Showing posts with label Defeat Autism Now. Show all posts
Showing posts with label Defeat Autism Now. Show all posts

Tuesday, October 7, 2008

Bernard Rimland, Ph.D., Winner of the Noble Prize

With yesterday's announcement of this year's winners of the Nobel Prize in Medicine, I think it is appropriate to honor the man who, sadly, will never see the full effects of his lifetime commitment to individuals and families impacted by autism. This man worked tirelessly and passionately in his quest for the true causes and effective treatments of autism to be accepted and widely applied so that more children could live free from constant pain and become independent, contributing members of society.

Today's post is dedicated to Bernard Rimland, Ph.D (1928 – 2006). The bulk of this post is a reprint of Dr. Rimland's testimony in 2000, before the House Committee on Government Reform. Given the current state of our economy and the recent 700 billion dollar buyout, I believe the timing of this post is especially relevant.

Here's to you, Bernie. Thank-you. You did not live long enough to receive the Nobel Prize, but if they gave one for being a Noble Man, you would have no competition whatsoever.


Testimony of Bernard Rimland, Ph.D. Before House Committee on Government Reform

April 6, 2000

The Autism Increase: Research Needed on the Vaccine Connection

My name is Bernard Rimland. I am a research psychologist (Ph.D.). and am Director Of the Autism Research Institute, which I founded in 1967. I am also the founder of the Autism Society of America (1965), and the editor of the Autism Research Review International. My book, Infantile Autism: The Syndrome and Its Implication for a Neural Theory of Behavior (1964) is widely credited with changing the field of psychiatry from its claim that autism is an emotional illness, caused by destructive mothers, to its current recognition that autism is a biological disorder. I have lectured on autism and related problems throughout the world, and am author of numerous publications. I served as primary technical advisor on autism for the film Rain Man.

My son Mark was born in 1956. It was obvious from birth that this perfectly normal-looking infant had something drastically wrong with him. I had earned my Ph.D in experimental psychology 3 years earlier and had never encountered the word autism. Our pediatrician, with 35 years of experience, had never heard of autism either. Autism was extremely rare then - it is extremely common now.

Some supposed experts will tell you that the increase reflects only greater awareness. That is nonsense. Any pediatrician, teacher or school official with 20 or more years experience will confirm what the studies tell us: there is a real increase in autism and the numbers are huge and growing. The epidemic is serious and world-wide.

Soon after my textbook on autism was published in 1964, I began to hear from other parents. Many parents told me that their children were normal until getting a triple vaccine - the DPT shot. In 1965 I began systematically collecting data on the symptoms and possible causes of autism: In 1967—33 years ago—I began querying the parents, specifically about the child's response to the DPT shot. Many had reported marked deterioration.

During the past few years the Autism Research Institute has been flooded with an upsurge in pleas for help from parents throughout the world - from wherever the World Health Organization vaccine guidelines are followed. The majority of these parents say their children were normal until getting the MMR - another triple vaccine.

Let me dispel several myths promoted by those who deny the autism-vaccine connection:

  1. They claim the vaccines are safe, but physicians are indoctrinated to disbelieve claims of harm and are not trained to recognize nor required to report any adverse reactions. From 90% to 99% of the adverse reactions reported to doctors are never reported by those doctors to the government's extremely lax Vaccine Adverse Event Reporting System, known as the VAERS.

  2. They say that the suspected linkage between the MMR vaccination and autism has been disproved by a study conducted by Brent Taylor and his colleagues in London, and published last year in The Lancet. The Taylor study is seriously flawed in many ways, as had been noted in a number of letters to the editor of The Lancet and in a number of additional letters on the subject which have been posted on the internet. It was subject to strong attack at a recent meeting of the British Statistical Society. I have been a full-time researcher my entire professional life, for almost 50 years, and I respectfully asked Dr. Taylor for a copy of the data so that I could reanalyze them. He refused this ordinary professional courtesy, and I have subsequently written to the editor of The Lancet requesting that an impartial committee be asked to reexamine Dr. Taylor's statistical methods. If he refuses again, I urged The Lancet to retract his paper.

  3. They say that autism has a large genetic component, and therefore vaccines must play a minimal, if any, role in the causation of autism. My book Infantile Autism, published in 1964, was the first systematic attempt to marshal the evidence for genetics as a contributing cause of autism, so I am certainly not hostile to that idea. However, genes do not begin to account for the huge increase in the incidence of autism, ranging from 250% to 500% in various places. I might add that we have just reviewed all of the recent genetic studies for the next issue of the Autism Research Review International, which I edit. The results are spectacularly inconsistent. The best guess is that there are at least 20 different genes involved in the causation of autism. Gene therapy is decades off, and may be infeasible.

  4. They claim that autism naturally occurs at about 18 months, when the MMR is routinely given, so the association is merely coincidental and not causal. But the onset of autism at 18 months is a recent development. Autism starting at 18 months rose very sharply in the mid-1980s, when the MMR vaccine came into wide use. A coincidence? Hardly! See the graph below.

Autism is not the only severe chronic illness which has reached epidemic proportions as the number of (profitable) vaccines has rapidly increased. Children now receive 33 vaccines before they enter school - a huge increase. The vaccines contain not only live viruses but also very significant amounts of highly toxic substances such as mercury, aluminum and formaldehyde. Could this be the reason for the upsurge in autism, ADHD, asthma, arthritis, Crohn's disease, lupus and other chronic disorders?

As a parent and as a full-time professional researcher, I am bitterly disappointed with the medical establishment's dismal record with regard to autism over the past 60 years. The medical schools, as well as the governmental agencies, have consistently supported outmoded, unproven and even disproven theories from the very beginning, and have actively opposed the most promising approaches for the treatment of autism. They supported the psychoanalytically-based theories which held the mother responsible for causing autism through her supposedly hostile attitude toward the child. They opposed the use of behavior modification, the most uniformly beneficial treatment for autism, by claiming that it neglected the deep-seated emotional blocks that were supposedly at the root of autism. They have ignored, and continue to ignore, the long series of studies conducted both in the U. S. and Europe showing that the elimination of foods containing gluten and casein from the diet brings about marked improvement in many autistic children. They have consistently ignored the series of 18 consecutive studies, conducted by researchers in 6 countries, which showed that almost half of all autistic children and adults respond favorably to high doses of vitamin B6 and magnesium., with no adverse effects. Eleven of these studies were double-blind placebo-crossover experiments. There is no drug that comes close to B6/magnesium in terms of safety, efficacy and positive research findings.

Tens of millions of dollars have been spent on non-productive lines of research, while virtually no money at all has been given to research on the methods of alternative medicine, which are far more promising in terms of both safety and efficacy.

The most interesting questions are not being asked: Why does the majority of the population survive such epidemics as autism, the bubonic plague, Legionnaires' disease, polio and AIDS, while relatively few succumb?

The answer is that the survivors have a healthy, effective immune system. Would enhancing the immune system decrease the likelihood of adverse reactions to vaccines (including the anthrax vaccine - DOD please note!)? Very probably. It is well known that the immune system must be adequately supplied with many nutrients if it is to function properly, including especially vitamins A, C, E, B6 and a number of minerals, including zinc, magnesium, and selenium. Nutritional levels of these substances are not only harmless, they are essential to good health. Since people do not change their diets readily, I believe that foods should be fortified with these nutrients - especially foods that will be consumed by infants and children. Research along these lines - as well as on the safety of the vaccines - is desperately needed.

As a parent and a researcher, I believe there should be a marked redirection of effort and funding, along the lines suggested above.

Committee on Government Reform

2157 Rayburn House Office Building

Washington, DC 20515

(202) 225-5074


Reprinted from:http://www.house.gov/reform/hearings/healthcare/00.06.04/rimland.htm

Monday, September 22, 2008

SUCCESS RATES FOR BIOMEDICAL TREATMENT OF AUTISM

The success rate experienced by families who undertake a biomedical approach for autism is often excellent, for those who stick with it. A major problem is that by the time people hear about Biomedical interventions for Autism, they have been convinced by their pediatrician or family doctor that there is nothing that can be done for autism, and since we live in a society that tends to value a physician's word as being on par with "the word of God" this can be a big hurdle to overcome.

A related problem is that most traditionally-trained physicians are not taught about nutrition or methods of disease prevention. They are taught to suppress symptoms with pharmaceutical drugs and to remove body parts when they decay or stop working - often because the symptoms of underlying disease are masked with pharmaceutical drugs while things continue to get worse.

Physicians and clinicians who employ biomedical treatments for autism (and ADHD, ADD, Bipolar Disorder, Chronic Fatigue, Fibromyalgia, etc.) subscribe to the belief that the most important thing is "FIRST, DO NO HARM." As is the case when considering any kind of intervention, we must ask ourselves if any risks associated are greater than any potential benefit that may come from taking the particular course of action. This is referred to as a “cost/benefit analysis.” In any cost/benefit analysis, you want to make decisions where the potential benefit outweighs the potential cost. I believe this is especially true when considering a treatment approach for a sick child.

The Autism Research Institute has been collecting data from parents for several years, regarding the success rates of various interventions, both biomedical and pharmaceutical. To view the complete list of parent ratings for biomedical and pharmaceutical interventions, click the following link: http://www.autism.com/treatable/form34qr.htm

Data from more than 26 thousand of parents indicates that biomedical interventions, such as dietary changes, antifungals, targeted supplementation with specific vitamins, minerals, amino acids, enzymes, and probiotics, and chelation therapy to remove heavy metals, organophosphates, and pesticides, are many times more successful than treatment with psychotropic medications AND they are far less likely to cause negative reactions in the children.

For example, Adderall, Ritalin, and Risperdal are three of the most frequently prescribed medications given to children with autism to help control behavior (suppress symptoms). Parent ratings regarding the success rates for these medications are as follows:

Adderall: of 775 cases, 43% got worse; 32% got better; 25% no effect.
Adderall: Better:Worse Ratio = 0.8:1

Ritalin: of 4127 cases, 45% got worse; 29% got better; 26% no effect.
Ritalin: Better:Worse Ratio = 0.7:1

Risperdal: of 1038 cases, 20% got worse; 54% got better; 26% no effect.
Risperdal: Better:Worse Ratio = 2.8:1

Note: "got worse" in these parental reports relates solely to the worsening of problematic behaviors. To read further information regarding potential side effects of these and other psychotropic medications click the following link:
http://www.autism.com/ari/adverse_reactions.html

Constipation and diarrhea are rampant in a vast majority of kids with autism, as are problems with eczema, skin rashes, and environmental and dietary allergies. Because 70% of the body’s immune system is located in the gastrointestinal tract, problems related to GI injury and inflammation are often the source of a domino-like cascade of issues as the child becomes immune-compromised and increasingly susceptible to bacterial, viral, and parasitic infections.

Dietary changes often help to correct issues in the gut and are therefore frequently targeted initially in biomedical treatments for autism. Parent ratings regarding the success of dietary interventions are as follows:

Remove Milk/Dairy: of 6360 cases, 2% got worse; 52% got better; 46% no effect.
Remove Milk/Dairy: Better:Worse Ratio: 32:1

Remove Wheat: of 3774 cases, 2% got worse; 51% got better; 47% no effect
Remove Wheat: Better:Worse Ratio: 28:1

Gluten Free/Casein Free Diet: of 2561 cases, 3% got worse; 66% got better; 31% no effect
GF/CF Diet: Better:Worse Ratio: 19:1

Candida Diet (Yeast-Free): of 941 cases, 3% got worse; 56% got better; 41% no effect
GF/CF Diet: Better:Worse Ratio: 19:1

Food Allergy Treatment: of 952 cases, 3% got worse; 64% got better; 33% no effect
Food Allergy Treatment: Better:Worse Ratio: 24:1

Yeast overgrowth (Candida Albicans) is a very common finding in children with autism, and is one of the effects of their weakened immune systems and resultant administration of antibiotics to fight recurrent bacterial infections. Physicians who adhere to the Defeat Autism Now! approach very often order laboratory testing to determine if yeast is problematic, and if so, will treat accordingly with antifungal prescriptions. Parental reports of success with antifungal treatment are as follows:

Antifungals: Diflucan: of 653 cases, 5% got worse; 57% got better; 38% no effect
Antifungals: Diflucan: Better:Worse Ratio: 11:1

Antifungals: Nystatin: of 1388 cases, 5% got worse; 50% got better; 44% no effect
Antifungals: Nystatin: Better:Worse Ratio: 9.7:1

Specific nutritional therapies and supplementation targeted for the individual child is a cornerstone of biomedical treatment of autism. One must be careful in giving vitamins and it is not advised to do so unless you know what you're doing. Having said that, one of the most frequently recommended supplements for autism is Cod Liver Oil or Fish Oil (must be treated to remove mercury - don't buy cheap fish oil!!!!). Other Fatty Acids are also supplemented, based on lab results and detailed developmental history and family history. Parent ratings for the success of these interventions are as follows:

Cod Liver Oil: of 1681 cases, 4% got worse; 51% got better; 45% no effect.
Cod Liver Oil: Better: Worse Ratio = 13:1

Fatty Acids: of 1169 cases, 2% got worse; 56% got better; 41% no effect.
Fatty Acids: Better: Worse Ratio = 24:1

Heavy Metal toxicity is a very common finding in children with autism, as is shown on hair analysis, through urine provocation testing, and now with porphyrin tests. Chelation (removal) of heavy metals and other toxins is often a very effective component of biomedical treatment for autism and is used when indicated, based on laboratory findings. Parent ratings for success rates of chelation treatments are as follows:

Chelation: of 803 cases, 3% got worse; 74% got better; 23% no effect.
Chelation: Better:Worse Ratio = 24:1

There are many other intervention strategies that are helping to recover children from an autism diagnosis and Defeat Autism Now! clinicians and researchers all over the globe are working tirelessly in their efforts.

If you ask a parent whose child disappeared for years, who made no eye contact, spoke no words, and spent hours each day watching his or her fingers and spinning in circles, that parent's response to the question, "How successful is biomedical treatment?" will depend on his or her own experience. If you ask one of the parents I met at a Defeat Autism Now! conference, who's children actually got on the stage, made eye contact with the interviewers, and answered questions in front of hundreds of other parents and professionals, the answer, I'm sure, would be "Extremely successful!"

Biomedical interventions do not work for everyone, and the results are varied, depending on the particular child. This is also why the GF/CF diet or SCD diet or LOD diet, or whatever, is not THE answer for everyone. Individual children need to be treated as individuals. Treatments need to be tailored, based on the child’s own developmental and medical history, observations of parents, and results of laboratory tests that assess specific areas for intervention.

Every child is different and EVERY CHILD WITH AUTISM IS DIFFERENT. That's why the standard medical response, "There's nothing you can do for autism" makes no sense.

Autism is treatable. Recovery is possible. One child at a time.

To view videos of some of the many children who have been successfully recovered from an autism diagnosis by implementing some of the above biomedical interventions, please click on the links below. Head’s up: You might want to grab a box of tissues for these.

This information is 4allofyou!

Blessings,
Marci

Baxter's Recovery from Autism:
http://www.youtube.com/watch?v=UsmBoGPzx9U&feature=related

Ethan's Recovery from Autism:
http://www.youtube.com/watch?v=aEw0Y5LJ6vg

Edward's Autism Journey and Recovery:
http://www.youtube.com/watch?v=jtHvtWBv7aM

Friday, September 19, 2008

NIMH Cancels Chelation Study While Dr. Proffit Heads for the Bank

Guess what? A couple of days ago the media announced, "A government agency has dropped plans for a study of a controversial treatment for autism that critics had called an unethical experiment on children. The National Institute of Mental Health said in a statement Wednesday that the study of the treatment - called chelation - has been abandoned."

I'm shocked. (that's sarcasm)

Okay. After about ten minutes of research, here's what I found:

First, the NIH study was called off because an experimental psychologist at Cornell University found that rats who were administered a chelating agent (succimer) specifically meant to chelate lead, suffered from learning disabilities that are long-lasting if they were administered the drug when they did not have lead poisoning to begin with. Towards the end of the article, it notes that the most likely reason for this is because succimer depletes zinc and iron and the resulting deficiencies of these minerals are what probably caused the cognitive problems. DUH!!!

Two problems with NIH calling off the chelation study as a result of the above:

1. ANY doctor trained by the Autism Research Institute (Defeat Autism Now!) KNOWS that one of the FIRST things to do is assess the child's nutritional status, including testing for zinc and iron levels. AND, they know that chelation with ANY agent is NOT an option unless the child has DOCUMENTED heavy metals in the body. This is WHY we do hair analysis AND urine provocation AND fecal metal tests. Any physician who uses chelation to treat heavy metals in the absence of proof that there ARE heavy metals should NOT be using chelation. This is akin to prescribing chemotherapy for cancer to someone who LOOKS like they may have cancer, without ever doing the tests to determine if the cancer really exists. Chemotherapy drugs are some of the MOST toxic drugs on the planet, but nobody is suggesting that we not use them! (At least nobody in "mainstream" medicine)

2. A more appropriate design for the NIH study, instead of administering chelating agents to children who do not have heavy metals, would be to document that ALL children in the study have heavy metals in their systems and then administer ALL of the same interventions, including addressing mineral and nutritional deficiencies in ALL participants. The experimental condition should be those children who receive chelation, while the control group should be a group of children who are matched on all other interventions but do not receive chelation. In this way, there would be no problems associated with the fact that the control group did not have heavy metals AND there would be no problems associated with mineral depletion because, just as it is in the clinical setting in hundreds of Defeat Autism Now! trained physicians, THE MINERAL LEVELS WOULD BE CONSISTENTLY MONITORED TO ENSURE THEY ARE NOT BEING DEPLETED BY THE DRUGS! AGAIN, DUH!!!!!!

Why can't NIH figure this out?

I suspect this is because the powers-that-be do not understand clinical nutrition. This is most likely because traditionally trained physicians practicing traditional western medicine are trained in medical schools that are funded by pharmaceutical companies, and most M.D.s have never taken a SINGLE course in nutrition. It is NOT REQUIRED. No WONDER we have so many drugs that have been pulled from the market after significant numbers of patients have DIED because of side effects of the drugs, which WERE approved by the FDA.

Care for some Vioxx, anyone?

It seems to me that the reason the powers-that-be do not want chelation to become more readily available is because if they did, more children with heavy metal poisoning would have access to this very effective (and very safe) treatment. That would mean that there would be hundreds of thousands of children whose levels of mercury (and lead and antimony) would be DOCUMENTED, and doctors like Paul Offit, who happens to sit on the IOM (Institute of Medicine), which has declared that an association between thimerosal (mercury) and autism does not exist, can continue to rake in the dough at the expense of our children. For those who don't know, Dr. Paul Offit is not only the most vocal opponent of the mercury/autism connection, he is also one of the recipients of 182 MILLION DOLLARS, for royalties to the Rotavirus Vaccine, of which Dr Offit is a patent-holder. HMMMMNNNNN.........

Has anyone ever heard the saying, "The Fox is Guarding the Henhouse?"

WATCH THIS:

http://www.youtube.com/watch?v=K1Hw-Q23S_s

Once again, I advise parents to DO YOUR OWN RESEARCH and do not rely on the misinformation being put out by those like Dr. Offit, who have SO MUCH to gain if our children remain poisoned by heavy metals.

To read more about chelation and the truth about the scare tactics, please visit the Autism Research Institute's website and read the following two articles:

http://www.autism.com/treatable/chelation/chelationsafety.htm

http://www.autism.com/ari/editorials/ed_chelationstory.htm

Marcella Piper-Terry

Saturday, August 16, 2008

Is There Thimerosal In the Flu Vaccine?

Yesterday I spoke at a local private school, where I talked about Executive Dysfunction and the change in what is considered "normal" as our society moves along the continuum in response to changes in our environment.

After my presentation, there were a few educators present who had some questions regarding my work as a Defeat Autism Now! provider. One of those questions was regarding the flu vaccine and if there is thimerosal in it. The woman who asked the question reported to me that her daughter had asked her pediatrician about the safety of the flu vaccine because she was considering whether or not to give it to her child. The woman before me (the grandmother of said child) indicated that the pediatrician in question responded to the concerned mother, "Of course the flu vaccine is safe! There hasn't been thimerosal in vaccines for six years!"

This is an outright lie.

Thimerosal was taken out of the CHILDHOOD vaccine schedule in 2004. The huge numbers of vaccines that were already stockpiled in pediatricians' and family practice docs' offices were NOT discarded - this means that unless a parent SPECIFICALLY REQUESTED their child be given INDIVIDUAL DOSE vaccines without preservatives, YOU DON'T KNOW if the vaccines given during and after 2004 were thimerosal-free or not. (You can research the vaccines yourself if you obtain a copy of your child's shot records and look up the particular vaccinations your child received.)

Of HUGE concern at this time is that the CDC and Pharmaceutical companies who develop the vaccines are pushing for ALL children, including infants and those yet unborn, be vaccinated against the flu. (Recommendations include vaccinating pregnant women during the second trimester of gestation.) A news story yesterday announced that flu vaccines have been produced and are being distributed in record numbers this year in the attempt to vaccinate every man, woman, child, and infant in the U.S.
THE FLU VACCINE DOES CONTAIN THIMEROSAL.

For those nay-sayers who believe this is misinformation reported by some radical wacko with an agenda or crazy conspiracy theory, here is the link to the CDC article declaring that yes, the flu vaccine contains mercury. Please read this very carefully and with the same skepticism I would hope you apply to everything you read online (including this blog):
http://www.cdc.gov/FLU/ABOUT/QA/thimerosal.htm

Note that the CDC uses terminology indicating that even in the vaccines that are labeled "preservative-free" THIMEROSAL IS USED IN THE MANUFACTURING PROCESS. The CDC states that the amount is so small and by the time the process is finished, it is untraceable. This is different from stating that IT IS NOT THERE. This is the same type of semantic trickery that has been played for years. Nothing has changed.

Please take the responsibility upon yourself as a parent to do your own research and find out the truth before you allow anyone to inject ANYTHING into your child. I don't know if the pediatrician mentioned above actually knows he is lying to the concerned parents of his young patients. If he does not realize this, it is his responsibility as a professional to research more closely the products he is declaring as safe. I encourage all parents reading this to ask your pediatrician about thimerosal in flu vaccines before having your child (or yourself) vaccinated. If your physician tells you there is no thimerosal in the vaccine, I suggest you find another physician. If he or she doesn't know about thimerosal, with all the media coverage on this issue, what is the likelihood that he or she researches any of the other drugs before writing out prescriptions?

Who is educating our doctors?
The pharmaceutical reps who peddle the prescriptions. The effectiveness of the sales pitch may be the determining factor as to which drugs a doctor prescribes. That's not about healing. That's about money.

As a Defeat Autism Now! provider, I am not taking the position (at this time) that you should not vaccinate your child at all. I am, however, suggesting that you become more proactive in the well-being of the children you have been blessed with and do not blindly follow advice just because the person dispensing it has the letters M.D. behind his or her name.

Posted below is a suggested schedule, for those who make the decision to vaccinate their children. This schedule includes the vaccinations that are protective against CHILDHOOD illnesses and is less likely to overwhelm their immune systems by greatly decreasing the number of antigens introduced into the body simultaneously. This allows the body to respond more appropriately to the invading antigen, and should decrease the likelihood of immune system confusion (which is related to auto-immune response).

Birth
Hepatitis B if mom is Hep. B Positive, otherwise wait
4 months
Hib, IPV
5 months
DTaP
6 months
Hib, IPV
7 months
DTaP
8 months
Hib
9 months
DTaP
15 months
Measles
17 months
Hib, IPV
18 months
DTaP
21 months
Rubella
24 months
Prevnar 1 dose
30 months
Mumps
4-5 years
Varicella (if not immune already)
4-5 years
Hepatitis B series
4-5 years
DTaP, IPV boosters
4-5 years
test titers for MMR and do not give unless not immune.

Please note that the above recommendations include not vaccinating a newborn against Hepatitis B unless the mother is positive. Hepatitis B is a sexually-transmitted disease. It is NOT typically a disease of childhood and should therefore NOT be given to all children as part of the CHILDHOOD vaccine schedule. Please also note that it is recommended that you NOT give a second round of vaccines for Measles, Mumps, and Rubella unless the child is not already immune. The reason the "Booster" vaccine was recommended in the first place is because 10% of children failed to establish immunity after the first vaccine. (I would argue this is a failure in the vaccine, rather than in the children themselves.) Rather than recommend testing for immunity to determine WHICH 10% of children actually NEEDED another dose of Measles, Mumps, and Rubella into their systems, the CDC recommended re-vaccinating ALL children, to be sure we catch the 10% still at risk. Ask yourself who benefits from that decision: Answer: The pharmaceutical industry and the companies who develop the vaccine.

Okay. Rant over for today.
Educate yourselves. We are humans - not sheep.

Marci

Tuesday, July 29, 2008

AUTISM IS TREATABLE

AUTISM IS TREATABLE


THE DIFFERENCE BETWEEN “STANDARD MEDICAL PRACTICE” AND

THE BIOMEDICAL APPROACH


I think the major difference between the more traditional medical point of view and those of us who employ biomedical treatments for children with autism is hope, coupled with our acceptance of the belief that we do not know if a child can be helped until we learn more about that particular child.


There are clues in every developmental and family history that guide the most important decision for your child, and that is, “Where do we start?” Once we know where to start, the process is one of growth and learning. We learn what the next step is, based on your child’s response to diagnostic trials and results of laboratory tests. In the case of regressive autism, because the diagnosis does not usually happen overnight, it is unrealistic to expect that the child you recognized previously will magically reappear as a result of a single intervention. It often takes considerable time and numerous steps to reverse the process that has resulted in the child who is presented to us at the initial appointment.

“Follow those who seek the truth but flee from those who have found it.” This quote from Vaclav Havel was shared with the room full of clinicians at the DAN! Physician’s Intensive Training I attended in April of 2007. I think this quote resonated with me personally for many reasons, not the least of which is my own stubborn resistance to accepting the status quo just because someone tells me to. (If my mother were still living she would readily attest to this aspect of my personality, which has been part of my makeup since early childhood.)


With regard to the diagnosis of autism, what this statement means to me is that if an “expert” tells you there is nothing that can be done for your child, before anything is even tried, you need to question where the “expert” came up with this information. In my opinion and experience, just because something has always been accepted as true does not necessarily mean it is true. Certain previously accepted “truths” come to mind, including those who “knew” the world was flat.


Within the world of medicine, for most of the 20th century it was “known” that ulcers were caused by stress and a hectic executive lifestyle. The medical mantra was, “No acid, No Ulcer.” In 1982, Australian gastroenterologist Barry Marshall, M.D., and pathologist Robin Warren, M.D., refuted the accepted “truth” when they showed that gastritis and ulcers were the result of a bacterial infection (Helicobacter pylori). The idea that a bacterial infection could be responsible for ulcers was heretical!


“Truth” changes very slowly; in the case of ulcers, it took 13 years before antibiotic treatment was accepted by the medical community as standard treatment for H. Pylori induced ulcers, something that was finally accomplished in 1995. (Drs. Marshall and Warren were awarded the Nobel Prize in 2005 for their discovery). I wonder how many people suffered needlessly from the pain caused by bacterial infection and inflammation during those 13 years while waiting for mainstream medicine to catch up to the science.


The “truth” about autism, according to mainstream medicine has been “There is no treatment.” I cannot tell you how many times I have seen the pain on the faces of parents as they relate their memories of how they received their child’s diagnosis. I have witnessed the tears falling down parents’ faces as they recall being told in the same breath, “Your child has autism. There is no treatment. I suggest you start thinking about institutionalizing him.” This “truth” is most often spoken by “experts” who have evaluated the child using standardized psychometric tests and questionnaires that were developed to measure intelligence, educational achievement, behavior, social skills, and developmental motor and speech milestones. All of these observations and impressions are important and they tell us a lot about how the child is functioning (or not) in his or her current environment and in response to particular situations. They do NOT, however, tell us ANYTHING about WHY the child is behaving in a particular way, or WHY the child is not growing properly, or WHY the child is not learning on par with his or her same-aged peers.

Dr. Sidney McDonald Baker has developed what he calls “The First Tacks Law,” which states, “If you are sitting on a tack it takes a lot of Risperdal to make it feel good. The appropriate treatment for tack sitting is tack removal.” Translation: If a child is in pain (due to bacterial infection, gastro-intestinal inflammation, or other systemic physical problems caused by exposure to toxins or from food allergies), the child may show a response to medication prescribed to decrease the behaviors, but that medication is not going to address the underlying issues, which will continue to get worse and require more and more medication to suppress the resulting symptomatic behaviors. Going back to the history of ulcers, stress, and H. Pylori bacteria, an analogous statement might be, “If you have an active bacterial infection in your gut, it takes a lot of antacids and pain medication to make it feel good.” It seems to me that a more appropriate way of addressing the pain is to do the laboratory tests that are most likely to determine WHY you have pain in your gut so we can figure out if there IS something that can be done about it. In the case of the ulcer, H. Pylori is the tack and antibiotic treatment is what is necessary to remove it.


Dr. Sid Baker has also developed what he calls “The Second Tacks Law,” which states, “If you are sitting on two tacks, removing one does not produce a fifty-percent improvement. Chronic illness is, or becomes, multi-factorial.”


Let’s talk again about our hypothetical adult with the ulcer. Let’s imagine that prior to developing his ulcer he was a successful entrepreneur and philanthropist whose life’s work was devoted to discovering a cure for cancer (or autism, or figuring out how to solve global warming, etc.) During the 13 years he was waiting for mainstream medicine to change the “standard of care” for his bacteria-related stomach inflammation, he was being “treated” with pain medications and antacids. He became addicted to opiates and developed chronic constipation and memory problems. As his overall health continued to deteriorate he decreased his social contacts and became basically house-bound; a shell of his former self. The antacids, which are high in aluminum, further contributed to his social and cognitive difficulties (he had trouble thinking straight) and his family members have now become concerned that he may have early-onset Alzheimer’s disease. An additional complication is that because his stomach hurts so much of the time, he has severely limited his diet and is only eating a small number of foods, which are poorly absorbed, resulting in significant nutritional deficiencies and a weakened immune system. He feels so bad most of the time that he lashes out verbally (and at times physically) at his wife and children, who have become convinced that he is suffering from not only Alzheimer’s disease, but depression and possibly a host of other psychiatric problems. When he is finally seen by a psychiatrist or psychologist, he is evaluated on the basis of his behavior and current cognitive functioning, and guess what? He may need to be institutionalized. What are the chances that anyone who “treats” this gentleman will understand the role his ulcer played in the process that led to his ultimate regression into the childlike state of dementia and accompanying social withdrawal and problematic behaviors?

The hypothetical story of the adult whose entire life course was changed as a result of his untreated ulcer is presented to give an idea of how we look at the treatment of autism from a biomedical perspective. If the gentleman in the story had received the appropriate treatment for his bacterial infection in the first place, the ensuing “train wreck” may have been avoided. Think about what could have been different for this man and his family. Think about how his life may have made a difference in his community and beyond. Now think about the fact that according to CDC reports (2007), 1 in 150 children in the United States meets the diagnostic criteria for autism. The cost of raising one child with autism is estimated to be in the range of $3 million over the lifespan. Much of the burden is borne by families with additional costs to society in general. Given what’s at stake, I cannot simply accept the “standard medical truth” that there is nothing that can be done. We owe it to our children and to our nation to do our very best to uncover the biological bases for the outward manifestations that lead to the diagnosis of autism. The only way to do that is on an individual basis, learning from one child at a time. Each child is different and there is no one-size-fits-all treatment for “Autism.” When we think about where to start, we have to learn as much as possible about the child in question: Your child.


Before I see your child for the first time, I will ask you to answer a LOT of questions. I want to know about the pregnancy. I want to know about your previous pregnancies and miscarriages. I want to know your blood type and if you have the Rh-factor. I want to know if you had the flu or took antibiotics during the pregnancy. Did you have dental work done? Did you crave particular foods, or crushed ice? Were you nauseous in the first three months, or did you throw-up every day from conception to delivery? I want to know about your family, particularly with regard to family medical history and previous history of exposures to environmental toxins. Did you grow up on a farm? Did your father own a gas station? Did you have recurrent bouts of strep or bronchitis as a child? Is there a high prevalence of thyroid disease, bipolar disorder, anxiety, or diabetes in your family? All of these questions are my way of fishing for clues about where to start when looking for the underlying issues that may need to be addressed with YOUR PARTICULAR CHILD.


I will ask you to tell me about your child – not just his or her current behavior and functioning, but EVERYTHING you can tell me about your child. I want to know if your child had reactions to vaccinations, and if so, what kind of reactions and to which vaccines. (NOTE: thimerosal (ethyl-mercury) is not the only issue with vaccines, and vaccines are not the only issue in autism. The information about vaccinations is important as ONE component of a VERY thorough investigation of your child’s lifetime experiences and medical history.)


I want to know if you notice behavior changes or if your child tends to get sick at certain times of the year. I will ask you to tell me about your child’s diet and what foods he or she tends to crave. Did he or she have problems with milk as an infant? Was soy formula used? Did he or she have trouble with constipation and/or diarrhea? Are those problems ongoing? I’ll also ask about things that you may think are totally unrelated – things like your child’s fingernails, number of cowlicks, and if he or she has little white bumps on the upper arms and legs. Again, these are all clues about where to look for further information through targeted laboratory tests for nutritional deficiencies and imbalances, which are often an essential component of biomedical treatment for Autism, Asperger’s Syndrome, ADHD, and Pervasive Developmental Delay (PDD).
With regard to the environment, I will ask where you live now and where you lived prior to the conception of the child. The age and composition of your home is important information as certain types of homes are more likely to be sources of toxin exposure than others. For example, a child who lives in an older home may need to be checked for lead exposure and a child who lives in a home with a basement that floods may be exposed to toxins from mold. Children who spend a lot of time in wooded areas may need to be checked for Lyme Disease or other tick-borne diseases. Other sensitivities to environmental toxins include exposures from parental occupations (uniforms being washed with children’s clothing, residue tracked in onto carpets, etc.), or geographic proximity to certain businesses and industrial sources of pollution (power plants, plastics, and by-products from manufacturing).


As you can probably tell, I like to be thorough. My greatest concern is not whether you will tire of answering questions; it’s whether I will miss something important because I failed to ask.

It may seem that there are so many possible factors involved here that we will never be able to determine a particular treatment for your child. Remember, the most important first question is, “Where do we start?”


While the overall number of possible factors to consider is vast, there are several issues that tend to be common among children with autism, regardless of the particular triggers involved. Among these commonalities, Gut Dysfunction (gastrointestinal problems or problems related to eating and pooping) are probably the most significant. The great majority of children diagnosed with an Autism Spectrum Disorder have significant histories of diarrhea, constipation, or other “poop-related” anomalies such as grainy stools, undigested food in stools, extremely stinky stools, floaters, or a combination of some or all of the above.


Another common finding in the histories of children with ASDs is previous administration of multiple rounds of antibiotics (and steroids), which are prescribed to treat their frequent bacterial infections (ears, strep, bronchitis, tonsillitis, pneumonia, etc.). In children with a history of antibiotic treatment we frequently find clues suggesting we should check for Yeast Overgrowth (candidiasis) that may need to be addressed with antifungal medications. Some indications that yeast may be an issue include: frequent rashes, peeling feet, ridged, discolored nails, inflamed cheeks, red ring around the anus, and history of thrush, ringworm, and cradle cap.


Children with Autism Spectrum Disorders frequently exhibit physical symptoms indicating Immune System Dysregulation, including eczema, allergic rhinitis, asthma, warts, viral skin infections, herpes, chicken pox, (and as noted previously) strep, bronchitis, tonsillitis, and recurrent ear infections. However, the opposite may also be true, where the child with autism seems to “never get sick.” Researchers are finding that in some cases, the child does not respond to viral or bacterial invaders appropriately because of underlying immune system dysfunction. Parental response to questions about the child’s health and medical history provides us with clues as to which laboratory tests may provide further information about what’s going on inside the child’s body.


In addition to common findings in the child’s medical history, there are a number of common Nutritional Deficiencies that are often present in children with ASDs. Among the most common are deficiencies in zinc, magnesium, essential fatty acids, and B-vitamins. It is important to note that when you think about treating a child (or adult) with chronic medical conditions, you need to be careful about vitamin therapy. This is why we use specific laboratory tests to gather the hard data before recommending high doses of a handful of supplements. Each vitamin, nutrient, mineral, amino acid, enzyme, and co-factor has a particular set of purposes it serves within the body and they are all inter-related. If one is not careful with supplementation, it is easy to induce a deficiency where one may not have previously existed. Given the complexity of issues involved in these children, it is my opinion that supplementation should be based on clinical impressions and in many cases, based on the results of laboratory analysis of the individual child. This is one example of the rationale behind the statement that There is no single Biomedical or DAN! Protocol for the treatment of autism (or any other neurodevelopmental disorder). The treatment is guided by the child and the information the practitioner learns from the child, the parents, and the data from labs.


The kinds of Laboratory Tests we order will depend on the information gathered from investigation into the child’s history and from the family history. That said, there are some labs that are almost always warranted, and these include urinalysis, CBC, liver and kidney function tests, tests to measure thyroid function, and assessment of minerals (iron, zinc, copper, and magnesium). We will also often want to check levels of B-12 and Vitamin A (retinol) and to assess viral titers and look for markers of autoimmunity and inflammation.

Some of the most common findings from laboratory analysis include mineral imbalances (high copper, low zinc, magnesium, calcium, and iron), deficiencies of Vitamins A and B-12, and increased markers for inflammation.


In addition to the more traditional labs, we will frequently order laboratory tests that are less commonly employed by “mainstream medicine” but which are very helpful in determining what’s going on inside the body, from a cellular perspective. These “Functional Medicine” tests include Urine Metabolic Analysis/Organic Acids, Comprehensive Digestive Stool Analysis, IgG Food Antibodies including antigliadin antibodies, Neopterin (Urine Immune Marker), and Porphyrin (Urine physiologic burden of metals).


Additional laboratory analysis very often includes tests to evaluate for Heavy Metal Exposure (urine, hair, & fecal tests), elemental nutrient analysis, plasma amino acids and fatty acids, and genetic testing.


With all of this information, the next important question involves Treatment and “Where do we begin?” The basis of the treatment plan is the foundation. In building the foundation we talk about “The Three R’s” – Remove, Replenish, & Repair.

Remove what?
Think back to Dr. Baker’s “First Tacks Law,” which can be restated with the following question, “Is there something within this child or to which this child is being exposed, that if removed, would result in improvement in functioning?”


When you have a child with chronic illness and ongoing environmental exposure to multiple toxins from air, water, preservatives, dyes, and other sources, it is important to get rid of as many sources of exposure as possible. I ask parents to consider, “What is it that you have control of?”


Dietary Changes are often one of the most important first steps to improving a child’s overall physical status. We begin by “cleaning up the diet” – removing sugars, junk foods, preservatives and dyes. By the way, there is no such thing as “junk food” – it’s either junk or it’s food. When I talk to parents about cleaning up the diet, I ask them to remember a couple of basic things. First, when you go to the grocery store, stick to the outer aisles. Stay away from things in cans and boxes. Second, read labels: The fewer ingredients something has, the easier it is for the body to break down and utilize (generally). Third, if you can’t pronounce it, don’t put it in your body (or in your child’s body).


While we are removing things, we want to think about environmental exposures and ongoing sources of toxic exposure. If you are investing all this time, money, effort, and emotional resources, you want to simultaneously eliminate toxins from the environment wherever possible. This might mean installing water and air filters, or it might mean tearing up carpet and ripping out moldy building materials in the basement. Again, the steps you take will be based on your own situation and information about your child.


In addition to these measures we often must remove specific foods from the child’s diet, in order to address food allergies, and in many cases to help promote healing of the gastrointestinal tract (regardless of allergy status). That does not always mean that the child has to be on such a strict diet forever! However, there are particular proteins that tend to be most problematic for children on the spectrum and these will need to be avoided, at least during the initial phase of treatment.


The second of the Three R’s is “Replenish.” This issue can be assessed by asking the question, “Is there something this child is missing, that if provided, would result in an improvement in function?” The answer to this question often comes from the results of laboratory testing. The most frequent recommendations involve supplementation with probiotics (to replace the “good” bacteria in the GI tract), digestive enzymes (to help break down certain foods and assist in supplying essential nutrients), supplemental nutrients (vitamins and minerals) and essential fatty acids.


The last of the Three R’s is “Repair.” This aspect of treatment is also based largely on the results of laboratory testing. Depending on the data gathered for a particular child, the reparation process may involve the administration of antimicrobials, antifungals, antivirals, antibacterials, Immunotherapy, and detoxification (naturally or with prescription medications).

As you can probably see, there are many different questions to be addressed in the Biomedical Treatment of Autism Spectrum Disorders and other neurodevelopmental disorders. I hope this information is helpful to you as you determine the appropriate course of action for your individual child. If nothing else, my fervent prayer is that after reading this article, you will at the very least begin to question the wisdom of accepting the standard medical “truth” about Autism. Don’t believe it. Autism IS TREATABLE. Recovery is POSSIBLE and it is happening every day. The most important first step for you is to choose whether or not to find out if it is possible for YOUR CHILD. I hope this article assists you in making that decision.


Marcella Piper-Terry, M.S.