Encephalomyopathy, Encephalitis Package Inserts Vaccine autism
Big Pharma Admits that Vaccines Cause Autism (Autism symptoms are identical to encephalomyopathy, listed on vaccine package inserts)
Am I seeing this right? *rubs eyes* Whoah! Big Pharma
actually admits (albeit in very fine print) that vaccines cause autism?
Says the insert from MedImmune's FluMist H1N1 vaccine, also known as Fluenz in
the UK (download
or read full document here):
http://healthbitesonline.blogspot.co.uk/
6.2 Postmarketing Experience
The following adverse reactions have been identified during postapproval use of
FluMist. [Translation: Our clinical trials involved too few people for too
short a time to catch these extremely serious adverse effects because we wanted
to rush this product through approval by our shareholders esteemed colleagues at
the FDA in a mere six months instead of the standard ten years—testing be
damned—so you paid to be our guinea pigs - more money for us, mwahaha!]
Because these reactions are reported voluntarily from a population of uncertain
size, it is not always possible to reliably estimate their frequency or
establish a causal relationship to vaccine exposure. [Since it happened
outside our controlled setting, you can't legally stick it on us, nyah nyah!]
Congenital, familial and genetic disorder: Exacerbation of symptoms ofmitochondrial
encephalomyopathy (Leigh syndrome).
What is mitochondrial encephalomyopathy and what's it got
to do with autism?
What is a mitochondrial disorder?
Mitochondria are the energy generators inside our cells.
Mitochondria are responsible for processing oxygen and
converting food into energy for essential cell functions.
The process of converting food and oxygen into energy requires hundreds of
chemical reactions, and each chemical reaction must run almost perfectly in
order to have a continuous supply of energy. When one or more components of
these chemical reactions does not run perfectly, there is an energy crisis, and
the cells cannot function normally. As a result, the incompletely burned food
might accumulate as poison inside the body.
This poison can stop other chemical reactions that are
important for the cells to survive, making the energy crisis even worse. In
addition, these poisons can act as free radicals (reactive substances that
readily form harmful compounds with other molecules) that can damage the
mitochondria over time, causing damage that cannot be reversed.
About 1 in 4,000 children in the United States will develop mitochondrial
disease by the age of 10.
(Source: Mitochondrial
Disease)
Mitochondria may not function correctly due to a genetic defect, damage
caused by drugs, or damage caused by free radicals. Neurotoxins (such as the
mercury in vaccines) disrupt
mitochondrial respiration.
As for encephalomyopathy, encephalo means brain and myopathy means
degeneration.
So mitochondrial encephalomyopathy means the malfunction of mitochondria
leading to the degeneration of the brain. (Better to just get the flu, no?)
Mitochondrial encephalomyopathy is listed as a side effect of the FluMist
vaccine. So the maker of FluMist admits that FluMist contains toxins potent
enough to permanently damage your mitochondria, leading to the death of brain
cells. In short, FluMist causes brain damage. If you know how Big Pharma
works, you know that for them to admit anything this serious means that they can
no longer get away with laughing it off or calling you a conspiracy theorist.
They printed it in their own insert!
Now, what's interesting is that they even specified the specific type of
mitochondrial disease that it causes exacerbates — Leigh Syndrome.
What is Leigh Syndrome?
Leigh Syndrome is a rare inherited neurometabolic disorder
characterised by degeneration of the brain, meaning that it gradually loses its
ability to function properly.
Leigh Syndrome usually occurs between the ages of three months and two years.
The disorder worsens rapidly; the first signs may be loss of head control, poor
sucking ability, and loss of previously acquired motor skills, meaning the
control of particular groups of muscles. Loss of appetite, vomiting, seizures,
irritability, and/or continuous crying may accompany these symptoms. As the
disorder becomes worse, other symptoms such as heart problems, lack of muscle
tone (hypotonia), and generalized weakness may develop, as well as lactic
acidosis, a condition by which the body produces too much lactic acid. In rare
cases, Leigh Syndrome may begin late in adolescence or early adulthood, and in
these cases, the progression of the disease is slower than the classical form.
(Source: Leigh
Syndrome)
If you are a parent of a child with autism, you might be forgiven for thinking
you were looking at the symptoms of autism. Here's a comparison:
(Click image to enlarge.)
Anyone diagnosed with Leigh Syndrome already more than fulfills the criteria for
autism. So, for Big Pharma to say that their vaccine causes "mitochondrial
encephalomyopathy" is to admit that it causes brain damage — not just any
garden-variety brain damage like epilepsy or dyslexia, but a very, very specific
type of mitochondria-induced brain damage — the type that meets all the criteria
for a diagnosis of autism. And more.
So, what has mitochondrial damage got to do with autism?
Hannah Poling (below) made medical history in 2008 when the US Vaccine Court
ruled that her regression into full-blown autism was caused by vaccines.
What happened to little, red-haired Hannah Poling is hardly
unique in the world of autism. She had an uneventful birth; she seemed to be
developing normally—smiling, babbling, engaging in imaginative play, speaking
about 20 words by 19 months. And then, right after receiving a bunch of
vaccines, she fell ill and it all stopped. "Something happened after the
vaccines," says her mom, Terry Poling, who is a registered nurse and an
attorney. "She just deteriorated and never came back."
A panel of medical evaluators at the Department of Health and Human Services
concluded that Hannah had been injured by vaccines — and recommended that her
family be compensated for the injuries. The panel said that Hannah had an
underlying cellular disorder that was aggravated by the vaccines, causing brain
damage with features of autism spectrum disorder.
(Source: Case
Study: Autism and Vaccines)
The case also thrusts the family into a national spotlight in the controversial
public debate over whether vaccines have played some role in the growing number
of U.S. children diagnosed with autism. Of particular concern to some families
is the mercury-based preservative thimerosal, not used in child vaccines (except
for some flu shots) since 2001.
The family turned to leading experts in neurology. “I had to know. My daughter
didn’t just suddenly develop autism for no reason,” Terry Poling said.
Hannah’s father co-authored an article about her case, which was published in
theJournal
of Child Neurology in 2006.
Hannah’s case was one of three vaccine-court test cases alleging that thimerosal
caused the children’s autism.
The government’s Division of Vaccine Injury Compensation concluded that five
shots Hannah received in July 2000, when she was 19 months old, “significantly
aggravated an underlying mitochondrial disorder” and resulted in a brain
disorder “with features of autism spectrum disorder.”
“The biggest question right now for the public is: How unique is Hannah’s case?”
said Jon Poling. Poling said he suspects there are other children like Hannah.
(Source: Georgia
Girl Helps Link Autism to Childhood Vaccines)
Indeed there are a whole lot more children like Hannah. A
population study (2005)found that the incidence of mitochondrial disorders
among autistic children is 7%.
In a recent
study (Apr 2010), researchers looked at a small group of children with both
mitochondrial disease and autism. Here are some interesting things they
found:
The frequency of autistic regression in the general population of patients with
autism was estimated to be 25%.
[Regression is defined as a loss of developmental skills within 2 weeks after a
fever.]
Autistic regression was identified in 60% of the study participants,
representing a statistically significant increase over the estimated 25%
reported in the general population of autistic spectrum disorders patients.
Autistic regression was not identified in 40%.
The rate of autistic regression in this highly selected group of individuals was
approximately twice the rate of regression reported in the general
population of patients with autistic spectrum disorder. Fever is associated
with regression in patients with many types of mitochondrial diseases as
well as in a broad array of other classes of metabolic disease. In no case
did we observe regression with vaccination unless fever was present.
Source: Full
text (PDF)
That is to say, children with mitochondrial diseases are
more than twice as likely as normal children to get autism after a
vaccination. 70% of them regressed after experiencing a high fever. Could the
raging fever be an indication that their bodies could not fend off the
simultaneous assault by multiple viruses and toxic vaccine components and
suffered damage as a result?
What would be interesting to know is:
• Do children with mitochondrial disorders already have the mitochondrial
disorder before getting vaccinated, or did they develop a mitochondrial disorder
as a result of getting vaccinated?
• What percentage of children who have a pre-existing mitochondrial disorder
develop autism after getting vaccinated? How many have a mitochondrial disorder
and but did not descend into autism after a vaccination?
• What percentage of normal, healthy children developed a mitochondrial disorder
as the result of getting vaccinated?
• Is it possible to have a mitochondrial disorder and not be autistic? Hannah
Poling's mother, Terry Poling, has
the same genetic disorder, but she's not autistic. Can we then conclude that
if you have a mitochondrial disorder, you can live a normal and healthy life
until the day you meet a vaccine you can't handle? Is Terry Poling an anomaly,
or are there many more adults like her? Remember that when Terry was a child,
she got only a quarter of the number of vaccines that the American child of
today gets.
Here is the US vaccination schedule of 1983 vs. 2007:
(See here for the latest
vaccination schedule and also that of past years - scroll down a bit.)
It would be difficult to find any child today who has not been vaccinated. It
would be near impossible to find children with rare mitochondrial disorders who
have also NOT been vaccinated. So don't count on seeing any such studies anytime
soon.
Do you think that the pharmaceutical companies producing these vaccines would
test their products this thoroughly before releasing them to the public? In the six
months that it took them to produce and push the H1N1 vaccine through FDA
approval? (Drugs normally go through 10 years of development and testing
before getting FDA approval, and even then, the testing is bloody hell shoddy -
I should know, I used to work in clinical trials.) Has any vaccine been
tested this thoroughly? (If you're wondering, the answer is no.) In 6 months,
there is no time to test anything. I doubt there were even human trials since it
usually takes more than 6 months just to get funding for the study! YOU are
their guinea pigs. And if you don't educate yourself, there is only one way to
find out—the
hard way.
Why do you suppose they don't give a crap about your child's safety? Because you
can't sue them, that's why. They're free of liability. You can sue the crib
maker if their crib choked your baby, you can sue the cigarette company if their
cigarettes gave you cancer, but you can't sue vaccine makers if their vaccines
harmed or killed your child. That's because they have colluded with their
friends in high places to change the law to protect themselves that way. Ask
yourself - why the need to do that? Could it be because they knew they were
making an extremely unsafe product in the first place? You don't see car makers
getting the government to change the law to exclude themselves from being sued,
do you? Those people protecting their interests (not yours) are the very people youelected
and pay. (Read Evidence
of Harm, by David Kirby, a very well-researched and truly superlative book
on how and why the US government allowed mercury to be added to your children's
vaccines.) Like you, I too thought that the FDA and CDC worked to protect us.
But I never thought I'd live to see the day when Big Pharma THEMSELVES ADMITthat
if your child has a mitochondrial disorder, you'd best not vaccinate them unless
you want to give them autism as well. And this is the sort of autism that is
lifelong because damage to mitochondria is permanent. If your doctor calls you a
nut or a conspiracy theorist, just ask him to read the insert.
(If you or your child have already suffered a vaccine injury, help
is available.)
---
Update - here is a vaccine insert that actually admits autism in plain English.
Tripedia’s DTaP (diphtheria, tetanus and pertussis) vaccine (December 2005). Read
the full document here (PDF).
No translation needed.
See also:
• Vaccine
Developer Would Not Vaccinate His Own Child
• To
Vaccinate or Not to Vaccinate?