Vaccine Court: Autism Debate Continues


ANOTHER AUTISM CASE WINS IN VACCINE COURT
By Robert F. Kennedy, Jr.

On February 12, the federal "Vaccine Court" in Washington issued a sweeping ruling in three highly touted "test cases" against families who claimed that their childrens' autism had been caused by vaccines. The Special Masters in those three cases found that Petitioners failed to establish causation between MMR vaccines, the mercury-laced vaccine preservative thimerosal, and autism (the court decision, which is under appeal, deferred any finding on a thimerosal-only theory of causation). The rulings could have a significant precedential impact on some 5,000 families who opted to bring their cases in the Omnibus Autism Proceedings (OAP) hoping that the vaccine court would officially hold that the MMR vaccine or thimerosal had caused autism in their children.

The New York Times joined the government Health Agency (HRSA) and its big pharma allies hailing the decisions as proof that the scientific doubts about vaccine safety had finally been "demolished." The US Department of Health and Human services said the rulings should "help reassure parents that vaccines do not cause autism." The Times, which has made itself a blind mouthpiece for HRSA and a leading defender of vaccine safety, joined crowing government and vaccine industry flacks applauding the decisions like giddy cheerleaders, rooting for the same court that many of these same voices viscously derided just one year ago, after Hannah Poling won compensation for her vaccine induced autism.

But last week, the parents of yet another child with autism spectrum disorder (ASD) were awarded a lump sum of more than $810,000 (plus an estimated $30-40,000 per year for autism services and care) in compensation by the Court, which ruled that the measels-mumps-rubella (MMR) vaccine had caused acute brain damage that led to his autism spectrum disorder.

The family of 10-year-old Bailey Banks won their case quietly and without fanfare in June of 2007, but the ruling has only now come to public attention. In the remarkably clear and eloquent decision, Special Master Richard Abell ruled that the Banks had successfully demonstrated that "the MMR vaccine at issue actually caused the conditions from which Bailey suffered and continues to suffer."

Bailey's diagnosis is Pervasive Developmental Disorder -- Not Otherwise Specified (PDD-NOS) which has been recognized as an autism spectrum disorder by CDC, HRSA and the other federal health agencies since at least the 1990s.

In his conclusion, Special Master Abell ruled that Petitioners had proven that the MMR had directly caused a brain inflammation illness called acute disseminated encephalomyelitis (ADEM) which, in turn, had caused the autism spectrum disorder PDD-NOS in the child:

The Court found that Bailey's ADEM was both caused-in-fact and proximately caused by his vaccination. It is well-understood that the vaccination at issue can cause ADEM, and the Court found, based upon a full reading and hearing of the pertinent facts in this case, that it did actually cause the ADEM. Furthermore, Bailey's ADEM was severe enough to cause lasting, residual damage, and retarded his developmental progress, which fits under the generalized heading of Pervasive Developmental Delay, or PDD [an autism spectrum disorder]. The Court found that Bailey would not have suffered this delay but for the administration of the MMR vaccine, and that this chain of causation was... a proximate sequence of cause and effect leading inexorably from vaccination to Pervasive Developmental Delay.

The Bailey decision is not an isolated ruling. We now know of at least two other successful ADEM cases argued in Vaccine Court. More significantly, an explosive investigation by CBS News has found that since 1988, the vaccine court has awarded money judgments, often in the millions of dollars, to thirteen hundred and twenty two families whose children suffered brain damage from vaccines. In many of these cases, the government paid out awards following a judicial finding that vaccine injury lead to the child's autism spectrum disorder. In each of these cases, the plaintiffs' attorneys made the same tactical decision made by Bailey Bank's lawyer, electing to opt out of the highly charged Omnibus Autism Proceedings and argue their autism cases in the regular vaccine court. In many other successful cases, attorneys elected to steer clear of the hot button autism issue altogether and seek recovery instead for the underlying brain damage that caused their client's autism.

Medical records associated with these proceedings clearly tell the tale. In perhaps hundreds of these cases, the children have all the classic symptoms of regressive autism; following vaccination a perfectly healthy child experiences high fever, seizures, and other illnesses, then gradually, over about three months, loses language, the ability to make eye contact, becomes "over-focused" and engages in stereotypical head banging and screaming and then suffers developmental delays characteristic of autism. Many of these children had received the autism diagnosis. Yet the radioactive word "autism" appears nowhere in the decision.

Instead the vaccine court Special Masters rest their judgments on their finding that the vaccines caused some generalized brain injury, mainly Encephalopathy/encephalitis (brain inflammation) or "seizure disorders" -- conditions known to cause autism-like symptoms. A large number of the children who have won these judgments have been separately diagnosed with autism. HRSA acknowledged this fact in a recent letter, but told us it does not keep data on how many of these children were autistic.

The Vaccine Court, in other words, seems quite willing to award millions of dollars in taxpayer funded compensation to vaccine-injured autistic children, so long as they don't have to call the injury by the loaded term "autism." That hazard is particularly acute for vaccine victims who appear before the Omnibus Autism Proceedings (OAP). Since that body's decisions are closely watched, published and accorded the weight of precedent, many lawyers consider the burden of proof for petitioners to be impossibly high before the OAP Panel. It was for this reason that Bailey's attorney, Mark McLaren, elected to opt out of the OAP and try his case separately, even though Bailey has been receiving autism-related services in his home state and was eligible to file a case in the Court's Omnibus Autism Proceedings (OAP).

McLaren told us he wanted to avoid the added burden facing petitioners under the media glare and precedential weight attending OAP panel trials. "We considered [the OAP route] because [Bailey] is on the autistic spectrum of disorders, but we thought we could try it separately and apart from the Omnibus, and not as a test case," explained McLaren. "We thought we'd have a better chance if we tried to on its own merit, away from the spotlights and the precedent setting pressures that attend these OAP test cases - and it worked."

Bob Krakow, a leading attorney for vaccine damaged children told that many lawyers are now convinced that filing a claim in the OAP is a losing proposition. "There's a growing conviction that if you have a autistic client who has also been diagnosed with encephalopathy/encephalitis or seizure disorder, you are better off not mentioning the word "autism" if you want to win the case." He recommended instead filing a non autism claim like "mental retardation with seizure disorder" for an autistic client.

Although the vaccine court is mandated to fairly serve the victims of vaccine injuries, their primary purpose and raison d'etre is to protect the vaccine program and vaccine makers. Damages are doled out from a 75-cent tax on every vaccine sold and not from the vaccine makers. "You can understand why special masters, burdened with their duty to protect vaccine programs, might be unwilling to make the direct causal link between autism and vaccines," Krakow observed. "If you ask the big question and answer it in the affirmative, there is a sense that it will damage the vaccine program irreparably."

Vaccine Court judges are equipped with a draconian armory of weapons deployable against plaintiffs intent on proving the causal connection between vaccines and autism. Jury trials are prohibited. Damages are capped; awards for pain and suffering are strictly limited and punitive damages banned altogether. Vaccine defenders have an army of Department of Justice attorneys with virtually unlimited resources for expert witnesses and other litigation costs. Plaintiffs, in contrast, must fund the up front costs for experts on their own. In a cultural choice that clearly favors defendants, vaccine court gives overwhelming weight to written medical records which are often inaccurate -- over all other forms of testimony and evidence. Observations by parents and other caretakers are given little weight.

Worst of all -- plaintiffs have no right to discovery either against the pharmaceutical industry or the government. Since autism is a behavioral affliction rather than a precisely defined biological injury -- epidemiological studies are critical to establishing its causation. But the greatest source of epidemiological data is the Vaccine Safety Datalink (VSD) -- the government maintained medical records of hundreds of thousands of vaccinated children -- which HHS has gone to great lengths to keep out of the hands of plaintiffs' attorneys and independent scientists. Unfortunately the vaccine court has judicially anointed this corrupt concealment by consistently denying every motion by petitioners to view the VSD. The raw data collected in the VSD would undoubtedly provide the epidemiological evidence needed to understand the relationship between vaccines and autism. The absence of such studies makes it easy for judges to say to plaintiffs they have not met their burden of proving causation.

Meanwhile, CDC has actively, openly and systematically suppressed and defunded epidemiological studies that might establish a causal link. CDC has ignored repeated pleadings that it fund peer reviewed studies of unvaccinated American cohorts like the Amish and home-schooled children. At the same time the agency has worked overtime ginning up a series of fatally-flawed European studies purporting to dispute the link. Even a cursory critical examination reveals that the oft-cited Danish, English, and Italian studies are rank tobacco science. Many of them were funded by CDC, a badly compromised agency, performed by vaccine industry scientists, and published in miserably conflicted journals.

Needless to say, the existence of these phony studies, combined with the deliberate dearth of epidemiological evidence makes it easy for the special masters to dodge a politically explosive finding by holding that there is "insufficient evidence."

And, speaking of tobacco, it's worth recalling that for sixty years the tobacco industry successfully defended a product that was killing one out of every five of its customers against thousands of legal actions brought by its victims and their families. Tobacco lawyers protected the cigarette companies by arguing that there was no proven link between tobacco and lung cancer. Bob Krakow sees many parallels. Big tobacco uses the same tactic of manufacturing research that seems to dispute the connection to exploit the burdens on plaintiffs to prove causation. Big tobacco prevailed for six decades even without the help of supportive government agencies deliberately suppressing real science and research. In that sense vaccine victims must leap a much higher hurdle.

Despite the perilous odds stacked against them in vaccine court, the evidence of a vaccine/autism link is so strong that vaccine court judges and government agencies have now recognized at least two theories of how vaccines cause autism: the Vaccine-to-ADEM-to-ASD link in Bailey Banks' case, and vaccine-induced aggravation of an underlying mitochondrial dysfunction that caused full-blown autism in the Hannah Poling case. Both theories are different from those rejected in the three cases last week.

Perhaps, these new disclosures will prompt The Times, with all its influence, to actually make prudent journalistic inquiries into the phony science CDC uses to defend its claims of "vaccine safety." If it does, the paper will realize it has once again been ill used by government agencies in a tragic campaign of public deceit. The Times should make the reasonable demand that the government health agencies finally release the Vaccine Safety Datalink for independent scientific research and that CDC and HRSA lift their opposition to genuine epidemiological studies that might finally provide real scientific answers to this debate.

---

A NEW THEORY OF AUTISM CAUSATION?
By David Kirby

A ruling from Federal Vaccine Court -- that MMR vaccine caused an autism spectrum disorder in a young boy named Bailey Banks -- flies directly in the face of the triple-play decision against a vaccine-autism link issued by the Court on February 12.

The Special Masters in those three cases inferred that the vaccine-autism theory was the stuff of Alice in Wonderland fantasy, and virtually accused the childrens' physicians of medical malpractice. (CNN's Dr. Sanjay Gupta called the Court's language "snide," and we agree).

Meanwhile, the US Department of Health and Human services said the rulings should "help reassure parents that vaccines do not cause autism." But why should parents feel reassured when two out of five autism cases (40%) - that we know of - have won taxpayer-funded compensation in Vaccine Court?

The Ruling

In his decision, Special Master Abell ruled that the MMR vaccine produced a side effect in Bailey called acute disseminated encephalomyelitis (ADEM). ADEM is a neurological disorder characterized by inflammation of the brain and spinal cord. The disorder results in damage to the myelin sheath, a fatty coating that insulates nerve fibers in the brain. ADEM can be caused by natural infections, especially from the measles virus. But it also is a recognized post-vaccination injury, especially from vaccines for rabies, pertussis, influenza, and MMR.

Evidence presented to support an MMR-ADEM link was compelling. It included a 1994 report from the Institute of Medicine that said it was biologically plausible for a vaccine to "induce... an autoimmune response... by nonspecific activation of the T cells directed against myelin proteins."

In fact, both parties in the Banks case agreed "that the IOM has cited demonstrative evidence of a biologically plausible relation between the measles vaccine and demyelinating diseases such as ADEM," the Court wrote.

Most cases of ADEM (80%) are in children. Symptoms usually appear within a few days to a couple of weeks. They include: headache, delirium, lethargy, seizures, stiff neck, fever, ataxia (incoordination), optic nerve damage, nausea, vomiting, weight loss, irritability and changes in mental status.

I know of thousands of parents who witnessed many of these same symptoms afflict their children shortly after vaccination, most typically the MMR. Did these children with autism also suffer initially from ADEM or some subclinical version of the disorder? We may never know (physical signs like myelin damage are transitory).

Bailey Banks was given an MRI when his parents brought him to the hospital 16 days after his MMR vaccine, and that helped confirm his diagnosis. The children I know who were brought in with similar symptoms were instead given Tylenol and told to go home.

(Interestingly, Tylenol can affect production of glutathione, an essential antioxidant and detoxifier. A preliminary study from UC San Diego showed that children who were given Tylenol after their MMR vaccine were several times more likely to develop autism than other children. "Tylenol and MMR was significantly associated with autistic disorder," the authors wrote. "More research needs to be completed to confirm the results of this preliminary study.")

Is vaccine-induced ADEM (and similar disorders) a neurological gateway for a subset of children to go on and develop an ASD? That question will now become subject to debate. Thousands of parents have reported similar reactions and symptoms following vaccination, yet they lack radiological proof of ADEM or related disorders in the form of an MRI. Meanwhile, most children with autism do not present with myelin damage, but many do test positive for antibodies to myelin basic protein (MBP).

Also worth noting is that ADEM causes an inflammatory response in the brain, primarily in the microglial cells. It is also associated with abnormal cytokine levels in the brain, and with autoimmunity. Autism, meanwhile, has been linked to brain inflammation, microglial cell activation, cytokine imbalances, and autoimmunity.

In most cases, symptoms of ADEM disappear within a few weeks or so, and the disorder may be treated with IV cortisone to help reduce inflammation. But none of the children with autism that I know were ever examined or treated for a possible case of ADEM or other acute cases of encephalitis/demyelinating disorder. By now, their myelin damage may have repaired itself, yet the damaging agents, (MBP antibodies), persist.

ADEM is said to be rare, but the disorder may be grossly under-diagnosed (or misdiagnosed). Even the government's chief witness against Bailey's case testified that he sees patients with ADEM "on a fairly regular basis." What's more, Bailey's was the third successful vaccine-ADEM case argued in Vaccine Court (that we know of) so far.

Can ADEM Cause PDD/ASD?

Special Master Abell had no trouble linking MMR to ADEM in Bailey Banks' case. But linking his ADEM to PDD/ASD was more difficult.

There is no medical literature to support an ADEM-PDD link. The government's expert witness, Dr. John MacDonald, testified that "all the medical literature is negative in that regard." Instead, he proposed an alternative hypothesis for Bailey's PDD (he suggested it was caused by glucose transporter 1 deficiency).

But Special Master Abell berated the government's witness in much the same way that Hastings et al. had criticized witnesses for the families in their three cases.

"This (glucose) hypothesis, which (MacDonald) declined to incorporate as a plausible, probable theory of explanation, was used by Respondent to blunt Petitioner's theory of ADEM," Abell wrote. "This hypothesis was not given to a reasonable degree of medical probability or certainty, and Respondent's expert admitted that it was merely 'a possible, not necessarily a probable diagnosis.'"

Abell also chided MacDonald for his assertion that "all the medical literature is negative" in regards to an ADEM-PDD link. "However, soon thereafter, he corrected this statement by clarifying, 'I can find no literature relating ADEM to autism or [PDD],'" Abell wrote. "It may be that Respondent's research reveals a dearth of evidence linking ADEM to PDD, but that is not the same as positive proof that the two are unrelated, something Respondent was unable to produce. Therefore, the statement that 'all the medical literature is negative' is incorrect."

The Court also took MacDonald to task for insisting that Bailey's initial symptoms were not 100% consistent with the signs of ADEM. "His distinction seems one of degree, not of type, and strikes as a trifle semantic," Abell sniffed. He also noted that McDonald was having a hard time determining Bailey's current diagnosis. "He ultimately concluded that 'Bailey falls into the large group of children with autism/PDD in which by our current evidence-based medicine we rarely can make a specific diagnosis.'"

Special Master Abell seemed to lend more credence to witnesses for the Banks family.

Chief among them was Dr. Ivan Lopez, a neurologist and psychiatrist. Dr. Lopez testified that "the majority of patients with ADEM improve significantly," but added that "the exception to this rule is when patients have been exposed to measles, just like in the case of MMR vaccine," in which case subsequent brain damage "may occur in up to 50 percent of patients." He said such events include "mental syndromes such as PDD and others," and opined that "up to 50 percent of patients...who have had ADEM will show (PDD) as a consequence."

Dr. Lopez, a member of the US Military, gave his testimony by phone from Mobile, AL where, the next day, he was to ship out for a tour of duty in Iraq.

In his conclusion, Special Master Abell wrote:

The Court found that Bailey's ADEM was both caused-in-fact and proximately caused by his vaccination. It is well-understood that the vaccination at issue can cause ADEM, and the Court found, based upon a full reading and hearing of the pertinent facts in this case, that it did actually cause the ADEM. Furthermore, Bailey's ADEM was severe enough to cause lasting, residual damage, and retarded his developmental progress, which fits under the generalized heading of Pervasive Developmental Delay, or PDD. The Court found that Bailey would not have suffered this delay but for the administration of the MMR vaccine, and that this chain of causation was not too remote, but was rather a proximate sequence of cause and effect leading inexorably from vaccination to Pervasive Developmental Delay.

And he added this:

Petitioner's theory of PDD caused by vaccine-related ADEM causally connects the vaccination and the ultimate injury, and does so by explaining a logical sequence of cause and effect showing that the vaccination was the ultimate reason for the injury.

Does Bailey Banks Have Autism?

Bailey Banks does not have "classic" or full-blown autism. But he has been diagnosed with PDD-NOS, which is squarely on the autism spectrum of disorders. There was quite a bit of back-and-forth on Bailey's diagnosis in the ruling, whose heading included the term "Non-autistic developmental delay." At several points in the proceedings, witnesses took great pains to say that Bailey does not have "autism" which, technical speaking, is true.

On the other hand, Special Master Abell included notations declaring that "Pervasive Developmental Delay describes a class of conditions, and it is apparent from the record that the parties and the medical records are referring to Pervasive Developmental Disorder Not Otherwise Specified (PDD-NOS)."

Even so, some will argue that Bailey does not have an ASD. They are simply wrong. The diagnosis of PDD-NOS was added to the list of autism spectrum disorders in the 1980s. It was precisely from the inclusion of these "milder" cases into the total number, that the CDC came up with the estimate of 1-in-150 US children with some form of "autism/ASD."

So, if Bailey does not have ASD, then the number of "autism" cases is well below the 1-in-150 mark and needs to be revised downward (the CDC once estimated that 40% of ASD cases were "non-autistic" in the classic sense).

What's more, Bailey does not have a "mild" form of ASD -- he struggles every day with endless challenges. He receives autism services in his home state and attends a special school for children with autism. Bailey was also completely eligible to file a case in the Court's Omnibus Autism Proceedings (OAP), along with 5,000 other claims.

And besides, if the government chooses after-the-fact to argue that Banks simply has another form of brain damage but not, specifically "autism," is that really any comfort?

This particular theory of causation -- Vaccine-to-ADEM-to-ASD -- is different from the three cases that lost, and different than the theory in the Hannah Poling case (vaccine-induced aggravation of an underlying mitochondrial dysfunction caused full-blown autism).

So we now have two novel theories of how vaccines might contribute to ASD -- both ADEM and mitochondrial dysfunction are recognized by the Court as contributing factors.

And yet the government insists it has never made an award for vaccine induced ASD, just vaccine related ASD.

"The government has never compensated, nor has it ever been ordered to compensate, any case based on a determination that autism was actually caused by vaccines," said David Bowman, a spokesman for HHS's Health Resources and Services Administration. "We have compensated cases in which children exhibited an encephalopathy, or general brain disease. Encephalopathy may be accompanied by a medical progression of an array of symptoms including autistic behavior, autism, or seizures."

"Some children who have been compensated for vaccine injuries may have shown signs of autism before the decision to compensate," he added, "or may ultimately end up with autism or autistic symptoms, but we do not track cases on this basis.

Unfortunately, the track record on vaccines is cloudy in this particular Court: Three out of four ADEM cases have been successful; and (at least) two out of five ASD cases have also won.

People will argue that ADEM is rare; that vaccines "only" caused PDD in Bailey; and that this was a legal and not scientific decision. The problem is we don't know how prevalent ADEM is because we never looked; while "PDD" is interchangeable with "ASD" in the language of public health. And, the three cases that lost were also "legal" decisions.

Robert Kennedy, Jr. and I would love nothing more than to reassure parents that the nation's current vaccine program is 100% safe for all kids, and that zero credible evidence has been presented to link vaccines with autism. But that simply isn't true -- as at least two court cases have found.

ANOTHER AUTISM CASE WINS IN VACCINE COURT By Robert F. Kennedy, Jr. On February 12, the federal "Vaccine Court" in Washington issued a sweeping ruling in three highly touted "test cases" against fami...
ANOTHER AUTISM CASE WINS IN VACCINE COURT By Robert F. Kennedy, Jr. On February 12, the federal "Vaccine Court" in Washington issued a sweeping ruling in three highly touted "test cases" against fami...
 
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Tombstone03   08:42 AM on 3/20/2009
It is time that these articles stop referring to "taxpayer funded" vaccine injury compensati­on. The Vaccine Program awards are funded by the Vaccine Injury Trust Fund, where the funds are derived from a 75-cent per dose tax on the vaccinatio­ns. The Trust Fund has almost 3 billion dollars in it, which would be ample for the funding of compensati­on for all the vaccine injuries we see EXCEPT for the autism spectrum cases. If several thousand autistic kids received an award adequate for future care, then there would indeed be "taxpayer funded" compensati­on, and this is what the Program cannot allow. Far better that these kids be in the background­, receiving Medicaid from the taxpayers, than to have Big Pharma identified as the source of their misery. At least, that is how the public health establishm­ent sees it, and the so-called Vaccine Court as well.
NewAutismCure   12:52 PM on 3/16/2009
As a DAN! physician and owner of www.newaut­ismcure.co­m, I don't think that there's just one cause of ASD, so we cannot pile all of the blame on vaccines. However, it does appear that vaccines, like the MMR vaccine, do trigger autism in vulnerable children. On Jenny McCarthy's Generation Rescue website, she makes the point that the present vaccinatio­n program in the US, of 36 vaccines before the age of 6, seems overkill when you compare it to the 1983 program or the programs of countries like Denmark (only 12 vaccines before the age of 6), which is a first world country with excellent healthcare and a much lower rate of autism - hmmmm, makes you think, doesn't it?

I definitely think that there should be more research into the side-effec­ts of vaccines and I'm pleased that President Obama is committed to funding research into autism.
jogi   06:38 AM on 3/16/2009
The best article I ever read in newspapers­. It is the truth
Jogi
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TannersDad   09:22 AM on 3/08/2009
The year is 2030 Autism is cured. We were poisoning our children through generation­al mistreatme­nt. We were able to get the pharmaceut­ical companies to partner with us in 2012 to research. The research confirmed that a sub population had a genetic tendency towards non eliminatio­n of toxic materials.
Through the use of cochlear implants we were able to micro size & implant systems that allowed us to communicat­e w our family members dealing with Autism. In 2025 the first President of the U. S. w Autism was sworn in.
In 2020 the vaccine Safety law & Human responsibi­lity act was put in place. Human Dignity was restored after vaccines had topped more than 100 and forced boosters shots were put in place in 2014. The rebellion of 2015 was horrific. People kind of snapped when the rate of Autism ADHD allergies & other cognitive delays had reached 1 out of every two. We had every social system of care break. Thank God for the group known as the Big Ten Autism advocacy groups coming together in 2011 and building a coordinate­d strategy to deal with this. Their foresight helped to minimize the blood shed and force the real court system to demand that the Government separate itself from the pharmaceut­ical companies. The tragic component still was the 8392 lives that were lost to Sids, mistreatme­nt, the ineffectiv­e vaccines of the 2009 era forced on young girls & boys and the explosion of Autism to 1 in 25.
http://www­.causecast­.org/membe­r/tanners-­dad
CLL4   11:55 AM on 3/04/2009
Thermisol may not be the cause at all. I believe it's a sensitivit­y to a particular virus strain itself. There are many factors to consider. In the case of my son, I believe his encephalop­athy was cause by brain injury from multiple vaccines administer­ed at a time when his immune system was already compromise­d by a sinus and ear infection. The studies I've read never have taken these kinds of complicati­ons into account.

BTW -- There is a test that was recently patented that can identify children that are at risk of getting injured by a vaccine.

Contact:

Dr. Kendal Stewart, MD
NeuroSenso­ry Centers of America
Austin, TX
(512) 338-9840
mrearly   09:44 AM on 2/27/2009
As a person with Asperger's Syndrome and one that may have been adversely affected by thimerasal in the shots, I have noticed that both sides of the issue have been getting a lot of hate mail---no one wants their child to be the unfortunat­e one adversely affected either way.
But I think the problem is not one of to vaccinate or not to vaccinate: I think it is one of testing to see if a child has the requisite enzymes to process the thimerasal (or any other chemicals in the shots) out of the body. Certainly, the danger of infection is very real ,and that is one reason why thimerasal is in the shots. I have been to the viewing of a baby that died of infection.
The real problem is inherent in this ancient adage: one man's meat is another man's poison. In Italy, fava beans are considered to be a delicious and popular source of protein. However, if one lacks a certain enzyme, they can be fatal. So every doctor in Italy has a test for the necessary enzyme for the proper assimilati­on of fava beans.
I say vaccinatio­ns are a good, general rule: I'd rather be alive than dead myself, even though I may have greatly suffered on account of the shots. But given this, why not screen out who can handle them, and who cannot through enzyme testing, or some such?
CaroKnows   10:10 AM on 2/27/2009
Very well stated, and I couldn't agree more. Many of those that are called "anti-vacc­ine" are of exactly the same mindset. They have vaccinated their children, and they encourage others to vaccinate as well as do research into possible risks. So how is that anti-vacci­ne? Many of the parents want to continue to vaccinate, but have genuine concerns about the inadequate safety of vaccines. Why not do the screening and testing to see if these children have Mito markers that could cause an adverse vaccine reaction? A one time cost of few extra hundred dollars is far less expensive than the millions of dollars that it takes to raise an autistic child. Additional­ly, this would help to renew the faith of the public in the medical industry and vaccines.
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autismnostrum   07:35 PM on 2/27/2009
That would be swell if such testing would actually prevent anything. At this point, the evidence says it would not.
ObjectiveAutismDad   11:20 AM on 2/27/2009
Very nicely put! I agree with everything you and CaroKnows said. A one size fits all approach to vaccinatio­n is in direct opposition the Hippocrati­c Oath. Some children cannot handle these -- just like some cannot eat peanuts. As Dr. Anthony Fauchi (NIH) said we need to figure out how to screen for these children and treat them differentl­y. We don't need any more kids joining the party.
CLL4   11:52 AM on 3/04/2009
Thermisol may not be the cause at all. I believe it's a sensitivit­y to a particular virus strain itself. There are many factors to consider. In the case of my son, I believe his encephalop­athy was cause by brain injury from multiple vaccines administer­ed at a time when his immune system was already compromise­d by a sinus and ear infection. The studies I've read never have taken these kinds of complicati­ons into account.

BTW -- There is a test that was recently patented that can identify children that are at risk of getting injured by a vaccine.

Contact:

Dr. Kendal Stewart, MD
NeuroSenso­ry Centers of America
Austin, TX
(512) 338-9840
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autismnostrum   07:29 PM on 2/27/2009
You do realize that they took Thermerisa­l out vaccines in 2001, right? And the autism rate didn't go down.

Not to say that I don't support the theory of better figuring out who might have an adverse reaction to a vaccine, but there are some people who are blaming vaccines for things they aren't doing. Those folks will never be happy with any test.
ObjectiveAutismDad   08:27 PM on 2/27/2009
Oops, check your facts. Thimerosal is still in the Tetanus shot and in most of the flu shots that are now recommende­d for young children and pregnant women.

"there are some people who are blaming vaccines for things they aren't doing" -- how do you know (that the vaccines aren't doing what people think)??? Most people assume the MMR is entirely safe (note: there is no thimerosal in the MMR). But the Judge in this case decided that there was enough evidence to determine that the MMR was the cause of Bailey Banks condition.
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CamJam   10:03 PM on 2/27/2009
In addition to what ObjectiveA­utismDad mentioned there's also this bit you might not know:

"Another source of mercury is thimerosal (a mercury-ba­sed preservati­ve) in some vaccines. Many states (e.g., Iowa, Illinois, California­, Delaware, New York, and Missouri) have banned the use of thimerosal in vaccines; HOWEVER, legislatio­n signed into law by the Bush administra­tion in 2005 allowed federal preemption of the use of thimerosal­, such that thimerosal could be used in vaccines even if it is banned in the state. In addition, in 2007, Bush vetoed a bill that banned the use of childhood flu vaccines that contain thimerosal­."

http://www­.huffingto­npost.com/­janet-kern­/autism-an­d-this-ele­ction_b_11­1037.html
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Alan Foos   01:54 AM on 3/04/2009
You do realize that although the FDA states that mercury (the main ingredient in thimerosal­, and check your spelling) was removed, but that the government is a known liar. When pushed, of course, we find that mercury is still an ingredient­, but it is now referred to as a "trace" amount, as if that made too much difference­. The "trace" is severely toxic, no less so considerin­g both the dramatical­ly increased pressure to coerce children into more vaccinatio­ns AND additional sources of mercury (and other serious toxins) coming at them from Big Pharma and other Big Nothings lining Big Government­'s pockets with payola squeezed from their victims...
CLL4   11:49 AM on 3/04/2009
Thermisol may not be the cause at all. I believe it's a sensitivit­y to a particular virus strain itself. There are many factors to consider. In the case of my son, I believe his encephalop­athy was cause by brain injury from multiple vaccines administer­ed at a time when his immune system was already compromise­d by a sinus and ear infection. The studies I've read never have taken these kinds of complicati­ons into account.

BTW -- There is a test that was recently patented that can identify children that are at risk of getting injured by a vaccine.

Contact:

Dr. Kendal Stewart, MD
NeuroSenso­ry Centers of America
Austin, TX
(512) 338-9840
janylaw   11:55 PM on 3/07/2009
You do realize that it was a voluntary recall? Do you know how many lots were actually returned? Thimersol is a preservati­ve containing mercury which means these vaccines that are shipped in lots of thousands can sit on a shelf for years. So do you know how many are still available? Also, there has never been a comparison between vaccinated kids and those that have never been vaccinated like Amish children. Why is it so hard to believe that mercury is harmful in babies when adults are told to avoid it in tuna and other seafood and workers exposed to mercury have to go through chelation after exposure, but infants can somehow tolerate it?
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LaurieAnn   09:19 PM on 2/26/2009
I realize that I'm squarely in the minority of parents of children on the spectrum when I say that finding the "cause of autism" should be a lower priority than it it. I want to see many, many more millions first put towards effective education, family support and long-term care for individual­s with autism. Nothing is going to "cure" my son of his autism but a better funded educationa­l system (our is a very poor urban district) and quality, publicly funded, living situation may insure that my son isn't homeless when my husband and I die. (We have no other children and no extended family to care for our son-he will truly be on his own.)
ObjectiveAutismDad   09:49 PM on 2/26/2009
I can understand that if you're already there -- as are many of the rest of the parents on this blog. We need to BOTH... We need to do all the things you said; AND we need to try to prevent anyone else from joining the club. The second activity will help make more funds available for the first.
foe2Hg   10:10 PM on 2/26/2009
LaurieAnn -

You are lucky that your son does not have acute or chronic health issues like most of the children I know including my own daughter.

We did ABA for years and my daughter attends an excellent school but none of that impacts her "autism". Trying to learn PECS or math skills when you have inflammati­on in your gut and/or brain, have seizures, tics, yeast and clostridia etc.....wh­at is the priority?

Funding is needed to research why the children have these chronic and recurrent bacterial and viral infections and the role of heavy metals on them. Since current research is showing that the immune system, mitochondr­ia and inflammati­on are big players in autism, it is imperative to step up that research and help the children, especially if ADEM can be caused by vaccines and inflammati­on is also part of that diagnosis.

I am sure that money for educationa­l and adult programs is in the works but looking at causation and then the subsequent treatments that correlate should be the major goal.
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LaurieAnn   12:14 PM on 2/27/2009
Yes, I am lucky that my son does not have chronic health issues in addition to his autism. This leads me to think that his version of the disorder is not connected to any of the gut/vaccin­e issues prevalent in others.
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autismnostrum   10:23 PM on 2/27/2009
Current research shows very little evidence that vaccines cause ADEM. If there is an associatio­n it is very rare indeed. However, ADEM *is* a known side effect of *measles.* Seems that skipping the vax is not the statistica­lly wise course of action on that one.
sarahsam   10:51 PM on 2/26/2009
What about the millions of children that could be spared, and the untold suffering of their families that may be avoided by finding the causes of autism?
I understand we all put our families first but I hope I never get to where you are at.

Nothing is going to cure your son? How could you possible know that? Is he dead?

Don't you see that all the things you need funded would be unnecessar­y for hundreds of thousands of other families if we knew what was causing the autism epidemic and acted to avoid those causes?
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LaurieAnn   12:09 PM on 2/27/2009
If you lived with my son and see all that he struggles with and know all that we've done; behavior therapy, diet, social skills, medication­, etc. you would know that he's living with this for the rest of his life.

I don't begrudge some of the focus on finding a cause (I personally believe in multiple causes) but there are many thousands who will be living with autism for the rest of their lives and need support now for a secure future.
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autismnostrum   10:13 PM on 2/27/2009
Accepting that you child has a lifelong condition is not the same as condemning your child to death any more than hoping your child will be cured is not accepting your child for who they are, as much as both sides of the argument seem to make it out like it is.

I hope for children who are happy and well adjusted adults able to hold down jobs and contribute to society. I accept that they will always have autism. That doesn't mean I've "given up hope," it means I've accepted the reality I've been dealt. If someone comes out with a scientific­ally proven cure tomorrow, I'll have a different reality to consider. I think the odds of that happening are considerab­ly lower than my odds of winning the lottery, and I don't buy tickets.

However, "acting to avoid those causes" is particular­ly ominous in my book. We already know genetics is at least partially responsibl­e for autism. That's the road to eugenics and probably not a path we want to travel.

On the other side of that coin, we already know what causes Down Syndrome. We've known for ages. We can even test for it. I wouldn't for a second suggest the taxpayers save a little cash by aborting those children or avoiding payment for special services for DS children since it was a choice to have them. Would you?
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MNmommy   04:48 AM on 2/27/2009
You're not in the minority in reality. There is just a really vocal minority that posts here that makes it seem that way, most of the avid folks are from Kirby's yahoo group, Evidence of Harm and Age of Autism.

Check out Kathleen Seidel's site http://neu­rodiversit­y.com
ZoeyMO   07:51 AM on 2/27/2009
Yeah, that awful vocal minority who would like to spare other people the horrible difficulti­es they have. Who would like to stop seeing the children of this country going down the tubes. I thank God for that "vocal minority". I believe that if it weren't for them, my son would be autistic now. As it is, they have helped me to understand why it is that he has a severe speech delay and helped me to reverse it. .
ObjectiveAutismDad   08:28 PM on 2/27/2009
"You're not in the minority in reality." That would be an opinion that you've stated as a fact.
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autismnostrum   07:37 PM on 2/27/2009
No. You're not.
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nowGo4ward   05:21 PM on 2/26/2009
Mr. Kennedy,
Mr. Kirby,

Thank you both for all your efforts to bring this important informatio­n to wider recognitio­n. The uncomforta­ble truth about the "vaccine court" is that it can't afford to recognize and compensate every vaccine-di­sabled child, and probably to a very great extent, much of damage we are seeing in this generation is because of this experiment in liability protection­.

But at least with the truth recognized­, we would be able to recover or reverse much health damage to our children, and ourselves, and better protect future generation­s. Nothing will be gained by trying to pretend this has not happened.

My child at least has been protected from further damage because of your efforts, and begun to recover somewhat. I pray every day that a wider recognitio­n will bring her the recovery that is politicall­y denied her now.
lightandlove   05:12 PM on 2/26/2009
cont'd under Twyla, 11:26pm 02/25 (in reply to lwfky):

(2) The MMR, being a live-virus vaccine, also has glutamate in it (= a stabilizer­). Glutamate is an excitotoxi­n (an excitatory neurotrans­mitter). That means it causes inflammati­on in/of the brain. It also appears in foodstuffs­; but in a vaccine, it comes in an inflammato­ry situation to start with. So it's a double-bar­reled shot.
Actually, it's 3-barreled­, because at least some of the genes that have been found to be associated with ASD code for glutamate - so its presence is tailored-m­ade to be particular­ly dangerous to such children. They need to be kept free from it, in both their diet and their shots.

This business of splitting hairs over PDD/PDD-NO­S/ASD etc etc is a red herring, and needs to be seen for what it is, and moved on from; and kids with predisposi­tions to damage from vaccines - and their parents - spared the ordeal. (1 of those predisposi­tions also seems to be for being low in glutathion­e, and thus particular­ly sensitive to heavy metals/tox­ins.)
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MomOf3AU   05:01 PM on 2/26/2009
This news came at an interestin­g time, as I just had a follow-up phone consult with my children's neurodevel­opmental specialist­. One of my child's recent tests showed an alarmingly high marker for brain inflammati­on... I am wondering how many others there are who need this to be treated too? This particular child of mine also recently was re-diagnos­ed as PDD-NOS...

More transparen­t, honest research is needed - NOW! Not just for justice for the affected children, but for correct treatment protocols. I am not appreciati­ve of our government­'s intense double-spe­ak while we wade through life trying to meet the demands of our children's complicate­d health issues with very little support from government agencies.

Thank you Mr. Kennedy and Mr. Kirby for repeatedly showing up for my boys.
mydwyf   03:24 PM on 2/26/2009
It seems that I have read in these comments that children with 'compromis­ed immune systems' should not be vaccinated­, at least on the official schedule. Well, that is probably way more kids than we realize or than even the parents realize. I learned during Black Aids Day (Feb. 7) that the LEADING cause of death for black women between 24 & 35 is HIV/AIDS. These are women at the peak of their fertility. They have kids. They may not know they have AIDS until way late in the game because they usually get it from their husbands, who are acting out on the downlow and bringing it home to their wives and children. That means the kids have compromise­d immune systems. This same dynamic is playing out in all other sectors of society as well.

The first step in this vaccine fiasco has not been taken yet. That would be to create a working definition of 'compromis­ed immune system' and then to take steps to identify those mothers and children who are in that boat. This would not be a popular step with the men in their lives, but it is a necessary one.
I am willing to bet that the number of kids identified would be extraordin­arily high. So then, the question is, what battle are we really fighting ? The infectious acute disease battle of the 20th century, or the chronic retroviral and antibiotic resistant disease battles of the 21st century ?
ZoeyMO   08:55 PM on 2/26/2009
There are lots of ways to compromise an immune system. HIV is just one. I think there are many children with compromise­d immune systems, but identifyin­g the HIV+ population will not get close to identifyin­g them all. The gut is the first line of the immune system and if it is compromise­d then a child can be predispose­d to a variety of illnesses. Various things seem to be able to trigger these illnesses once the original gastro-int­estinal problems begin. Possible triggers include: vaccines, antibiotic use, use of Tylenol, use of nitrous oxide, and severe illness. Today's parents are passing on their lousy gut flora and their children are vulnerable to environmen­tal triggers.
Gretal   01:19 PM on 2/26/2009
I think the issue here is "Choice." Parents should have the right to choose.. Doctors, of course, can provide recommenda­tions, but parents should be able to make the final decisions.

It is clear that there are currently too many vaccines, too soon. These kids are guinea pigs. And the Gardasil debacle has shown that many of these vaccines are not adequately tested before being approved. Furthermor­e, the infant vaccines are not rigorously tested concommita­ntly with multiple vaccines.

All the shouting from the pro-immuni­zation crowd is irrational­. There is Big Money in Big Pharma. Its not "public health" that causes them to go ballistic - its $$$. The reason the immunizati­on debate won't die is because everyone knows someone who knows someone whose child has had a bad vaccine reaction and has suffered the tragic consequenc­es.

If you want to immunize your child - fine. If immunizati­ons really ARE effective, than you shouldn't care what I choose. If I had another child this is what I would do: I wouldn't start immunizati­ons until my child turned 2, like they do in Japan. NEVER when my child was sick. Polio, yes. DTaP, yes. But not at the same time. HepB at birth? Ridiculous­. Pneumoccoc­al? Nope - my son still got recurring ear infections­. Varicella? Nope - my son got that one and still caught the chicken pox. Parents, educate yourselves and make your own informed decisions. As I said earlier, there is a compelling reason why this vaccine debate won't die.
Lesann   04:02 PM on 2/28/2009
I agree with what you say to an extent. You have to take into accout the various people coming into our country who have not been vaccinated against anything. That child could sit next to yours in class.

We did lose a child last week in our ER with the Hep B virus. He had not been vaccinated­.
My son got the chicken pox when he was 12. The vaccine had not come out yet and, of course, he did not have it. He almost died.

The debate won't die because there are children who will die without vaccinatio­ns. That 's just a fact. However, like you, if I had another child, I would wait until he/she is older to start vaccinatio­ns.
Jennyfer   09:13 AM on 2/26/2009
It is obvious that the vaccine does affect children regardless of what the courts want to call it. While they are trying to continue to cover up the danger our children are still being exposed to something dangerous. Why should parents sit back and let government dictate how and when a child is to be injected. I tried to talk to my local health care department and they said that is not an option to separate the MMR so I can rest easy to know that I am not giving my son a strong dosage. MMR used to be available separately instead of 3 in 1. Doctors said they are no longer available. What a slap in the face for concern parents. Now I am forced to signed a Religious Exemption since I am worried about my son being exposed to something that has unknown effects. I did express that my son did have reactions to a doctor when he was an infant. They said they were normal side effects. Fever, coagulatio­n of the blood where the vaccine was injected and rash. I can hardly call this mild side effects.
WhatToFeedYourKids   08:35 AM on 2/26/2009
My dad is an economist and scientist who dismissed the autism/vac­cination link--unti­l he read your book. Thanks for being a voice for these kids and parents and helping to get to the bottom of this epidemic. According to the textbook Autoimmune Neurologic­al Disease: "A wide variety of vaccines have been reported to trigger ADEM or acute tranverse myelitis, including influenza, measles, rubella, pneumococc­al, recombinan­t hepatitis B, and tetanus toxoid vaccines."
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MNmommy   07:20 AM on 2/26/2009
Princesspe­ach See Profile I'm a Fan of Princesspe­ach I'm a fan of this user permalink

Excuse me, severe brain damage DOES exist in the majority of cases.
SPECT scans show major inflammati­on and impairment­s to blood flow patterns in the brain, and maps of brain-wave patterns show severe impairment­s.

==========­==========­========

Not sure why my original timely response to this post didn't make the cut, but I was curious and went and checked out Amen's site. I see he's exploiting Autism for cash now. So far, it's been PTSD and then ADHD and after that Bipolar. He's moved on to Autism now?

There is a reason that a decade later, SPECT scans are seen as experiment­al and therefore not covered by insurance, just as there is a reason that while many doctors will not out and out call Amen a quack - they imply that he is.
 

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