The purpose of this website is to provide material supplementary to the update review (not yet published) of the 1993-published autism theory paper (linked in header above). All the posts here serve that purpose in one way or another, but some are more worthwhile or necessary than others. So here is a brief guide to the contents here.

Click here to read discussion of whether there is a relationship of vaccines to autism.

"Skeptical" people will generate plenty of supposedly clever reasons for rejecting the whole basis of the antiinnatia theory. That's despite the fact that any such "skeptics" must therefore be instead gullibly taking seriously one of a handful of utterly absurd alternative theories as explained in the update paper.

An answer to one of these "skeptical" notions is this one about being supposedly impossible for mercury to get to the DNA. And this one about supposedly the history of Pink Disease (acrodynia) proving that mercury doesn't cause autism. But perhaps you're a sheep?

Autism research is now becoming seriously distorted by official charlatanism similar to that of which the proof is shown here. And that distortion directly affronts the truths to which this theory relates. One of the leading sources of extreme misinformation is the book by Paul Offit, which is being distributed free to parents of victims via the American Academy of Pediatrics.

The myths:

1. that there has been no autism increase,
2. that mercury is not associated with autism, and
3. that removal by chelation cannot help,

are all addressed in the articles linked above and therefrom (and more fully in conjunction with the update review paper).

Turning to less militarised corners of the autism research field, I'll first point out that theories are often not in conflict even when they superficially may appear to be.

And there is only one autistic/ASD/etc syndrome, not several or many "autisms".

You can find the link to the spectacularly-predicted Purgatorius video here, along with some further evidence relating to my explanation of the hand-flapping.

Some other peoples' excellent graphs of the increase in the US can be found here, particularly the ones with multiple differently-coloured curves. They basically confirm my interpretation of the California DDS data as essentially a simple exponential-shaped increase.

Here is a link to my comment on close-spaced pregnancy findings of Keely Cheslack-Postava, Kayuet Liu, and Peter S. Bearman.

I've added yet another amazing new prediction, that the Flynn Effect (rising IQs increase) affects non-human animals as well.

Mitochondrial dysfunctions could be caused by antiinnatia (both within and without the brain), or they could be a non-antiinnatia "side effect" of mercury toxication. They could be part of some processes whereby antiinnatia affects neuronal function. So the reports about mitochondria appear to give neither support nor challenge to antiinatia theory.

Data on a "photoninthedarkness" blog leads me now to thinking that the increase has involved some diagnostic substitution, but not in the way that is assumed by pro-vaxxers. More later, but I reckon when there was a rapid real increase of autism c. 1985-1995, much of it was incorrectly diagnosed as non-autistic retardation. Thereafter the diagnoses substituted to the correct autism diagnoses. This leads me to suspect that the autism increase actually stopped increasing about ten years ago and since then it's just been an artifact of substitution.

“We’re finding that the immune system seems to function at a lower level in autism,” says Hertz-Picciotto. Which could be because the dental mercury that caused the autism increase is well-known to also impair immune functioning.

July 2011: Powerful yet further evidence of mercury involvement in autism - 6-fold increased autism in children whose grandparents survived Pink Disease.

(I'll continue work on this intro menu in due course, so be sure to check back later.)

What evidence there is of effectiveness of chelation for autism, and what evidence that there is no mercury-autism connection anyway.

It is impossible to exist as a human with IQ above 50 or so without forming theories; for instance the theory that one should go to sleep at night, or that there's something called chocolate which tastes nice.

Those superiors who beam down their contempt for conspiracy theorising may be unduly believing in the opposite which we might call "integrity theorising". And the older I get the less and less evidence I see for any truth of such integrity theories!

Conspiracy theorising is limited in the contribution it can make towards resolving medical questions, but I think it can help. Here are two relevant “conspiracy theories” that are supported by so much evidence that I can’t even begin to present it here.
(1) Those who cause a great harm are inclined to go to great lengths to deflect blame from themselves. The medical establishment is well-aware that some of the sources of mercury exposure are from themselves, not least dental amalgam. So it has great hostility to any suggestion of mercury involvement in autism.
(2) One of the most profitable industries in history is Big Pharma. They have for numerous decades engaged in dirty tricks propaganda designed to suppress competition from alternatives to their own patented products. A million dollars spent on propaganda is peanuts to them. And just think how much more you could achieve if you had just one of those millions of dollars to deploy.

There has been a lot of misrepresentation of chelation therapy, not least because it is a whole new approach to treatment, not properly fitting into the categories of either nutrients or conventional drugs. Just as you would not lump together all pharma-drugs or all nutrients as if they were just one treatment, so you should not lump together all chelation treatments. Huge numbers have been killed by prescribed drugs, but we do not seriously argue that therefore all drugs should be banned.

There’s also been a lot of misrepresentation of chelation because even many of those who promote it are incompetent, having little understanding of what is involved.

In my experience the unequalled mercury chelation expert is Andrew Hall Cutler who worked out how to cure himself of “amalgam illness” as he calls it. There’s no substitute for reading his slightly pricey book titled “Amalgam Illness”. But you can get to the key part of it by finding it on Amazon.com (not co.uk), and clicking the “Look inside”, then searching for the word “avid” which will take you to page 201. Page 199 onwards explains the essence of competent chelation, and of why incompetent chelation can be rather harmful. It’s simply the difference between brute ignorance and knowledge of the simple principles, not some amazing rocket-science expertise or great skill.

The purpose of chelation is, as per the diagrams on pages 200-201, to remove the toxin from the body. EDTA is not good for mercury detox; AHC explicitly condemned its use in this 1999 book. For adult amalgam illness he recommends only a specific protocol of (optional) DMSA for lowering the general body levels, followed only later by the (necessary) use of ALA which enables transport out from the brain (but also into it which is why the outside-of-brain levels must be lowered first). ALA is a nutrient, an amino acid, so not really comparable to a synthetic drug -- except that in mercurised persons it has that great potential negative (as I experienced myself before I understood I was mercury poisoned; I certainly didn’t take a second tablet of it).

Elsewhere in his book AHC explains how to counteract the tendency of chelators to remove required elements alongside the toxic ones. Again this isn’t exactly rocket science, unless of course your job depends on not understanding it.

Thus you can see now why inappropriate chelation can certainly be harmful, just as you can easily kill yourself with some commonly available pills from the pharmacy. And the sensationalist propaganda anecdotes by Offit and Fitzpatrick of one death caused by an incompetent’s use of EDTA casts not the slightest light on the question of safety of competent chelation protocols.

AHC’s recommendation for chelation of autistics is roughly the same (DMSA–)ALA protocol as for adult amalgam illness, except with shorter intervals. He’s been critical of the protocols recommended by ARI/DAN people, but I don’t know the exact details (as therapy is not something I reckon to have comprehensive expertise about).

Hopefully the above has adequately explained the proper and improper uses of the widely differing protocols applied to the various chelators.

~~~~~~~~

Meanwhile, the medical corporo-establishment is hostile to the idea of mercury involvement in autism, for those two reasons of denying blame for causing it and opposing a non-pharma treatment for it.

You probably already know that it began with the thimerosal hypothesis, itself soon after Wakefield’s MMR hypothesis. These vaccine hypotheses were rightly debunked (at least as major autism factors), but once the debunkers got started they got carried away into falsely debunking everything else to do with autism-mercury -- in the context of those two prejudicing motives.

That included seeking to debunk chelation for autism. Both Offit’s and Fitzpatrick’s books deploy a number of fallacious critiques of chelation, accompanying their lurid highlighting of the irrelevant EDTA-related death anecdote. That latter is as logical as condemning the use of anti-depressants (“drugs”) on the basis of an anecdote of one death resulting from a pain-killer (“drugs”) overdose.

Meanwhile, what about the evidence of effectiveness?

Years ago the ARI instigated a whole load of carefully-designed studies which established the value of vitamin B6 in ameliorating autism in about half of cases. And then all that peer-reviewed, double-blinded, multi-replicated research was utterly ignored and pretended away anyway by the medical establishment.

Thereafter Rimland and Co understandably decided to let the “proper” scientific publishing process go to hell and the ARI concentrated on doing its own publishing via internet and conferences.

Non-establishment science faces increasingly severe obstacles to reaching the official recognition of a PubMed number. Researchers find funding unavailable; they fear having their careers trashed; and many journal editors and referees then deploy their own unsound hostilities. And then even if it does manage to get published it just gets ignored by the sheep and sheepdogs of the establishment anyway, like those B6 studies and my own theory paper.

The CDC, NIMH, MRC etc have not exactly been racing against one another to set up chelation trials with the millions at their command. It appears that eventually SafeMinds etc managed to pester them into setting up a trial, but it, oh, --so regettably!-- "had to be" halted due to supposedly some safety concerns. It couldn’t of course really even possibly be just because they were in danger of getting the “wrong” result and proving that chelation cures autism.

Meanwhile, in the real world, yes there are all those many videos of recovered children, which a lot of "experts" seem incapable of even mentioning, including for instance Simon Baron-Cohen, and "Research Autism" which pretends to be a charity trying to help autistics. And the plural of anecdote eventually does become scientific evidence despite all the efforts of sham scientists. Scientific American recently suggested that 75% of parents are now using the treatments decried as life-threatening quackery.

It is very analogous to the case of adult amalgam illness (which ironically is caused by the same amalgams that caused the autism increase). Many thousands of cases of spectacular “miraculous” recovery from serious intractable illness are on record; plus there’s my own stupendous case and the official lies and evasions to prevent me getting treatment; the internet is getting more and more flooded with such stark testimonies. Amalgam’s even been banned now in Sweden, Norway, and Denmark. And yet parts of the med establishment and their slimey assistants such as Ben Goldacre insist on just churning out yet more lies and patently pseudo-science reports such as the SCENIHR one.

Evidence that the real quackery is coming from the medical establishment:
their defence of mercury is demonstrably a pile of rubbish.

Senior names in the research bureaucracy such as Linda Birnbaum assert that an autism-mercury connection has been found to be lacking. The putative evidence of this lack of involvement of mercury rests on three studies, namely Ip et al, Soden, and Hertz-Picciotto et al. 2010. But the first two have been shown to be flawed beyond repair, and indeed evidencing the opposite, by DeSoto and Hitlan 2010. And the remaining study has meanwhile been shown by myself to be worthless rubbish malfounded on a most elementary error.

Oh, and now we have this further would-be contribution: http://www.ncbi.nlm.nih.gov/pubmed/19027035, which purports an ignorance of even the most basic principle of chelation therapy (namely removing the toxin from the body) and substitutes a straw-man fallacious in-situ “detoxification” concept of its own. It is just as impossible to carry out a test of chelation in vitro (or in this case "in tissue") as it is impossible to venture out on a test drive of a car engine which is standing isolated from the car body on a mechanic's bench. When a dentist drills your tooth it instantly creates more pain than was there already. But we don't validly infer from that that dental treatment is counterproductive; because the treatment has to be evaluated as a whole.

That’s four out of four piles of rubbish constantly cited by the very-well-qualified professional defenders of mercury.

On the one hand there is that fourfold pile of rubbish supposedly showing no involvement of mercury. On the other hand the evidence that mercury is involved in autism is now so substantial as to be far beyond reasonable doubt (as reviewed in my update review forthcoming).

Wouldn't it be wonderful if researchers in capitalist countries were paid to find out the truth rather than to cover it up and oppress victims?
More pages relevant to chelation denialism are linked here.

(This post has been written in response to a question asked on the lbrb blog - search for the second comment by "daedalus".)
Two more studies apparently showing a mercury connection (though I've not read them as I concentrate my reading on things that don't agree with my current conclusions): http://www.informaworld.com/smpp/content~db=all~content=a916457948 and http://www.medscape.com/viewarticle/730552

There is only one autistic/ASD syndrome!

There are many thousands of autistics, and each one is unique.

But I resolutely reject the notion suggested by some, that there are "many autisms", for the following reasons.

The world has been aware of the autistic syndrome/Asperger syndrome for nearing 70 years now. Many people have spent much time trying to delineate separate subdivisions within that syndrome. The result has been a resounding lack of finding any such subdivisions. Even attempts to show any certain distinction between "Aspergers" and "high-functioning autism" have drawn a blank [as per Tony Attwood's review linked at end here].

Meanwhile there are certainly great variations in how autism manifests. And there is much reason to believe that the etiological (causal) factors can be quite different in different cases.

Years ago when I was first writing down the antiinnatia theory of autism I wrote a paragraph which explained about this. But because the paper (as published in 1993) was already rather long, I cut that paragraph out before publication. I'll now reinstate it here, in concept at least (as I don't remember the original wording).

Autism(/ASD etc) is like a tree. Just as a tree has many roots, so autism has many causes. Just as a tree has many branches, so autism has many characteristics and signs (notwithstanding the dumbing-down to a "triad of impairments"). But also, just as a tree has only one trunk, so autism/ASD/Aspergers/etc has only one central causal, definitional mechanism/concept, namely antiinnatia.

We can elaborate this metaphor of a tree by thinking of it as grounded in some rather peculiar soil. At the northwest corner there is a lot of (say) uranium in the soil, whereas at the southeast corner there is none at all. In consequence of this the leaves of one corner of the tree contain a lot of uranium while at the opposite corner there is little or none. But all are part of the same tree.

But....!
Notwithstanding the above, it would be wise for autism research to recognise various distinctions, such as male/female, and late/early onset. And another distinction I would suggest to be particularly important.

The evidence concerning this is is more fully elaborated in my update review, but I will briefly outline it here. According to my update of the theory, the autism increase has been caused by mercury (from non-gamma-2 amalgams); whereas the pre-increase autism had generally minimal involvement of mercury. (But it couldn't be zero as no-one has ever lived in a zero-mercury environment.)

It follows that within contemporary autism/ASD/Aspergers/etc we are looking at two substantially different things. On the one hand the minority (10-20%?) who would have been autistic/etc even if the increase had not taken place. These would be the "true" autism/etc, so to speak. On the other hand, those cases caused by mercury intake. These latter are very likely to have a variety of mercury-specific symptoms accompanying their antiinnatia-caused symptoms.

It follows that any research that just lumps together both these groups is liable to learn little about either. Indicators towards distinguishing between the two are likely to include: age of onset, number of maternal amalgams, level of indoor mercury vapor, results of porphyrin tests or hair mercury tests. Meanwhile, mercury levels in blood or urine are most unlikely to be worthwhile distinguishers.

It may be possible to discern the two categories in bimodal distributions and or scattergrams, getting beyond overly simple averaging of the whole autistic category.

Review of Asperger's/Autism relationship by Tony Attwood.

Abstract of the draft of the update review of the antiinnatia theory

While I cannot post here the actual full paper (as that can breach the pre-publication policies of some journals), I think it will be ok to put here just the abstract (summary), as currently drafted. It's important to understand that this abstract has space only to merely assert the conclusions therein stated, but the full paper presents the evidence and reasoning through which those conclusions are reached.

The causes of autism: A theory now further supported by four predictions;
why dental amalgams caused increased autism;
and why mercury pollution caused the Flynn effect IQ increase

The gene-expression theory of autism and IQ (antiinnatia theory) is further supported via others’ findings relating to four predictions:
1. Correlation of body symmetry with IQ.
2. In autism, rationality less reduced by innate predispositions.
3. Autism being caused by molecules which erratically, dose-dependently bind to DNA and thereby reduce gene-expression (e.g. mercury).
4. Shared causality of raised IQ (the Flynn effect) and autism.
The hitherto-puzzling Flynn effect is explained in terms of varying atmospheric mercury. The Flynn effect has reversed because mercury pollution has reversed. Mercury pollution is probably causing harm additional to that currently recognised. Fetal testosterone is only a minor antiinnatia factor. Autism partially coincides with “extreme-male-brain”. The concept of “developmental instability” is unsound.
Summary of the amalgam case:
· Autistic behaviours are shown to have increased about tenfold in Western capitalist countries.
· Mercury was definitely involved.
· Mercury vapor from amalgams is the main source of mercury in the body.
· No other tenable sources of the mercury are available.
· Non-gamma-2 amalgams emit 30-50 times more mercury vapor, which is highly absorbed by lungs and infant brain.
· Exponential increase started promptly after the introduction of non-gamma-2 amalgams.
· A marked change of ratio of age of onset coincided closely with the increase. Yet the ratio remained low in Poland, where data did not show any increase either.
· Number of maternal amalgams is a risk factor for autism in the US, but maybe not in Poland.
· The antiinnatia theory had unknowingly pre-explained how mercury would cause autism.
· Accords with the antiinnatia theory causality of maintained suppression rather than knockout blow.
· The late onset is explained as due to accumulation when infants regularly inhale the vapor.
· The new ventilation prediction has already been supported by correlation of rainfall/snowfall with autism.

I cannot put this update paper on a website in advance of it being accepted by a journal. But in the interim I can send you a draft copy by email if you email a request for it to rpclarke{att]autismcauses{dott]info .

Abnormalities of the "resting network" and of language lateralisation

In my most recent draft of the update review of the theory, I wrote:

Pisula (2010) lists numerous areas of the brain which are known to be normally (and by implication innately) associated with specified psychological functions, and which function abnormally in autism. She notes that these findings cannot be adequately accounted for in terms of “theory of mind” or “executive dysfunction” or “lack of central coherence”. But they all rather obviously fall very clearly within the concept of innatons being affected by excessive antiinnatia. So Pisula’s review can be re-read in retrospect as even further testimony to the empirical soundness of the antiinnatia theory...."

I'd now add to that list two more instances of a similar kind.

Firstly the "resting network", which in neurotypicals activates while not concentrating on a task, and becomes inactive when task-engaged. Whereas in autistics it tends to just have a similar level of activity in both circumstances. Ref: Failing to deactivate: Resting functional abnormalities in autism. Daniel P. Kennedy, Elizabeth Redcay and Eric Courchesne

Secondly, here is Dr Courchesne speaking before the ASF's 2010 meeting:
“We discovered that autistic infants and toddlers displayed a pronounced abnormality of language activation and cortical development.” “At each age studied from infancy to young childhood, most autistic subjects had greater activation on the incorrect side, namely, the right temporal cortex, compared to the left side and this incorrect activation pattern did not change or “normalize” even by 3 or 4 years of age. The abnormal pattern was strong in a substantial percentage of autistic infants and toddlers....".

More evidence on the autism increase

Uta Frith is one of the most notable names in what we might call the autism research 'establishment'. She has recently stated [1] that autism in earlier decades was usually of the classic, severe variety, whereas nowadays most or many cases are of the mild to moderate or high-functioning variety. Putting that in the context of my view that there has been a major global increase due to a certain identified environmental factor, her observation poses the question of why that environmental factor should have produced generally less extreme autism than the preceding "genetic" form did.

And that is a question that is very happily answered by my explanation of the increase. Because the cause I invoke accumulates postnatally, it only impacts at a later age, whereas the classic genetic causation would impact from long before birth. And so one would indeed expect the new causation to commonly be less severe than the earlier variety.
1. Uta Frith, Autism: A very short introduction, OUP 2008