Transcript: AWA interview with Ari Ne’eman and Paula Durbin-Westby of ASAN

This is a transcript of the November 2, 2009 appearance of ASAN’s Ari Ne’eman and Paula Durbin-Westby on AWA Radio with Sharon daVanport.

Sweetie

When I am alone, in public, this thing happens.

“You look like a lost puppy!” said a friend as I was looking for my seat in the college cafeteria. Once someone offered me a glass of water as soon as I walked in. Another time, a man pulled me off the street and forced me to sit down at an outdoor table and didn’t even ask me about the water—he just gave me a glass. And yes, there was that really bizarre time when I was in high school, and a teacher grabbed me by the shoulders, shook me and said to me V-E-R-Y S-L-O-W-L-Y: “The Sophomores. Are meeting. In the gym.” But what usually happens is, people—other white women, not much older than me, if they are older than me at all—call me “sweetie.”

Transcript: AWA interview with Melissa Barton

This is a transcript of Sharon daVanport’s interview with Melissa Barton for the Asperger Women’s Association. Melissa’s son Alex was voted out of his kindergarten class Survivor-style by his teacher, Wendy Portillo, in May 2008; Alex has Asperger Syndrome. The Bartons have recently filed a federal lawsuit.

*Squeak!* It’s open thread time!

TRIGGER WARNING for people with phobias of mice and rats

Rosemary

From True Compass by Edward M. Kennedy:

“My eldest sister, Rosemary, was twenty-three in 1941. Luminously pretty and round-faced, with a widow’s peak, dark brows, and a great smile that dimpled her cheeks, Rosemary was the one sibling with whom all the others were unfailingly gentle. Her affliction, diagnosed as mental retardation, left her struggling to comprehend things as quickly or as clearly as other people. She was a sweet and loving human being.

Rosemary enriched the humanity of all of us. Our sister Eunice seemed always to be near her, helping her through simple childhood games such as dodgeball, inviting her along and giving her assignments in sailing races. As she grew into adolescence, Rosemary knew she could count on Jack or Joe to escort her to dances at the Yacht Club at the Cape, or to the Stork Club in New York. I looked out for her too, when I could, although I was fourteen years younger–she was my godmother, after all. Dad wrote affectionate letters to her from abroad, and Mother actually altered her own handwriting from the swirling ‘fine Spencerian hand’ on which she’d prided herself, to a simpler style that imitated typographic print, so that Rosemary would have less trouble following it.

But in the fall of that year, our father, concerned that Rosemary’s condition would pose insurmountable dangers to her as an adult woman in the world, listened to doctors who assured him that a new form of neurosurgery would greatly benefit her and improve her quality of life. The doctors were wrong, the surgery further injured Rosie, and my parents were devastated. I, of course, knew and understood nothing of what had happened. Rosemary spent her remaining sixty-three years mostly in comfortable supervision at her home in a Catholic community in Wisconsin. Over the years, through her regular visits to Eunice’s home or her summer days on Cape Cod or wintertime in Florida or Thanksgiving at Jean’s, Rosemary remained a loving and inspirational presence in our family, not just for her siblings, but for the next generations as well.” (pp. 25-6)

New blog of awesomeness

FWD/Forward is a new group blog of/for feminists with disabilities. From the Mission Statement:

It is a place to discuss disability issues and the intersection between feminism and disability rights activism. The content here ranges from basic information which is designed to introduce people who are new to disability issues or feminism to some core concepts, to more advanced topics, with the goal of promoting discussion, conversation, fellowship, and education.

This site does not claim to speak for all feminists with disabilities. However, we are trying to cultivate a broad perspective which incorporates as many experiences and viewpoints as possible. We have attempted to assemble a diverse team of contributors with a broad spectrum of disabilities who come from different cultural, racial, religious, and class backgrounds, as well as age groups, and we welcome contributions such as guest posts, suggestions for article topics, and engagement in the comments from people interested in disability issues, disability feminism, and related topics, especially if those contributions will broaden our perspective.

We are very committed to accessibility; we want everyone to be able to enjoy our content. To that end, we commit to fully captioning and describing any images published here, transcribing text in images and audio content, and taking any other steps which can improve accessibility. We also welcome translation of our content into other languages. If you identify an accessibility issue here, we most definitely want to hear about it.

The site has just started up, but there’s lots of really excellent stuff there already, including an Ableist Word Profile series, and a series “about representations of disability in movies, television shows, and books.” (The series’s inaugural post examines the television show Joan of Arcadia.)

It’s awesome. Get thee over to disabledfeminists.com and check it out.

Trailer dump:Avatar

The Googlerati asks: “Orphan” Edition

Last week Sweet Perdition had its busiest day ever, and the past two days have each been busier than the previous winner:

This development is partly thanks to this post about the film Orphan. There’s a lesson for me somewhere about organization, managing my mental spoons, and writing about things in a timely manner. (I’d been planning on using Orphan to write about the “bad seed” sub-genre in general and cultural anxieties about disabled children. so was gathering my thoughts in a disability analysis direction seriously for days–and, much less intensely, for months–before I saw the movie).

The other lesson is that people want to know things–and, unfortunately, many searchers’ Orphan-related questions weren’t answered at all. While I hope some of them stuck around for the analysis of disability anyway, it totally sucks to not get the answers you seek. So, Internets, I apologize. And I’m here to make it up to you. Let’s begin, shall we?

Transcript: Tony Attwood’s July 21 appearance on the AWA podcast (Part 2 of 2)

Here’s a transcript of Tony Attwood’s appearance on the Asperger Women’s Association podcast at Blogtalk Radio. This is the second half of the podcast; part 1 is here. If you’ve noticed any errors I’ve made, please let me know:

“There’s something wrong with Esther”: Disability, deception, and Orphan

WARNING: Major spoilers for the movie Orphan, including the twist.