Lyme Cryme in the News- How to Diagnose it, really
Mort Zuckerman
Durlan...@yale.edu, Aa...@columbia.edu, gary_w...@nymc.edu,
scientifi...@ostp.gov, pkru...@princeton.edu,
Stanle...@fiu.edu, emcsw...@niaid.nih.gov, afa...@niaid.nih.gov,
Spin...@yahoogroups.com, kshe...@calea.org, fit...@gmail.com,
patrick.f...@usdoj.gov, model...@sbcglobal.net,
jdr...@nejm.org, let...@courant.com, Jgerb...@cdc.gov,
michae...@po.state.ct.us, con...@po.state.ct.us, executive-
edi...@nytimes.com, managin...@nytimes.com, news-
ti...@nytimes.com, biz...@nytimes.com, for...@nytimes.com,
nati...@nytimes.com, dv...@cdc.gov, brigidc...@optonline.net,
tr...@hotmail.com, illino...@aol.com, jle...@courant.com,
tinaj...@yahoo.com, jhorn...@fff.org, thomas...@usdoj.gov,
thoma...@po.state.ct.us, kur...@washpost.com,
georg...@washpost.com, p...@allegorypress.com,
commissi...@po.state.ct.us, brans...@comcast.net,
vts...@comcast.net, o...@po.state.ct.us, freet...@charter.net,
scott....@po.state.ct.us, govern...@po.state.ct.us,
attorney...@po.state.ct.us, randall...@usdoj.gov,
Robert....@yale.edu, edi...@greenwich-post.com,
harol...@yale.edu, sedm...@nswbc.org, rrmcg...@aol.com,
fr...@nytimes.com, dpr...@stmartin.edu
Cc: fra...@ucia.gov, dr-ahma...@president.ir,
eugener...@washpost.com, afa...@niaid.nih.gov,
bmi...@newstimes.com, tr...@hotmail.com, rast...@aol.com,
billc...@gmail.com, amcg...@rms-law.com, rjmu...@aol.com,
paulcrai...@yahoo.com, sidney_b...@yahoo.com,
criminal...@usdoj.gov, karla.d...@usdoj.gov,
christophe...@usdoj.gov, richar...@yale.edu,
harol...@yale.edu, james.p...@yale.edu, inq...@aldf.com,
ly...@idsociety.org, meganm...@theatlantic.com
Subject: Lyme Cryme in the News- How to Diagnose it, really
Date: Jan 19, 2010 12:38 AM
ARTICLE BELOW ABOUT A RICH
FAMILY'S LYME SAGA
=====================================
The Infectious Diseases Society of America
cannot re-write any guidelines because now
they have no data. They used to rely on
the scientific fraud study of Mark Klempner
which was to say:
"The arbitrarily assigned 30 days of
intravenous ceftriaxone for meningitis
Lyme was not enough IV ceftriaxone."
http://www.actionlyme.org/MKLEMPNER.htm
Now Klempner has been debunked by Brown's
Alison DeLong (she revealed that it was
scientific crap), and the CDC itself, which
has finally dropped their insane idea
"that one had to have late Lyme arthritis
in a knee (with no other illness signs), and
in the early stages of Lyme."
http://www.actionlyme.org/CRYMEDISEASE_CHP3_B.htm
The entire skit (Dearborn, and the falsification
of the Lyme testing by Allen Steere in Europe
http://www.actionlyme.org/STEERE_IN_EUROPE.htm
alone) was designed around acquiring
a monopoly on grants, testing kits, and
tick borne diseases vaccines for Yale
and Allen Steere's company, Imugen.
McSweegan and Fish, not being real scientists,
were the henchmen. McSweegan and Fish
trashed anyone who stood in their way, like
myself, an analytical chemist with kids
with congenital Lyme and support group
leader, Karen Forschner of the Lyme Foundation
(has a degree in biology and whose son
died of congenital Lyme
http://www.lyme.org
http://www.actionlyme.org/Schoen.htm
and Lisa masterson who understood the whole
scame from a scientific point of view,
being a nurse, and was thus charged with
poisoning her own children:
http://www.actionlyme.org/MUNCHAUSENS.htm
These "social workers" are routinely deployed
against the New Erin Brockowichs of the New
World, because of their notorious evil and
even more notorious ignorance. These are
the dumbest people I have ever met, and I
know some pretty *dumb* people, having been
raised by them. (Think of it like this:
If you as a kid watched cartoons, you get
a sense of what it is like to be raised around
kooks and retards- you don't pay attention
or take them seriously, because you can't;
it's all brainscramble and *goes* *nowhere.*)
Lisa Masterson made the mistake of saying
the very important thing about dark field
as a way to detect real illness. This
would include the detection of fungal infections
in the blood (mycoplasma, which is responsible
much of the time, for the chronic fatigue
http://www.actionlyme.org/BIOMARKERS2.htm
especially once it develops into activated
Epstein-Barr, or chronic mono. The Lyme crooks
are aware of the chronic mono-connection with
Lyme because they downplay it, and because of
what they did to Lisa Mastersone to shut her
up:
http://www.actionlyme.org/MCSWEEGAN_AND_MUNCHAUSENS.htm
- - - -
So: How to Detect Lyme:
The only scientifically valid way to detect
ALL BORRELIOSES, and not just "Strain B31 with
the no OspC in it" which is called "Lyme Disease"
is to use recombinant flagellins from all the
known local Borreliae.
Yale owns the patent for "Lyme Borreliosis,"
Flagellin, which again, is strain B31's flagellin
DNA, or the OspA-Borreliosis, or the Mycoplasmal
Borreliosis.
CDC Officer Alan Steere owns a patent for
the DNA for Southern Lyme Disease or
Masters' Disease or STARI.
http://www.actionlyme.org/CENTRAL_LYME_RICO_PATENTS.htm
and he has known for over 15 years that "Lyme"
is all over the country, and not limited to
the northeast, because it's all just
BORRELIOSIS, or Relapsing Fever from a tick.
Therefore, if these criminally insane assholes
won't license their DNA - no one can have their
diseases, because they own the DNA necessary
to identify them - then the only thing to
do is to combine several Borrelia in a Western
Blot mix, and compare the intensity of the
flagellin band (41) to that of the Syphilis
spirochete:
http://www.ncbi.nlm.nih.gov/pubmed?term=magnarelli[All%20Fields]%20AND%20%28%22flagellin%22[MeSH%20Terms]%20OR%20%22flagellin%22[All%20Fields]%29&cmd=DetailsSearch&log$=details
(Search for Magnarelli and Flagellin)
That - what I just explained would be a standard
test since evil murderous bastards don't want to
go to jail for falsifying the testing at Dearborn
in order to not diagnose the worst cases, like the
ALS cases.
(look for a new article on Tony Judt
to see how miserable this disease is).
Many people are under the mistaken impression
that they have to do what the CDC says, and
ILADS.org's Nick Harris (IGENEX) is not in the
business of giving himself any lab business
competition by revealing to the world that he
knows Dearborn was a FRAUD.
Additionally Pat Smith of the
Lymediseaseassociation.org is not in the business
of giving herself any competition for Lyme Activist
Queen becuase she is a bona fide sociopath:
http://www.facebook.com/#/pages/Lyme-Disease-Association-Inc-LDA/134708722163?ref=mf
Look at the kinds of people she recuits:
"You're great because now you're a fan of the Lyme
Disease Association (LDA)."
- - - - -
At the present time, and within the present
criminal/fraud/Lyme Queen atmosphere, the
one practical thing you can do is to use
Igenex, and if you have band 41, chronic
fatigue, and not syphilis (according to
Allen Steere:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC423723/pdf/jcinvest00109-0086.pdf
"This observation suggests that the
41 -kD antigen of B. burgdorferi may give better results in an
ELISA for early Lyme disease than the current test, which uses
sonicated whole spirochetes (1 1, 12). Furthermore, in this study,
IgM antibodies to the 41-kD polypeptide were usually apparent
by immunoblots before IgM titers were elevated by the current
ELISA (12). ***Although antibodies reactive against this antigen
may be present in patients with relapsing fever or syphilis (1 1,
14), these diseases can be distinguished clinically from Lyme
disease and therefore should not cause diagnostic confusion.*** The
binding of this antigen by IgM from rheumatic disease controls
was typically very weak and could potentially be blocked to
avoid false-positive results in this group of patients."
(Page 938)
= = = = =
Yale's Lyme patent:
http://patft1.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=5618533.PN.&OS=PN/5618533&RS=PN/5618533
"They are capable of detecting B. burgdorferi-specific antibodies in
the vast majority of confirmed seropositive samples tested."
17 out of 18 patients in early
and late Lyme, and in neurologic
Lyme, were positive by this method, or, it
detects 94-95% of ALL CASES.
As far as the activation of latent viruses
and to look in/at the blood for other
pathogens, good luck. No one does this
testing to look for all the strains
of mycoplasma, and no one routinely
performs dark field, although it only
makes sense for all hospitals to have
their own labs and perform their own
analyses. You can't trust Quest and you
can't trust the FDA or the CDC, and ILADS
and Igenex don't want anyone to know all
their non-secrets because then they can't
selectively only treat rich people.
Right now, Lyme, the Yuppie Flu, or the
Yuppie AIDS, or North American Borreliosis
or Relapsing Fever is still that. Only the
very wealthy Yuppies can afford it:
http://www.actionlyme.org/BLUMENTHAL_FORSCHNER.htm
NOBODY INVOLVED, except myself and my handful
of comrades are doing something about it that
does not involve personal profit or self-
promotion:
http://www.lymecryme.com
Weintraub, I trained. But when she
no longer could rely on me, had nowhere
to go, and published a book called
"Cure Unknown":
http://www.actionlyme.org/Actionlyme_History.htm
Use band 41, alone, to diagnose Borreliosis
or Relapsing Fever.
If it is positive and you don't have syphilis,
you have some kind of illness. AND, You have
Allen Steere, Lou Magnarelli, Erol Fikrig
and Richard Flavell, and CDC officer Alan
Barbour saying so.
As far as developing the rest of the
testing, we had hoped that that would
be accomplished once the crime was
prosecuted by the USDOJ, not knowing the
USDOJ was hanging with the likes of
Kroll Associates, who performed the
911 stunt for AIG:
http://www.actionlyme.org/USDOJ_COMPLAINT_RICO.htm
and who was also closely involved in
duh DCF Whorey-Glories' RICO, for
a "national chain of juvenile prisons"
http://www.actionlyme.org/RAGAGLIA_GRANDJURY_DETAILS.htm
I am a scientist. How would I know
such whores even existed? I do not
play in that lying scumbag world.
KMDickson
http://www.actionlyme.org
http://www.relapsingfever.org
============================
http://www.germantownnews.com/articles/2010/01/18/top_stories/doc4b54785c7efd8147944128.txt
Family crusades against disease
Wilson and Shelby Nanney, both students at Germantown High School,
have been in a two-year battle with this disease and still have a way
to go.
By Maxine Hunter
Published: Monday, January 18, 2010 10:18 AM CST
The Lee and Kelly Nanney family of Germantown are on a personal
crusade to bring the dangers of lyme disease to everyone’s attention.
Their children, Wilson and Shelby Nanney, both students at Germantown
High School, have been in a two-year battle with this disease and
still have a way to go. Last year the family had to move to Kansas
City, Kansas for seven months to a doctor who used I.V. antibiotics to
treat the disease. There the teenagers received daily I.V. infusions
through a picc line. “This treatment was five hours a day, seven days
a week with hardly a break in between, costing our family upwards of
$200,000.00,” Kelly Nanney said. “They are much better and we feel as
if we may finally be looking at calmer days ahead.”
Lyme disease is treatable and may be even curable when diagnosed at
the right time, Kelly said. “Unfortunately because of a flawed set of
guidelines, doctors are not looking for this and are diagnosing many
people with the following syndromes that have no cure: MS (Wilson was
diagnosed with MS his freshman year when he was just 15); chronic
fatigue syndrome (Shelby’s prior diagnosis), lupus, fibromyalgia (with
this, you are going to feel as if you have the flu the rest of your
life, on pain meds, this is a horrible diagnosis); ALS, Bells palsy,
the list goes on.”
For this reason, Kelly points out, Lyme disease awareness has to begin
with the patient. “When it comes to lyme disease the Infectious
Disease society of America gets an F,” she says. “The guidelines for
lyme disease are under scrutiny at this time and there is supposed to
be an answer by the end of the year as to whether they will be
rewritten to help the patients, not the insurance companies.”
Lyme disease begins with the bite of ticks; in the Nanney children’s
case, seed ticks. The family feels they were bitten some eight or 10
years ago on a camping trip in Arkansas. There they encountered
hundreds of the tiny seed ticks, which are deer ticks in the nymphet
stage.
The bacteria they implanted stayed in the blood and smoldered and grew
slowly. Then two years ago the slow-growing bacteria made their
presence known.
It started with flu-like symptoms, but unlike flu, it did not get
better. Wilson, now 19, was diagnosed with MS and Shelby, now 16, with
chronic fatigue syndrome. They were treated with oral antibiotics, but
they were not strong enough to rout the tenacious underlying bacteria
whose symptoms came and went.
Then Wilson had a seizure in a river and nearly drowned. He aspirated
the river water and developed pneumonia. In a hospital, on I.V.
antibiotics he became better and his family noticed the other symptoms
also improved. Wilson’s history and symptoms led them to believe he
had lyme disease, and this was later proved by a combination of blood
tests and documentation of his medical history.
“Diagnosis depends on both,” Kelly said. “That is the thing that makes
lyme disease so difficult to pinpoint.”
Both the youths are on oral antibiotics now, along with supplements to
build up their immunity, and they are doing well. Blood tests are sent
to Kansas City about every six weeks to monitor their progress.
But the Nanneys want to help others recognize the complex symptoms of
lyme disease in order to avoid the years of worry they have gone
through. There are some 10 cases of lyme disease in the Memphis area
now, and perhaps others that have been incorrectly diagnosed. There is
a current documentary movie entitled “Under Our Skin” that follows
several families and goes into why diagnostic guidelines for the
disease are flawed.
“The documentary has won several awards and has just made the Oscar’s
short list of favorite documentary. Out of around 100 films it was in
the top 15. All of this is huge for the lyme community. The more
awareness from the general population, the more doctors will get on
board. Lyme disease will stop you dead in your tracks without a clue
as to treatment, and this needs to change,” Kelly said.
The Nanneys have copies of the documentary and would be glad to have
others view it. To contact them go to www.caringbridge.org/visit/wilsonnanney
and follow the link there.
It could save you years of uncertainty and worry.
"[Real] scientists are *fiercely* independent. That's the good
news."-- NIH's Top Fool, Anthony Fauci