell in replication of mitosis, only instead of
there being 2 centrosomes there are 4 centrosomes. Let us call that
the visual demonstration proof. And compare that to the Statistics
means of proving in science.
Statistics were done by researchers at Arizona State
University and published in the journal Biological Trace Element
Research.
--- quoting ---
http://www.naturalnews.com/039492_autism_children_heavy_metals.html
<http://www.google.com/url?sa=D&q=http://www.naturalnews.com/039492_autism_children_heavy_metals.html&usg=AFQjCNFqIyeWKDgdTMqNB4_25-zfRc8ygA>
Based on three separate scales of autism severity, the researchers
also found that higher blood levels of toxic metals were associated
with more severe cases of autism. In fact, between 38 and 47 percent
of all variation in autism severity could be explained by varying
heavy metal levels, particularly cadmium and mercury. This made toxic
metal burden the single "strongest factor" predicting severity, the
researchers said.
--- end quoting ---
So what we have is eye witness proving that Chromium-6 causes cancer
since it pulls apart centrosomes in mitosis. And we have Statistics
proving that the severity of Autism matches the amount of mercury
levels in the body of autistic children.
For chromium-6 we actually see the havoc of the metal in making 4
centrosomes and so we easily conclude it causes cancer. The proof is
in the seeing.
For mercury in Autism, we do not eye witness what the mercury actually
does, and what we have is math numbers of autism severity matching the
math numbers of the amount of mercury in the body.
Now the eye-witness proof is preferable than the numbers matching
proof. But sometimes we just have to wait for the technology to see
how the mercury causes autism.
Now let us run the chromium-6 through the Statistics way of proving,
for it offers us a lesson in reasoning.
Suppose we had a village in China that had many cases of stomach and
kidney cancer and we measured the bodies for metal in all those
patients and found that they had a lot of chromium-6 compared to
normal people. So, can we say that such a statistic is a proof that
chromium-6 caused the cancer? No, for we need a additional statistical
link-up. We need to show that if the chromium-6 amount in one patient
that had advanced cancer was a amount that matches the state of
advanced progression, compared to a smaller cancer and less
chromium-6, and compared to a normal person with no cancer and little
to none chromium-6 in the body.
So we can say Statistics is a proof method, if it links up with a
metal, and the rate of progression of the disease links up with the
amount of metal.
In the eyewitness proof, seeing is believing and chromium-6 is the
cause of cancer.
In the Statistics proof, we need two link-ups:
(i) the metal is present in a large quantity in the disease and not
present or small quantity in the non-disease.
(ii) the severity of the disease matches the statistics of increasing
levels of quantity. So that if we had a mild autistic child with x
amount of mercury and a severe case of autism of 2x amount of mercury
and a normal child with a tiny amount of mercury, that those numbers
serve as a proof that mercury causes autism.
So in a Statistics proof, it is not sufficient to have mercury present
to prove autism is caused by mercury, but that the amount of mercury
present matches the severity of the disease. So if you have both (i)
and (ii), then we can say mercury causes autism.
However, we would rather have the visual demonstration of where
mercury in cells, makes a normal child into autistic child.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/85fbe2db0e58776c%3Fhl%3Den&msg=f194e71c1a69eb18>
@gmail.com>
Date: Sat, 23 Mar 2013 13:20:29 -0700 (PDT)
Subject: cadmium versus mercury in Autism: Math-Statistics proving method:
Metal Causation Diseases
Now I probably need a 3rd category of a **Scientific Proof Method**
since in that
Arizona State University research they indicate two metals of cadmium
and mercury.
So how can (i) and (ii) standing alone distinguish whether the cadmium
is the cause or
whether mercury is the cause or whether the two combined is the cause
of autism.
Now if we used just (i) and (ii) we could eliminate all the other
metals such as aluminum
or copper or iron etc etc because none of them would match a severity
level of autism with a quantity of that metal. However, (i) and (ii)
could not eliminate cadmium.
So, do I need a third criterion? I think so, and the third would
involve toxicity. How much cadmium alone is a noticeable toxin on a
human body and how much is mercury?
Well, for mercury the answer is very simple in that just one drop of
mercury is enough to kill a human being. Is one drop of cadmium
enough? At Dartmouth College in the 1990s, a chemistry professor Dr.
Wetterhahn died of mercury poisoning from a single drop accidently
spilled, and her gloves were incapable of protecting her as the
mercury went straight through the glove.
Mercury is perhaps the single most dangerous non radioactive toxin on
Earth, yet, we humans as a society continue to fill our houses, homes,
hospitals with all sorts of devices and implements that contain
mercury. Walk into any hospital across the USA and you will find
fluorescent lamps filled with mercury for which when they cease
working, a workman has a chance of breaking the lamp and filling the
hospital floors and rooms with mercury poison, and when these lamps
are discarded, end up in the landfill where the mercury leaks out and
contaminates the water we drink.
So I need a third category:
(iii) A tiny amount of the toxin is able to do vast damage to a
individual human being.
So if I ran cadmium through (i), (ii) and (iii) then it would fail at
(iii), although cadmium is toxic, it requires more cadmium to cause
death in humans.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/85fbe2db0e58776c/0697d885216c83f8%3Fhl%3Den%26lnk%3Draot&msg=0697d885216c83f8>
@gmail.com>
Date: Sat, 23 Mar 2013 21:44:22 -0700 (PDT)
Subject: more on cadmium Re: Math-Statistics proving method : Metal
Causation Diseases
On Mar 23, 3:20 pm, Archimedes Plutonium
<plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/85fbe2db0e58776c/0697d885216c83f8%3Fhl%3Den%26lnk%3Draot&msg=0697d885216c83f8>@gmail.com>
wrote:
> On Mar 23, 1:57 am, Archimedes Plutonium
(snipped)
> Mercury is perhaps the single most dangerous non radioactive toxin on
> Earth, yet, we humans as a society continue to fill our houses, homes,
Sorry, mercury is probably not the most dangerous non-radioactive
element
but it is certainly dangerous.
And, I am learning about cadmium and it appears to be similar to
mercury, although not as toxic.
Cd even forms mercuric cadmium compounds.
I was reading where cadmium is taken into the body via smoking of
cigarettes. So like mercury, cadmium
is commonly found in human bodies.
Cadmium is often found in batteries and when they are thrown in trash
landfills they likely leak out and
get into the water supply.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/3e5065c6b930f64c%3Fhl%3Den&msg=e9fc6e6aa976e23e>
@gmail.com>
Date: Sun, 24 Mar 2013 00:30:18 -0700 (PDT)
Subject: Arizona State U research run on Alzheimers, Schizophrenia,
Parkinsons, et al: Math-Statistics proving method : Metal Causation Diseases
Alright, what was done in research by Arizona State University for
Autism, and thus proving by statistics that autism is caused by heavy
metals in the body, the same sort of research needs to be done for
Schizophrenia, Parkinsons, Prion, Depression, and Alzheimers.
> Statistics were done by researchers at Arizona State
> University and published in the journal Biological Trace Element
> Research.
> --- quoting ---
http://www.naturalnews.com/039492_autism_children_heavy_metals.html
<http://www.google.com/url?sa=D&q=http://www.naturalnews.com/039492_autism_children_heavy_metals.html&usg=AFQjCNFqIyeWKDgdTMqNB4_25-zfRc8ygA>
> Based on three separate scales of autism severity, the researchers
> also found that higher blood levels of toxic metals were associated
> with more severe cases of autism. In fact, between 38 and 47 percent
> of all variation in autism severity could be explained by varying
> heavy metal levels, particularly cadmium and mercury. This made toxic
> metal burden the single "strongest factor" predicting severity, the
> researchers said.
> --- end quoting ---
Now autism has severity levels and those levels can be correlated by
the quantity of mercury or cadmium in the body.
I do not know if Alzheimers, Parkinsons, Schizophrenia, Prion and
Depression have levels of severity. I would think Alzheimers,
Parkinsons and Prion have progressive stages of the disease where it
continually gets worse as the plaques build up or Parkinsons tremors
increase, but I would suspect the heavy metal build-up is not
increasing.
So in the case of Alzheimers Parkinsons and Prion, there maybe a
accumulative load of heavy metal that starts the onset and the disease
then feeds on that load. Now I do remember a report in England in the
1990s where a group of people contracted an accelerated form of CJD, a
prion disease, and where all had one thing in common, eating at a
restaurant. That sounds like a classic case of getting too much
mercury or other heavy metals. I do not suppose autopsies can be run
on those individuals to see if they had excess mercury in their
bodies.
A research into how much heavy metals in Schizophrenia and in
Depression patients needs to be carried out.
So it looks as though ASU has started some big, good, and new science
research in medicine, and now we need to expand it from just Autism to
that of these other diseases-- Alzheimers, Parkinsons, Schizophrenia,
Prion, Depression.
Now I wonder if Depression comes in severity levels?
And I wonder from the map in Wikipedia on Schizophrenia having the
highest rates in Asia showing 273 to 295 cases per 100,000 while the
USA and Canada have just 197 per 100,000, whether Schizophrenia has a
high quantity of heavy metal and whether that is due to the higher
rates of cigarette smoking in Asia. So it looks as though what ASU has
started in measuring metals in the bodies of disease patients, needs
to be extended to a broader class of diseases-- all of them brain
diseases.
And we should not stop with human disease of heavy metal, but notice
that bees have what is called
"Colony Collapse Disorder", with something gone wrong with the bee's
mind in orientation which sounds like mercury. So can someone do a
research as to the heavy metal load in bees suffering from CCD?
Also, many whales and other sea creatures get disoriented and beach
themselves. And here again we need a research study to see if it is
caused by heavy metals.
And also, the Mad Cow Disease, the prion disease is highly likely to
be a mercury causing disease and we need to run the same tests on MCD
as Arizona State University ran on Autism.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/01bb9206e4be1a1d%3Fhl%3Den&msg=46fdff6ff5f95c18>
@gmail.com>
Date: Sun, 24 Mar 2013 21:40:25 -0700 (PDT)
Subject: moths gone extinct due to mercury? is the honeybee next?
Math-Statistics proving method : Metal Causation Diseases
Moths gone extinct and is the honeybee next due to mercury
Like the parrot in the coal mine to alarm us of danger. The honeybee
maybe the parrot of the insect world. The main thesis of this book is
that these 6 diseases are caused by heavy metals in the body, mostly
mercury. Autism, Alzheimers, Parkinsons, Prion, Schizophrenia,
Depression.
But since mercury is made so common in our environment from coal fired
power plants, burning fossil fuels, that every living body on Earth is
likely to take in many atoms of mercury each and every day. If this
mercury can cause those 6 diseases, then imagine what that mercury
would do to a small creature like insects.
So I went to look up what insect species have gone extinct recently
and was guessing that mercury would affect moths and flies more than
any other insect. And sure enough according to this report, moths take
the majority of extinctions.
http://www.petermaas.nl/extinct/lists/insects.htm
<http://www.google.com/url?sa=D&q=www.petermaas.nl/extinct/lists/insects.htm&usg=AFQjCNEziIrcTNqZk9fzJYb7be-K9K_suA>
If it takes just a little mercury to cause those 6 human diseases then
imagine how devastating it would be on honeybees.
Now I remember a report in China where a community had pear trees that
had to be hand pollinated because all the bees were absent. So I
wonder if there is a nearby coal fire power station spewing mercury
into the air?
Now I remember that France did not have the Colony Collapse Disorder
of bees that the USA has, and whether the fact that France has mostly
nuclear power generation and few coal fired plants to spew mercury
into the air.
Now the Arizona State University conducted a research into how much
mercury in the bodies of Autism children. I wonder if they could
conduct a research into telling us how much mercury is in the "air
around the campus of Arizona State University".
Now I remember a few years back reading a report that Utah had one of
the highest rates of autism in the country and that Utah was downwind
of Nevada, one of the most heavy mining and smelting of mercury in the
USA. So can Utah conduct a air test for mercury?
And of course, can someone conduct a ASU type research into how much
mercury is in the bodies of these honeybees and whether the diseased
bees have more mercury than normal bees.
Newsgroups: sci.med, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/01bb9206e4be1a1d/3cc6bbde325c8ad4%3Fhl%3Den&msg=aa2c9f454cb5d201>
@gmail.com>
Date: Mon, 25 Mar 2013 15:15:29 -0700 (PDT)
Subject: Re: moths gone extinct due to mercury? is the honeybee next?
Math-Statistics proving method : Metal Causation Diseases
On Mar 25, 2:27 pm, Rosario1903 <Rosa...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/01bb9206e4be1a1d/3cc6bbde325c8ad4%3Fhl%3Den&msg=aa2c9f454cb5d201>@invalid.invalid>
wrote:
> On Sun, 24 Mar 2013 21:40:25 -0700 (PDT), Archimedes Plutonium
> <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/01bb9206e4be1a1d/3cc6bbde325c8ad4%3Fhl%3Den&msg=aa2c9f454cb5d201>@gmail.com>
wrote:
> >Moths gone extinct and is the honeybee next due to mercury
> >Like the parrot in the coal mine to alarm us of danger. The honeybee
> >maybe the parrot of the insect world. The main thesis of this book is
> >that these 6 diseases are caused by heavy metals in the body, mostly
> >mercury. Autism, Alzheimers, Parkinsons, Prion,
> but prion are not pieces of dna? are not virus but as virus... right?
Well, in my scientific opinion, Stanley Prusiner is one of the worst
cranks and
crackpots in biology to ever come along with his idea that Prions are
self replicating
proteins to cause CJD, spongiform encephalopathy and BSE mad cow
disease and scrapie in
sheep. To account for all of these prion-diseases, we need only heavy
metals such as mercury poisoning.
And now that Arizona State University researchers have paved the clear
and pretty way of measuring metals in the bodies of diseased
individuals (Autism in humans) it is obvious that we should test for
mercury in BSE, scrapie, CJD and other alleged prion diseases.
Prusiner committed the worst sin of all sins in science thinking--
assuming something to be true without proving it to be true --
proteins causing the disease and thus narrowing his field of causative
agents -- yet never scientifically eliminating heavy metals as a toxic
substance that can cause protein plaques. And to such poor and pitiful
science work that Prusiner has given, they award him a Nobel prize.
May as well give a Nobel prize to Ed Conrad for man as old as the
Devonian Age coal. What Stanley Prusiner teaches us about science in
the past 100 years, is that the prizes given to scientists is not for
merit, but for those connected to a religion.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/f9aa92c15597072d%3Fhl%3Den&msg=1e200348fb601842>
@gmail.com>
Date: Tue, 26 Mar 2013 13:37:54 -0700 (PDT)
Subject: mercury as a catalyst in Prion and Alzheimer : Math-Statistics
proving method : Metal Causation Diseases
The disease sequence-progression of Prion and Alzheimers
Now in the PBS Newshour of Friday, March 15, Miles OBrien went to the
Wise Laboratory of Univ Southern Maine to see how dangerous Chromium
6
was to health and he shows a slide of a cell in replication of
mitosis, only instead of there being 2 centrosomes, there were 4
centrosomes-- very very dangerous.
Now we can take a clue or link to Alzheimers and Prion disease where
we have a waste build-up of plaques in the brain. Plaque build-up is
where protein filaments stick together in clusters and thus unable to
be removed.
So now, if Chromium 6 can mess up centrosomes so that there are 4
centrosomes when there should be only 2, means that metals can cause
a
clumping of proteins when no clumping is wanted. In other words,
the
metal caused two more clumps of genes. So if chromium 6 can
cause
centers of clumping when none should clump, then metals can be
the
same mechanism that causes plaques in Alzheimers or Prion.
Now let us spend some time with Prion disease and what its likely
mechanism is when mercury is its causative agent.
Chromium-6 is not involved in Prion disease, at least that is my
present understanding since hexavalent chromium cannot pass through
the blood-brain-barrier but mercury compounds easily pass through.
If I recall correctly the normal body makes prion proteins as
substance for the walls of cells. And pictures of these molecules
shows they contain metals such as copper and zinc as normal prions. In
the case of the disease, the body makes too much of the protein and
the overload starts clumping together. Much like Alzheimers where it
starts clumping into beta amyloid or tau plaques, only in the case of
Prion disease, it clumps in prion proteins. So that Alzheimers is very
similar in its mechanism of an unwanted protein, where the body makes
too much and where the body clean-up cannot get rid of the protein
build-up.
So far, it sounds like mercury or compound of mercury acting like a
catalyst. If you remember a catalyst in chemistry speeds up a reaction
and ends up leaving the catalyst untouched at the end.
So for Prion disease, or Alzheimers, some mercury compound, let us
guess mercuric-cesium or mercuric cadmium or mercuric fluorine, some
other compound gets into the brain of an individual and meets the
processing of prion proteins where it becomes incorporated into the
processing that then spews out misshapen prion proteins instead of
normal proteins. In the case of Alzheimers, the mercuric compound gets
into the manufacturing process of normal tau and beta molecules and
becomes part of that manufacturing process where it produces misshapen tau
and beta molecules.
And because it is a catalyst, wrecking the manufacturing of proteins,
the dangerous disease causing mercury keeps going around altering the
protein manufacturing process.
If I remember correctly both Prion and Alzheimers require a threshold
of bad proteins to initiate the disease, which if true, rings of the
idea of a toxin threshold. And in the case of Prion disease, when
other animals eat the brains of an infected animal, it is not the
prions that are the danger, but the mercury compound that started the
disease.
Now that makes a startling prediction that if the brains of an
Alzheimers victim were eaten, that the mercury compound could cause
the disease all over again in the person doing the consuming. Or, it
may predict that some rare cases of people who contract both Prion
disease and Alzheimers simultaneously due to the mercury catalyst
involved.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/f9aa92c15597072d/e5b646808bdb5771%3Fhl%3Den&msg=e5b646808bdb5771>
@gmail.com>
Date: Wed, 27 Mar 2013 08:25:34 -0700 (PDT)
Subject: sleep involved in these 6 diseases : Math-Statistics proving
method : Metal Causation Diseases
Math Statistics of Sleep involved in Autism, Alzheimers, Parkinsons,
Depression, Schizophrenia, Prion.
Now let me list those 6 diseases according to when in life, they have
onsets.
1) Autism is first since it comes soon after birth
2) Schizophrenia is second since it attacks in the teenager years
3) Depression is next since it attacks from age 20s to throughout the
remainder of life
4) Parkinsons comes slightly before Alzheimers at about 50 years age
5) Alzheimers arrives at about 60
6) Prion such as CJD arrives a little later than Alzheimers
Now the Mathematical Statistics way of proving these diseases are all
a heavy metal based disease is that we measure the metals inside the
bodies of diseased individuals and we compare the severity level of
disease with the amount of metal in the body. If there is a
correlation such as the Arizona State University matching cadmium and
mercury with Autism severity, means Autism is caused by mercury
poison.
But if all 6 diseases are mercury poison related, then there should be
a obvious sign in symptoms of all 6 diseases. Such an obvious sign is
disorientation and the proneness of sleeping. In Autism, we have
failure of eye contact and a proneness to wanting to go to sleep. In
Alzheimers and Depression we see extensive sleeping for it is sleep
that counteracts the disease. I am not sure about Schizophrenia
whether the patient is prone to sleeping, but in Parkinson's the
physical handicap of shaking forces sleeping.
Sleep and disorientation are one and the same affliction and
counteraction of the disease.
Now if you encounter a person poisoned by mercury, their behavior is
one of sleeping and disorientation.
So these symptoms do not prove that mercury causes all 6 diseases, but
supports the claim that mercury is likely to be the underlying
causative agent. What proves it is that we need the same research of
ASU run upon the other 5 diseases.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/f9aa92c15597072d/1c8a56ef580fbe48%3Fhl%3Den%26lnk%3Draot&msg=1c8a56ef580fbe48>
@gmail.com>
Date: Wed, 27 Mar 2013 23:13:10 -0700 (PDT)
Subject: why lithium and electric shock treat Depression : Math-Statistics
proving method : book Metal Causation Diseases
Now I see that lithium is helpful in treating depression. So if
mercury is the causative agent of clinical depression, we should find
some link with lithium and mercury.
Now one treatment for depression is electric shock therapy, and we
know that mercury is extremely good at electrical conduction. So the
link there would be that electric shock focuses on the mercury content
in the body.
But is there some link up of lithium with mercury?
I was able to find this piece of information, which implies some
special connectivity of lithium and mercury.
--- quoting from Wikipedia on isotopes of lithium ---
Colex separation
Lithium-6 has a greater affinity for the element mercury than lithum-7
does. When an amalgam of lithium and mercury is added to solutions
containing lithium hydroxide, then lithium-6 becomes more concentrated
in the amalgam and lithium-7 more in the hydroxide solution.
This is the basis of the colex (column exchange) separation method, in
which a counter-flow of amalgam and hydroxide passes through a cascade
of stages. The fraction of lithium-6 is preferentially drained by the
mercury, but the lithium-7 flows mostly with the hydroxide.
--- end quote ---
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/961c53b0524ef12d%3Fhl%3Den&msg=57e921cef10182ea>
@gmail.com>
Date: Mon, 1 Apr 2013 00:56:26 -0700 (PDT)
Subject: Metal Causing Diseases (Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion)
Since I cannot start over but rather, am adding to an existing book, I
am going to number these in negative numbers where I feel they should
belong when I do the 2nd edition.
The title of the book is:
Metal Causing Diseases (Autism, Schizophrenia, Depression, Parkinsons,
Alzheimers, Prion)
This book was started in 1996 when I started to tackle the disease
prion disease. Back in 1996, I thought the cause was a fungus, for I
had seen a disease in ants where fungus end up killing the ants with a
brain disease. As the years wore on, I slowly began to end up with the
cause being metals in the environment and included 5 more diseases
along with prion disease.
Usenet book 1996-2013 (assimilated
in April 2007 in sci.med,sci.chem,sci.bio.misc)
(a) History of this book
(b) earlier metal diseases: lead then mercury then asbestos
(c) experimental math-statistical proof that autism is caused by
mercury and cadmium and the mechanism is similar to chromium-6
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/961c53b0524ef12d%3Fhl%3Den&msg=6f0fe944d2330720>
@gmail.com>
Date: Mon, 1 Apr 2013 01:46:41 -0700 (PDT)
Subject: Metal Causing Diseases (Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion)
History of this book
This book started on Usenet of 1996 posts in science newsgroups as
seen by the three posts below.
I made some remarks and commentary on Prion disease in 1996 and then
launched a research into what causes it-- hearing about a TV story on
ants.
In 2007 I assimilated my Usenet posts on the subject as a book. I
never counted up the posts I made on the subject from 1996 to 2007,
but I would hazard to guess it was approximately a 1,000 to 2,000
posts on the subject.
--- quoting my early 1996 posts that started this book ---
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/961c53b0524ef12d%3Fhl%3Den&msg=6f0fe944d2330720>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,alt.sci.physics.plutonium,sci.bio.misc
Subject: .5 of UK infected by CJD? solution is CLONING
Date: 12 Apr 1996 01:47:11 GMT
It was reported in the NEW SCIENTIST 30MAR96 that the highest rate of
infection of the prion CJD or BSE for humans for UK could reach almost
1/2 of the population. That is most alarming. Instead of a viral attack
on humanity it may turn out to be a cocktail mixture of virus and prions.
And how we thought that a solution for AIDS was a cocktail of drugs.
The little beasties may be playing us at our own game.
Our Maker, our Creator seems to want to end wars for humanity,
perhaps for alltime. Perhaps we will never need another WW1 or WW2, and
that a WW3 will never come about, because population control will now
be taken on by the little beasties of the world. The prions and the
virus and the bacteria and the protozoans will mount attacks on
humanity that will make the bubonic plague of olden times look like a
Sunday picnic.
Imagine if 1/2 of the UK population is smitten with the prion
disease and has less than 10 years of life.
Pharmaceutical companies are merely a cry in the dark with prion
disease. Prion disease is almost a mineral. Sort of like radioactive
nuclear waste.
The answer is not drugs to combat the next prion outbreak or viral
outbreak. The answer is human cloning. Clone humans and should a
disease wipe out 90 percent of the population, clone the resistant
humans.
If one thing biology has taught us, is that we are impotent in
exterminating diseases. So we have to play to the diseases weaknesses.
Never does a disease exterminate all of humanity, likewise, never does
humanity exterminate a disease. Thus, we must increase the resistant
humans to all viral and prion diseases that ever infest humanity.
That is why cloning is a great weapon in the arsenal against
diseases. Should a disease become so aggressive as to wipe out huge
populations, we must be ready to clone in large numbers the resistant
humans.
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/961c53b0524ef12d%3Fhl%3Den&msg=6f0fe944d2330720>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups:
sci.bio.technology,misc.invest.stocks,alt.sci.physics.plutonium,sci.bio.mis
c,sci.chem
Subject: Patent on a cure for prion spongiform; Chiral chemistry
Date: 16 Apr 1996 18:00:34 GMT
I am posting what I suspect will be the cure and a treatment for prion
spongiform.
The science behind this is that of chiral chemistry. To detail the
prion spongiform protein and then make the opposite twist to both the
dangerous prion and the normal prion. The opposite twist, ie, chiral
chemistry should attract and defuse the dangerous prion. Since I do
not
have the lab, it could be the chiral of the normal protein which
defuses the bad protein.
Also in this patent claim will be claims for treatment of existing
spongiform in mammals. The technique involves the protein bad prion
and
existing plaques in the brain. Use monoclonal magic bullets and
develop
a molecule which as a scissors cuts the existing plaque.
If memory serves me, Bayer of Germany is the worlds premiere company
working in chiral chemistry. I have until April 16, 1997 to submit
patent claims on chiral chemistry of antiprion pharmaceuticals.
--- end quote ---
Now one of my early first on guesses as to what caused prion disease
was a fungus as seen in this 1997 post:
--- quoting a post ---
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/961c53b0524ef12d%3Fhl%3Den&msg=6f0fe944d2330720>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,sci.bio.misc
Subject: Cordyceps Ascomycetes Clavicipitacea; ant checked for prion
disease?
Date: 10 Oct 1997 23:55:34 GMT
I wrote yesterday:
> The fungus disease that infects ants is somewhat similar to the
> symptoms of prion brain disease. Does anyone know the name of the
> fungus that causes the ant disease?
And thank goodness someone else gave me the information:
Name of the ant fungus you are thinking about is probably the genus
_Cordyceps_
(Ascomycetes: Clavicipitacea)
Here is what is said about it in "The Ants" (Wilson & Holldobler,
1990):
"...the largest of the entomophagous fungi and often brightly colored
as well.
The multicellular mycelium pervades the host thoroughly, killing it.
It
often produces asexual spores or conidia, in which the case the
specimen has been placed in "_Isaria_", a genus of convenience
classified as one of the imperfect fungi. Eventually the mycelium
sprouts a boll- or club-shaped organ on a stalk that protrudes as much
as 10 centimeters outside the body of the host. The swollen terminus
of
this structure contains numerous ascocarps, each generating spores
within elongate cells or asci. It is a startling experience to
encounter a large ant, dead yet standing rigidly at attention with a
_Cordyceps_ sporophore raised above it like a flag. At least some
species of this genus occur on more than one species of insect host."
+++++
Has anyone checked ants who have been infected by such for prion
brain
disease? I do not know how little of a brain an ant has. But, has
anyone checked ants infected by this fungus for spongiform
encephalopathy
--- end quote ---
Newsgroups: sci.chem, sci.med, sci.bio.misc From: Archimedes Plutonium
<plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/bc416ea595939f0a%3Fhl%3Den&msg=dbaded2cb99ca7b4>@gmail.com>
Date: Mon, 1 Apr 2013 14:08:06 -0700 (PDT) Subject: Metal Causing Diseases
(Autism, Schizophrenia, Depression, Parkinsons, Alzheimers, Prion)
Metal Causing Diseases (Autism, Schizophrenia, Depression, Parkinsons,
Alzheimers, Prion)
Chapt1: History of this book
Chapt2: earlier metal diseases: lead then mercury
Chapt3: asbestos diseases
Chapt4: experimental math-statistical proof that autism (ASU report)
is caused by mercury and cadmium and the mechanism is similar to
chromium-6 (PBS report)
Chapt5: Autism
Chapt6: Schizophrenia
Chapt7: Depression
Chapt8: Parkinsons
Chapt9: Alzheimers
Chapt10: Prion
Now I could not call asbestos a metal so I gave it its own chapter.
Now the reason I list the diseases the way I do, is because of
chronology age in which the diseases are likely to occur where autism
is the first disease to often unfold and prion is usually in very old
age.
Now this morning I was thinking of the gender difference between the
diseases, for I do recall that boys are more prone to autism than
girls by a ratio of 4 to 1 or 3 to 1.
So if mercury poisoning or some other metal poisoning is the cause,
what accounts for the gender ratio?
Well, the best I can do for the gender difference is to say that the
site in which the mercury attacks an infant is a difference in growth
between a male child and a female child. We all know that females seem
to mature in growth faster than do males, so the site in which the
mercury manipulates in the body is easier to manipulate in a boy child
than a girl child.
Now we have to look at the other 5 diseases to see if the metal
poisoning affects male and female differently.
At one time in my writings, long time ago, I said the gender
difference was that boys are more active and exploring and so if you
put boys and girls in a environment of too much mercury present, the
boys will breathe in more mercury than the girls staying in doors.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>
@gmail.com>
Date: Mon, 1 Apr 2013 23:35:15 -0700 (PDT)
Subject: My history on metal diseases: Metal Causing Diseases (Autism,
Schizophrenia, Depression, Parkinsons, Alzheimers, Prion)
This book started in 1996 when I decided to take on the disease Prion
and solve its causation. Unfortunately from 1996 to 1999, I still
clung to some biology explanation, not thinking it was purely a metal
caused disease, and even though I started to consider metals as the
cause, it took me much longer to drop everything and say it is all
metal caused disease.
As I look back now at my own history of these 6 diseases, I am
somewhat saddened of how long it took for me to come out of the "shell
I was in" and not realize quicker that it is a metal caused disease,
especially after reading Collinge report in 1999 and then a week later
writing about Wilson's disease which is a copper poisoning disease.
I pride myself on my logic as my main asset in doing science, but I
failed in June of 1999, to have thence, right then and there, realized
that Prion disease was a metal poison disease. And in fact, it took me
until August of 2003 to have a subject title stating that prion
disease was caused by metal poisoning:
Subject:
prion disease is a Metal-Ion disease/poisoning Re:
Prion:
Date:
Fri, 29 Aug 2003 12:18:48 -0500
But here, now let me relist three posts of 1999. And any reader can
Google search all my posts to Usenet, several thousands on Prion and
the 6 diseases from 1996 to present.
----------------
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.med,sci.bio.technology,sci.chem
Subject: copper/zinc involved with Prion Disease
Date: 13 May 1999 06:46:45 GMT
Organization: prion disease news
Lines: 76
Distribution: world
Message-ID: (7hdsgl$qph$3...@dartvax.dartmouth.edu>
--- quoting NEW SCIENTIST, 8MAY99, p. 22 ---
Shape Shifters
Prions, the twisted proteins thought to cause BSE, Creutzfeldt-Jakob
disease and other related conditions need metal atoms to maintain
their deadly shapes, say researchers in London.
Prion diseases start when the shape of a brain protein called PrP
changes. In this form the protein is insoluble and begins to form
clumps in the brain, killing nerve cells. Many biologists think these
misshapen proteins are the infectious agent that spreads the disease--
although some think a virus is involved.
Some prion diseases exist in several different strains. People who
support the "protein-only" theory believe that each strain represents
a prion with a slightly different shape. Now a team led by John
Collinge of Imperial College, London, has evidence that metal ions
maintain the shape of the prion. "We've been trying to understand this
for some time," he says.
To study prion strains, researchers use an enzyme that digests protein
to break down infected brain tissue and reveal the characteristic
patterns of PrP fragments. Collinge's team has now found that changing
the amounts of copper or zinc in a solution bathing tissue from
patients with CJD seems to cause prions to shift shape from one strain
to another (NATURE CELL BIOLOGY, vol 1, p.55).
If these lab-created strains of CJD could infect animals, and produce
symptoms typical of the strain in question, says Collinge, that would
be the best evidence yet for the protein-only theory.
Collinge says his lab is already working on the necessary animal
experiments, and he expects results within two years. "If they could
do that, I'd definitely be impressed," says Laura Manuelidis of
Yale.., a long-standing sceptic of the protein-only theory.
--- end quoting NEW SCIENTIST, 8MAY99, p. 22 ---
Well, I do not know what to make of this news. I did say in that long
debate with Messr. Bruner, Bennett, and Pelletier that prion disease
mechanism maybe something like a radioactive decay mode in the protein
molecule, although copper and zinc are not radioactive decay. Then
again, it may be a form of radioactive copper and zinc that start the
prion disease. Has Collinge inspected the copper and zinc atoms?
And, even if metal ions are involved with the Prion disease, which
maybe protein only, but they do not explain how one prion protein
alters the form of another. Such that the metal ions may explain the
many forms and shapes of prion molecules, but have little to do with
the multiplication of bad prions from good prions.
And, in the above, the protein only theorists are in trouble with a
statement such as this: "People who support the "protein-only" theory
believe that each strain represents a prion with a slightly different
shape." For that statement implies that the multiplication mechanism
of prion disease is not that a bad prion alters the shape of a good
prion, but rather that something else in the prion environment, such
as strains of foreign DNA/RNA is acting as a catalyst to change the
shapes of other good prion proteins, and perhaps even an immune
reaction started by a fungus or virus or bacteria.
It may well come to pass that different shapes of Prion proteins are
due to different content of copper or zinc or other metal ions. But
the role of these metals is only the role of different shapes, and is
not the causative agent of the Prion disease nor a major mechanism of
the disease.
In fact, this report is rather negative to Mr. Prusiner's theory where
the proteins alter the shape of other proteins. If bad prions altered
the shape of good prion into more bad prions then this would become
difficult to impossible to carry-out if every prion had different
shapes from one another. You would need standard forms of prions and a
numerous quantity of them for the Prusiner scenario to work
More later
--------------
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.med,sci.bio.technology
Subject: Re: Prion is the sickle cell disease of proteins; iron to
copper/zinc
Date: 6 Jun 1999 03:57:24 GMT
Organization: getting to the heart of prion disease
Lines: 52
Distribution: world
Message-ID: (7jcrj4$1g...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
References: (7ib0kf$lv...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
(7ins95$hh...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
(7invu4$jbk
$...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
(7is48o$ek...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
(7j9tuq
$ql...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartvax.dartmouth.edu>
(7jco03$v0...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>
@dartvax.dartmouth.edu>
In article (7jco03$v0...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>
@dartvax.dartmouth.edu>
Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartmouth.edu
(Archimedes Plutonium) writes:
> But is the
> prion protein the world's newest mutated form of blood cell?
I had a long debate with Bruner, Bennett and Pelletier early in 1999
about prion disease. Amazing that the subject of copper/zinc metal
ions
role in prion disease never came up. I first learned of this
copper/zinc role in the NEW SCIENTIST article of 8MAY99.
Anyway, I believe this report of 18DEC97 is the turning point in
prion
disease theory. I believe this copper/zinc role will destroy the
Prusiner prion theory.
I believe that prion protein disease is connected to some agent of
virus/fungus/chlamydia/bacteria that starts an Immune system response
in the body which then goes to signalling an excess production of
prion
proteins and in conjunction signals these prion proteins to function
like white blood cells to engulf the virus/fungus/chlamydia/bacteria
debris. In the engulfing of the debris the prion protein engulfs
copper/zinc metal ions.
Some forms of arthritis are like this, where the body's own immune
system goes awry and the body attacks its ownself. In prion disease,
the immune system signals an excess production of prions and then
signals these prions to act like white blood cells upon the copper-
zinc
laden virus/fungus/chlamydia/bacteria debris.
--- quoting NATURE 18DEC97, pp 684-687 ---
The cellular prion protein binds copper in vivo
The normal cellular form of prion protein (PrP^C) is a precursor to
the
pathogenic protease-resistant forms (PrP^Sc) believed to cause
scrapie,
bovine spongiform encephalopathy (BSE) and Creutzfeldt-Jakob disease.
Its amino terminus contains the octapeptide PHGGGWGQ, which is
repeated
four times and
is among the best-preserved regions of mammalian PrP^C. Here we show
that the amino-terminal domain of PrP^C exhibits five to six sites
that
bind copper (Cu(II)) presented as a glycine chelate. At neutral pH,
binding occurs with positive cooperativity, with binding affinity
compatible with estimates for extracellular, labile copper. Two lines
of independently derived PrP^C
gene-ablated (Prnp^0/0) mice exhibit severe reductions in the copper
content of membrane-enriched brain extracts and similar reductions in
synaptosomal and endosome-enriched subcellular fractions. Prnp^0/0
mice
also have altered cellular phenotypes, including a reduction in the
activity of copper/zinc superoxide dismutase and altered
electrophysiological responses in the presence
of excess copper. These findings indicate that PrP^C can exist in a
Cu-metalloprotein form in vivo.
--- end quoting NATURE 18DEC97, pp 684-687 ---
--------------
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.med,sci.bio.technology
Subject: Re: Prion is the sickle cell disease of proteins; iron to
copper/zinc
Date: 12 Jun 1999 08:08:57 GMT
Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/0fa1452fb7347646%3Fhl%3Den&msg=cc6a5a7f3ad4bc43>@dartmouth.edu
(Archimedes Plutonium) writes:
> Wilson's disease: copper disease and copper deposited in iris of eye,
> other copper diseases, and zinc diseases.
--- quoting in parts http://gi.ucsf.edu/alf/alffinal/infowilsons.html
<http://www.google.com/url?sa=D&q=http://gi.ucsf.edu/alf/alffinal/infowilsons.html&usg=AFQjCNECgsGV5Sq_JFlrft5XGzByzhR-_Q>
---
WILSON'S DISEASE
What is Wilson's Disease?
Wilson's disease is an inherited disorder in which excessive amounts
of
copper accumulate in the body. This rare disorder affects
approximately
one in 30,000
individuals. Wilson's disease is inherited as an autosomal recessive
trait, which means that the affected individual must receive the
abnormal gene for Wilson's disease from both parents. The genetic
defect in Wilson's disease
results in failure of the liver to rid the body of copper. The copper
then builds up in the liver, the brain and other organs.
What are the Symptoms?
... Approximately 40% of all patients with Wilson's disease are first
seen because they have symptoms of liver disease. Blood tests show an
elevation in liver enzymes, and symptoms of acute hepatitis, fulminant
hepatitis, chronic hepatitis or cirrhosis, with all of its
complications, may be present.
Copper also accumulates in other body organs, particularly the brain,
and may result in difficulty with speech, trembling, writing problems,
an unsteady walk, depression, suicidal impulses, and loss of mental
functions. Other body organs may also be damaged by copper overload.
Copper may accumulate in the cornea of the eye and cause a
characteristic brown pigmentation called Kayser-Fleischer rings.
Hemolytic anemia, a low blood count related to damage of red blood
cells,
may occur in patients with Wilson's disease. There may be injury to
the
kidneys due to copper overload. Finally, severe bone disease from
osteoporosis may occur in patients with Wilson's disease.
What is the Prognosis and Treatment?
Wilson's disease that is untreated results in increasing damage to the
liver and brain. Until the late 1940s, patients typically died before
reaching 30 years of age. The treatment improved substantially after
the introduction of the copper chelating agent, D-penicillamine. This
drug removes excess copper from the body and prevents future
accumulation and damage to body organs. D-penicillamine treatment must
be continued for life. A small number of patients are unable
to tolerate D-penicillamine because of side effects and another
chelating agent, trientine may be used. When either chelator is used,
pyridoxine (vitamin B6) should be administered.
A third drug that is used to treat Wilson's disease is zinc which
promotes excretion of copper in the stool and has been shown to be an
effective long-term therapy. Some physicians recommend long-term
maintenance therapy with either D-penicillamine or trientine, while
others believe that patients can be switched to zinc after an initial
treatment with one of the above two chelators.
Foods high in copper such as shellfish, nuts, liver, chocolate, and
mushrooms should be avoided. Patients with advanced liver disease who
do not respond to medical therapy should be considered for liver
transplantation.
--- quoting in parts from
http://www.ncrr.nih.gov/newspub/sep97rpt/wilson.htm
<http://www.google.com/url?sa=D&q=http://www.ncrr.nih.gov/newspub/sep97rpt/wilson.htm&usg=AFQjCNEIUcndrC8qL2FqeO2PhkLgfbHHMQ>
---
Research Highlight
Exploring Therapeutic Options for Wilson's Disease
... Two years ago she was told she had multiple sclerosis, and her
condition had grown steadily worse since then. But Dr. Brewer paid
particular attention to
the state of the young woman's liver and issued a diagnosis of his
own:
Wilson's disease...
Wilson's disease is an inherited disorder of metabolism in which the
body is unable to excrete excess copper. "Most of us take in about one
milligram of copper per day in our diet, and that's about 25 percent
more than we need," says Dr. Brewer. Under normal circumstances, a
protein in the liver binds the excess copper and shepherds it along an
excretory pathway into the bile. In Wilson's disease patients this
crucial protein is defective. As a result, says Dr. Brewer, excess
copper builds up in liver and brain, leading to jaundice or liver
failure. Copper may also cause neurological disorders that interfere
with swallowing, speech, and movement, or cause psychiatric symptoms
that include impaired cognitive performance, depression, and
uncontrollable anger.
....
------------
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/7385e25b781e1ca4%3Fhl%3Den&msg=c2499360871cda69>
@gmail.com>
Date: Tue, 2 Apr 2013 22:09:51 -0700 (PDT)
Subject: My history on metal diseases: Metal Causing Diseases (Autism,
Schizophrenia, Depression, Parkinsons, Alzheimers, Prion)
So in 1999, I was mixing Alzheimers with Prion as metal causing
diseases. And I should have spent more time on Wilson's disease for it
is a copper excess disease. But apparently I was stifled and stifled
by being in the mindset of something going around in the brain and
altering good proteins into bad proteins. If instead, when I reached
Wilson's disease in 1999, if I had said the brain had excess copper
and the prion proteins were being manufactured to sort of go around
and mop-up the copper and get rid of it. That would have explained the
disease but not explained how it is transmissive. And that would have
involved research into whether Wilson's disease turns into Prion
disease. Trouble with this scenario is that eating infected brains of
prion would be eating copper and we generally do not consider copper
to outright cause a disease, so it lacked transmission abilities.
A different mechanism would have been to say that copper with mercury
is the cause and it goes around in the brain altering good prion
proteins into bad prion proteins, like a catalysis reaction. And when
an infected cow brains is eaten by others, what is transmitted is a
number of CuHg molecules that cause the disease over again. So this
scenario has transmission abilities.
Here are some posts of 1999 showing where I was going in thought.
--------------
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/7385e25b781e1ca4%3Fhl%3Den&msg=c2499360871cda69>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.med,sci.bio.technology,sci.chem
Subject: protein folding around copper/iron also found in Alzheimers,
and of course prion disease
Date: 24 Jun 1999 08:38:07 GMT
Well it appears to be wrapping up quite nicely that Prion disease like
Alzheimers disease is mostly a protein folding around metal ions
disease. I still feel strongly that the Immune system is involved and
some foreign DNA/RNA involved in this protein folding around metal
ions.
--- quoting New Scientist, 19 June 1999, page 10 ---
Peroxide is to blame for the degenerating minds of Alzheimer's
patients
THE ABNORMAL PROTEIN deposits that clog the brains of Alzheimer's
patients probably damage nerve cells by producing the toxic chemical
hydrogen peroxide, new research suggests. Experts say this raises
hopes
that it might be possible to treat the disease by blocking this fairly
simple chemical.
In Alzheimer's disease, an abnormal form of beta-amyloid protein forms
in the brain. Scientists already knew that cells containing this
protein also have raised levels of the powerful oxidising agent
hydrogen peroxide. However, it was unclear why this was. To find out
more, scientists from Harvard Medical School and the University of
Heidelberg looked at the chemical reactions in these cells by studying
changes in the way they absorbed light and fluoresced.
The researchers discovered that when abnormal beta-amyloid binds to
iron and copper, the metal ions donate electrons to dissolved oxygen
(Biochemistry, vol 99, p 438). Oxygen molecules with two excess
negative charges then react with hydrogen ions to form hydrogen
peroxide. The team also showed that the type of beta-amyloid
associated
with the most aggressive form of Alzheimer's was the best at binding
copper and iron--and hence at generating peroxide--suggesting that
this
reaction is a major factor in causing the brain damage.
"Ultimately we would like to be able to interrupt this process," says
team member Ashley Bush of Harvard Medical School in Charlestown,
Massachusetts. "The sites where the copper and iron bind could be an
easy target." He adds that scientists will first need to figure out
the
three-dimensional structure of the binding site.
The new evidence that the generation of peroxide may be involved in
the
disease process fits in with other observations, Bush says. Earlier
studies showed that antioxidants such as vitamin E offer significant
protection to people who are developing Alzheimer's.
--- end quoting New Scientist, 19 June 1999, page 10 ---
--------------
From: Archimedes.Pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/7385e25b781e1ca4%3Fhl%3Den&msg=c2499360871cda69>@dartmouth.edu
(Archimedes Plutonium)
Newsgroups: sci.med
Subject: copper & zinc roles in prion disease
Date: 7 Jul 1999 23:25:36 GMT
The below is a summary of my theoretical musings on prion disease.
When I first heard about the Prusiner mechanism 1980s I was in favor
of
it, for I like new ideas, new things. Then somewhere in the mid 1990s
I
began to realize that this mechanism is a fake. That how can one
molecule reproduce itself upon that of another molecule, the energy
flows made no sense and violated energy principles of 2nd law
thermodynamics and conservation of energy. This disfavor caused me to
search for a better explanation of Prion disease. And after a long
thread with several biochemists and biologists I came to the opinion
that prion disease is a metal ion folding problem of copper/zinc and
that the autoimmune system was involved and triggered by some foreign
DNA/RNA particle or debris.
I suspect in the next several years the dominant role that copper and
zinc play in prion disease will be so well understood, that the
Prusiner theory is trashcanned. And just today I was reading in New
Scientist 3 July 99 "Spot the prion Europe approves three tests for
BSE
" where a test for the disease is highly reliable. I was wondering if
these tests were based on the metal ions of copper and zinc?
[rest deleted]
---------------
From: plutonium_archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/7385e25b781e1ca4%3Fhl%3Den&msg=c2499360871cda69>@yahoo.com
(Archimedes Plutonium)
Newsgroups: sci.med,sci.bio.technology
Subject: Any more news on Copper causing prion disease? Any on human
cloning
Date: 18 Jul 1999 17:52:40 GMT
It looks as though England's scientists will resolve the prion
disease.
The last I read on the progress on prion disease was that England's
scientists (Collinge et al, forgive the spelling) needed about 2 years
to test how the copper metal ions folded the normal prion molecule.
Two years is a long time to wait. So, in the interim is anyone else
doing the metal ion research? It would be sad if only one group of
scientists worked on the metal ion research.
And human cloning research seems to have moved to Hawaii. It is nice
to see how the gods change the scenes of science. First in Scotland
and
now Hawaii. I think though, soon, a news flash of the first human
clone. If I had to guess, I would say somewhere in the Orient.
----------------
AP
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/a5992874dab971a6%3Fhl%3Den&msg=f0aae862959e2e5d>
@gmail.com>
Date: Sun, 7 Apr 2013 12:15:31 -0700 (PDT)
Subject: showing that mercury poisoning can cause a 5 to 1 Autism rate
Chapt4 Math Statistics as proof in science: Metal Causing Diseases (Autism,
Schizophrenia, Depression, Parkinsons, Alzheimers, Prion)
Chapt4: experimental math-statistical proof that autism (ASU report)
is caused by mercury and cadmium and the mechanism is similar to
chromium-6 (PBS report)
Now why would even medical doctors or some scientists even deny
mercury as a poison that can cause all 6 of these diseases Autism,
Schizophrenia, Depression, Parkinson, Alzheimer and Prion? Why would
they deny mercury? Well obviously for doctors who do not want lawsuits
or blame from vaccine administrations that contained mercury and to
continue applying vaccines laden with mercury, and for scientists who
are funded to do genetic research, not wanting to have to examine for
mercury. If you are working as a geneticist, you want these diseases
to be caused by genetics, not by a environment toxin.
Now I listed the 6 diseases in an order of when those diseases attack
the human body starting with Autism of its first years of life.
Now it is alarmingly sad that medical doctors do not apply scientific
reasoning in this debate. And sad that many research scientists do not
apply logical reasoning in the debate.
What I mean is that often a doctor or researcher will say some
incredibly antiscience opinion like this:
"Well, if autism occurs 5 times more often in boys than in girls,
proves autism is a genetic caused disease."
Now a statement like that is sad to come from the lips of a doctor or
scientist. Can you spot the horrible logical error?
Mathematical Statistics can prove that autism is caused by mercury
poisoning as the recent Arizona State University research report
proclaimed:
> In a recently published study in the journal Biological Trace Element
> Research, Arizona State University researchers report that children
> with autism had higher levels of several toxic metals in their blood
> and urine compared to typical children. The study involved 55 children
> with autism ages 5–16 years compared to 44 controls of similar age and
> gender.
> The autism group had significantly higher levels of lead in their red
> blood cells (+41 percent) and significantly higher urinary levels of
> lead (+74 percent), thallium (+77 percent), tin (+115 percent), and
> tungsten (+44 percent). Lead, thallium, tin, and tungsten are toxic
> metals that can impair brain development and function, and also
> interfere with the normal functioning of other body organs and
> systems.
> A statistical analysis was conducted to determine if the levels of
> toxic metals were associated with autism severity, using three
> different scales of autism severity. It was found that 38-47 percent
> of the variation of autism severity was associated with the level of
> several toxic metals, with cadmium and mercury being the most strongly
> associated.
> In the paper about the study, the authors state “We hypothesize that
> reducing early exposure to toxic metals may help ameliorate symptoms
> of autism, and treatment to remove toxic metals may reduce symptoms of
> autism; these hypotheses need further exploration, as there is a
> growing body of research to support it.”
So, let us summarize that report with the logic of Mathematical
Statistics.
If the report had said there is just a correlation of more mercury
with autism individuals, it would not prove mercury is the cause. But
since the report showed that the severity of Autism that the spectrum
of autism matches the amount of mercury in the body, then that
suffices to prove mercury is the cause.
So, let us look at the facts of gender ratio. I have assembled a ratio
for all 6 diseases and the most striking differences are with Autism
where 5 times more boys are diagnosed than girls. One answer is that
boys mature by about 2 years slower than girls. So that if a boy had
the same amount of mercury in his body and that mercury attacks a
special site of the brain, then girls, with their faster maturity
would be able to ward off the mercury. Another explanation would be
that boys are more apt to be outside and play around in a mercury
laden environment.
But now look at the statistics of where females are more likely
stricken in that of Alzheimers where 2 times as many females than
males. But is that logical science? Because we all know that in old
age, many of the men have died off earlier in life than their women
contemporaries. So by old age, there are far more women survivors. So
to say that 2x times more women get Alzheimers has to be
scientifically incorrect.
Now Parkinsons disease has a gender difference of about 1.5 times
greater in men. But when we ask questions of that statistic, does it
hold up scientifically for or against mercury poisoning? Parkinsons
has become known as "welders" disease. If you are a welder, you have
an increased chance of ending up with Parkinsons because most metals
contain mercury and when applied heat in a welding torch that mercury
is transformed into a more toxic state. So, if the Statistics of
Parkinsons were to include how many men were ever welding compared to
how many women ever held a arc welding torch, we can easily see that
Parkinsons would have a 1.5 ratio.
But now, if you are a scientist payed to research genetics, you would
be inclined to say that since Autism is 5 to 1 or Parkinson's is 1.5
men to women, you would say such silly things as "those numbers prove
it is a genetic disease".
If we went back to the 1980s where the statistics of asbestos related
diseases were being diagnosed and found that the gender ratio was 5
times more men than women or 10 times more men than women would the
medical doctors and geneticists come forth hollering that asbestos
diseases are genetic diseases? Of course not, since it is men that
were mining and processing asbestos far more than women exposed to
asbestos.
So we have to be careful in how Mathematical Statistics is used to
prove or disprove a science issue.
Here is a list of the 6 diseases and what the gender ratio is:
1) For Autism
http://www.cnn.com/2012/04/04/health/mental-health/autism-sex-differe...
<http://www.google.com/url?sa=D&q=http://www.cnn.com/2012/04/04/health/mental-health/autism-sex-differences&usg=AFQjCNGB3jo6rLw3rEPosuyptbyZVsjIAw>
A striking finding of the recent Centers for Disease Control and
Prevention report, showing a 78% increase in cases over the past
decade, is that the ratio of boys to girls in ASD is about 5-to-1.
That is higher than what is usually reported in other studies, where a
ratio of 2-, 3- or 4-to-1 is more common.
2) For Schizophrenia
http://www.health.am/psy/more/schizophrenia-and-gender/
<http://www.google.com/url?sa=D&q=http://www.health.am/psy/more/schizophrenia-and-gender/&usg=AFQjCNGZIEp8OeDVKw7xN-g7CQWnQbqWyg>
Because the pace of cerebral development is slower in males than in
females, the male fetal brain is considered more susceptible to
environmental adversity than the female brain, due at least in part to
estrogen. By activating common intracellular signaling pathways and
initiating “cross-talk” with neurotrophins, the female hormone
estrogen is known to play an influential role in promoting neuronal
survival after environmental insult. More symmetrical brain
organization in females is also considered protective, in that the
other side of a symmetrical brain can compensate for functions
unilaterally disrupted. During adolescence, sex-specific (hormonally
induced?) reductions in synaptic density may additionally contribute
to the extra vulnerability of the male brain at that critical time.
Incidence rates
Recent meta-analyses of incidence risk report a mean ratio of 1.42 for
men over women, an excess for males that is only slightly reduced when
studies of lower quality are excluded.
3) For Depression:
http://deepblue.lib.umich.edu/bitstream/handle/
<http://www.google.com/url?sa=D&q=http://deepblue.lib.umich.edu/bitstream/handle/&usg=AFQjCNEZJ7tmiqqeJ5sC28RZOUF9K2Ksow>
Abstract:
From early adolescence through adulthood, women are twice as likely as
men to experience depression.
4) For Parkinson's disease:
http://jnnp.bmj.com/content/75/4/637.full
<http://www.google.com/url?sa=D&q=http://jnnp.bmj.com/content/75/4/637.full&usg=AFQjCNGhO4YWijEl8Dq5JqzipJwsTDwaUg>
Abstract
Parkinson’s disease seems to occur more commonly in men than women
based primarily on studies of death rates and prevalence. In recent
years, several population based incidence studies of Parkinson’s
disease that included sex data have been conducted in a variety of
populations around the world. To investigate whether these incidence
studies suggest an increased risk of Parkinson’s disease in men, a
meta-analysis was performed of the differences in incidence of
Parkinson’s disease between men and women reported in seven studies
that met the inclusion criteria. A significantly higher incidence rate
of Parkinson’s disease was found among men with the relative risk
being 1.5 times greater in men than women. Possible reasons for this
increased risk of Parkinson’s disease in men are toxicant exposure,
head trauma, neuroprotection by oestrogen, mitochondrial dysfunction,
or X linkage of genetic risk factors.
5) Saw one report where 2 times as many women get Alzheimers than men
http://www.ncbi.nlm.nih.gov/pubmed/18381051
<http://www.google.com/url?sa=D&q=http://www.ncbi.nlm.nih.gov/pubmed/18381051&usg=AFQjCNEjtUMs0b5C032QiWarFwnCOIDouQ>
Abstract
The prevalence of Alzheimer disease is higher in women than in men. In
the age group 65-69 years 0.7% of women and 0.6% of men suffer from
the disease with increasing frequencies of 14.2% and 8.8% in
individuals aged 85-89 years. The incidence is also higher in demented
women. In Austria 74.1% of Alzheimer patients older than 60 years are
women.
6) For Prion CJD
1. Creutzfeldt-Jakob disease and related diseases ... -
Eurosurveillance
www.eurosurveillance.org/ViewArticle.aspx?ArticleId=395
<http://www.google.com/url?sa=D&q=www.eurosurveillance.org/ViewArticle.aspx%3FArticleId%3D395&usg=AFQjCNHqtHq56t6szsQeMja816E_FQiA9w>
Jan 1, 2003 – The distribution by sex of CJD reports is similar for
all three years studied: sex ratio (male/female) was 1.05. The
proportion of reports of ...
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/a5992874dab971a6%3Fhl%3Den&msg=38f2cd2422b58951>
@gmail.com>
Date: Sun, 7 Apr 2013 12:40:50 -0700 (PDT)
Subject: Re: showing that mercury poisoning can cause a 5 to 1 Autism rate
:Math Statistics as proof in science: Metal Causing Diseases (Autism,
Schizophrenia, Depression, Parkinsons, Alzheimers, Prion)
Now several quick solutions for why 5 boys are diagnosed with autism
per every girl
are these:
1) If in hospitals, the boys are separated from the girls in separate
rooms and where there has been more fluorescent lamps broken and more
mercury present in the boy room
2) Where boys are given a vaccine laden with mercury that the girls
are not given.
3) Where boys are given a infant formula or food which contains more
mercury than girls.
4) Where boy toys contain more mercury.
5) Where boys are exposed to more cigarette smoke than girls, since
cigarettes have mercury content.
But I think the best answer for the 5 to 1 gender ratio is that boys
mature so much slower than do girls and that a "autism critical level"
is easily reached in boys and the girls have already outgrown that
critical level of exposure.
*10) Homosexuality*
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=857899476d93cc6f>
@gmail.com>
Date: Tue, 16 Apr 2013 23:20:06 -0700 (PDT)
Subject: Is Homosexuality a metal poisoning caused disease like Autism?
Metal Causing Diseases
Is Homosexuality a metal poisoning disease? Chapt1 my history of metal
causing diseases
Metal Causing Diseases (Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion)
By August of 2001, I was not yet fully in tune with the idea that
these diseases were 100% caused by metal poisons of the environment.
Then by 2002 I was fully in tune with the idea that these diseases
were caused by metals alone, and that genetics had no significant
role, such as lead poisoning or mercury poisoning, and that these
diseases were caused by the Industrial Revolution that unleashed
torrents of harmful chemicals and metals into our daily environment.
----------
Subject:
research news on Alzheimers and Prion
Date:
Wed, 01 Aug 2001 04:24:04 -0500
From:
Archimedes Plutonium (pluto...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=857899476d93cc6f>@willinet.net>
Organization:
whole entire Universe is just one big atom
Newsgroups:
sci.bio.technology, sci.med
--- quoting in parts SCIENCE NEWS, 30JUN01, page 406 ---
In the presence of copper atoms in the brain, beta-amyloid
can act as an enzyme that generates free radicals in the form of
hydrogen peroxide. When concentrations of free radicals soar,
zinc in the brain interacts with beta-amyloid and plaques result.
.....
The copper then can catalyze the formation of more free
radicals. Bush's team reports in the June NEURON. When
this happens, the initially protective plaques do in fact become
part of the problem...
--- end quoting in parts SCIENCE NEWS, 30JUN01 ---
I want to mention several points of fact. That prion disease, much
like Alzheimers is a disease of plaque buildup. And prion disease
is connected with copper and zinc and other metals.
One aspect of Prion disease is its multitude of variants. And it
is this multi-variance that destroys the Prusiner protein only
theory.
But I am not quite sure if Alzheimers also has multi-variations
as does prion disease.
Apparently metals are involved in a critical way in both
Prion and Alzheimers.
And although the above quote hints of a means of generating
more plaque, a better generator would be that of a virus
or bacteria or fungus. A microbial organism would also
offer the best explanation for the multitude of variants in
Prion disease. Does Alzheimers disease come in variants
and has anyone researched the differences or similarities
between the Prion variants and the Alzheimers variants.
Such a study focused on variants in the two diseases
may yield clues as to the generators of both diseases.
-----------
It is now February of 2002 and here is where I enter a pure metal
causing mechanism of these diseases. So that by February of 2002, I
started looking at these diseases as metal poisoning from the
environment, no different than if you had been smitten by lead
poisoning or mercury poisoning, or asbestos poisoning provided that
asbestos is a metal for it is not a metal in reality, and coming from
the environment. Now it is extremely difficult for scientists to
separate whether a disease is environment or genetic when a family
contracts the disease because all family members are likely to be
exposed to the metal poisoning, if it is in the air or in the food or
in contact by members of the family. Recently on the BBC was a nasty
report of lead poisoning of many of the infants of a small Nigeria
Africa village where their fathers were coated in lead from gold
mining and brought the lead home in their clothing coated from the
dust and dirt. So here we see how geneticists would be terribly
mistaken to think because families get the disease that it is genetic.
So that because several family members get the disease, the adherents
of genetics will bark that it is genetic, but it could just as easily
be 100% environment.
Now, one thing working against these 6 diseases being genetic diseases
is that often the parents do not have the disease but just the
offspring. For example, nearly 100% of the cases of Autism are from a
mother and father that do not have autism. So if autism were really
genetic disease, we would think that the parents should have the
disease, such as sickle cell disease must come from parents who have
the disease.
I am going to interrupt this post, for at this very moment, I think I
have a 7th disease to add to the list of diseases-- homosexuality as a
metal poisoning disease. Now I am going to be cautious in adding
homosexuality and by that I mean I need to dig up some facts and
statistics of homosexuality. After writing the above, I realized that
if you have a metal poisoning while in the womb, such as mercury, that
it is not genetics that cause homosexuality, but rather, a specific
quantity of mercury in the womb that alters the brain for sexual
orientation. Now autistic children can catch the disease after birth,
especially males since their brains mature about 2 years slower than
the female brain and so that if a critical quantity of mercury or
cadmium or some other dangerous metal enters their bodies, they
succumb. Now can we say that autism behavior is sort of like
homosexuality? Are there 4 or 5 times as many boys homosexual as
girls, for in Autism, boys are 4 or 5 times more likely to be
Autistic, as a gender preference of the disease.
Are autistic people more inclined to homosexuality?
I need to write a separate chapter that Homosexuality is likely to be
caused by a metal poisoning, and is not a genetic disease. It can
happen in the womb and comes earlier than Autism. It can happen in
infancy as does Autism, say when a tuna fish sandwich laden with too
much mercury is ingested, or living near by, or down wind of a coal
electricity station spewing out mercury.
Now I have to check up on the statistics of whether Homosexuality is
on the rise or not on the rise, for that Autism surely is on the rise
since of last report there are 1 in 50 infants with Autism when a few
years back it was 1 in 110.
Now one fact that lends credence to the idea of homosexuality being a
metal poisoning is that many animals display homosexual tendencies and
homosexuality has no evolutionary benefit, but rather is contradictory
to evolution theory. So that homosexuality as a metal poisoning
disease along with Autism and Alzheimers makes a lot more sense.
----------
Subject:
CELL, 16NOV01 Re: possible mechanism for Alzheimers,
Prion, Parkinson, et al
Date:
Sun, 10 Feb 2002 16:40:32 -0600
From:
Archimedes Plutonium (pluto...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=857899476d93cc6f>@willinet.net>
Organization:
whole entire Universe is just one big atom
Newsgroups:
sci.bio.technology, sci.med
Thanks to Bob Bruner for telling me about these articles.
--- quoting from CELL, 16NOV01 ---
When the Message Goes Awry: Disease-Producing
Mutations that Influence mRNA Content and Performance
Up to 30% of mutant alleles that contribute to human
disease harbor a premature signal for the termination
of translation, either through nonsense or frameshift
mutations. The most intuitive consequence of such mutations,
which continues to be widely predicted, is the production
of protein products truncated at the C-terminal end.
--- end quoting from CELL ---
My main interest in all of this is that I intuit that the diseases
of Prion, Alzheimers, Parkinsons and many others are
diseases wherein the body manufacturing site of proteins
has *gone awry* and that the body accumulates these
unwanted proteins and results in the disease.
Whether it is purely a chemical mutation where no
bacteria or virus is involved, or whether a microbe is
involved is inconsequential. The disease pathology
is that the body over-manufactures unwanted proteins
that accumulate and cause the disease.
Reading that article I was struck by the fact that *iron*
in the body can lead to mutational disease. Called the
L and H-ferritin transcripts.
Some decades back it was guessed that Alzheimers maybe
influenced by aluminum in the body. That guess has been
debunked recently, but I am not so sure whether that debunking
was premature. Does anyone know if Alzheimers is an
Industrial Revolution disease that runs in tandem with the
aluminum industry and the prevalence of aluminum in cooking?
And also, with Prion disease, it is noted that the disease is in
association with copper and other metal ions.
Could it be that Prion, Alzheimers and Parkinsons are relatively
modern diseases which have increased in frequency due to the
increase in metal contamination of the environment? Whereas
tobacco smoking can lead directly to lung cancer that Prion and
Alzheimers and Parkinsons is our modern diseases due mainly
to the increase in metal contaminants in the environment. That
they facilitate the mutations of mRNA and lead to diseases
of protein manufacture that accumulate in the body.
------------
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.math/browse_thread/thread/14ad9aa3e2558ed2%3Fhl%3Den&msg=b3397fc32929259c>
@gmail.com>
Date: Tue, 16 Apr 2013 23:43:01 -0700 (PDT)
Subject: math-statistics proof that Homosexuality is caused by metal
poisoning: Metal Causing Diseases
Now the Arizona State University research that found the severity of
Autism coincides with the amount of cadmium and mercury inside the
bodies of Autistic children is a mathematical statistics proof that
Autism is caused by these two metal poisons. Our modern day
environment is saturated in mercury poison from all those coal fired
electric stations to the fish to the cigarette smoke to the
fluorescent lamps in our homes to the teeth fillings and to the
mercury laden vaccines. Probably every breathe we inhale today
contains some atoms of mercury. So it should not be any surprise to
anyone that the rates of reported Autism has gone from:
So we have this historical data:
1970s to 1990 the Autism frequency was 1 in 110
1990s to 2010 the Autism frequency was 1 in 88
2010 to present the Autism frequency was 1 in 50
But now, I want a Mathematical Statistical proof that Homosexuality is
caused by a metal poisoning such as mercury. The trouble here is that
the metal may just affect a fetus in the womb or a young child, affect
him or her in a moment in time to alter the sex preference and not be
measured in the same way as Arizona State University measured severity
of autism matched with concentrations of mercury and cadmium.
So I need a different Math-Statistic proof measure. What I propose is
to see if Autism is linked to Homosexuality. See if there is a
significant statistic that autistic children have a homosexual sex
preference. Or whether they have no sex preference. So that the metal
reverses the sex preference in making homosexuality, but keeps Autism
sex preference as neutral.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=cbd14c51aaa5aec7>
@gmail.com>
Date: Wed, 17 Apr 2013 00:54:03 -0700 (PDT)
Subject: direct science evidence that Homosexuality is caused by metal
poisoning: Metal Causing Diseases
Well it looks as though we need no math statistic proof that mercury
can cause homosexuality because here is a list of direct science
proofs:
--- searching in Google under "homosexuality caused by mercury" gives
me these hits ---
1. Mercury causes homosexuality in male ibises : Nature News
www.nature.com/news/2010/101201/full/news.2010.641.html
<http://www.google.com/url?sa=D&q=www.nature.com/news/2010/101201/full/news.2010.641.html%E2%80%A8&usg=AFQjCNFGT0ufUn8Yt8KepczEKHowONiELA>Dec
1, 2010 –
Exposure to mercury pollution could be hitting some wild birds'
reproductive prospects hard by causing males to pair with other males.
2.
3.
Pollution Causes Homosexuality in Birds, Study Suggests | Fox
News
www.foxnews.com/.../pollution-causes-homosexuality-birds-studies/
<http://www.google.com/url?sa=D&q=www.foxnews.com/.../pollution-causes-homosexuality-birds-studies/&usg=AFQjCNEsChHS9J698ofAs6Ofxgaow9Pzpw>
Dec 2, 2010 – Mercury pollution is causing homosexuality among
American white ibises, studies show.Wikipedia. The nature versus
nurture debate just took ...
4.
5.
High exposure to Mercury = Homosexuality?
www.escapistmagazine.com
<http://www.google.com/url?sa=D&q=www.escapistmagazine.com&usg=AFQjCNHPD7uUQRTNTuUj7zfFJnZhiQG_rA>
› ... › Religion and Politics
35 posts - 24 authors - Dec 1, 2010
If
mercury in the environment could really be a cause, does that mean we
will see a decline in the occurrence of homosexuals in the next ...
6.
7.
Mercury Poisoning Makes Birds Act Homosexual
news.nationalgeographic.com/.../101203-homosexual-birds-mercury...
Dec
3, 2010 – The biological mechanism for how the metal causes homosexual
actions is not totally understood, Frederick added. Mercury is a
known ...
8.
9.
Study: Mercury pollution causes birds to act gay
content.usatoday.com/communities/.../post/.../mercury...causes-
gay.../...
Dec 6, 2010 – Mercury pollution causes a surprising
tendency of male white ibis birds to mate with other males, finds a
new University of Florida study.
10.
11.
Fossil Fuel Mercury Causes Unnatural Homosexuality | Irregular
Times
irregulartimes.com/.../fossil-fuel-mercury-causes-unnatural-
homosex...
Dec 1, 2010 – Now the facts are in that mercury pollution
from burning fossil fuels can cause homosexuality in the natural
world. Shouldn't that lead right wing ...
12.
13.
This discovery that homosexuality is a disease of Nature, caused by
metal poisons of the environment makes sense in the fact that the
theory of evolution is violated or contradicted by homosexuality for
it leaves no benefits to the genetics of the individual. In
sociobiology, they have a corrupted and warped opinion of altruism to
try to patch up the fact that homosexuality confers some benefit, when
in truth, homosexuality confers no benefit to the genes involved. So
that, if we see homosexuality, what we are seeing is a disease, not
much different from Autism or Parkinsons, and we would be silly to
think that a mechanism of Altruism is conferring some advantage to the
victim of the disease. So that homosexuality is a victim of a disease
caused by mercury or metal poisons in the womb or early in life.
Now we know the Gay males have mannerisms that we easily identify with
homosexuality. Mannerisms as seen by the actor on PBS of the British
comedy Are You Being Served of a British store with a gay salesman.
Now the question I have, is whether Autism males ever show mannerisms
as what Gay men have mannerisms? I am not aware of them have similar
behaviors, but I never met with many autistic children. I am aware
that autism seems to not want to socialize or make social contact at
all, yet Gay men are rather super-social and thrive in social contact.
So that leaves me with the question of when in development does a
mercury poisoning cast the male as going to be homosexual and when
does the mercury cast the male to be autistic? So here I suspect
mercury in the womb is likely to yield Homosexuality and mercury in
the first few years of life is going to be casting autism.
Now I have enough evidence to include Homosexuality as the 7th metal
poisoning disease.
--
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=db4eebdebfa2a2bd>
@gmail.com>
Date: Wed, 17 Apr 2013 13:30:20 -0700 (PDT)
Subject: methylmercury causes Gay Re: math-statistics proof that
Homosexuality is caused by metal poisoning: Metal Causing Diseases
On Apr 17, 5:15 am, "John H. Gohde" <john.h.go...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=db4eebdebfa2a2bd>@gmail.com>
wrote:
> On Apr 17, 2:43 am, Archimedes Plutonium
> <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=db4eebdebfa2a2bd>@gmail.com>
wrote:
> > On Apr 17, 1:20 am, Archimedes Plutonium
> > <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=db4eebdebfa2a2bd>@gmail.com>
wrote:
> > > Is Homosexuality a metal poisoning disease? Chapt1 my history of
metal
> > > causing diseases
> Obviously something is causing Homosexuality.
> One thing that you can take to the bank is that unlike the lies of ALL
> liberals; Homosexuality is positively NOT caused by genetics.
> ALL you have to do is think about Darwinism for about five seconds to
> figure that big lie out. If it was genetics, then Homosexuality would
> have been breed out of existence millions of years ago, since
> Homosexuals do NOT reproduce.
Yes I agree, and sadly the biology community has invented a utterly
silly and false patch-over
with their daffy Altruism as a excuse to have homosexuality as a
benefit. The true answer is that homosexuality has no Evolutionary
benefit to its genetics and is a disease caused by the environment.
Before metals were mined and put into the fireplace some thousands of
years ago in the Bronze Age there were no homosexual humans, but once
the Bronze Age then the Iron Age began, so thus we start the history
of homosexuality. Now it may have started even earlier with fire
because as we burn materials, the smoke contains mercury from the
release of mercury in the sulfur of living tissue or in fossil fuels
if prehistoric man burned fossil fuels and in Volcano emissions. But
as the Bronze Age and then the Iron Age introduced more mercury into
humanity's environment, the rate of homosexuality started to increase.
I do not see any present day frequency of homosexuality, but I do see
it for Autism as being 1 in 50 when it was 1 in 110 for a decade ago.
So what is the frequency of Homosexuality? Would I be terribly off the
mark if I guessed 1 in 200 is homosexual, considering that autism is 1
in 110 a decade ago?
Now Autism has a gender preference for males who get the metal
poisoning about 5 times more than females, but we realize that females
have about a 2 years increase in maturity lead over males and would
thus require a very potent mercury dose to make a infant girl be
autistic. Perhaps the mother of boys eats too many tuna fish
sandwiches.
Now the ibis research report of where MethylMercury caused the
homosexuality of ibises is enough proof that methylmercury causes
homosexuality and causes it in humans. But what we need to do is make
further proof that methylmercury causes homosexuality in humans. The
way to do this is to set up research around fish eating societies and
monitor the math-statistics of the fish eating society and a society
that rarely eats fish. Then we need a research on a smoking cigarette
society versus a non smoking society. Finally we need a research on a
coal fired electric power station and downwind of that station versus
a geography where mercury is not so much in the breathing air.
Unlike the research of autism where the autistic child is analyzed for
mercury content in his body, for homosexuality, the mercury caused the
harm in the womb or shortly after birth and is no longer around. So
that in homosexuality, the mercury did its dastardly deed in a one
time event and turned the switch of
sex preference in the child.
One fact that may help in the research is the fact that homosexual gay
men far outnumber lesbian women, much like the 5 times more autism in
boys than girls.
So we need charts and graphs as we have of Autism showing the rise of
frequency from 1 in 110 to 1 in 50 be done for homosexuality, because
as we continue to fill the oceans and the fish with more mercury and
pollute the sky and air with more mercury, the rise and increase of
these 7 diseases will continue to plague humanity -- Homosexuality,
Autism/Asperger, Schizophrenia, Depression, Parkinsons, Alzheimers,
Prion.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/89423a30a10aa394%3Fhl%3Den&msg=1f38b7db5001973a>
@gmail.com>
Date: Wed, 17 Apr 2013 14:25:57 -0700 (PDT)
Subject: 4-6% of USA & Briton are gay: Metal Causing Diseases
Yes I was terribly off the mark there. After googling around for rates
of gay, I see a figure of 6% of Briton
is surveyed to be homosexual and 4% for France and USA.
So that would translate into 1 in 17 in Briton and 1 in 25 in the USA
whereas we have (recently) 1 in 50 for Autism.
So in the USA, we have homosexuality as the most common disease when a
youngster and the second most common disease is autism.
So we would expect 1 in 25 children to be gay and 1 in 50 children to
be autistic.
Now it does not surprise me at all that Briton would be far higher
rate of homosexuals than USA because Briton burns a lot of coal and
eats a lot of ocean fish, two prime sources of mercury poison. Briton
is also the historical home of prion disease, of sheep scrapie and mad
cow disease and that fits in to the picture of "so much mercury in the
environment."
Now we should see that China, as it becomes more and more industrial
and the worst polluter in the world, we should see China have a spiked
increase in homosexuality, in autism/aspergers, in schizophrenia, in
depression, in Parkinsons, in Alzheimers and in Prion disease all due
to the fact that China burns the most fossil fuels releasing the most
mercury into the air. And please, reader, do not be fooled into
thinking that that mercury that China releases will stay in China.
Remember, that in the Japan tsunami that much of that material ended
up in the USA hours and days later, so that as China releases more
mercury into the air, that in a few days all the continents have an
increased mercury in the air that they breathe.
Pollution is global, especially mercury pollution for mercury has the
two insidious features of being spread far and wide and a small
quantity is lethal and disease causing. With those two
characteristics- spread far and wide and only a little can do great
harm, it is no wonder at all that mercury is to blame for 7 major
diseases.
Now if Homosexual gay is 4% of the world population, has anyone
surveyed what the old age diseases of mercury-- Alzheimers percentage
is of old people. I had heard that at age 90, that 90% of the people
who live to be 90 or older have Alzheimers? If that is true then at
what old age do 6% or 4% of the population of old people have
Alzheimers? Is it age 60 where 6% of the people that survived to age
60 have Alzheimers?
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/73158acab24b820f%3Fhl%3Den&msg=a033ad5159b11bcc>
@gmail.com>
Date: Wed, 17 Apr 2013 16:50:31 -0700 (PDT)
Subject: asbestos a semi-metal for silicon is a semi-metal: Metal Causing
Diseases
I am going to include asbestos and asbestos diseases in this book, for
it is a metalloid or a semi-metal. If you look at elemental silicon,
you would be hard pressed to not call it a metal.
I am going to include it in this book for asbestos diseases are
obviously 100% environment caused diseases and asbestos is far easier
to model or compare as a disease than is lead disease.
Now this book is about brain metal diseases and asbestos is a cancer
disease not a brain disease so I will not include it as a brain
disease of this book. Also, chromium 6 is a body disease but not a
brain disease.
Now lead and mercury do cause brain diseases.
So let me include asbestos as a metal disease, semi-metal disease.
--
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/b8a007146532142a%3Fhl%3Den%26&msg=b8a007146532142a>
@gmail.com>
Date: Wed, 17 Apr 2013 22:18:56 -0700 (PDT)
Subject: My history; asbestos as causing disease: Metal Causing Diseases
This is still Chapter1 where I go over my history of formulating this
theory of diseases caused by metal poisoning.
The below two posts were in 2003 and are key to my
development of the theory that many of the modern day brain diseases
such as autism, alzheimers, parkinsons and recently, homosexuality are
caused by the environment of toxic metals. Now asbestos causes
asbestos diseases such as cancer not brain diseases, but asbestos can
be taken as a semi-metal and included in this textbook for comparison
of asbestos to another metal such as mercury or cadmium or lead.
One of the huge problems of modern day medicine is that the doctors
are blindsided by advances of genetics that to them, every disease is
a genetic caused disease and never any room to consider the toxins of
the environment as the likely cause of most of the brain diseases.
----------
Subject:
asbestos disease related to Prion disease??
Date:
Sat, 22 Feb 2003 21:18:07 -0600
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/b8a007146532142a%3Fhl%3Den%26&msg=b8a007146532142a>
@dtgnet.com>
21 Feb 2003 09:31:38 -0800 Kevin Eanes wrote:
> Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/b8a007146532142a%3Fhl%3Den%26&msg=b8a007146532142a>@dtgnet.com>
wrote in message news:(3E55D53E.66348...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/b8a007146532142a%3Fhl%3Den%26&msg=b8a007146532142a>
@dtgnet.com>...
> > Now I wonder why asbestos is so cancerous yet fiberglass is not so.
> > Seems to
> > me that the two are almost identical in shape and characteristics.
> > Anyone have
> > a quick short answer for what makes asbestos so bad.
> Archimedes,
> I did some internet research, and found out that we can not say with
> certainty that fiberglass is safe, because the scientific evidence on
> fiberglass is contradictory and inconclusive. However, fiberglass is
> probably safer than asbestos. To be on the safe side, I would suggest
> that when handling fiberglass, one should take the same precautions as
> when handling asbestos.
> There is less research on fiberglass than on asbestos. Some studies,
> often those funded by the fiberglass and insurance industries,
> indicate that fiberglass is not carcinogenic. However, other studies
> by the International Agency for Research on Cancer, National Cancer
> Institute, and World Health Organization indicate that fiberglass may
> be a potential carcinogen.
> With regard to the shape and characteristics of the two materials, two
> significant differences between asbestos and fiberglass are the size
> and the way the fibers break down. Unlike most minerals, which turn
> into dust particles when crushed, asbestos breaks up into fine fibers,
> which are often mixed with a binding material. Asbestos fibers are
> always present in bundles, never as a single fiber. Asbestos fibers
> fracture only lengthwise when the bundles break apart, releasing
> thousands of long tiny fibers. Because asbestos fibers are long,
> sharp, and irritating, the alveoli close up and trap them in the
> lungs.
> Fiberglass contains cylindrical single fibers, larger than asbestos
> fibers, which never split lengthwise. They only break across the
> fiber, forming fragments that no longer have the properties of a
> fiber. The tissue response is very different when these particles are
> inhaled. The larger size of the fibers makes it less likely that they
> will bypass the respiratory defense system and become embedded in the
> lungs. When fiberglass fragments are inhaled, the particles are more
> readily expelled and there is a more rapid clearance of fiberglass
> dust particles from the lungs.
> With regard to identifying asbestos, unless the manufacturer has
> labelled the material, visual examination only allows one to suspect
> that a material contains asbestos. A definite determination can only
> be made by instrumental analysis.
> Best Regards,
> -Kevin
Thanks for that informative response. Someone else in this thread
spoke
of a chemical reaction to the presence of asbestos in the lungs.
21 Feb 2003 07:39:55 -0800 al kemist wrote:
> AP
> One qualitative method that I have used to determine the possibility
> of a material being asbestos is to view a sample at 100x. Please be
> aware that this method has high inherent exposure risk while
> collecting, preparing and viewing the test specimens.
> Asbestos fibers have much longer (~150x) length than diameter.
> Transmitted light microscopy can reveal the appearance of asbestos to
> be not unlike a whisk broom.
> The inherent danger of this crystal family is this high L to D aspect
> ratio that allows the fibers to align themselves in air currents and
> thus penetrate deeply into the lungs.
> The balance of the toxic equation is the physiological reaction of the
> hydrous magnesium silicate fibers with the body.
> I achieved final confirmation of the crystal component via XRD. Again,
> be aware of the high potential risk of exposure during communition of
> the material that is required to prepare the sample(s) for analysis.
> "If it looks like a duck and quacks like a duck..."
> The principal variety is chrysotile - fibrous form of serpentine;
> other commercial varieties are amosite and crocidolite. Reference -
> Kingery, Introduction to Ceramics, 1960, pg. 24.
> -al
Which got me to thinking that there seems to be quite some analogy
or similarity of asbestos disease and that of Prion disease.
If we think of the bad prion entering the body and the good-prions as
sort
of like white-blood cells seeking to remove the bad-prion.
I do not think anyone has yet fully found out what the function of
good-prions
are. Perhaps their function is somewhat of a white-blood cell to
encapsulate
foreign material. They play some role in cell-walls of the brain.
Perhaps it
is a combined role of cell wall and removal of foreign matter in the
brain.
But that bad-prions like asbestos are unremovable. And when a bad
prion
comes in contact with the site production of new good prions, the bad
prion can disrupt the manufacturing site which then spews out only
more bad prions.
Asbestos causes disease because it is unremovable. Perhaps this
unremovable
characteristic is what causes Prion disease.
I should not push this analogy too far, but I see some benefits in
making this
analogy.
AP
----------
Subject:
BSE of a cow in Canada recently
Date:
Thu, 22 May 2003 11:50:28 -0500
From:
Archimedes Plutonium
Newsgroups:
sci.bio.technology, sci.med
Saw an interview with a Dr. Crawford about this mad cow disease in
Canada.
He said the state of affairs of the science of spongiform was such
that
it is comparable to what Ancient Rome knew about measles. I concur,
but
to the rest of modern society, they are hypocritical and antiscience
in
their ironic awarding of a Nobel to Prusiner over his falsehoods.
Imagine the
Ancient Romans of Caesar awarding Hypocrates III for saying that
measles
was caused by worms in old meat.
Dr. Crawford did mention some interesting features of spongiform, that
most scientists have closed their eyes and minds to. The feature that
it
is unknown how the vector of disease goes from the stomach to the
brain.
Because that feature is virtually unknown, suggests that the theory
that
all forms of spongiform are not caused by prions, but that prions are
the
end result. And that these diseases are triggered by some chemical
whether organic or inorganic that the individual of a species succumbs
to
spongiform because it's own body has been set to contract the disease.
We all know about Cancer of cells as a rapid multiplication of cells
that are unwanted. That is what cancer is. It is rapid multiplication
of unwanted cells.
Spongiform is *Cancer of Proteins* and specifically the prion protein.
It is rare because only a few individual bodies will set the
contraction in
motion once exposed to other prions. The prions themselves are not
like viruses or bacteria as Prusiner would believe but the prions are
like
asbestos that fosters the likely inception of cancer of cells. Prion
proteins do not alter the shape of other prions but rather instead,
they
induce the body to alter the manufacturing site of where normal
prions
are made. Alter that site to spew out prions in abnormal quantity.
Cancer is the spewing out of abnormal cells in overabundance.
Prion or Spongiform is the spewing out of abnormal prion proteins from
manufacturing sites of normal-prions in the body.
Even Dr. Crawford admits that the science of Spongiform is about as
developed as what the Ancient Romans thought of the measles, and yet,
how so ironic that the Nobel Prize Organization has awarded a prize
to Prusiner over a model that is a falsehood. Modern Biology
entertained
another false award during the Russian rule of the early 20th century
when they accepted the Lysenko thoughts. Prusiner is the Lysenko
equivalent for the modern world of biology.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/356702db0ef73f07%3Fhl%3Den%26&msg=356702db0ef73f07>
@gmail.com>
Date: Wed, 17 Apr 2013 22:29:07 -0700 (PDT)
Subject: exploring aluminum: My history: Metal Causing Diseases
Now the below three old posts of 2003 starts to explore whether the
metal aluminum is the cause of brain diseases such as prion or
alzheimers.
----------
Subject:
Re: handle on pots, rivets & strength
Date:
Sat, 23 Aug 2003 00:46:09 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/356702db0ef73f07%3Fhl%3Den%26&msg=356702db0ef73f07>@dtgnet.com>
Newsgroups:
sci.materials, sci.chem, sci.bio.misc
r norman wrote:
> On Fri, 22 Aug 2003 12:45:57 -0500, Archimedes Plutonium
> (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/356702db0ef73f07%3Fhl%3Den%26&msg=356702db0ef73f07>@dtgnet.com>
wrote:
> >I need to avoid contact of food with aluminum because I do not want a
single
> >atom of aluminum going through my body. Especially cooking tomatoes for
> >canning.
> >I am finding the T-Fall cookware that is teflon coated is the best
modern day
> >cookware. However, I am not certain whether the aluminum can leak
through the
> >teflon coating.
> >Anyone have any data on whether aluminum can leak through teflon?
> I hope you don't breathe air that contains any dust particles
> whatsoever. Moreover, I hope you only drink distilled water and never
> eat any plant material that was grown on soil or any animal material
> that ever ate plants that grew on soil. That is the only way you will
> avoid getting a single atom of aluminum going through your body.
Norman, I think we have to distinguish between aluminum compounds
and complexes from elemental-aluminum such as found on pots and pans.
Aluminum soda cans even have a laquer coating so that elemental
aluminum
does not get into the body.
I believe toothpaste has some aluminum complexes but not elemental
aluminum.
The troubling thing about elemental aluminum is that it is so
widespread and
abundant in the USA and industrial world. Last night I heard that 1 in
2 people
over the age of 75 will contract Alzheimers.
I am suspicious that elemental aluminum in the body, like lead, can
cause
disease and the disease I am most suspicious of is Alzheimers or even
Parkinsons.
That too much elemental aluminum can trigger a brain disease.
Maybe elemental aluminum triggers prion disease also.
If you have an aluminum pot with exposed elemental aluminum and
cooking
very acid foods such as rhubarb or tomatoes in such pots, I suspect
that the food
is laden with elemental aluminum.
I have heard some people break out into a rash or skin disease after
eating
rhubarb cooked in an aluminum pot.
> Aluminum makes up about 8% of the surface of the earth. As long as
> you live here, you are going to get aluminum, whether you like it or
> not. You might want to minimize your exposure, which is fine, but
> worrying about the rivets in a pot is a bit extreme. Why do you
> prefer fluorinated hydrocarbons? Aren't you afraid of those, also?
> There are real hazards in our life that we should minimize but we
> accept in the normal routine of our life. Then there are quite
> innocuous theoretically potential hazards which play no real role in
> our lives that we spend inordinate amounts of time, effort, and money
> in eliminating. I suggest that you take reasonable steps to limit
> aluminum intake. Then accept a certain background level which is
> inevitable.
I suspect, but have no evidence, that a country that uses a lot of
aluminum
cookware has a higher rate of Alzheimers than does a country that uses
nothing but stainless steel cookware.
It has taken humanity 2,000 years to realize the danger of using lead
in the food
and water supply of people. Similarly, I suspect the exposure to
elemental
aluminum is not a safe thing but that it accumulates and perhaps
triggers a
disease in the body.
With that said, it is not wise to cook with elemental aluminum
cookware. I
suppose the safest cookware is pure iron. Perhaps the enamel coated
steel
is safe. I am guessing that the alloys of stainless steel are safe and
that it is
difficult for those alloys to enter the food. I am guessing that
teflon coating
is safe and that even if ingested that it will be stooled out. But is
elemental
aluminum stooled out or does it accumulate like lead and mercury?
I believe that science has never really questioned the safety of
aluminum as per
the food and water supply. It is so ubiquitous, but that does not mean
it is
safe.
Aluminum in compounds and complexes is probably safe, but Nature does
not have
aluminum in elemental form spread all over the environment.
In fact, I know of no case where elemental aluminum was filed and
eaten and
whether any health damage accrued.
Prudence tells me that since elemental aluminum is not found in the
environment
then I certainly do not want exposure to elemental aluminum in my food
and water
from pots and pans exposed to high heat.
----------
Subject:
Re: Prion: An Active / Receptive Chemical Paradigm
Date:
Thu, 28 Aug 2003 02:45:20 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/356702db0ef73f07%3Fhl%3Den%26&msg=356702db0ef73f07>@dtgnet.com>
Newsgroups:
sci.chem, sci.bio.technology
"Jo‹o Antonio" wrote:
> I'm not an expert but I have stumbled more than a few times on articles
> claiming that
> the 'bending" of a prion (i.e. conversion of helix to sheet) is promoted
by
> metal ions.
> I read things about copper, but aluminium can work too.
> The metals can interact with pending basic sites and change both
> the secondary and tertiary structures
> So it's not just a worry, it's a fair research project...
The metal connection makes sense also in the fact that in recent years
some
drugs have been discovered to be effective in prion disease, yet the
way the
drugs work is a total unknown.
If one considers that the 2 drugs found effective against prion
disease have
some
means of binding with metal ions in the brain and thus interfering
with the bad
prion formations, well, perhaps we are coming closer to a better
understanding
of prion disease.
Now I wonder if too much mercury in the body, not enough to kill
outright but
too much mercury has a disease that can be considered say the "prion
disease of
mercury poisoning"
And also, if aluminum is the culprit as a carcinogen for prion
disease, makes
one wonder if England grass fields where scrapie for sheep or Mad Cow
Disease,
whether there is more aluminum in the grasses and vegetation that they
eat. And
that in the USA where prion disease is rather rare, whether there is
much less
aluminum in the vegetation and grasses. Obviously copper is a vital
element for
life, but I think aluminum was never a vital element.
AP
Subject:
quinacrine & chlorpromazine act to disengage aluminum in
Prion Disease
Date:
Thu, 28 Aug 2003 04:56:58 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/msg/356702db0ef73f07%3Fhl%3Den%26&msg=356702db0ef73f07>@dtgnet.com>
Newsgroups:
sci.chem, sci.bio.technology, sci.med
Archimedes Plutonium wrote:
> The metal connection makes sense also in the fact that in recent years
some
> drugs have been discovered to be effective in prion disease, yet the way
the
> drugs work is a total unknown.
> If one considers that the 2 drugs found effective against prion disease
have
> some
> means of binding with metal ions in the brain and thus interfering with
the bad
> prion formations, well, perhaps we are coming closer to a better
understanding
> of prion disease.
Now I wonder if aluminum is the catalyst for creating Prion disease, I
wonder if
the effectiveness of these 2 drugs of quinacrine and chlorpromazine
act as a
"getter" of aluminum? I wonder if these 2 drugs have a similar
chemical reaction
as a aluminum pot with rhubarb in that the rhubarb absorbs and gets
aluminum.
Does any chemist know if these drugs of quinacrine and chlorpromazine
react
with aluminum in the brain tissue?
And if part of the above is true, then even more effective drugs can
be found to
conquer prion disease because it would only require a drug to "get
aluminum".
Now I wonder if the history of prion disease is only a modern history
because
aluminum manufacture was only some few hundred years. And perhaps the
kuru
victims were given modern day aluminum cookware.
And perhaps sheep scrapie is so prevalent in England because of some
aluminum
based compound applied to sheep in England? Who knows? I do remember
that some
hair ointment or lotion has a lot of aluminum in it and perhaps sheep
are given it.
Or that some plant in England in the pastures contains too much
aluminum?
Anyone know when the first aluminum pots and pans can into being?
Then again, it maybe copper and not aluminum. Perhaps too much copper
causes good prions to turn into bad prions. And perhaps those 2 drugs
"get copper" and not aluminum.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/356702db0ef73f07%3Fhl%3Den&msg=1049060b96b2af8c>
@gmail.com>
Date: Thu, 18 Apr 2013 12:17:30 -0700 (PDT)
Subject: subject contained the words metal & poison: Metal Causing Diseases
Alright, it was still 2003 and then my posts started the subject line
with the key words of "metal" and "poisoning" as seen in these two
posts of 2003.
----------
Subject:
Re: prion disease a chelation process Re: quinacrine &
chlorpromazine act to disengage
aluminum in Prion Disease
Date:
Thu, 28 Aug 2003 12:50:22 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/356702db0ef73f07%3Fhl%3Den&msg=1049060b96b2af8c>@dtgnet.com>
Newsgroups:
sci.chem, sci.med, sci.bio.technology
Now here is an idea that is very pretty because of its simplicity.
It is well known that the prion molecule is not understood for its
function or
role. It is not known why prions exist at all. Some have suggested
that the
molecule is cell-wall-building. But the point I am making is that the
_function_
of prion molecules was never really well understood.
Perhaps that function of prion molecules is that of mopping up or
cleaning out
or balancing overabundant metal ions in the brain region.
In other words, perhaps the animal body creates prion molecules as a
natural
Chelating agent. Perhaps that was one of the major roles of prion
molecules
was to chelate excess metal ions such as copper. But when the brain
gets too
much metal ions of say perhaps aluminum, that the good prions are
doing their
job of trying to rid the body of these bad metal ions and in the
process of
trying to remove the metal ions that the good prions have now been
turned
into bad prions.
So that one garbage removal of excess metal ions has now become a
different
garbage of malformed prions.
And that when chemists add quinacrine and chlorpromazine to an animal
body
that has too much metal ions and its good prions are trying to remove
the
metal, that these drugs of quinacrine are further help in getting rid
of the
metal.
AP
Subject:
prion disease is a Metal-Ion disease/poisoning Re:
Prion:
Date:
Fri, 29 Aug 2003 12:18:48 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/356702db0ef73f07%3Fhl%3Den&msg=1049060b96b2af8c>@dtgnet.com>
Newsgroups:
sci.chem, sci.med, sci.bio.technology
Wyrin wrote:
> I hate feeding trolls, but thats just rubbish
But you do not hate feeding a genius, eh.
> Try looking into Transthyretin - and the mechanism by which that forms
> amyloid, just like prion protein does.
Try making a simple calculation for chemistry. How much of a
difference in
energy within molecule A in order for molecule A to transform molecule
B
into a duplicate of A? What is the minimum amount of energy difference
for
this reaction to occur:
Molecule A + Molecule B ---> 2 Molecule A
Shape of molecules is part of their intrinsic energy. The shape of bad
prions
versus good prions makes for an energy difference of less than 5%
between
the bad prion. So, can a molecule with 5% energy difference remake
another
molecule into identical?
Even the physics of photocopy machines would disprove the Prusiner
prion theory
because if Prusiner is correct then the future copy machines will be
prion activated where there is no electricity but just a vat of prion
chemicals
and you just put the paper in and a photocopy comes out. And, if
Prusiner is
correct then in the million year future, prion technology will
eliminate
cloning
as wasteful of energy. This is where in a million years you have a
person and
next to that person a block-of-prion matter and overnight you have 2
prion
blocks.
> Try looking at how crystallisation happens; how clay banks grow in rivers
> Try doing any scientific research rather than spouting off all this
rhetoric
> without anything to back it up save supposition and bad logic
I know of no clay A that changes clay B into another clay A.
Try thinking about real science instead of being buffaloed and
hornswoggled by
fake bandwagon science of Prusiner.
> Now, to help guide you along with the metal ions stuff - it has been
shown
> that mice treated with copper chelators - ie things that strip copper
from
> the cells - develop a brain pathology very similar to that in prion
disease,
> but with no amyloid formation.
A glimmer of science thinking on your part!
Chemistry has chelation. Chemistry has ligand. Chemistry has
thermodynamic
operators. Chemistry does have metal ion mobility. Chemistry does have
catalysis.
Chemistry does not have molecule duplication by another molecule.
Experiment (a) Take a healthy sheep and inject metal ions of copper,
aluminum.
Inject enough that you do not have to wait 10 years for scrapie. If
the sheep
develop scrapie in fast order, then the cause of prion disease is not
prion
molecules but rather instead it is Metal Ions and the prions are just
a side
reaction to the metal ion presence.
Experiment (b) Take a scrapie sheep and inject metal ion chelates that
removes
various copper and aluminum ions. See if the sheep become healthy
again.
Experiment (c) Measure the difference of metal ion body content of
scrapie
sheep from normal sheep. Is there a difference in metal ion content?
Experiment (d) What metal ions does quanacrine and chloropromazine
chelate??
And is there a more powerful chelator? If so, do we have a better cure
for
Prion diseases in all animals by finding the best chelator.
Trouble with the above writer is that he cannot understand that in
science
there comes a time to stop defending the current bozo theory and
instead start
prying into the real truth and mechanisms of the subject.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/b169209bb8253035%3Fhl%3Den%26&msg=b169209bb8253035>
@gmail.com>
Date: Thu, 18 Apr 2013 12:33:09 -0700 (PDT)
Subject: hot oven incineration in Mad Cow Disease, means mercury is the
likely culprit: Metal Causing Diseases
Alright, in my history of posting this metal causing diseases, it is
seen that by 2003, I was firmly in the camp of metal causing
mechanism.
The obviousness of having to burn in hot ovens, Mad Cow disease means
that the disease is not living tissue of the Prusiner Prion silliness,
but rather is a inorganic chemical element like mercury or a mercury
compound.
----------
Subject:
Re: prion disease is a Metal-Ion disease/poisoning Re:
Prion:
Date:
Tue, 02 Sep 2003 01:43:35 -0500
From:
Archimedes Plutonium (a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/b169209bb8253035%3Fhl%3Den%26&msg=b169209bb8253035>@dtgnet.com>
Newsgroups:
sci.med, sci.bio.technology, sci.chem
doe wrote:
> Using that theory then one would wonder how after all these millions of
years
> .. there would be any animals .. left .. ?
> How could a system so easily unbalanced .. simply eating .. EVER survive?
> Simply .. eating .. is going to kill them ..?
> COULD the fact BE something has been introduced to a herbivore population
which
> would CAUSE the absorption of too many metals ..?
> Below ..
> The American Heritage¨ Dictionary of the English Language: Fourth
Edition.
> 2000.
> blood meal
> NOUN: The dried and powdered blood of animals, used in animal feeds and
as a
> nitrogen-rich fertilizer for plants.
> Blood Meal 13-1-0
> Kiln dried Blood Meal has been used for years by organic gardeners as a
> natural, slow release source of nitrogen, plus trace minerals. Use 1-3
lbs. per
> 100 sq. ft. before planting, or side dress later in the season.
> #869 5 lb. Bag (6 lb) $6.95
> This heme-iron gets right into the water and this heme-iron leads to
absorption
> of minerals at a HIGH RATE .. higher than NORMALLY POSSIBLE in a
herbivore who
> NORMALLY WOULD NOT CONSUME BLOOD AT ANY TIME .. ?
> Heme-iron has the unique ability to ENHANCE the absorption of other
minerals
> ingested with it.
> At high rates WHETHER THE BODY NEEDS IT OR NOT .. at "all times of
minerals
> status" ..
Prion disease is rare, very rare, except for scrapie in sheep. That
immediately
rings an alarm bell, or should ring a alarm as to why these animals.
The answer
is likely to involve the food they eat.
Sheep probably eat more metal ions in their grazing than other
grazers.
Has anyone done a field test samples of England grazing fields of
sheep where
scrapie is numerous and compared the metal ions to a field say in New
Zealand or
Australia where scrapie also occurs.
Has anyone done tests as to the incineration of prion carcasses. Heat
so high that
it incinerates the proteins, but does not alter the metallic ions.
Has anyone researched whether the sheep farming of England introduces
more
metallic ions into the sheep whether from increased aluminum or copper
implements.
And the question of whether the English countryside has more metal
ions due to
industrial pollution.
Prion disease is rare and its rarity conforms to the idea that a
concentration of
metal ions in older age leads to death. As for human CJD prion disease
is
hereditary because the genetics of a few people are more susceptible
to a protein
response by the body due to an excess of metal ions in the brain. The
cause of CJD
would then be the excess metal in the brain and the response or
symptoms would be
the prion proteins trying to remove the metal ions. As they attempt to
remove the
metal some good prions become altered in shape. Just as white blood
cells become
altered in shape once they engulf and try to remove bacteria.
Prions are the garbage removers of the brain that white blood cells
are the
removers the body of foreign invaders. When good prions come in
contact with metal
ions, many of them are changed in configuration.
How many different aluminum and copper ions exist? At least 6. And
there are
some 6 varieties of bad prions. So for each metal ion of aluminum in
excess in the
brain can lead to those numbers of varieties of bad prions.
These are not really bad prions for they are just prions trying to
remove the
metal ion excess in the brain.
Prion disease is a fairly new disease in the history of time because
before the
industrial age of numerous metal production and thus pollution, the
chances of the
body ingesting metal ions was low.
And if this theory is correct then the areas in the USA that should
have more
scrapie are areas of high pollution of metallic ions to grazing
animals. And areas
in the USA much like England where a lot of mosses and lichens are
found and sheep.
If memory serves me, in the USA the states of Oregon and Wisconsin are
the most
scrapie prone states which coincides with the fact that they are two
of the
highest moss and lichen states.
Does CJD have a geographical concentration? If this theory is correct
then it
probably does increase in areas where metal ions are in high
pollution.
In the case of the 4 victims in England in the early 1990s, I wonder
if anyone did
an autopsy on the amount of metallic ions in the brain tissue of the
victims. The
supposed blame is on a restaurant with tainted meat. And the victims
were
unusually young to contract prion disease. So I am suspecting that if
this theory
is correct then some metallic ions are more deadly than others such as
perhaps a
rarer aluminum ion or a rarer copper ion.
So that if you ingest a rarer metal ion can have a Prion disease in
fast forward.
It would be nice if an autopsy of those England victims were
conducted.
As I said before, the gravest trouble with Prion disease knowledge is
the time it
takes to get any sort of answers since the date of infection and the
date of
disease symptoms is 30 years apart. Much like horticulture in that you
have to
wait 30 years to find out answers about trees.
Archimedes Plutonium, a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/b169209bb8253035%3Fhl%3Den%26&msg=b169209bb8253035>@hotmail.com
whole entire Universe is just one big atom where dots
of the electron-dot-cloud are galaxies
--------------------
From: a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/b169209bb8253035%3Fhl%3Den%26&msg=b169209bb8253035>@hotmail.com
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,sci.chem,sci.med
Subject: BSE in USA today and priondisease is really caused by metals
in the environment
Date: 24 Dec 2003 00:07:08 -0800
Bob (xyzbbru...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/b169209bb8253035%3Fhl%3Den%26&msg=b169209bb8253035>@uclink4.berkeley.edu>
wrote in message
news:(73hfuvsn2tvhqravrrv77qacfm2rgg9__BEGIN_MASK_n#9g02mG7!__...__END_MASK_i?a63jfAD$z...@4ax.com
<http://groups.google.com/groups?as_umsgid=(73hfuvsn2tvhqravrrv77qacfm2rgg9__BEGIN_MASK_n#9g02mG7!__...__END_MASK_i?a63jfAD$z...@4ax.com>>...
(huge snip)
>
> But some of the elements are just too scarce. The level of
some,
> including Hg and Pb, makes them essentially invisible. That
doesn't
> preclude that some special case might have arisen where such an
> element is used, but it offers a fine explanation of why they
are not
> used commonly. It isn't hit or miss, but simply that heavy
elements
> are invisible (too low concentration). (Abundance loosely
correlates,
> inversely, with heaviness, for the heavy elements.)
>
> Even among the abundant elements, there are differences in how
much
> they are used. Aluminum and silicon are abundant crustal
elements, and
> have at least reasonable (tho low) abundance in the oceans. Yet
there
> is no known biol role for Al and only specialized roles for Si
(as in
> diatom skeletons).
>
> bob
Bob, after responding to your above I remembered in the news
today of
the first known USA outbreak of BSE in cattle in the state of
Washington.
The last time I visited Prion disease I was of the firm opinion
that
the disease is purely a metal contamination of the environment
which
nicely accounts for the huge variety of prions and accounts
nicely for
why those proteins are indestructible unless enormous hot oven
fires.
Accounts nicely for the noted hereditary affliction where entire
families catch it. And accounts nicely for the catching by
eating.
Bob, several questions:
(1) Has anyone linked the 2 metal ions of copper to 2 different
strains of prion disease. Has anyone linked the 2 metal ions of
zinc
to 2 different strains of prion disease so that copper and zinc
account for a total of 4 different varieties of prion disease.
Also
for the 2 of iron, 2 of nickel etc etc
(2) Bob, do cattle ingest more of some metal ions such as say
cobalt
or cadmium
or some other metal ion which neither sheep nor humans eat? I am
thinking that perhaps the Prion disease of cattle can be blamed
more
on one specific metal than the prion disease found in humans,
sheep,
other animals. Such that the metal ion that causes most human
prion
disease is a different metal from that of sheep scrapie.
Prion disease mechanism: I suspect that all prion diseases are
when a
metal ion gets into the brain it alters the manufacturing site
for
normal prions and leaves a template that is a rogue template
which
then spews out deformed prion proteins.
So the entire cause of this disease are metal ions in the
environment.
Bob, has any scientist started to make links between metal ions
of
copper, iron, zinc and the various strains of prion molecules???
If I am correct, then it is a waste of time and money to burn
prion
cattle and other livestock. That Prion disease is not a living
organic
contagion but is rather inert physical metals that are ingested.
When
eating a BSE meat, it is the metal ion that is ingested that
causes
the disease.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/6a05fdb164c63847%3Fhl%3Den&msg=f3c288680bf7350f>
@gmail.com>
Date: Thu, 18 Apr 2013 13:00:36 -0700 (PDT)
Subject: chapters of this textbook written on the Internet; Mosley's 2nd
brain gut: Metal Causing Diseases
Before I get to the main topic, let me note that I watched on PBS
Mosley's Gut show where he swallows a camera and watches it travel
through his gut. Now I learned something new from that program that I
was not aware of before and could possibly come in useful in my Brain
Locus theory or this metal causing disease theory. For it was
explained that the intestine has over 100 million neurons that
composes a small brain, a second brain so to speak. So I was not aware
of that. And in the Brain Locus theory that would come in aid in the
idea that neurons are just the output of the brain not the input which
would be photons shot from the Nucleus of the Atom Totality and our
brain is just a radio-receiver antenna type of apparatus.
Here is a current outline of this textbook and its chapters. It is a
textbook written exclusively on Usenet and is one of the first
textbooks written on the Internet. I probably am the first person to
write my science books exclusively and in total by using the Usenet
Internet. All my posts and replies can be dug up by the search
engines.
Metal Causing Diseases (Homosexual, Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion)
Chapt1: History of this book
Chapt2: earlier metal diseases: lead then mercury then asbestos and
now mostly mercury
Chapt3: asbestos diseases, a semi-metal disease
Chapt4: experimental math-statistical proof that autism (ASU report)
is caused by mercury and cadmium and the mechanism is similar to
chromium-6 (PBS report)
Chapt5: Homosexual
Chapt6: Autism
Chapt7: Schizophrenia
Chapt8: Depression
Chapt9: Parkinsons
Chapt10: Alzheimers
Chapt11: Prion
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/c782f90d96788c79%3Fhl%3Den&msg=f2dc3a8be47c4dca>
@gmail.com>
Date: Thu, 18 Apr 2013 13:30:08 -0700 (PDT)
Subject: similarities between Homosexual, Autism and Schizophrenia:
Homosexual metal caused disease: Metal Causing Diseases
Now it is likely that mercury and cadmium and their compounds are the
primary causes of all 7 of these brain diseases:
Homosexual, Autism, Schizophrenia, Depression,
Parkinsons, Alzheimers, Prion
Now I have listed them in chronological order of when the disease is
usually attacking the human body of a human age. Homosexual preference
is likely to have been set in place in the fetus in the womb. Too much
mercury, perhaps far too many tuna fish sandwiches. Perhaps far too
much mercury in the air we breathe, especially near coal fired
electric plants.
Now are there any similarities between the first three chronologically
listed diseases? Can we sort of see some blending of features or
merging of features from homosexuality to autism/asperger to
schizophrenia?
I think we can safely say there is one huge similarity. A similarity
that the poison of mercury creates.
Mercury as a poison creates a disconnect with reality. We see it in
the case of Schizophrenia of "hearing of voices" that are non-
existent. In Autism/Asperger we see it in the disconnect with reality
of
making social-contact.
And we see it in the unreality of sex preference of male to male or
female to female when sex is designed for only male to female.
So, what can we conclude from this analysis? We can conclude that what
causes Homosexuality, Autism/Asperger, and Schizophrenia has the power
to alter the brain/mind so that it no longer is able to see reality
but rather sees unreality. Is it genetics? Obviously not, but rather
it must be a chemical from the environment that makes the brain
altered to see unreality.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>
@gmail.com>
Date: Thu, 18 Apr 2013 22:35:40 -0700 (PDT)
Subject: phosmet and then magnetic manganese: Metal Causing Diseases
Now in the below two old posts we see me talking about phosmet in
December 2003 and magnetic manganese in January 2004.
--------------------
From: a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>@hotmail.com
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,sci.chem,sci.med
Subject: phosmet the cause of England Prion density Re: BSE in USA
today and priondisease is really caused by metals in the environment
Date: 29 Dec 2003 22:39:44 -0800
Mark Thorson (nos...@sonic.net> wrote in message news:
(3FF0EB25.F3686...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>@sonic.net>...
> Bob wrote:
>
> > a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>@hotmail.com
(Archimedes Plutonium) wrote:
> > >
> > >The last time I visited Prion disease I was of the firm
opinion that
> > >the disease is purely a metal contamination of the
environment
> >
> > There is no basis for that -- and no particular reason that
metal ions
> > couldn't be one factor among many.
> >
> > (I vaguely recall one paper on yeast prions, which showed an
effect of
> > metal ions on certain prions and not on others. I don't
remember any
> > details beyond that, but it generally agrees with my previous
point.)
>
> This site has an interesting review of the main theories
> on the causal mechanism of BSE:
>
>
http://www1.umn.edu/eoh/hazards/hazardssite/prions/prionmetabolislm.html
<http://www.google.com/url?sa=D&q=http://www1.umn.edu/eoh/hazards/hazardssite/prions/prionmetabolislm.html&usg=AFQjCNF_tFVxarlwpYnA7DFzagNv2bOBsg>
>
> One of these theories involves copper deficiency and
> manganese overload as possible cofactors with exposure
> to a certain insecticide.
Thanks for that pretty Univ. Minnesota reference. I am going to
quote
a sample
paragraph from your above reference website:
--- quoting Univ. Minnesota ---
A copper deficiency may predispose cattle and humans to PrPc
transformation and misfolding. This theory
states that the BSE variant in
humans
(vCJD) is caused by a low copper and high manganese content in
soil
and
food consumed by humans.(14) When
PrPc
binds manganese instead of copper it becomes more protease
resistant over time and loses
superoxide dismutase activity.(22) It is believed that excess
manganese entered the
soil by the use of sewage sludge
as
fertilizer and manganese-based pesticides. A group of researchers
have
concluded that PrPc plays a role
in
copper metabolism or transport and that disturbance of this
function
may be
involved in prion-related
neurotoxicity.(16)
In conclusion, phosmet may have
caused
an initial mutation of PrPc
--- end quoting ---
I call it pretty because it surprized me. I was thinking all
along
that it was a Metal Ion excess that was generating the Prion
disease
never dawning on me that it could be a Metal Ion Deficiency.
And the ominous role of pesticide phosmet. So it was phosmet that
created the huge concentration density of prion disease in
England. I
wonder if Canada and its cattle industry where the recent
Canadaian
and now USA outbreak of prion disease.
But I wonder if scrapie sheep have analogous pesticides used on
them
as phosmet on cattle? And whether it is copper and manganese
metal
ions that causes scrapie?
And whether the plethora of variants of Prion disease matches the
variety of both Copper and Manganese ions??
Prion disease is finally being reckoned and solved
scientifically,
unlike the last decade of the 20th century which could be
described as
a decade by economists as the science-irrational-exuberance with
Enron
and Stanley Prusiner the eye of that irrational exuberance.
Yes, indeed, it looks as though the science of Prion disease is
beginning to be a "science" and not a "Stanley Prusiner decade of
publicity stunts".
AP
From: a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>@hotmail.com
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,sci.chem,sci.med
Subject: magnetic manganese affecting yeast; the cause of prion
diseases
Date: 18 Jan 2004 11:12:03 -0800
delc...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>@uniserve.com
(Del Crow) wrote in message news:
(6b500d90.0401171246.63a77...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/4fa440bc6417cf72/5f1bb05d2635d885%3Fhl%3Den&msg=5f1bb05d2635d885>
@posting.google.com>...
>
> #### Not just brain, whole body, every cell, hundreds to
thousands of
> mitochondria per cell require trace minerals to function. Some
> substitutions are commonly made Faulty prions, mainly
carrying (I am
> adding this word in here)"magnetized" Manganese on the amino
acid
> Tyrosine where 4 molecules of copper should be becomes a
"wrong"
> breakpoint creating a bottleneck of processes. Manganese has
the
> interesting ability of being able to oxidize several times
I have told Bob that yeast studies are irrelevant to Prion
disease
because yeast does not carry the diseases of prion.
But perhaps yeast studies can now be useful.
Experiments: I believe no-one has experimented with yeast where
they
inject magnetic manganese ions and measure the affects thereof.
It is quite possible to turn perhaps yeast into dangerous disease
infecting yeast by the infusion of magnetic manganese ions.
And in those cases in past history that were given a description
of
"spontaneous prion disease" were perhaps not really spontaneous
but
cases in which an individual ate both yeast plus magnetic
manganese
ions and the combination of the two into the body began the prion
disease.
Question to DelCrow: How does the ion of magnetic manganese hold
up as
far as stability is concerned? Because we know that prion
diseases is
very persistent and needs high temperatures of burning carcass to
extinguish the disease. So, does high temperature burning destroy
the
Magnetic Manganese?? How stable and persistent is Magnetic
Manganese
in the environment??
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/1bdb8754cbc1c335%3Fhl%3Den%26&msg=1bdb8754cbc1c335>
@gmail.com>
Date: Thu, 18 Apr 2013 22:44:47 -0700 (PDT)
Subject: all types of metals, mercury, cesium: Metal Causing Diseases
Now in the below two old posts of mine
First time in a title subject of January 2004, do I mention
Alzheimers, Parkinsons, and Prion caused by metals in the subject
line.
And after a poster in January 2004 added magnetic manganese to my
prion thread, I let the floodgates open with all types of metals--
mercury, cesium etc.
Now this is the last post of a overall review of some of my history in
writing this book. There are thousands of post made by me concerning
this textbook. This is now 2013 and I am hoping to consolidate this
book spurred on by the recent evidence of Arizona State University
that correlated the severity level of autism with mercury and cadmium
levels found inside the autistic child. And by the recent PBS coverage
of chromium-6 and how it damages the body.
--------------------
From: a_pluton...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/1bdb8754cbc1c335%3Fhl%3Den%26&msg=1bdb8754cbc1c335>@hotmail.com
(Archimedes Plutonium)
Newsgroups: sci.bio.technology,sci.chem,sci.med
Subject: metal-ions cause modern diseases of Alzheimers, Parkinson,
Prion Re: does Canada use Phosmet on their cattle??
Date: 7 Jan 2004 11:43:43 -0800
Bob (xyzbb...@uclink4.berkeley.edu> wrote in message news:
(fmdkvv0l03vif2utmi67m17btljfm1m...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/1bdb8754cbc1c335%3Fhl%3Den%26&msg=1bdb8754cbc1c335>@4ax.com>...
> On Mon, 5 Jan 2004 16:16:29 +0100,
"DP" (joze.daro...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/msg/1bdb8754cbc1c335%3Fhl%3Den%26&msg=1bdb8754cbc1c335>@guest.arnes.si>
> wrote:
>
> >
> >some people believe that BSE could be the cause of vJCD in
human?!
>
> There is pretty good evidence for that -- though hard to know
for
> sure.
>
The more likely answer is that in our modern environment where
industrial chemicals, especially to the food supply of herbicides
and
pesticides, have created "modern diseases" of Alzheimers,
Parkinsons,
and Prion. They all take long periods of time to develop
coinciding
with accumulation buildup in the body.
They all affect the brain which is the most sensitive portion of
the
body to Metallic Ions.
The place where the pesticide Phosmet is most dense is England
and
England has the most severe sheep scrapie plus BSE. I do not know
if
England has the most dense population of Alzheimers and or
Parkinsons.
Then again, I do not know if phosmet is responsible for
Alzheimers and
Parkinsons.
I do know that the Midwest farm states in the USA has the highest
USA
concentration of Parkinsons. I am thus guided into thinking that
the
reason is because of the higher concentration of herbicide and
pesticide in the air and in the water and in the food. Some
scientists
and politicians and commercial people have tried to hide this
Parkinson density under the quiet rug. And when they cannot hide
it,
they then make the absurd claim that the genetical background of
most
people in the Midwest USA are Scandinavian origin who are more
prone
to Parkinson which is a hogwash argument.
>
> >but they also say that incubation period of vJCD is /much /
shorter than
> >in the case of the 'classical' JCD. which could be about 10 to
20 years.
> >question: why haven't we got an epidemic vJCD in great
britain, for
> >instance?
>
>
> Well, that is a very interesting question. In fact, we do not
know two
> key things. We do not really know how long the incubation
period is,
> and we do not know how transmissible it is (that is, what is
the
> probability that a human who eats a BSE prion will get the
human
> disease). In general, there is a barrier of transmitting prions
from
> one species to another, but there is no way to know how big the
> barrier is. People have computer models for the vCJD epidemic
-- but
> the models give widely varying predictions because of the
unknowns.
> Some people think there will be a big epidemic later, allowing
for a
> long incubation time. And some people are beginning to back
away from
> the more pessimistic predictions.
>
From what I remember in my readings of prion disease is that vCJD
is
equally susceptible by all age groups not just the young. Only
that
CJD seems to attack only the old. The vCJD attacks young equally
as it
attacks old. I suspect the reason is because metal-ions cannot
differentiate whether a human is young of age or old of age. And
that
if the dosage of metal-ions is big enough it matters not whether
the
person is young or old. CJD maybe a different ion of say copper
or
manganese or iron from vCJD. Not only do we have the various
different
ions to cause prion disease but we also have the two variables of
whether the metals are excess in the body or a deficiency in the
body.
If a disease is caused by excess then it maybe a fast attacking
disease whereas if the disease is caused by deficiency it is slow
acting.
>
> >and again: why should be we -people over 55-60/y - immune
against vJCD?
From my readings, old people are susceptible to both CJD and
vCJD, but
young people are susceptible to vCJD. A possible chemical answer
is
that young people often are more susceptible to a chemical in the
environment more so then old people whose body mass is larger and
whose cells are hardened by age. When you spray phosmet over
human
populations the young are usually the first to see symptoms.
>
> I'm not sure what the data is. I have heard that vCJD strikes
younger
> people. Do you know whether that means it strikes all ages
"equally"
> (which would be very different from "natural" CJD), or whether
it
> occurs _mainly_ in younger people?
>
> If the former, it could be due to it being to an infection. The
> infectious vCJD could hit all ages "equally". In contrast, the
regular
> CJD requires some odd event to initiate in the body, and so the
older
> one is, the more likely.
>
> If the latter is true... Hm, I wonder whether that initial
uptake of
> the protein from the digestive system works better in younger
people??
> But take that as speculation from me, not knowledge.
>
> bob
Bob, granted many of my questions or trial experiments are
"irrelevant", which is usually the norm for research in
explorative
mode. But I also must lay a "irrelevancy" on your thinking
regards to
yeast prions. In that yeast prion research is irrelevant for
Prion
disease because yeast prions are not disease forming. To talk
about
yeast prions in prion disease is like talking about apples
compared to
golf balls. And if the science journals deleted or cut out all
articles on yeast prion then they would cut out 99/100 of all the
research related to prion disease.
If it turns out that Prion disease is a chemical disease caused
by
metal-ions, then the time period of the 1980 to 2004 will have
been
seen as years in which the biology community had wandered astray.
And
that they had filled NATURE and SCIENCE and the literature full
of the
yeast research that was utterly irrelevant as regards to the
disease.
Bob, if I take my clothes out to dry in the sun, then the
wrinkles are
altered. Likewise, if I take a protein from one solution into a
different solution and because the geometry is altered, does not
allow
for a scientific conclusion that some misfolding had taken place.
In
this sense the decade of the 1980s and 1990s or yeast prion
misfolding
or of animal prion misfolding is no more of science merit then to
think that clothes drying in the Sun is "misfolding".
AP
superoxide dismutase and ALS disease resembles Prion; cesium/rubidium
the disease agent? Re: function or role of Prion proteins is copper
transport
From: a_plutonium
Date: Sat, Aug 26 2006 1:53 pm
Groups: sci.med, sci.chem, sci.bio.technology
a_plutonium wrote:
>Well, I am glad to announce that from reading this website:
>--- quoting http://srs.dl.ac.uk/Annual_Reports/AnRep00_01/prion.htm
<http://www.google.com/url?sa=D&q=http://srs.dl.ac.uk/Annual_Reports/AnRep00_01/prion.htm&usg=AFQjCNFMspzmcuzQ6m5MWkg81XIwaM8VAQ>
---
> The research indicates that the normal isoform of PrP has the
>necessary properties, in the form of histidine residues 96 and 111, to
>transport copper from outside the cell through the process known as
>endocytic cycling.
>--- end quoting ---
>That the function of prion proteins is *surprize* the transportation
of
>copper.
>All of a sudden the Metal Causation theory becomes a million times
more
>easy and becomes very much more the true theory.
>From that website above it is mentioned that superoxide dismutase
closely resembles prion proteins. Even the geometry of the molecules
resemble one another.
The function of superoxide dismutase is to oxidize the copper ions
from
say +2 and +1.
But this brings up an interesting question as to what the "infectious
agent" would be in prion disease, since superoxide dismutase is
related. The most reactive alkalis effect superoxide dismutase such as
cesium and rubidium.
How much cesium or rubidium in an animal body before it is toxic?
All along I am thinking it is mercury that is corrupting the prion
proteins. Perhaps I should look into these most reactive of alkali
metals.
And another reference says that infectious prion proteins are
sterilized by autoclaving at 600 degrees C for 15 minutes. I looked up
the boiling point of cesium and rubidium which are 671 degrees C and
688 degrees C respectively.
So is cesium or rubidium in tiny quantity in the brain the causing
agent of Prion diseases, and not mercury?
The above researchers used some fancy X-ray scanning. I wonder if that
same method can reveal whether diseased brain of a CJD victim
contains-- mercury, or cesium or rubidium?
What modern day instrumentation would best take a diseased BSE or
scrapie or CJD and tell us the amounts of metals in the brain tissue?
Is it mass spectroscopy or some form of X-ray diffraction?
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/d5445d944e571bf9%3Fhl%3Den&msg=c0e921f745903219>
@gmail.com>
Date: Thu, 18 Apr 2013 23:41:59 -0700 (PDT)
Subject: why Homosexual cannot be a genetic disease, but a environment
metal: Metal Causing Diseases
Earlier I made some statements that were wrong, saying that before the
Bronze age there was no homosexuality in human populations. But it is
more complicated then that. Because methylmercury and other mercury
compounds are collected in living tissue and when they are burned,
such as forest fire or ancient human fireplaces, methylmercury can be
inhaled.
And homosexual children should have a higher rate of incidence in
mothers who are close to fireplaces breathing smoke and smoke
cigarettes.
Here is a quote from Wikipedia on methyl mercury, the same substance
in the ibis research proving that methyl mercury turned ibises into
homosexuals.
--- quoting in various parts of Wikipedia ---
Methylmercury (sometimes methyl mercury) is an organometallic cation
with the formula [CH3Hg]+. It is a bioaccumulative environmental
toxicant.
(snip)
It also has very high affinity for sulfur-containing anions,
particularly the thiol (-SH) groups on the amino acid cysteine and
hence in proteins containing cysteine, forming a covalent bond. More
than one cysteine moiety may coordinate with methylmercury, and
methylmercury may migrate to other metal-binding sites in proteins.
(snip)
Currently there are few anthropogenic sources of methylmercury
pollution other than as an indirect consequence of the burning of
wastes containing inorganic mercury and from the burning of fossil
fuels, particularly coal. Although inorganic mercury is only a trace
constituent of such fuels, their large scale combustion in utility and
commercial/industrial boilers in the United States alone results in
release of some 80.2 tons (73 tonnes) of elemental mercury to the
atmosphere each year, out of total anthropogenic mercury emissions in
the United States of 158 tons (144 tonnes)/year. Natural sources of
mercury to the atmosphere include volcanoes, forest fires and
weathering of mercury-bearing rocks.
Methylmercury is formed from inorganic mercury by the action of
anaerobic organisms that live in aquatic systems including lakes,
rivers, wetlands, sediments, soils and the open ocean.
(snip)
Fish and other aquatic species are the only significant source of
human methylmercury exposure.
--- end quoting in parts ---
I am going to argue with the above last sentence of Wikipedia by
saying that the air we breathe and cigarette smoking probably rivals
or out rivals the fish eating source.
Now in the case of asbestos semi metal diseases, we can say that at
some point in past history, there were few if any cases of asbestos
diseases, and the reason is obvious because we never used the material
in any human contact. But then when asbestos was found to be useful
and money-making then it was mined and frequently in contact with many
people and so the rise in asbestos diseases.
Now at some time in ancient human history we can say that few
homosexuals were borne because the contact with methylmercury was a
rare contact especially by pregnant women. Unless they lived near a
smoky fireplace and smoked cigarettes or ate fish that was
concentrated in methylmercury. So in the past history of humanity,
homosexuality was a rare disease. But then comes the Industrial
Revolution with the burning of fossil fuels and in that burning are
many atoms of mercury and the compound methylmercury are released into
the air.
So much so is mercury in the air we breathe that perhaps every breathe
we breathe in 2013 contains atoms of mercury and mercury compounds.
With the widespread presence of mercury by 2013, it is no surprise
that in the UK some 6 percent of the population is homosexual and 4
percent of France and USA is homosexual. Now as the quantity of
mercury and methylmercury increases in the environment as China and
India increase their coal burning and the USA continues to burn huge
amounts of coal and as billions more people drive cars with gasoline,
that perhaps the percentage of homosexuality in human society can
reach 20, 40, 50 percent of populations.
Now why can homosexuality not be a genetic caused disease and must be
a environment metal caused disease? Well, there are two answers that
have to be taken together as one answer. The first answer is that
Darwin Evolution theory is violated by
genetics causing homosexuality. A homosexual person just does not
produce offspring into the next generations so homosexuals should
decrease over time, and instead, homosexuality has increased in world
populations. And the second answer is that we have science research
proof, such as the ibis experiment that methylmercury causes
homosexuality. Now both of those answers together show us that
homosexuality is not a genetics caused feature.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/290a211cba9b062f%3Fhl%3Den&msg=070f506c595ab4f2>
@gmail.com>
Date: Sat, 20 Apr 2013 23:53:41 -0700 (PDT)
Subject: gay and lesbians in Japan since they eat so much fish: Metal
Causing Diseases
Now I was curious about Japan since the figures for UK is 6% gay,
France and USA 4% gay, whether Japan had a higher figure than 6% of
population. And also I was looking to see if the people around
Minamata saw a rise in homosexuality and in autism due to the
methylmercury spill circa 1956. Seems like they are awfully quiet as
to data on gay/lesbian, autism, alzheimers in the Minamata area.
Japan seems rather secretive of statistical data of gay/lesbian
numbers and of autism. The only hint that Japan's numbers are high and
higher than most countries is that one website said that the density
of gays and lesbians is highest in Japan than other countries such as
USA, China, India, UK.
But it appears that in Japan, gays and lesbians can easily get married
and that the social culture is not hostile towards gays and lesbians,
probably because there are so many there in Japan.
Now of the means of intake of methylmercury are basically three means:
1) coal fired plant that releases it into the air breathed
2) eating seafood high in methylmercury
3) smoking cigarettes
Now of those three, Japan is a country where seafood is perhaps its
major food along with rice. And so I would suspect that Japan is very
high in gay/lesbian and autism and if the UK is 6% then I would easily
guess that Japan is 6% in gay/lesbian.
Now the very worst condition to get autism or alzheimers or
homosexuality, is to live near a coal fired electric plant and to
smoke cigarettes and to eat a lot of fish, especially tuna.
Now the lowest rates of homosexuality, autism, schizophrenia,
depression, parkinsons, alzheimers, and prion would be a country that
has no coal burning going on and few gasoline pollution and hardly any
smoking and rarely any fish to eat. This sounds like interior of
Africa or the interior of Russia or the interior of South America.
Newsgroups: sci.chem, sci.med, sci.bio.misc, sci.math
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/f9aa92c15597072d/8ddd6499bdb34168%3Fhl%3Den%26lnk%3Draot&msg=8ddd6499bdb34168>
@gmail.com>
Date: Sun, 28 Apr 2013 11:17:18 -0700 (PDT)
Subject: homosexuality is the 7th Re: sleep involved in these 6 diseases:
Math-Statistics proving method: Metal Causation Diseases
On Apr 27, 6:06 pm, hab...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.bio.misc/browse_thread/thread/f9aa92c15597072d/8ddd6499bdb34168%3Fhl%3Den%26lnk%3Draot&msg=8ddd6499bdb34168>@anony.net
wrote:
> But they are all genetic which manifest at certain ages when the
> genes uncoil
Get a real name before you post to the sci newsgroups. The sci
newsgroups should only allow
real names, no hiding with fake names, for that reduces spam and anti-
science.
When you drink a poison and 2 years old, you will die in minutes. The
same poison drunk by a 40 year old takes 3 weeks and ends up not in
death but debilitating health.
Take the recent example of gold miners in Nigeria whose fathers spent
the day in the camps and their clothes covering in lead. They survived
with debilitation but the children at home in contact with the lead
made them mentally retarded. And you call it genetic.
Now since I wrote the above, I found a 7th disease of metal poisoning
by the environment-- homosexuality.
Now none of these diseases is genetic, and the only interface of
genetics, is that genetics plays a role in what body parts are most
vulnerable to the poison given age of the human. Other than that,
genetics is besides the point. But the horrible thing about modern
medicine is that the funding grants in medicine is given to those who
scream "genetics, genetics, genetics" and then they are given millions
to waste and throw away.
--
Now let me say something about fake named posters.
When you post with a fake name, you can say almost anything anti-
science.
Recently Google made New Google Newsgroups where they hire either paid
or unpaid moderators to throw out abuse such as in sci.math. Trouble
is, that Google should not be wasting the time and energy of these
moderators, because all Google really needs to do is to put in place
two simple rules:
Rule 1: only full legal names of all posters in science newsgroups
Rule 2: no more than 5 posts in a 24 hour interval
With those two rules, the science newsgroups would be clean and
improved and would rival the best science peer reviewed journals.
Because Rule 1, eliminates almost all posters except those actually
doing science. For if someone spams with a real name, then people will
start involving that person's employer or family. So with real names
taking responsibility of their posts, then the poster is more apt to
focus on doing "real science".
And Rule 2 eliminates more spam but also eliminates what can be called
the Sam Wormley circus trick of hogging the first page of a newsboard.
The Wormley trick is to make numerous 1 liner posts that bumps
everyone off the first viewing page. So that if there was a 5 maximum
posts per 24 hours, Wormley could only faintly bump others off.
Newsgroups: sci.chem, sci.med, sci.bio.misc
From: Archimedes Plutonium <plutonium.archime...
<http://groups.google.com/groups/unlock?hl=en&_done=/group/sci.chem/browse_thread/thread/8cc02e13f43e22a1%3Fhl%3Den&msg=9e859e8ef40f9ddf>
@gmail.com>
Date: Sun, 12 May 2013 15:44:34 -0700 (PDT)
Subject: Alexander the Great and Homosexuality: Metal Causation Diseases
Now my last post in this book was this one titled:
homosexuality is the 7th Re: sleep involved in these 6 diseases Chapt3
Math-Statistics proving method: Metal Causation Diseases
And since I wrote that page, I was wondering why so much homosexuality
in the history of Alexander the Great? Seems like a bit of too much
homosexuality if we are to believe the movies rendition of the history
and in the case of the Greek Spartans. However, if we look at the
history of mercury, or quicksilver as it was called in ancient Greece,
that they revered mercury, even calling a God after mercury and they
used mercury in medication. If my memory serves me, the first Chinese
emperor drank mercury and died of it shortly thereafter. But for
Alexander the Great and Spartans, they used mercury very much so for
ailments of the body, and that use could have been for pregnant
mothers. So, if we put that in perspective that in Ancient Greek times
they actively sought out mercury and used it as a health potent, then
we can readily see that of an increase in homosexuality. Now in places
in the world where mercury was rare and never mined nor refined and
people would rarely come in contact with mercury from burning fuels,
then we would expect rarity of homosexuality. Places like Australia or
parts of Africa
or North America. Now correct me if wrong, but I have never heard of a
homosexual Australian aboriginal, nor a African bushman, nor American
native Indians. So that in history, where there was concentrations of
mercury pollution in air, food, water there was a rise in cases of
homosexuality.
*11) Future commentary.*
AP
zzzzzzzzzz
plutonium dot archimedes at gmail dot com. Looking for a College or
University press to hardcover publish all 318+ AP books of science, likely
to become 500-600 maybe even 700 books by the time I die. E-books are too
prone to unbalanced-unhinged censor-editors, who can easily make your books
vanish by pulling a switch. Science should never have gatekeepers, who
thwart access to true science.
| /
| /
|/______ hardcover or paperback
PAU newsgroup is this.
https://groups.google.com/forum/?hl=en#!forum/plutonium-atom-universe
Archimedes Plutonium
Archimedes Plutonium
Jun 7, 2026, 5:34:57 PM (9 hours ago) Jun 7
to Plutonium Atom Universe
Some new news on Parkinson's Disease and, I offer a good new Experiment, after reading "Science News-- New hope for Parkinson's" June 2026.
Archimedes Plutonium
Jun 7, 2026, 6:21:39 PM (8 hours ago) Jun 7
to Plutonium Atom Universe
So I had a cursory reading of this article in Science News, June 2026, which well describes the disease of shaking of body, especially hands, the tremors.
I had reread partially my book above on Parkinson's and saying in a remarkable paragraph that Autism was Parkinsons at a young age while Parkinsons is autism at an old age, from the viewpoint that a chemical like mercury causes, or is the underlying cause of both diseases.
Let me briefly look up how many different forms of mercury compounds exist.
1) elemental mercury
2) methylmercury
3) ethylmercury (thiomersal)
4) mercury chloride
5) cinnabar, mercury sulfide
6) fluorescent lamps, mercury oxide
What SCIENCE NEWS reports is that relief from Parkinsons is found in UltraSound which burns a lesion into the Brain in the site of Parkinson's disease.
--- quoting SCIENCE NEWS---
In opting for this treatment, called high-intensity focused ultrasound, ... has joined a small but growing number of people choosing to control their Parkinson's symptoms with permanent lesions in their brain.
--- end quoting SCIENCE NEWS---
Alright that insight gives AP a new experiment to perform. For sure--- no-one knows what causes Parkinsons, but AP thinks it is mercury. So the Ultrasound treatment makes way for a new experiment.
If AP is correct, we can take a sample of the mentioned 6 types of mercury listed above and implant them into a dead animal tissue. Then we ultrasound that dead animal tissue. We then look to see if any lesions had formed of the implanted mercury.
By lesions, I mean a reshaping of the mercury (elemental or compound). In this sense, if the experiment turns out in favor of AP, would mean that Mercury causes Parkinsons and means that the Ultrasound relief treatment is going to be only as good as what the ultrasound energy had done upon the mercury compounds.
Another Insight
------------------------
Since I wrote my mercury caused diseases starting 1996, I was never in view or contact with people who contracted these diseases. But since 1996, I have had some contact with people who caught these diseases. And sadly it seems as though a predominant number of Alzheimers comes to females-- 2/3 to 1/3; while a predominant number of Autism 4 to 1, and Parkinsons almost 2 times more common in men than women-- comes to males.
AP writes: these statistics lean toward AP's hypothesis that mercury is the underlying agent of the disease, in that the XX chromosome of female has more mercury acceptance to Alzheimers while the XY chromosome of males has more mercury acceptance to Autism and Parkinsons. It maybe the case also, that a specific compound of mercury is more conducive to linking up with XX or to XY.
AP, King of Science
Reply all
Reply to author
Forward
0 new messages