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Infant Primates Given Vaccines On U.S. Children's Immunization
Schedule Develop Behavioral Symptoms Of Autism 20 May 2008
[input]
A primate model for autism using the U.S. children's immunization schedule was
unveiled at the International Meeting For Autism Research (IMFAR) this weekend.
The research underscores the critical need for studies into vaccine safety and
the immune and mitochondrial dysfunction of autistic children. The National
Autism Association (NAA) questions why the government hasn't undertaken these
vital studies and why researchers have had to depend on private money to
perform this critical science that will surely impact the health of millions of
children worldwide.
While the authors and organizations associated with this study are withholding
comment until publication, University of Pittsburgh's Dr. Laura Hewitson,
Ph.D., described at the IMFAR meeting how vaccinated animals, when compared to
unvaccinated animals, showed significant neurodevelopmental deficits and
"significant associations between specific aberrant social and non-social
behaviors, isotope binding, and vaccine exposure."
Researchers also reported at the scientific meeting that "vaccinated animals
exhibited progressively severe chronic active inflammation whereas unexposed
animals did not" and found "many significant differences in the GI tissue gene
expression profiles between vaccinated and unvaccinated animals."
Gastrointestinal issues are a common symptom of children with regressive autism.
NAA calls for the NIH to conduct large scale, non-epidemiological studies into
the biomedical symptoms surrounding young children and all vaccines, including
those containing the mercury-based preservative thimerosal and other additives
like aluminum.
This request for further research echoes that of Dr. Bernadine Healy, Former
NIH Director in a CBS interview earlier this week. "I think public health
officials have been too quick to dismiss the hypothesis as 'irrational,'
without sufficient studies of causation... without studying the population that
got sick," Healy said. "I have not seen major studies that focus on 300 kids
who got autistic symptoms within a period of a few weeks of the vaccines."
Recently the government's vaccine court conceded the case of Hannah Poling,
admitting that vaccines triggered her regression into autism by exacerbating
mitochondrial dysfunction. "The recent Poling case and this new research
provide further evidence that the CDC has fallen down on their job to protect
children from harm. The biomedical research to date suggests that parental
reports of regression following vaccination is not only plausible, but likely
in certain individuals," said Scott Bono, NAA Chairman. "To date, the CDC has
conducted no safety testing on the possible harmful effects of simultaneously
administering multiple vaccines to infants, and has steadfastly refused to
state a preference for mercury-free vaccines to be given to children and
pregnant women. It's time for HHS and Congress to step in and take vaccine
safety away from the CDC."
On June 4th, parents of vaccine-injured children will rally for toxin-free
immunizations in Washington, DC. For more information visit
http://www.nationalautism.org.
National Autism Association
http://www.nationalautism.org
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