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No, gastrointestinal symptoms are not a sign that autism is environmentally caused

21 Jan

There is a great deal of misinformation in the vaccines-caused-an-autism-epidemic message. The most commonly discussed misinformation is the fear that is spread about vaccines. But there is also a great deal of misinformation about autism causation and biology. For example, it is often stated that environmentally derived disabilities can be treated and that genetically derived disabilities can not. Some of the recent proposed treatments for autism have come from studies of fragile-X syndrome (a genetic condition with a high prevalence of autism). People with Down Syndrome are living longer and more healthy lives due to improvements in treatment. Another misunderstanding that get promoted is that co-morbid conditions, especially gastrointestinal symptoms, in an individual indicate that his/her autism is a result of environmental influences. Much of this impression likely results from the work of Andrew Wakefield, who tried to tie autism, GI disease and the MMR vaccine together.

While it has been long known that this “GI disease means environmental causation” idea is false, a recent paper helps to illustrate that. Gastrointestinal problems in 15q duplication syndrome discusses how gastrointestinal problems are very prevalent in individuals with the genetic 15q duplication syndrome. 15q duplication syndrome, like fragile-X, is a condition with a high prevalence of autism. About 80% of people with 15q duplication syndrome have GI problems, and this number is the same whether or not the individuals also have an autism diagnosis.

Chromosome 15q duplication syndrome (Dup15q syndrome) is a neurodevelopmental disorder involving copy number gains of the maternal chromosome 15q11.2-q13 region, characterized by intellectual disability, developmental delay, autism spectrum disorder (ASD), and epilepsy. Gastrointestinal (GI) problems in Dup15q syndrome have been reported only rarely, mostly focused on neonatal feeding difficulties. A retrospective review of the medical records of 46 patients with Dup15q syndrome was conducted to assess GI issues and their treatments in this population. GI symptoms were present in 76.7% of subjects with an isodicentric duplication and 87.5% with an interstitial duplication. There was no clear association between GI issues and ASD, with symptoms occurring in 78.9% of all subjects and 78.2% of ASD subjects. The most commonly reported symptoms were gastroesophageal reflux (56.7%) and constipation (60%), with 30% of subjects reporting both. The most common treatments were polyethylene glycol for constipation and proton pump inhibitors for reflux. Behaviors such as irritability and aggressiveness improved with treatment of GI symptoms in several subjects. The results indicate that GI symptoms are common in Dup15q syndrome and may have an atypical presentation. Diagnosis may be difficult, especially in individuals who are nonverbal or minimally verbal, so increased awareness is critical for early diagnosis and treatment.

Genetic conditions are frequently multisystemic. Consider Down Syndrome:

People with Down syndrome have an increased risk for certain medical conditions such as congenital heart defects, respiratory and hearing problems, Alzheimer’s disease, childhood leukemia, and thyroid conditions. Many of these conditions are now treatable, so most people with Down syndrome lead healthy lives –

It seems to be a relatively small point I know. It is a topic that I see come up a great deal. And given the guilt that is instilled in parents and the way that the vaccine-causation idea is used as a hook for people selling useless and often risky alternative treatments, it really isn’t such a small point.


By Matt Carey

If MMS, CD, chlorine dioxide, “parasite protocol” is safe, why does ClO2 dissolve tissue?

15 Jan

One of the marketing ploys for MMS* is that it somehow attacks viruses, bacteria, parasites, heavy metals, toxins and more but doesn’t affect human tissue. It’s safe! Of course this is from the same people who said that it isn’t a bleach. Emily Willingham did a very simple and elegant demonstration that, MMS: Yes, It Is Bleach. Put a few drops on a black cloth and, lo an behold, it bleaches it.

photo+%25286%2529[1]

I thought about taking this to the next step–putting some drops on raw meat to see how much tissue would be bleached. Then I thought, I wonder if there’s a study on this already? Consider this paper, Comparison of Organic Tissue Dissolution Capacities of Sodium Hypochlorite and Chlorine Dioxide (full paper here).

Organic tissue dissolution capacity. In other words: how well do these solutions dissolve tissue.

According to the main site promoting MMS as an autism cure:

What is MMS?

MMS stands for Master Mineral Solution. It’s chemical name is Chlorine Dioxide (ClO2). ClO2 is a gas that is produced as a result of combining 2 liquids, Sodium Chlorite (NaClO2) and citric acid. When added to the sodium chlorite, the citric acid brings the combined pH level to under five, causing the sodium chlorite to become unstable and release chorine dioxide. (ClO2) Chlorine dioxide is an oxidizer with a lower oxidation potential (.95 V) than any of the other oxidizers in the human body.

MMS starts out as sodium chlorite, not the hypochlorite as mentioned in the paper. But the final solution contains ClO2, the same as one tested in the above paper. In that paper they were exploring whether these solutions (sodium hypochlorite and ClO2) could be used in dental work. They wanted to test whether ClO2 solutions would have an effect on tissue, in this case the pulp from the inside of teeth. They already knew that sodium hypochlorite dissolved tissue.

What did they find? When they put tooth pulp (taken from cows) into these solutions, after 20 minutes about 28% of the tissue was dissolved.

Dissolved.

In ClO2 solution.

But wait, you say. That’s a paper using cow teeth, published in Turkey. Realizing that this argument would come up, I searched for more papers. Such as Effect of chlorine dioxide and sodium hypochlorite on the dissolution of human pulp tissue e An in vitro study. Which concludes

5% Chlorine dioxide is capable of dissolving human pulp tissue but sodium hypochlorite was more effective.

Or

Comparison of Organic Tissue Dissolution Capacities of NaOCl and ClO2

Conclusion: Within the limitations of this in vitro study, it was concluded that ClO2 is efficient as well as NaOCl in dissolving organic tissue.

Not all tissues are the same. Skin, especially the dead skin in the outer layer, is likely more resistant than tooth pulp. But, how about the intestinal lining (a consideration for those using this as an enema solution)? Or once absorbed in the stomach (for those taking an oral route) or the esophagus?

OK, it dissolves tissues. But why go to these papers? How about just looking at the MSDS? People have long brought out the MSDS for thimerosal to tell us that it should be removed from vaccines. The MSDS for thimerosal shows that the LD50 level (the exposure where 1/2 of the test animals died, lethal dose 50) is Acute oral toxicity (LD50): 75 mg/kg [Rat] for thimerosal. A chlorine dioxide solution of 0.054 weight% Chlorine Dioxide is less toxic than thimerosal, with an LD50 (oral) rats: 292 mg/kg. So, it would take about 4 times as much chlorine dioxide solution at this concentration to kill a rat as thimerosal.

The thing is, people don’t drink thimerosal solutions. Or do so repeatedly. People are encouraged to drink MMS.

Consider what happens if we increase the concentration of ClO2. Up the concentration to 3% ClO2 in water and it is as toxic as thimerosal. But, again, dose makes the poison and the dose of ClO2 from MMS is much higher than the dose of thimerosal from a vaccine.

The idea that MMS, or CD or Chlorine Dioxide is somehow a magical solution which rids the body of harmful substances while having no effect on human tissues is just flat out incorrect. It dissolves organic tissue. It’s toxic and the doses are significant.

(*MMS is “miracle mineral solution”, a relatively new bit of alternative medicine that is being sold as an autism cure. It has been promoted at parent conventions such as Autism One and by the blog The Age of Autism. It is a scam and if the discussion above wasn’t clear: it should be avoided.)


By Matt Carey

Yes, it may be illegal to sell MMS

14 Jan

A few years ago a new “treatment” appeared in the alternative medical world: MMS or Miracle Mineral Solution. As just criticism came out on this treatment, the name has morphed. One can now find it called CD (chlorine dioxide) or CDS (chlorine dioxide solution) or even the “parasite protocol). It goes by many names and it’s a scam. It is a well marketed scam and it’s taken in a lot of smart people. If you haven’t heard of it before you may be wondering what it is. Essentially, it’s a bleach (sodium chlorite) which is supposed to be mixed with a weak acid to make another bleach (chlorine dioxide). There are some effective marketing materials posing as scientific talks that use the classic alt-med sales techniques: testimonials and science-like discussions. In the autism world, this means claiming that it makes autistic kids non-autistic. Usually they avoid the “c” word (cure) because that is a quick way to get noticed by the people who are supposed to protect us from such scams.

MMS is sold often with a wink and a nod as a water purification solution. Such appears to be the case with a team charged with defrauding regulators and the sale of MMS as a cure or treatment. Per the press release below, it seems that this U.S. based team was importing their materials from Canada. At some point they “smuggled sodium chlorite into the United States from Canada using fraudulent invoices to hide the true end use of the product. In these invoices, according to the indictment, they falsely claimed that the ingredients they were purchasing for MMS were to be used in wastewater treatment facilities.” Their website shows them selling 4 ounce bottles of the solution. It would take a lot of those bottles to supply a wastewater treatment facility.

Here’s a point I haven’t seen made about MMS. One can purchase the base material, sodium chlorite, for about 50 cents a pound. Alibaba shows the liquid selling for $100-300 per metric ton. (click to enlarge)

Alibaba Sodium Chlorite

But, let’s look at the website of this team selling the sodium chlorite solution. For only $20 you could get a 4-ounce bottle. That’s a savings of $5 off the regular price! Anyone want to do the calculations of how many 4-ounce bottles could be filled with a metric ton purchased for a few hundred dollars?

If one doesn’t want a ton shipped from China, Canada (where this team was sourcing their material) has sellers selling seven pound jars of the solid for $200. Not as big a profit margin as buying by the ton, but still a notable markup.

pgl

The “project green life” team point out that they are selling it as a water purification product only. If, by chance, you are planning on doing the “MMS protocol” they will provide you with information “for your safety and convenience”. And just in case, they have a one-stop shop in that they will sell you the second part of the MMS protocol, citric acid.

pgl2

Wink. Nod. It’s just a water purification product, right? Sold at a huge profit. And for a small additional fee, one could also get the second part of the MMS product.

Apparently after this one team had their production facility inspected by the FDA, they moved production on to the property of one of their team members. There’s a silicon valley legend about companies starting in garages. It’s one thing for making electronics or computers. It’s another thing when we are talking about something sold (even with the wink) for human consumption.

Here is the press release from the Justice Department about when the charges were made.

Louis Daniel Smith, 42, and Karis Delong, 38, both of Ashland, Ore., were charged with defrauding regulators and suppliers in a scheme to manufacture and sell industrial bleach as a cure for numerous illnesses, including arthritis, cancer, and the seasonal flu. Also charged were Chris Olson, 49, and Tammy Olson, 50, of Nine Mile Falls, Wash. A federal grand jury returned an indictment, unsealed yesterday, charging Smith, Delong and Tammy Olson with one count of conspiracy, four counts of interstate sales of misbranded drugs, and one count of smuggling. The grand jury charged Chris Olson with one count of conspiracy, one count of the interstate sale of a misbranded drug and one count of smuggling.

The indictment alleges that Smith and Delong operated a business called “Project GreenLife” (PGL) from 2004 to 2011. PGL provided various health products for sale over the internet. According to the indictment, Smith and Delong arranged the manufacture and sale of the “Miracle Mineral Supplement” (MMS), a mixture of Sodium Chlorite and water. Sodium chlorite is not meant for human consumption. Suppliers of the chemical include a warning sheet with the chemical that states that it is harmful if swallowed.

According to the indictment, PGL provided consumers directions to combine MMS with citric acid to create Chlorine Dioxide, and the instructions told consumers to drink this mixture to cure numerous illnesses. Chlorine Dioxide is a potent agent used to bleach textiles, among other industrial applications. In humans, Chlorine Dioxide is a severe respiratory and eye irritant that can cause nausea, diarrhea and dehydration.

As part of the scheme to manufacture MMS, the indictment alleges that Smith, Delong, and others smuggled sodium chlorite into the United States from Canada using fraudulent invoices to hide the true end use of the product. In these invoices, according to the indictment, they falsely claimed that the ingredients they were purchasing for MMS were to be used in wastewater treatment facilities.

According to the charging documents, Smith and Delong were the managing members of PGL Smith co-founded the company, and Delong frequently handled financial transactions for the company and recruited friends and family to participate in the business. The indictment alleges that Smith and Delong paid Tammy Olson to handle all customer inquiries regarding the product. It is alleged that Tammy Olson continued selling MMS on her own website after federal agents shut down the Project GreenLife website and production facilities.

The indictment also alleges that Smith and Delong paid Chris Olson to clandestinely manufacture MMS in a building on his property after regulators from the Food and Drug Administration (FDA) inspected PGL’s original manufacture and shipping locations.

“The Department of Justice is committed to protecting the health and safety of people with cancer and other serious medical conditions,” said Stuart F. Delery, Principal Deputy Assistant Attorney General for the Justice Department’s Civil Division. “Our most vulnerable citizens need real medicine – not dangerous chemicals peddled by modern-day snake oil salesmen.”

Charges contained in the indictment are simply accusations, and not evidence of guilt. Evidence supporting the charges must be presented to a federal trial jury, whose duty it is to determine guilt or innocence.

The case was investigated by agents of the FDA’s Office of Criminal Investigations and the U.S. Postal Inspection Service. The case is being prosecuted by Christopher E. Parisi, a Trial Attorney at the Department of Justice’s Consumer Protection Branch in Washington, D.C.

The defendants have made a number of motions and at least one appears to be defending himself (filing pro se). Here’s an example of one such motion:

In his motion to strike for lack of standing, ECF No. 37, Mr. Smith disputes whether the “United States” and the “United States of America” are “legally one and the same.”

I’d want a real attorney if I were a part of this group, but that’s me.


By Matt Carey

Unethical DAN doctor to be supervised by acupuncturist

31 Dec

An Illinois doctor who subjects autistic children to “unwarranted, dangerous therapies” must have her work reviewed by an acupuncturist. The state medical board also fined Dr. Anju Usman $10,000, ordered her to take additional medical education classes, and placed her on probation for at least one year, as part of her plea agreement with state regulators.

The acupuncturist, Dr. Robert Charles Dumont, is a pediatrician, and a member of the faculty of the Integrative Medicine Department of Northwestern University School of Medicine. According to the consent decree, Usman “shall submit ten active patient charts on a quarterly basis” to Dumont. When asked if Usman is allowed to select which charts will be reviewed, a medical board spokesperson referred the reporter to the language in the consent decree.

Usman suggested to regulators the doctor who will be reviewing her charts, according to Usman’s attorney.

drusman

Usman is director of True Health Medical Center in Naperville, Illinois and owner of Pure Compounding Pharmacy. She a is regular presenter at Autism One, an annual gathering of vendors, providers, quasi-researchers and desperate parents.

The Illinois Department of Financial and Professional Regulation says Usman provided “medically unwarranted treatment that may potentially result in permanent disabling injuries” to a boy that Usman started seeing in the spring of 2002, when the child was not quite two years old. Records indicate Usman diagnosed the boy with a calcium-to-zinc imbalance, yeast, “dysbiosis”, low zinc, heavy metal toxicity, and abnormally high levels of aluminum, antimony, arsenic, cadmium, copper, lead, nickel, silver, tin, titanium and selenium. Usman prescribed chelation, a hormone modulator, and hyperbaric oxygen therapy, which regulators describe as an “extreme departure from rational medical judgment.”

The complaint against Usman was filed by the boy’s father in 2009. A year later, he sued Usman and Dr. Daniel Rossignol of Melbourne, Fla. for harming the child with “dangerous and unnecessary experimental treatments.” A Chicago-area lab, Doctor’s Data, was also sued. The plaintiff voluntarily dismissed the suit in 2014, but will reportedly reinstate it in 2015 or later.

Usman was the subject of a 2009 Chicago Tribune investigation into questionable medical practices aimed at treating autism. The article noted that Usman and Rossignol “are stars of Defeat Autism Now!, having trained thousands of clinicians…  They are listed on the group’s online clinician registry, a first stop for many parents of children with autism seeking alternative treatment.”

Usman’s name is also connected to the 2005 death of Tariq Nadama, a five-year-old boy who died at the hands of Dr. Roy Kerry. Usman diagnosed the boy with high aluminum levels, then referred him to Kerry, an ear-nose-throat specialist in Pennsylvania. Kerry treated the child for lead poisoning, even though his blood lead levels were below that which indicates the need for chelation.

Cross posted from Autism News Beat

IACC Presentation by Lisa Croen: Psychiatric and Medical Conditions Among Adults with ASD

20 Nov

The last meeting of the previous Interagency Autism Coordinating Committee (IACC) was a workshop on under recognized co-occurring conditions in ASD. One of the speakers was Lisa Croen of Kaiser Permanente. She spoke about psychiatric and medical conditions among adults with ASD. Much of this work (and more) was presented as a webinar at SFARI. This work was also presented at IMFAR.

If you can find the time to watch the video (it’s 17 minutes long), it’s well worth it. This is the sort of work we just haven’t seen before now–a look at medical needs of autistic adults. If you don’t have that time, here are a few highlights.

First consider the sort of medical conditions that get a lot of attention in the pediatric population: Sleep, GI and immune. For the pediatric population, one can watch the presentation by the Lewin group that was also given at the IACC workshop: IACC Co-occurring conditions workshop: Lewin Group presentation on co-occurring conditions in autistic children in the U.S..

In adults, GI, sleep and immune conditions are found more often in the autistic population than in the general population. Moderately more often. Interestingly, thyroid conditions are 2.5 times more common (compare this to GI disorders, which are 1.3 times more common).

croen 3

By contrast, psychiatric conditions like anxiety, depression and suicide attempts are even more common in the autistic population. Schizophrenia is 22 times more common.

croen 1

Neurologic conditions are also more common in the autistic population. Parkinson’s is 32 times more common in autistics. Dementia is 4.4 times more common.

croen 2

This is the sort of work I’ve been calling for since even before I was appointed to the IACC. The autism parent community and the research community spends a lot of time talking about learning about kids and getting tools into the hands of pediatricians. But what about adults? We know that epilepsy often has an onset about puberty for autistic kids. We know that for another developmental disability, Down Syndrome, early onset dementia is relatively common. But what is going on right now with adults? What is do we, parents and autistics, have to plan around for the future?

If I recall correctly, the last comment I made as a member of the IACC had to do with this study.

Those are exactly the kind of things that frankly scare the heck out of me and I would like to know more about. And know there’s something on the horizon I need to know about and if there is a way to intervene with adults.


By Matt Carey

IACC Co-occurring conditions workshop: Lewin Group presentation on co-occurring conditions in autistic children in the U.S.

4 Nov

Anjali Jain of the Lewin group presented on data they have collected from medical records about the prevalence of co-occurring conditions found in autistic children in the U.S.. This presentation was made to the Interagency Autism Coordinating Committee in Sept. 2014. (the original video is here, and the Lewin Group talk started at about timestamp 17:50.  The original has closed captioning).

Some of the most common co-occurring conditions are anxiety and depression. In fact, mental health conditions are found in about 70% of autistics. Similarly, neurological conditions and neurodevelopmental disorders are found in about 70% of autistics. By comparison, GI+nutritional disorders (which include areas like allergies), which get a great deal of attention, are found in about 20% of the autistic population. While large, this is much less common than the 70% rates found for mental health and neurodevelopmental disorders.

Another interesting finding was that autistic children are seen more often for treatment of infectious diseases. If the risk for serious problems from infectious diseases is higher in autistic children, this makes the decision of many autism parents to stop vaccinating their children even more problematic.

The full video (with closed captioning) can be found here:

http://videocast.nih.gov/launch.asp?18636


By Matt Carey

Globanews.ca reports:Health Canada seizes dangerous health product

20 Oct

The article is very short but the news is good–Health Canada has gone beyond issuing warnings about MMS (also known as CD protocol, CDS, Chlorine Dioxide Solution, Magic Mineral Solution). They have seized the product from one supplier:

According to Health Canada, MMS contains sodium chlorite, which is used as a textile bleaching agent and disinfectant. An alternate form of MMS, which is called CDS, is also being sold on the same web site. It would have the same risks associated with it as MMS.

Health Canada has now seized the product since sodium chlorite is not approved for human consumption.

If you have been using the product, it is recommended you stop immediately and go see your doctor.

MMS is a scam, plain and simple. And a dangerous scam. More discussion of it can be found at the Thinking Person’s Guide to Autism in: Dangerous Interventions: MMS and Autism by Emily Willingham, Ph.D..


By Matt Carey

The Quacks behind the Warrior Moms

13 Oct

I accept Dr Carpenter’s opinion that there is no evidence that any of these treatments were individually beneficial for M and that collectively they were intrusive and contrary to his best interests.  M’s life was increasingly dominated by the programme of treatment to the exclusion of other activities.  I find that E has implemented a programme of diet, supplements and treatments and therapies indiscriminately, with no analysis as to whether they are for M’s benefit, and on a scale that has been oppressive and contrary to his interests.  She has exercised total control of this aspect of M’s life.’

Mr Honourable Justice Baker, In the Court of Protection, Judgment, In the matter of the Mental Capacity Act 2005 and in the matter of M, 11 August 2014

Brian Deer has once again done a service to the autism community, by putting in the public domain the judgment of Mr Justice Baker in the case arising from a dispute between a local authority and the mother (E) and father (A) of a young man (M) with autism.

http://briandeer.com/solved/mother-lied-protection-news.htm

Deer’s report, published in the Sunday Times on 12 October, focuses on the judge’s scathing judgment on E, a prominent supporter of the claim by the discredited Royal Free researcher Andrew Wakefield of a link between the MMR vaccine and autism. Mr Justice Baker concluded that E had fabricated evidence of an adverse reaction to MMR in her son, invented a range of associated diagnoses, subjected her son to unnecessary tests and treatments, neglected a dental abscess and indulged in fantasy conspiracy theories.

This Court of Protection case offered a rare opportunity to ventilate in public some of the controversies that have raged in the world of autism over the past decade. In the USA, the Omnibus Autism proceedings in 2008-9 provided a public forum in which claims regarding vaccine-autism links and associated alternative treatments were exposed as scientifically baseless and clinically irresponsible.

http://www.spiked-online.com/newsite/article/6283#.VDqLgWd0yUk

Though Mr Justice Baker did not address the MMR link or alternative treatments in general, his 92 page report provides a devastating indictment of the role of a range of therapists in relation to M, some of whom appeared as witnesses. In addition to exclusion diets and supplements, M received homeopathy, cranial osteopathy, reflexology, naturopathy, light and sound therapy, auditory integration training and hyperbaric oxygen therapy. It is clear that E’s descent into irrationality and paranoia was supported and encouraged by a number of dubious authorities and therapists, with damaging consequences for her son and her family.

Three therapists gave evidence in support of E’s treatment of her son. Shelley Birkett-Eyles, an occupational therapist working in a private clinic, was accepted by Mr Justice Baker as a ‘responsible practitioner’, though he noted that her reliability was challenged by Dr Peter Carpenter, a consultant psychiatrist with a special interest in learning disability, the expert witness called by the local authority.

Dr Peter Julu describes himself as ‘autonomic neurophysiologist’ (based at the private Breakspear Clinic), though Mr Justice Baker questioned whether this was a legitimate speciality and noted that his diagnosis of ‘neurodevelopmental dysautonomia’ was disputed by Dr Carpenter, who also challenged the reliability of his assessments and treatments, particularly his recommendation of hyperbaric oxygen therapy.

Ms Juliet Hayward, a nutritional therapist, was censured for giving ‘advice well beyond her expertise’, in endorsing a diagnosis of Lyme Disease and in prescribing a dietary protocol without taking an adequate medical history. Mr Justice Baker concluded that he ‘was left with a profound anxiety about Ms Haywood’s influence on E and her role in the treatment that M has received.’

Mr Justice Baker was particularly concerned that none of these three had received training in issues of ‘mental capacity’ as codified in the 2005 Mental Capacity Act. He observed that ‘it was clear from their evidence that none of them had given proper consideration to the question whether M had capacity to consent to their assessments or the treatment they were prescribing’.

In addition to these therapists, E called as expert witnesses two veterans of the Wakefield anti-MMR campaign: Dr Ken Aitken, a clinical psychologist formerly associated with the (now defunct) Autism Treatment Trust providing alternative treatments in Edinburgh; and Mr Paul Shattock, a retired pharmacy lecturer from Sunderland, a long-standing promoter of exclusion diets and unorthodox biomedical therapies.

http://www.spiked-online.com/newsite/article/5992#.VDqNsWd0yUk

By contrast with other expert witnesses (including Dr Peter Carpenter, Dr Alison Beck, Professor Robin Williamson, Dr Gwyn Adshead, Mr Keith McKinstrie), whom Mr Justice  Baker found to be ‘wholly reliable and professional’, he expressed considerable reservations about Aitken and Shattock:

‘I was concerned at times as to their qualifications to opine on some of the matters about which they gave evidence.’

In his conclusion, Mr Justice Baker categorically rejected the approach advocated by Aitken and Shattock in relation to M:

‘I stress, again, that I am not making any definitive findings on the efficacy of alternative treatments generally.  That is not the subject of these proceedings, which are about M.  I do, however, find that: (1) there is no reliable evidence that the alternative treatments given to M have had any positive impact on people with autism generally or M in particular and (2) the approach to prescribing alternative treatments to and assessing the impact of such treatments on people with autism in general and M in particular has lacked the rigor and responsibility usually associated with conventional medicine.’

Mr Justice Baker repudiated ‘the fallacy’ of E’s belief that there are two parallel approaches to the diagnosis and treatment of autism, each of which is equally valid:

‘The evidence in this hearing has demonstrated clearly that there is one approach – the clinical approach advocated by Dr Carpenter – that is methodical, rigorous and valid, and other approaches advocated by a number of other practitioners, for which there is no evidence of any positive impact and which (in this case at least) have been followed with insufficient rigor.  Whilst each treatment may be harmless, they may, if imposed collectively and indiscriminately, be unduly restrictive and contrary to the patient’s interests.  These disadvantages are compounded when, as in several instances in this case, insufficient consideration is given by the practitioners to the question of whether a mentally-incapacitated patient has consented to or wishes to have the treatment.’

Given his characterisation of E’s performance in court as controlling, manipulative, duplicitous and obstructive it was perhaps not surprising that Mr Justice Baker expressed some sympathy for the long-suffering family GP, Dr W. This ‘older-style family GP’ had been ‘tolerant and sympathetic’ and had maintained a good relationship with the family ‘until he went into the witness box’, when it became clear to E and her husband that, though Dr W had been attentive to the family needs and had responded to her requests to arrange investigations that he did not consider clinically indicated, he did not endorse her wilder theories and diagnoses. Though the parents later expressed ‘disillusionment’ with Dr W, Mr Justice Baker found his evidence ‘responsible, truthful and humane’.

Michael Fitzpatrick

13 October 2014

Michael Fitzpatrick has an autistic son close in age to M; he is a doctor, former GP and the author of MMR and Autism: What Parents Need to Know (2004) and Defeating Autism: A Damaging Delusion (2009)

Since bleach wasn’t enough, let’s start adding hydrochloric acid to MMS?

27 Aug

MMS. Miracle Mineral Solution is dangerous bunk. They’ve taken such a hit with people exposing it as bunk that they’ve started rebranding themselves as “CD” of “Chlorine Dioxide”.

The basic idea is that there are bad things inside you that make you sick. And by sick, they include autistic. If you ingest something that kills the bad things, or take enemas that kill the bad things, you will no longer be sick. There’s a lot of handwaving about how this only works on the bad things and not the good things like, say, the tissues in your body.

It’s nonsense. Dangerous nonsense.

MMS stands for Miracle Mineral Solution. It’s not a miracle. It’s not a mineral. It is a solution made by combining two other solutions to get chlorine dioxide in solution. The two starter solutions are sodium chlorite (a powerful bleach) and citric acid.

Well if citric acid is “good”, how can we make it “better” some have asked?

A New Simpler MMS: CDH – Chlorine Dioxide Holding (01-04-2014)

Here’s what they say:

While CDS has no raw materials left in the final product, CDH does, making it similar to classic MMS. The main difference between classic MMS and CDH, however, is that the sodium chlorite is allowed to react with the acid for a much longer period of time which reduces the amount of unactivated sodium chlorite and activator left in the final CDH solution. Then, since CDH is more fully activated outside of the body, it causes little or no stomach upset in most people. Also, CDH made with 4% HCl tastes much better. (Note: For those who still have a problem with the taste, “Sweetleaf” brand liquid stevia has been tested and is compatible with MMS, thus can be used to make it taste even better.)

If you took high school or college chemistry you probably remember the very sharp aroma of HCl. You may remember how it can burn skin and the lining of your nose. It’s nasty stuff. Sure, they’ve got relatively dilute HCl (4%), but, still, WHAT ARE THEY THINKING? (and after that–people are looking at 10% HCl! There is something seriously wrong here)

MMS/CD/CDH, whatever you want to call this, it’s a scam. People post to Facebook pictures of the intestinal linings of their disabled kids, passed with the help of MMS enemas. They caption these pictures with statements about how MMS killed “worms”. Rather than go to a doctor and see if there are real parasites, they are self-diagnosing and self-treating and causing harm.

One of the main avenues for promoting this to the autism community is the AutismOne parent convention, where MMS pracitioner Terri Kerri Riviera sells her services under the guise of “scientific” presentations.

And all the people presenting at AutismOne stand by and don’t say a word. The supposed leaders in that community don’t seem to have the ability to spot scam artists (which is pretty obvious given the years they have spent promoting Andrew Wakefield, to give just one example). They also lack courage. They rarely if ever stand up to anyone who is promoting obvious and dangerous nonsense.

The all show up, promote themselves, their goods and services, and go home. It’s time for them to show some courage. They can put a stop to this. Instead they lend their names and credibility to this obvious scam.


By Matt Carey


By Matt Carey

Recent Autism Gastrointestinal research funded by NIH

24 Jul

There are many parent advocates asking for research into gastrointestinal disorders and autism. My own anecdotal observations have been that these same parent advocates are of the belief that no work is ongoing. There are a number of projects ongoing and I’ve tried in the past to make that point (What projects are being funded in autism research? Part 1: vaccines and GI issues). I found 14 projects, nearly $3M in 2010. I found 11 projects for $1.7M in 2009.

I thought it time to revisit this question. I’m using a different data source–the NIH RePORTER database. Because of that these projects are those funded by NIH. Other Federal groups can and do fund autism research. Also private organizations like Autism Speaks

Below are the projects I found for the past few years. There are projects on epidemiology, treatment and biology.

While I think that the funding agencies could do a better job informing the communities about these projects, I sincerely wish that the parent advocacy groups calling for this research would inform their members that it is going on. I am actually very curious as to why they have not done that.

MECHANISMS OF AUTONOMIC BRAINSTEM DEVELOPMENT ($243,000)

Brainstem and autonomic circuitry, though understudied in neurodevelopmental disorders, are implicated in pathophysiology and co-occurring medical conditions, such as gastrointestinal disturbances (GID). The goal of this R21 project is to fill this knowledge gap, based on significant preliminary data.

CASEIN KINASE 1 INHIBITORS FOR TREATMENT OF AUTISM $349,610

The overall goal of our program is to (1) identify CK1 [Casein Kinase 1] inhibitors suitable for development as therapeutic agents and (2) to use these agents to investigate the suitability of CK1 inhibitors for addressing specific behavioral features of the complex, multi-symptom disorder known as autism.

The CADDRE SEED studies are multiyear but I haven’t listed all the grants. So the amount is much higher than even the substantial sums noted below.

MD CADDRE: STUDY TO EXPLORE EARLY DEVELOPMENT, SEED PHASE II $91,706

MD CADDRE: STUDY TO EXPLORE EARLY DEVELOPMENT, SEED PHASE II $1,600,000

CALIFORNIA CADDRE-SEED PHASE II $1,100,000

NC CADDRE: STUDY TO EXPLORE EARLY DEVELOPMENT (SEED) PHASE II $1,100,000

COLORADO CADDRE STUDY TO EXPLORE EARLY DEVELOPMENT CADDRE_SEED II $1,100,000

PA-CADDRE: STUDY TO EXPLORE EARLY DEVELOPMENT (SEED) PHASE II $1,100,000

SEED will address hypotheses including: ASD phenotypic variation, including the pattern of clustering of core symptoms, timing of onset, cognitive status, and presence of medical and psychiatric co-morbidities; gastrointestinal features; genetic variation and interaction with environmental risk factors (GxE); infection, immune function, and autoimmunity factors; hormonal factors and maternal reproductive characteristics; and sociodemographic and lifestyle factors.

INVESTIGATING THE GUT MICROBIOME FOR NOVEL THERAPIES AND DIAGNOSTICS FOR AUTISM $558,136 (also funded in 2013 for $558,136)

Based on compelling preliminary evidence, this project aims to explore the potential connection between GI barrier defects and altered behavior in preclinical models of autism. Our long-term goal is to explore possible serum biomarkers for ASD diagnosis, and potentially develop a novel probiotic therapy for at least a subset of children with ASD with GI issues.

2013 projects

TREATMENT OF MEDICAL CONDITIONS AMONG INDIVIDUALS WITH AUTISM SPECTRUM DISORDERS $488,568 (also, $339,591 in 2012, $264,726 in 2011, $578,006 in 2010, $535,209 in 2009, and $465,840 in 2008)

The life-long impairments in communication and social function are often complicated by the presence of medical comorbidities, including epilepsy, (and epileptiform discharges), gastrointestinal disturbances and sleep disorders.

REGULATION OF GASTROINTESTINAL NEUROMUSCULAR FUNCTION BY NIBP/NFKB SIGNALING $320,576 (and 2012 $343,747)

The proposed research is relevant to public health because the discovery of a novel function of NIBP/NFkB signaling in enteric neurons and glial cells is ultimately expected to increase the understanding of the pathogenesis of gastrointestinal diseases. It also shed light on the therapeutics for gastrointestinal inflammation and functional disorders.

ARE AUTISM SPECTRUM DISORDERS ASSOCIATED WITH LEAKY-GUT AT AN EARLY CRITIACAL PER $292,221 (and 2012 $302,820, and 2011 $302,820)

This project seeks to answer fundamental questions about the connection between early development of gastrointestinal (GI) problems (constipation, diarrhea, vomiting, etc.) and autism spectrum disorders (ASD)

From 2011

NEUROIMMUNOLOGIC INVESTIGATIONS OF AUTISM SPECTRUM DISORDERS (ASD) $264,726

A number of anecdotal reports have linked autism with gastrointestinal (GI) dysfunction; most notable among these are reports that autism is associated with “leaky gut” syndrome. Microbial translocation (MT) is the process by which bacteria or microbial byproducts permeate through the wall of the GI Tract (or other abnormally porous mucosal barriers) into the bloodstream. The microbial byproducts would then stimulate the immune system, which could have secondary effects on CNS functioning, or the byproducts could have a direct neurotoxic effect. We conducted assays of MT products in children with autism (from blood and CSF), as well as typically developing children (blood samples only).

and

Our ongoing phenotyping studies will be used to identify a cohort of children with autism who also have significant gastrointestinal symptoms in order to address this potentially important subgroup of patients.

A PRIMATE MODEL OF GUT, IMMUNE, AND CNS RESPONSE TO CHILDHOOD VACCINES $156,634


By Matt Carey