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The Next Big Autism Bomb: Are 1 in 50 Kids Potentially At Risk?

The Next Big Autism Bomb: Are 1 in 50 Kids Potentially At Risk?

http://www.huffingtonpost.com/david-kirby/the-next-big-autism-bomb_b_93627.html

Posted March 26, 2008 | 09:30 PM (EST)
Read More: Autism, Autism Mitochondria, Autism Thimerosal, Autism Vaccine Mercury, Autism Vaccines, Breaking Living News

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On Tuesday, March 11, a conference call was held between vaccine safety officials at the US Centers for Disease Control and Prevention, several leading experts in vaccine safety research, and executives from America’s Health Insurance Plans, (the HMO trade association) to discuss childhood mitochondrial dysfunction and its potential link to autism and vaccines.

It was a sobering event for all concerned, and it could soon become known as the Conference Call heard ’round the world.

The teleconference was scheduled by a little known CDC agency called the Clinical Immunization Safety Assessment (CISA) Network, a consortium of six research centers working on “immunization-associated health risks,” in conjunction with the CDC’s Immunization Safety Office and the health insurance lobby — whose companies cover some 200 million Americans.

The hot topic of the day was mitochondria – the little powerhouses within each cell that convert food and oxygen into energy for use by the body. Recent news events have implicated mitochondria in at least one case of regressive autism, following normal development.

Some researchers on the call reported that mitochondrial dysfunction is probably much more common than the current estimate of 1-in-4,000 people. The potential implications for autism, then, are staggering.

“We need to find out if there is credible evidence, theoretically, to support the idea that childhood mitochondrial dysfunction might regress into autism,” one of the callers reportedly told participants.

“THE CLOCK IS TICKING”

One person on the call (those interviewed for this article asked to remain anonymous) told me that, “the CDC people were informed, in no uncertain terms, that they need to look into this issue immediately, and do something about it.” The clock is ticking, they were told, and if they don’t respond, the information will be made public.

Still, the doctor said, he was enormously impressed by the “seriousness” with which CDC officials treated the possibility of a link between mitochondria, autism and possibly vaccines as well.

In the recent landmark Hannah Poling case, filed in Federal “Vaccine Court,” officials conceded that Hannah’s underlying mitochondrial dysfunction was aggravated by her vaccines, leading to fever and an “immune stimulation that exceeded metabolic reserves.”

But on March 6, CDC Director Dr. Julie Gerberding claimed that Hannah’s case was a rare, virtually one-of-a-kind incident with little, if any relevance to the other 4,900 autism claims currently pending in the court — or to any other case of autism for that matter.(There were conflicting accounts about whether Gerberding was on the call or not).

Since then, however, Dr. Gerberding and other CDC officials were made aware of a Portuguese study, published last October, which reported that 7.2% of children with autism had confirmed mitochondrial disorders. The authors also noted that, “a diversity of associated medical conditions was documented in 20%, with an unexpectedly high rate of mitochondrial respiratory chain disorders.”

“Apparently, the Portuguese study really got their attention,” one of the participants said. “It’s a highly significant finding. And it’s worrisome enough to definitely look into. I think the CDC people know that.”

They also know that some reports estimate the rate of mitochondrial dysfunction in autism to be 20% or more. And the rate among children with the regressive sub-type of autism is likely higher still.

Vaccine safety officials on the March 11 call may have been open to discussing mitochondria and autism, but they were probably highly unprepared for what was to come next.

One doctor reported his findings from a five-year study of children with autism, who also showed clinical markers for impaired cellular energy, due to mild dysfunction of their mitochondria.

The biochemistry of 30 children was studied intensively, and in each case, the results showed the same abnormalities as those found in Hannah Poling, participants said. Each child had moderate elevations or imbalances in the exact same amino acids and liver enzymes as Hannah Poling.

All thirty children also displayed normal, healthy development until about 18-24 months of age, when they quickly regressed into clinically diagnosed autism (and not merely “features of autism”), following some type of unusual trigger, or stress, placed on their immune system.

Researchers explained on the call that some data show that mitochondrial dysfunction can convert into autism “in numbers that make it not a rare occurrence,” one participant told me. They explained this as “a distinct syndrome; not a mixed bag at all. Every kid had mild mitochondria dysfunction and autistic regression.”

Another surprise came when one researcher announced an “inheritance pattern” that linked each case through the genetics of the father: In families where two cousins had autism, the genetic link was always through the father.

This unexpected discovery would clearly implicate nuclear DNA inheritance, and not mitochondrial DNA, which is inherited only through the mother.

Gerberding and others had previously insisted that Hannah and her mother, Teri Poling, both had the same single point mutation in their mitochondrial DNA. CDC officials asserted that Hannah had a pre-existing disease, a rare genetic glitch in her mitochondria, that may well have manifested as “features of autism” on its own, perhaps even without an environmental trigger.

“It’s not in the mitochondrial DNA, and it’s not rare,” one participant confirmed. In fact, he said, many people probably carry the nuclear DNA mutation that confers susceptibility to mitochondrial dysfunction, they just don’t know it.

1-in-50 GENETIC RISK?

On the call, speculation on the prevalence of a genetic mutation that could confer mild mitochondrial dysfunction in the general population ranged from about 1-in-400, to a staggering 1-in-50, or 2% of all Americans.

There was talk about the urgent need to do mapping studies, and find the locus of this gene. Some of the researchers said they want to test all 30 children for the actual DNA mutation. There was some expectation that they might discover that the mutation goes back generations, so parents and grandparents might be tested as well.

One belief is that a particular mutated gene may have become prevalent over the centuries, because of selective advantage. Mild mitochondrial dysfunction reportedly has been associated with intelligence, because it can increase activity of the brain’s NMDA receptors. A large number of receptors can produce increased intelligence, but it can also increase risk of brain disease, one doctor explained to me. It’s possible that increased receptor activity acts in same way.

But not everyone agrees that mitochondrial dysfunction is a purely inherited affair. Some researchers believe that, while a susceptibility gene for mitochondrial problems certainly exists, some type of environmental trigger, or “adversity,” as one doctor put it, is needed to turn the mutation into a dysfunction.

The medical literature is replete with studies on mitochondrial health and the adverse impact of mercury, aluminum and other toxins. Even AIDS drugs like AZT and prenatal alcohol consumption can damage mitochondria and impact cellular energy.

The mercury-containing vaccine preservative, thimerosal, for example, “can definitely kill cells in vitro through the mitochondria,” one teleconference participant told me. “And some people are beginning to suspect that the dose of hepatitis B vaccine given at birth might be interfering with proper mitochondrial function in certain children.”

While the cause of mitochondrial dysfunction is up for the debate, so too is its potential effect on regressive autism.

All the researchers I spoke with agreed that, in many cases, there was an underlying, asymptomatic mitochondrial dysfunction, aggravated by some other stressful event imposed on the child’s immune system, resulting in autism.

Such “metabolic decomposition” occurs when a child’s system simply “cannot meet the energy demand needed to fight the stress of illness,” one doctor explained.

But what causes the stress? That is a very big question.

Apparently, in only two of the 30 cases, or 6%, could the regression be traced directly and temporally to immunizations, and one of them was Hannah Poling. In the other cases, there was reportedly some type of documented, fever-inducing viral infection that occurred within seven days of the onset of brain injury symptoms.

All 30 of the regressions occurred between one and two years of age, at a time when the still-developing brain is particularly vulnerable to injury.

But if a significant minority of autism cases was caused by mitochondrial dysfunction aggravated by common childhood illnesses, then shouldn’t we see fewer cases today than, say, at the beginning of the 20th Century? And wouldn’t developing countries likewise show far more prevalence of autism than the United States?

Not necessarily, some experts said. They noted that many viral infections are still quite prevalent in modern-day America, and many children still get these types of viral infections about once a month, on average.

If that is the case, then why doesn’t every child with “mito” dysfunction regress into autism? Surely, they must encounter viral infections during their yearlong window of neurological peril.

Again, not necessarily: Some doctors said it would depend on the severity of the dysfunction, the type of virus encountered, and perhaps other factors that are still not understood.

But at least two of the 30 kids with mito deficiencies were pushed over the edge into autism by their vaccines, and some researchers feel the number is probably much higher than that in the larger population.

“Vaccines, in some cases, can cause an unusually heightened immune reaction, fever, and even mild illness,” one participant said. “A normal vaccine reaction in most kids would be very different in a kid with a metabolic disorder. We know it happened to at least two kids in this study, and I’m certain there are many more Hannahs out there.”

One theory currently in circulation about what happened to Hannah and other children like her, is an apparent “triple domino effect.” According to this hypothesis, it takes three steps and two triggers to get to some types of autism, and it goes like this:

STEP ONE: Child is conceived and born healthy, but with an underlying nuclear DNA genetic susceptibility to mitochondrial dysfunction, inherited from dad.

TRIGGER ONE: An early environmental “adversity” occurs in the womb or during the neonatal period, perhaps caused by prenatal exposure to heavy metals, pollutants, pesticides and medicines. Or, it occurs in early infancy, through environmental toxins, thimerosal exposure, or even the Hepatitis B vaccine “birth dose.” This trigger results in:

STEP TWO: Child develops mild, usually asymptomatic mitochondrial dysfunction (though I wonder if the ear infections and eczema so common in these cases might also be symptoms of mito problems).

TRIGGER TWO: Child, now with an underlying mitochondrial dysfunction, suffers over-stimulation of the immune system beyond the capacity of his or her metabolic reserves. This stress is either via a viral febrile infection, or from multiple vaccinations, as in the Poling case. This trigger results in:

STEP THREE: Acute illness, seizures, encephalopathy, developmental regression, autism.

Such a scenario might help explain why autism has increased right along with the addition of more vaccines to the national schedule.

And it might help explain why autism rates are not plummeting now that thimerosal levels have been significantly reduced in most childhood vaccines.

It’s possible that exposures from the flu shot, and residual mercury left over in other vaccines — perhaps in synergistic effect with aluminum used as an “adjuvant” to boost the immune response – might “contribute to the toxic mix that causes childhood mitochondrial dysfunction in the first place,” one of the doctors said.

But like many hypotheses, this one has competition. Some researchers believe that the modern American diet is largely to blame for an increase in the number of children whose underlying mitochondrial dysfunction is “triggered” into autism by febrile infections.

The answer, they hypothesize, is corn.

The American diet has become extraordinarily dependent on corn oil and corn syrup used in processing, these experts contend. They say that corn oil and syrup are inflammatory, whereas fish oil is anti-inflammatory. Could our diet be a factor in making this mutated gene become more pathogenic? It’s a biochemical defect that leads to biochemical disease, supporters of this theory say: The gene itself becomes more of a problem.

WHAT NOW?

This information raises so many questions it makes your head swim.

First and foremost among them: What to do about vaccinating children with known mitochondrial dysfunction?

In many respects, these kids should be first in line for vaccination, to prevent some illnesses that might trigger an autistic regression during the window of vulnerability. On the other hand, with multiple vaccinations, such as the case with Hannah, there is also a risk of overtaxing the immune system, and likewise triggering regression into autism.

What’s needed most urgently, if possible, is a quick, affordable and efficient method of testing children for low cellular energy, perhaps before vaccination even begins.

There was some discussion on the conference call about altering the vaccine schedule in some way, to lower the risk of immune over-stimulation in susceptible children. Certainly, pressure will grow for a change in the schedule – the question is how, when, and if such changes will be made.

Some of the suggestions may not be popular among public health officials. They include:

1) Establishing a maximum number of vaccine antigens to which any child could be exposed on any given day.

2) Permitting the option of separating out the measles-mumps-rubella (MMR) live virus combination vaccines into three distinct “monovalent” shots.

3) Not giving the varicella vaccine (chicken pox) on the same day as the MMR injection – the CDC recently withdrew is recommendation for the Pro-Quad MMR+Varicella vaccine because it doubled the risk of seizures.

Another option is to create new “recommendations for administering multiple vaccines to children who have fallen behind in the recommended childhood immunization schedule,” according to the website of the Institute for Vaccine Safety at Johns Hopkins Bloomberg School of Public Health.

Hannah had missed some shots and her doctor decided to “catch up” with the schedule by administering five shots, containing nine vaccine antigens, at once. But some autism activists have pointed out that giving five shots in one day is not that uncommon.

Moreover, they claim, many children regressed into autism following normal vaccination, when the parents religiously adhered to the official schedule.

According to the Johns Hopkins site, “Additional research is needed to determine if other children with autism, especially those with ‘the regressive form’ of autism, have the same or similar underlying mitochondrial dysfunction disorders.”

It adds that, “the advisory groups who make recommendations regarding vaccines will undoubtedly examine this case carefully and make decisions regarding the potential need for changes.”

That day may come sooner than you think. It was just announced that, on April 11 in Washington, DC, the National Vaccine Program Office at HHS will convene a meeting of the National Vaccine Advisory Committee’s Vaccine Safety Working Group. The Working Group was established to go over the CDC’s Immunization Safety Office draft research agenda, and to, “review the current vaccine safety system.”

The meeting is open to the public, and I have my seat reserved. But I honestly don’t envy the Working Group’s very tricky task at hand.

It remains to be seen how all this plays out. And many important questions still lie ahead.

For example, if mitochondrial dysfunction turns out to be as common as 200-per-10,000, and autism is now at 66 per 10,000, did anything bad happen to any of the other 134-per-10,000 children, apart from autism (i.e., ADD, ADHD, speech delay, etc.)?

Moreover, if 10-20% of autism cases can actually be traced to an underlying mitochondrial dysfunction, then what about the majority of autism cases where this did not come into play?

And, if 20% of autism cases are mito related, and 6% of those cases regressed because of vaccines, that would mean that at least 1% of all autism cases were vaccine related. Some estimates of autism go as high as a million Americans – that would mean 10,000 people with vaccine-triggered autism, and billions of dollars in the cost of lifetime care.

(While we are on the subject, isn’t it time to fund a study of vaccinated and unvaccinated children, to settle this debate once and for all?)

Finally, the goals of the CISA Network, (which convened the teleconference) are rather progressive and far reaching. It remains to be seen how well the Network fulfills its stated mission, which includes:

Conduct research into “the role of individual variation” on vaccine injury;

“Empower individuals to make informed immunization decisions;”

Help policy makers “in the recommendation of exclusion criteria for at-risk individuals,” and;

“Enhance public confidence in sustaining immunization benefits for all populations”

Let’s see how long it takes before Network members hang out the proverbial banner: “Mission Accomplished.”

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April 2, 2008 Posted by | Autism | , , , , , , , , , , , , , , , , , , | Leave a comment

BLOOD LEVELS OF MERCURY ARE RELATED TO DIAGNOSIS OF AUTISM –FACT

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BLOOD LEVELS OF MERCURY ARE RELATED TO DIAGNOSIS OF AUTISM –

(House of Representatives – December 11, 2007)
The SPEAKER pro tempore. Under a previous order of the House, the gentleman from Indiana (Mr. Burton) is recognized for 5 minutes.

Mr. BURTON of Indiana. Madam Speaker, it’s late at night here in the Capitol, and most of my colleagues are in their offices or have gone home. But I want to talk about an issue that’s very, very important that we’ve been talking about now for the last 8 years.

I was chairman of the Government Reform Committee for 6 years, and during that time, my grandson became autistic; and we checked to find out what was the cause, trying to find out, because my daughter and her husband were just extremely upset about it, as we were as grandparents. And we found that he had received nine shots in one day, seven of which had a product called themarasol, a preservative, in it. And the themarasol was 50 percent ethylmercury. And so I decided to have hearings to try to find out if the ethylmercury in those vaccines had anything to do with the autistic problem my grandson had. And we found, by having many, many hearings over a 4-year period, we found that scientists from all over the world and leading doctors and educators here that work with autistic children, that the mercury in the vaccines did contribute to the autistic epidemic that we had.

We used to have one in 10,000 children that were diagnosed as being autistic. One in 10,000. Today the Centers for Disease Control will tell you it’s one out of 150. It’s an absolute epidemic in this country. And we have been fighting and fighting and fighting to make sure that those families who have been damaged and those children who have been damaged by autism get some kind of compensation. And that’s why, and I think in 1986 we passed what was called the Vaccine Injury Compensation Fund, and it took some of the money from the pharmaceutical companies when they sold their vaccine products to put into this fund to take care of people who are damaged by vaccines. And one of the reasons we did that was because of the issue of autism, although at that time I didn’t know much about it.

In any event, the Vaccine Injury Compensation Fund has about $3 billion in it, and the people who’s children have been adversely affected by mercury and have autism have not been able to get anything out of that. They have to go through a process and see a special master, and he has to judge whether or not the information that he has and the information they have lead them to believe that the mercury in the vaccines caused autism. And so far the special masters have not been able to ascertain, according to them, that the mercury in the vaccines does cause autism.

Well, last week, 2 years ago, let’s see, 4 years ago there was a report, 2004, that said that there was definitely no connection between the mercury and the vaccinations and the children getting autism. Well, this past November, just last month, two doctors, Dr. Catherine DeSoto and Dr. Robert T. Hitlan, both very renowned doctors across this country, they have Ph.D.s in medicine, they wrote an article in the Journal of Child Neurology. And you can’t discount this. What they’re saying is fact. I want to read to you the summary of what they said. They said: “The question of what is leading to the apparent increase in autism is of great importance. Like the link between aspirin and heart attack, even a small effect can have a major health implication. If there is any link between autism and mercury, it is absolutely crucial that the first reports of the question are not falsely stated and that no link occurs.”

Now, get this: “We have reanalyzed the data set forth originally reported in 2004 and have found that the original P value was in error and that a significant relation does exist between the blood levels of mercury and diagnosis of an autism spectrum disorder. Moreover, the hair sample analysis results offer some support for the idea that persons with autism may be less efficient and more variable at eliminating mercury from the blood.”

The fact of the matter is the mercury in the vaccines causes autism. It’s not the only cause of autism. But now we have scientific evidence by two leading doctors in the Journal of Child Neurology that says without doubt, the mercury in the vaccines does cause autism, is a major contributing factor.

Well, I’ve written, contacted Congressman Kucinich, who’s chairman of the subcommittee that deals with this in the Capitol, and I’ve also contacted the special masters that decide these cases and have urged them to re-evaluate all of these cases where people who have autistic children have found that the mercury in the vaccines may have been a major cause.

Now we know that it is a cause of autism, and those people who have suffered, and those kids who have suffered need to be compensated out of the Vaccine Injury Compensation Fund.

So I’d like to say to my colleagues, I hope you will join me in making sure that the information I just read gets out to everybody. These kids are going to live to be 50, 60, 70 years old, and unless there’s some help for them, they’re going to be a real burden on the taxpayers and on society. We have an obligation to make sure they’re taken care of.

I hope all of my colleagues will read this statement tonight and help us to change the attitude of our health agencies and the special masters dealing with this problem.

In November 2007, the well-respected scientific journal, the Journal of Child Neurology, published an article authored by Drs. M. Catherine DeSoto and Robert T. Hiltlan (PhDs), detailing their findings on the relationship between mercury and autism spectrum disorders. The article was entitled “Blood Levels of Mercury are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set.”

To summarize the article, Drs. DeSoto and Hiltlan reanalyzed a data set the subject of a 2004 study that found no relationship between mercury and autism. By reexamining the data set, Drs. DeSoto and Hiltlan determined that the conclusions of the 2004 study were wrong,

and that a relation does exist between the blood levels of mercury and diagnosis of an autism spectrum disorder.
As Drs. DeSoto and Hiltlan noted in their article, there has been a marked increase in the diagnosis of autism in this country over the last 20 years. In fact we have gone from an autism rate of 1 in 10,000 to 1 in 150. So, answering the question of what is (and is not) a possible contributing cause of autism is crucial, not only to the millions of American families currently affected by autism but to future generations.

We simply cannot dismiss or downplay scientific research, which has the potential to unlock the mysteries surrounding what is causing our Nation’s autism crisis. We owe it

to the thousands of families living with autism to follow the science wherever it may lead.

That’s why in late November, I wrote to the Chairman of the House Subcommittee on Domestic Policy, Representative Dennis Kucinich; and the Special Masters assigned to the Congressionally-created Office of Vaccine Program within the U.S. Court of Federal Claims, alerting them to the findings in Drs. DeSoto and Hiltlan’s latest research.

Specifically, I asked the Special Masters to take Drs. DeSoto and Hiltlan’s latest findings into consideration as they carry out their mandate of managing and adjudicating childhood vaccine claims. I asked Chairman Kucinich to hold a hearing on the environmental risks of mercury in childhood vaccines before the 110th Congress ends.

Given the high stakes involved, scientific reports discussing a connection between blood mercury levels and autism deserve serious consideration and review by the medical and scientific community.

During my tenure as Chairman of the House Committee on Government and Reform, I spent 6 years researching and hearing testimony from the autism advocacy and scientific communities about the autism epidemic sweeping our country. Over and over again, questions of causation, namely the use of thimerosal–the mercury-based vaccine preservative–in childhood vaccines were raised.

Here’s what I learned:

A number of credible national and international scientists testified before the Committee that mercury in vaccines is a contributing factor in developing neurological disorders, including, but not limited to, modest declines in intelligent quotient, autism, and Alzheimer’s disease. And the body of evidence to support that conclusion gets larger everyday.

Experience tells us that, as with any other epidemic, while there may be underlying genetic susceptibilities, there usually is also some type of environmental trigger as well–be it exposure to a virus, fungus, heavy metal, or pollutant. There has never, to the best of my knowledge, been a purely genetic epidemic.

Genetics alone cannot explain how we went from 1 in 10,000 children with autism spectrum disorders 20 years ago to 1 in 150 today. The increase happened far too quickly for a genetic shift.

As mercury is a known bio-accumulative neurotoxin, it is biologically plausible that it is a contributing factor to our Nation’s autism epidemic.

Autism has no cure, and while it is a life-changing condition, it is not a life-threatening disease. This means that the autistic children of today will be the autistic adults and autistic seniors, 20, 30, 50, even 70 years from now. Our Nation is ill prepared to deal with the complex educational, financial, housing, and health care challenges posed by a generation of autistic individuals.

My only grandson is autistic, so this is an issue that is very close to my heart; and for the last several years I have fought hard to raise awareness of this disease, and increase research into the causes of autism, as well as new treatments for those suffering with autism.

As a Nation, I believe, we have a collective responsibility to do everything we can to not only stop the further spread of this disease but to help the millions of children, adults and families afflicted with it.

http://a-champ.org/index.html

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December 14, 2007 Posted by | Autism, Vaccines | , , , , , , , | Leave a comment

Autism:Overwhelming Evidence Vaccines Play a Role in Autism

Although a connection to Autism from Vaccines has been dismissed repeatedly in the current media(no surprise), scientific studies that are based on biological processes show a significant link. CDC epidemiological studies also show a strong link of Thimerosal to ADD, Learning Disabilities, Speech Delay and Autism.

It is apparent that critical medical decisions for an entire
generation of American children are being made by small committees
whose members have incestuous ties with agencies
that stand to gain power, or manufacturers that stand to
gain enormous profits, from the policy that is made.
Jane Orient, M.D.

Link to Video on Google

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December 4, 2007 Posted by | Autism, Vaccines | , , , , , , , , , , , | Leave a comment

Secret Government Database of Vaccine-Damaged Children

Secret Government Database
of Vaccine-Damaged Children

The general public is essentially unaware of the true number of people — mostly children — who have been permanently damaged or killed by vaccines. In fact, most parents would be surprised to learn that the government has a secret computer database filled with several thousand names of disabled and dead babies, children who were healthy and alive just prior to receiving the vaccines. Of course, the medical establishment and federal government don’t readily disclose this information because they know it’s likely to frighten parents into seeking other ways to protect their children. In other words, parents just might think this issue through on their own and decide to reject the shots.

Federal Admission of Vaccine Risks:

In 1986, Congress officially acknowledged the reality of vaccine-caused injuries and death by creating and passing The National Childhood Vaccine Injury Act (Public Law 99-660). The safety reform portion of this law requires doctors to provide parents with information about the benefits and risks of childhood vaccines prior to vaccination, and to report vaccine reactions to federal health officials. Doctors are required by law to report suspected cases of vaccine damage. To simplify and centralize this legal requisite, federal health officials established the Vaccine Adverse Event Reporting System (VAERS) — operated by the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA).

Ideally, doctors would abide by this federal law and report adverse events following the administration of a vaccine. However, the FDA recently acknowledged that 90 percent of doctors do not report vaccine reactions. They are choosing to subvert this law by claiming the adverse event was, in their opinion, not related to the shot. In fact, every year between 12,000 and 14,000 reports of adverse reactions to vaccines are made to the FDA (data initially accessible only through the Freedom of Information Act). These figures include hospitalizations, irreversible brain damage, and hundreds of deaths. Considering that these numbers may represent just 10 percent, the true figures could be as high as 140,000 adverse events annually. However, even this figure could be conservative. According to Dr. David Kessler, former head of the Food and Drug Administration, “Only about 1 percent of serious events [adverse drug reactions] are reported to the FDA.” Thus, it is entirely possible that millions of people are adversely affected by mandatory vaccines every year.

Maybe it doesn’t matter that doctors won’t report vaccine reactions, because the federal government won’t investigate them. Government officials claim VAERS was designed to “document” suspected cases of vaccine damage. No attempt is being made to confirm or deny the reports. Parents are not being interviewed, and the vaccines that preceded the severe reactions are not being recalled. Instead, new waves of unsuspecting parents and innocent children are being subjected to the damaging shots.

Who Pays for Compensation?

In order to pay for vaccine injuries and deaths, a surtax is levied on mandated vaccines. When parents elect to have their children vaccinated, a portion of the money they spend on each vaccine goes into a Congressional fund to compensate them if their child is hurt or killed by the shot.

The compensation portion of the law awards up to $250,000 if the individual dies, or millions of dollars to cover lifelong medical bills, pain, and suffering in the case of a living (but brain-damaged) child. To date, more than $1 BILLION has already been paid out for hundreds of injuries and deaths caused by mandated vaccines. Thousands of cases are pending.

Vaccine Injury Compensation Claims do not include private settlements, or the many families that become dependent on public assistance for medical and living expenses because of vaccine injuries. Therefore, taxpayers subsidize vaccine manufacturers and the federal government by paying for their vaccine-liability expenses.

How Are Vaccines Made?

Vaccine production is a disgusting procedure. To begin, one must first acquire the disease germ — a toxic bacterium or a live virus. To make a “live” vaccine, the live virus must be attenuated, or weakened for human use. This is accomplished by serial passage — passing the virus through animal tissue several times to reduce its potency. For example, measles virus is passed through chick embryos, polio virus through monkey kidneys, and the rubella virus through human diploid cells —-the dissected organs of an aborted fetus! “Killed” vaccines are “inactivated” through heat, radiation, or chemicals.

The weakened germ must then be strengthened with adjuvants (antibody boosters) and stabilizers. This is done by adding drugs, antibiotics, and toxic disinfectants to the concoction: neomycin, streptomycin, sodium chloride, sodium hydroxide, aluminum hydroxide, aluminum hydrochloride, sorbitol, hydrolized gelatin, formaldehyde, and thimerosal (a mercury derivative).

Aluminum, formaldehyde, and mercury are extremely toxic substances with a long history of documented hazardous effects. Studies confirm again and again that microscopic doses of these substances can lead to cancer, neurological damage, and death. Yet, each of them may be found in childhood vaccines.

In addition to the deliberately planned additives, unanticipated matter may contaminate the shots. For example, during serial passage of the virus through animal cells, animal RNA and DNA — foreign genetic material — is transferred from one host to another. Because this biological matter is injected directly into the body, researchers say it can change our genetic makeup.

Undetected animal viruses may jump the species barrier as well. This is exactly what happened during the 1950s and 1960s when millions of people were infected with polio vaccines that were contaminated with the SV-40 virus undetected in the monkey organs used to prepare the vaccines. SV-40 (Simian Virus 40 — the 40th such virus detected since researchers began looking), is considered a powerful immunosuppressor and trigger for HIV, the name given to the AIDS virus. It is said to cause a clinical condition similar to AIDS, and has been found in brain tumors, leukemia, and other human cancers as well. Researchers consider it to be a cancer-causing virus.

What happens next, once this foul concoction — live viruses, bacteria, toxic substances, and diseased animal matter — is created? This witch’s brew is forced into the healthy child.

Satanic Rituals:

Dr. Robert Mendelsohn often criticized modern medicine for its sanctimonious doctrine. He argued that “doctors are the priests who dispense holy water in the form of inoculations” to ritually initiate our loyalty into the larger medical industry. Dr. Richard Moskowitz agrees: “Vaccines have become sacraments of our faith in biotechnology. Their efficacy and safety are widely seen as self-evident and needing no further proof.”

Others see a link between vaccinations and satanic rituals or witchcraft, where animals are sacrificed and their organs brewed in a hellish concoction of horrid substances: voodoo medicine by 21st century mad scientists. Sadly, our children are their unwilling subjects as society is slowly devoured by their insatiable appetite for human experimentation.


SECRET DATABASE!

FDA/U.S. GOVERNMENT VACCINE DATABASE (Years 1990-2004)
Every year, the FDA receives thousands of reports of adverse reactions after vaccines. These include brain damage and death. This information is stored in a secret government database and is available through the Freedom of Information Act — or right here from Thinktwice/New Atlantean Press! Serious researchers can now study and analyze 15 years of data — tens of thousands of adverse events filed with the FDA/CDC Vaccine Adverse Event Reporting System (VAERS). You will receive the data on a CD disc. The data is easily read with popular word processors, such as Word and Word Perfect or imported into common database programs such as Borland’s Paradox and Microsoft’s Access or Excel. The information can be filtered, sorted, and analyzed in many ways. Categories include vaccines administered, types of reactions, dates of hospitalization or death, and more. Data from 1990 thru August 2004. Code DB15 (1 CD Disc) $25.

http://www.thinktwice.com/secret.htm

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December 3, 2007 Posted by | Vaccines | , , , , , , , , , , , , , , , , , , | 1 Comment

Time For The CDC To Come Clean

Robert F. Kennedy Jr.   Robert F. Kennedy Jr.| BIO

 Time for CDC to Come Clean

Posted March 1, 2006 | 12:09 AM (EST)




Correspondence newly obtained under the Freedom of Information Act raises troubling new questions about CDC’s role in the Thimerosal scandal. Thimerosal is the mercury-based vaccine preservative that has been linked to epidemics of neurological disorders, including autism, in American children born after 1989.

Responding to scientific studies linking dangerous levels of mercury to a range of health disorders, the CDC in July 1999 recommended that the nation’s vaccine makers eliminate Thimerosal as a preservative, “as soon as possible.”

But the newly released documents show that behind the scenes CDC was quietly discouraging Thimerosal’s removal. In a July 1999 letter, vaccine producer SmithKline Beecham tells CDC that it is ready to produce non-Thimerosal DTP (Diptheria/Tetanus/Pertussis) vaccines immediately and has sufficient inventories to supply the entire U.S. market during the remainder of 1999 and the first half of 2000, by which time other vaccine manufacturers would have their Thimerosal-free DTP vaccines on line.

Thimerosal-laden DTP vaccines containing 25 micrograms of mercury apiece were then being administered to American infants at two months, four months and six months — far exceeding EPA’s recommended safe level for mercury. Had CDC accepted SmithKline’s offer, it could have immediately reduced the mercury exposures to vaccinated six-month-old children by 40%.

However, in November, CDC mysteriously sent a letter back rejecting SmithKline’s offer. Then, on July 14, 2000 CDC published a deceptive press release promising to require that all vaccines be Thimerosal-free as soon as “adequate supplies are available.” This was a full 12 months after the agency had denied SmithKline’s proposal.

“If CDC were basing its decision on safety alone, it would have taken SmithKline up on its offer. That’s a no-brainer,” said a federal health official who requested anonymity. “So there were other considerations beside safety that were guiding their decision making.”

Among these “other considerations” were CDC’s important concerns for the preservation of the vaccine program, a bureaucratic impulse for self-preservation, and protecting the economic interests of its vaccine industry friends.

“Immediate withdrawal would send a strong message; ‘We messed up!'” the health official told me. “And I don’t think they wanted to send that message to parents, the public or those considering legal action.”

“There was also concern,” says the federal official, “that an immediate withdrawal might discredit the international vaccine programs for which CDC is an important partner.” The World Health Organization has urged CDC against the banning of Thimerosal in U.S. vaccines since that prohibition might discredit WHO’s third world inoculation programs. WHO, with U.S. funding, is now injecting children in developing countries with the same amounts of Thimerosal we were giving American kids at their highest exposures, but in a shorter time period. In May 2001, WHO committed to “develop a strong advocacy campaign to support the ongoing use of Thimerosal.”

But CDC insiders argue that CDC’s primary concern was the economic impacts on its pharmaceutical industry partners. “The big consideration was cost,” says the federal health official. “A lot of CDC’s friends in the vaccine industry had stockpiled Thimerosal-based vaccines. If they couldn’t sell them the costs would total in the tens of millions of dollars.”

On July 14, 2000 CDC promised to complete the transition to Thimerosal-free vaccines for children by first quarter 2001. But, probably for the reasons stated above, its commitment sometimes seems half-hearted. CDC continues to promote the use of Thimerosal in vaccines. The agency continues to send its top spokesman Roger Bernier around the country to testify before state legislatures to derail state efforts to ban Thimerosal in vaccines. Last week Bernier was testifying against a proposed Thimerosal ban in Maryland.

CDC continues to exert muscular efforts to derail studies of American cohorts — the Amish, Christian Scientists, and home-schooled children — who were not exposed to Thimerosal vaccines. Preliminary studies of these groups indicate very low levels of the neurological disorders, including autism, that have been associated with Thimerosal in vaccinated populations.

It’s time for the CDC to come clean with the American public. Its tactics of deception and obfuscation are jeopardizing the credibility of the entire vaccine program, and therefore posing an enormous danger to public health.

http://www.huffingtonpost.com/robert-f-kennedy-jr/time-for-cdc-to-come-clea_b_16550.html

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December 3, 2007 Posted by | Autism, Vaccines | , , , , , , , | Leave a comment