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Upcoming IACC Subcommittee on Safety Meeting – November 29, 2010

17 Nov

The Interagency Autism Coordinating Committee (IACC) has a number of subcommittees to concentrate on various specific areas which may need research focus. The IACC subcommittee on Safety is a new subcommittee and it will hold a meeting on November 29.

Here is the roster of members:

Co-Chairs

Lyn Redwood, R.N., M.S.N.
Co-Founder and Vice President
Coalition for SafeMinds
Tyrone, Georgia

Alison Tepper Singer, M.B.A.
President
Autism Science Foundation
New York, New York

Members

Coleen Boyle, Ph.D.
Director
National Center on Birth Defects and Developmental
Disabilities
Centers for Disease Control and Prevention
Atlanta, Georgia

Ari Ne’eman
Founding President
Autistic Self Advocacy Network
Washington, DC

Peter van Dyck, M.D., M.P.H.
Associate Administrator
Maternal and Child Health
Health Resources and Services Administration
Rockville, Maryland

Here is the meeting announcement:

Interagency Autism Coordinating Committee (IACC) Subcommittee on Safety

Please join us for an IACC Subcommittee on Safety conference call that will take place on Monday, November 29, 2010 from 10:00 a.m. to 12:00 p.m. ET.

Agenda: The subcommittee plans to discuss issues related to autism and safety.

Members of the public who participate using the conference call phone number below will be able to listen to the meeting, but will not be heard.

Conference Call Access
USA/Canada Phone Number: 800-369-1754
Access code: 5105457

Individuals who participate using this service and who need special assistance, such as captioning of the conference call or other reasonable accommodations, should submit a request to the contact person listed above at least seven days prior to the meeting. If you experience any technical problems with the conference call, please-mail IACCTechSupport@acclaroresearch.com.

Please visit the IACC Events page for the latest information about the meeting, including registration, remote access information, the agenda and information about other upcoming IACC events.

Contact Person for this meeting is:

Ms. Lina Perez
Office of Autism Research Coordination
National Institute of Mental Health, NIH
6001 Executive Boulevard, NSC
Room 8185a
Rockville, MD 20852
Phone: 301-443-6040
Email: IACCpublicinquiries@mail.nih.gov

Upcoming Interagency Autism Coordinating Committee (IACC) Services Subcommittee Conference Call

16 Nov

The Interagency Autism Coordinating Committee (IACC) will be holding a subcommittee meeting on Monday. This particular meeting is for the services subcommittee.

Here is how the services subcommittee is described:

The IACC Services Subcommittee was created in 2008 to assess and improve services and supports for people with Autism Spectrum Disorder (ASD). Its vision is that one day, all people with ASD will have the services and supports they need and desire throughout their lifespan, helping them to reach their fullest potential.

The current array of services and supports available through Federal, state, and local government agencies and private organizations is a patchwork that varies greatly based on where the person with ASD lives, creating unique challenges for people with ASD and their families as they navigate what is often a fragmented system. As the number of children with ASD increases, the nation’s health, education, and social service systems must respond in turn to meet the needs of this growing population. Many adults with ASD remain undiagnosed and underserved, adding further complexity to meeting their needs.

Government agencies, private service organizations, and families must partner to improve and coordinate services to serve a broad spectrum of needs as, ultimately, the success of people with ASD will be largely dependent on the availability and quality of services and supports offered in their communities. The Services Subcommittee recognizes this fact and is working to support a strong services research base, and to raise the profile of ASD services and supports, and to ensure that appropriate, effective, and cost efficient service systems are developed and implemented in communities to improve the quality of life for people with ASD and their families.

Here is the announcement for the meeting:

Interagency Autism Coordinating Committee (IACC) Services Subcommittee

Please join us for an IACC Services Subcommittee conference call that will take place on Monday, November 29, 2010 from 2:00 p.m. to 4:00 p.m. ET.

Agenda: The subcommittee will discuss recommendations from the IACC workshop on services and supports that was held on November 8, 2010.

Members of the public who participate using the conference call phone number below will be able to listen to the meeting, but will not be heard.

Conference Call Access
USA/Canada Phone Number: 888-456-0356
Access code: 1427016

Individuals who participate using this service and who need special assistance, such as captioning of the conference call or other reasonable accommodations, should submit a request to the contact person listed above at least seven days prior to the meeting. If you experience any technical problems with the conference call, please e-mail IACCTechSupport@acclaroresearch.com.

Please visit the IACC Events page for the latest information about the meeting, including registration, remote access information, the agenda and information about other upcoming IACC events.

Contact Person for this meeting is:

Ms. Lina Perez
Office of Autism Research Coordination
National Institute of Mental Health, NIH
6001 Executive Boulevard, NSC
Room 8185a
Rockville, MD 20852
Phone: 301-443-6040
E-mail: IACCpublicinquiries@mail.nih.gov

Special ed students could bankrupt districts

16 Nov

At least according to a television station in San Francisco, California. In Special ed students could bankrupt districts Lyanne Melendez lays out a simple thesis:

The budget problems facing schools across California are getting even worse. There has been a dramatic increase in the number of special education students in recent years and the added cost of teaching them could bankrupt some school districts.

Starting with a bad premise, the story is bound to come to a bad conclusion. First, there are no “added costs” to teaching special education students. There are costs to educating students. We as a country decided, rightfully so, that one can not deny a student an education because doing so would cost more than the average.

We often hear how special education budgets “encroach” on the general education budgets. That is a false idea. Special Education students *are* students. General funds money spent on Special Education students *is* appropriate.

The rest of the piece by Lyanne Melendez is a classic example of scapegoating. Sorry to put it so bluntly, but that is my take.

Scapegoat (noun): a person or group made to bear the blame for others or to suffer in their place.

Why do I say this? Let’s look at one of the examples given in the story, Gilroy Unified School District. Google Maps puts Gilroy 80 miles south of San Francisco. Not to pick on Gilroy, but the idea that Special Education is bankrupting them doesn’t hold water.

Gilroy Unified School District is one of those districts that is struggling to cover the costs of educating special needs students.

“In 2002, our unfunded special ed costs were about $170,000, this school year it’s $3,200,000,” district spokesperson Deborah Toups said.

First, this irks me. There is no “unfunded” Special Education costs. The schools may not be reimbursed specifically for all special education costs, but they aren’t supposed to. Yes, there was a commitment by the Federal government to pay 40% of the costs (this is a sore point for me), but that doesn’t mean that local communities shouldn’t be funding whatever the Federal government doesn’t pay. Special education students are a part of the student population. It is the responsibility of the people to educate all students.

Let’s check some simple numbers. In the past 8 years, the budget for Gilroy Unified has been going down and the enrollment has been going up.

The website for the district has a number of documents relating to the budget. Here is the 2010-2011 budget book and here is a table of the budget and projected budgets (click it to enlarge):

The total budget is $82M this year. $3M for special education would be a big chunk of that budget. But, is that the whole story? I couldn’t find the 2002 budget numbers, but in 2005, the budget for Gilroy Unified was $119M .

So, the budget is down $37M in 5 years. Could this, perhaps, be part of the financial problem for Girloy Unified?

How about student population? The number of special ed kids has actually dropped. Gilroy had 882 special ed students in the 2009-10 school year and 923 2002-03 school year.

Note that overall student enrollment went up from 9,630 students in 2002/03 to to 11,116 in 2009/10. So, total student enrollment is going up, revenues are down.

Also, if I did my math correctly, that means that Gilroy Unified saw a *drop* in the percentage of Special Education students from 9.2% to 8.3%.

If you are interested in some more detail: from 2002 to 2009, the number of students in the “autism” special education category went up from 10 to 63. At the same time, students in the “mental retardation” category went down from 60 to 36. These numbers were dwarfed by the big drop in the number of children in the “specific learning disability” category (from 443 to 218).

Back to the budget. Here is a quote from the budget book:

The 2010-11 Revised State Budget defers $12.6 billion in revenue limit funding for K-12 education, including $5 billion in payments which are being postponed from one fiscal year to the next. The District will not receive approximately 25% of the State portion of Prop. 98 Revenue Limit funding for 2010-11 until the following year (July & August 2011). These cash deferrals are expected to be ongoing.

.

Yes, the State Government, in an effort to balance its own budget, isn’t paying school districts on time all the money they are committed to.
.
When I looked for more information on Proposition 98 funding, I found this paragraph:

The Governor has stated that education has been “protected” in his proposed budget. It is important to note that “protected” does not mean that school districts will be spared further reductions. The District’s largest source of revenue, Prop. 98 Revenue Limit, has a funding deficit of 18.355%. In addition the Governor’s Proposed budget “fully funds” the cost of living allowance (COLA) at a negative 0.39% and adds an ongoing “targeted” funding reduction of 3.85% of school districts base revenue limit. The chart below shows the dollar amount per Average Daily Attendance (ADA) the District is entitled to under current funding formulas and the estimated funded amount.

So, the State is assuming that the cost of living is going down? Funding from Prop. 98 sources is down.

Another document that came up on the Gilroy Unified website for the search “budget” was Staff Letter re: 2010/2011 Budget. Here’s the opening paragraph:

The Governor released the proposed 2010-11 State Budget last week. Prior to its release, we were planning for budget reductions in the $3-4 million range. Unfortunately, the Governor’s budget significantly reduced funding for public schools and the amount we now need to cut is in the $6.3 million range – which is 11.4% of our unrestricted general fund budget. This unprecedented level of cuts follows two years of significant reductions in revenue from the State.

So, the State government “defers” paying the district, and “protects” education by reducing the payment they do make. How do we get from that to “special education students are bankrupting the district”?

Yes, California is having hard times. Yes, many special education students cost much more to educate than the average student. But, please, do we have to scapegoat these students with the label that they are “bankrupting” districts?

I am Bonnie Offit!!

16 Nov

AoA have a hilariouslybizarre post up this morning.

Is Dr. Bonnie Offit masquerading on the web as an autism parent and prolific blogger named “Sullivan”?

And why do AoA think this?

The primary answer seems to be that they found a comment from Liz Ditz on Squidalicious blog that _seems_ (if you’re not too bothered about reading the context) to refer to Sullivan as ‘her’. In fact what Liz was doing was referring to the subject of the post she was commenting on – Holly Robinson Peete.

AoA’s next piece of evidence is that Bonnie Offit surfs the blogosphere late at night. Erm…so what?

Their third piece of evidence seems to be that Sullivan is a smart guy. This is undeniable. I’ve had the good fortune to chat to him via Skype and he is indeed one smart cookie. Is he a doctor of medicine as Bonnie Offit is? No. No he’s not.

Their fourth piece of evidence is that Sully defends Paul Offit. Well so what? I know of lots of bloggers, including myself, who defend Paul Offit.

Their fifth piece of evidence (why does this remind me of ploughing through Age of Autism the book) is that Sullivan appears to know Paul Offit. Again, so what? I’ll be frank, I’ve swapped emails with Paul Offit and charming man that he is, he’s always very friendly and courteous , going out of his way to be helpful and guess what – he gives proof copies of his books to people he think would be interested in reading them!! I have one myself. Dan Olmsted, Mark Blaxill et al also indulge in this practice. That takes care of another piece of ‘evidence’.

Yet another piece of evidence produced by AoA is that Sully goes to great lengths to clarify what Paul Offit earned from his vaccines. Let me give you a little lesson AoA – this is something called ‘clarity’ and it is coupled with something called ‘tenacity’. When you have these things, as Sullivan does, you are interested in the actual truth as opposed to the surface appearance.

Yet another piece of evidence (and we’re really scraping the barrel here) is that Sully didn’t discuss the suit against Paul Offit until the day it was dismissed, despite the fact that Orac had. Not really sure what to say about that one, except this is getting very silly indeed.

AoA closes this piece of hilarity with:

You know, I’m starting to hope this is Bonnie Offit, because if it isn’t we have one really, really troubled father on our hands. Get a life, father of a child with autism, Paul Offit is not going to help your child…unless Paul Offit is the father of your children, and then, once again, it all makes sense.

Which is a weird statement to make given that the author of this whole piece, JB Handley, said in an email to Sullivan:

…you are entitled to your own opinion, and I find your writing to be thought-provoking.

So on one hand Sully is a really, really troubled father and on the other JB Handley finds Sully thought provoking. Hmmm.

However, as I said, its plain to me that Sullivan is not Bonnie Offit for one clear and simple reason. I’ve spoke with HIM.

And there’s one other factoid AoA clearly missed. Sully can’t be Bonnie Offit because I am!!

Update:Orac claims he’s Bonnie Offit. Clearly this can’t be true because I AM!!!

Callous Disregard: “That Paper”

16 Nov

We recently discussed here on LeftBrainRightBrain some sections of the transcripts from the GMC fitness to practice hearing that was held for Andrew Wakefield. I’ve recently added Mr. Wakefield’s book, Callous Disregard to my reading mix. Frequent visitors to LeftBreainRightBrain may have noticed that my blogging output has dropped. There is just so much, so much, to respond to in that book that it has become difficult to find good and somewhat brief examples of the misinformation that Mr. Wakefield is attempting.

As you can see, even this example isn’t so brief. But it does show a clear example of Mr. Wakefield’s methods, past and present.

Mr. Wakefield likes to use citations. They look good and, if you don’t look closely, they make it seem like he has data to back up his claims. Catherina at JustTheVax blogged that Andrew Wakefield uses references to support his ideas, but if you follow those references you get a very different story. Catherina’s example showed that Mr. Wakefield claimed that his work has been replicated by others when, in fact, his references showed nothing of the sort. No surprise: he does this again in his book. The citations don’t prove his point. Much to the contrary, in fact.

Following that sleight of hand, as I followed some of his references and checked with the GMC hearing transcirpts I kept finding more and more examples of exactly why he lost his license to practice medicine.

For example:

1) Mr. Wakefield knew full well that many of the parents of the children being seen at the Royal Free were on the road to litigation. Not only that, but Mr. Wakefield’s stated goal was “…to make sure that their legal cases are presented in the best possible light”.

2) Mr. Wakefield did not make his activities with the legal aid board public. He informed one of his authors, but there isn’t evidence he informed the other 11. If he knew it was important to inform one author, why leave the rest in the dark about his activities?

3) Mr. Wakefield claims that a news story made his activities public. The news story never mentions his name. In fact, it tends to prove just what Mr. Wakefield denies. The news article states that the study at the Royal Free was being organised by silicitors.

Orac over at Respectful Insolence would call “Callous Disregard” a “target rich environment”. At some point, when every page, every sentence, every reference has a high probability of being false, it becomes something worse. I have to pull in a popular culture reference–the Princess Bride–as this is what comes to mind as I read “Callous Disregard”: it is a land war in Asia.

This comes to mind because I am bogged down and it is only chapter 1.

Chapter 1 of his book is entitled “That Paper” and focuses on the 1998 article in the Lancet. Mr. Wakefield published essentially the same discussion of “That Paper” in the magazine The Autism File.

Let’s just pick a couple of the so-called “myths”, shall we? From Callous Disregard:

My involvement as a medical expert was kept “secret”[14].

False– at least one year before publication, I informed my senior coathors[15], the head of the department, the dean of the medical school[16], and the CEO of the hospital. This fact was also reported in the national press 15 months prior to publication.

He informed his “senior” coathors? Why not everyone? Let’s take a look at citation 15, shall we?

[15] Correspondence between Dr. Wakefield and Professor Waker-Smith, February 3, 1997 and February 20, 1997.

Do you know based on that what letters he is talking about? They are in the transcripts for the GMC hearing, and they are in the press complaints commission (PCC) complaint that Mr. Wakefield filed (is he actually moving on that at all, by the way? It seems to be hanging for a long time with no activity).

The letters are reproduced below.

Note a few things here. This is in February 1997. That’s a year before the Lancet study was published. Mr. Wakefield’s letter is not to his “senior coauthors”, plural, but to one coauthor. He had 13 authors. So were eleven co-authors left in the dark? Why only let one author know?

Also note that the children in the Lancet study had already been seen at the Royal Free. Child 1 was admitted in July 1996. Mr. Wakefield had seen the children and he knew that many were pursuing claims. Mr. Wakefield felt it his duty to “…make sure their legal cases are presented in the best possible light”.

That is a very clear conflict of interest.

Here is the letter:

“Dear John

re: Enterocolitis and regressive autism

Further to our meeting on Tuesday 21 January, I thought it important to write to you to clarify my role in the legal issues. I fully appreciate your desire not to become involved in the legal aspect of these cases, but I feel that it is important to express the reasons that I do feel obliged to become involved.

The future for the children with whom we are dealing is very bleak indeed. Not only are the provisions for these children within the community inadequate at present, but looking ahead to the future, there will come a time when the parents of these children die, and the patients, as chronically disabled adults, left to fend for themselves in an extremely hostile world. Were there any long-term institutions left for such children, then that is where they would end up. Since these hospitals are being closed on an almost weekly basis around the country, these hopeless individuals will be left to ‘care in the community’. One does not like to imagine how it will all end. Maybe their only hope is in people taking the possible organic basis of their disease seriously enough to investigate it and institute the appropriate therapies where possible.

Vaccination is designed to protect the majority, and it does so at the expense of a minority of individuals who suffer adverse consequences. Although the case against MMR is far from proven it is one that we are obliged to investigate in view of the consistent history given by these patients’ parents and by the observations made in the United States. If this disease is caused by the MMR vaccination, then these children are the few unfortunates that have been sacrificed to protect the majority of children in this country. If this is the case, our society has an absolute obligation to compensate and care for those who have been damaged by the vaccine for the greater good. This is an inescapable moral imperative and is the principal reason that I have decided to become involved in helping these children pursue their claims. I have considered this issue in great depth and, whilst it may not be the wish of others within the group to become involved, it falls to me to make sure that their legal cases are presented in the best possible light. Fortunately, this is entirely consistent with best clinical practice which, I believe, you are providing for these children. I felt it important, however, to let you know of my feelings on this, and the position that I feel I am obliged to adopt to support these children. Without our help, I genuinely believe that the medical profession would otherwise put them to one side, as it appears to have done in many cases already. My present fears for these children are much less than the horrible imaginings if they do not receive the appropriate help that is due to them at this stage. However, I am an optimist, and I believe that this project will turn out to be both enlightening and rewarding for all those who have been involved, and I am most grateful for your help and encouragement.

Kindest regards & best wishes,

Yours sincerely”

Here is Prof. Walker-Smith’s response. Note this sentence (with emphasis added): “It is clear that the legal involvement by nearly all the parents will have an effect on the study as they have a vested interest.”

“Dear Andy

Re: Enterocolitis and Regressive Autism

Many thanks for your letter of 3 February concerning the legal issues. I can exactly understand your position and I can appreciate the compassionate human side of your argument.

My position as with measles, MMR and Crohn’s disease is that the link with MMR is so far unproven. It is clear that the legal involvement by nearly all the parents will have an effect on the study as they have a vested interest. I myself simply will not appear in court on this issue.

I would have been less concerned by legal involvement if our work were complete and we had a firm view. Never before in my career have I been confronted by litigant parents of research work in progress. I think this makes our work difficult, especially publication and presentation.

I am very excited by this work and it is very worthwhile. Simon Murch and I met today and have drawn up a draft for patient selection for your comment please.

I also feel that Dr Harvey’s contribution to the study should now be concluded and Dr Andrew Lloyd-Evans asked to join us. Do you agree with this?

With Kind Regards
Yours sincerely”

Prof. Walker-Smith made a very good comment here: I would have been less concerned by legal involvement if our work were complete and we had a firm view. Never before in my career have I been confronted by litigant parents of research work in progress. I think this makes our work difficult, especially publication and presentation.

Another “myth” which Mr. Wakefield chose to address:

Children were litigants[19].

False–at the time of their referral to the Royal Free, the time material to their inclusion in The Lancet paper, none of the children were litigants.

I don’t know what definition of “litigant” Mr. Wakefield is using, but “nearly all” of the parents were involved in preparing legal action, according to Dr. Walker-Smith. Also, Mr. Wakefield was working to “…make sure their legal cases are presented in the best possible light”.

Mr. Wakefield can define terms and redefine the English language however he wishes. I deserved to hear that the parents were pursuing legal action and I deserved to hear that Mr. Wakefield was working to help those families in their cause.

Let’s go back to another statement by Mr. Wakefield.

This fact [Mr. Wakefield’s involvement as a medical expert] was also reported in the national press 15 months prior to publication[17].

As evidence of this He cites this article in the Independent. The article doesn’t mention Andrew Wakefield at all, much less mention his side job as a paid expert for the MMR litigation:

The article [17] can be found on Brian Deer’s website. I copy it here, but will replace it with a link should he make that request.

Law: A shot in the dark; The complications from vaccine damage seem to multiply in the courtroom, writes Grania Langdon-Down

The Independent (Law, Page 25) November 27 1996

Rosemary Kessick has watched her son William deteriorate from a bright, active toddler to a destructive eight-year-old who cannot talk, play or feed himself and who lives in a frantic, rushed world of his own. She blames the MMR (measles, mumps and rubella) vaccine for the devastating changes in William, now diagnosed as autistic and suffering from a debilitating inflammatory bowel disorder which can leave him screaming with pain.

William is one of 10 children taking part in a pilot study at the Royal Free Hospital in London, which is investigating possible links between the measles vaccine with the bowel disorder Crohn’s Disease, and with autism. The study is being organised by Norfolk solicitors Dawbarns, one of two firms awarded a contract in 1994 to co-ordinate claims resulting from the MMR vaccine.

Mrs Kessick, 42, had to give up her job as a business manager to look after William, the middle of her three children. William joined the other 300-plus children bringing claims through Dawbarns only in February, because the doctors she saw during her traumatic search for answers dismissed her fears about the vaccine out of hand.

“Within weeks of the vaccination, his development slowed down, then it stopped and then he regressed. Seeing what has happened to him has broken our hearts. It means so much to finally be listened to and to find people to stand up and say the safety of these vaccines must be investigated,” she says.

Concern about vaccination has resurfaced with the Government’s campaign to introduce a new MMR booster for all four-year-olds. Most of those children will have had their first MMR at about 15 months.

The Department of Health dismisses suggested links with autism and Crohn’s disease as the work of just one researcher, and argues that children are at far greater risk from measles than from the vaccine. The latest campaign, launched on the advice of an independent committee of doctors, was needed to stop the build-up of unvaccinated children, which would inevitably lead to new outbreaks of measles.

Dawbarns partner Richard Barr is co-ordinating the families’ claims. Depending on the results of the scientific study and counsel’s advice, he intends taking on the vaccine manufacturers using the Consumer Protection Act, 1987.

The Act was introduced to offer a system for dealing with no-fault liability without the need to prove negligence, and was intended to help cases such as those involving vaccine damage.

However, critics argue that it has not been widely used because of the extensive defences offered to manufacturers. These include the “development risks” defence which says manufacturers will not be liable if, with reasonably diligent research, they would not have been able to find the fault that is now causing the problem.

The development risks defence is being challenged in the European Court as being outside the terms of the European Directive on consumer protection legislation, because it effectively incorporates negligence back into the strict liability provision.

Mr Barr also intends to pursue the medical negligence aspect but, to date, there has never been a successful compensation claim for vaccine damage under negligence laws.

Mr Barr said: “The whole field of vaccine litigation was brought to a shuddering halt by the High Court judgement in Loveday and Renton in 1988, which involved the whooping cough vaccine.

“The case centres on whether the vaccine caused brain damage, but it went horribly wrong and the outcome was the judge concluded it did not. The case was based mainly on expert opinion rather than scientific evidence and the manufacturers were able to marshal massive resources to defeat the plaintiff’s experts. We will have to try to make sure we do not fall into the same traps.”

One result of the Loveday case was that the Legal Aid Board applied the result to all vaccine damage cases and generally refused to grant aid.

Mr Barr said: “For a year, we were without legal aid but we battled on until we were eventually granted it to pursue the possibility of bringing cases under the Consumer Protection Act.

“The benefit is you do not have to prove negligence – you simply have to prove the vaccine caused the damage and that it is an unsafe product. We will also have a strong argument that parents were given no, or insufficient, information or warnings about the possible risks of the vaccine to be able to give informed consent to its use.

“I am sure the manufacturers will try to discount any causal link between the vaccine and the damage suffered by the children. They will also argue that the benefits of being immunised far outweigh the risks from the vaccine. But we will argue that the dangers of these childhood disease have been exaggerated to terrorise parents into vaccinating their children.

“I also do not think the ‘development risk’ defence is a runner, because we would argue the mechanisms of how the damage is caused have been known since the Sixties when the measles vaccine was first being tested.”

He said another line of attack would be to focus on clusters of similar side-effects associated with particular batches of vaccine, although the main thrust remained against the vaccine as a whole.

Mr Barr, who refused to let his children be vaccinated, said their research was being helped by having an in-house scientist working on the cases. Kirsten Limb initially came to them as a client after her daughter was left severely disabled through medical negligence.

Jack Rabinowicz, a partner at Teacher Stern Selby, has been involved in vaccine damage cases for a decade and is chairman of the solicitors’ steering group dealing with whooping cough claims.

He was pessimistic about the likely success of cases brought against the vaccine rather than a specific “bad batch”.

“My view is that you have to show a child was damaged by vaccine from a bad batch, as happened in a case in Ireland in 1994 which resulted in more than pounds 2m compensation. The court found in favour of the claimant after hearing that the vaccine had failed internal toxicity tests but was still put on the market.

“A full frontal attack against the vaccine itself is much more difficult. The steering group is waiting for advice from counsel and, if it is reasonably optimistic, will issue writs early next year. They will involve product liability claims against manufacturers over specific ‘hot lots’ of the vaccine and medical negligence claims against individual doctors who ignored the contraindicational warnings about having the vaccinations.”

He said the cases were at the frontiers of medicine and law and the Legal Aid Board was rightly worried about committing public money unwisely. “There have been a number of disastrous product liability cases and these will be David against Goliath because the manufacturers and doctors have unlimited resources to fight their corner.

“I think the only thing that will change the situation is if Richard Barr and I get our cases off the ground and the manufacturers and doctors scream merry hell at the prospect of paying millions in compensation and put pressure on the government of whatever hue to provide state aid.”

The only help currently offered by the government is through the Vaccine Damage Pay Unit. Since it was set up in 1979, it has received 3,749 claims and made 883 awards. However, these have been capped at pounds 30,000 since 1991, and apply only if a child is 60 per cent disabled.

Mr Rabinowicz said: “If these children were birth victims they would receive about 2m each. These vaccine-damaged children would be looking probably for upwards of pounds 1m.”

There is no reference to Andrew Wakefield in the above article. The reference to the study at the Royal Free is this paragraph:

William is one of 10 children taking part in a pilot study at the Royal Free Hospital in London, which is investigating possible links between the measles vaccine with the bowel disorder Crohn’s Disease, and with autism. The study is being organised by Norfolk solicitors Dawbarns, one of two firms awarded a contract in 1994 to co-ordinate claims resulting from the MMR vaccine.

“The study is being organised by Norfolk solicitors Dawbarns….”

So, an article which Mr. Wakefield cites in his defense states that there is a study ongoing, organised by solicitors, on the link between mealses vaccine, bowel disorder and autism.

Keep that in mind when you read this other so-called “myth”:

Children were “sourced” by lawyers to sue vaccine manufacturers.

False– children were referred, evalueated and investigated on the basis of their clinical symptoms alone, following referral from the child’s physician[18]

I’ve only covered some of the “myths”, and that is only part of chapter 1 of “Callous Disregard”. There are 13 chapters, an afterword and an epilogue. There are hundreds upon hundreds of pages of GMC testimony.

It is a land war in Asia. I don’t plan to drag myself or LBRB through it all. My hat is off to the people who sat through the entire GMC hearing, read and reread the transcripts and boiled it down to a decision, only to have Mr. Wakefield attempt to rewrite history, complete with citations.

Another mother kills her autistic child

15 Nov

In what’s turned out to be a terrible year for autistic children, survival wise, another ‘mother’ has killed her autistic child.

A mother forced her 12-year-old autistic son drink a cup of bleach because she feared social services would take him, a court heard.

Satpal Kaur Singh, 44, killed her son Ajit just hours after she refused to cooperate with council staff at a meeting over his care.

This time it is clear that Singh was

…suffering a mental disorder.

And so I have to wrestle with my feelings. My immediate feeling is that if she had a mental disorder she cannot be held accountable for her actions. However, my other feelings are revolted not just be the murder but by the horribly cruel way she murdered her son. Making him drink a cup of bleach must’ve been a long drawn out and horrendously painful process for young Ajit.

At the end, this time searching questions must be asked of Social Services. If they had concerns over Singh’s parenting skills and her behaviour which they apparently did why was Ajit Singh not placed on the ‘at risk’ register. Or were they already beginning that process and it was this that set Satpal Kaur Singh on her murderous course?

Its an appalling story and at the bottom of it is a little boy who was killed by the one person he should’ve been able to put all his trust in and in a manner so awful it makes me shudder.

Planting a tree in Isreal

15 Nov

If you read Orac’s blog, Respectful Insolence, you would have seen the post, Requiem for a friend I’ve never met. I too “knew” Mark. I’ve been trading emails with him for a few years now. I’ve never met him in person, or even heard his voice.

Mark was a fighter. He was fighting the good fight before I even knew about it. Mark was working to make life better for my kid before I had a kid. He was intensely proud of his kids.

Mark’s son let a comment on Liz Ditz’ facebook page:

Please plant a tree in my dads honor in Israel. He would want that to show a sign of growth. Thank you

I took Liz’s suggestion and made a donation to the Jewish National Fund.

Farewell Mark. I wish your family peace in these times.

Reading Age of Autism – All I can handle, I’m no Vladimir Nabokov

13 Nov

I read Dan Olmsted’s latest post on Age of Autism and was reminded I had yet to publish a closing post on my experiences with the book. Here’s a quote from Dan:

It’s doubly disappointing to see traditionally progressive outlets – from Salon to Daily Kos to The Atlantic to National Public Radio and PBS – ignore the evidence presented in our book and so many other places, twist the facts they can’t deny, belittle those who believe otherwise including beleaguered autism parents, and glibly trumpet tired reassurances that the concern over vaccines has been “asked and answered,” that “study after study” has refuted any relation, and that continuing to point out disturbing patterns of evidence to the contrary endangers children and infants.

Quick translation for you: “Waaah, nobody liked our book or thought it was valid. What a bunch of pooh-pooh heads!”

The embarrassing truth for Dan Olmsted and Mark Blaxill is that their book has been still-born. Take a look at the Amazon rankings compiled by Broken Link and its hard to come to any other conclusion. But why has this happened?

First off, the book is badly written. Its not an easy read in the way that Evidence of Harm was. Of course the style is different but Age of Autism is not even a well written poor story.

Secondly, the content is – well – embarrassingly one sided. Whilst B & O claim to be not anti-vaccine, the whole book – particularly part II is rife with anti-vaccine sentiments designed not so much to lead the reader to a conclusion but to batter the reader over the head with the conclusion B & O reached before sitting down to write even.

Thirdly, the content is old hat. There is literally nothing new in the book. For those of us who have followed the the whole story, AoA has nothing _new_ to add to the overall scenario. Whereas Defeating Autism, Autism’s False Prophets and Evidence of Harm all had something _new_ to add to the story, AoA merely dully repeats truthiness from 3 or 4 years ago and couples it with a retelling of historical speculation that simply reiterates what everyone already knew – mercury isn’t so good for you.

So thats that for me reading purgatory. I’m reading something very much better now that I think Sullivan and I will be blogging at length in the new year.

Autism-vaccine books, an indication that the tide has turned?

13 Nov

We recently discussed here on LeftbrainRightBrain two books, both due out in January. The first, The Panic Virus: A True Story of Medicine, Science, and Fear, is by a new name to the discussion, Seth Mnookin. The second book, Deadly Choices: How the Anti-Vaccine Movement Threatens Us All, is by Dr. Paul Offit, a name well known in the autism/vaccine discussion.

With these two books due out in the near future, it is only natural to look back at the recent past. I am thinking of two other books on autism and vaccines, Dan Olmsted and Mark Blaxill’s “The Age of Autism: Mercury, Medicine, and a Man-made Epidemic“, and Andrew Wakefield’s “Callous Disregard: Autism and Vaccines: The Truth Behind a Tragedy. Both of these books continue the old story of autism caused by mercury in vaccines and autism caused by the MMR vaccine. There is really no new science and there never was much in the first place. Sure, Age of Autism tries to apply their same “correlation is causation” arguments about mercury to other medical conditions in history, but that isn’t science. Callous Disregard is more about Andrew Wakefield’s excuses for his own misdeeds than about the science anyway. The books have been given a lukewarm reception by their target audience (neither has really sold in large numbers, and the trends are clear that the books are selling through the promotion by “friendly” blogs and book signings). Even Dan Olmsted himself recently blogged about how the formerly friendly press is now ignoring his book.

Jenny McCarthy has moved on, at least for now. The same can be said for David Kirby (but he is still giving appearances at autism-parent conventions as some sort of expert.) But, the days when Evidence of Harm: Mercury in Vaccines and the Autism Epidemic: A Medical Controversy could hit the New York Times best seller list are in the past.

This isn’t about some sense of schadenfreude or an “our author’s books are doing better than your author’s books” sort of competition. Rather, this is a time to ask (once again), has the tide turned? Do two flops tell us that the heyday of the movement over?

Sure, there will always be a SafeMinds and a Generation Rescue out there pushing the idea of a vaccine-induced autism epidemic. But one researcher I know has told me that vaccines just aren’t even coming up as a point of discussion any more. Not in conferences (the real kind, not the parent-convention kind). Not even in public lectures.

Has the tide turned? I hope so. I really do.

Deadly Choices: How the Anti-Vaccine Movement Threatens Us All

13 Nov

I recently wrote about the book, Panic Virus, which is set to come out in January, 2011. Another book which includes sections on the autism/vaccine story is also scheduled for January: Deadly Choices: How the Anti-Vaccine Movement Threatens Us All, by Paul Offit.

The “product description” is very brief:

How did we get to a place where vaccines are viewed with horror rather than as life-saving medicine? The answer is rooted in one of the most powerful and disturbing citizen activist movements in our nation’s history—a movement that, despite recent epidemics and deaths, continues to grow. Deadly Choices is the story of anti-vaccine activity in America—its origins, leaders, influences, and impact—and is a powerful defense of science in the face of fear.

While the word “autism” doesn’t appear at all on the Amazon.com page for the book, it will come as no surprise that the autism/vaccine parent groups play a prominent role in the book’s discussion of the modern anti-vaccine movement.

Dr. Offit’s books get read. By important people. I have little doubt this one will too.

As I said with my discussion of Panic Virus, there is no joy in realizing that some of the vocal autism-parent groups are being chronicled in this way. There is, however, relief that books such as these signal that perhaps the worst is over. The public and the press are no longer giving the idea of the vaccine-induced-autism-epidemic the credibility it enjoyed only a year or two ago.