It's a Lie that Vaccines Don't Cause Disease and Disability (Johns Hopkins MD and Mitochondria)
Kathleen
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Subject: It's a Lie that Vaccines Don't Cause Disease and Disability
(Johns Hopkins MD and Mitochondria)
Date: Feb 6, 2011 4:28 AM
Bill Gates says the reverse is
true:
http://gizmodo.com/5752880/bill-gates-says-its-an-absolute-lie-to-link-vaccines-and-autism
I wonder when Bill Gates became
a Biochemist?
Article below
=======================
As we all will recall, a Johns Hopkins
MD won a no-mitochondrial-disorder
screening before vaccination lawsuit
regarding his own daughter.
The disease known to be the result of
vaccinations is called subclinical
encephalitis. See the Monographs
of the vaccines, where they refer
to "Neurological Adverse Outcomes."
In other words, "Infection from the not
completely-heat killed viruses Without the
Spots."
re: Kids with Immune Deficiencies:
While the US Govt et al (including
the Lyme Cryme Israelis, perhaps
through bioweapons blackmail of the
US), only in a round-about way admit
that LYMErix was a crime, and that
there is no Tuberculosis vaccine
for the same reason the LYMErix OspA
TLR2 agonist vaccines failed
http://www.actionlyme.org/101016.htm
- these lipoproteins inhibit antigen
presentation, and also activate viruses
like Epstein-Barr, one of the two main
culprits in the production of the New
Great and the Regular Great Imitator
Outcomes of spirochetal diseases:
http://www.actionlyme.org/CHP_9_IDSA_REVIEWS.htm
(ALS, Lupus, Dementia, Cancer, MS, etc).
It is also true that these fungal
antigens adhere to mitochondrial
membranes:
http://www.actionlyme.org/101016.htm
(Search for mitochondria in ^^ the page)
"In addition, M. fermentans total proteins LPMf and MALP-2, but not
AqMf, downregulated the formation of active caspase-8. NF-kappaB was
transactivated in cells treated with M. fermentans lipoproteins, and
was essential for host cell survival, but not for the inhibition of
TNFalpha-induced apoptosis by LPMf. Our results suggest that the
inhibitory effect exerted by M. fermentans on TNFalpha-induced
apoptosis in U937 cells is due to the membrane lipoproteins of these
bacteria." http://www.ncbi.nlm.nih.gov/pubmed/16889623
"The modulation of host cell death pathways by bacteria has been
recognized as a major pathogenicity mechanism. Among other strategies,
bacterial pathogens can hijack the cell death machinery of host cells
by influencing the signalling pathways that converge on the
mitochondria. In particular, many bacterial proteins have evolved to
interact in a highly specific manner with host mitochondria, thereby
modulating the decision between cell life and death. In this Review,
we explore the intimate interactions between bacterial pathogens and
mitochondrial cell death pathways."
http://www.ncbi.nlm.nih.gov/pubmed/20818415
http://www.nature.com/nrmicro/journal/v8/n10/full/nrmicro2421.html
So, think: There are epidemics
of Asthma and Autism in America,
which only a liar or a retard would
deny.
There are also huge epidemics of
cancers, leukemias, MS, Lupus, ALS
Chronic Fatigue, Lyme, etc.
Get it?
You get both ends of the immune
spectrum happening in epidemic
proportions.
With children who are immune compromised
by molds (or HIV or Lyme-like OspA)
http://www.ncbi.nlm.nih.gov/pubmed?term=9639369
IMPORTANT - THIS IS THE MMWR, NOW:
MMWR Recomm Rep. 1998 May 22;47(RR-8):1-57.
Measles, mumps, and rubella--vaccine use and strategies for
elimination of measles, rubella, and congenital rubella syndrome and
control of mumps: recommendations of the Advisory Committee on
Immunization Practices (ACIP).
Watson JC, Hadler SC, Dykewicz CA, Reef S, Phillips L.
Abstract
These revised recommendations of the Advisory Committee on
Immunization Practices (ACIP) on measles, mumps, and rubella
prevention supersede recommendations published in 1989 and 1990. This
statement summarizes the goals and current strategies for measles,
rubella, and congenital rubella syndrome (CRS) elimination and for
mumps reduction in the United States. Changes from previous
recommendations include: Emphasis on the use of combined MMR vaccine
for most indications; A change in the recommended age for routine
vaccination to 12-15 months for the first dose of MMR, and to 4-6
years for the second dose of MMR; A recommendation that all states
take immediate steps to implement a two dose MMR requirement for
school entry and any additional measures needed to ensure that all
school-aged children are vaccinated with two doses of MMR by 2001; A
clarification of the role of serologic screening to determine
immunity; A change in the criteria for determining acceptable evidence
of rubella immunity; A recommendation that all persons who work in
health-care facilities have acceptable evidence of measles and rubella
immunity; Changes in the recommended interval between administration
of immune globulin and measles vaccination; and Updated information on
adverse events and contraindications, particularly for persons with
severe HIV infection, persons with a history of egg allergy or gelatin
allergy, persons with a history of thrombocytopenia, and persons
receiving steroid therapy."
CHILDREN WHO ARE IMMUNE INCOMPETENT
SHOULD NOT BE GIVEN LIVE, ATTENUATED
VACCINATIONS; THE VACCINES SHOULD
CONTAIN FULLY HEAT-KILLED VIRUSES.
Follow?
We have epidemics of asthma from airborne
fungi - which is the opposite end of
the immune response, and less common
(see Harding in this page, explaining
how Steere's version of allergy works,
since it is novel):
http://www.actionlyme.org/101016.htm
2010, Dec, Clifford Harding: Mycobacterium tuberculosis synergizes
with ATP to induce release of microvesicles and exosomes containing
major histocompatibility complex class II molecules capable of antigen
presentation.
Major histocompatibility complex class II (MHC-II) molecules are
released by murine macrophages upon lipopolysaccharide (LPS)
stimulation and ATP signaling through the P2X7 receptor. These studies
show that infection of macrophages with Mycobacterium tuberculosis or
M. bovis strain BCG enhances MHC-II release in synergy with ATP. Shed
MHC-II was contained in two distinct organelles, exosomes and plasma
membrane-derived microvesicles, which were both able to present
exogenous antigenic peptide to T hybridoma cells. Furthermore,
microvesicles from mycobacterium-infected macrophages were able to
directly present M. tuberculosis antigen (Ag) 85B(241-256)-I-A(b)
complexes that were generated by the processing of M. tuberculosis Ag
85B in infected cells to both M. tuberculosis-specific T hybridoma
cells and naïve P25 M. tuberculosis T-cell receptor (TCR)-transgenic T
cells. In the presence of prefixed macrophages, exosomes from
mycobacterium-infected macrophages provided weak stimulation to M.
tuberculosis-specific T hybridoma cells but not naïve P25 T cells.
Thus, infection with M. tuberculosis primes macrophages for the
increased release of exosomes and microvesicles bearing M.
tuberculosis ***peptide-MHC-II complexes*** that may generate
antimicrobial T-cell responses."
http://www.ncbi.nlm.nih.gov/pubmed/20837713
Peptide MHC-II complexes and not
Peptide-antibody complexes, drive
chronic inflammation in some
cases. (Allen Steere proposes
the latter, as the cause of his
"only a bad-knee is Lyme.")
Now you see. There is plenty of
scientific evidence and even successful
lawsuits which demonstrate that all kids
should be screened for immune competence
to all vaccines.
If we have an epidemic of *asthma*
and moldy homes in America, and if
we have an epidemic of POLLUTION
(discuss as such and not global
warming),... and if the DHHS.gov has
had to admit that you can't make
vaccines against the fungal antigens
OspA, the Tuberculosis fungal antigens
and LYMErix-HIVgp120 (same thing, apparently)
http://www.actionlyme.org/101016.htm
And if the GOVT ITSELF has stipulated
that immune compromised children should
not get live attenuated vaccines, and if
a Johns Hopkins MD won a lawsuit againts
vaccine manufacturers over the claim of
a MITOCHONDRIAL DISORDER (which could
be induced from exposure to fungi or
mycoplasma in the blood or in the
vaccine vial), then vaccines-associated
dementias are very, very likely.
No one can deny the mechanisms of
immunosuppression and immune dysregulation
now seen as true - Fungal-Viral Synergy -
identified by many sources, all over
the world
http://www.actionlyme.org/101016.htm
Bill Gates ought not be such an arrogant
dick as to be playing any role here.
He may be rich, and he may be nerdy,
but he is not a scientist.
Fungal infections (mycoplasma) in the blood
make a healthy adult physiologically
delirious. They CAPTURE membranes, in
one way or another. They're hydrophobic
and in the case of OspA, have a very
electronegative core. The body can't
handle them. What's happening is
we're dumping extra viruses into that
environment with vaccinations in the
case of children.
The rest of us acquire the kissing
disease - Epstein-Barr - usually
when we're almost-adults.
*This* is the cause of most
chronic illness in all of
Western Society.
Feel free to start at any point here
http://www.actionlyme.org/101016.htm
and do your own explorations, because
this *science* is non-linear,
Kathleen M. Dickson
http://www.actionlyme.org
http://www.relapsingfever.org
=======================
Dr. Wakefield's study once showed a link between vaccinations and
autism. Too bad it was based on fraudulent data and "an absolute lie".
Bill Gates has pledged 10 billion dollars to make it the "year of the
vaccines".
Specifically, Gates' $10 billion will be spread over 10 years. In an
interview with Dr. Sanjay Gupta for CNN, Gates has some ideas on how
to improve vaccination:
We have to do three things in parallel: Eradicate the few that fit
that profile — ringworm and polio; get the coverage up for the
vaccines we have; and then invent the vaccines — and we only need
about six or seven more — and then you would have all the tools to
reduce childhood death, reduce population growth, and everything — the
stability, the environment — benefits from that.
As for the Jenny McCarthys of the world who stand against vaccines,
well, he has some choice words for them as well.
"Well, Dr. Wakefield has been shown to have used absolutely
fraudulent data. He had a financial interest in some lawsuits, he
created a fake paper, the journal allowed it to run. All the other
studies were done, showed no connection whatsoever again and again and
again. So it's an absolute lie that has killed thousands of kids.
Because the mothers who heard that lie, many of them didn't have their
kids take either pertussis or measles vaccine, and their children are
dead today. It's a very sad thing, because these vaccines are
important.
I'm with Bill. Check out the whole Bill Gates interview at CNN. [CNN]
Send an email to Casey Chan, the author of this post, at
cc...@gizmodo.com.
KMDickson