Daily Archives: 9 September, 2010

Recommended Reading for 09 September 2010

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.

Raising my Boychick: Musings on mental health, in-patient therapy, and ableism: or, why isn’t there a “Hooha Behavioral Center”?

There is so much broken in mental health services, I hardly know where to begin unraveling it. Should I have sought this sort of care? Certainly in a less-ableist society, it would have occurred to me far sooner. But what sort of “care” would I have received, even with relative protections of being a male-partnered middle-class white woman? What sorts of traumas might I have risked acquiring through the experience? Would I even have been admitted, or dismissed as not-crazy-enough, and what would the pain of failed help-seeking have done to me?

Jack and Dilley: Thoughts on Therapy: Right Livlihood: Veteran Farms (Thanks to SavvyChristine for the link!)

Veterans Farm, an organic blueberry farm in the Jacksonville area of Florida, takes a life-affirming approach to empowering disabled veterans to heal, return to work, and reintegrate into American society. It was begun by Adam Burke, a veteran who came back from Iraq with PTSD and a closed head injury. Seeking to come to terms with his disabilities and wartime experiences, he remembered peaceful and satisfying work on his family’s farm growing up. He realized “horticulture therapy” provided an ideal environment for rehabilitation, and talked his wife into buying a small farm.

JF Activists: ‘The Closed Digital Door:’ State Benefits’ Websites Inaccessible to PWD

The report, “The Closed Digital Door: State Public Benefits Agencies’ Failure to Make Websites Accessible to People with Disabilities and Usable for Everyone,” describes barriers to access for people with disabilities when applying for cash and other benefits online, requesting an application, searching the website, or contacting the agency by email. These accessibility problems violate the Americans with Disabilities Act, Section 504 of the Rehabilitation Act, and many state web accessibility laws and policies.

The Globe and Mail: Caregivers suffering depression, rage

“The message here is that if we’re going to help seniors stay in the community – and we should – then we critically have to look at the needs of caregivers,” said Linda Jackson, executive director of community and ambulatory programs at Baycrest, a Toronto health-care facility that specializes in care of the elderly.

CBC News: OxyContin worries misplaced: pain experts

In Quebec, opioid use doubled over 14 years, said Kristen Reidel, a master’s student in epidemiology at Montreal’s McGill University.

When Reidel presented her findings on opioid prescribing trends in Quebec at the World Congress on Pain in Montreal this week, she said she didn’t find an increase for the youngest age group.

Rather, the highest increase in opioid use was among people over the age of 80, who tend to suffer more chronic pain.

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 at disabledfeminists dot com. Please note if you would like to be credited, and under what name/site.

Body Image & Disability: An Entry Into The Conversation

A long time ago, I said this:

People with disabilities, especially women, have all the same pressures currently non-disabled people do to look “good enough”, with added bonus of being either non-sexualised or hyper-sexualised, as well as having people infantize them to an incredible degree.

Talking about disability and self-esteem and body image is very difficult for me. People look at me and see a woman without a disability (or a woman with a non-evident one), and I pass. I don’t get the odd looks that a woman of my age (or younger, or older) using a cane or crutches would. I don’t get the pats on the head that women who use wheelchairs report, and I don’t have people leaping out of the way when I’m using a motorized scooter.

But at the same time, women like me are often used as stand-ins for “horrible”. Whether that’s the simple of “she took off her glasses and suddenly she was beautiful!”, or the more complicated of “oh my gosh! the woman I had sex with is actually a crazy person! Quick, let us make many movies about crazy = bunny-boiler = grotesque!”, I’m well aware that women like me are bad, ugly inside, and unacceptable.

These things add a whole other layer to the conversations that many women, feminist and non, have about self esteem and body image. We are all inundated with the constant barrage of White, Long-Haired, Slender (But Not Too Slender), Tall (But Not Too Tall), Unblemished, Healthy-looking, Young women in most advertising and fashion spreads, television shows, movies, and even on our book covers.[1. The last one is so ubiquitous that until just now I didn’t realise that of all the non-fiction books on my desk about disability, only one has an actual image of visibly disabled people on it. Most of them have very plain covers, or abstract-type art on them.]

At the same time, though, poster children and the pity parade are a fairly common image of disabled children – whether with visible or non-evident disabilities – that present people with disabilities as weak, as undesirable, as needing of pity – and always, always, always, as children. Very rarely are images of self-possessed, happy, disabled adults shown, unless they are in one of the “he’s so brave” “look at what she’s overcome” news stories.

I don’t know how this affects other people, or how they deal with it. I know that when Don first got his cane, and then his wheelchair, his self-esteem and image of himself took a hit, and it took a while for me to convince him that yes, I still found him attractive (and I can’t tell you how much I love that wheelchair, since my sexy sexy husband now has energy!). I know for me it would be nice to see images of Actual Crazy Women who aren’t mockeries of women like me, but treated like actual people. It would be nice to see casual fashion spreads with people with evident disabilities in them, rather than only seeing “diversity matters!” posters that include maybe one (male) wheelchair user, usually white.

As I said, I find these things very hard to talk about, because in many ways I don’t even know where to start. While to some extent discussing pop culture and representations there is important, how do we, as individuals, deal with our own self-esteem issues? How do we, as a group, tackle the constant attacks on people with visible disabilities to hide parts of themselves? Make yourself more approachable by putting sparkles on your cane! Soup up your wheelchair and maybe someone will ask you a question! Hide your obvious aid-devices so that they don’t offend people! Cake on make-up so no one can see your scars!

I think there’s so much here to talk about. Please, tell me your thoughts.