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WXYZ and bad "investigative" reporting

11 Jul

Wouldn’t you love to move on from the thimerosal debate? Yes, I mean that as part of the greater move away from the vaccine/autism debate. But we are closing in on the end of the thimerosal era and, let’s face it, the nebulous arguments about “toxins” will be around for a while. People have learned the lessons of not making clearly falsifiable claims or setting deadlines for the “autism rate to decline”, so they will be able to keep the general vaccine discussion alive for some time to come.

But, we aren’t there yet with thimerosal. And, to prove the point, Steve Wilson at station WXYZ in Detroit has managed to regurgitate the standard thimerosal arguments. That would be not surprising. I expect a these aftershocks. What I is really annoying is the methodology. Orac has referred to it as “yellow journalism”, and I quite agree.

I will note that Orac and the Denialism Blog have both covered this in greater detail than I can. AutismNewsBeat has a journalist’s viewpoint as well.

Why am I annoyed with Steve Wilson? First off, he starts out by claiming that the “prevailing strategy seems to be to downplay the possibility of any link so that parents will continue to vaccinate their children”. (rough quote, sorry, I just don’t want to listen to that over and over again).

Sounds like a page from the Bernadine Healy playbook. Let’s imply something sinister is going on. Let’s imply that the AAP is hiding evidence. Steve: how about acknowledging that the “prevailing strategy” is to tell people what the science actually says? Doesn’t that seem like the “prevailing strategy” that the AAP and others are using? It does to me.

Another big chunk of the Steve Wilson’s report is based on this statement:

“..the truth is, there is still as much as ever..in 11 vaccines”

At this point, it’s worth reading Orac who lists the actual pediatric vaccines and their thimerosal levels.

You see, Steve Wilson pulled a classic con. Sorry to call it so bluntly, but that’s what I see. He talks about vaccines that aren’t being given to children young enough to develop autism. I don’t even know if the 11 vaccines he is talking about really do have thimerosal. Because, it doesn’t matter in this discussion. What matters is the pediatric vaccine schedule.

The part that bugs me is that Steve Wilson knows it. He gives as an example the thimerosal in tetanus boosters given to 11 year olds. Yes, he actually talks about 11 year olds.

Yep, the goalposts have moved so far, we are building new stadiums. 11 year olds being given tetanus boosters might develop autism. Except for Jim Carrey, who has ever implicated Tetanus shots? Even Jim Carry didn’t indicate that it was the booster given at age 11.

It appears to me that Mr. Wilson isn’t even going to the actual sources for his information. His report is a nice smattering of the standard vaccines-cause-autism line. One bit that caught my attention is when he talks about statements in the congressional record.

A congressional committee that studied the matter has already concluded: “Thimerosal…is directly related to the Autism epidemic.”

I was pretty sure that was a Dan Burton quote, so I Googled it to find the source. I came up with Deadly Immunity, by Robert Kennedy Jr, but I didn’t find the part of the congressional record with it. I looked a bit harder and found that the congressional record shows the statement as:

“Thimerosal used as a preservative in vaccines in [sic] likely related to the autism epidemic.”

I don’t agree with the above either. But, compare “likely related” (Steve Wilson) and “directly related” (congressional record). Somewhat different meaning, don’t you think?

I can’t resist putting out some of the list of “what do we know about mercury”? As it turns out, a lot. A lot more than I ever wanted to know, I’ll tell you that. A lot more than actually helps my family. But, here are some examples of what we know:

1) the dose makes the poison. Absolutely. There has to be a dose small enough that it would not cause toxicity.

2) mercury is everywhere. It was in the organic cinnamon-applesauce cup I just ate. It was in the organic lemonade juicebox I just drank. (sounds like I am the one on the playground, eh?).

3) When used in vaccines, it doesn’t increase the risk of most neurological disorders. Most? Yes, they didn’t include autism (see (5) below). Also, there were disorders that were indicated as possibly associated. Then again, there were some positive outcomes that were indicated as possibly associated with thimerosal. It looks like random chance–association is determined by statistics, and if you test enough associations, some will appear to be statistically significant.

4) when injected into pregnant women in RhoGaM type shots, it does not increase the risk of autism.

5) indications are that the upcoming CDC report on thimerosal and autism will show no increased risk.

6) Autism symptoms are not the same as mercury intoxication…autism is not “a novel form of mercury poisoning.

We could go on for a long time with the evidence against the concept that autism is caused by mercury. But, this is just a small list of the many things that somehow didn’t get into Steve Wilson’s investigative report.

New clues to autism's cause

10 Jul

Time report on a new study that found yet more genetic clues to what causes autism.

A paper published in the current issue of Science by researchers at Children’s Hospital Boston and members of the Boston-based Autism Consortium identifies five new autism-related gene defects. Already, more than a dozen genetic defects have been found to be associated with autism spectrum disorders, which affect about 1 in 150 children, according to the Centers for Disease Control and Prevention. But the good news, say the Boston researchers, is that many of the genes are beginning to fit into a pattern. “While it might seem discouraging that it’s a growing list of genes, we can be encouraged that a common pathway is emerging,” says Dr. Christopher Walsh, chief of genetics at Children’s Hospital Boston and an author of the paper.

I haven’t read the paper yet but it sounds pretty interesting. They eschewed US and European people and elected to study Turkish and Middle East autistic people because these families have a high incidence of cousins marrying cousins. The end product of this paper is that the authors believe autism may:

…fundamentally amount to molecular defects in learning.

I have issues with the word defect. Some research indicates clearly that autistic people learn differently and not in a way that should be classed as a defect. However, I understand that scientists use terminology pertinent to their training. Hopefully, lessons can be learnt in this arena.

One fascinating thing – and one long suspected by many of us:

There may be hundreds of varieties of autism. From what researchers have seen so far, says Morrow, “It looks like almost every child with autism is different from the next — a different gene is mutated in almost every child.”

A different gene in every child. That – to me – is one more confirmation of what I once thought of as a spectrum and now imagine as an ever-shifting Aurora of autism. And not just autism but _all_ neurological differences.

Amanda Peet says it like it is

10 Jul

From Cookiemag.

Peet’s analytical urges are comical when she’s talking about kids’ gear, but not when she’s discussing a subject she feels is among today’s most pressing public-health issues: infant vaccinations. “As soon as I was pregnant, the neuroses kicked in,” says Peet, 36, who is married to screenwriter David Benioff. She began calling her older sister’s husband, a Philadelphia pediatrician, “every five minutes” with all kinds of questions, especially about shots. “I asked him, ‘Why are all of these necessary? Why are some people staggering them?’?” Eventually her brother-in-law arranged a series of phone calls between Peet and his own mentor, Paul Offit, M.D., who is chief of infectious diseases at the Children’s Hospital of Philadelphia, a co-inventor of the rotavirus vaccine, and a board member of Every Child by Two, a pro-vaccine organization cofounded in 1991 by former first lady Rosalynn Carter.

“Once we had spoken, I was shocked at the amount of misinformation floating around, particularly in Hollywood,” says Peet, who quickly boned up on the hot-button controversies surrounding the topic, including the unproven link between certain vaccines and autism; the safety of preservatives like mercury-based thimerosal; and the fear that the relatively high number of shots kids receive today can overwhelm young immune systems. Her conclusion? Well, not only is Frankie up-to-date on her vaccines (with no staggering), but her mom will soon appear in public-service announcements for Every Child by Two. “I buy 99 percent organic food for Frankie, and I don’t like to give her medicine or put sunscreen on her,” says Peet. “But now that I’ve done my research, vaccines do not concern me.” What does concern her is the growing number of unvaccinated children who are benefiting from the “shield” created by the inoculated—we are protected from viruses only if everyone, or most everyone, is immunized: “Frankly, I feel that parents who don’t vaccinate their children are parasites.

Amanda Peet

Why should I go bumping against people who were jogging?

10 Jul

I am once again thrilled to present LB/RB readers with something from Tito Rajarshi Mukhopadhyay.

Born in India, Tito is a non-verbal autistic person with a considerable talent for writing. His first book is (as I understand it) soon to be followed by a second. Enjoy.

Why should I go bumping against people who were jogging?

“Tito, don’t go that way. You are interrupting the people who are jogging.” I could hear my aide’s voice – loud and clear coming from a very fragile part of the world that I was trying to save at that moment.

I had a responsibility of saving a very scared and fragile world from the load of the sky that was threatening to drop any moment on it, if not for me and my responsible shoulders on which the sky had settled down, while I was walking around the trail.

Since I was feeling very responsible I did have my reasons for not obeying petty commands like, “Tito you need to walk this side of the trail,” or “Tito you need not run into any one jogging across from the other direction!”

The load of sky made me drift to the other side towards them who were coming towards my direction. Balancing the sky is never easy!!!

Since my aide did not see how I was saving the planet, he suspected that I was deliberately trying to block the passage of those serious-body-workers who have goals of sweating profusely so that they can mark the trail with distinguished vapours that evaporate from their individual biological fluids with independent chemical compositions.

Carrying the load of sky is not an easy and anybody’s work. And if people with whom I constantly bumped into had a problem comprehending it, that is not my problem.

Here's a story you won't see on Age of Autism

10 Jul

Not without substantial spin anyway.

The measles outbreak continues to push through the US:

The biggest U.S. outbreak of measles since 1997 has sickened 127 people in 15 states, most of whom were not vaccinated against the highly contagious viral illness, federal health officials said on Wednesday.

These are the consequences of not vaccinating.

Oh but measles is nothing right? Just a bit of a rash and then you’re done, right?

Maybe not.

A teenage boy has become the first person in the UK to die from measles for two years as cases of the disease continue to rise, Government scientists have said….The teenager, from West Yorkshire, who has not been named, had been born with a poor immune system, leaving him susceptible to infections and unlikely to have been able to be immunised. However, he would have been protected if there had been high vaccination rates in the community.

Because of the MMR scare in the late 1990s when the measles, mumps and rubella jab was linked to bowel disorders and autism, vaccinations levels have dropped below the threshold required to control the diseases.

Its really not difficult.

MMR doesn’t cause autism.
MMR helps raise herd immunity against measles, mumps and rubella.
High herd immunity means weakened members of ‘the herd’ don’t die.

Take MMR.

When is Jenny McCarthy Honest?

9 Jul

Is she honest in April 2008?

There are some who wonder what we mean when we say “recovering” from autism.

……

….we think there are treatments that often bring about such healing, so that the observable symptoms of the condition no longer exist.

……

We believe what helped Evan recover was starting a gluten-free, casein-free diet, vitamin supplementation, detox of metals, and anti-fungals for yeast overgrowth that plagued his intestines.

Or is she honest in June 2008?

A lot of people are scared to chelate, which is the process of pulling metals out of the body, but it has triggered many recoveries. … Everyone has their own recipe to recovery, but your child might need chelation to get there. With a DAN doctor, I mean these guys are so good, they will help, you know, make sure your child is safe, your child has the minerals it needs to do it. … I’m, of course, scared to do it with Evan, but I plan on doing it this summer because Evan still suffers from seizures……

(Contributor from Autism One Conference wishes to remain anonymous).

So, in April 2008, Evan McCarthy is recovered (‘we believe what helped Evan recover…’). Not recovering but recovered. We can also see that among the treatments the helped Evan ‘recover’ is ‘detox of metals’.

Fast forward two months later and apparently Even needs chelation. Why? Back in April he’s recovered. Now he’s not? Now he needs chelation? And what for? Back in April, one of the ‘treatments’ that ‘recovered’ Evan was ‘detox of metals’. So why does he need to be chelated?

Can we add this to the other things that McCarthy has been slightly, ummm, vague about? Such as the fate of her indigomoms.com website? It existed in May 2007 as I blogged about it. But by July 2007 it had disappeared. Jenny’s explanation (from June 2008)?

SS: “You mention the word Indigo. What happened to your Indigo Moms website?”

JM: “You know I had to take that down and I was so sad to take it down, for a while anyways, it’ll be coming back up. People got really confused because I was coming out with Evan’s autism at the same time. And, they thought that I was healing Evan through Tarot cards instead of biomedical treatments.

So I realized I had to separate my messages and I had to take down one message which is the indigo and crystals, for now. I said, ‘oh the world is getting confused with these two different paths,’ you know. I consider them to be one. But people aren’t quite there yet and I kinda had to, not lower my vibration, change my vibration to focusing on the world hearing that message. Hearing that biomedical treatment does help these kids.

Right, right – oh the world is getting confused….so Jen just lowered her vibration and took her indigomoms site down.

Jenny McCarthy - Indigo Mom

Is it just me, or is anyone else starting to have a really bad feeling about this person’s involvement in autism advocacy?

Chelation study to be 'released'?

9 Jul

AP print an even-handed account of the current state of a Chelation study. This study which was approved and then put on hold:

….for safety concerns after an animal study, published last year, linked DMSA to lasting brain problems in rats.

I’m really torn about this study. On one hand, it would put to rest once and for all the issue of whether chelation benefits autistic children (except it won’t. When it finds chelation does nothing it will simply be attacked as crap by the anti-vaccine/autism groups). On the other hand, it will mean putting a whole load of kids at risk for no purpose whatsoever.

“I don’t really know why we have to do this in helpless children,” said Ellen Silbergeld of Johns Hopkins University’s Bloomberg School of Public Health, who was invited to comment on the study to a review board of the national institute.

Quite.

Lets be clear. This study is being touted about for one reason and one reason only – to appease the anti-vaccine/autism groups. In the mainstream medical/scientific community (and notably in the toxicology community) it is well known that autistic kids aren’t toxic. Here is a few snippets from the testimony of Dr Jeffery Brent – a sub-specialty board certified medical toxicologist. He is an active member of the medical school teaching faculty and is an attending physician on the clinical pharmacology/toxicology consultation service at the University Hospital. Currently he holds the rank of Clinical Professor of Medicine at the University of Colorado Denver. Dr. Brent has a long list of publications, virtually all related to clinical toxicology. He is senior editor of Critical Care Toxicology: The Diagnosis and Management of the Critically Poisoned Patient and serves as Editor-in-Chief of Toxicological Reviews, a major international state-of-the-art review journal devoted to human toxicology.

Q: Dr Mumper discussed today some key aspects of chelation therapy….as a medical toxicologist do you see any reason for the chelation to remove mercury from either Jordan King or William Mead in these cases?

A: Absolutely not….there is no test in medicine that is more valid for for assessing mercury toxicity than an unprovoked urine mercury concentration.

[For Jordan King and William Mead]…their unprovoked urine concentration is exactly in the normal range.

On the other hand, they have been chelated. And the justification for that chelation with regard to mercury comes from what you see in the right hand column where in both cases, 4 out of 5 provoked examples have been…uh…increase urine mercury. Well, you’re supposed to have increased urine mercury with provoked examples! Therefore there is absolutely no indication based here or anywhere else I saw in the medical records that suggest that there is any mercury effect in these children and therefore that was absolutely no reason to chelate them for any mercury related reason.

The standard way of chelating autistic kids is to do a provoked challenge test. As Dr Brent says – you’re _supposed_ to have increased levels with provoked examples.

Q: There’s nothing here that would be out of the ordinary – from your experience – absent, even in the absence of a standard reference range.

A: Well, in truth we don’t (?) urine/leads because the ‘gold test’ is blood/lead so I haven’t looked at many urine/leads in children that I have chelated. So I can’t speak to that in my experience. But I have seen a number of patients now come to me because of these ‘doctor’s data’ type of laboratories which are based on urines – chelated urines – and they always have high leads in their chelated urines and I tell them ‘well, lets just do the gold standard test, lets get a blood/lead level and so far, 100% of the time they’ve been normal.

So basically, when you do the provoked, non-standard tests from labs that make a good living from charging for these tests, they come back positive. When experts like Dr Brent do the gold standard tests, 100% of the time they come back normal.

*There is no reason to chelate autistic children* .

And here in this report is part of the problem. There seems to be a type of scientist who wants to short-circuit the scientific process:

Insel said he has come to believe after listening to parents that traditional scientific research, building incrementally on animal studies and published papers, wasn’t answering questions fast enough.

Well, boo-hoo. Its slow for a reason. Its slow to be as accurate as possible and to be as safe for humans as possible. Insel needs to remember that his patients – his duty of care – is not to parents, but to the autistic people in his case load.

And one more thing….in this piece, Jenny McCarthy says:

Actress Jenny McCarthy, whose bestseller “Louder Than Words” details her search for treatments for her autistic son, Evan, told thousands of parents at a recent autism conference outside Chicago that she plans to try chelation on him this summer.

I thought Evan McCarthy was recovered? Surely Jenny McCarthy isn’t – can’t be – wrong?

Neurodiversity on show

9 Jul

I think I’ve talked before about how the concept of neurodiversity is – as well as being heavily personal – not necessarily something that most people know actually exists as a defined word. What I mean is, some people do things or hold views that are quite obviously neurodiverse but might never have heard of the word or concept.

Googe Alerts sent me a fantastic blog post this morning which was about a story I’d missed due to personal illness. It seems a young autistic girl had gone to a restaurant with her family and were ejected because the girl had a meltdown and another family refused to pay for their meal until the family of the autistic girl were removed.

Renee, the blog owner, makes it clear how repugnant the attitude of both the restaurant (and this intolerant person who demanded the girls family were ejected) were:

Now I will admit that I don’t know much about autism but I do know enough to realize that those that have it deserve the same respect and dignity as anyone else.

I would _love_ it, if that was everyones starting point. How nice would it be to have that attitude as the prevailing one when it comes to autism (or disability in general)?

Thats Neurodiversity right there folks.

Renee, goes on to detail some very intolerant responses to the reported story. They’re nothing that most of us who are either autistic or parents of autistic people have not heard in one shape or other before:

I don’t care if a child is autistic or what, the child needs behaviour modification. In this case, the child should have been removed from the restaurant by a parent until the child calmed down.

Thats someone who doesn’t get it. Thats someone whos probable priority as far as disability goes is not to respect the persons essential difference but to try and ignore it and make sure it does’t inconvenience them.

Thats what Neurodiversity challenges.

I’ll leave the last word to Renee, along with my thanks:

When we refuse to see people who are living with a form of disability whether it be physical, or mental as worthy of sharing our space we are constructing them as less than. It is in this disharmony of worth and value that ‘othering’ occurs. Our ability to project difference onto others leads to dire consequences for those that are unable to fit into a model of what society has accepted as “normal.” Despite the fact that we are individuals and no true norm exists, socially what we expect is conformity to preconceived ideas of what validates personhood.

Bias, Stigma and Stereotyping and their Effects on Autistic People

8 Jul

One of the presentations I made at the University of San Diego Summer Autism Conference was titled Bias, Stigma and Stereotyping and their effects on Autistic People. In the talk I explained that one tool researchers use study bias is called the Implicit Association Test or IAT . I don’t have extensive knowledge about IATs but I know a little about them because when I was an undergrad at UC Davis (a couple of years ago) I had a volunteer position as a research assistant to a professor who used IATs to study bias, specifically bias against particular ethnic groups.

My job was to interact with the research participants (who were likewise undergraduates), one of my most important duties was to get a signature from each participant on a release form that explained their rights as test subjects. I also had a little memorized statement to tell them about what they they were to do and what they should expect while taking the test (on a computer). Afterward, I was supposed to answer any simple questions that they had and tell them how to contact the professor or a post-doc to answer more complicated questions.

Occasionally the students really wanted to talk about what the material used in the experiment or about how the experiment was designed, and occasionally I had time to talk about it with them. Besides directing them to direct their questions to the researchers, I told them that if they wanted to learn more about the IATs, in general, there was a popular book called Blink, by Malcolm Gladwell, that would give them a little more information. I also told some of them about the Harvard University website called, Project Implicit which is dedicated to sharing information about the Implicit Association Test and is also used to gather data from the (anonymous) people who take the tests online (for free).

The experiment with which I was assisting wasn’t designed didn’t give the “results” of the tests to each individual participant, their data were not “attached” to them as a person with a name, but it was aggregated, more or less, with dozens of other people’s data. But, if you take an IAT on the Project Implicit site, the computer tells you your “results”. Here’s a link to the Project Implicit website:
https://implicit.harvard.edu/implicit/demo/takeatest.html

Near the beginning of this presentation in San Diego I read the following quote:
Every man has reminiscences which he would not tell to everyone but only to his friends. He has other matters which he would not reveal even to his friends but only to himself, and that in secret. But there are other things that a man is afraid to tell, even to himself, and every decent man has a number of such things stored away in his mind. – Fyodor Dostoyevsky
Dostoyevsky was writing about what people know at different levels of consciousness. I would say that he was pointing out that there are things that people believe that they would prefer not to believe, and those things are sometimes subconscious. I got the quote from the Project Implicit website.

If you read the book Blink, you may remember that he explained that everyone has biases and we don’t all like or agree with our biases. We may even have subconscious biases against people of our own group or ethnicity. Those biases might be there because of negative portrayals of people of our own group in the media and in the dominant culture we are surrounded with.

This picture is a sample of a page from one of the IATs on the Project Implicit website. If you saw this particular page during a test you would have been instructed to place the face in the category on the left or the one on the right, and as quickly as possible. Basically, you hit the “e” key on your keyboard if you think the picture or word in the middle if the screen belongs in a category that is listed on the left of the screen, and you hit the “i” key if you think that picture belongs in a category that is found on the right side of the screen.

For this particular IAT photographs of faces of White Americans or Native Americans (all the photos of faces were from late 1800s as far as I could tell). So for this particular page you would probably want to hit the “i” key because this fellow looks like a Native American and that category is on the right side of the page at this point in the test. The photos of faces were interspersed with modern color pictures of places that were located either in America or in a Foreign country. I don’t remember which places they showed, but for instance, a picture of the Eiffel Tower, or the Great Wall of China, might be shown and if you were taking this IAT you’d decide quickly if it was a photo of an “American” place or if it was a “Foreign” place.

Project Implicit offers free access to some journal articles about IATs, as far as I could tell, they don’t have any that touch on bias and autism. But they did have a paper there called: Implicit and Explicit Stigma of Mental Illness: Links to Clinical Care. It’s by Peris et al. It is “in press.” Obviously, keeping in mind that this is not a paper about stigma and autism, but about stigma and mental illness, I think it’s still worthwhile looking at what these researchers found.

In total, 1,539 participants were interviewed online and took an IAT (not unlike what I described above, using a keyboard to categorize words as quickly as possible as belonging to a category shown on the left or right side of the screen. More than half of the participants had studied psychology. This group ranged from undergrads studying psychology up to practicing psychologists. The bulk of the participants were professionals who not only had training in psychology, but presumably lots of experience of being around people with varying sorts of mental illness. They also had a control group of people without psychology training.

If you download the paper you can get the details, but to give you a very brief idea of what they did. The experiment the participants were asked to report what they thought about mentally ill people. Quoting the paper:

Participants rated their attitudes toward “mentally ill people” on a 7- point semantic differential scale (1 = bad to 7 = good). Analogous scales were completed for two other common stereotypes about persons with mental illness: blameworthy/innocent and helpless/competent. Note, the same ratings were also made regarding “people on welfare” to match the relative comparison category used on the IAT measure. In this way, we could more readily evaluate the relationship between the implicit and explicit bias measures.

They took an Implicit Associations Test designed to look for implicit associations or biases that the participants might have that would tend to link mental illness with negative words.The test compared judgments about people with mental illness with judgments about people who are on welfare.

In the first sorting condition, items representing the category Mentally Ill People (e.g., diagnosis, disorder) were categorized with the same response key as items representing the category Good (e.g., wonderful, joyful), while items representing Welfare Recipients (e.g., unemployed, poor) were categorized with the same response key as items representing Bad (e.g., terrible, awful). In the second condition, Mentally Ill People and Bad items were categorized with one response key, and Welfare Recipients and Good items were categorized with the other.

You may have to read the whole paper and perhaps some other background information on IATs to understand how they are designed and scored in order to get the rationale behind the study design.

The participants were also shown clinical vignettes which were “DSM IV based” clinical descriptions of people with problems who could be diagnosed as mental illness. They also looked at one vignette of a person with “general psychological difficulties” that didn’t really fit into any mental illness category.

This study reported the interactions between explicit and implicit biases and “clinical decision making”. Explicit biases are ones that the participants self-reported. Implicit biases were those not stated openly, but were “implicit associations” that were revealed by the IAT.

The were some findings that I thought were possibly applicable to the experience of autistic people being treated or diagnosed in “clinical settings.” The more training a person had in psychology, and presumably the more exposure that person had to people with mental illness, the more positive view they tended to have of mentally ill people. Which is good news. The bad news, which is old news to most people, is that the controls which are meant to represent the average person on the street without particular training in psychology (when compared to those with training) had more explicit and implicit bias against the idea of mentally ill people. Mental illness carries with it a heavy load of stigma. It may seem natural enough for us to fear and stigmatize mental illness, but it’s not so fun for those with mental illness to deal with being treated badly and thought of badly simply because of a label, not necessarily because of anything in particular that they have done.

Back to the study’s findings, even though people with training in psychology tended to have relatively less bias the mentally ill, there was still enough bias among them to measure and make correlations with how they tended to see those in the clinical vignettes. Peris et al found that if a clinician openly expressed a bias against mentally ill people, that he or she would tend to give a worse prognosis for a person whose description he had read. A bad prognosis might look something like, “this person is unlikely to be able to remain employed,” or “this person is likely to harm himself or others.”

On the other hand, if the person openly expressed no bias against mentally ill people, but nonetheless showed a perhaps hidden bias against the mentally ill via the IAT, that person tended to give a better prognosis, however tended to “over pathologize” or add on extra labels, the paper called this, “over-diagnosis”. In over-diagosis the person described in the clinical vignette got additional labels that the writers of the vignettes didn’t intend. For instance, the person in a clinical vignette who had symptoms best fitting a single diagnosis of alcohol dependence might get additional inappropriate labels like, anxiety disorder or major depression.

To quote the paper’s authors: “… the finding of a link between bias and clinical decision-making is striking and suggests that negative views toward mental illness may influence clinical care, even among individuals with considerable mental health training.” Of course, the authors say that the study should be extended to see if the way the psychologists reacted to the clinical vignettes is the same as they would diagnose and give prognoses in their practices.

Coming back to autism, maybe we need the think about whether or not bias against autistic people could likewise influence clinical care of autistic people. It’s well known that parents will work to get clinicians to either give or not give particular autism spectrum diagnoses. A parent of a child with bipolar disorder may prefer that their child be diagnosed with Asperger’s since Asperger’s is still a recognized disorder or disability, but maybe it has a cachet of “genius” that bipolar doesn’t have. And if you are very much involved with autism at all you probably know that people will try to get a kid who generally would be seen as “Asperger’s” to get an “autistic disorder” diagnosis so that the kid can get more services paid for by some entity. And some parents of obviously autism spectrum kids pressure diagnosticians to take the label off their kid because they don’t want the child to be ….uhm… stigmatized. And, unfortunately some parents want to have their efforts at curing their child to be officially recognized as successful, so maybe they’d like to say, “See I gave my kid 5,000 methyl B12 shots and she had 40 rounds of IV chelation and 300 dives in an HBOT tank and it all paid off!” or maybe they’d like to say, “Selling our home and taking on extra jobs and begging money from all our relatives to pay for ABA therapy has left us in tatters financially, but we got our real boy back.” Of course, it is appropriate to re-diagnose autistic kids sometimes. Some do start out looking very autistic and end up looking close to normal, at least some of the time. You can watch a couple of talks by Deborah Fein on the MIND Institute website about this very thing. She points out that kids sometimes move from looking autistic to looking ADHD, perhaps plus OCD, or plus ODD or anxiety… which makes me wonder about how much the clinician’s biases are influencing the desire to rid the kid of a single diagnosis or PDD,nos and replacing it with mulitples like “ADHD plus social anxiety plus depression.” Hmmm?

We know that clinicians sometimes give negative prognoses for very small children, such as, “this two year old child is autistic. He will never marry, never have a job, you might as well lock him up now in an institution and get on with your lives….” and we also know that some autistics have lots of different diagnoses on top of an ASD. We might ponder about why that is, is it because of bias against autistic people and autism in general? We don’t know because, as far as I can tell no one is studying it. Autism clinicians are pretty much all assumed to be blank slates who don’t bring to the table their own biases that influence their ability to judge a situation fairly or accurately. Autistic people are, in my opinion, inherently “irritating” to most folks. We aren’t so ingratiating or charming, we aren’t precisely acting on typical social rules, generally speaking, to say the least. Still if you learn more accurate things about autism as opposed to stigmatizing misinformation such as is commonly found on the Autism Speaks website or from the mercury parent organizations where you may read that autistics destroy families and are walking toxic-waste carrying “train-wrecks,” or you may hear that autistic teens are tsunamis of fiscal devastation, thank you Stephen Shore.  If you learn the true things about autism and autistic people you may actually start to like autistic people. You might think we are pretty fabulous. I think we are pretty fabulous. If you listen to people like me say things like, “autistics are pretty fabulous,” you can actually start to think differently about autism and perhaps change your biases.

I also found three other papers that I thought were interesting, they were referred to in this book chapter on IATs. (Lane, K. A., Banaji, M. R., Nosek, B. A., & Greenwald, A. G. (2007). Understanding and using the Implicit Association Test: IV: Procedures and validity. In B. Wittenbrink & N. Schwarz (Eds.), Implicit measures of attitudes: Procedures and controversies (pp. 59-102). New York: Guilford Press.) You can request this chapter from the project implicit website.  It’s free.

Could similar problems caused by bias against autistic people be affecting autistic people now?

In one study, physicians who held stronger negative stereotypes of African American people were more likely to give them less adequate care after a heart attack. Or you could say, “Belonging to a group your doctor has a bias against can be bad for your health.”

People with a bias against African Americans score lower on a test of intelligence in the presence of an African-American person. Or, if you are in the presence of someone who has a bias against you you can expect them to behave less intelligently.

Stronger implicit stereotyping of members of a group was associated with more negative judgments of ambiguous actions by a member of that ethnic group. Or, if people have a bias against you they will tend to interpret your neutral actions as negative.

What biases or attitudes about the autism spectrum, autistic children and autistic adults might we be hiding from ourselves? Is this important to ask?

Does 'autism' disrupt? And what does it disrupt?

8 Jul

Interesting post in the Seattle Times today. The title is _”Autism disrupts work and pay, article says”_ .

The article in question is a new study from Pediatrics:

<blockquote>An emerging body of work is showing the impact an autism diagnosis has on a family….<blockquote>….families with a child with ASD were 7 times more likely to report that child care problems affected employment than comparable families with typically developing children. These accommodations probably result in lower household income.</blockquote></blockquote>

Now, I’ll be upfront and say that I know those circumstances to be true. A combination of my own diagnosis (of manic depression) and my child’s diagnosis of severe autism with associated learning difficulties has made things very difficult at times. It is a simple truth that I cannot progress in my chosen career (I am a web developer) much past the stage I am at now because doing so means committing myself  (excuse the pun) to a schedule of work I cannot possibly meet, given our home circumstances. A lot of my professional friends and colleagues who are about my age and are of a similar skill level to me are now either owning their own companies or heading up teams of designers.

But…is it right to say that autism is the disrupting influence? Obviously In my own life there are my own personal medical issues but even so, I do not think it is right to say that it is _this_ which is the disruptive influence.

It is a simple truth that much more is expected of workers of this generation. People of my parents age never had the work pressures we do now. Employees are expected to work ‘above and beyond’ if they want to progress. To work hours beyond – way beyond – their contracted hours, to never be ill, to keep holidays to a time that is non disruptive to the employer. We in the West have started to live to work rather than working to live.

For a family with a special needs child (of any age) it is simply not realistic that they can meet this expectation. And so we _do_ need to expect a less financially comfortable life.

But what is the disrupting influence? Is it autism? Is it manic depression? Is it Down’s Syndrome? Is it Cerebral Palsy? Is it any other physical or mental difference?

Or is it the demands of a society that is putting less and less stock on the family and more on work?