Biomedical Treatment was Too Expensive and Too Late

This post is in memory of Isaac. This little boy died on Saturday when his heart finally gave out. He was waiting for his third heart surgery, which would have taken place in September. Unfortunately, the strep and staph infections in his blood were too much for him to fight off and the attack of multiple infections was ovewhelming.

I never met Isaac. I did meet with his parents a few months ago when they came to Cady Wellness Institute to meet with a colleague. Because Isaac was a child who had received an Autism Spectrum Diagnosis, I was asked if I had time to talk with the parents about what might be done to help improve their son's overall state of wellness by implementing biomedical interventions. As best I can recall, I spent about an hour with Isaac's parents. This was not an official appointment and they were not charged anything, since they were not patients and we were simply having a "chat."

I talked with Isaac's parents about biomedical interventions for autism, and made several recommendations regarding steps they could take on their own, to improve his body's ability to fight off the multiple environmental and immune system assaults that are common in children on the spectrum. Unfortunately this family, like so many others, did not have the funds to pay out-of-pocket for biomedical treatment in the tri-state, and they were also unable to travel to one of the larger clinics around the country.

Because I never met Isaac and because his parents were not able to have their son seen on an official basis due to the financial strain of doing so, much of what I am writing in this post is speculation. However, it is speculation based on experience. I have seen and spoken with MANY parents and families in the last four years whose children clearly needed biomedical help, but who simply could not afford it. (I have also seen families whose children clearly needed biomedical help, and they COULD afford it but believed it was too expensive and not worth dedicating the resources.)

There are many children - no, there are MANY children on the spectrum (including kids diagnosed with autism, Asperger's, ADHD, PDD, Bipolar disorder, OCD, and ODD) that have underlying medical problems that are never diagnosed and treated. One of the MOST frequent of those problems is Strep infection. When a child has a strep infection that is untreated, it can damage the heart. I don't KNOW that this is what happened with Isaac. All I know is he died because his heart gave out while waiting for his third heart surgery, AND he had Strep and Staph infections in his blood. I cannot recall the exact conversation I had with Isaac's parents, but based on the conversations I have had with EVERY parent of a child with ASD who has sought my help, I would bet the farm that I brought up the importance of checking his Strep titer. This is something I routinely recommend for ALL kids I see, and for ALL kids on the spectrum, especially those with anger outbursts and OCD tendencies. The reason is because PANDAS (Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcus) can be treated! And it is often EASY to treat with antibiotics. That is, if you can get your pediatrician or family practice doctor to run the test and give the monthly shots of bicillin. There have been many cases when I have talked with families who could not afford to have their child seen at my former place of employment, and for whom I have recommended they ask their primary care physician about running a strep titer, and for whom the response has been, "That's experimental. There's no proof. I'm not going to do it." For those physicians who think obtaining a blood test to check for strep is "experimental," I take this opportunity to say, "Shame on you." I wonder how many other children with autism have died from heart problems, simply because their physicians refused to check their strep titers - or because they never thought to do so.

Children with autism are not hopeless and they do not deserve to be ignored by the medical professionals simply because they have received an autism diagnosis. These children are medically sick and if we do not care enough about them to do the tests that are necessary and to treat the infections that are wracking their bodies, then WE are responsible when something like this happens.

To Isaac...and to all the other children who currently cannot afford to get the treatment you so desperately need and deserve: I am so sorry. I pray you will have an eternal life in heaven that is completely joyous and free from pain. God knows you deserve it, especially after the way we have failed you on earth. Eternal blessings to you, Isaac.

A Tale of Autistic Blood - Article from Age of Autism, by Kent Heckenlively, Esq.

There is a very interesting article on the Age of Autism website, entitled "A Tale of Autistic Blood." The article contains a link to a fascinating video and slide show that compares the blood of six autistic children. I highly recommend you watch this and read the article (Click the title to go to the Age of Autism site and read the entire article). My comments about the article and video are posted below.

A Tale of Autistic Blood
By Kent Heckenlively, Esq.

This may be the most important article about autism I’ve ever written. But first I need you to do a little work. I need you to go to this site (HERE) and watch the approximately five minute long video comparing the blood of six autistic children put together by Mark Squibb.

Marci's Response:
IMO, I believe this is another physiological marker of the multiple factors involved in autism and pretty much all of the comments posted are on track.

Stress will cause aggregation in preparation for clotting in case of injury. Think "fight or flight" - when you are preparing for battle or to run away, there is a significant chance you may get hurt. When the the balance of stress hormones is disrupted (shifted) due to high anxiety or panic, the body doesn't differentiate between real or perceived danger and prepares to clot. So thats ONE factor at work.

Heavy metals like lead and mercury (and aluminum which is not technically a "heavy" metal) also damage the circulatory system and lead to problems like Raynaud's Syndrome, atherosclerosis, hypertension, stroke, and aneurysm.

Metals and other toxins have something else in common - a single valence electron in their outermost ring. This makes them very attractive to each other - they don't like to be alone but like to travel in pairs so they will "hook up" with other toxins. This is one reason (along with impaired detoxification due to depletion of metallothionein) why our kids, once shot up (pun intended) with aluminum or thimerosal (flu vaccine, rhogam, etc.) become like magnets for other toxins. It's also why when chelating, mercury does not come out until after aluminum, antimony, and lead. The magnets (our children) hold onto the metals because their electrical charges have been altered. This was for me, probably the most fascinating thing about the video by Mark Squibb - he actually points out the alteration in electrical fields in the blood patterns of autistic children.

The comment about babesia (a bacteria associated with Lyme disease) is also correct, which is why adults with chronic Lyme exhibit many of the same behavioral and neurological issues as do children with "autism."

Infections in the blood (from systemic yeast, viruses, strep, staph, etc) will also cause clumping, as what is left of the immune system tries to kick in and fight off the infection. Remember that one of the first things the immune system does is to send extra blood (and oxygen) to the sight of injury or infection. This is part of the healing process and is why we get the swelling, heat, and itching when we get a minor cut or scrape. That's the body's attempt to heal.

The problem is, in our children there are so many different things to fight that their bodies become confused and shift over into autoimmunity. The analogy I use is like the old Space Invaders game where you start of shooting at one bad guy and it's relatively easy, but as things speed up, there are too many bad guys to shoot at accurately and you end up crashing and burning.

Finally, the genetic link is (again, IMO) often associated with metals (especially lead) that is passed from mother to child. In the family histories of my patients I frequently see higher than expected occurrance of things like stroke, blood clots, hypertension, bipolar disorder, heart-valve problems, and heavy bleeding/clotting with menses. All of these things, (and autoimmune thyroiditis) are associated with lead poisoning. When I check further, these parents and grandparents grew up with coal-burning stoves, lived near or worked in coal mines, or in some cases owned gas stations (before gasoline was unleaded.)

Very interesting article and video - thanks so much to the folks at Age of Autism for your wonderful work, and to my friend Lori for bringing this article to my attention!

Marci

NIH Study Shows Anti-Depressants Don't Work for Autism

Below is an article from today's Los Angeles Times, reporting on the results of a recent NIH study looking at the effectiveness of Celexa in Autism. What a waste of money that could have (and should have) been spent researching treatments that really work - like those aimed at healing the gastrointestinal tract.

(Thanks Lori for posting this on C.A.R.E. Keep 'em coming!)

My response to the article, which follows:

This is not surprising at all. Look at the money involved - between 2 & 3 billion per year for drugs that have not been tested on children with autism, and whose side effects are 2-3x worse in kids with ASD. Interesting that the pharmaceutical companies who make the drugs to "treat" the symptoms are also the ones who make the vaccines that contribute to autism in the first place - the perfect storm. Before you pay big bucks for a pyschiatrist to "treat" your child with drugs that don't work, please consider looking deeper to heal the underlying problems.

SSRIs don't work because 95% of serotonin is in the gastrointestinal tract. If the gut is injured then serotonin will not be produced in the first place, so it cannot be utilized in the brain.

SSRI stands for Selective Serotonin Reuptake Inhibitor - meaning that what it does is keep Serotonin in the synapse (the gap between two neurons) longer so it can work longer before being taken back up by the neuron that released it. If there is no serotonin for an SSRI to work on (because the gut is injured and it's not being produced) all you are going to get is side-effects from the fillers and dyes used in the capsules.

DUH. I wonder how much money was wasted on this study?
(Click the title to read the article in its entirety)

Study Finds Antidepressant Doesn't Help Autistic Children
Nationwide research finds that citalopram is no more effective than a placebo and that its side effects are twice as bad. About a third of autistic kids take the drug, known as Celexa in the U.S.
By Karen Kaplan June 2, 2009

An antidepressant commonly prescribed to help autistic children control their repetitive behaviors is actually no better than a placebo, according to a report published today.Roughly a third of all children diagnosed with autism in the U.S. now take citalopram, the antidepressant examined in the study, or others that are closely related. The results of the nationwide trial, published in Archives of General Psychiatry, have some experts reconsidering the appropriateness of antidepressants and other mind-altering drugs used to treat children with autism spectrum disorders.

Memorial Day: Remembering the Children of War, Political and Private

The front page of today's Courier & Press newspaper is a tribute to Kalab Lay, the three year-old boy who was beaten to death by his parents after being failed by the system that was supposed to protect him. Kalab's parents, like many in the Tri-State and beyond, were involved with methamphetamine. Click the link below to read the article in its entirety (please click the "back" button to return to this article).

http://www.courierpress.com/news/2009/may/23/a-life-tainted-by-meth/

It is fitting that Kalab's face adorns the front page of the C&P today, the Sunday before Memorial Day. We most often think about soldiers at this time, especially those who lose their lives while fighting to protect our freedoms. However, there is a large portion of our society whose lives are also impacted by war, and whose traumas most often go unrecognized: The children of veterans serving in Iraq and Afganistan. With the numbers of veterans returning after sometimes multiple tours of duty, and many of them not receiving assistance for their own traumas, the numbers of children who are abused by their military parents continues to grow.


A while back I wrote an article about the effect of PTSD on military families, and given the timing, I believe it is worth reposting. This is the bulk of today's post. Resources for more information about PTSD and military families are posted at the end of this artcle.

The Effect of PTSD on the Family:

One of the scariest things for someone suffering from PTSD is when something in the present happens that "triggers" memories of the past. This is the same thing that happens when a Viet-Nam veteran suddenly drops to the ground, covering his head or assuming the fetal position when a car backfires (or when the "pop" and "flash" of exploding fireworks catches him off- guard). While we are probably all aware of the difficulties suffered by combat veterans, I have come to realize that as a society we are very unaware of the impact trauma has on adult survivors of child abuse. This needs to change. To illustrate my point, I will use an analogy, as I often do when working with clients in therapy. For the purpose of this example, I will refer to Viet-Nam veterans, as it was only after that war that PTSD was officially recognized. (Before Viet Nam soldiers suffered the same devastating symptoms, but it was referred to as "Shell Shock.")

Imagine yourself as a combat soldier in Viet Nam. You and your buddies are hunkered down, rifles at the ready, creeping through thick jungle foliage. Your body is tense. All your senses are on high alert for any sign of danger. Suddenly a bullet whizzes by you so fast you can feel the breeze on your face as it slices through the air. Then another one flies by. And another. You call on your heightened senses, frantically trying to figure out where the bullets are coming from but the jungle is so thick you can't see your attacker. Another bullet zings by and hits your best buddy. He falls, bleeding from his belly and writhing in pain. You go to him, kneeling, trying to help stop the bleeding. Meanwhile, the onslaught of bullets continues and you have to make a decision to stay and help your friend or retreat and try to keep from becoming another war statistic. As you are trying to figure out what to do, your friend dies in your arms. You are still under attack. You do not have time to think about your friend or to experience the painful emotions of losing him. You refocus your attention on the situation at hand and do what you can to avoid being killed.

Now imagine that this scenario repeats itself over and over again for several months or even years on end. It is easy for us to see how the lives of combat veterans would be impacted, with the ongoing traumas they face. Not only are they facing horrendous conditions and repetitive traumas, they can't get away from it. They can't just say, "I've had enough. I'm outta’ here." They are, in effect, trapped.

Imagine you are the child of a combat veteran returning from the war. You have missed your daddy terribly and have spent many hours dreaming of the day he would come home again. You remember how he used to play catch with you in the yard or crawl around on the floor with you on his back squealing with delight, shouting, "Yee-haw! Giddy-up!" As a child, you expect things to return to the way they were and life will continue as it was before Daddy left. But Daddy is not the same. He doesn't laugh. He hardly even talks to you. When he does, he sounds angry or annoyed. You try to figure out why he's mad at you and you work hard to be good so maybe, you can make him happy. Maybe you can make him smile. Time goes by and Daddy doesn't smile. He is even more quiet than before and gets angry over the littlest things. Unlike before, when Daddy gets upset, he yells. Sometimes he throws things. Sometimes he hurts you. Or Mommy. Sometimes he storms out of the house and drives away in his car with the tires squealing, and you cry because you're afraid he won't come back. Or you cry because you're afraid he will. The man who came home looks like Daddy but it isn't Daddy. Like the combat soldier, you are living in a war zone. Like the combat soldier, you don't know when the attack will come, what will set it off, or how bad the damage will be. You just know it will happen and you have to be ready for it when it does. Like the combat soldier your body goes on high-alert, always watching out for signs of danger. You can't sleep and when you do you have nightmares but you can't wake up Mommy and Daddy to tell them because Daddy might get angry. So you keep it to yourself. It's hard for you to concentrate on your schoolwork and your grades start falling. You are afraid of what will happen when Daddy sees your report card. Like the combat soldier, bad things are happening all around you. Like the combat soldier, you are trapped. Because you are a child, you can't just say, "I've had enough. I'm outta’ here."

The human brain is a wonderful thing. It has the ability to go on autopilot when necessary, shielding us from awareness when things get too overwhelming. This is what we call a "defense mechanism" and it is a very important coping skill that allows us to survive even the most terrifying of experiences. As we all know, many veterans of the Viet-Nam War basically accomplished the same thing through self-medicating with drugs and alcohol, which allowed them to "zone-out" and escape the pain, if only for a while. Others did not turn to substance abuse, but became sullen, withdrawn, and unable to interact with others or hold a job. Many families were split and the suicide rate among veterans skyrocketed. If there is anyone who does not see parallels between Viet Nam and Iraq, at least in this regard, he or she has simply not been paying attention.

Many people, even those who have little faith in the necessity or effectiveness of mental health based interventions, can and do accept that the lives of our veterans are often immeasurably changed as a result of their experiences. Tragically, we as a society do not afford the same compassion for adults, who as children experienced their own terrifying battles, in many cases continuing for several years without any end to the conflict. For many adult survivors of child abuse (war-related or not), their "tours of duty" extended far beyond anything this nation would require of even the strongest, most well trained adult soldier. For many survivors of child abuse, the consequences of their experience have never been acknowledged. Not even by themselves. If there is any hope of changing the cycle and helping today’s military children, we must learn from the past.

There are many good sources of information on the web. A few very relevant websites are listed here, in case you wish to read further.

http://www.medscape.com/viewarticle/565407

http://aje.oxfordjournals.org/cgi/content/abstract/165/10/1199

http://coalitionforveterans.org/2009/01/invisible-wounds/

http://www.ncptsd.va.gov/facts/specific/fs_children_veterans.html

http://www.ncptsd.va.gov/index.html

http://www.ptsdalliance.org/

http://www.sidran.org/

Vaccines and Autism: Your Child and "The Greater Good"

Yesterday's episode of "The Doctors" was worth watching, if only because it is sure to stir more debate and controversy about the link between vaccines and autism. Hopefully, this will help to keep the vaccine/autism connection from fading away as the AAP and "99.9 % of pediatricians" (according to Dr. Stork) would like. For anyone who did not see the show, let me set the stage.

Jenny McCarthy, Dr. Jerry Kartzinel, J.B. Handley, and Stan Kurtz were guests. Probably everyone knows by know that Jenny McCarthy is the mother of Evan, a little boy who was diagnosed with autism and who is now recovered. He no longer has autism. Dr. Jerry Kartzinel is the Defeat Autism Now! Pediatrician who helped Jenny McCarthy and Evan by utilizing the Biomedical Approach to address the underlying medical problems that led to the autism diagnosis. Jenny Documented Evan's recovery in her book, "Louder Than Words." Jenny and Dr. Kartzinel have recently written a book together, "Healing and Preventing Autism: A Complete Guide." J.B. Handley and his wife Lisa founded Generation Rescue, a non-profit organization that provides information and support to families who are working to recover their children from an autism diagnosis.

I don't usually watch "The Doctors" and wouldn't have seen it yesterday if I had not been given a heads' up via email from a friend who is also the parent of a child diagnosed with autism. I don't know anything about "The Doctors" other than the two who were most involved in the debate were Dr. Stork and Dr. Sears.

At the beginning of the show, Dr. Stork introduced the topic by saying, "Some of the theories you’re about to hear we may not agree with, but we know as doctors, this is an important issue to discuss."

As the discussion began, Dr. Lisa Masterson was supportive of Jenny McCarthy's work and gave her kudos for standing up, not only for her own kid but for so many other kids in this country and beyond. However, as the discussion heated up, Dr. Masterson disappeared from the stage and we were left with Dr. Sears and Dr. Stork. Dr. Sears, a pediatrician and member of the AAP, was reasonable and asked thoughtful questions about the science behind the GF/CF diet, specifically questioning, "Why doesn't it work for ALL kids?" Dr. Kartzinel responded that while the GF/CF diet does not work for ALL kids, it DOES work well for a significant percentage, and we CAN test to see if children have allergic reactions to certain foods and we CAN TEST to see if an individual child is making opiates from gluten and casein proteins. This is what medicine is supposed to be about. You base the treatment on the results of laboratory tests.

Dr. Sears then asked Dr. Kartzinel about his opinion with regard to whether or not there is a genetic component to autism. As Dr. Kartzinel responded, we talk about a "genetic predisposition" - something that makes an individual child more vulnerable to having a bad reaction to particular environmental insults - including toxins, and including toxins that are injected into the child's body via vaccinations.

Dr. Kartzinel: "What thing can we do in medicine to an entire population, and not expect a certain small group not to do well with? There is nothing in medicine that we do…lidocane, anesthesia, certain surgical procedures...Why would we think that we can give every child in the nation not one vaccine, but multiple vaccines and not suspect anything to go wrong with them. So, genetically, whether it be penicillin, or vaccines we have to understand there are going to be some children who will not do well with it…That’s probably one big reason we have a problem with this…we don’t look at the children as individuals…we look at them as a population."

As Dr. Kartzinel pointed out, in medicine, nothing works for everyone, so why would we expect that a universal vaccine schedule would work for ALL kids, without a certain percentage of them having problems as a result? Jenny joined in to say that the message is, there are too many, too soon and that the increase in the number of vaccines from 10 in 1983 to 36 in 2009 is unwarranted and IS related to the increase in autism. This is when things turned ugly. Here is a link to a discussion you may want to see (or see again): http://www.thedoctorstv.com/main/procedure_list/269

What I noticed is that when J.B. Handley stated that he is tired of physicians telling parents that vaccines are safe when the physician has not personally looked at the science, Dr. Stork blew a gasket. Dr. Stork began yelling at J.B. Handley and accusing him of "antagonizing me" and "personally attacking me on MY stage." Dr. Stork then switched the topic away from vaccines and started talking about environmental toxins and dietary changes that may be contributing to autism. He was willing to entertain the idea that there are other toxins and seemingly benign things that may be problematic for our kids, but to question vaccines? That is out of bounds. Wait...I thought he wanted to have an open debate...

Here is a link to the next segment of the show: http://www.thedoctorstv.com/main/procedure_list/271

Again, let's have an open discussion, but not about vaccines, since we "Know the Truth" that "Vaccines have been studied and scrutinized" so let's stop talking about that. Did anyone else hear Jenny McCarthy, Jerry Kartzinel, and J.B. Handley saying over and over again "They've looked at 2 vaccines and only one ingredient (mercury)." Drs. Sears and Stork continued to talk over their guests as if they could not hear what they were saying. They just continued to tow the party-line, from the AAP and the CDC. During the break, after the above "discussion," Dr. Stork stated that they contacted the AAP and had recieved a statement from the American Academy of Pediatrics. This is the official party-line:

• “It is upsetting for families not to know what caused their child’s autism. While it is likely that there are many environmental factors that influence the development of autism, because of very careful and repeated studies we know that vaccines do not cause autism. We share the concern that additional research is needed to investigate genetic and environmental factors that may affect the developing brain.”
  

J.B. Handley: "It’s maddening for them to put out a statement like that…scientific dishonesty."

Who are you supposed to believe?

To boost The Doctors' position that vaccines have been proven safe, Dr. Stork showed a clip from a previous episode where the expert, Harvey Karp, M.D. declared: "A dozen or so large studies that have shown zero association between vaccines and autism."

That might be pretty convincing, IF any of those studies had included children with autism as part of the subject pool. But wait...this "expert" is declaring that 36 vaccines have been "proven" safe and to have "zero association" with autism, and ALL of that information has been gleaned from "A dozen or so" studies. In order for that to be true, each study would have had to cover 3 different vaccines, since "a dozen" goes into 36 (the number of childhood vaccines) 3 times. I would like to see those studies because I've looked at PubMed and they aren't there.

If you have never researched this issue for yourself, let me give you a few suggestions on where to look for more information. I suggest you begin by asking, "Has the vaccine-autism question been answered?"

Why don't we ask Dr. Bernadine Healy, former director of the National Institutes of Health (NIH). Click here to see what Dr. Healy has to say. Please be patient and wait for the advertisement at the beginning to play through. Dr. Healy's interview is well worth the wait.

According to the former director of NIH, not only has the question NOT been answered, it has not even been addressed. Injured children have not been studied because the government is afraid of what they will find. “The public health officials have been too quick to dismiss…”

Aha! you may say...Dr. Healy is only ONE physician and she is no longer the director of NIH anyway. Why should we believe her?

The problems with mercury have been known for decades, and it's not just mercury. Aluminum does many of the same things that mercury does. If you want to learn more about this read the article by Dr. Russell Blaylock, reporting on the cover-up at the Simpsonwood Conference.

If you have read much about vaccine safety, you may be familiar with Dr. Paul Offit; the biggest proponent of vaccines, and member of the Institute Of Medicine (IOM), which has declared with a great degree of certainty that vaccines are safe. I encourage you to watch this video clip of Dr. Offit, promoting his latest book about the subject.

Dr. Offit is pretty impressive. Unfortunately he doesn't understand neuroscience. If he did, he would realize that his argument about problems with the synapse being the cause of autism, he is actually MAKING the CASE for vaccine injury, since mercury and aluminum (both vaccine additives) are both NEUROTOXINS and damage the ability of one neuron to communicate with another by way of the SYNAPSE.

Dr. Offit makes a big point of the fact that in the last year there has been the largest oubreak of measles in decades. 135 cases of measles, and 10% of those children had serious complications. For clarification: 10% of 135 is 13.5, meaning that when Dr. Offit is cautioning about the impact of measles, he is talking about complications that impacted less than 14 children in the United States in the last year - which was "the largest measles outbreak in years." What Dr. Offit doesn't tell you is that more than 50% of the measles cases he talks about have been determined to be from the vaccine strain of measles, meaning the children who got measles either got them from the vaccine, or from being exposed to someone who was shedding the virus after being vaccinated. This is the same thing that happens with many of the polio cases, but Dr. Offit is not going to tell you that. Why would he want to be...less than honest about these facts? Watch this video clip and draw your own conclusions.

Remember the American Academy of Pediatrics' statement on "The Doctors?" Why would they declare 36 vaccines "safe" when only "a dozen or so" studies have been done and none of them have included children with autism? Follow the money.

Fifty-five doses of vaccines by age six. Wait, you might say...I thought it was 36! Thirty-six vaccinations or shots, but because so many are multi-dose shots (DTaP, MMR) when you add them all up, it's actually 55 doses of vaccines.

Remember, it's not just mercury that is neurotoxic, aluminum is a huge problem that most people haven't even considered at this point. Here is a link to a very informative article about aluminum, and why we should be concerned. This article is written by Dr. Robert Sears. Dr. Robert Sears happens to be the brother of Dr. James (Jim) Sears of "The Doctors." Both are pediatricians, but they apparently have some different views on the issue of vaccine safety. If you saw the episode of "The Doctors," you may have noticed that at one point after being asked by Dr. Jim Sears about "the scientific studies" showing that diet is effective in treating autism, Dr. Kartzinel spoke about how so many doctors are questioning if diet works, but they are not coming to his clinic and actually talking to parents of kids who are improving. He also made reference to Dr. Robert Sears, saying something along the lines of, "Those who are saying there are no studies are not talking to your brother about what he sees at the clinic." My hunch is that the reason Dr. Jim Sears appeared more rational and reasonable than Dr. Stork on the subject of vaccine safety is because he has had this conversation many times within his own family. Unlike Dr. Stork, who seems to be married to his position of "Devil's Advocate." Interesting choice of terminology.

Dr. Stork is okay with talking about ENVIRONMENTAL TOXINS as a possible contributing factor in autism, but he adamantly denies that toxins in vaccines (which are injected directly into the bloodstream of a tiny infant) could have anything to do with autism. Let's ask another pediatrician (one of the .1% who disagrees with Dr. Stork, according to his own estimate) about her experience with autism. Dr. Stephanie Cave is a Defeat Autism Now! pediatrician in Louisiana. She is also author of the book, "What Your Pediatrician May Not Tell You About Vaccinations." In an interview with Mothering Magazine, Dr. Cave stated:

• We started testing hair, urine and blood samples…we found low levels of mercury in the hair and high levels of several other metals like aluminum, antimony, arsenic, and tin in the blood and urine. These children retain mercury, which is toxic to them.

…these children don’t have to be around a high exposure to metal – they just have to be around metal, per se, because they do not have the biochemistry to aid them in the removal of metals. I believe that’s because we have overloaded them with metal through the vaccines. We give them so much metal early in life, specifically through the hepatitis B vaccine given at birth, that their bodies keep producing metallothionein, which is what helps us to remove metals from the body. After their biochemistry is depleted, they end up with an inability to handle any metal at all.

Biochemist Bill Walsh of the Pfeiffer Treatment Center tested 503 autistic children…91% had deficiency of metallothionein. Neurotypical children did not.

To read the interview with Dr. Cave in its entirety, click here.

So, what is the source of the mercury and aluminum? There are many environmental sources of mercury and aluminum, especially here in the midwest. We have a lot of coal-burning power plants, and they put a lot of heavy metals into our environment. When it's in the air, water, and soil, it's hard to avoid it, which is exactly why it is so important to be able to detoxify. If your metallothionein is depleted, that's not going to happen and metals are going to build up in your system. As a side-trip, this might be a good time to mention that when we talk about genetic predisposition and considering which children might be most at risk, we need to consider where the parents live and how many toxins are built up in the mother before she gets pregnant. The message is, "It's all ADDITIVE." It's not JUST the vaccines, but if the mercury and aluminum that is injected into an infant on the first day of his or her life shuts down the baby's ability to detoxify AND that infant lives in an area with a lot of toxins, ENVIRONMENTAL toxins are going to pose more of a problem for that child.

The problem is, Dr. Stork is thinking just like a traditionally trained physician who practices traditional western medicine and is not open to considering any other points of view because that would be inconsistent with the party-line. He does not see the cumulative effect of toxins, but only wants to attribute the effects of poisons to those he is not involved in administering. This is the same kind of thought process behind his statement that there are increases in autoimmune diseases and all kinds of other diseases, and using that argument to establish as "truth" the "fact" that there is no connection between vaccines and autism. As Jenny McCarthy and Jerry Kartzinel pointed out, those other diseases are ALSO related to vaccines.

I found it interesting that nobody on the show brought up aluminum, or the increase in Alzheimer's disease since the administration of yearly flu vaccination (which not only has a lot of aluminum, they also contain mercury). On this subject I encourage you to go to PubMed and search for "aluminum with alzheimer's" - I just did and I got 775 studies.

Do you know anyone with Alzheimer's Disease? or "Alzheimer's type dementia?" If you do, I would ask you to envision that older person as a young child with the same problems: memory problems, communication problems, disturbed sleep and wake cycles, anxiety and irrational fears, behavior problems, etc... Sounds like autism, doesn't it?

Many pediatricians will tell you there is "No mercury in the childhood vaccines" anymore. This is not true. For a list of childhood vaccines that still have mercury (thimerosal) click here. When you are evaluating how much poison is safe for your infant to have injected into his or her body, the following information may be helpful: 12.5 mcg. of ethyl mercury (thimerosal) is 25 times the EPA "safe level" for an adult. When Dr. Cave gave her interview in 2002 she talked about the vaccine schedule at that time, pointing out that at 2 months of age, children were receiving 62.5 micrograms of ethyl mercury from just two vaccinations (Hep B & Hib). 62.5 micrograms in a 10 pound infant is up to 125 times the EPA "safe level." Dr. Cave went on to explain that mercury is a neurotoxin and as such, inhibits brain function. It also suppresses the immune system.

Dr. Cave relates, "When Hepatitis B began to be administered at birth during the 1990s, we started seeing ear infections beginning around two weeks of age, which was almost unheard of before that…they have antibodies to the basic myelin protein in brain tissue. These antibodies disappear after the children are treated and the mercury is eliminated.”

As noted, this interview was given in 2002, and according to the current information from the FDA and AAFP (American Academy of Family Practitioners) there is no longer 62.5 mcg. of ethyl mercury in the Hep B and HiB vaccine combination. However, as you will see if you check the information for yourself, there is still plenty of mercury to damage your child's brain, particularly if you follow the newest "guidelines" and get the flu shot every year, beginning in utero. If 62.5 mcg is 125 times the "safe limit" for a 10 pound infant, I wonder how many times the "safe limit" 25 mcg is to a 1 or 2 pound fetus.

Okay, so you now know that mercury is a neurotoxin and it also damages the immune system. If you watched "The Doctors" show yesterday, you will recall that the first thing Jenny McCarthy and Dr. Kartzinel talked about was dietary changes - specifically the Gluten Free/Casein Free Diet. Jenny stated that when she removed casein from Evan's diet "his eye-contact returned."

You also heard Dr. Kartzinel talk about how some children produce opiates from certain foods (gluten and casein) and how removing those foods from their diet often leads to improvement in the "symptoms" associated with autism. Here is an explanation of how all of this is related to mercury:

• Mercury and other heavy metals deactivate DPPIV
• DPPIV is an enzyme that breaks down gliadomorphin and casomorphin peptides in the body.
• Casomorphin comes from casein, the protein in milk and dairy products.
• Gliadomorphin comes from gluten, the protein in wheat, oats, barley, and rye
• Casomorphin & gliadomorphin are endogenous opiates – morphines – that make children spacy & irritable
• Children with autism are spacy & irritable

This is why the GF/CF diet works. It is also why it is necessary. Mercury and other heavy metals deactivate the enzyme that breaks down the peptides that are formed from gluten and casein. When they are not broken down, the kid is making his or her own opiates and is therefore spaced out and irritable - just like any other drug addict. This is also why so many kids on "the spectrum" are such picky eaters - they will often ONLY eat things that contain gluten and casein (bread, pizza, pasta, cheese, milk, ice cream, etc.). The reason is because they are not seeking food for nourishment, they are drug-seeking. Just like any other drug addict, they are not interested in eating, they are only interested in obtaining their fix - and they get it from foods that supply gluten and casein. BUT, the important thing to remember, in this conversation, is that mercury inactivates the enzyme that breaks down those two proteins, so if it weren't for the mercury, would these kids be addicted in the first place? Probably not.

The explosion of autism cases coincided with the doubling and then tripling of the number of childhood vaccines during the 1990s. Mercury was finally removed from the "childhood" vaccine schedule in 2002-2004, although there were still stockpiles of vaccines in doctors' offices after that time. The only way to know if your child was given vaccines containing mercury is to review the vaccine insert information. But, remember, if you are giving the "recommended" annual flu vaccine, your child is still getting 25 mcg. of mercury each year, unless you specifically request a mercury-free vaccine. And there is still mercury in a number of other vaccines, but you have to really look to find it. The language has been changed. Sometimes it is referred to as "a trace" amount that is used in the manufacturing process, but NOT as a preservative. What does that mean? It's still there - it's just not labeled as a preservative. So, get the vaccine insert and read it BEFORE you allow anyone to inject anything into your child.

Back to aluminum:

Remember Dr. Offit said that delaying or altering the vaccine schedule would expose more infants to disease...Of particular concern is the Hepatitis B vaccine given at birth. This has whopping amounts of aluminum, which hyperstimulates the immune system and shifts the balance from TH1 to TH2 - towards hyper-responsiveness (allergies, asthma, RSV, ear infections, and autoimmunity). One primary way to avoid this is by not giving the Hepatitis B vaccines unless Mom is positive for Hep B.

But you just heard on "The Doctors" that delaying vaccinations during the first year will expose millions of babies to diseases that are preventable by vaccines. What to do????!!!!

What to do is research for yourself and not buy into the hysteria promoted by those who have so much to gain, monetarily, from vaccinating your children.

Remember, mercury and other metals (including aluminum) damage the immune system and impair the body's ability to detoxify, making it more vulnerable to damage from environmental toxins and viral and bacterial infections.

The Hepatitis B vaccine is recommended for ALL children on the FIRST day of life. Does your child REALLY NEED to be vaccinated against Hepatitis B as an infant? If you (mother or father) are positive for Hepatitis B, then the answer is "Yes." If someone in your immediate family, or someone who will be caring for your child on a consistent basis and from whom your child might be exposed to infected blood, then the answer is "possibly - your child is at increased risk." Otherwise, the answer is "No."

INFANTS ARE NOT AT RISK FOR HEPATITIS B! In 1991, there were 18,003 cases of hepatitis B reported in the U.S. out of a total U.S. population of 248 million. According to the October 31, 1997 Morbidity and Mortality Weekly Report published by the CDC, in 1996 there were 10,637 cases of hepatitis B reported in the U.S. with 279 cases reported in children under the age of 14 and the CDC stated that "Hepatitis B continues to decline in most states, primarily because of a decrease in the number of cases among injecting drug users and, to a lesser extent, among both homosexuals and heterosexuals of both sexes."

But Dr. Offit wants ALL babies vaccinated for Hepatitis B, not once but three times. I wonder if that's because if they are going in for their Hep. B shots, they are also more likely to receive the Rotavirus Vaccine, for which HE developed the patent, which sold for 182 MILLION dollars. Hmmmnnn....

If you think babies should be vaccinated against a sexually transmitted disease at birth, with a vaccine that contains up to 125 times the "safe" limit of aluminum (according to the EPA regulations), watch this: http://www.youtube.com/watch?v=hNy5VmeaGNw

and this: http://www.youtube.com/watch?v=78b1rFJgyXI

Wow! That's some scary stuff. It must be the media exaggerating things, right? Yes. And No.

Remember when Dr. Kartzinel talked about how there is nothing in medicine that can be utilized universally without some percent of the population having problems? This is an example of what he was talking about. Aluminum is a neurotoxin and it damages the immune system.

So just how much aluminum is in vaccines that are "recommended" for ALL infants living in the United States? And what is the "safe level" of aluminum?

According to the FDA, the "safe level" of aluminum for full-term babies with healthy kidneys is 5 micrograms per kilogram per day. As Dr. Robert Sears points out, using this "safe level" determined by the FDA, a 12 pound, 2 month-old infant should be able to handle "at least" 30 mcg. of aluminum in one day. A 22 pound one year-old infant should be able to handle "at least" 50 mcg. of aluminum in one day. As Dr. Robert Sears states, the FDA "safe level" was determined from studies of premature infants with immature kidneys, so full-term infants with healthy kidneys should theoretically be able to handle more than the "safe level." However, we don't know because there haven't been any studies done - at least none Dr. Sears (or I) could find.

Okay, so how much aluminum is really in the childhood vaccines?

• DTaP (for Diphtheria, Tetanus, and Pertussis): 170-625 mcg, depending on manufacturer
• Hepatitis A: 250 mcg
• Hepatitis B: 250 mcg
• HIB (for meningitis; PedVaxHib brand only): 225 mcg
• HPV: 225 mcg
• Pediarix (DTaP/Hepatitis B/Polio combination): 850 mcg
• Pentacel (DTaP/HIB/Polio combination): 1500 mcg
• Pneumococcus: 125 mcg

The above information is from Dr. Robert Sears' article, "Is Aluminum the New Thimerosal?"

So what does this mean for your child, living in the United States and complying with the "recommended" childhood vaccine schedule?

Dr. Robert Sears does the math:

• Newborn gets Hepatitis B injection on day one of life would get 250 micrograms of aluminum.
• Repeated at one month of age with the next Hep B shot.
• When a baby gets the first big round of shots at 2 months, the total dose of aluminum can vary from 295 micrograms (if a non-aluminum HIB and the lowest aluminum brand of DTaP is used) to a whopping 1225 micrograms if the highest aluminum brands are used and Hep B vaccine is also given.
• These doses are repeated at 4 and 6 months.
• A child would continue to get some aluminum throughout the first 2 years with most rounds of shots.

Okay, so going back to the issue of metals depleting metallothionein, and basically shutting down the body's ability to detoxify other environmental toxins, you may want to ask yourself, is the Hepatitis B vaccine really something my child needs, if I do not have Hepatitis B?

Is your child really at risk for Hepatitis B? And is the risk worth the consequences of injecting aluminum (a neurotoxin and immunotoxin) into your child at levels that are exponentially higher than the "safe level" determined by the FDA?

Question: Is your child really at risk for Hepatitis B?

Hepatitis B

• Is not common in childhood and is not highly contagious.
• Is primarily an adult disease transmitted through infected body fluids, most frequently infected blood
• Is prevalent in high risk populations such as: needle using drug addicts; sexually promiscuous heterosexual and homosexual adults; residents and staff of custodial institutions such as prisons; health care workers exposed to blood; persons who require repeated blood transfusions; babies born to infected mothers.

According to the CDC Guide to Action publication on Hepatitis B (1997):

"the sources of [hepatitis B] infection for most cases include intravenous drug use (28%), heterosexual contact with infected persons or multiple partners (22%) and homosexual activity (9%).”

Although CDC officials have made statements that hepatitis B is easy to catch through sharing toothbrushes or razors, Eric Mast, M.D., Chief of the Surveillance Section, Hepatitis Branch of the CDC, stated in a 1997 public hearing that: " although [the hepatitis B virus] is present in moderate concentrations in saliva, it's not transmitted commonly by casual contact." (National Vaccine Information Center)

Once again, you as a parent are faced with a difficult question: "Who am I supposed to believe?"

Another question you need to ask yourself is "Just how serious is Hepatitis B?" You need to ask this question in order to make an informed decision about whether the risks associated with vaccination outweigh the risks of actually contracting the disease. The following information comes from the National Vaccine Information Center.

Hepatitis B is not a killer disease for most people.

Symptoms of Hepatitis B infection include nausea, vomiting, fatigue, low grade fever, pain and swelling in joints, headache and cough that may occur one to two weeks before the onset of jaundice (yellowing of the skin) and enlargement and tenderness of the liver, which can last for three to four weeks. (YUCK)

Fatigue can last up to a year. (Again, YUCK)

Translation: You will feel REALLY YUCKY for 6-8 weeks, and it may take you a year to recover your energy level to pre-illness status.

According to Harrison's Principles of Internal Medicine (1994): in cases of acute hepatitis B most patients do not require hospital care; 95 percent of patients have a favorable course and recover completely; case-fatality ratio is “very low (approximately 0.1 percent).” (1/10th of 1% or 1 out of 1,000); and Those (95%) who recover completely from hepatitis B infection acquire life-long immunity (this is a good thing).

According to Robbins Pathological Basis of Disease (a medical textbook published in 1994), of those who do not recover completely, fewer than 5 percent become chronic carriers of the virus with just one quarter of these in danger of developing life threatening liver disease later in life.

Translation: Of the 5% of people who do not recover completely from hepatitis B infection, 5% will become chronic carriers and ¼ of them will eventually die from Hep B related liver disease.

What does this mean? It depends on which statistics you look at. Let's take the worst-case scenario and go with the "200,000 new cases yearly" cited in the 1999 video from ABC's 20/20 show.

• 200,000 x .95 = 190,000 will recover completely (95% will recover completely)

Of the 5% of people who do not recover completely from hepatitis B infection, 5% will become chronic carriers and ¼ of them will eventually die from Hep B related liver disease.

• 10,000 will not recover completely
• 10,000 x .05 = 500 will become chronic carriers
• 500 x .25 = 125 will die in later life due to liver disease

Are we over-reacting and over-vaccinating as a result? Remember, it's not just the Hepatitis B we have to worry about, it's the aluminum. We, as parents, have to weigh the actual threat of disease against the cost of "protection." Given the amount of Aluminum contained in Hepatitis B vaccinations, AND the very low risk of young children becoming infected (if Mom is not infected), this particular vaccine does not seem worth the risk.

If Hepatitis B is not worth the risks associated with injecting aluminum directly into the bloodstream, AND if those who adamantly state that by delaying the Hepatitis B vaccines we, as parents are putting our children's health at risk, maybe we should start questioning further the advise we are getting from those who rigidly follow the party-line put out by the American Academy of Pediatrics (AAP) and the Centers for Disease Control (CDC). Despite the declarations of the AAP and the CDC that the huge amount of money they recieve from the vaccine manufacturers does not influence the advice they give to parents, delving further into the facts about Hepatitis B (one vaccine out of MANY the AAP and CDC have declared as "safe") leads me to believe that these sources may not be completely vested in the best interest of my child - or yours.

PLEASE - do not follow blindly everything you are told by your pediatrician or family physician. Ask first if he or she has actually looked at the science, or if your trusted health advisor is simply following the party-line. And remember - ultimately you, as the parents, are the ones who are responsible (and who will live with the consequences) for the decisions you make about your child's health. The pediatrician may order the shots, but he or she is not the one who will be raising your child for the rest of his or her life.

Educate before you vaccinate.

Marci

Swine Flu - Why Mexico City? It's Evansville in July

I have been working nonstop this month doing a series of presentations about biomedical interventions for autism. So far, I've finished and presented seven different talks, which presented information about immune disregulation, gastrointestinal illness, labs, diets, supplements, and the association of environmental toxins in the epidemic of autism. Tomorrow night I will be talking about vaccines. In preparation for tomorrow night's talk, I have been learning about why things like aluminum and mercury are put into the vaccines in the first place. It has to do with their effects on preserving and enhancing viral activity. This worries me, because I also know from my research and presentations, that there are several other toxins, including heavy metals like arsenic, lead, and cadmium, that also change the way the body handles viruses. This is what has been bothering me all day today.

Today, instead of preparing for tomorrow night's talk, I am consumed with the breaking news about the Swine Flu. As of the afternoon there are 40 confirmed cases in the United States. Apparently the largest cluster is among a group of students in New York, who had traveled to Mexico for Spring Break. There has been much commentary on the news about the fact that the cases in the U.S. (thus far) have been mild compared to the spectrum of illness that is currently ravaging Mexico City. This begs the question, "Why is it so bad in Mexico City?" We need to figure out the answer to that question if we are to predict where the pandemic will be most severe in other parts of the world, including here in the U.S.

As I have been pondering (obsessing about) this question today, I keep getting a sinking feeling in my gut. The reason is because I know too much. That's not a compliment to myself, it's a statement that explains why I have so much trouble sleeping some nights. I have an incessant need to know "why" things happen. In this case, you will have to judge if this is a good thing.

The sinking feeling in my stomach is related to something I remember from the second Defeat Autism Now! Conference I attended (April 2007). There was a presentation given by Dr. William Rea, from the Environmental Health Center in Dallas, Texas. The presentation was entitled, "The Environmental Aspects of ASD; The Early Mechanisms of Chronic Degenerative Disease and Hypersensitivity." I know, that's a long title. Much of the presentation was about the impact of toxins (heavy metals, pesticides, organophosphates, etc.) on the immune system and the subsequent link to autism. This will not sound like Greek to anyone who has researched the issue of thimerosal (mercury) or aluminum in vaccines and their effects on viruses.

Anyway, the main thing I remember from Dr. Rea's presentation was a photograph of Mexico City and the smog there. When I got home this afternoon, I pulled out my binder from that Conference and looked up Dr. Rea's presentation. I found the photo of Mexico City, and written above it, in my handwriting, is "Evansville in July."

So, I googled "Mexico City" and "Air Pollution." Here is what I found:



Mexico City ranks at the top of the list of "Most Polluted Megacities" in the world, according to Maricela Yip and Pierre Madl, authors of an interesting paper, completed while they were students at the University of Salzburg in Austria. It appears the paper was published under the direction of Dr. W. Hofmann, and the Department of Biophysics, "in Cooperation with the Afro-Asian Institute (Salzburg, Austria) and International Laboratory for Air Quality and Health at QUT (Australia)."

I honestly don't know how impressed I should be by these authors or whether or not the source is a "valid" one. However, when I read the article (actually skimmed it, due to time constraints), several bells went off. Why is this relevant to Southwestern Indiana?

The article talks about the specific toxins that are ranked "severe" and "heavy" in Mexico City: Sulfur Dioxide, Particulate Matter, Lead, Carbon Monoxide, Nitrogen Dioxide, and Ozone. These are some of the same toxins that cause Southwestern Indiana to have more PPM and Ozone Alert days in the summer than they have in Los Angeles. If you think I'm joking, check out the EPA website for yourself. And, like Mexico City, we live in a valley, so the toxins get trapped here. If you have ever read this blog before, you have probably read some of my "rantings" about these toxins and the health effects of living in the "Coal Burning Power Plant Capital of the World."

I am not going to reprise my rants here, but if you would like to learn about what's in our environment and how it relates to this discussion and your children's health, please read the previous posts: It's In the Air In Southwestern Indiana and Environmental Toxins and Autism. (click on the title to go to the original post.)

To learn about how the air pollution in Mexico City may be contributing to the high levels of deaths from the Swine Flu, please read the article, Air Pollution in Mexico City by Maricela Yip and Pierre Madl.

If there really is a connection here, we need to take steps now to beef up our immune systems by taking antioxidants and natural anti-virals like grapefruit seed extract and olive leaf extract. This will be especially important for groups whose immune systems are already compromised by persistent viral infections (herpes, HIV, Epstein-Barr, etc.). This includes children with autism, ADHD, asthma, and allergies. It also includes adults with chronic fatigue and fibromyalgia.

Don't panic, but now is the time to prepare. If there is a connection between the air pollution and the flu virus, places like Southwestern Indiana may have a lot more to deal with in the near future than high rates of autism, cancer, and suicide.

I hope I'm wrong.


Marci

Preparing Your Body for Pregnancy; Preparing Your Child for Vaccination

If you have read much about biomedical interventions and recovery from autism, you may be familiar with the analogy of being hit by a bus. As Stan Kurtz writes, “You cannot be cured of being hit by a bus, but you can recover from it. You might even be able to recover enough that you do not need to park in special parking spaces when you go shopping. If you are fortunate enough you might recover well enough that you gain back so much of your functioning such that no one would know you were ever in an accident.” This is a great analogy, especially for those children who have already received a diagnosis of autism. In many cases, while we may not be able to “cure” the autism, if we address the underlying conditions through appropriated testing and treatment, we may be able to recover the child to the point where he or she no longer meets the diagnostic criteria for autism. In many cases, no one would ever guess the child had been “hit by the bus” in the first place.

But wait…

What if we could prevent your child from being hit by the bus in the first place?

Let’s think about pregnancy. When a fetus is growing in the womb, it is incubating. We have been told for some time now that pregnant women should not smoke and should not drink alcohol, because these behaviors are known to be damaging to a developing fetus. The peer-reviewed medical literature is bursting at the seams with paper after paper, documenting the research findings about the teratologic effects of tobacco and alcohol.

Teratologic: the scientific study of visible conditions caused by the interruption or alteration of normal development

Marci’s note: Teratological effects may well include effects that are not “visible” and which may not become known for a long time after the exposure that caused the damage. Examples:

• Babies who were fed soy formula. Soy is a source of estrogen. When fed as the sole source of nutrition, the amount of estrogen taken in can disrupt the balance between hormones, and may contribute to the early onset of puberty in girls, and delayed onset of puberty in boys.
  
• Terbutaline administration. Terbutaline is a medication given to women to stop preterm labor. It has been linked to later onset of learning disabilities and social deficits in children whose mothers took the drug during pregnancy.
  

By now, everyone has heard that there is an epidemic of autism in this country. There are some people who still want to deny this fact, but the evidence is overwhelming, and it is real. It’s not just because of more inclusive diagnostic criteria. It’s also not purely genetic. There is no such thing as a genetic epidemic. So what’s going on? And why can’t the researchers figure out the cause of autism?

The clue is in the previous question. As long as researchers are looking for “the cause” of autism, they are not going to find it. Why? Because multiple factors working together synergistically is the source of the epidemic. There is no single “smoking gun.” If you are not familiar with the concept of synergism, you need to understand this key concept. Here is the definition:

Synergism: the phenomenon in which the combined action of two things such as drugs or muscles is greater than the sum of their effects individually. In the case of drugs, the result may be dangerous to the patient.

Marci’s note: in the case of toxins (heavy metals, toxic chemicals, pesticides, organophosphates, food additives), the combined action of two (or more) things is greater than the sum of their effects individually. The result may be dangerous to the patient. Alternatively, the synergistic effect of a genetic predisposition and an environmental exposure (to metals, pesticides, medications, etc…) will be more damaging than the effects of either situation (genetic or environmental) alone. The result may be dangerous to the patient. (Remember that in this case, the patient is the infant in the incubator.)

Synergy is an extremely important concept when it comes to autism and other neurodevelopmental disabilities. The concept of synergy is precisely why families who have sought relief through “The Vaccine Court” have not been successful in establishing that their children’s regressive autism was caused by the combination of thimerosal (mercury) and the MMR vaccine. (Note: the basic premise of the argument is that the child’s immune system is compromised by mercury (a heavy metal, which damages multiple systems in the body, including the enzymatic processes, and detoxification pathways), predisposing the child to be more vulnerable to the effects of the MMR vaccine (a vaccination which simultaneously injects three separate viruses into the blood stream, bypassing the body’s primary immune defense mechanisms (gastrointestinal and respiratory), ultimately resulting in a situation which overwhelms the body’s defenses and leads to chronic illness (fever, vomiting, diarrhea, constipation, ear infections, respiratory infections, chronic tonsillitis, strep, bronchitis, allergies, asthma, & seizures), which later results in the behavioral and cognitive symptoms that lead to an “autism spectrum disorder” diagnosis.

Please remember that the fever, diarrhea, constipation, vomiting, seizures, etc… tend to occur prior to the behaviors that lead, ultimately, to the “autism” diagnosis. This is an important piece of information, especially since most parents I have spoken with report that the “experts” who diagnosed their children with “autism” often state (with considerable authority) that the physical symptoms (diarrhea, constipation, vomiting) the parents are reporting are “just part of autism.” The physical symptoms are therefore ignored. This is PRECISELY why professionals who do not look further than the obvious behavioral and cognitive presentations, can and do state (with considerable authority), that “Autism is a lifelong condition and there is nothing you can do about it.” From where I sit, it looks like the authorities have it backwards. The physical symptoms happen first and the behavioral and cognitive symptoms happen as a result of the physical symptoms. Therefore, the lack of eye-contact, reduced awareness of the environment, inattention, aggression, and poor social skills are “just part of the gastro-intestinal disease” and if we do something to fix the GI problems, the symptoms associated with the child’s “autism” diagnosis will improve. If this sounds like voodoo science to you, let me phrase it differently.

Consider, for a moment, symptoms that you yourself might have had. Have you ever had a migraine? Have you ever had a “stomach virus” with nausea, pain in your gut, diarrhea, constipation, achy joints, headache and ‘brain-fog?’ If you have, please try to recall at this moment what it felt like. Now, imagine you are in a room full of four year-olds – a preschool environment. Do you feel “social?” Can you concentrate? Are you likely to learn and “achieve on par with your potential?”

If you only consider “autism” – which is a behavioral and cognitive-based diagnosis – and do not look further, the professionals who tell you with so much authority, “There is nothing you can do” are probably correct. If you don’t look beyond the behaviors and the label, it is likely that you are facing a lifelong diagnosis, for which you will not see significant improvement. In other words, your child will most likely never get married or have children, will probably not be able to live independently, will most likely not be able to support himself or herself, and will require full-time support from you until the day you die – which will probably happen prematurely due to all the stress you will endure in the interim. And your marriage? Statistics indicate that the divorce rate among couples with autistic children is 85%. Is this a good time to talk about the economy and the difficulties of single parents raising a child with autism?

I realize I am being brutal. I apologize for that, but not for the need to be honest. Grab a tissue, have a good cry, and suck it up because this discussion is relevant to your life. It is especially relevant if you are considering having children in the future.

“Current Events” time!

On February 12, 2009, the National Vaccine Injury Compensation Program (Vaccine Court) Special Masters ruled against three families of autistic children, whose histories were chosen as “test cases” in the plaintiffs’ efforts to legally establish causality between thimerosal, MMR, and the children’s regression into autistic symptoms, which happened to occur shortly after receiving the vaccinations.

It was reported that one factor which helped sway the decision against the families is that they claimed their children were “developing normally” prior to the administration of the MMR vaccine. The Masters, upon review of photographs, videos, and medical records of the children in question, concluded that the parents’ claim that their children were “developing normally” was untrue. As I recall, the opinion of the special masters cited things like videos and photographs showing inconsistent eye-contact prior to the MMR administration. This concept of “normal development” hit me like a ton of bricks when I read it.

What does this statement mean, “Developing Normally?”

When I think about this question, the first thing that comes to mind is how shocked I have been and continue to be, when I ask parents the following question, “Did your child have a lot of ear infections during the first four years of life?”

The answer I frequently receive is, “Not a lot. No more than any other children.”
My response: “How many ear infections does your child typically have in a year?”
Typical response: “Three or four.”

What is important about the conversation, as reported above, is that most parents I interview report that their child is having three or four ear infections per year (which are treated with antibiotics) and the parents are also reporting that their child is no different from other children who are “developing normally.”

This is a problem.

Another area where I see a problem involves constipation. My developmental history form specifically asks about constipation and the majority of children I see have had significant problems with the frequency of bowel movements. Several have had to go to the hospital multiple times because their bowels have become impacted. Many parents have told me that they have expressed concerns to their pediatricians or family doctors, regarding their children’s infrequent bowel movements (often once a week or less), only to be told by their trusted physician, “In some children, that’s normal.”

Bowel movements are the body’s way of clearing toxins. (The body also clears toxins through urination and sweating.) Some toxins will ONLY clear the body through bowel movements. If you have toxins building up in the body and the half-life of that toxin is, let’s say 3 days, and the child in question is only having a bowel movement every 7 days, then if that toxin is taken into the body (perhaps through vaccination) and the child does not have a bowel movement for four or five days after taking the toxin it, where do you suppose the toxin goes? It gets stored in the body. Some of it goes into the soft tissues like kidneys and bone marrow. Some of it goes into the brain. Once it’s stored, it’s hard to get it out.

The gist of this is that our children are NOT developing normally if they are having chronic constipation (or diarrhea), or if they are having chronic bacterial and viral infections, upper respiratory infections, bronchitis, tonsillitis, strep, allergies, and asthma. We have an entire generation of children who are more prone to illness than children who are truly “developing normally.” The problem is, we have become so accustomed to this that we now accept this situation as “normal.” This needs to change.

So, going back to the concept of teratology – things that disrupt normal development … In order to prevent more children from being “hit by the bus,” we need to pay closer attention to the things that may disrupt “normal development,” starting before conception even occurs. We need to prepare the incubator. For those children who are already here, we need to assess the status of their overall health and development BEFORE we inject them with multiple viruses simultaneously, and BEFORE we allow anyone to inject them with substances (thimerosal, aluminum, formaldehyde, etc.) that are KNOWN to have teratologic effects. Remember, the first rule of vaccinations is “do not vaccinate a sick child.” The problem is that when we view children with chronic conditions (viruses, bacterial infections, etc.) as “normal,” our perception of what constitutes “a sick child” has been skewed. Those are the children who are being “thrown in front of the bus.” My point: If we identify (accurately) those children who ARE sick, and get them healthy BEFORE administering vaccinations, we are likely to decrease the numbers of children who subsequently regress and end up receiving an autism diagnosis.

Back to the main question at hand – what do you need to do to increase your chances of having a healthy baby – one who stays healthy and does not become part of the estimated 1 in 67 American children with an autism spectrum disorder?

1. Don’t wait until you are pregnant to start preparing your body. Remember, you are the incubator. Imagine for a moment that you have just delivered a baby that was born premature, and had to be placed in the NICU (Neonatal Intensive Care Unit) of the hospital. When your precious infant is taken from your womb and placed in the incubator in the NICU, you expect that the incubator will be a healthy environment for your fragile infant. By healthy, I mean, you expect that the incubator is free from bacteria (strep, staph, clostridia), viruses (Herpes, Measles, Varicella [Chickenpox], Human Papilloma Virus, Epstein-Barr, Cytomegalovirus), yeast (candida albicans and others), and parasites. You also expect that the incubator your infant is placed in will not be contaminated with heavy metals (lead, mercury, antimony, arsenic, cadmium, aluminum [not technically a ‘heavy metal’]), and that the incubator will not be sprayed with pesticides or contaminated with organophosphates. In essence, what you expect, is that your precious baby will be placed in a pristine environment, in which he or she will be able to develop, to his or her full potential.
   

If you expect strangers to care for your baby this way, shouldn’t you do everything you can to care for your future child with the same concern?

This entire thought process should start at least one to two years before you become pregnant.
If you are a patient at Cady Wellness Institute (CWI) or considering becoming a patient here, you probably live in the Tri-state (Indiana, Kentucky, Illinois). If you have lived here for any length of time, you have been exposed to heavy metals (from coal-burning power plants), pesticides and organophosphates (from farming). If you get annual flu shots and have not specified that you want thimerosal-free flu shots, you have had a yearly dose of mercury injected directly into your bloodstream.

If you live in an area where you are regularly exposed to heavy metals and other environmental toxins, you owe it to your future children to find out what toxins have built up in your system, before you make it an incubator for your future child. You would not want your child to be placed in a hospital incubator contaminated with bacteria, viruses, and toxins (metals, pesticides, organophosphates), so why would you allow your child to spend the most important growing stage in just such an environment. If you do not pursue primary intervention that assesses your own body stores of these toxins, that is exactly what you are doing. The incubator is contaminated.

Clean it up before you trust it with the future of your precious baby.

2. If you are the parent of a young child and you are concerned about whether or not to vaccinate him or her, you need to become informed about your options as a parent. One of those options I would encourage is to have your child evaluated first to determine if there are physical problems that should be addressed, prior to vaccination. This may be especially important if your child has gastrointestinal problems, or recurrent viral and/or bacterial infections.

To learn more about assessment for genetic vulnerability and toxic exposures before you get pregnant, or before vaccinating your child, contact Marcella Piper-Terry, M.S.; Biomedical Consultant; Cady Wellness Institute.

Rappoport Raises Important Questions About Vaccines

First, let me say that prior to today, I have never heard of Jon Rappoport.

I have been catching up on emails, which have been sorely neglected during the Christmas break. This evening I clicked on a post from one of the groups I shadow, and followed the link to this, which is said to be an interview of a former vaccine researcher, who does not want to use his own identity because of the consequences of doing so. (If this is true, his decision is completely understandable.)

If this is not true, I still believe it is worth posting, as there are many questions that need to be asked, which may come from more interested people having access to the dialogue (scripted or not).

I encourage parents to research the vaccine issue and make informed decisions before injecting anything into their child's body. Make your own decisions.

Marci


http://avropa.spaces.live.com/blog/cns!5F6877002CEECEB3!1964.entry

O'Bama: Please Change Government Stance on Autism!

Hello All:
There is currently a forum on Change.org - which will allow you to submit or vote for ideas that you believe President-elect O'Bama needs to address for change when his administration is ushered into power. Please go to the following link and vote for change for our children with neurodevelopmental disabilities, including autism:

http://www.change.org/ideas/view/bodies_in_rebellion

And visit the Bodies in Rebellion site to learn more:

http://www.bodiesinrebellion.com/

Here is one of the latests posts on the Change. org site: (Lots of information well worth your time to investigate.)

Blessings.
Marci


For all those that want to understand the realtionship between mercury and autism read the article "Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set.

http://bodiesinrebellion.com/BloodLevelsofMercuryRelatedtoAutism1.pdf

The symptoms of mercury toxicity and autism are almost identical: Thimerosal and autism? A plausible hypothesis that should not be dismissed . Medical Hypotheses , Volume 62 , Issue 5 , Pages 788 - 794 M .

Blaxillhttp://www.nomercury.org/science/documents/Med_Hypoth_Blaxill_Redwood_Bernard.pdfFor

Those that do not understand how serious a problem autism is... just read all these comments parents and relatives are making. Do a search for Dr. Boyd Haley, University of Kentucky, Dr. Mady Hornig, Columbia University, Dr. Thomas Burbacher, University of Washington; Dr. Mark Geier, President of The Genetic Centers of America and David Geier, Vice President of The Institute of Chronic Illnesses, and Dr. Jill James, University of Arkansas. They're just a few of the independent scientists whose findings link unsafe vaccines to neurological damage in our children. Research on vaccines can also be found on this link:

http://www.generationrescue.org/studies.html

The National Autism Association has said that while officials continue to claim that there is no science linking vaccines to autism, many peer-reviewed published studies confirm the connection between vaccinations and neurological injuries.

http://www.national%20autismassociatio%20n.org/library.%20php

Look at what the former head of the NIH has to say:

CBS News Exclusive: Former Head Of NIH Says Government Too Quick To Dismiss Possible LinkSEE VIDEO

http://www.cbsnews.com/stories/2008/05/12/cbsnews_investigates/main4086809.shtml

Healy said that officials have been too quick to dismiss a link between vaccines and autism without ever studying the group that got sick. There never have been studies done on the kids that developed symptoms of autism within a few weeks of being vaccinated. She furthermore pointed out that the Institute of Medicine which produced the cumulative study on vaccines and autism in 2004 refused to 'pursue susceptibility groups.' In other words, they didn't want to find any evidence that linked vaccines to autism. She left us with the haunting statement: 'The question has not been answered.'

In the current issue of U.S. News and World Report, A Government Call for Vaccine Research, Dr. Healy again calls for more research into vaccine safety. This ad ran in USA Today on Feb 12 and 29: Green our vaccines. And administer them with greater care.

http://www.generationrescue.org/pdf/080212.pdf .

It shows what happened to the vaccine schedule since 1983 and it lists the toxic ingredients like mercury, aluminum, MSG, ether, formaldehyde, and anti-freeze commonly found in vaccines. The soaring increase in autism directly coincided with the dramatic escalation of the number of vaccines. It's important to note that there has never been a study done on the cumulative effect of so many vaccines with toxic ingredients so soon on the health of a baby. This is also the time period in which autism went from one in 10,000 children to one in every 150 on average in the U.S. The official autism rate is one in 150 children. In the 1970s, the rate was one in every 10,000 kids. The CDC gave us the figure of one in 150 in Feb. 2007, but it was based on studies of eight year olds done back in 2002 and 2000. Those children are now 14 and 16 years old. This can hardly be considered a true picture of the autism disaster. In Minnesota, the recognized rate is one in every 81 kids. Others put the national average rate at one in every 67 children. Among the Somali immigrants in Minneapolis, the autism rate for American-born Somali children is one in every 28 kids. And these children are ones with classic autism. They could hardly have been misdiagnosed. One in every six schoolchildren now has a diagnosis of a learning disability.

Autism, once a rare disorder, is now so common that everyone knows someone with an autistic child and no one can reasonability tell us why. When we read about autism, it's always about kids with autism. Where are the 30, 50, and 70 year olds with autism like we see in our children? We should all be worried about what will happen when hundreds of thousands of children with autism age out into the welfare system. They'll become the responsibility of the taxpayers. We do not currently have a significant adult population with autism, but that will soon be changing and the cost of their support and care will be massive. Findings by Michael Ganz at Harvard make a chilling prediction of the future cost to our society. Ganz projects that it will cost about $3.2 million to take care of ONE autistic person over his or her lifetime. His findings are felt by others to be a gross underestimate of the eventual autism price tag.

Autism Has High Costs to U.S. Society, press release of Tuesday ...

The words of Laura Bono of the National Autism Association are a grim forecast for the future: "As those children reach adulthood, the U.S. is ill-equipped to care for them. Not only do we not have enough services for adults now, the light at the end of the tunnel is a train. Frankly, we don't know what we're going to do."

Click the link below to view this discussion.

http://www.change.org/ideas/view/bodies_in_rebellion

Lead in Wild Game, Venison, Be Careful What You Eat!

The following article is important, especially for those of us with sick children, who also live in areas of the country where wild game consumption is part of how families get by.

The take-home message is: Think about every aspect of your life, especially if you have a child with autism or other developmental disability. Also, please remember that lead only shows up in blood for a short period of time after exposure. It is stored in soft tissues, including bone marrow and the brain, for decades after initial exposure, and the effect is cumulative. In other words, it adds up. Just because it doesn't show up in blood doesn't mean it's not in your body (or your child's body).

Lead is also passed from mother to child in utero and through breast milk, so if you have eaten a considerable amount of wild game in your life and are thinking about getting pregnant, you may want to have a hair analysis and urine provocation test prior to conception. Get the lead out before you pass it on to the next generation.

Take care.
Marci

Study links lead in blood to wild game consumption

By JAMES MacPHERSON, Associated Press Writer James Macpherson, Associated Press Writer – Wed Nov 5, 8:58 pm ET

BISMARCK, N.D. – North Dakota health officials are recommending that pregnant women and young children avoid eating meat from wild game killed with lead bullets.

The recommendation is based on a study released Wednesday that examined the lead levels in the blood of more than 700 state residents. Those who ate wild game killed with lead bullets appeared to have higher lead levels than those who ate little or no wild game.

The elevated lead levels were not considered dangerous, but North Dakota says pregnant women and children younger than 6 should avoid eating venison harvested using lead bullets.
Those groups are considered most at risk from lead poisoning, which can cause learning problems and convulsions, and in severe cases can lead to brain damage and death.

The study, conducted by the federal Centers for Disease Control and Prevention and the state health department, is the first to connect lead traces in game with higher lead levels in the blood of game eaters, said Dr. Stephen Pickard, a CDC epidemiolgist who works with the state health department.

A separate study by Minnesota's Department of Natural Resources previously found that fragments from lead bullets spread as far as 18 inches away from the wound.

"Nobody was in trouble from the lead levels," Pickard said. However, "the effect was small but large enough to be a concern," he said.

Pickard said the study found "the more recent the consumption of wild game harvested with lead bullets, the higher the level of lead in the blood."

Officials in North Dakota and other states have warned about eating venison killed with lead ammunition since the spring, when a physician conducting tests using a CT scanner found lead in samples of donated deer meat.

The findings led North Dakota's health department to order food pantries to throw out donated venison. Some groups that organize venison donations have called such actions premature and unsupported by science.