The Vaccine Hoax is Over
Freedom of Information Act in the UK filed by a doctor there has revealed 30 years of secret official documents showing that government experts have
1. Known the vaccines don’t work
2. Known they cause the diseases they are supposed to prevent
3. Known they are a hazard to children
4. Colluded to lie to the public
5. Worked to prevent safety studies
Those are the same vaccines that are mandated to children in the US.
Educated parents can either get their children out of harm’s way or continue living inside one of the largest most evil lies in history, that vaccines – full of heavy metals, viral diseases, mycoplasma, fecal material, DNA fragments from other species, formaldehyde, polysorbate 80 (a sterilizing agent) – are a miracle of modern medicine.
Freedom of Information Act filed in the US with the CDC by a doctor with an autistic son, seeking information on what the CDC knows about the dangers of vaccines, had by law to be responded to in 20 days. Nearly 7 years later, the doctor went to court and the CDC argued it does not have to turn over documents. A judge ordered the CDC to turn over the documents on September 30th, 2011.
On October 26, 2011, a Denver Post editorial expressed shock that the Obama administration, after promising to be especially transparent, was proposing changes to the Freedom of Information Act that would allow it to go beyond declaring some documents secret and to actually allow government agencies (such as the CDC) to declare some document “non-existent.”
Simultaneous to this on-going massive CDC cover up involving its primary “health” not recommendation but MANDATE for American children, the CDC is in deep trouble over its decades of covering up the damaging effects of fluoride and affecting the lives of all Americans, especially children and the immune compromised. Lawsuits are being prepared. Children are ingesting 3-4 times more fluoride by body weight as adults and “[t]he sheer number of potentially harmed citizens — persons with dental fluorosis, kidney patients tipped into needing dialysis, diabetics, thyroid patients, etc — numbers in the millions.”
Continue Article Here: http://foodfreedomgroup.com/
Full Study Here: http://www.ecomed.org.uk/
REGARDING VACCINES, THE
U.S. COURT OF FEDERAL CLAIMS FOR VACCINE DAMAGES, AND HHS/FDA
Attorney Walter Kyle of
Cape Cod, Massachusetts, began representing Plaintiffs with vaccine injuries
ten years before the Vaccine Injury Act began, and has argued more than forty
cases before the Special Masters of the United States Court of Federal Claims
[under the Vaccine Injury Compensation Act] - 42 U.S.C.A. §300aa, et.seq. As a
result, Attorney Kyle has unique insight into the nuances of vaccine injury
law.
TO START OUR INTERVIEW,
MAY I ASK HOW YOU BECAME INVOLVED IN VACCINE LAW?
I began representation
of vaccine-injured clients in Arkansas in 1977. My first case out of law school
was representing a paraplegic mother who acquired paralytic polio from mutated
Sabin live trivalent oral polio vaccine [TOPV] viruses shed from her
three-month-old infant’s diapers. Centers for Disease control classified the
woman in the “immune deficient” category of “vaccine associated contact cases”
from Type 2 Sabin vaccine.
Walter, you just
mentioned the phrase “vaccine viruses shed.” For those who are not familiar with
such terminology I’d like to say it means certain types of vaccines contain
certain viruses that are alive and once injected into [orally administered to]
an individual can infect others via contact with bodily fluids, excrement, and
sometimes coughing or sneezing. In your first vaccine case, the mother
contracted paralytic polio from viruses “shed” in her infant’s diapers soiled
with urine and feces.
WALTER, HOW DID YOU
PRESENT THAT CASE AT COURT?
In the first case
against the manufacturer, American Cyanamid, which defended based on the fact
that the woman was categorized as “immune deficient” and implied the reaction
was her fault, I countered with the position that the Type 2 vaccine caused her
immune deficiency since she had never been sick in her life before contact with
that vaccine. After settling that lawsuit against the manufacturer for failure
to warn, I instituted a Federal Tort Claims Act (FTCA) lawsuit against HEW for
regulatory violations in the license and release of OPV, in general, and the
individual Lot of polio vaccine, in particular. In addition, I challenged the
FDA’s intention to use Sabin’s live oral polio vaccine (OPV) for immunization
of unwitting contacts of vaccine recipients as an unconstitutional invasion of
their privacy (see Loge v. United States, 662 F.2d 1268 8th Cir. 1981), which
evolved into civil actions of “battery” against the sole manufacturer of the
Sabin vaccine –American Cyanamid.
CAN YOU TELL US WHAT
HAPPENED IN THAT CASE?
From my perspective I
gained a profound disrespect for the FDA and pro-vaccine defense experts who
pretended the case could have been from wild polio in spite of the fact that
most, if not all of the polio in the United States at that time, arose from
parents coming into contact with the polio viruses shed in their child’s stool
or saliva.
Their justification
then, similar to their justification now, arose from an unwritten CDC/FDA
policy to “sacrifice some for the good of the whole” – a comment related to me
by a senior CDC physician, Dr. Michael Gregg, in a private conversation.
This explains why zero
funding is available to do clinical studies of vaccine reactions in the United
States.
Both of the lawsuits
settled before trial. The trial judge dismissed the FTCA lawsuit and was
overturned on appeal in the decision cited above.
Before you go further,
can you please explain what a Vaccine Injury Table is?
According to HHS Health
Resources and Services Administration, “The Vaccine Injury Table makes it
easier for some people to get compensation.” [1]
It makes it easier for
some and impossible for others. Certain reactions within a set time period are
automatically compensated. For example, the parent of a child who became
paralyzed by polio within 60 days of the child’s receiving the live polio
vaccine would automatically be compensated. This was the most common reaction
to both live and inactivated polio vaccines.
However, a child
acquiring an encephalitis where the Colburn strain of CMV (cytomegalovirus) was
isolated from his brain at the age of six, would not be compensated unless his
lawyer were clever enough to discover that the Colburn strain of CMV is
actually simian in origin and came from the African green monkeys used to
produce the live polio vaccine.
Recently Baboon endogenous
retrovirus (BERV) was discovered in MMR vaccine, but no one has access to the
tests to detect it in children with possible vaccine reactions. Since it is a
live vaccine, one would expect the onset to occur within 3 days to three years,
nor would anyone know how to correlate it to the particular Lot of vaccine
given as FDA keeps such information secret.a “commercial privilege” protection under FOIA.
Walter, what I find
interesting about the Vaccine Injury Table is something most proponents of vaccines/vaccinations
probably are not aware and it is “The Table lists and explains
injuries/conditions that are presumed to be caused by vaccines.” [1] So, in
effect, HHS/CDC/FDA agree vaccines can cause damage. I suggest every parent
becomes familiar with the Vaccine Injury Table in the link at reference [1].
The Table is per se
inadequate and a mother or father should follow their gut instinct when faced
with a vaccine reaction most of which are probably not on the Vaccine Injury
Table. Currently there are laboratory-testing methods developed, but withheld
from diagnostic use by FDA that can quickly and cheaply link reactions to
vaccines. I do not feel anyone should subject their child to an immunization
unless faced with an actual, not a CDC forecast, epidemic of a life-threatening
pathogen. That is, until those testing procedures are made available to the
general public for diagnostic evaluations of both the injured and of the
vaccines which are administered.
I am not anti-vaccine
but strongly oppose FDA/CDC/NIH B.S. (rhetoric and hyperbole) when it comes to
evaluation of vaccine reactions. For example: Dr. Jonas Salk, developer of the
inactivated polio vaccine (IPV) gave unchallenged testimony before the Senate
Committee establishing the Vaccine Injury Table that there had been no
paralytic reactions to the Salk vaccine in 450,000,000 doses resulting in a
Table that provided no compensation for IPV-caused polio. The FDA stood by and
said absolutely nothing, but had good reason to know Salk’s testimony was not
true. Really!
Salk had provided expert
assistance and consultation to me for 12 years while the ongoing feud between
Sabin and Salk brewed over which vaccine should be used in the United States.
When the Chief Special
Master appointed me to head an Attorneys Committee to investigate the
possibility that Salk’s vaccine had caused hundreds of cases of polio that had
never been linked to the vaccine by FDA, I truly believed that Salk’s vaccine
had never caused polio except in one isolated manufacturing problem in 1955.
After the Committee
investigated and discovered that not only had Salk’s IPV caused polio, it had
probably started epidemics, and the famous “Frances Field Trials,” which the
FDA’s predecessor touted as proving IPV’s absolute safety, were “rigged” and
probably caused as much polio as they prevented.
Walter, that’s something
that isn’t well known and apparently pushed under the carpet, as they say.
Under the carpet would
have been nice, HHS pushed the attorneys on my committee out the door. The
Justice Department attorney began attacking members of the Committee on trivial
issues, objected to our being paid promptly in all matters including other
cases and ultimately all of us stopped practicing in the Vaccine Injury
Compensation Program.
Walter, thank you for
pointing out that important fact, something vaccine safety advocates are
concerned about to this very day—unknowns in vaccines. It’s happened several
times and constantly gets pushed under the ‘scientific carpet’, it seems. Please
continue.
By 1988, I concluded,
based on evidence discovered from the OPV manufacturer’s files and FOIA
litigation against the FDA, that FDA allowed release of live Sabin oral polio
vaccines that also contained live simian retroviruses and/or viable genetic
sequences of such retroviruses within the polio vaccine itself – a fact
admitted by the Director of the Bureau of Biologics on April 15, 1980 in the
Federal Register.
In 1992 a world renowned
medical journal, The Lancet, published my paper, “Simian retroviruses, polio
vaccine and origin of AIDS” 339:600-601 (Mar. 7 1992), which linked the 1981
AIDS outbreak in the United States to the nationwide use of OPV for treatment
of genital herpes in homosexual men by dermatologists. Following multiple oral doses
of OPV, the viruses passed in their stools along with the then unknown simian
retroviruses and herpes viruses (i.e., SIV and KSHV – Kaposi’s Sarcoma Herpes
Virus – and CMV – Cytomegalovirus). Curiously, this panorama of simian herpes
viruses also infected the first AIDS victims.
That article identified
specific lots of contaminated OPV and suggested independent testing, which FDA
refused to retest, but “pretended” that it had through false press releases in
1996. The FDA faced huge liability here so they spent millions sending someone
to find AIDS-like virus in chimpanzees which is more genetically similar to HIV
than any of the other simian viruses, problem was, the chimps would eat the
same African green monkeys, the source of all SIVs, which were used in the oral
polio vaccine.
Curiously, Sabin’s Type
II oral polio vaccine, most frequently (of the three Types in a single dose of
Sabin OPV) associated with the immune deficient category of paralytic polio was
administered to and ultimately isolated from the stool of a chimpanzee.
I believe an honest
evaluation of the science would place AIDS under the vaccine injury table, and
what a massive expense that would be.
So Congressional
oversight of the issue may be hard to acquire, but should be sought, all
parents should ask for is “the whole truth,” the portions of truth FDA releases
often times mislead.
Although I have not
actively practiced law for several years, I have followed the scientific
developments in the vaccine injury debate. Furthermore, I feel it is possible
to eliminate the Vaccine Injury Table and simultaneously streamline the onerous
litigation process HHS has devolved for vaccine injury cases, but only if the
FDA provides:
1.Vaccine injury
claimants have access to the deep sequencing technology and microbial detection
arrays capable of identifying every known and sequenced virus, pathogen, fungus
and parasite that might be associated with the onset of illnesses following
vaccinations, and
2.similar sequencing
data on every lot of vaccine distributed in the United States for comparison of
illnesses following immunization with pathogens present in the vaccines and the
medium (substrate) used to generate the vaccine, or;
3.for recombinant DNA
vaccines (rDNA), studies on the viability, propensities, and evolutionary
tendencies of the genetic vaccine agent when introduced into an appropriate
species or cell line free of any other portions of the original putative agent
toward which the vaccine is targeted.
PLEASE FOLLOW LINK FOR
MORE
http://globalpoliticalawakening.blogspot.com/2012/08/exposing-fdas-vaccine-injury-cover-up.html
BANKERS NOT JUST CALLING
THE SHOTS, THEY ARE GIVING THEM (vaccine shots that is)
Goldman Sachs, known for
its integrity around the bailout and around food markets, is also invested in
vaccines.
"Lloyd Blankfein, a
major shareholder in the Goldman-Sachs/AstraZeneca partnerships] is co-chairman
with media mogul Rupert Murdoch in the David Rockefeller-founded Partnership
for New York City (PFNYC), chartered by the Royal Family of England. This group
is currently advancing a world leading biotechnology trust, heavily invested in
genetopharmaceuticals and flu vaccine genetic engineering."
Lloyd Blankfein, Rupert
Murdoch's Co-Chairman of the PFNYC, directed Goldman-Sachs/AstraZeneca's $15
billion acquisition of MedImmune, the H1N1 FLUMIST maker. ....
Goldman Sachs and the
Rockefellers are international bankers. And it is the international bankers, in
country after country, whose financial misdeeds surpass any ever seen before in
history. The same, it seems, can now be said of their vaccines. For the
international bankers so currently beloved of people around the world are not
only deeply invested but deeply involved in vaccines.
In the UK, Dr Lucija
Tomljenovic used Freedom of Information to uncover 30 years of secret official
documents exposing a coverup of the hazards of their vaccines and the names of
those present, including manufacturers, were redacted:
".... the
documentation .... appears to show that the JCVI made continuous efforts to
withhold critical data on severe adverse reactions and contraindications to
vaccinations to both parents and health practitioners in order to reach overall
vaccination rates which they deemed were necessary for “herd immunity, a
concept which with regards to vaccination, and contrary to prevalent beliefs,
does not rest on solid scientific evidence as will be explained. As a result of
such vaccination policy promoted by the JCVI and the DH, many children have
been vaccinated without their parents being disclosed the critical information
about demonstrated risks of serious adverse reactions, one that the JCVI
appeared to have been fully aware of. It would also appear that, by withholding
this information, the JCVI/DH neglected the right of individuals to make an
informed consent concerning vaccination. By doing so, the JCVI/DH may have
violated not only International Guidelines for Medical Ethics (i.e., Helsinki
Declaration and the International Code of Medical Ethics) [2] but also, their
own Code of Practice.
Goldman Sachs, known for
its integrity around the bailout and around food markets, is also invested in
vaccines.
"Lloyd Blankfein, a
major shareholder in the Goldman-Sachs/AstraZeneca partnerships] is co-chairman
with media mogul Rupert Murdoch in the David Rockefeller-founded Partnership
for New York City (PFNYC), chartered by the Royal Family of England. This group
is currently advancing a world leading biotechnology trust, heavily invested in
genetopharmaceuticals and flu vaccine genetic engineering."
Lloyd Blankfein, Rupert
Murdoch’s Co-Chairman of the PFNYC, directed Goldman-Sachs/AstraZeneca's $15
billion acquisition of MedImmune, the H1N1 FLUMIST maker. ....
Goldman Sachs and the
Rockefellers are international bankers. And it is the international bankers, in
country after country, whose financial misdeeds surpass any ever seen before in
history. The same, it seems, can now be said of their vaccines. For the
international bankers so currently beloved of people around the world are not
only deeply invested but deeply involved in vaccines.
In the UK, Dr Lucija
Tomljenovic used Freedom of Information to uncover 30 years of secret official
documents exposing a coverup of the hazards of their vaccines and the names of
those present, including manufacturers, were redacted:
".... the
documentation .... appears to show that the JCVI made continuous efforts to
withhold critical data on severe adverse reactions and contraindications to
vaccinations to both parents and health practitioners in order to reach overall
vaccination rates which they deemed were necessary for “herd immunity, a
concept which with regards to vaccination, and contrary to prevalent beliefs,
does not rest on solid scientific evidence as will be explained. As a result of
such vaccination policy promoted by the JCVI and the DH, many children have
been vaccinated without their parents being disclosed the critical information
about demonstrated risks of serious adverse reactions, one that the JCVI
appeared to have been fully aware of. It would also appear that, by withholding
this information, the JCVI/DH neglected the right of individuals to make an
informed consent concerning vaccination. By doing so, the JCVI/DH may have
violated not only International Guidelines for Medical Ethics (i.e., Helsinki
Declaration and the International Code of Medical Ethics) [2] but also, their
own Code of Practice.
Rupert Murdoch's mother,
Elizabeth, Dame Commander of the Most Excellent Order of the British Empire,
and daughter-in-law, Sarah Murdoch, steward the Royal Women's Hospital and
Murdoch Children's Research Institute, respectively, in Australia. They oversaw
their staff conduct H1N1 vaccine trials on infants, children, and pregnant
women in 2009, collaborating with Merck's subsidiary, CSL.
It might be noted that
"Overall, the number of vaccine-related "fetal demise" reports
increased by 2,440 percent in 2009 compared to previous years, which is even
more shocking than the miscarriage statistic [700%].
Members of this group
[Goldman-Sachs, Rupert Murdoch, David Rockefeller, the Royal Family of
England], along with George Soros-directed assets, virtually monopolized the
genetics industry during the 1990s, culminating in the corporate privatization
of the Human Genome Project.
Involvement of these
economic leaders in the vaccine industry is most revealing and even shocking as
the following facts evidence:
The Baxter Corporation,
indicted for spreading:
[1] HIV contaminated
blood products during the late 1970s through the 1980s;
[2] a cheap lethal
heparin substitute in 2008; and
[3] H5N1 contaminated
seasonal flu vaccines in early 2009, was
directed by Mr. Tony
White, Soro's appointee to lead the privately owned Applera Company following
their obvious heist of the Human Genome Project during the late 1990s. The
sudden privatization of what had previously been public, non-profit, patentable
property, also implicated co-sponsors the U.S. Department of Energy and The
Wellcome Trust of London.
Today, the American
Baxter Company is a major H1N1 vaccine maker for European nations, and at the
center of controversy concerning the expanding outbreak of recombinant
H1N1-hemorrhagic pneumonia. Many experts conclude the 2009 H1N1 triple
reassortant sourced from a lab, similar to its 1977 relative.
Why hasn't the public
heard that the UK government has been covering up hazards of vaccines, for
example the controversial MMR vaccine?
Rupert Murdoch's son
James runs the Times of London and oversees GlaxoSmithKline. In fact, the
CSL/Merck H1N1 vaccine was "tested in Murdoch-family directed
facilities." The MMR (measles, mumps, rubella) vaccines are produced by
GSK and Merck. A reporter for the Times of London character-assassinated Dr.
Andrew Wakefield after his work on mitochondrial dysfunction in autistic
children and the possibility it was linked to the MMR vaccine.
"Taking down
Wakefield in a big way became a means of discrediting anyone questioning
vaccines. Wakefield was cast as a fraud and so all those voicing concerns were
dismissed by reference to him. This Alan Golding documentary gives background
which can allow people to judge the credibility of Murdoch's reporter for
themselves."
The Bankers have been
thrown out of Iceland. They are being arrested in numbers of countries. They
are not high on credibility.
To know the Bankers is
to know who is behind children's vaccines. In knowing that, one can see
understand more easily the UK's 30 year coverup around vaccines, and why it is
significant that a lawsuit had to filed against the CDC, for they are still
refusing to tell the American public what is really going on there with
vaccines and mercury.
Curiously, in 2008, The
Wellcome Trust of London’s Biocentre, the UK’s largest non-governmental source
of funds for biomedical research, created a special grant program to heavily
fund research into alleged mysterious neurodegenerative diseases linked by
censored science to thimerosal mercury.
And why isn't media in
the UK and here reporting on these huge stories?
Besides James and Rupert's
News Corp directing film makers Twentieth Century Fox and Warner Brothers, the
Western World's mass-mediated mind-set is reinforced by PFNYC €œpartner and
Reuters News Service CEO, Thomas H. Glocer. [Emphasis added.]
Read more: http://www.newpartiotsblog.com/news/bankers-not-just-calling-the-shots-they-are-giving-them/
"Glocer sits on the
Board of Directors of Merck & Company, whose (CSL) H1N1 vaccine, and
(Merck's) Pneumovax vaccine, is broadening markets as the main ingredient
laboratory engineered H1N1 virus mutates, as in the Ukraine, becoming more
deadly.
"Additionally,
those poorly-paid inadequately-trained pharmacists administering vaccines in
supermarkets, draining doctors' revenue streams, reflect the 'hostile takeover'
of clinical medicine by Goldman-Sachs' limited partner, PFNYC ˜Corporate
Partner", [David Rockefeller] and world-leading ˜buyout firm, Kolberg,
Kravitz, Roberts & Company (KKR) This ˜immunization" industry-altering
practice is promoted as a cost-saving invention according to KKRâ's director of
Safeway supermarkets, Steven Burd, founder of the Coalition to Advance
Healthcare Reform (CAHR), popularly called ˜Obamacare."
Perhaps the Bankers
might institute another cost saving measure and parents forced to take their
children for mandated shots (now known to be ineffective and dangerous) can do
so at banks and the bankers could be paid directly, skipping the hoax of
medical treatment. Children are a captive market for vaccines which are a
trillion dollar industry, and health is as unwelcome as cancelling a fat debt,
whereas vaccine induced illnesses expand financial markets.
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