Sharyl Attkisson's 3rd autism/vaccine concession

26 Aug

A few days ago, I posted an entry about Sharyl Attkisson’s breathless parroting of ‘facts’ regarding a case from 1991 based on a child born in 1974. This case was settled in favour of the child. It transpired (of course) that the Special Master had in fact said nothing about autism whatsoever.

However, an interesting comment was left by ‘M’ who said:

Dravet syndrome? It is a genetic disorder, de novo mutations of the sodium-channel gene SCN1A. Children with these mutations are seemingly normal until they have the first high fever episode (it could be post-vaccination fever as well) – then the syndrome manifests with epileptic syndrome and subsequent developmental delay (encephalopathy). The genetic diagnosis was not possible until recently – the mutation was first identified in 2001.

An intriguing possibility that I read and then with my usual stunning foresight, totally forgot about.

However, I got an email yesterday that raised the issue once more. I cannot share with you who its from, a fact that is rather annoying (but understandable, this person doesn’t want to expose themselves to the loving care of the mercury militia) but I assure you, you would recognise this name.

The writer assumes that this is a vaccine injury because the special master determined that this was a compensable case. However, this event occurred in 1974 and the hearing in 1990-91. Now, in 2008, it is obvious that the epilepsy and resultant developmental impairment and “autism” are not caused by DTP but, rather, are due to Dravet syndrome (or severe myoclonic epilepsy of infancy), which is a genetic epilepsy with a mutation or change in the SCN1A gene. The evolution is typical of this disorder. It is a very temperature sensitive epilepsy (a 1 degree Celcius elevation is sufficient to trigger a seizure) and is not caused or aggravated by any immunization. Berkovic et al described this entity as a cause of vaccine encephalopathy in their Lancet Neurology 2006 paper.

I am concerned about the superficial investigatory actions of this writer (actually no real investigation was done – she assumes everything to be true). I thought I would share this information with you and let you use the information as you wish.

I can’t find a copy of the entire transcript, but from the parts Attkisson transcribed and quoted and comparing the evolution to the Dravert Syndrome home page, it certainly does look like a good match.

So what does that imply? Well, if its _not_ Dravert Syndrome then, nothings changed – still not autism though. If it _is_ Dravert Syndrome then it goes to show how little we know about genetic disorders and how careful we should be about rushing to judgements.

Endemic in the UK

25 Aug

Endemic:

Adj. 1. endemic – of or relating to a disease (or anything resembling a disease) constantly present to greater or lesser extent in a particular locality; “diseases endemic to the tropics”; “endemic malaria”; “food shortages and starvation are endemic in certain parts of the world”

Or, another example is measles in the UK.

How very shameful in the year 2008 that we have allowed one person to create an all-encompassing atmosphere of fear – groundless fear at that – that has allowed a disease that 10 years ago was virtually unheard of to return with such vengeance that two children have died in the past two years and many more have been hospitalised.

There are two reasons I find this shameful. Firstly, there is the fact that as an autism parent I am ‘judged’ every time I leave the house. We all are. The people who stare, the people who do double takes, the people whispering behind their hands. What are they saying now? How long will it be before the general public cotton on to the fact that measles _is_ now endemic is largely due to autism parents and the quacks they pay huge amounts of money to? As a community of parents we are divided and when people ask why that is or ‘can’t we just come together?’ on this issue, this is why.

*I cannot condone or stand by quietly whilst the autism community sinks into becoming a convenient media scapegoat. Neither can I stand by and say nothing whilst autism parents sink deeper and deeper into anti-vaccinationism and pretend that hospitalisation and death in the name of chasing a belief for which there is no proof is OK.*

The CDC’s Jane Seward (deputy director of the division of viral diseases) is interviewed today by Scientific American.

…in the 1960s, right before the vaccine was developed, it killed 400 to 500 children every year out of 500,000 reported cases at that time.

That’s a death every 1,111 reported cases. The current US measles epidemic has 163 cases. You’re nearly 15% there already.

Seward also says there were 4,000 cases of encephalitis a year resulting from measles in the 60’s and goes on to describe some of things that can follow on from encephalitis. Quite a lot of anti-vaccine believers say that encephalitis can lead to autism. Taste the irony.

Kelli Ann Davis doesn't get it

23 Aug

Over on Orac’s blog, a discussion is ongoing about (you guessed it) thiomersal.

One of the usual antivax canards is played beautifully by Kelli Ann Davis when she says:

So Phoenix Woman [another commenter], can you explain to me what the skull and crossbones is doing on the Material Safety Data Sheet (MSDS) if thimerosal is not a poison

This is top notch antivax stupidity. Not only does she entirely miss the point of ‘Phoenix Woman’s’ comment (which was not that thiomersal was not a poison) she also infers that the fact that thiomersal is a poison means that its automatically going to cause damage. She conveniently forgets – or doesn’t care – that the adage ‘the dose makes the poison‘ always applies.

And of course we have the scare tactic of mentioning the skull and crossbones.

Thing is, there are plenty of other Toxic substances used routinely in medicine. Lets have a look at Warafrin – which is at one level rat poison and at another level an anticoagulant. And hey – look at that – the MSDS sheet has a skull and crossbones on it.

Common clinical indications for warfarin use are atrial fibrillation, the presence of artificial heart valves, deep venous thrombosis, pulmonary embolism, antiphospholipid syndrome and, occasionally, after myocardial infarction.

And also

To this day, coumarins are used as rodenticides for controlling rats and mice in residential, industrial, and agricultural areas. Warfarin is both odorless and tasteless, and is effective when mixed with food bait, because the rodents will return to the bait and continue to feed over a period of days until a lethal dose is accumulated.

So, lets spell it out nice and slow for Kelli Ann – the dose makes the poison.

And so, lets have a look at the current dose levels of thiomersal in vaccine shall we?

For an ‘average’ person of 154 pounds, there is 6mg (miligrams) – or 6000 micrograms(µg)) of mercury occurring naturally in the body. So, roughly, a person of 25 pounds has 1mg (1000µg) of mercury (or, to put it another way, 1 pound of body mass gives us 40µg). A healthy newborn weighs on average about 7.5 pounds which gives a mercury body burden of approximately 303µg of mercury.

When we look at the FDA thimerosal content of vaccines currently mandated and add them all up we see that we get 239.2µg of mercury – way under what occurs naturally in the body of a healthy 7.5 pound newborn.

Now, this is not even a fair comparison. I have added up all the vaccines for a child of 6. Including doubling up on doses of a vaccine made by different manufacturers. Quite obviously a child won’t get a Td jab from two different manufacturers at one time. I have also included all the flu jabs – again, no one will get all flu jabs in a single flu season.

The maths is quite clear. There is more mercury existing naturally in our bodies – even those of a 7.5 pound newborn – than the combined total of every single thiomersal containing vaccine on the market.

Dear civilised world

22 Aug

Hi, I’m parent to an autistic child. I want to write a letter to apologise for the actions, inactions and unerring stupidity of some of my fellow parents of autistic people.

You see, we have become something of a scapegoat, us autism parents. But – it has to be said – a scapegoat who really can’t protest too much that we are so designated. A sizeable minority of us have done exactly what you accuse us of and what you are so irritated about. In fact, I know it goes beyond irritation to fear and I can understand that.

‘Measles Cases Grow in Number, and Officials Blame Parents’ Fear of Autism‘ says the New York Times. Officials have a good point. In the last two years, two teenagers in the UK have died from measles. In 2006, a 13 year old boy became the first person to die from measles in 14 years. In 2008, he was joined by a seventeen year old. Of particular poignancy was the fact that both of these children were genuinely unsuitable candidates for vaccination and were thus relying on herd immunity.

How sad that these children were victims of grown adults negligence and irresponsibility.

In the first six months of this year, 131 people in the US have contracted measles. Fifteen people were hospitalised. Thankfully, none have died. Of those 131 people, 63 chose (or their parents chose for them) not to vaccinate.

I guess what I really need to apologise for is the attitude displayed in the face of a disease that can kill. Some say that they’d rather measles than autism. One parent I know of said:

…..15 American children were hospitalized with Measles. None died. How many children with autism drowned least year? Deadly indeed.

Drowning would seem to be an elevated risk for autistic children (if anyone can get that paper I’d like to read it – got it now – thank you 🙂 ) however, I think that’s really besides the point. This is year one of what looks like the _start_ of a measles epidemic in the US. Over here, its about year four. If things continue at this pace, measles deaths will easily outstrip drowning deaths or any other accidental deaths of autistic kids. It should also be noted that its highly probable that the drowning deaths will be much more common in populations that have domestic pools. That’s a very uncommon feature in the UK for example.

So please civilised world, please remember that this vocal minority do not speak for us all. Please remember before we are all tarred with the same brush that many of us believe in and accept our social responsibilities as well as our parental responsibilities. We know vaccines don’t cause autism. We need you to make more noise about how unacceptable it is to live amongst those who _choose_ not to vaccinate.

IACC Wants to Hear From You

21 Aug

The IACC was formed after the Combating Autism Act was passed last year. Their role is to help formulate the direction of future scientific research.

As I have blogged about previously,autism/antivax groups are attempting to short circuit this process. These groups include SafeMinds and Generation Rescue. They claim to want to represent autistic people and the parents of autistic people.

The only way actions and groups like this can be stopped is for as many people as possible to contact the IACC with their own thoughts on the draft plan the IACC have. The plan is as follows:

Children with or at risk for ASD will be identified by 24 months and receive appropriate interventions.

Discover how ASD affects development, which will lead to targeted and personalized interventions.

Causes of ASD will be discovered that inform prognosis and treatments and lead to prevention/preemption of the challenges and disabilities of ASD.

Interventions will be developed that are effective for reducing both core and associated symptoms, for building adaptive skills, and for preventing the disabilities associated with ASD.

Communities will implement high quality, evidence-based and cost-effective services and supports across the lifespan for people with ASD.

Advances in intervention, education and services will support and enable individuals on the autism spectrum to lead fulfilling and productive lives in the community.

I personally like the bare bones of this plan a lot.

You need to respond. It is imperative that autistic people and parents of autistic people that do not believe in the unscientific agendas of certain groups allow their voices to be heard.

Full details of how to make your points and who to send them to (please note – the deadline is 30th September) is on the NIH website.

Sharyl Attkisson – are you sure?

19 Aug

Searchingly diligent and totally impartial CBS reporter Sharyl Attkisson has managed to uncover a third case of autism/vaccine related activity via the the Vaccine Courts. Never mind that Kathleen found it 5 months ago eh?

This case originates from a person born in 1974 who had a DTP shot that very same year, exactly 4 months later…..and thats about all we know.

Comparing autism in 1974 with autism in 2008 is not comparing apples to oranges. Its more like comparing apples to trains. In 1974, the DSM, didn’t even contain the _word_ autism. This is the existing DSM in use at the time:

DSM II (1968)
295.8 Schizophrenia, childhood type

This category is for cases in which schizophrenic symptoms appear before puberty. The condition may be manifested by autistic, atypical and withdrawn behavior; failure to develop identity separate from the mother’s; and general unevenness, gross immaturity and inadequacy of development. These developmental defects may result in mental retardation, which should also be diagnosed.

So, in 1974 autism was not even a defined disorder. It was a behaviour. A symptom of Schizophrenia. That’s worth remembering as we go forward.

Atkinson says:

In excerpts from the case below, the government agreed the child suffered “a residual seizure disorder” after his second Diphtheria, Tetanus & Pertussis (DPT) vaccine but attempted to argue that the child’s mental retardation and brain injury were unrelated to the seizure disorder and were, instead, caused by his autism. On the other hand, the court found that the autistic behavior, brain injury and mental retardation were all part of the vaccine injury.

Did they? Is this accurate? Did the court find that _the autistic behaviour_ was part of the vaccine injury?

Atkinson quotes at length from the transcript of the case.

CHILD was born on August 23, 1974, the 9 lb. 9 oz. product of an uncomplicated pregnancy and delivery. CHILD developed normally until the age of four months when he was administered his second DPT vaccination on December 23, 1974… That evening, he experienced a grand mal seizure. CHILD’s mother… took CHILD to the… emergency room where he was found to have a fever of 101.8 degrees at that time and a *bulging fontanelle* …CHILD had a *seizure* on March 25, 1975, with a temperature of 102 degrees. The next day, he had another *seizure* with a *fever* less than 102 degrees…On April 15, 1975, CHILD experienced a *petit mal seizure* without an associated fever… CHILD apparently did well until mid-July 1975, when he had four *seizures, with fever* around 100.7 degrees… CHILD had *additional seizure activity* in November 1975. Again in February 1976, CHILD had *seizures*. At that time, a repeat EEG was grossly abnormal…when CHILD was 21 months of age, (CHILD’s doctor) noted that CHILD had a vocabulary of only two to three words. At that time, (CHILD’s doctor) discussed… the *possibility that CHILD was mentally retarded and developmentally delayed*. CHILD currently is severely mentally retarded and has an intractable seizure disorder.

(The government) respondent has conceded that CHILD suffered a residual seizure disorder as set forth in the Vaccine Injury Table, but argues against a finding that CHILD also suffered an encephalopathy (brain injury). Moreover, (the government) contends that CHILD suffers from autism, which has produced his severe mental retardation and developmental delay. Consequently, (the government) urges that compensation in this case be limited to those expenses that reasonably might be incurred for CHILD’s residual seizure disorder, not for expenses he might accrue because of his mental retardation, developmental delay and autistic behaviors.

The question of encephalopathy.

*(Government physician) believes that CHILD currently suffers from autism and mental retardation that are the result of an independent underlying neurologic condition that pre-dated the vaccination*. However, all tests that were conducted to determine possible causes for CHILD’s condition have revealed none. Furthermore, (government physician) has posited no origin of any underlying neurologic condition. (Government physician) would have us believe that CHILD’s grand mal convulsion following his second DPT vaccination was simply a manifestation of benign febrile seizures and that CHILD had another concurrent underlying (but etiologically undetermined) neurological disorder which later produced his severe mental retardation and autism.

I reject this theory for several reasons. First, the Vaccine Act’s defines encephalopathy as “any significant acquired abnormality of, or injury to, or impairment of function of the brain.” Section 14(b)((3)(A). This definition is extremely broad. CHILD’s initial grand mal seizure indicated an impairment of function of the brain. The question becomes whether this was a benign event unrelated to any lasting neurological sequelae. In my view… (CHILD’s treating pediatric neurologist) is in a better position to accurately assess CHILD’s illness than (government physician). Beginning in 1980, when he first evaluated CHILD, (CHILD’s neurologist) diagnosed CHILD as having static encephalopathy probably related to the time of his first seizure at four months of age.

Based on the foregoing, *I find that there is a preponderance of the evidence that CHILD suffered an encephalopathy within 72 hours of the administration of a DPT vaccination on December 23, 1974, and that no alternative cause for such encephalopathy has been satisfactorily shown*.

Read all that carefully? Good. Now, where in that summation does the Special Master find ‘that the autistic behavior, brain injury and mental retardation were all part of the vaccine injury’

Brain injury – yes. mental retardation – yes. But where is ‘autistic behaviour’ mentioned by the court? In fact, the truth is that the only person who raised the issue of autism at all were the government. They tried to explain away CHILD’s injury by blaming it on autism (which bizarrely wasn’t an actual diagnosis in 1974).

Bottom line: the court did not, I repeat *did not* find that this child (a grown man now) had autism, autistic features or autistic behaviours as a result of vaccines. The closest we get is the phrase ‘static encephalopathy’ which basically means that a child doesn’t develop. This can _lead_ to autism (as well as a whole host of things such as cerebral palsy, learning disabilities, Schizophrenia) but it is not autism. When this diagnosis was given (1980) the child would’ve been 6 and thus well past the age at which autistic symptoms must appear.

An interesting sidenote. We can guesstimate the 1974 schedule. Well, maybe not the schedule but we can at least see which vaccines were in use.

In 1960, the US was using Smallpox, DTwP and Polio. By the mid-80’s, the schedule was made up of DTP, MMR and Polio.

Smallpox was dropped in 1971 and MMR stared in 1963. Therefore we can guesstimate that in 1974 the schedule was the same as the 1980 one. DTP, MMR and Polio. At some point however, the Polio switched from injection to Oral. I can’t find out when.

So – how is this ‘too many too soon’? How is a case from when there wasn’t even an autism category relevant? How is a case where the claim is that one single vaccine caused autism in any way similar to the idea of ‘too many too soon’?

Seeing the obvious

19 Aug

Two months ago I passed the half decade mark in running a blog about autism. I hoped when I started that I would be able to document my autistic child’s progress as xe developed and grew.

Somehow, through the efforts of others I got sidetracked. I no longer feel comfortable about blogging about xyr and that is nothing but a damn shame but it is still a reality. My wife is scared by the invective and hatred she reads in some people who disagree with me and we have an agreement now that I will not mention by gender or name any of my children.

This runs directly counter to my philosophy of trying to raise awareness of the good that can be available to parents and families of autistic people. Of the fun times – and there are many of them – as well as the heartbreaking times (and there are some of them too). I feel frustrated and angry that I have been forced by the irresponsible actions of others to not talk about the good thing I see in my life with autism. Maybe that was their reason for doing it. Who knows.

So, it was lovely this morning to see a story in my newsreader from someone who could see the good things. Who could see the obvious. Someone who chose to see the glass as half full.

The music was being performed live by two female artist of exceptional talent. Their music was sort of 70´s and 80s. They even took the risk of performing a Barry White Song, “My first , My Last, My everything” (I´m not sure that´s the real title), and they shocked me with how well they complemented his music. People were dancing. Old people and young people, but is was the “special” people who caught my eye; The down Syndrome people. They danced to the music and seemed so filled with the joy of the moment that it was contagious. I found myself dancing with them in my mind. They were laughing and moving, touching each other and their partners right at the moment when a spin or a turn was dictated by the music. As I watched I could not help but think of my own grandson, Anthony Adame, who is Autistic.

So maybe this writers choice of words wouldn’t be mine but there is no mistaking the vision of someone _who got it_ .

As I watched the crowd I noted many who looked upon these special people with sympathy and sorrow for them and their families. I know the look. I have often seen it while in the company of my own grandson Anthony. Only few ever intentionally mean to offend. Most simply do not understand the nature and condition of Down Syndrome, or Autistic people. They do not know the joy that many of these very special people have in their lives, or the wonder of living with, or being close to one of them.

Those words could’ve been lifted right out of my heart and mind. The joy is there. It exists. There is a choice that we can make as parents – do we fight a psuedo-war? A war which is simply psychological transference? Or do we see the fact that autistic (or Down Sydrome or Tourettes or Manic Depressive) people can see and experience happiness and bring joy to their families?

This isn’t a matter of religious style happiness. You don’t have to join hands with the world, hug a tree and sing Kumbya. Its really the simplest thing in the world. Its saying ‘my life is not like most peoples. I have hardship beyond what most do. My choices are limited. But look at the joy that my child/friend/grandchild/niece/nephew/cousin/child of a blogger from far away brings! Should I turn away from that? Or should I choose to participate in it?’

Its obvious isn’t it?

Leaky gut aka intestinal permeability

18 Aug

Leaky Gut syndrome is a hypothesis associated with autism by people who believe that toxins (particularly those caused by vaccines – notably the MMR) weakens the lining of the bowel letting various rubbish thorough (undigested food, toxins, whatever) and triggering an immune response and/or leading to Wakefield’s much-hyped but never backed up Autistic Enterocolitis.

This unverified condition has (of course) been found by any number of Wakefield supporters and yet, curiously, no researchers external to Wakefield’s peers have found any evidence for it and the phrase exists as a diagnosis within that AltMed community.

In fact, its not curious at all as the only groups that _did_ find evidence for ‘Autistic Enterocolitis’ used the now discredited Unigentics lab run by John O’Leary.

Anyway, in Feb of this year a team from the University of Calgary published a Pilot study into the ‘leaky gut’ (posh name: ‘intestinal permeability’) issue.

They enrolled 14 autistic kids (all of whom had parents who reported gastric issues), 7 NT siblings of these kids, and 8 NT non-related controls.

In the ‘leaky gut’ opioid-excess theory, it is proposed that increased intestinal permeability in children allows for increased absorption of dietary peptides, which ultimately leads to disruption of neuroregulatory mechanisms and normal brain development.

The reason for choosing autistic kids who were reported by parents to have gastric issues is that the researchers reasoned that these kids would be more likely to have ‘abnormal gastrointestinal tests’.

In this population, the researchers found:

we neither demonstrate abnormal small intestinal permeability, nor abnormal postprandial responses of the enteroendocrine peptide GLP-2.

…..

It has been suggested that increased permeability may be causally related to the onset of the inflammatory bowel disease and not just a consequence of inflammation. Our data does not support a similar hypothesis in autism.

…..

Our study did not detect differences in the functional gastrointestinal parameters measured in a group of children with autism. Although there may be a subset of children with autism with a specific gastrointestinal abnormality there is no firm evidence yet of a role for gastrointestinal dysfunction in
the etiology of autism.

One of the things the authors reported that struck me was:

The subtle endoscopic and histological findings of lymphonodular hyperplasia in the colon and ileum previously described in ‘‘autistic enterocolitis’’ (Wakefield et al. 1998, 2005) are also seen in normally developing children with similar gastrointestinal symptoms (Furlano et al. 2001).

This is only a pilot study of course so not too much can be read into the results but if the study is expanded upon and replicated then the results would be interesting to see. Its certainly a smallish spanner in the works of the ‘autistic enterocolitis’ believers.

Tags:

Politics of Mitochondrial-PDD

15 Aug

For most people reading this blog, the story of Hannah Poling is very familiar. She was diagnosed with a condition called “Mitochondrial-PDD” by Richard Kelley of the Kennedy Kreiger Institute (*according to the document David Kirby blogged)

That, of course, is not what makes her well known. A year ago, I doubt many if any readers here would have heard of Mitochondrial-PDD. What makes her well known is that her case before the Federal Court of Claims (the “vaccine court”) was conceded by the U.S. Department of Health and Human Services (HHS).

What did they say? According to David Kirby’s post:

In sum, DVIC has concluded that the facts of this case meet the statutory criteria for demonstrating that the vaccinations [Hannah Poling] received on July 19, 2000, significantly aggravated an underlying mitochondrial disorder, which predisposed her to deficits in cellular energy metabolism, and manifested as a regressive encephalopathy with features of autism spectrum disorder. Therefore, respondent recommends that compensation be awarded to petitioners in accordance with 42 U.S.C. § 300aa-11(c)(1)(C)(ii).

The HHS conceded that vaccines caused an injury. In specific, the injury was an “aggravation of an underlying mitochondrial disorder”

It’s worth asking a series of questions at this point, I think

Q) Do all mitochondrial disorders result in autistic features or autism?
A) No.

Q) Do all the children in the 30-child study have vaccine injury?
A) No. It appears that Hannah Poling is unique in that group.

Q) Is mitochondrial medicine a highly specialized field?
A) Absolutely.

Q) Are autism doctors/researchers experienced with mitochondrial disorders?
A) Only a few, and not likely to the depth that the mitochondrial doctors/researchers are

Q) Is anyone going to look at the potential role of vaccines with mitochondrial disorders?
A) Yes.

And that is a key point that deserves some extra attention. Dr. Poling in his letter to the NEJM noted that

Also commendable is the new 5-year research plan of the National Vaccine Advisory Committee, which will entail the study of minority subpopulations, including patients with mitochondrial disorders.

In doing so, he cites the Centers for Disease Control and Prevention’s Immunization Safety Office Scientific Agenda: Draft Recommendations.

Which states:

CISA has formed a working group to identify key research questions and consider study methods related to mitochondrial disorders and immunization, in collaboration with partners.

CISA being the “Clinical Immunization Safety Assessment (CISA) Network”

The document further states as the first lines of the first two bullet points under this proposed study:

Mitochondrial disorders are a heterogeneous group of disorders characterized by impaired energy production.

and

Children with mitochondrial disorders commonly present with a range central nervous system findings.

*Again, note that autism/autistic-features are not the only outcome of mitochondrial disorders.

*I think this proposed study is a good idea. The government has conceded a case, mitochondrial doctors state that the question is open as to whether vaccines could be a stressor that causes a metabolic crisis.

People are pushing for this to be a part of the IACC’s Strategic Plan.

Why?

A group of people, experts in vaccine safety studies, are already going to look at the whole question of the potential role vaccines and mitochondrial disorders. Why carve out the even smaller subset with autism? Or, to put it more directly, why call for a second study, and, at the same time, leave out people who don’t have autism?

The answer is simple: politics. People want the idea of vaccine induced autism in the Strategic Plan. To do so, they are willing to ignore the fact that the study is already being planned and, worse, they are willing to sacrifice a large segment of the potential target population.

It’s just not right. Let the correct groups do the correct study. It’s in the planning stage. If people really care about the question of vaccines potentially causing crises in people with metabolic disorders, support the CISA study.

Why do I have a feeling this isn’t going to happen?

* added on edit.

Fools rush in – Wakefield's race

15 Aug

In today’s Hampstead and Highgate Express there’s an interesting little piece on Andrew Wakefield’s ongoing legal altercation with the GMC.

A ROYAL Free doctor accused of serious professional misconduct during controversial MMR research admitted that short cuts were made in the quest for fame.

…..

Asked whether Dr Wakefield had pushed him into it, Prof Walker-Smith said: “I think that’s true. If we had not had any urgency to get on with it, we would not be in the muddle we are in now because we would have done it in the usual way by getting a referral. Dr Wakefield was a man in a hurry and in full-time research.

Damn. You know things aren’t going well for you when your co-accused is willing to push you under a bus.

Walker-Smith performed completely unnecessary (in my opinion) lumbar punctures on these kids and lo and behold:

Ms Smith said out of the 12 children, complications materialised in two. “I’m not suggesting that the complications were serious, but you would accept that having a child admitted to hospital overnight with a fever and feeling unwell is worrying for parents,” she said.

Performing lumbar punctures and consequently hospitalising 17% of your case load is not great. Neither is it great to perform blood draws at birthday parties and make children pass out and vomit.

But, we know Dr Wakefield is an impatient man. Remember this testimony given by Dr Nick Chadwick?

Q Okay. Did you personally test the gut biopsy samples for measles RNA?
A Yes.

Q What tests did you perform?
A A PCR test, a polymerase chain reaction.

Q What results did you receive from the gut biopsy materials for measles RNA?
A They were all negative.

Q They were always negative?
A Yes. There were a few cases of false positive results, which I used a method to see whether they were real positive results or false positive, and in every case they turned out to be false positive results. Essentially all the samples tested were negative.

…….

Q So you personally tested while you were in Dr. Wakefield’s lab gut biopsy material, CSF and PBMCs?
A Yes, that’s right.

Q And all the results were either negative, or if they were positive it always turned out that they were false positives?
A Yes, that’s correct.

Q Did you inform Dr. Wakefield of the negative results?
A Yes. Yes.

This was the test to ‘prove’ that measles virus was in autistic kids guts and hence cause their autism. Seems Dr Wakefield was too impatient to listen to his own team.

We expect Doctors to have our primary care interests at heart. We should not expect for them to sacrifice scientific integrity and our children’s wellbeing in order to make themselves famous.

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