Daily Archives: 7 May, 2010

Chatterday! Open Thread.

This is our weekly Chatterday! open thread. Use this open thread to talk amongst yourselves: feel free to share a link, have a vent, or spread some joy.

What have you been reading or watching lately (remembering spoiler warnings)? What are you proud of this week? What’s made your teeth itch? What’s going on in your part of the world? Got any questions for your fellow FWD commenters?

Today’s chatterday backcloth, a teeny tiny octopus, comes via I Can Has Cheezburger.

very tiny octopus on a person's fingers

UK Signal Boost: Study about Disability & Benefits at the University of Leeds

Are you a person with a disability?

Do you currently receive disability benefits?

Do you want to work?

If so, we want to talk to you! A research project at the University of Illinois at Chicago is interested in your experiences in and views of employment programs associated with work-related activities under reform to Incapacity Benefits or the Employment and Support Allowance.

We would like for you to participate in a focus group and share your experiences with the researchers and a group of people like you.

Who?

To be eligible, you must:

live in the city of Leeds or receive services there;

be between the ages of 18 and 64;

receive Incapacity Benefits or the Employment and Support Allowance; or be participating in or eligible for employment services through Pathways to Work or the New Deal for Disabled People

Continue reading UK Signal Boost: Study about Disability & Benefits at the University of Leeds

An Open Letter to Ms Magazine Blog

Dear Ms Magazine Blog:

My name is Anna. I’m what some people in North America would call a person with a disability, and some people in the UK would call a disabled person. My husband, many of my friends, all of my co-bloggers, and a large number of our commenters are also people with disabilities/disabled people.

Your blogger, Carol King, would instead refer to us as “the disabled”, and as pawns of the religious right. In her blog post Kevorkian and the Right to Choose , she wrote:

The “right-to-lifers” enlisted the disabled in their cause when they cautioned that allowing people to choose to die would soon become their “duty to die.”

I’m pretty angry about that. Not offended, Ms Magazine, angry. You see, I’m really tired of “the disabled” being treated like we’re unthinking masses. I’m especially tired of the feminist movement – you know, one that allegedly wants equal rights for all people, including women with disabilities – doing this. It makes me angry because I’m a feminist as well as a woman as well as a person with a disability as well as someone who is not the pawn of anyone, thank you very much.

Some people with disabilities support the right to die. Others do not. Others do in some cases and not in others. Each of us has come to the conclusions we have because we are reasoning individuals. Gosh, some of us are even feminists who use a feminist lens to come to our decisions, regardless of which of the many places on that particular spectrum of opinion we find ourselves.

People with disabilities deserve better treatment than you have given them. We are not a throw-away line so you can score some sort of points. We are people, and I’m appalled that a feminist blog like Ms would publish something that would treat us as otherwise.

Frankly, I am so fucking tired of this shit. I’m tired of smiling while feminist organisations treat people with disabilities like they’re afterthoughts and problems to be solved. Like we’re just pawns in politics, like we need to be appeased but never spoken to or considered, like we’re too angry or not angry enough, like we have to push this fucking rock of dis/ableism uphill while you – our “sisters” – stand by and politely look away.

Do you remember Beijing, Ms Magazine? You’ve talked about it a lot lately. You know what I know about Beijing? I know the accessibility tent was inaccessible to people with disabilities. [transcript follows]

“We will achieve our rights and the respect we deserve as women with disabilities.” “Because the issues of women with disabilities have often been excluded, the goal this year was to make sure the concerns of disabled women were addressed.” Oh, hell, just watch the whole damned thing – it’s subtitled – and see the commitment feminists made to women with disabilities. Ask yourself, seriously, Ms Magazine, why your new blog has decided not to talk much about women with disabilities. “No woman who attends this conference should be able to leave Beijing without thinking about the rights of women with disabilities.” Do you?

You know what? If that’s something you can’t do, let me sum it up:

Nothing about us without us.

You wanna talk “about” “the disabled”? How about talking to us? How about letting us talk for ourselves?

How about treating us – people with disabilities – the way you would like women like yourselves to be treated? As though we have some understanding of our own experiences, our own opinions, our own thoughts. As though our thoughts do not belong to anyone but ourselves?

As though we are thinking beings?

Again, my name is Anna. I, like you, am a woman, and I am also a person with a disability. And we deserve better from you.

Sincerely,

Anna.

Please note: This thread is meant to be about the continued marginalization of people with disabilities in the Feminist Movement. I won’t be approving any comments about Kevorkian or related discussions.
Continue reading An Open Letter to Ms Magazine Blog

Signal Boost: Disenfranchisement at its Worst

Jady Lady describes her experience as a blind vote in today’s election in the UK

It was only whilst walking home with my partner that we compared notes. It appeared that my template had been placed fairly close to the left hand edge of the form, and my partner’s had been nearer the middle of the form. We phoned a friend and asked where the boxes appear on the ballot paper and were told that they are down the right hand side.

It would therefore appear that both our bballot papers are spoilt and we haven’t had a vote in this very important election.

If I never campaign for anything else in my life, I’m determined to get my voice heard on this one.

If you read this, I would urge you, please circulate it as widely as possible. I want as many people to realise how open to error the voting system is for blind people.

Our right to independence relies wholly on a sighted person to line the template up for us, and we have no way of checking that the vote has been cast properly.

I wonder how many other blind people’s ballot papers have been unknowingly spoilt today?

Read the whole thing.