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‘Neurodiversity’ in New York Magazine

26 May

The journalist and author Andrew Solomon (author of the truly excellent and personally recommended Noonday Demon) has written a long piece for New York Magazine entitled The New Wave of Autism Rights Activists in which he paints us a picture of the heavily fractured tripod of autism activism.

Its far, far too long for me to summarise but I will try and give a very brief overview of how Solomon sees these three groups:

There are in reality three sides in this debate: those who believe autism is caused by environmental toxins (especially vaccines) and should be cured by addressing those pollutants; those who believe it is genetic and should be addressed through the genome; and the neurodiverse, who believe that it is genetic and should be left alone. These camps are blatantly hostile to one another. Gerald Fischbach, the scientific director of the Simons Foundation, one of the largest private funders of autism research, says, “I’ve never seen an advocacy community as intense and demanding. The mercuries get livid when people talk about genetics. The geneticists get furious when people talk about environmental toxins. And these activists get angry at both.”

That is a fairly accurate picture although not without it faults (ND’s believing autism should be ‘left alone’….not sure about that – and Solomon does qualify that statement later on)

I don’t really want to talk that much about Solomon’s piece. Its very, very good overall in my opinion. What I _do_ want to talk about is my reaction to it and how my slightly changed view of what ‘neurodiversity’ means to me is.

Ever since I had a large public disagreement with certain people last year about how I and other parents on the Autism Hub allegedly advocated (this disagreement led me to ‘outing’ myself as a manic depressive, handing over ownership and control of the Autism Hub and taking time away from blogging for a week or two), I have been thinking off and on about ‘neurodiversity’ as a practical construct.

I will come clean and say that Andrew contacted me for a statement about what I thought about neurodiversity as someone both neurologically different and also parent to someone neurologically different. That I didn’t make it into the final piece is testament to his skills as a journalist and my own growing ambivalence regarding neurodiversity. I started off by saying:

I felt that I had a good handle on the meaning of neurodiversity – to me it was simple: the diversity of neurology or, to lengthen that out to a truly epic state of pedantry, the many differing states of being that could be neurologically encompassed.

and I still do think that. I also said:

…what neurodiversity was, was a concept that could be embraced by people who valued difference and respected those who were different. It didn’t matter to me that those who embraced the concept were parents or professionals or autistic people or blind people or bipolar people or any mixture of the above. The important thing was that here was a group of people who were saying that being different wasn’t bad. That it (whatever ‘it’ happened to be for you) was a state of being worthy of respect in its own right. It is vital to me that my child grows up to think of xyrself as a person who is entitled to respect.

Beyond that, I am unsure what – if any – of the other things associated with neurodiversity apply to me. I am not ‘anti-cure’. I agree with Alex Plank who states in the article:

Alex Plank, who founded the Wrong Planet Website, which has over 19,000 members, says, “Since no cure exists, I don’t have to be opposed or for it. The thing now is to deal with the autistic people who are already on this planet.

What I want to do is raise my child to a point where xe can advocate for xyrself. If there was a cure invented tomorrow I would want xyr to able to ask the question xyrself: ‘Do I want this?’. This is because, as a parent, just as it is not my right to make xyr not autistic, it is neither my right to keep xyr autistic against xyr own wishes. I am a parent first and advocate second. Let me go even further. If a cure was discovered tomorrow I would not advocate against it. I would try and debate its use as something that should be used with extreme caution but I would not advocate against it point blank.

I come from a viewpoint that views a cure for autism as something that should not be necessary, not as something that should not exist.

What I mean by that is that I do not think it should be _necessary_ for someone who was autistic to be made not autistic in order to enjoy their life. I see plenty of autistic people clearly enjoying their lives and who they are. I want to see respect, tolerance and caring to come _first_ – not only after someone has been ‘cured’. This is (to me) at the root of the recent issue involving Alex Barton. One argument is that because Alex is autistic this is only to be expected. I disagree with that totally. I think that Alex was/is worthy of respect whatever his neurology. Its the same reason I don’t really like the heavy NT bashing that goes on at some ASD forums – two wrongs never make a right.

I also come from a belief that science is important. I therefore recognise that we cannot pick and choose what science we like and what we don’t. Science is either valid or it isn’t. So, when a scientist writes a _good_ paper that states MMR doesn’t cause autism I have to (by definition of science) agree with it. Likewise however, if a scientist writes a _good_ paper that states that Facilitated Communication is not valid, I have to accept that also. I do think that some neurodiversity activists are guilty of picking and choosing what science they like and saying its good and vilifying science that they don’t agree with. Which is fine if the criticism is valid. But not if it isn’t.

If a scientist works on a cure for autism should he be stopped? No way. To me, that’s pointless. If science is interested in a subject they’ll do it. Not always in the best interests of humanity I grant you but all the same – the debate about what to do with the results of said science are more practical than simply trying to stop it.

So, I’m not sure if I am ‘ND’ anymore. Or maybe I’ve just re-interpreted what I think being ‘ND’ means for myself. I don’t know.

Edit: Missed a bit

The closing of Andrew Solomon’s piece is a bit of a dichotomy.

Severe autism is a ghastly affliction that should be cured

I’m afraid that I entirely disagree with Andrew there. They key word is ‘should’. To me, the sentence would be more representative of my own personal definition of ‘nd’ if it read:

Is it important to cure ‘severe’ autism or look more carefully at how the rest of society operates around ‘severely’ autistic people?

.

However, it seems as though Andrew was reading my mind when he wrote:

It is unproductive to rail against the incurable; if you can learn to love it, that’s your best chance of happiness. For some people, the love is self-evident; for others, it is acquired through struggle; others cannot do more than pretend to it. Though neurodiversity activists can get in the way of science and sometimes wrap themselves up in self-important, specious arguments, they also light the way to such love—a model of social acceptance and self-acceptance that has the capacity to redeem whole lives.

Laura Hewitson’s Stinker

18 May

Sorry about the title, I couldn’t find a word to rhyme with her last name to infer wrong-doing a la Age of Autism’s ‘Grinker’s Stinker. Anyway….

Meet Laura Hewitson. Laura is the lead and joint author of a trio of papers presented at this years IMFAR as posters.

These papers (also shredded by Orac) purport to show how it is possible to mimic the 1999 US vaccine schedule and give monkeys autism as a reult. Never mind the fact that the results reported don’t sound or present anything like autism (<em>”survival reflexes, tests of color discrimination and reversal, and learning sets”</em> huh??), lets look at Laura Hewitson a bit more closely then I managed to in a quick 10 min post last time.

As I mentioned at the time, Laura Hewitson claims affiliation with DAN! Thats enough in my book to place a rather large red flag against her impartiality.

Now I’ve learnt that her entanglement with the vaccine/autism hypotheses goes very much further than that.

It turns out that Hewitson’s partner is Dan Hollenbeck, an Age of Autism contributor. Hollenbeck owns the website FightingAutism.org and in the top right hand corner of the FightingAutism website are the words:

FightingAutism is now part of Thoughtful House Center for Children.

And we all know who is the big cheese at THoughtful House don’t we? That’s right – one Andrew Wakefield. He’s also the co-author to the three studies poster presented at IMFAR.

Hollenbeck’s asociation with Thoughtful House goes beyond just having a website affiliated with them however. He’s also an employee of Thoughtful House.

Director of Information Technology for Thoughtful House, Dan Hollenbeck received his Bachelor of Science degree in Electrical and Computer Engineering from the University of Wisconsin-Madison in 1992

….

When their son was diagnosed with autism in 2001, the Hollenbecks relocated from Oregon to Pittsburgh in order to accept employment as an Information Technology Manager for a large NIH (National Institutes of Health)-funded medical research organization

….

He is also on the Board of Directors, as well as the Research Committee, for SafeMinds…

So, here we are with three poster presentations from a woman who has an autistic son, affiliated with DAN!, is married to the Thoughtful House IT guy (who also happens to be on the Board of Directors of SafeMinds) and these afore-mentioned poster presentations are also co-authored by Andrew Wakefield.

I wonder just how impartial this science can be?

How about when we throw one more fact into the equation?

437. Laura Hewiston (sic) and Dan Hollenbeck on behalf of Joshua Hollenbeck, Dallas, Texas, Court of Federal Claims Number 03-1166V

That’s right. Hewitson and Hollenbeck are suing HHS for vaccine injury visited upon their son Joshua.

Now, lets turn our attention to IMFAR where Hewitson made her three poster presentations. INSAR have regulations governing the papers and abstracts submitted.

INSAR requires authors to disclose their sources of contributed support (commercial, public, or private foundation grants, and off-label use of drugs, if any). INSAR also requires authors to signify whether there may be a real or perceived conflict of interest. Any potential for financial gain that may be derived from reported work may constitute a potential conflict of interest.”

Now, maybe Hewitson did note the fact that:

a) Her husband is an employee of an organisation that makes money from treating what they allege is vaccine caused autism.

b) She has an autistic child.

c) Said child has been registered for compensation for alleged vaccine damage resulting in autism (I assume they’re part of the Omnibus proceedings then?)

But if she did, then it isn’t recorded in the abstracts posted on the Age of Autism website.

Monkeying Around

16 May

Its IMFAR time again and over on Age of Autism (thanks to Kelli Ann Davies for this priceless hat tip) they’re getting all het-up:

SICK MONKEYS: RESEARCH LINKS VACCINE LOAD, AUTISM SIGNS
The first research project to examine effects of the total vaccine load received by children in the 1990s has found autism-like signs and symptoms in infant monkeys vaccinated the same way. The study’s principal investigator, Laura Hewitson from the University of Pittsburgh, reports developmental delays, behavior problems and brain changes in macaque monkeys that mimic “certain neurological abnormalities of autism.”

Autism signs? Not just ‘autism? Research hasn’t linked vaccine load to autism?

I’d love to tell you more about this (and the other two accompanying studies on the same subject) but I can’t. Why? Well, because they’re not actually _studies_ as such. They’re poster presentations.

So, what’s a poster presentation? Well, its exactly what it sounds like – its a researcher, making a poster of their research and standing beside it for an hour, hoping other people find it enough of interest to look at. A few popular ones are sometimes asked to be presented orally. There are usually at least a hundred different poster presentations at a conference. It mostly depends on teh size of the conference hall.

Age of Autism’s Dan Olmsted says:

Poster presentations must go through a form of peer review before they are presented at the conference; the papers have not yet appeared in a scientific journal.

One of those two statements is true. The other is sadly not. Here are ‘the rules’ for poster presentations at IMFAR 2008.

Posterboards will have a display area 194cm wide X 84cm high. We suggest that you produce posters in A0 landscape format (120cm wide X 84cm high). Posters will be fixed to boards using sticky-back Velcro that will be supplied on site. Poster Numbers 1-60 will be located in the Champagne Terrace room, and Numbers 61-120 will be located in the Bordeaux room. In the programme a time is allocated for each poster presenter to be standing by their poster.

The page goes on to provide some helpful tips such as: ‘Less is more’ (probably no worries on that score) and ‘Use an appropriate font’. Hopefully, the team will have taken onboard the services a real typography expert such as Dr Paul King of CoMeD.

So – I can tell you next to nothing about these poster presentations. The good folk at AoA seemed oddly reluctant to link through to the abstracts.

However, I can tell you a little about the authors. The primary author seems to be Laura Hewiston of Pittsburgh University. She is registered on that page as a DAN! Doctor. She (I think its the same person) also appears here (see 953) and here.

Also listed as an author according to AoA is one AJ Wakefield. Enough said about that!

Lastly, is Steve Walker who did a poster presentation at an IMFAR in the past (can’t recall which one) which also appeared to offer support for the MMR hypothesis. Oddly, that poster presentation never made it into any kind of peer reviewed journal.

Best comment on Age of Autism comes courtesy of David Ayoub who begins with:

someone slap me!

I tell you, if that man didn’t exist, someone would have to invent him.

No such thing as a genetic epidemic

15 May

Since the Autism Omnibus started up again, I’ve been talking about how the Petitioners have pulled the tablecloth out from under the feet of the mercury militia. Its been a mainstay of the militia that there has been an epidemic of autism since the early 1990’s, caused by vaccines, most notably thiomersal and MMR (hence the strapline of mercury militia bible Evidence of Harm – Mercury in Vaccines and the Autism Epidemic and the ‘M’ in SafeMinds (Sensible Action For Ending Mercury -Induced Neurological Disorders).

In fact, lets be clear, SafeMinds believe in an Autism Epidemic, Generation Rescue believe in an Autism Epidemic, the NAA believe in an Autism Epidemic, Jenny McCarthy believes in an Autism Epidemic.

And yet this week, we had petitioners expert witness (i.e. _for the families_) in the autism omnibus destroying the idea of an epidemic. According to him, the number of children throughout the 1990’s/early noughties was in the hundreds.

That’s ‘hundreds’ from a population of 40 million.

He went on to say:

Q: So if the risk is confined to that group, clearly regressive autism, are you assuming then that there is no elevated risk to any other group – any other cases of autism?

A: In the calculations I made, yes.

This is a deliberate strategy on behalf on Petitioners. They want to destroy the idea that all the epidemiological evidence regarding autism and vaccines has shown thus far – that there is no association between autism and any vaccine. They cannot challenge the quality of the science itself so they have moved the goal posts. They are now saying _not_ that vaccines cause autism, but that _some_ vaccines _may_ cause autism in a population of children so tiny it cannot be detected by epidemiology.

That is in direct opposition to the very idea of an autism epidemic which, by definition, must be large and ‘unmissable’ – a tsunami of autism.

Amusingly, the beloved science editor of the Age of Autism blog decided the best way to deal with _his own sides_ expert testimony was to pretend it had never happened.

‘You cannot have a genetic epidemic’ – that’s another mainstay of the mercury militia. The idea that there has been an epidemic is used to support the idea that genes play a small, negligible role in autism (if they play a role at all) because ‘you cannot have a genetic epidemic’ and as we all know there has been au autism epidemic right? Therefore, genees can’t have played any role _in_ that epidemic.

Except that the families in the Autism Omnibus are now relying almost totally on the idea that there never _was_ an autism epidemic.

The genetic role in autism science came to the fore again yesterday when Yale announced a new study that found Genetic links to impaired social behavior in autism:

With the help of Yale’s Autism Center of Excellence, led by Drs. Ami Klin and Fred Volkmar, and many families of individuals with ASD, we have registered a possible association between some of the genes identified in animal studies as controlling affiliative behaviors in ASD.” The strongest statistical findings of the study implicate the prolactin gene, the prolactin receptor gene, and the oxytocin receptor gene in these affiliative behavior deficits.

I haven’t read the paper yet (and I’ll probably need help to understand all the highly technical gene talk) but I’ll probably have nore to say once I have. For now, its interesting that in the week that expert witness for the families in the Autism Omnibus gutted the epidemic hypothesis, yet another study was released linking genes to autism.

Enforced Vaccination

11 May

I don’t like this, I really don’t.

I know I advocate for the undoubted and scientifically established benefits of vaccination and will continue to do so, but the news that the influential Fabian Society have recommended a policy of enforced vaccination is not good.

In an article for the Fabian Society, leading public health expert Sir Sandy Macara called for child benefit to be linked with vaccination uptake.

And Labour MP Mary Creagh said children should have to prove they are vaccinated before they start school to improve uptake of MMR.

Call for vaccine opt-out penalty

I’m all up for improving the uptake of MMR, I think that is a worthy and vital goal. But is this – educationally and financially punishing children – the right way to do it? Because make no mistake, the parents won’t particularly care that their kids are home schooled. And the type of parent who doesn’t vaccinate (wealthy, white middle class) won’t miss the child benefit. But the child at the heart of these penalties may well miss scholastic education. As a home schoolers ourselves (less through choice than lack of any other option) one of the things we are keenly aware our child misses is the company of her peers in an educational setting.

For those who don’t know, the Fabian Society is a ‘middle-left’ think tank that recommends policy to Labour Party members, particularly influential whilst we have a Labour government (as we do now). They reached this recommendation apparently after:

A poll by YouGov for the Fabian Society suggested that the public would back government action on MMR to address large rises in mumps and measles’ cases. It found that 63% of the public felt that immunisation only worked if everyone was covered, and only 31%felt if was purely up to families to make the choice.

MMR press release

YouGov are a well thought-of (in terms of results accuracy) market research agency. I’ve little doubt the figures they collected are correct. I still don’t like it though. I think that something needs to be done, but this? The penalties seem targeted to ‘hit’ the kids. It also seems tantamount to admitting that attempts to utilise the excellent, freely available science that has killed the MMR hypothesis is pointless.

I’m also frankly disturbed by this quote from Fabian review author Sir Sandy Macara:

One ought to recognise that mothers have a responsibility for ensuring their children are protected.

Mothers? Not parents?

This seems ill thought out, knee-jerk-ish and guaranteed to play into the hands of the conspiracy theorists. We need to do better – much better – than this.

Age of Autism Excels Itself

4 May

It’s my opinion that the blog Age of Autism has not ever once published a post that has contributed anything to the sum of human knowledge in a general sense, nor has it ever published a post that is designed to actually help autistic people live their lives.

However, every once in awhile, it publishes a post that is so monumentally stupid that I literally think the worse of myself for wasting time reading it. And here I am actually blogging about one. Sigh.

Such a post appeared today. It is entitled ‘CDC triggers measles outbreak’. The author of this post, ex-UPI journo Dan Olmsted says:

I’m starting to think we should rename the CDC the Centers for Disease Contagion. You’ve all seen the news that there are suddenly more measles cases in the United States and the CDC is blaming it in part on the increasing reluctance of parents to vaccinate their kids.

But it’s the CDC’s fault, and no other. Getting the “measles shot” means getting the MMR, and the MMR is “the autism shot” in the minds of many, many parents.

So, let me get this straight. It is the CDC’s fault that measles is making a return across the US? I see.

Its not, for example, the fault of the non-vaccinating upper-middle class soccer-mommies and daddies, for example:

Of the 64 people infected by the measles virus, only 1 had documentation of prior vaccination. Among the other 63 case-patients were 14 infants who were too young to be vaccinated. Many of the cases among US children occurred in children whose parents claimed exemption from vaccination due to religious or personal beliefs, or in children too young to be vaccinated.

Hell, no. _That_ couldn’t be the issue, right? Its obviously the CDC’s fault. Damn them for providing the vaccines and a schedule that has led to serious measles epidemics being held at bay in the US and the UK prior to the last 10 years of utter complacency and idiocy.

And why is Dan Olmsted happy to blame the CDC?

Let me tell you one reason why I’m not shy or circumspect about squarely blaming the CDC for this — because Jon Poling, Hannah’s dad, predicted something like this, or much worse, just a few week ago

And as we all know:

Dr, Poling is the real deal, educated at Johns Hopkins, devoted both to his daughter and his patients, tempered by reality. He’s mild-mannered. He’s mainstream. He’s credible.

Riiiiight. This is the same Jon Poling who was recently described by his co-authors as ‘muddying the waters’. The same Jon Poling who’s wife has been a subscriber to the vaccine hypothesis since at least 2001. The same Jon Poling who knowingly uses incorrect epidemiology.

I’m afraid that Jon Poling is right now in the process of extricating himself from the mainstream. And also from any concept of credibility. His refusal to approve access to information that would provide more accuracy to public statements members of his clique have made about the situation is testament to a man who is not governed by any reality other than a desire to push a pre-conceived agenda.

But really, the attempt to point the finger elsewhere by Dan Olmsted is nothing more than a childish ‘It wasn’t me! Its not my fault!’ when both logic and morality show quite clearly that if people decide to eschew something that might not only save their kids lives but the lives and/or well-being of the society in which they live then the finger of responsibility can only point in one direction.

US Reports Biggest Measles Outbreak Since 2001

2 May

The biggest U.S. outbreak of measles since 2001 is unfolding in 10 states, with at least 72 people ranging from infants to the elderly becoming ill — most of them unvaccinated, U.S. health officials said on Thursday.

The U.S. Centers for Disease Control and Prevention said none of those who caught the highly contagious viral illness has died, but at least 14 people have been hospitalized, most with pneumonia triggered by measles.

Lets hope that none of these 14 actually get any worse or (god forbid) die. Lets hope that no one else gets sick. The last time people dies of measles in the US was 1991, the year before that pesky vaccine schedule was strengthened – not that that has any bearing on the matter I’m sure.

1989 to 1991, when 55,000 people got measles and 123 died.

On this recent outbreak, the CDC said:

Of the 64 people infected by the measles virus, only 1 had documentation of prior vaccination. Among the other 63 case-patients were 14 infants who were too young to be vaccinated. Many of the cases among US children occurred in children whose parents claimed exemption from vaccination due to religious or personal beliefs, or in children too young to be vaccinated.

Anti-vaccinationists inflict the coolest things on their kids. Illness, hospitalisation, death….

I wonder if any of these things will make it onto the no doubt completely rational signs the parents attending the ‘Green our vaccines’ rally will be waving around. After all, when the organiser of the event says:

I am surely not going to tell anyone to vaccinate. But if I had another child, there’s no way in hell…….for my next kid—which I’m never going to have—there’s no way.

Then you can rest assured that this will in no way be an anti-vaccine event.

Right?

Frustration

20 Apr

One of the most frustrating things about blogging the unfolding vaccine>mitochondria>autism hypothesis is that a lot of the doctors who are experts in the field of mitochondria don’t want to publicly comment. A lot of them feel quite rightly that there is a certain element who are not the most balanced of individuals and they don’t really want to expose themselves to these people. That I can definitely empathise with.

However it does, as one of them has admitted themselves, leave the field wide open to (and I quote directly from one of these doctors):

….legions of mountebanks eager to pad their retirement funds at the expense of desperate parents…

So when a very well respected mitochondria researcher says the following all I can do is post it and not attribute it and hope that it can be read and believed. Of course, the fact it appears on this blog will no doubt cause some to dismiss it entirely but I would urge them not to do so. Please remember that kids with mitochondrial issues are a whole new ball game. Talking their parents out of vaccinating them could very well kill them.

…..I do not know of any evidence connecting mercury and mitochondrial disease. There is no evidence connecting vaccination with mitochondrial diseases: certainly vaccinations do not cause mitochondrial diseases. Whether they may act as transient stressors, like intercurrent URIs do, remains to be determined. Clearly, energy-challenged children with mitochondrial diseases need to be protected from potentially deadly infections through vaccination.

Wakefield Admits Fabrication

17 Apr

Here:

The doctor whose study triggered a collapse in public confidence in the combined measles, mumps, and rubella (MMR) vaccine told a disciplinary panel last week that he made up details of his son’s birthday party—at which he took blood samples from several children—when giving a speech in California.

……

Last week the GMC panel saw video footage of a speech Dr Wakefield gave in 1999 at a meeting of parents of autistic children called by the Mind Institute of the University of California, Davis, where he jokingly described children fainting and vomiting after giving blood.

“Two children fainted, one threw up over his mother,” he told his laughing audience in the clip. “People said to me, you can’t do that— children won’t come back to your birthday parties. I said we live in a market economy; next year they’ll want £10.”

But Dr Wakefield told the GMC panel that he had made up these details to amuse his listeners. “It was the end of a long and rather exacting talk for the parents, and it was an attempt to introduce a little bit of levity,” he said. “It was a quip, just a story. The way these stories are told, if the audience responds you tend to respond back.
So the story was told. But it had no bearing on the truth at all.”

“Clearly, if it has caused any distress then I am extremely sorry for that,” said Dr Wakefield. “That wasn’t my intention.” He added that he had been “naive” to think he could take the samples without the permission of an ethics committee.

So – the first confirmation from Wakefield himself what a lot of us suspected – Wakefield makes stuff up.

Why? What possible reason could he have for making up such a thing? Is it to make himself the centre of attention? To become the darling raconteur? God knows that some Americans think that Brits are all witty mini Oscar Wilde’s (I am living proof we’re not). Did he feel obliged to play up to that image?

Or is he lying now to escape censure for what he actually _did_ do?

Who can know? Its all getting a bit tacky.

Anti-vaccination and autism

16 Apr

I need to reproduce this comment from Amy Tuteur, MD on Autism News Beat. Its perfect.

“How does Dr. Tuteur explain parents who fully vaccinated and trusted the vaccination policy and then became disenchanted with it only after seeing their children seriously injured?”

Disenchantment is not the standard. The scientific evidence is the standard. It is not as though this hasn’t been studied. The purported link between vaccines and autism has been studied extensively and repeatedly. The scientific evidence indicates no difference in the incidence of autism between those who are vaccinated and those who are not. There is also no difference in the incidence of autism between those who received vaccines containing thimerosal and those who did not.

We’ve looked and the link simply isn’t there. That’s not surprising when you consider that the classic descriptions of the onset of autism, elucidated long before the use of multiple vaccines, is exactly the same as the onset of autism today. Vaccines do not increase the incidence of autism. Thimerosal does not increase the incidence of autism. The natural history of autism has not changed since the introduction of vaccines. It cannot be any clearer than that.

The conspiracy theories are a bunch of baloney. In order for there to be a conspiracy, someone must be hiding information. Doctors are vaccinating their children. Vaccine manufacturers are vaccinating their children. Immunologists are vaccinating their children. Who, precisely, is conspiring to keep information from the public and are we really supposed to believe that they would sacrifice their own children just to preserve the conspiracy?

Moreover, it isn’t as though doctors, immunologist and vaccine manufacturers are denying that vaccines have risks. It is well known that vaccines can and will cause small numbers of deaths and cases of brain damage. We have set up a compensation system precisely because we know about and acknowledge these risks. If doctors, immunologists and vaccine manufacturers are forthcoming about the risk of DEATH, isn’t it a bit absurd to suggest that they would hide the risk of autism?

One thing is certain, vaccine rejectionists do not understand immunology. Immunology is extremely complicated, so it’s not surprising that many people don’t understand it. However, the fact that they don’t understand it tells us nothing about immunology or vaccines, just like the fact that most people do not understand Einstein’s theories of general and special relativity tell us nothing about whether they are true.

Autism is a very serious problem. To the extent that we waste time, money, attention and effort on something that is not causing autism, we are diverting time, money, attention and effort from finding the real cause for autism. That is the saddest aspect of this incredibly sad situation.

I also recently read ‘Trusting blindly can be the biggest risk of all’: organised resistance to childhood vaccination in the UK which has some fascinating things to say on the anti-vaccine movement and their history. Consider this:

There is a small but fascinating social history literature which looks at the birth of resistance during this period in the form of groups like the Leicester Anti-Vaccination League and critical publications like the Vaccination Inquirer . Several of the accounts demonstrate the successes of organised campaigns which inspired marches of up to 100,000 people, riots, public burning of effigies of Edward Jenner, and the celebration of martyrs (Beck 1960, Porter and Porter 1988, Durbach 2000)…..Other accounts of this period stress the impressive ability of the anti-vaccinators to harness the power of the press (Howard 2003) and the important role of key individuals in pushing forward the movement.

Sounds familiar huh?

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