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Rashid Buttar And the Autism Industry

17 Jun

Its a few days short of a year since I wrote my original piece on Rashid Buttar – a piece that drew equal amounts of amusement and hostility depending on one’s viewpoint. I received many comments regarding how nasty I was to a poor, dedicated doctor and so I thought it fit to take another look at Dr Buttar and re-examine some of my comments and look at some things I didn’t previously look closely at.

TDDMPS Revisited

In my previous posts I was skeptical of the efficacy of Buttar’s TD-DMPS product, however I noted that Buttar had stated that:

In a study due to be released by the winter of 2004, conclusive data was accumulated regarding the efficacy of a specifically formulated transdermally applied combination of DMPS conjugated with a number of peptides, called TD-DMPS

And yet, a search of PubMed still – 18 months after the stated release date – reveals _no_ such study. If anyone has a copy of this elusive study I would love to see it.

Interestingly, as I (and Orac) also reported, Dr Buttar seems to be moving away from TD-DMPS, once lauded as the holy grail of autism treatments, in favour of an IV EDTA protocol. The reader can make up his or her own mind about why that might be.

Rashid Buttar: Man Of Letters

Rashid Buttar has an impressive amount of letters after his name and an equally impressive amount of fellowships and board certifications on his CV.

Fellow – American Academy of Preventative Medicine
Fellow – American College for Advancement in Medicine
Diplomat – American Academy of Preventative Medicine
Diplomat – American Board of Chelation Therapy
Board Eligib – Board Certification in Emergency Medicine
Diplomat – American Board of Clinical Metal Toxicology
Diplomat – American Association of Integrative Medicine
Diplomay Candidate – Board Certification in Emergency Medicine
Diplomat Candidate – American Board of Anti-Aging Medicine
Member – National Metals Task Force
Member – American Association of Physician Specialists
Member – International College of Integrative Medicine
Member – International Hyperbaric Medical Association
Member – International Hyperbaric Medical Association Foundation

Wow! Thats pretty impressive. Until we actually look a little closer.

In the US, its the American Board of Medical Specialities who oversee which boards are legitimate and which are not. They have a full list of accepted board certifications online. Of the ten individual associations listed as being ‘American’ or ‘national’ above, *only one – the American Board of Emergency Medicine – is recognised* and this is one that Buttar lists himself as simply being eligible for, not a member, diplomat or fellow of.

So the ‘veneer of respectability’ Rashid Buttar has constructed for himself reveals itself as not in anyway officially recognised. Is such official recognition important? I guess that would depend on who you asked. If you asked autism/thiomersal believers then its not important at all. they would say that such omissions reflect the ongoing conspiracy to ensure only mainstream medicine keeps itself in business by excluding pioneering mavericks like Rashid Buttar. If you asked everyone else they’d probably say it was important because recognised board certification reflects the fact that a member, diplomat or fellow has a certain, scientifically valid level of expertise within a given subject. Or that a given subject is recognised to have a beneficial effect. There is a lengthy document explaining what a medical specialty has to do to gain ABMS approval.

Boards not recognised by ABMS are self appointed and thus free to offer membership based on whatever criteria they see fit.

I did note that there were a few certifications Dr Buttar has missed out on – however he can easily rectify that situation with certification that is as equally – if not more – credible as his current certification.

Rashid Buttar: Man of Science

One of the most intriguing statements on Rashid Buttar’s CV is this:

Visiting Scientist, North Carolina State University

So I popped along to NCSU to have a look and sure enough, Rashid Buttar is listed in his role as ‘visiting scientist. However, what his CV fails to mention is that his chosen specialty is ‘Food Science’, a science that up until now I’d never heard of. Luckily, NCSU have a handy page that defines it for me:

Food Science is what happens to food from the time it’s harvested (or from it’s beginning in a lab) until you swallow it

I think we can all see just how vital this sort of science would be in autism research. Why do I get the feeling that at some point we’ll be seeing the emergence of Buttar Bread? Tasty and Gluten Free!!

Rashid Buttar: Crusading Maverick

In an amusing piece of one-sided propaganda, Rashid Buttar is portrayed as a poor, hard done by hero:

Buttar and eight other integrative doctors from across the state decided they’d had enough. They formed the North Carolina Integrative Medical Society and hired their own lobbyist to work on changing state law. At an April press conference attended by a mere three members of the media, plus lawyers for the medical board and members of the medical society, Buttar’s hand shook as he blistered the medical board for the way it treated integrative doctors.

Two weeks after Buttar’s blistering testimony at the legislature, a letter arrived in the mail from the medical board inviting him and his attorney to appear before the board to answer questions about his practice of medicine and advising him that his rights would be read to him when he appeared. When Buttar declined the invitation, the board subpoenaed him to appear before them.

After two years of harassment and $20,000 in legal fees, Buttar emerged from the hearing poorer but with his clean record intact.

Poor Rashid couldn’t quite seem to grasp why he and his fellow ‘integrative practitioners’ should have to answer to medical authorities like everyone else. And how about that $20,000 legal fee? Ouch.

Rashid Buttar: Fairly Recompensed?

So there’s our hero, 20 grand out of pocket. What does a crusading maverick with an interest in picking food and invented board certifications do? Why he starts getting some money of course! He either set up or joined V-SAB medical labs, which is again listed on his ‘autism buster’ CV….except that just like his ‘visiting scientist’ status, this position doesn’t seem to have much to do with autism. Chemidex lists V-SAB under _’Personal Care & Cosmetics’_ . Go figure.

He has also established ‘Advanced Medical Education & Services Physician Association’ (AMESPA), which is essentially a training facility to allow other practitioners to learn at the feet of Rashid Buttar all the secrets he knows to cure autism, cancer and reverse old age. For this service he charges $20,000 for a five day course. Coincidentally the same amount as two years worth of legal fees when being investigated by North Carolina health authorities. Dr Buttar has no less than 15 testimonials on his site from satisfied practitioners. Thats a cool $300,000 – but not to worry, I’m sure those practitioners will easily recoup their investment from their patients – the autism industry is a growing one after all!

But Buttar hasn’t forgotten his patients. Oh no.

Rashid Buttar: Caring and Sharing

While Dr. Buttar….is also one of those practitioners who receives a lot of complaints. In my opinion, Dr. Buttar’s latest chelation protocol is too invasive and risky. His rates are obscene, too.

(Autism-Mercury Yahoo Group)

Obscene rates? Surely not! Lets take a further look.

Dr. Buttar is asking for $800 for consultation fee (1 hr max) on his Dallas conference on June 16th-17th. I fell off my chair when I heard it.

(‘dingwendy’ CK2 yahoo Group)

We started with Dr. Buttar and $20,000 out-of-pocket expenses later (yes,in a little over a year!)…

(‘plumbrok’ CK2 Yahoo Group)

Wait, $20,000 _in a year??_ Thats…what….the same amount as _two_ years worth of legal fees when being investigated by North Carolina – guess Buttar was easily able to get that money back.

‘plumbrok’ continued:

..he had an unusually strict set-up, as Tracy put it, “My way or the highway” – every supplement had to be purchased through his office and at the time we saw him, he would not accept any substitutes.

Well of course! Only his products = only his profits. This is not a stupid man. However, for that $800 per hour I bet these people get _great_ service!

I do want you to become aware Dr. Buttar treats Cancer and Heart Disease patients. It is his Nurse Practioner that handles all the Autism children and Dr. Buttar reviews the files each week. Very rarely do patients get to see Dr. Buttar. I understand he is trying to see new patients the first time they are in the office, but there is no guarantee as he travels around the country lecturing on various topics and may not be around.

(‘punkinsmama1999’ CK2 Yahoo Group)

Yes, Dr Buttar does not see a lot of his autism patients more than once but oversees the protocol.

(‘Susan Fund’ CK2 Yahoo Group)

So it seems that your $800 per hour gets you an hour with Buttar’s nurse and that you probably won’t get to see Buttat himself above once. It also transpires that to be on his protocol you must buy _all_ supplements from him and him alone. Is his reputation suffering?

Is he really reversing Alzheimer’s? I find that Dr. Buttar talks a lot but produces little evidence.

(‘noaholiviaian’ CK2 Yahoo Group)

The crown seems to be slipping.

Im sorry, but I cant help but to think that with such an outrageous hourly rate, it is praying on parents who are desperately seeking the comforting assurance of a medical practitioner….I know that most parents would willing cut off their own right hand if it would help their kids… and Dr. Buttar knows that as well.

(‘rheaton_stormcast’ CK2 Yahoo Group)

As touched on above, Dr Buttar also treats cancer. I made mention of this in my first blog post about Buttar and discusses his biggest fan – Cajun Cowboy – who had this to say about Dr Buttar:

He (Dr Buttar) told me that most of his patients were much worse off than I and that God had Blessed me by giving me a wake up call and that he could enable my body to heal itself! Now that is the first time I have ever heard a Doctor say he could enable my body to heal cancer.

So I thought I’d drop in on Cajun Cowboy’s site to see how things were going. I was a little surprised by what I found:

All the information about Dr. Buttar is still on this site but I no longer am one of his patients and I do not recommend him to any one for any reason. If you go to him for treatment BEWARE, BEWARE and read Roger Mason’s books first and go to QuackWatch.org first!

Seems like Cajun Cowboy has had something of a change of heart.

Now as far as Dr. Buttar goes read what is said about almost every modality that he practices at QuackWatch.org. Now I new (sic) what was on this site and I new (sic) you have to take it with a grain of salt but for me, most of their opinions concerning Dr. Buttar’s treatment may be true! What I can say for sure is that they did not work for me after over $150,000.00 dollars and two years of treatment!

$150,000 worth of ‘treatment’ that appears to have done nothing at all. Cajun Cowboy sounds quite bitter about the whole thing. Why for $150,000, Buttar could afford to be pursued over 7 times over 14 years by the North Carolina medical authorities and _still_ make a $10,000 profit.

Rashid Buttar: Living The American Dream

Business and free enterprise are the American ideals. On a much smaller scale we could easily equate the level of success Rashid Buttar has had with say a company like…oh I don’t know…Enron. They were successful for quiet some time.

Rashid Buttar is making a very very good living out of his autism cottage industry and so far he’s managed to do it on the back of some fake respectability generated from meaningless board certifications, without publishing any studies (despite repeated promises to do so) into the efficacy of his treatments and by charging people who consider themselves as desperate a lot of money for receiving an ‘interesting’ level of personal service. Along the way he’s keeping his friends sweet by teaching them his methods and is also getting a good slice of money from them too.

Wonder what things will be like a year from now?

A Dateline Participant Speaks

14 Jun

_This comes from Autism Street. The whole post is here. I’m going to reproduce the post then shut off comments here. Please comment at Autism Street._

My wife recently told me about an acquaintance of ours (through a local online parent group) who had just withdrawn from the Arizona chelation study at the Southwest College of Naturopathic Medicine. It had been I long time since I had exchanged any sort of messages with her or the group, so I sent her an e-mail to ask her about it.

Boy was I in for a wonderful surprise – a return message full of love and acceptance for a wonderful child! This was interesting to me, because I was curious how the influence of media like NBC’s Dateline or Autism Speaks may or may not have played a part in her decision, especially since her daughter had actually appeared in the Dateline segment. I did not specifically mention Dateline or Autism Speaks in my original e-mail to her, but did ask if media was an influence.

We exchanged several more e-mails and discussed her guest blogging about this. Without any further ado, I’d like to welcome a guest blogger to Autism Street who will go by the name Belle. She’ll refer to her daughter as Mulan. I’ll ask Belle two questions, and she’ll provide her answers. Whether or not she fields any comments will be entirely up to her.

*Belle, what influenced your decision to participate?*

_”I had read a lot on chelation, and I was at one point in my life, ready to do “whatever” it took! It’s easy for parents to get hooked on all the hype and “doom and gloom” out there. If at one point I had read that I could get a child as cool and great as Mulan, then maybe I wouldn’t have been so quick to do “whatever” it took.”_

*How did you arrive at the decision to withdraw Mulan from the study?*

_”Thanks to time, discussion with friends, and Mulan herself, I decided to withdraw. I signed up for this about a year ago, got approved for it, and started the process. Since signing up, I had a lot of time to listen to others and to think more about what I was doing.”_

_”Then there’s Mulan. Mulan is doing soo well! I couldn’t ask for a child to be doing as well as her. If I had been told that she’d be doing as well as she is, I wouldn’t have believed what anyone was telling me. I know another local research nurse who has a son who is also doing really well. Sometimes it seems she’s the only one I know who doesn’t talk “doom and gloom”. I am taking her attitude. I do believe that with a lot of hard work on the parents’ part, discipline, and reality, your child can do a lot!”_

_”When I read about someone’s child who is doing such and such, and they attribute it to pills or chelation, I think, oh yeah, Mulan is doing that. And it’s not because of a pill or chelation, it’s because of good old-fashioned hard work! There’s a short movie that someone at [name removed] suggested I watch. It’s about how chelation has supposedly helped their children. It’s horrible! I thought that Mulan could easily be on that as well – I have pictures of her freaking of getting her picture taken, and then I could use her kindergarten picture, before hours of therapy and hard work, etc.”_

_”After seeing the piece on Dateline, and that clip from autism speaks, I am sick and tired of the “doom and gloom” attitude. Dateline showed Mulan for approx. 4 seconds. Both times, it appeared they tried to make her look like a freak. The first time she was up close to the camera and making a face. Those of us who know her, know that she’s vain and loves the camera. My dad always has the video camera and will turn it around so Mulan can see herself. Mulan was just doing her thing in front of the camera. I could see any and all of my kids doing what Mulan was doing, especially if it’s edited carefully. I’m sure I could find all three of my kids looking like freaks – they’re kids! Then they showed her getting her ears checked and she’s hand flapping. Yes, because of autism Mulan is a hand flapper when she’s excited. They couldn’t show the whole story let alone the fact that she’s a child with autism that has never seen this Dr. before, and was excited to have a check up.”_

_”They could have shown Mulan socializing with her siblings or communicating with the doctor, but they didn’t do that. Apparently Dateline would think it okay to have people believe that people with autism don’t socialize or communicate! Now I am going off on a totally different tangent, but I was sort of hoping that after seeing the show I would have changed my mind and decided to “go for it” with Mulan. Instead, it just made me more adamant that I wasn’t going to do this to Mulan. Before the show I just had a lot of fear.”_

_”Mulan has always been healthy. I’ve had her at the Dr. more than once convinced she had strep, and she didn’t. Actually, her siblings get strep, and she doesn’t. It’s weird in a way, but I’m not complaining! Mulan also hasn’t had any surgeries since she’s been diagnosed. She’s had nothing medical done to her, so I have fear of doing anything medically unnecessary to her. Not that I wouldn’t do anything for her medically, I would in a heart beat if she needed it. She doesn’t need DMSA, so I am choosing not to give it to her.”_

_”I want to clarify that I don’t blame the medical community for Mulan’s autism – she was born with it, I know that. I have seen my child take such great steps forward, that I fear giving her anything that might hurt her. I still give her McD’s, and candy with all the food coloring in the world. She will get an Icee at Target on occasion, just like her siblings. I guess some might say those things might hurt her, but that’s called living, and Mulan is living and functioning in her own cool way.”_

_”I just had Mulan’s first habilitation worker quit. This woman is the coolest woman ever. I thanked her for helping Mulan become the weird free spirit that she is. I love my weird free spirit, and I hope others can see how her free spiritedness is actually pretty cool, and not necessarily as weird as they first might think!”_

Creatinine, Chelation and Lupron…Oh my!

6 Jun

A recent news segment on NBC in America covered Chelation therapy as a treatment for autism. The response was as predicted. The pro-cure/biomed side went into raptures. Everyone else winced. As a UK resident I have to say that (sorry America) this seems to be a furtherance of the dumbing down of science in the US that has led to both this sort of report appearing on a serious news show and the joke of creationism being taught in science classes.

Anyway, thankfully, these types of things are still viewed by most people (over there and over here) as marginal and not representative of the truth. However, that doesn’t negate the fact that there is a lot of experimentation going on by so called ‘scientists’ and by some parents. My favourite quote so far from some retorting to the Dateline segment is:

A treatment used prior to proof is called an experiment.

ACSH.

So what can be said to be poorly understood and yet still be used?

Lupron for Autism

I recently had an interaction with a number of people on an Autism Biomed board after they stated that Lupron was ‘working miracles in recovering my child’. At least one of these people was someone who had assured me about a year ago that chelation was ‘working miracles in recovering my child’. A part of me fully expects to hear that car battery acid is ‘working miracles in recovering my child’ from the same person a year from now. After that? Tongue of Toad? Eye of Newt?

It was clear that the ‘scientists’ advising these people had not informed them of basic facts about the condition that was allegedly affecting their kids autism. Neither of them had had their childrens hand and wrist radiographed which is the standard way of determining if a child is undergoing Precocious Puberty or not. Basically, If bone age is within 1 year of chronological age, puberty has not started. If bone age is advanced by 2 or more years, puberty likely has been present for a year or more or is progressing more rapidly.

The single most basic fact about Precocious Puberty is that it is immediately subdivided into Central Precocious Puberty (CPP) or Pseudo Precocious Puberty (PPP). It is vital to make this difference as the treatment is different in each division. The division can only be made by testing for premature activation of the hypothalamic-pituitary-gonadal axis. When I asked one of these people if the Geiers (yes, it was they) had subcategorised into CPP or PPP they did not know what I was talking about. They were entirely ignorant of these terms. It was clear neither of the two people I had spoken to had undergone this sub-categorisation.

They claimed it was ‘enough’ to ‘know’ that their children had excess testosterone. One of these children is female. This child’s parent was utterly ignorant of the fact that excess testosterone in females was not called ‘precocious puberty’ but indicative of ‘Androgen excess’. Lupron is not mentioned as a treatment for Androgen Excess.

One other interesting fact about increased testosterone is that in patients diagnosed with PPP, this can result from an excess of vitamins and other dietary supplements. Its common knowledge that this is a common part of DAN! and DAN! style treatment regimes. Yet again, the Geier’s patients parents were entirely unaware of this fact.

Sources

http://www.emedicine.com/ped/topic1882.htm
http://www.emedicine.com/PED/topic1881.htm
http://www.androgenexcesssociety.org/signs.html
http://www.healthatoz.com/healthatoz/Atoz/ency/sex_hormones_tests.jsp

The Role of Creatinine in Relation to Porphyrins and Chelation to Creatinine

I’m not going to go over this subject as well as Not Mercury recently did but I want to highlight a few key concepts from that paper that it seems the authors either missed or didn’t account for.

The paper’s essence is that it is significant the their are elevated levels of Porphyrins in autistic kids. However, they fail to account for the likelihood that this is a false elevation. The study attempts to measure the amount of porphyrins in the urine of their subjects. However, because collecting urine of a standard volume, content and dilution is next to impossible, its necessary to use a stable compound to express the porphyrins as a ratio of – which is where creatinine comes in. So, the paper claims that, relative to creatinine, porphyrins are high in autistic kids.

However, as Not Mercury also highlights, its fairly accepted amongst DAN! practitioners:

Creatinine is often found to be marginal in the urine of autistics, and low creatinine can skew urine analyte results to high levels. So, also take note of creatinine levels if the laboratory results include ratioing to creatinine.

PDF translated to HTML from ARI

And Andrew Wakefield’s colleague, Paul Shattock, also reports low creatinine in autistic kids (see source on Not Mercury blog entry). So why does that matter? Now, I’m no scientist so I was struggling to find a way to visualise this in my head and I came up with the bar chart below. The thin black line is an arbitrary ‘baseline’ (where the creatinine stops and the Porphs start) below which in purple is creatinine levels and above which is Porph levels. Now, in the autistic representation note how the decrease in creatinine has led the baseline measurement for Porph to falsely raise the amount of Porphs. In other words, relative to the baseline, there are not more Porphs as such, but less creatinine. I’m open to interpretation on this by the way – I don’t want it to be misleading.

There are also anecdotal reports of various chelators reducing creatinine further:

my son’s creatinine has come down to 11 by round 3. why is it going down?how can i bring it back to normal? i have been giving glycine to him also during rounds – every 3hrs dmsa+ala

Onibasu.

And:

Importantly, recent data suggest that oral NAC administration > transiently lowers creatinine levels.

PubMed

So here we seem to have a situation wherein autistic children are already noted to have low creatinine levels and that these levels could be even further reduced by the chelators used either in the study itself or by parents externally to the study and still the study authors claim it is significant to epxress Porphs _as a ratio_ of creatinine.

Autism One

Meanwhile, over in Chicago, Autism One has been in full force (or should that be farce?). I’m reliably informed that one of the big draws was David ‘crowd pleaser’ Kirby so I downloaded his slides to have a looksee.

Incredibly, it seems that David Kirby has magically ‘forgotten’ everything he conceded to blogger Citizen cain regarding the use of CDDS data. Lets remind ourselves of what Kirby told Citizen Cain:

…if the total number of 3-5 year olds in the California DDS system has not declined by 2007, that would deal a severe blow to the autism-thimerosal hypothesis. He [kirby] also conceded that total cases among 3-5 year olds, not changes in the rate of increase is the right measure….

And yet, here we have slides showing Kirby demonstrating the change in the rate of increase, something he has conceded is inaccurate as a measure. He also refers to the increase in cases as ‘new’ cases when its been demonstrated time and time again that these are _not new cases_ . All in all, this is simply more dishonesty from David Kirby.

Autism and autistic people deserve better than this hodge-podge of sloppiness and dishonesty.

Pediatrics Letter – More Misrepresentation

10 May

On the 5th May a Letter from Kenneth P Stoller appeared in Pediatrics.

UW-Madison researcher Paul Shattuck concludes that special education figures being used are “faulty and do not substantiate such a claim” (that there is an autism epidemic). Paul Shattuck seems to be saying that all the reported autistic children have always been here, they were just called something else.

Shattuck makes no such conclusion. In a clarifying comment on Scienceblogs, Paul Shattuck stated:

Unfortunately, the media and some advocacy groups have distorted what my article was all about. I was quite explicit in the article that A) my work does not prove or disprove the existence of an epidemic and I think that is still an open issue….My number one goal was to raise awareness about the limitations of the special ed. data.

As a pediatrician, who has been in practice for over two decades, I find it more than a little insulting as well as disturbing to have someone say that these children were always there.

Several pediatricians do not find it insulting. Suniti Chakrabarti for example – who diagnosed my own daughter – co-authored a paper with Eric Fombonne which confirned a high but stable prevalence for autism. There are also several interesting studies that indicate that ASD has historically been very underdiagnosed.

In 2004, an ‘autism audit‘ was performed in Scotland. One of the questions the audit asked was how accurate they thought the prevalence rate estimates were for their area. 45% of authorities who responded made a point of noting that they felt diagnosis for adults was very underrepresented. For example, Perth and Kinross council stated

Figures for adults reflect the national findings that the numbers known to services/diagnosed represent a significant underestimate of those individuals likely to be affected. For example day centre managers locally consider a number of people to be on the spectrum who have had no formal diagnosis.

Also, in a New Scientist piece last year, the findings of the University of Nottingham were reported. The team reexamined data from the 1970’s which resulted in five diagnosis. Using modern diagnostic criteria, the team found 56 cases, a ten-fold increase.

Lastly, earlier this year, Health Minister Liam Byrne reported figures that demonstrated autism diagnoses for children have nearly doubled in 8 years from 3100 to 6170. Meanwhile adult diagnoses have nearly tripled in the same period from 1120 to 3000.

The idea of ‘insult’ is irrelevant to the substantiation of a case. And yet again, Shattuck made no claim that ‘these children were always there’. Such purposefully misleading statements entirely invalidate Stoller’s case.

As a scientist, I find the current approach to the autism epidemic – “The Emperor’s New Clothes” approach – to be deeply disturbing.

Appeals to authority do not make one automatically correct. I’m sure there are several people who could say that ‘as scientists’ they question the idea of there being an epidemic of autism at all. That wouldn’t automatically make them right either. What does lend their viewpoint some weight as the fact that the science supports their opinions.

For years the vaccine division at the CDC and others have said the reason for the dramatic increase in autism is due to “better diagnosing” and “greater awareness.””They have encouraged those like Paul Shattuck to manufacture uncertainty.

This is quite simply yet more purposefully misleading rubbish. This study was funded largely by the Autistic Society of America. Paul Shattuck has also stated his affiliations with the CDC quite clearly:

As for the $540,000 from the CDC…it’s not entirely clear what they are talking about. I certainly don’t have a grant that big from anyone. They are probably talking about the autism surveillance grant that our center received from the CDC…a proposal which I helped prepare but am not listed as a co-investigator and am not funded from….I do have a small grant for about $12,000 from the CDC to investigate racial and socioeconomic disparities in the timing of autism diagnosis and service utilization.

Why Stoller indulges in such flagrant misrepresentation is not apparent. I am forced to conclude in the absence of a good reason, that Stoller has nothing to fall back on other than annoyance that Shattuck’s conclusions did not meet his beliefs and thus he felt it necessary to resort to distortion and spin.

There are no studies that have found the previously undiagnosed or misdiagnosed autistic individuals among older Americans. They simply aren’t there.

Mr Stoller is once again making assumptions. I have found no studies in PubMed that even attempt to pose this question, let alone answer it. How Stoller concludes there are none when no studies have sought an answer to this question is bewildering. I would like to suggest Mr Stoller examines the evidence from the three UK sources I quote from above. The US and the UK have a near identical autism prevalence. It seems reasonable that older patterns of prevalence might follow suit.

Now, the increase of autism has been linked to the increase in mercury exposure through fish and industrial sources, amalgam and additionally, through increased parenteral exposure to ethylmercurithiosalicate.

Its also been linked to alien invasion and plastic cups. Surely a scientist understand the concept of correlation not equaling causation?

A recent study, using infant Macaca fascicularis primates exposed to injected ethylmercury or those exposed to equal amounts of ingested methylmercury, showed that ethylmercuy was retained twice as much inorganic mercury in their brains in comparison to the methylmercury exposed primates.(Burbacher T, et al. Comparison of blood and brain mercury levels in infant monkeys exposed to methylmercury or vaccines containing thimerosal. Environmental Health Perspectives, 2005 Aug:113(8):1015-21.)These primates were exposed to mercury levels at a rate equal to what children in the United States received via standard childhood vaccines from 1991- 2003.

What’s not often discussed about the Burbacher study is the interesting point that the group did not use thiomersal containing vaccines. They used non-thiomersal containing vaccines and then added thiomersal to them. It is difficult to know how this fresh preparation compares with vaccine formulas when thimerosal is part of the manufacturing process and may have suffered some degradation to inorganic Hg in the vials before administration.

Cysteine and glutathione synthesis are crucial for mercury detoxification, and are reduced in autistic children, possibly due to epigenetic polymorphisms.

The Deth paper made no such claim. The basic gist of the Deth paper is that various toxins, including thimerosal, affect methionine synthase activity (a process that helps in building proteins) and that this can adversely affect children. In short, the Deth paper alleges that thimerosal causes methionine synthase dysfunction (MSD). However, autism and MSD are entirely dissimilar.

Therefore, autistic children have 20% lower levels of cysteine and 54% lower levels of glutathione, which adversely affect their ability to detoxify and excrete metals like mercury. (James, S.J. et al.: Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism. Am. J. Clin. Nutr. 80, 1611-1617 2004).This leads to a higher concentration of free mercury in blood, which then transfers into tissues and increases the half-life of mercury in the body, as compared to children with normal levels of cysteine and glutathione. As was shown by Bradstreet et al (Bradstreet, J et al.: A case control study of mercury burden in children with autistic spectrum disorders. J. Am. Phys. Surg. 8, 76-79 2003) in a study involving 221 autistic children, vaccinated autistic children showed about 6 fold elevation of urinary mercury than normal controls after appropriate mobilization with the chelating agent DMSA.

And so we get down to it – Bradstreet and JAPANDS. A man who recommends exorcism and a journal who don’t publish errata or retractions. Great. Next!

Stoller then goes on to describe a whole host of things thiomersal apparently does without ever stating the fact that none of these things appear in the diagnostic criteria for autism.

This is an unconscionable oversight failure at best, at worse it is an example that we have left consensus reality to be created by the liars, thieves, cheats, killers, and the PR junk scientists they employ.

Quite a statement from someone who has actively misled people regarding Paul Shattucks connections with the CDC. I would put forward the idea that a PR junk scientist is one who isn’t even able to research the simplest of facts and instead concentrates solely on misrepresentation and spin. As for killers, its my opinion that Dr Roy Kerry is a great example of a DAN! protocol follower.

We are living in a time where an incredible overplay and lies and self-aggrandizing behavior and non-science is the norm.

Stoller has no argument from me there. He would seem to me to be living embodiment of that statement. He cites studies from people like Burbacher who’s ‘science’is funded by SafeMinds – a group whos mission statement is to establish a causal relationship between vaccines and autism. He cites people like Deth who are listed as expert witnesses for the prosecution in the omnibus proceedings against vaccine manufacturers.

Is it stretch to realize that by putting our heads in the sand about the autism epidemic we have made it possible for the groundwork to be put in place for Marshal Law?

Er, yes. Yes it is.

No something easy to contemplate? Then ask why haven’t pediatricians come forward to demand the end of the use of ethylmercurithiosalicate once and for all, and to advocate for the treatment of these children before it is too late?

Simple: they realise that the science doesn’t support your beliefs Mr Stoller. They understand the massive societal benefits of vaccination – a benefit being well demonstrated now that vaccine uptake is falling thanks to your scare mongering as Mumps epidemics sweep your country and measles epidemics resulting in 12% hospitalisation and at least one death so far sweep mine.

Stoller declares no conflicts of interest and yet in his signature he describes himself as a member of the International Hyperbaric Medical Association. This treament is a favourite of DAN! practitioners – people who profit by ‘treating’ autism – and yet there have been no published randomized controlled trials for low-pressure hyperbaric oxygen therapy as an autism treatment yet. Only one paper exists in Pub Med relating to HBOT and autism which blogger Dad of Cameron found at least one significant error in.

Mr Stoller establishes once more his propensity to bend or totally shatter facts by claiming no conflict of interest when it is clear he supports a therapy being widely utilised for profit on autistic children. Throughout this whole letter he willfully and (one must assume) knowingly misrepresents people like Paul Shattuck, relationships between people and institutions. He quite clearly has little knowledge of the limitations of the science he quotes as backing up his beliefs and then goes on to rage about ‘PR junk scientists’ whilst he promotes the use of a very expensive treatment with no established – or even reliably investigated- appreciable effect on autistic children.

DAN! Protocol For Dummies

20 Mar

Whenever anyone else hears the word ‘DAN!’ with that little exclamation mark do they go ‘DAN! – DAN! – DAN – DAN!’ to the opening four bars of the theme to ‘Dragnet’? No? Ah well, just me then.

Ken Aitken is a psychologist. He’s also a DAN! Doctor. One doesn’t need to be an actual Doctor to be a DAN! Doctor apparently:

As for choosing a DAN!, it just depends on what type of treatment you are looking for. DAN!’s that are MDs or DOs are typically going to be much more into testing and genetics and lots of expensive and invasive stuff. This, of course, is a gross generalization and isn’t necessarily true of all DAN! MDs, but rather something to be cautious of. A DAN! who is a homeopath or naturopath is typically going to do things more naturally and less invasive. Again, it’s a generalization. There are chiropractors, allergists and other types of doctors that are DAN!s as well, so it is really the type of doctor and treatment that best suits your needs. Many people go with a MD or DO because they can get insurance coverage for some of the services.

Homeopaths and Naturopaths doing things ‘naturally’. Heh. Does this lack of training in medical matters prevent them from performing things like chelation (source as above)?

…which is why we went with a homeopath/naturopath…….We decided to get the mercury out because I knew that Seth had had way too much put into him and it wasn’t coming out at all (he’s a non-excretor).

Homeopaths and Naturopaths doing chelation. Cool.

I talked to one yesterday (a DAN doctor mind you) and how he got qualifications to be one is beyond me. He told me has a couple of autistic patients and knows of the chelation process. If this is all that is required to be a DAN doctor then I don’t see a distinct advantage to them either.

Source.

Is your mind boggling yet? Here’s the reply to this commenter (source as above):

I think that being on the DAN list (in the past) meant something like that the person had attended some DAN training– or something rather general like this. Someone (in some post, somewhere) who went to the recent DAN conference wrote about that there is/was some discussion afoot to try to improve on this and make the
info on doctors more useful (or more detailed….or something??)

This doesn’t sound like a recipie for disaster at all. Was Roy Kerry a DAN! Doctor? I don’t know.

I came across some priceless websites pushing the DAN! protocol. They had numerous things in common, chiefly the disclaimer – all variations on the theme of:

this is not medical advice

Which is odd because from that point on, they mostly plough into what can only be thought of as _advice_ about what _medication_ an autistic child should take. There’s a fairly representative sample of what a dutiful DAN! Doc should do on the website of Miriam Jang MD. First, the usual copout from responsibility:

At this point, I would like to point out that this is not medical advice, even though I am a Medical Doctor. Rather, this is a wish for your child or your loved one(s) to have the advantage of what took us eight years to discover. Please take this as a medical disclaimer. All suggestions here should be done at your own risk.

‘Own risk’. Right. Or actually – wrong. She means the risk of the child receiving the treatment. Thats whos health will suffer when if it all goes wrong.

Dr Jang decides to lead off with some impressive science:

In both Chinese medicine and Ayurvedic medicine, the sages believed that there were only two ways to health: one was to correct deficiencies; the other was to get rid of toxicities.

Ayurvedic? What the hell?

This ancient art of healing has been practiced continuously for over 5,000 years. The principles of many natural healing systems now familiar in the West, such as Homeopathy and Polarity Therapy, have their roots in Ayurveda. Ayurvedic practices restore the balance and harmony of the individual, resulting in self-healing, good health and longevity.

So, DAN! Doctors are homeopaths and naturopaths who practice er, Polarity Therapy. Polarity Therapy? What the hell?

Polarity Therapy is a comprehensive health system involving energy-based bodywork, diet, exercise and self-awareness. It works with the Human Energy Field, electromagnetic patterns expressed in mental, emotional and physical experience.

Riiiight. OK. Back to er, Doctor (?) Jang. Basically, there’s a load of stuff with no cites – such as:

An important finding is that about 85 percent of Autistic kids are high in Copper and low in Zinc. Furthermore, these kids are very low in an important protein call Metallothionein, or MT Protein.

Hmm. Searching PubMed for ‘Metallothionein autism’ reveals two results. One is an inaccessible review and one is a free PDF published in the confidence inspiringly named ‘Alternative Medecine Review’. A Google search for the same reveals the predicted circus of quackery.

Except….another one of the mercury/autism darlings, Vijendra K. Singh has a paper that states:

serum level of MT did not significantly differ between normal and autistic children. Furthermore, autistic children harboured normal levels of anti-MT, including antibodies to isoform MT-I (anti-MT-I) and MT-II (anti-MT-II), without any significant difference between normal and autistic children.

A dilema, no? (You can read more on this paper here.)

Dr Jang continues with:

I will include a list of supplements that Marky is taking. There are many protocols, with many rationales. When we write down the dosages, please take into consideration that Marky is 11 years old and weighs 75 pounds. Please adjust your dosages according to your child’s weight.

Marky is her son. But isn’t it amazing how a DAN! Doctor is assuming parents know *how* to adjust medications for weight – and is happy to trust them to do so without medical supervision or even consultation!

Towards the end of her piece she says:

Please remember that, if you introduce your child to a new supplement, it is not unusual for the child to experience some adverse effects for a short while…When this happens, it does not necessarily mean that you should discontinue the supplement, unless the adverse effects are dangerous, or persistent….If there are adverse effects, stay at this dose until the adverse effects are gone, then proceed to a slightly higher dose, etc.

So there may be adverse effects but don’t stop unless the adverse effects are dangerous, instead stay on the same dose until the adverse effects are gone. I can’t imagine any Doctor thinking this is good advice. Interestingly, the following appeared from Dr Jang as part of an email newsletter:

I would like to start with some very serious news: we do have to be careful of Vitamin A toxicity with our sweet kids. There is a child with reported Vitamin A toxicity that was so severe that the child had to be hospitalized for 12 days.

Her patient? I wonder. Maybe the practitioner (whomever s/he was) read her advice to ‘stay on the same dose until the adverse effects are gone’.

Dr Jang tells us in relation to supplements that:

We noticed a difference in Marky in less than a week.

And yet later on she says:

In addition, you may not see the beneficial effects of these supplements for a period of time.

Something of a glaring contradiction. Which is true?

Anyway, having expounded all this good advice, Dr Jang closes with:

So, be curious and be persistent. Take good care of yourselves so that you can endure this arduous journey called “Autism”!

Yes, be curious – try everything that takes your fancy. Be persistent – whats a little Vitamin A poisoning between friends? And above all take good care of _yourselves_ so that _you_ can endure this journey…..except, its not _you_ who’s undergoing all these treatments is it? Its your child.

Dr Jang is also a big clay bath fancier (clay baths cure autism? Who knew?)

“…I have put a huge number of patients on these clay baths and the levels of heavy metals – mercury, lead, arsenic, aluminum, and cadmium have come down dramatically…I have been monitoring the levels of metals using all three methods (TD DMPS, oral DMSA and clay baths)and the clay baths are way faster in the removal of metals”.

Hoooo boy! Rashid’s going to be plenty pissed with her. Better than TD DMPS? Surely not! Why not use both? Smother your child with TD DMPS and then wash that stuff off in a nice clay bath? At least your child will have a nice happy splash in a bath.

So, Ken Aitken – welcome to your new role as a Dan! Doctor. I feel sure you can uphold the strong scientific standards your colleagues demonstrate.

Lupron: An Alternate View

17 Mar

I think it was Prometheus who first used the phrase:

You can’t reason someone out of a belief they haven’t reasoned themselves into.

By which he meant that proponents of the mercury/autism hypothesis were acting out of belief, innuendo and poor science rather than scientifically valid science and that subsequently trying to use reason to dissect their arguments was of limited use.

What I intend to do in the rest of this post is use the tactics, sources and methods commonly used by proponents of the autism/mercury connection to justify their belief systems. before I do I want to assure you that _nothing_ in this post is fabricated.

As we all know, Lupron has been big news recently. The Geiers love it, the mercury/autism crowd are clamouring to use it and the likes of Orac, Kathleen, Autism Diva, Prometheus and myself have all blogged comprehensively against its use.

However, we were using science and reason and as we know, there are people who are impervious to these things. However, when I received a fascinating email from a middle aged American woman who wanted to talk to me about Lupron I read her words with interest. As all proponents of the mercury/autism hypothesis know, anecdotes trump science. With that in mind I read her opening statement.

I am extremely concerned about the use of the drug Lupron being used on autistic children. As a former consumer of this drug, I can tell you firsthand how harmful it is. I understand the desperation people may experience trying to do all they can to heal their conditions, but we must not forget that Lupron is actually chemotherapy, and leaves the same conditions other forms of chemo do on patients. You wouldn’t give chemo to someone who didn’t have cancer, so how Lupron made the jump to all these other patient groups is purely manufactured by Abbott Labs, the parent of TAP who makes Lupron.

Lupron is chemotherapy. Lupron is manufactured by Big Pharma’s TAP – owned by Abbot Labs. A little digging on the Internet turns up lots of bad things about Abbot Labs:

ABBOTT LABS OBESITY DRUG KILLS 32 PEOPLE AND IS PULLED OFF THE MARKET IN ITALY

Source.

Abbott Laboratories, the world’s 12th largest drug company, has been suspended for a minimum of six months from membership in the Association of the British Pharmaceutical Industry (ABPI).

Source

If there was ever any reason to squash human beings like a bug, the decision makers at Abbott Labortories have provided a perfect one with their decision to increase the cost of the anti-AIDS drug Norvir by 500% (from $1500 to $7800 per year).

Source.

Thats just the tip of the iceberg. My anonymous emailer continued….

Any child already harmed by vaccinations does not deserve a second pharmaceutical insult, which is what Lupron will
do. TAP/Abbott is a filthy company, and thinks nothing about the harm they do to patients. It was just published how 800 people have died from another drug they make.

Pretty convincing stuff, I think you’ll agree. Its obvious that Lupron is manufactured by the same sort of bottom-feeding evil scum Big Pharma types that inject autism-causing thiomersal into healthy babies. My anonymous emailer continued:

It just horrorfied me to read about these kids being encouraged to take this drug. Do you know, there was a National Lupron Victims Network with over 2 million hits that suddenly just disappeared off the net? The data is on Way Back Machine or Archive.org under “lupronvictims.com”. We have Abbott employees who follow us around the internet trying to discredit us. It’s like science fiction.

So I checked it out – the domain ‘lupronvictims.com’ was registered in August of 1999 and is hosted by Forest a Seattle company – the same city that the domain registrant specified. I’ve sent an email to the admin contact at Forest to enquire about why the site vanished in early 2005 but have thus far recieved no reply.

As proponents of the Simpsonwood conspiracy will readily recognise, this reeks of corruption and Big Pharma meddling.

The site is indeed archived on the WayBack Machine but fascinatingly, even though the Way Back Machine continued to archive up until March 2005, one has to go back to late 2003 to find actual archived content. the most complete archive is the first one from 1999.

And still my anonymous emailer had more to say:

Whether this happens to all patients I don’t know, but I do know there are many, many people living in hell from using it. Some of us have contracted terrible deseases from having our immune system compromised, and we all battle many diseases: CFS, Fibromyalgia, EBV, arthritus, severe memory problems, clinical depression, liver problems, high cholesterol, trabecular bone loss creating disc herniation and osteoporosis, etc.

She also mentioned the name ‘Lynne Millican’:

In 1999 I went public in the Boston Herald with my story trying to prevent more poisonings. One person, Lynne Millican, has testified before the senate. We have fought and fought to bring awareness to no avail.

A quick search reveals some impressive sources:

When we first met Lynne Millican in January, when this series on Lupron was launched, we learned that she still suffers a range of serious ailments more than a decade after injections of the drug, Lupron, for treatment of endometriosis. Millican, a registered nurse and paralegal, believes her problems are associated with Lupron. Millican’s numerous symptoms have included the development of a noncancerous tumor, breast cysts, cardiac arrythmias, pain, dizziness, swelling and fatigue. She is one of many women treated for endometriosis who have complained over the years about these and other lingering symptoms they believe are related to Lupron. Other symptoms include depression and confusion, bone pain, vision loss, high blood pressure, and nausea.

Red Flags Weekly

“There are thousands in the United States who say they have been victimized by this drug,” Millican said, emphasizing that symptoms can be severe, such as tremors, seizures and memory loss. “Many women I know say their symptoms didn’t stop when they stopped taking the drug.”

Mercola

Proof indeed. My anonymous emailer closed with the following:

They just got bagged doing the same dirty tricks in England that they were levied the largest fine in US History for doing
here. They have so much money they just pay everyone off. Get the word out. Prevent more poisonings because the FDA does not care.

I think supporters of the thiomeral/autism connection will testify to the truth of that. The FDA are in the pocket of Abbot Labs, Big Pharma Agents of the Apocolypse.

Truly, its stupid to put Lupron into kids. When their bodies start to break down, we can all march on Washington – the placards will read ‘It was the Lupron, stupid’.

No need for science. No need for investigation. As a regualr commenter here says ‘Because its obvious…’

McScience

3 Mar

Yesterday, my fellow countryman Mike Stanton left the following comment in response to a previous commenter about his belief regarding how his child had become autistic:

There may not be a single answer. But that does not mean we can pick any answer we like. There has to be some scientific validity to any hypothesis.

This is such a good comment. It reflects something I’ve felt increasingly over the last year or so – the increase in pseudo-scientific theories posed as a ‘menu’ for parents to choose from. It reminds me of sauntering up to the counter at McDonalds and saying – “I’ll have one of those, one of those and one of those.”

I recently came across a post made on the Onibasu list which illustrates my point. This is the signature of the poster in question. Its a list of treatments she’s trying on her child:

My son is using M-B12 (Hopewell) since Dec 2003, Wellness Essential GSH (had been using TD-Glut but levels were always low), TD-DMSA (3 on and 4 off – 8 hr schedule) (Lee Silsby) since Oct 2005, (Used TD-DMPS Jan 2005 ?Oct 2005) TD-ALA (Lee Silsby) since Oct 2005, TD-LDN (Wellness) Since Oct 2005, (High Tech Health) FIR sauna, Magnetico bed, High Tech Health’s water machine, and a lot of supplements.) GFGFSF diet.

The post in question is also asking about Lupron. Thats a total of 12 separate treatments, ‘a lot of’ supplements and she probably is in the process of adding Lupron to that list as we speak.

And can you Supersize me please?

What worries me is even a bog-standard bottle of Asprin has a warning on it about responsible use. Is it really sensible to risk giving one’s child such a massive cocktail of drugs on the word of someone who quite obviously is more interested in money than science?

Medicine shouldn’t be such a pick and mix affair. Its quite worrying about what this reveals about how the West’s perception of doctors has changed. Doctors who have undergone 7 years plus of training are viewed with suspicion and sued at the drop of an opinion whilst ‘doctors’ who have shops rather than practices are lauded as heroes.

How did it come to this? When did McScience start to replace science? How did it come to pass that the process of peer review (designed to give a good _starting point_ to a paper) meant nothing and the process of buying an entry in a pseudoscience rag or buying a misleading advertmeant everything?

I’m nobodies scientist. It takes me longer to understand the science because I need to go through it time after time so I understand all the words and understand the implications. I ask questions of actual scientists and get them to translate for me so it stands to reason to me that for an article to be peer reviewed in a decent journal assures that the standard of science in that article will be fairly high. It might not make the paper _right_ , but at least we can be sure its been thought through properly.

Surely that needs to be the absolute baseline of quality we should come to expect for papers that discuss such important questions. Otherwise we really do end up at the counter of McScience – like kids in a sweet shop, taking what we think we’ll like rather than what we need.

Lupron Rears Its Head

22 Feb

The issue of Lupron finally raises its head above the parapet of autism. I’m going to attempt to ‘bring together’ the various discussions that have sprung up and then have my say on the subject. But before I do, lets just clarify what we’re talking about.

There is an unsubstantiated theory put about by Boyd Haley and the Geiers that testosterone levels are raised in autistic people. There is a further unsubstantiated theory that high testosterone counteracts the bodies ability to be chelated of its mercury efficiently. That the excess mercury got there is also due to an unsubstantiated theory that thiomersal in vaccines is responsible.

The use of chelating agents (which alter the body’s chemistry) have never been tested for safety or efficacy for autistic people (who have chemically different brains than non-autistic people).

So, in my opinion, we have a potentially dangerous and thus far non demonstrably necessary treatment being administered to autistic people. It was put about awhile ago that a typical course of chelation should last 18 months to two years. Now we seem to be approaching that time scale for a lot of children and there seems to be little to no response (unless you believe the unverified claims of Generation Rescue), there’s now a casting about for a reason why the chelation isn’t working as was first thought.

Yes, I have my own opinion as to why it isn’t working. I’m sure you can guess what that opinion is.

But whats _their_ opinion? The chelationistas? Why, that all that pesky testosterone is impeding the chelating of all that pesky mercury. And what reasons are given for that idea? Why, that there are four times as many male autistics as female autistics.

Now that the testosterone theory is out in the wild, suddenly the chelationistas are ‘remembering’ that their kids seem to be developing quickly, that they have a lot of body hair, that they become violent during chelation.

Yes, I have my own theory why they become violent during chelation. I’m sure you can guess that opinion is.

And thats it. Thats why there’s a sudden mad dash for Lupron. So lets now look at how its used.

Quite simply, its being used because the Geier’s are ‘excited’ about using it.

Try going to the NAA website and ordering the DVD or CD from the Geier’s lecture this past weekend. You’ll learn about their work with testosterone and Autism. This research is in its’ infancy, but the Geiers are SO excited about this topic.

Onibasu.

Dr. Geier now has a testosterone study going on, I think it’s Lupron injections every 45 days? until age 12, while chelating with DMPS-TD. there’s some other stuff, too, he’s got I think 8 kids in the study, we’re working on getting all the stuff out of the way for allie Kat to participate, last I knew he had no girls.

EoH.

My daughter will be seeing the Geiers this winter/spring and we’re about to have her tested to see if their protocol is appropriate for her. I’ll report the results when we have them…but in the MEANTIME, you can watch the Reverend Lisa Sykes discuss her son Wesley’s progress after receiving Lupron treatments!

EoH.

Kathleen at Neurodiversity has a very thorough round up of this side of things which I strongly suggest you read. But lets not pretend – children are already being treated with Lupron.

So, just to recap – an unsubstantiated treatment is now being used to treat an unsubstantiated condition which allegedly aids an unsubstantiated process.

But what _is_ Lupron? Whats it used for?

Its used to chemically castrate sex offenders in the US and also to treat Prostrate cancer. Basically it inhibits testosterone. In females it can cause a drug induced menopause. Its only legitimate sue for children is to treat precocious puberty.

There’s been at least one lawsuit associated with Lupron.

Many women with endometriosis who have been given Lupron injections have had severe side-effects, including cardiac arrhythmias, dizziness, swelling, chest pain, depression and confusion, bone pain, extreme fatigue, vision loss, high blood pressure, and nausea. Some of the women claim their side- effects last long after treatment is completed. The plaintiffs in the lawsuit against Tap claim, for example, to have experienced serious injury after Lupron injections, “resulting in pain and suffering, disability, disfigurement, mental anguish, loss of the capacity for enjoyment of life, expense of medical care and treatment, loss of earnings, loss of the ability to earn money.”

This is a serious drug. Nothing to make assumptions about – nothing to treat _children_ with unless they have a diagnosis of Precocioous Puberty which can be tested for without needing to inject Lupron.

The science that underpins the Geiers is practically non-existent and based pretty much on either their assumptions regarding mercury or their assumptions regarding testosterone – neither of which are authenticated. You can view an overview of the bad science behind the Geiers suppositions at Bartholomew Cubbins site and at an ongoing discussion at the Not Mercury site.

What happens when Lupron is deemed ‘inefficient’? What will be the next inhibitor? What will be the next unnecessary chemical pumped into autistic kids to ‘uninhibit’ the chelation process? And lets not even start on the bizarre cognitive dissonance necessary to refuse to trust Big Pharma regarding thiomersal and yet rush to embrace it regarding Lupron.

Into The Unknown With The Unknowing

31 Jan

The unknown is exciting. As a species we seem innately curious about seeing whats over the next hill, beyond the next valley, what happens if we heat this liquid to its boiling point, etc etc. But fairly obviously, we quickly realised that if we didn’t exert some level of control over the things we were curious enough about to examine closely then the results were arbitrary and meaningless.

“Hey, look at that!” we exclaimed to ourselves, “we’ve just invented the scientific method. How cool are we?”.

Unfortunately, as well as being logical, nuanced creatures capable of appreciating such things as the pathos in satire we’re also reactionary and blinkered. As someone recently remarked:

Too many people on all sides of the debate(s) seem to wear blinders that prevent them from acknowledging how little we all know.

Wade Rankin.

A statement I fully support. However, there are certain things that we need to be certain about when we treat autistic children.

Is chelation safe? Here’s Wade again, quoting a commenter called Random John:

At any rate, it’s still pretty unclear why chelation therapy seems to be successful for some children, but not for others. The polarity of the thimerosal and chelation debates does not seem to cover the ground necessary to understand what’s really going on.

Which is very true. Unfortunately, its yet another example of shutting the barn door after the horse has bolted. To worry about these things after you’re already treating an autistic child with something like chelation is quite simply stupid. If there are people who are concerned about what effects chelation may or may not have on autistic children then basic medical principles need to be applied: first, do no harm.

That means you need to conduct safety trials before using something that has the following warning on it:

The use of this drug [EDTA] in any particular patient is recommended only when the severity of the clinical condition justifies the aggressive measure associated with this type of therapy.

Recently such people as Dr. Mary Jean Brown, Chief of the Lead Poisoning Prevention Branch of the Centers for Disease Control claimed that if chelators were used properly then they’d be safe. I take extreme issue with this viewpoint.

Chelation is essentially a chemical process – it alters the chemical composition of the body. Bearing that in mind, consider the following:

This review focuses on recent advances in the in vivo study of the whole brain in idiopathic autism…..Diffuse abnormalities of brain chemical concentrations, are…found. Abnormalities of ….brain chemistry…are evident by early childhood….

Source

So, the brains of autistic people are chemically different then the brains of non-autistics. Given that fact, is it a) stupid or b) clever to use a process that alters the chemical composition of the person and which has never undergone any safety trials in regards to autism?

There’s a whole bunch of people here who need to take a drastic step backwards and do some basic safety trials on what is, irrespective of their beliefs, a poorly understood and potentially dangerous/fatal process.

Chelation Death: The Coroner Speaks (subtitled: Look Before You Leap)

6 Jan

A few months ago, Abubakar Tariq Nadama, a 5 year old autistic boy died at the office of Dr Roy Kerry after undergoing IV EDTA chelation therapy. I wrote about it extensively at the time, as did Autism Diva and Orac.

Today, the coroners report has come in:

In layman’s terms, the administration of ethylene diamine tetra-acetate, commonly known as chelation, resulted in a lack of oxygen to the brain as well as irreversible heart damage, said Allegheny County Deputy Coroner Ed Strimlan.

We determined there’s a direct correlation between the EDTA and the lack of oxygen to the brain and the heart muscle damage. It’s a total package, based on the autopsy, the histology [tissue sampling] and the toxicology [blood sampling],” Mr. Strimlan said.

Source.

At the time, anti-vaxxers, anti-thiomersalers and pro-chelators said we should wait for the results of the report before issuing judgment. However, they failed to extend that same criteria to Dr Rashid Buttar who decided to include EDTA in his new treatment protocol. Dr Buttar is frequently described as a hero amongst the anti-vac’s, anti-thiomersal and pro-chelators and yet they seem strangely reluctant to comment on the efficacy and/or safety of his new protocol. I have repeatedly asked commenter’s to this site the following question:

Given that we don’t know the exact role that IV EDTA played in young Tariq’s death, on what level is it a good idea for Rashid Buttar to start using it in a new protocol?

I have never received an answer to this question. The question has been shirked by at least four separate comments on approximately 6 separate occasions.

Now, of course, we _do_ know that EDTA has ‘a direct correlation’ to the lack of oxygen and heart muscle damage that poor Tariq sustained and which killed him. And still no one is prepared to stand up from the pro-chelationist side and state they think Buttar is being (once again) dangerously irresponsible. He (Buttar) has a reputation as a forceful man – a bit like a bull in a china shop. As we know from recent experience from another man with a similar reputation – such people seldom stop to look before they leap. So convinced they are in their own ‘rightness’ they they plough ahead without pause or consideration.

Now we know for sure that Chelation did play a role in a young boys death – a boy who’s dead _solely because he was autistic_ – I invite commenter’s from an anti-vax, anti-thiomersal, pro-chelation perspective to call for investigations into Dr Roy Kerry under who’s treatment Tariq died and to call for Rashid Buttar to exercise more care.

Speaking of ‘more care’ and ‘looking before one leaps’, yet another anti-thiomersal activist, Dan Olmsted, recently wrote a column lauding Gold salts as a potential chelator of mercury. It seemed he was inundated with emails from scientists expressing grave concern. So much so that he wrote an obviously unplanned and somewhat panicky reaction piece which included the line:

Clearly, given the serious risks, figuring this out is a job best left to the experts.

What a stunning piece of ‘shutting the barn door after horse has bolted’ syndrome. You’re absolutely right Mr Olmsted, this _is_ a case best left to experts. And yet you didn’t let that stop you in any of your previous pieces. Lets hope that no one read your first piece without reading your second one. Lets hope they didn’t go out and pump their kids full of Gold salts and lets hope that no one gets hurt.

Roy Kerry, Rashid Buttar, Dan Olmsted – next time , look before you leap.