Daily Archives: 14 July, 2010

What a Lovely Surprise

I was recently reminded of the importance of noticing, appreciating, and celebrating “good disability moments” – those times when someone responds to me or treats me in a non-ableist way. This is more than the lack of discrimination or oppression, this is someone treating me as I want to be treated. Although these moments aren’t as routine as I would like them to be, they certainly come along, and I think it’s important to remind myself that not everyone will respond to my disability negatively or with fear or anger. Another side benefit is demonstrating how easy it is for people to act with compassion and caring on disability issues.

I read a post at Rolling Around that highlighted a recent “good moment”:

A Wheel-trans driver just came to pick up one of our members (a bit late, but understandable). While loading the member onto the bus, this driver took the opportunity to have a conversation with our member (she didn’t even realize that I was there). This member has a profound disability, he’s also blind and can’t answer back verbally. She spoke to him with kindness throughout the loading procedure, reassuring him he was going home, letting him know what she was doing and she was joking around with him. This driver has a huge heart and smile and made sure that no matter how stressed she was feeling due to traffic, she didn’t let that ruin someone else’s day. Too often people with disabilities are passed off and are not seen as “normal human beings” that have emotions and feelings. It’s a wonderful thing to see it when someone takes time out of their day to talk to members, be friendly, maintain professionalism and make someone smile with such a simple act of kindness.

I recently had a “good moment” of my own. I was at work, eating lunch with a few of my co-worker friends, people who know my disability status and whom I trust enough to feel comfortable discussing my disability issues. I mentioned how I had seen a lot of recent articles about lithium mining, spurred by the recent discovery of huge lithium deposits in Afghanistan, which prompted lots of articles analyzing lithium mining industries in Bolivia, and so on. I laughed that every time I see one of these articles, I have to consciously remind myself that the lithium they’re getting is to use in electronics and industry and that it isn’t being mined for pharmaceutical reasons. Partway through the story, I realized that one of my newer co-workers was sitting with us and remembered that I had not discussed my disability status with her, so continuing my story would basically be outing myself to her, but I was so far into it I couldn’t stop without also calling attention to my disability status. So I plunged ahead, saying that my reaction to those headlines is always to think “I don’t need that many pills! You all can stop mining the stuff now! I’m all set! Thanks!”

New co-worker laughed at the punchline and then the conversation moved on to other things. She didn’t stop the conversation to say, “wait, you’re on lithium? Isn’t that for crazy people?” or any other questions. She didn’t ask me what I take it for. She didn’t ask me anything, in fact, but continued to chat and laugh with me and the others with absolutely no change or shift at all. Since then, she’s continued to treat me exactly the same as before – griping about World Cup officiating, wondering if the A/C in our office will ever work reliably – and hasn’t mentioned or questioned my disability issues at all.

It is difficult to say how much this means to me. The ability to talk about myself, to share those jokes, without encountering negativity, curiosity, or even stares, made me feel like my disability did not set me apart from the group. That mentioning my medication in that context was equally mundane and non-notable as mentioning I have a cat, or drive a Honda, or don’t like beets. It was the feeling of acceptance. Of equality. And it was amazing.

Recommended Reading for July 14

Warning: Offsite links are not safe spaces. Articles and comments in the links may contain ableist, sexist, and other -ist language and ideas of varying intensity. Opinions expressed in the articles may not reflect the opinions held by the compiler of the post and links are provided as topics of interest and exploration only. I attempt to provide extra warnings for material like extreme violence/rape; however, your triggers/issues may vary, so please read with care.

Via Delicious:

RMJ at Bitch Magazine Blog: TelevIsm: Ableism, Appropriation, and United States of Tara

There are a lot of things that USOT does with its conceptual portrayal of disability that I like as a woman with disabilities. The producers did a lot of research—they consulted and worked with a DID specialist. In my [subjective] reading, main character Tara’s disability is not framed as a tragedy or particularly pitiable. It’s something that she lives with, and in my reading of the first season it’s explicitly used as a tool to cope with the repercussions of trauma. It’s something that she and her family work with and through on a day-to-day basis. She rejects medication that would “cure” her, reflecting the complexity of making decisions about medical care and pills. She experiences discrimination, and often argues against it.

But the show’s depiction of disability is inherently problematic because while it’s somewhat relatable, it’s not normalized. The point of the show is “look at this woman with multiple extra-wacky personae! Isn’t that hilarious and crazy and weird?” Furthermore, Tara’s form of DID is representative of only about 5% of all DID cases—instead of normalizing DID, the producers have chosen the most sensational form of the disorder.

RMJ at Deeply Problematic: Disability is Relevant to Feminism Part Infinity: Study Shows that Long-Lived Women have higher rates of disability:

Disability is naturally ocurring, and not something to be eliminated. But when women experience disability at disproportionate rates, it is indicative not of a wide variety of different human experiences and bodies. It’s indicative of sexist demands placed on women’s bodies throughout our lifetime.

Blogs:

terajk has done up another thorough transcript at Transcripts for Everyone: Transcript of interview with Neli Latson’s mother

This is a transcript of Nicole Flamer’s (of “You Aut to Know!” on Blogtalk Radio) interview with Lisa Alexander, whose autistic son Neli Latson was arrested after being harassed by the police.

Maria at the Hathor Legacy: WISCON 34: Activism: When to Speak Up, When to Let it Go

BCH pointed out that it’s sometimes easier to engage when you’re not seen as personally invested, and also said it’s good to know exactly what your rights are. The BUST card from the ACLU is useful for this. CTJ said she needed to ask herself the following: “Do I feel safe? Do I have backup? Will they listen? Is there someone nearby for whom I want to set a good example? I’ll only try to teach a pig to sing if there’s someone nearby who might find that song useful.”

Nebby at Hopeful Nebula: On Erasure in the Eureka Season 4 Premier SPOILERS!

So, just watched Eureka 4.01 “Founders Day.” Loved it, right up until the last few minutes.

Jedifreac at Racebending: Tinkerbell’s Amazing Ethnic Friends

So if when animated characters are made flesh, they become real, then what does it mean when an animated character with indigenous ethnicity and an anorak–one of the very few animated female heroines to ever be depicted with dark skin–is transferred into the real world, but looks and is portrayed by someone who is white?

At Racebending.com we hear a lot about what this might mean from an adult perspective, ranging from “racism” to “cultural appropriation” to “nothing to get your panties in a twist over.”

But I want to know what it means to a kid. Because children notice skin color. And they quickly notice, from observing how adults treat one another, that skin color clearly matters.

Alias-sqbr: A question for people who use image descriptions (Comments are of interest)

I always try and add alt tags, descriptions, and (when relevant) transcripts to my images. But I thought it was worth checking to see if anyone who uses these things (because of visual impairments, text-only browsing, speaking English as a second language etc) has any preferences for me doing them differently (and thus I ask here, where I post my art, rather than at my Serious Business journal). If I’m going to do them I might as well make them as useful as possible.

I guess my main questions are…

If you’re on Delicious, feel free to tag entries ‘disfem’ or ‘disfeminists,’ or ‘for:feminists’ to bring them to our attention! Link recommendations can also be emailed to recreading[@]disabledfeminists[.]com