Daily Archives: 1 April, 2010

No, It’s Not As Easy As You Think

When I talk to people in the United States about disability and the need for accommodations, I am usually met with a bit of bewilderment. “You mean there’s still more work to be done on accommodations? I thought all that had been taken care of.” These are people who are used to seeing wheelchair ramps at the entrance to government buildings, used to seeing the hand switch for wheelchair users to open automatic doors, used to seeing the braille at the ATMs. Given their observations of those existing accommodations and a minimal awareness of the Americans with Disabilities Act (ADA) that mandates those accommodations, they assume that there’s been a consensus on the need to provide accommodations, a law mandating those agreed-on accommodations, and general compliance with that law.

As we well know, that is far from the truth. None of those assumptions are as true or are interpreted as broadly as people tend to assume. There is no general consensus on the need to provide accommodations for the broad range of disabilities that exist – there is general agreement that people who use wheelchairs should have access to government buildings, but there is nothing even close to general agreement on how to accommodate people with depression or even whether depression is a disability “deserving” of accommodation. The US does have a law mandating accommodations – but there are not equivalents in every country and there are significant holes in the ADA itself, often putting the burden of requesting accommodations and demonstrating a need for them on the person with a disability. Finally, the idea that agencies and businesses affirmatively comply with the ADA, obviating the need for enforcement, is just patently false.

A recent federal court decision in underlines all of these realities. In 2005, the American Council of the Blind filed a lawsuit against the Social Security Administration (SSA) “to compel SSA to provide alternative formats of communication that would enable [people with visual impairments] to have more equal access to participate in SSA programs.” (Court documents and information available through DREDEF’s site.) It took until 2009 for a court to agree and order SSA that it is required to issue notices to people with visual impairments in a format they can read – in Braille, large print, e-mail that can be read by a screen reader, computer disks, or audiotape recordings.

This lawsuit undercuts each of the assumptions above. First, there is clearly not consensus on providing accommodations, even to what would be considered a relatively “easy” impairment to accommodate – it is easy to anticipate the functional difficulties that a person with a visual impairment would encounter when presented with a written notice. A lot of these people – 250,000 of them – are getting benefits from SSA specifically because they have a visual impairment, so they’ve given SSA extensive documentation of those impairments and information on the functional limitations caused by the impairments. A much larger group – about 3 million in total – get retirement benefits from SSA. At any rate, SSA knows that these people have visual impairments and has detailed information on how those impairments affect them. And it still has not provided accommodations.

But what about the second assumption – there’s the ADA, right? It turns out that the SSA is not subject to the requirements of the ADA! The ADA applies only to state and local governments and agencies that receive federal funding – it does not apply to federal agencies such as SSA. (Raise your hand if you knew that – few people do!) The only disability rights law that applies is a precursor to the ADA, Section 504 of the Rehabilitation Act of 1973. While the requirements regarding accommodations from government agencies are largely similar, the Rehabilitation Act does provide limited rights in comparison to the ADA.

It’s also very clear that the SSA – despite being the primary provider of cash and medical benefits for people with disabilities – did not consider that it had any obligation to provide accommodations. When individual plaintiffs with visual disabilities requested that they be given notices in alternative formats, they were simply told that no other formats were available. This included notices to which people must respond within 10 days or risk losing their benefits. Even when they were initially sued in 2005, SSA argued that the Rehabilitation Act “did not even apply” to the issue of notices to people with visual impairments. Similarly, SSA did not consider itself obligated to let benefits recipients know that they had accommodation rights under the Rehabilitation Act and laying out a process for them to request and enforce those rights.

The result of the litigation is that SSA is now required to develop a procedure to 1) notify benefits recipients of their rights to accommodations for visual impairments  and 2) provide notices in alternative formats when recipients request them. Which is certainly a good thing – but one that I would simply expect from a government agency that administers disability benefits, rather than having to be ordered by a federal court after 5 years of litigation. And if accommodations that are this common sense, from a federal agency set up to deal with people with disabilities, are so hard to obtain and enforce, that demonstrates how very far we are from a society where PWDs are meaningfully accommodated.

Recommended Reading for April 1, 2010

A painting done showing hands in the Signs for A-S-L

Shit I Hate: Models as the Face of ED Survivorhood

Let me be clear – I do not hate models who are suffering from eating disorders, have come out as ED sufferers or survivors, or who have turned to advocate for other sufferers. That is a good thing to do, it comes from a place of kindness and intelligence, and it is an admirable use of privilege in order to help others. Model moral behavior, you might even say. However, I do not like the way the models’ narrative seems to be the dominant or even only story that is recognized in our wider media as the neatly-packaged beginning-to-end textbook case of an eating disorder. I’m focusing on women here because women’s bodies are, overwhelmingly, the target of these narratives. I’m also focusing on those women who have made it to tell their stories – though we know many will not make it, and we do not forget them. I’m talking specifically about media portrayal of ED survivors.

Nursing at the Keyboard [NAK]: How to give boob and type too

When my kids were little, they nursed a lot. A LOT. They were both evening cluster feeders, which meant that my options for the evening were to sit on the couch and watch TV or read a book, or I could NAK. Nursing at the keyboard was often the best choice for me. Television was sometimes too loud and the Internet was just too compelling. But as someone who has mastered the art of typing, trying to type messages one-handed while nursing a baby quickly got old. Something had to be done about it.

So I worked out a system.

“Let’s Go Talk to Patio Furniture”

One day Wanda refused to assist me in the bathroom and gave no explanation why. I was in class (college) so it was not like I had my mom there and none of my friends knew how to transfer me (why would they?). So there I was at lunch, needing to pee but my aide refusing. So I had to ask one of my friends. My aide wouldn’t even help explain how to transfer me or do anything else. I had to eyespell how to do everything to my poor friend.

Dear Michael & Brian, You Were Lied To

At i09, M. Night Shylaman answers questions about The Last Airbender Live Action Move (aka, that Racist Mess). And he shows not only that he’s the South Asian equivalent of an Uncle Tom; he shows that he doesn’t get the optimism and hope of Avatar – that it wasn’t that it started young and skewed older, but that it has a foundation of joy and hope and friendship that carries all through; just as it has a foundation of being non-white fantasy.

Remember the interview that’s now unfortunately on the official animated series DVD? About how he ‘got’ it all?

M. Night Shylaman lied.

Judge Quentin D Corley

Another disability history image thanks to the Flickr Commons project. This one is from the Library of Congress’s set from the George Grantham Bain Collection, news photos from 1910-1915. Here we see Judge Quentin D. Corley (as the title suggests), driving a very early model car with steering wheel adaptations for his prosthetic left hand; the right sleeve of his jacket appears to be empty. Corley looks to be a young man wearing a white summer hat.

Life is Too Short

Brandy, a large yellow Labrador worked faithfully by her partners side for 11 years. She was the first service dog for people with physical disabilities I ever met and I still remember meeting her and her human on while we were stuck on a plane having electrical difficulties on a tarmac in a plane going nowhere anytime soon. As the crew allowed other passenger to exit to plane if they wish for a bit, this gentleman and I bot made the decision to sit tight because it was too much of a hassle to get of the plane and risk not getting back in time.

Does Diagnosis Matter?

In the recovery movement, which is the zeitgeist in the delivery of mental health services at this time, we are supposed to look past someone’s diagnosis. I am not “a bipolar” or “depressive” or “schizophrenic.” I have been diagnosed with such, but the relevance of that diagnosis is highly suspect. Because aren’t I just Liz? Liz who is addicted to Dunkin Donuts hazelnut coffee, Liz who likes chihuahuas in sweaters, Liz who tries to do gluteal exercises to increase her butt’s circumference — without success. So many things make up my Liz-ness, right? So who cares what some doctor said?

Generally speaking, I agree with this approach. For many years we have been labelling people in an attempt to treat them, and the results aren’t exactly stellar. So why not change protocols, DSM by damned?

This Situation Is Not Unique DISCUSSES SEXUAL ASSAULT

When I was in middle school, around the same age as this little girl is, and freshly diagnosed with Aspergers, I was also a victim of sexual harassment/assault, repeatedly, by my classmates. Innapropriate touching, lewd comments about my body, and bragging about taking advantage of me because I was too “retarded” to understand what was going on. This continued for three years uninterrupted, and only slightly lessened when I entered high school. Nobody did anything, not teachers, nor my parents, nor the administrative staff at the private school I attended. Whether it was due to them being oblivious to the bullying, whether they thought that because I was bigger than the other students that I should “take care of myself”, or because the students who tormented me were wealthy and came from good families and I didn’t, I’ll never know. I suffered in silence. In fact, until today, I’ve never talked candidly about the fact that I was sexually assaulted. I simply labelled it “bullying”.