Archive by Author

Brian Deer challenges Andrew Wakefields words

5 Apr

Andrew Wakefield has recently published a series of videos on YouTube (the only media outlet still left interested in his ramblings). Fascinating in largely no aspect, they do however remain riddled with innaccuracies which Brian Deer has challenged in his own response video which is below.

Specialist People: looking to find 1 million jobs for autistics

1 Apr

ABC News has a story that caught my eye: Software Company Only Hires People who Have Autism. The company, Specialisterne, is a Danish company that is looking to capitalize on the strengths of autistics in the workplace.

On the name of the company:

The company name ‘SPECIALISTERNE’ is a danish word for ‘The Specialists’ and alludes to that we are the opposite of ‘Generalists’. Our strength is in the details where our employees have a special skill for immersing themselves in their work.

We use the company name internationally though the term ‘specialister’ is phrased differently in different languages.

In the graphics of the company name the I’s are highlighted with the colour of the Dandelion flower.

and the idea behind the company:

Thorkil Sonne’s son was given the diagnosis “infantile autism with normal intelligence” at age 3. This gave Thorkil the chance to get to know a fascinating and vulnerable handicap world.

Thorkil has been behind many of the initiatives in the area of autism and was president of the local chapter of Autism Denmark in the West Zealand County for three years.

Thorkil got to know many adolescents and adults with autism spectrum disorders (ASD) – and he wondered why these intelligent young people couldn’t use their energy and skills in the business community, doing what they do best and yearn to do.

Thorkil concluded that out welfare system works best if you have a visible handicap – but lacks much in experience and knowledge when it comes to handling invisible handicaps like ASD.

There was obviously a shortage of job opportunities where people with ASD can meet understanding and support and through that get the opportunity to use their special skills. Thorkil didn’t see enough opportunities within the existing system.

After 15 years in the world of tele-communications Thorkil knew the value of the skills he saw in young people with ASD.
Thanks to the support of his family Thorkil was able to start SPECIALISTERNE based on a loan on their house and his family’s belief in his vision.

If I can get the embed code for the video on the ABC News site, I’ll post it here.

Specialisterne has expanded to the UK, with a website SpecialstPeople.com and a plan to create 60 jobs in Glasgow. This was discussed on the BBC website last year. A video is on the Specialst People website.

George Takei in a PSA (not autism related)

1 Apr

Orac over at Respectful Insolence posted about this in One more reason why George Takei is still awesome after all these years…

I’ve watched it a few times now and I thought maybe, just maybe, the readers here would like it as well.

It is time for the Census in the U.S.. Mr. Takei and his husband, Mr. Altman, are asking people to be counted if they are married–even if the laws of the land don’t grant them a legal marriage certificate.

There are many things I hope are different in the future in the U.S.. Recognizing marriage is one of them.

An example of where I disagree with Rodney Peete

1 Apr

Rodney Peete is the husband of Holly Robinson Peete and the father of two autistic kids. Mrs. Peete recently wrote a blog post on the Huffington Post that was fairly reasonable. It was also promoting her family’s upcoming books.

Mr. Peete has a book out, Not My Boy, and there is an excerpt at the Today Show’s website as

Facing the trauma of autism diagnosis
Former NFLer Rodney Peete writes about his son’s condition

The choice of the title, “Not My Boy”, is not one I would make. The picture on the cover makes it clear that he is not saying, “This child is not my boy”, but I’d still have picked something different.

The excerpt on the Today Show’s website has a section about vaccines. Too bad. I bet there are big sections of the book that don’t dwell on vaccines at all. Mr. Peete isn’t as bad as, say, Jenny McCarthy in terms of quantity of misinformation and his approach is better. He is still not well informed. As in, “The symptoms of mercury poisoning look an awful lot like what children with autism suffer”.

For the record, autism is not at all like mercury poisoning. I’d suggest people who want to explore this idea talk to toxicologists, people who have experience with those who have mercury poisoning. DAN doctors (who don’t treat actual cases of mercury poisoning and have little or no training in toxicology), actors and football players are not my first line for medical advice.

That said, I probably would have skipped discussing this if that was all. A title that’s, well, not so great. Information that’s, well, not so great. One line I read, though, sticks in my mind. This one line is why I am writing this. Keeping it in context for the moment, in talking about the early years with his son before the autism diagnosis, Mr. Peete writes:

We asked our pediatrician what was happening with R.J., and he acted as though what we described was no big deal. He reminded us that boys develop differently than girls. Growing up isn’t a straight line, he said. He’d catch up just like Ryan had pretty much caught up with him physically.

I see now that we were willing to accept this because he was telling us what we wanted to hear. There was nothing wrong with R.J. He was just going through a phase, a temporary setback that he’d recover from before he started school in the fall. We were overjoyed when we found out that Ryan and R.J. had been accepted into our top choice for preschool. The teachers there were well trained and compassionate, and we expected that they would help R.J. learn more social skills and encourage him to make friends.

I thought that trying to keep up with the other kids would be a huge motivation for R.J. to snap out of whatever phase he was going through. Maybe once he was around the other kids he’d start to do what they did. That would help with speaking too, I thought. If R.J. really was a member of the Robinson-Peete family, there wasn’t anything that could have prevented him from talking. Our pediatrician confirmed everything I had hoped about how getting R.J. out into the world would be a way to break his isolation.

And here is the statement out of that that bothers me:

If R.J. really was a member of the Robinson-Peete family, there wasn’t anything that could have prevented him from talking.

I’m certain I have written and said things I don’t want my kid to hear or read someday. I believe the above statement is supposed to tell us Mr. Peete’s feelings at that time and his opinion has evolved. It probably reads well to other pro sports players. But, assuming his thoughts have evolved, I wish Mr. Peete had made that evolution more clear.

I just can’t imagine thinking, “if my kid were really a member of the family…” for a kid that young. I guess if an older kid (or adult) is doing things that are harming others, yeah, sure, not part of the family.

I thought that sitting for a few hours to think it over would result in the line making sense and I wouldn’t be writing this. I was wrong.

Urge the GMC to strike off Andrew Wakefield

31 Mar

On April 7th, the GMC reconvene to decide what is to be done with Andrew Wakefield.

You can play a part in helping to make sure that the GMC know the feelings – the anger – of the true autism and autistic community and by urging them to strike Wakefield off.

We all know how Wakefield has lied, grabbed money, attempted to conceal his role in murky dealings and covered up results that he knew would counteract his ‘science’. He still holds sway over a few hardcore antivax/autism believers and for his continued lying to them and relying on their belief alone he deserves to be struck off. His abuse of their inability to understand science is shameful.

Please email Kate Emmerson, the GMC solicitor concerned on KateDOTEmmersonATffwDOTcom stating how you feel about Andrew Wakefield and urging the GMC to strike him off.

White House Remains Steadfast In Support Of Disability Council Nominee

30 Mar

Disability Scoop has a new article about the nomination of Ari Ne’eman to the National Council on Disability.

Mr. Ne’eman’s appointment has been on hold in the Senate, as noted in a New York Times article and on this blog (and others).

“We are still behind Mr. Ne’eman and hope for a quick confirmation,” a senior White House official told Disability Scoop on Monday.

The appointment has the support of multiple disability advocacy groups. Again, from Disability Scoop:

Nonetheless, more than a dozen disability advocacy groups including the Autism Society of America, Easter Seals, Special Olympics and the American Association of People with Disabilities have expressed support for Ne’eman’s appointment.

Ari Ne’eman’s appointment to the National Council on Disability on hold

28 Mar

In a piece in the New York Times, Nominee to Disability Council Is Lightning Rod for Dispute on Views of Autism, Amy Harmon discusses Ari Ne’eman and his nomination to the National Council on Disability (NCD).

Mr. Ne’eman’s name was submitted by the White House as part of a group of nominees to the NCD. His nomination is to succeed Robert Davila, whose term has expired. Mr. Ne’eman’s nomination was “ordered to be reported favorably” by the Senate HELP committee on March 10th and sent to the full senate. At present, the nomination is on hold.

Mr. Ne’eman is an autistic adult. If his nomination is confirmed he will be the first autistic to serve on the NCD. He is probably best known his efforts with the Autistic Self Advocacy Network (ASAN), which he founded. ASAN seeks to advance rights of autistcs as reflected in its mission statement:

The Autistic Self Advocacy Network seeks to advance the principles of the disability rights movement in the world of autism. Drawing on the principles of the cross-disability community on issues such as inclusive education, community living supports and others, ASAN seeks to organize the community of Autistic adults and youth to have our voices heard in the national conversation about us. In addition, ASAN seeks to advance the idea of neurological diversity, putting forward the concept that the goal of autism advocacy should not be a world without Autistic people. Instead, it should be a world in which Autistic people enjoy the same access, rights and opportunities as all other citizens. Working in fields such as public policy, media representation, research and systems change, ASAN hopes to empower Autistic people across the world to take control of their own lives and the future of our common community. Nothing About Us, Without Us!

I will repeat for emphasis: “ASAN seeks to advance the idea of neurological diversity, putting forward the concept that the goal of autism advocacy should not be a world without Autistic people. Instead, it should be a world in which Autistic people enjoy the same access, rights and opportunities as all other citizens”.

I find that a position difficult to argue with. Who wouldn’t support access, rights and opportunities for autistics?

This mission statement is fully in line with the purpose of the National Council on Disability, which also promotes rights and opportunity:

The purpose of NCD is to promote policies, programs, practices, and procedures that guarantee equal opportunity for all individuals with disabilities, and that empower individuals with disabilities to achieve economic self-sufficiency, independent living, and inclusion and integration into all aspects of society.

As the parent of an autistic child with very significant disabilities, I can say without reservation we need groups working on improving the rights and access and opportunities of autistics. I believe Mr. Ne’eman and the National Council on Disability would be an excellent match.

In her piece in the Times, Ms. Harmon notes that it is unclear who put the hold on the nomination and what the reason may be. Senate rules allow for a single senator to place a hold, anonymously, for any reason (including just plain obstructionism):

Mr. Obama’s seven other nominees to the council were confirmed this month. But parliamentary procedure in the Senate allows one or more members to prevent a motion from reaching the floor for a vote by placing an anonymous hold on the action, which an official with knowledge of the proceedings said had been done in Mr. Ne’eman’s case.

The Senate has been rather obstructionist in approving many Obama administration appointments, leading the President to employ recess appointments in order to get some of his nominees into jobs. Recess appointments are not the sort of action the President takes lightly, indicating the level of obstructionism in place.

Mr. Ne’eman’s nomination to the NCD generated some discussion within the online autism communities when it was announced. For many people this centered on a question of whether Mr. Ne’eman viewed autism as a disability. Many went so far as to outright claim that he does not see autism as a disability. It would seem clear that Mr. Ne’eman views autism as a disability merely from ASAN’s mission statement which places ASAN as a disability rights organization. For those who remained unsure, Mr. Ne’eman answered this claim quite clearly in a recent piece he wrote for Disabilty Studies Quarterly:

It should be stressed: none of this is meant to deny the very real fact that autism is a disability. It is only to point out that disability is as much a social as a medical phenomenon and that the “cure” approach is not the best way forward for securing people’s quality of life.

Mr. Ne’eman and ASAN have been very active in united efforts by multiple disability groups, such as the recent request for an investigation into the methods employed by the Judge Rotenberg Center (which includes electric shocks and seclusion). One thing lacking in most autism organizations, in my view, is the recognition of our place within a larger disability community. Mr. Ne’eman’s track record of collaborations within this broader community is another sign that he would be an excellent candidate for the NCD.

The Times article concludes with:

But the split among autism advocates, suggests Lee Grossman, director of the Autism Society of America, may simply reflect the unmet needs of a growing population, for both research into potential treatments and for programs to support jobs and independent living.

“We have this community out there frustrated and bewildered and reaching out for any assistance, and that makes us battle-hardened,” Mr. Grossman said. “We need to reframe the discussion. From our perspective, it’s great to have a person on the spectrum being nominated to this committee.”

I agree with Mr. Grossman that this is a great thing to have an autistic nominated to the NCD. As I’ve already pointed out, Mr. Ne’eman’s goals fit those of the NCD quite well.

One notable piece of irony in this story is that the organizations which are critical of Mr. Ne’eman’s nomination have no positions held by autistics. The notable exception is Autism Speaks, which only recently added an adult autistic (John Elder Robinson) to an advisory position. As an additional irony, it is very likely that Mr. Ne’eman’s own advocacy efforts were partly responsible for Autism Speaks giving a position to an adult autistic.

Autism represents a “spectrum” of disabilities. All to often, Mr. Ne’eman’s efforts are framed as being part of some divide between the “high functioning” and “low functioning” ends of the spectrum.

The New York Times piece noted this in this section:

But that viewpoint [neurodiversity], critics say, represents only those on the autism spectrum who at least have basic communication skills and are able to care of themselves.

“Why people have gotten upset is, he doesn’t seem to represent, understand or have great sympathy for all the people who are truly, deeply affected in a way that he isn’t,” said Jonathan Shestack, a co-founder of the advocacy group Autism Speaks, whose mission is to help finance research to find a cure.

Neurodiversity certainly does not represent only “high functioning” autistics as its critics would imply. I will not speak for Mr. Ne’eman nor ASAN, but from my own perspective. First, neurodiversity is not limited to autism. Second, within autism, neurodiversity does not apply only to the “high functioning” autistics. In my opinion, the neurodiveristy “viewpoint” is one that stresses rights for all, regardless of the level of “functioning” or presence or lack of any neurological “disorders”.

There are those who try to downplay Mr. Ne’eman’s disability. Keep in mind, we are talking about a man who spent part of his education in a segregated special education program. The fact that he was able to self advocate his way out of this program is to his credit.

For the record, my perspective is that of the parent of a young child with multiple disabilities including very significant challenges due to autism. I would argue that it is precisely children like my own who most need other people to fight to protect their rights. It is from that perspective that I welcome the nomination of Mr. Ne’eman and look forward to his confirmation in the full senate.

Social Security to run a deficit this year

27 Mar

The U.S. social security system is predicted to run a deficit this year. The government will pay out more money in benefits than they will take in taxes.

Social Security has two main functions: a retirement system for the elderly and a support system for the disabled. Throughout my adult life two things have been ongoing. First, social security has been taking in extra money. Second, people have been predicting a time when the number of “baby boomers” retiring would put the system into a deficit sometime in the future. The problem arises that the extra money taken in hasn’t really been saved. It has been “borrowed” by the rest of the government.

So, again with the two things theme: for parents of disabled children, we have two things to look forward to. First, a retirement when our social security benefits will likely be dramatically reduced. Second, a retirement where we get to watch the social security support for our children be dramatically reduced.

The Atlantic Online has a story Social Security is Not in Crisis, and We Don’t Need to ‘Fix’ It. The crisis is years away, we don’t need to do anything now:

In any case, there is really no reason to do anything about Social Security this year, for at least three reasons. First, this deficit isn’t even projected to last five years. Second, Social Security is an entitlement, but it’s also a ‘stimulus.’ It is money paid to retired folks who are likely to spend because the old have a lower savings rate and many of their savings have been gutted by the downturn. Third, fixing Social Security will always be tough politics, but delaying, cutting or reforming benefits the same year you’ve announced half a trillion in Medicare cuts is downright crazy.

We are not in a crisis yet, you see. That’s because the current deficit is due to the bad economy. No, the real red ink won’t start to flow until 2016, according to Atlantic Online writer Derek Thompson.

Some of us are looking a bit farther down the road than 2016. Try 2080, for example. Somehow I’d like to think that my disabled kid will have support well after I am gone.

The Stupid, It Barks.

26 Mar

When I told a few friends about this link I said that words failed me in regard to the utter stupidity of these people. They still do so all I’ve done here is repeat the news article below:

Anxious parents might be breathing easier as research dismissing the purported link between childhood autism and vaccines continues to pile up.

But we’re not done hearing about the vaccine-autism connection just yet: Some U.K. pet owners are convinced that vaccines do more than just trigger autism in people — they’re adamant that shots do the same thing to canine companions.

Canine Health Concern (CHC), a U.K.-based nonprofit, is calling on the country’s government to investigate potential risks of vaccinations recommended by veterinarians. Among the alleged dangers? Doggie autism.

According to CHC founder Catherine O’Driscoll, vets who vaccinate their canine patients once a year are guilty of overdoing it, with potentially devastating consequences.

Dogs are vaccinated against a handful of illnesses, including Lyme disease, distemper and influenza. Most also receive routine booster shots into adulthood.

“There is a massive group delusion within the veterinary profession, with members’ eyes glazing over as they numb out to the known science and perform veterinary procedures that are unnecessary,” O’Driscoll told the U.K.’s Veterinary Times. “[Some] veterinary bodies around the world have called a halt to the practice of annual vaccination. Why is the U.K. lagging so far behind?”

But the British Small Animal Veterinary Association is adamant that all science points to the effectiveness of annual vaccines. Spokesperson Mark Johnston told Veterinary Times that he’s seen hundreds of animals die because they weren’t vaccinated, but only witnessed two deaths from side effects of an injection.

Despite dismissal from veterinary experts, O’Driscoll and company are garnering more attention from U.K. pet owners. O’Driscoll has published two books on the subject: “What Vets Don’t Tell You About Vaccines” and “Shock to the System.”

The Daily Mail covered the group’s autism-vaccine position in early March.

O’Driscoll founded the CHC in 1994, after her two golden retrievers — Oliver and Prudence — died unexpectedly. She blames commercial pet food and a vaccine overload for their demise.

CHC advocates a raw-meat diet for dogs and cats, along with “natural remedies” like garlic for parasite control and flaxseed oil combined with cottage cheese as a cancer cure for ailing canines.

In the United States, vaccination decisions are largely left up to pet owners and their vets. The American Veterinary Medical Association acknowledges that once-a-year vaccines can “increase the potential risk of post-vaccination adverse events.”

Among the potential risks listed by the association are transient infections, autoimmune disorders and even localized tumors. Autism didn’t make the cut.

It’s also not on the radar of the United Kingdom’s Veterinary Medicines Directorate. An agency spokesperson reported that more than 80 million doses of different vaccines have been administered to dogs since 1985, but it has received fewer than 7,000 reports of side effects, according to the Daily Mail.

The CHC’s chief complaint is that dogs who’ve been vaccinated often suffer from “dramatic changes in behavior.” The group claims that those personality changes are a symptom of autism.

Most veterinarians, however, have several other explanations. A dog’s sudden personality changes have been attributed to hypothyroidism, diabetes, brain tumors and, perhaps most likely, to hormonal fluctuations, as Fido copes with surging, preneutered teenage hormones.

Autistic girl assaulted by elementary school classmates

26 Mar

From CBS News: Three Florida Elementary Students Charged in Sexual Assault of Autistic Girl in School Bathroom.

Three elementary students were charged Wednesday in connection with a shocking alleged sexual assault March 3 on an 11-year-old classmate whose mother says suffers from a high functioning form of autism called Asperger’s

Two kids acted as lookouts. Add the school as accomplices, in my view:

The girl’s mother and her attorney told CBS affiliate KFOR that she wasn’t notified by Norland Elementary School officials about the incident for two days, but her mother could tell something was wrong.

Two days?!?

Here’s a comment that I wish didn’t have to be said:

The victim’s mother said her daughter is “very aware of what happened to her.”