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Jean Shaw© -
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In 1993 my son was four years old and received a diagnosis of autism. It was probably
the worst day of my life.
At the time autism was quite rare. I couldn't find anyone
in my local area who had it and most people had never heard of it. Those that had
automatically thought of Dustin Hoffman in Rain Man. The statistics then were 4 out
of 10,000.
Fast forward to 2006 and autism is a word on everyone's lips. You may
not know what it is but you will have heard of it or know some family affected. Statistically
it now stands at 1 out of 156.
And the big question is WHY?
Could it be mercury,
the second most toxic substance on the planet used in many childhood vaccines as
a preservative under the name of thimerosal?
I think so, and what if a bit of aluminium
and formaldehyde is mixed in for good measure? How can a young child's developing
immune system possibly cope?
Vaccines play a very important role in eradicating preventable
communicable diseases. The theory is if you put a weakened version of a live virus
into someone their immune system will send out antibodies to fight. Hopefully, after
a bit of a tussle the antibodies win, the body remembers the foe and should the virus
attack in its full strength at a later stage it's prepared for battle.
What happens
though if your immune system is too weakened to fight?
When someone contracts a virus
naturally it passes through the skin or mucous substances in the nose and throat.
The body has a bit of a warning. Childhood vaccines are injected directly into supposedly
healthy babies. There is no warning.
Vaccines contain the weakened live virus and also preservatives and stablisers including
aluminium hydroxide, aluminium hydrochloride, formaldehyde and thimerosal -
Is it just coincidence that the amount of children falling under the
autistic spectrum has increased with the introduction of more and more recommended
childhood vaccines?
In UK in 1968, Polio and DPT vaccines were given at 6 months
and 7 ½ months. Autism was very rare.
In 1988, Polio and DPT was given at 3 months,
DPT at 5 months and MMR was introduced at 13 months+. Autism rates were still low.
In 1996, Polio, DPT/HIB injections were given at 2,3 and 4 months, followed by MMR
at 13 month +. Autism rates rising rapidly.
In 2006 -
The Autism
Research institute have an interesting article saying:
"The characteristics of autism and mercury poisoning are so
similar as to suggest
that many cases of autism are a form
of mercury poisoning. For these children the
exposure route
is childhood vaccines, most of which contain thimerosal.
Exposure
to more than 62.5 micrograms of mercury within the
first three months of life significantly
increases a child's
risk of developing some form of neuro-
such
as speech and language, autism, stuttering and
attention deficit disorder".
It appears a child born in the USA in the 1990's would have had 75 micrograms by
the time it was 2 months old, and if this vaccinal mercury was not excreted it migrates
to the brain.
Thimerosal is 49.6% ethyl mercury and has been around for over 70 years
but appears never to have been tested for safety, only efficacy. Amazingly it was
banned from vaccines in dogs in USA in 1992 so why did it take until 2002 ( USA)
and 2004 (UK) for children?
Could the answer be that to remove it as "a precautionary
measure" might just suggest the autism pandemic we are currently experiencing was
indeed man made? If so, the governments and medical profession have a lot to answer
for.
California boasts the best record keeping systems in the world. In 2004 it reported
the first ever nine month sustained reduction in diagnosis of autism for children
between 4 and 6 years of age.
These children were born from 1999 onwards from which
time the USA made a serious effort to reduce the amount of thimerosal in childhood
vaccines.
Makes you think, doesn't it?
Note from Jean
Mercury poisoning can be confirmed by means of a porphyrin test. This
can be carried out by a urine sample sent by post. Unlike the well-
