Hello Wednesday my old friend. Why I can’t remember that it’s Wednesday until late in the day (at least in my time zone), I will never know.
I was going to link an article about a showcase of artwork by Deaf and Hard-of-Hearing artists, and then when I re-read the article realised the only artist the article highlighted was a person who is neither d/Deaf nor hard of hearing, but wanted to show art in support of the project. I find that a really…. interesting…. way of framing a show that’s supposed to be about highlighting the work of artists with disabilities.
Instead, I’ll point your attention towards a presentation that Deaf photographer Stacy Lawrence gave to the Rochester School for the Deaf.
Katie at Muni Diaries: My Disability on Muni
I get on the train in the Sunset/Parkside district and ride it all the way in. My disability is largely invisible unless I’m barefoot or wearing a skirt that exposes my scar-covered right leg. I get dirty looks from older riders when I don’t get up to allow them a seat; I look like a perfectly healthy 22-year-old woman. I sit in the seat, repeat to myself “you’re handicapped and have a right to sit here” and stare at my foot-and-a-half while clutching my cane with white knuckles.
Citizens with FASD make up only 1% of the Canadian population but account for an estimated 40% to 50% of all prisoners. People born with FASD have difficulty learning new behaviours and controlling behavioural impulses.
Theatre Blog: How captions stopped plays being seen and not heard
Captioning is offered on a regular basis by major subsidised and commercial theatres all over the country. You’ll see “CAP” or “STAGETEXT” in the flyers. Stagetext is the name of a charity that made captioning happen big time. Over the past 10 years they have delivered captioned shows, and trained theatres in how to provide captioning in-house. Captioning has meant a big growth in deaf or hard of hearing theatregoers, for whom theatre is accessible like never before. Stagetext also offers deaf and access awareness training to theatre staff, including front of house staff, to help make a theatre visit more enjoyable and less stressful for deaf people. Clear communication and a friendly face work wonders. It’s great to see deaf and hard of hearing people talking passionately about shows with family and friends, and even daring to say what utter rubbish they’ve just seen.
Minister Responsible for Disability has Inaccessible Office Diane Finley, you are driving me up the wall.
Yes she piloted the Registered Disabilities Saving Plan through Parliament. That helps the children of upper-middle class Canadians save for the time when the parents have passed on. Those lucky few children with disabilities, then adults, face the bleak future of struggling to exist in Canada’s disability wasteland. The program is useless for most Canadians with disabilities who are struggling to survive. Where are they going to find disposable income to save for their childrens’ income?
Canadians with disabilities who can no longer work are subject to the worst conditions of poverty of any group. They form the largest number of people in Canada on social assistance.
The only Federal income program that helps them is the Canada Pension Disability which maxes out at $13,000 annually. Most Canadians on disabilities and CPP are receiving less than $10,000 a year. It doesn’t take an economist to understand survival on $10,000 is punishing poverty.
[Don has a RDSP. Don is also the child of upper-middle class parents. It’s also really really firmly designed with parents of children with disabilities in mind, much like the Registered Education Savings Plans. For example, our bank refused to allow Don to manage his RDSP over the phone, through ebanking, or anything else except in person. The bank building is only “wheelchair accessible” in certain areas, which doesn’t include the areas you need enter in order to manage your RDSP in person. Other banks have different policies, of course, but there’s nothing quite like being told an investment is “for you” when you can’t even get into the building to manage it.]
Mariness: Body scanners and pat downs
With the body scanner, however, you have to be able to stand still. Since I can’t do this without at the very least wobbling and swaying, I now have to do the patdown in my wheelchair.
Smackie the Frog:My TSA Experience
This got me to thinking, though. Am I going to always be subjected to the “enhanced pat down” because of my medical device? I don’t even so much object to the backscatter x-ray machines, and I don’t have any problem with them doing the swab on the device. So I did some research and talked to other people with the insulin pumps who have also flown, and they have had to deal with the same thing I did. One lady was even told by a TSA supervisor that if you have a medical device like an insulin pump, you have to go through the “enhanced pat down”. No choice.
American Coalition of Amputees: ACA calls for Improved Screening Procedures for TSA
“I had just been put in the Plexiglas screening booth,” said Peggy. “My 4-year-old son was made to sit across from me, crying because they would not let him touch me. Everyone was looking at us. Then the TSA agent asked for my prosthetic leg. I knew they could wand my leg, but he insisted on taking it from me. And if that wasn’t humiliating enough, he asked for the liner sock that covers my residual limb, saying I had to give it to him. I felt pressured to give him my liner even though it is critical to keep it sanitary. I was embarrassed to have my residual limb exposed in public.”
There have been several news stories about how the changes in the TSA in the US have affected passengers with disabilities. Here is only a sample, I assure you: