That Shouldn't Happen: The Just World Fallacy and Autism

Everyday, we hear about tragedies, some that hit too close to home for comfort, and our reactions...

Heaviness: Euthanasia For Expediency

It's all over the internet now, the story of the twin brothers in Belgium who were deaf and going...

What's the Harm: When Reality and Wishful Thinking Clash

I'm digging around for posts people have written on what to say/what not to say to autistic people...

Facilitated Communication: Same As It Ever Was (Same As It Ever Was)

In the past couple years, I’ve written over a dozen articles examining facilitated communication...

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Kim WomblesRSS Feed of this column.

Instructor of English and psychology and mother to three on the autism spectrum.

Writer of the site (where most of these articles will have first appeared) and co-administrator

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Spend anytime in the online autism community, and you'll find a rich cast of characters offering a diverse perspective on what it means to be autistic. From clinically diagnosed autistics in early adulthood to late middle age to individuals who have self-identified as autistic, I've had the chance to read over 130 autistic bloggers on the directory, in addition to other autistics whose writings appear in print, on websites, forums, and facebook. 

Moon and Sky

Moon and Sky

Mar 20 2011 | comment(s)

Friday night a storm moves in.

Raindrops start to lazily fall.

In the category of "Duh?" for the week, we have a new article from France looking at how parental beliefs regarding autism dictate treatment choices. Dardennes et al. (2011) put 78 parents through a questionnaire called "the Lay-Beliefs about Autism Questionnaire (LBA-Q; Furnham&Buck, 2003). This questionnaire explores beliefs regarding the etiology and treatment of autism. LBA-Q’s authors considered two main academic theories of the possible causes and treatment of autism: the psychogenic model and the biomedical model" (Dardennes et al.).
ASAN and the IACC

On Monday, I went through an ASAN petition to the CDC that appears to have been intentionally hyperbolic and meant to get supporters foaming at the mouth. Since I posted the piece, I've continued to look into the ICD-9-CM, IACC's take on wandering, and when it was first mentioned at the IACC, of which Ari Ne'eman is a committee member.

This morning, Wendy Fournier commented at the article on Science 2.0, providing information that placed when Ari Ne'eman would have been first informed of the CDC's interest in wandering:
The online disability rights and autism advocacy movements intersect, with appeals from the autism advocacy movement appealing to the larger disability rights movement. Recently, a new petition has been started by the Autistic Self-Advocacy Network calling for individuals to "Tell the CDC 'No' on Abuse-Enabling 'Wandering' Code!" 
Because occasionally, it's important to stop and enjoy the flowers.