Banner
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...

User picture.
picture for Robert H Olleypicture for Helen Barrattpicture for Gerhard Adampicture for Mark Bermanpicture for Vikki  Cvichieepicture for David  Andrews
Kim WomblesRSS Feed of this column.

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

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

... Read More »

Blogroll
How a society treats the disabled, especially those in need of specialized care due to aggressive behaviors and self-injurious behaviors, says a lot about the morality and compassion of that society. Are they locked away out of sight, left to live in horrendous conditions, abandoned not only by society, but by family members as well? The United States does not have a good record when it comes to the care provided to the mentally and physically disabled. From lobotomies to forced sterilization, from electric shock therapy and restraint systems that resemble the horrors of a torturer’s chamber, we as a society have wreaked havoc on those unable to defend themselves.
Yesterday, I wrote a post about how facebook is a rapid, easy way to spread misinformation and pseudoscience, and the difficulties in figuring out how to respond to pseudoscience when you see it. I wasn't specific about what triggered it, but I reached out to a few who shared the link and provided additional information, I placed a comment where I was invited to do so, and I flooded my facebook wall with information about facilitated communication.
We engage in wishful thinking all the time. Infomercials continue to exist because people continue to buy the products. Diet pills fly off the shelves because we want an easy fix. The HCG diet is popular because, of course, the weight falls off when you restrict your calories to 500 a day--drops be damned.
We grieve in our own ways and in our own time. Some of us push the losses into the dusty recesses of our mind and refuse to go there. Some of us cannot and remain in the immediacy of the loss, continually bombarded with it so that we are sucker punched throughout the day.

Part guidebook, part workbook, Ariel's book for neurotypical partners is sure to be considered a boon for spouses who know almost nothing about Asperger's Syndrome. Written by  Cindy Ariel, a licensed psychologist who provides therapy for a variety of issues, including relationships, it is an easy-to-read guide to understanding Asperger's Syndrome and why partners on the spectrum behave in ways that may be hard for those unfamiliar with the syndrome to understand.

It's been a rough two weeks--tears galore, bright spots, strep, then mono, and days passed in bed, sleeping hour after hour, as if in a week, I managed to make up for 22 years of child-created sleep debt. I'm pretty sure there's still some sleep debt remaining, as I remain wiped out, with a shower and getting dressed this afternoon taking all the energy I had and depleting it.