Posted by: shesabibliophile | 01/31/2010

Comfort, Safety, and Internalized [dis]Ableism

A while back, I joined a website for people with disabilities called Disaboom. There was a chat room, message boards, and articles written by PWD, doctors, and carers. While I did make a couple of friends there, it was mostly filled with internet drama and points-of-view that I couldn’t deal with.

In a space that was supposed to be comfortable and safe for PWD, it wasn’t. It certainly wasn’t one for me, being a disabled mixed-race woman.  There were posts by devotees looking for a little action, posts about  “illegal aliens” and any people of color who immigrate to the US, how women were inventing and perpetuating sexism, about Obama only winning because he is black, and more. Of course, there were people who did not think these things (my friends), but we all started to leave as the bigotry grew.  I eventually left.

Even though I would like to forget that whole experience, I did take away two things from it. One is that, besides being with good friends, my boyfriend, and some family, I will probably never feel totally comfortable in any space. This is something I knew before, subconsciously, but I didn’t start to analyze it or think about it until post-Disaboom. At zine fests, I’m usually the only (visibly) disabled person; I mean, at most social events, this is true. But even in spaces with other disabled folk, I am the woman, or the stealth Latina. Or the atheist. Whatever. There’s always something that sets me off from the crowd. I’m used to feeling like I’m on the fringe (and not in a cool, punk-rocky way), so I roll with it. It’s there, it will always be that way, so I deal. My activism is something that I hope will change this, but realistically, it’s beyond just me.

The second thing I took away from Disaboom is that there is a lot of internalized (dis)ableism going around. I know that, when I was younger, I was one of those “I’m not DISABLED like THEM!” people. I guess that’s because the only images of disabled people I’d ever seen were “inspirational” (which I never felt) or “sad” (which I also never felt). I used to go to the Muscular Dystrophy Association parties, and I would be uncomfortable with the attitude that permeated the room. It seemed like everyone there was so obsessed with their disability and being poster children and finding a cure to FIX them, and I wasn’t raised like that. I was raised in a home where my disability was rarely a topic of conversation, and all my friends were able-bodied. It was alien to me to think of myself as something that needed to be fixed. But this is what disability was to me because this is what I was exposed to.

It wasn’t until I reached adulthood that I started to view disability as something that wasn’t inherently bad. I learned more about disability rights and activism – the internet and books opened that world for me – and I began using “disabled” as a word to describe myself. I knew there were people out there who were fighting for rights and getting together to do protests, whether they were in the streets or online through blogs.

So, when I joined Disaboom, I was at that point in my life – accepting and appreciating who I am. But this website wasn’t like that. Even the people with disabilities talking about how they weren’t disabled (sound familiar?), but differently-abled, how they would never be able to accomplish anything in life and they needed to be fixed or cured. I wanted to tell them, and tried to tell them,  that, no, you don’t need to be fixed – society needs to be fixed! Your disability isn’t the problem, it’s society’s inability to include us in everyday life!

While I would definitely want parts of my disability to go away (stomach issues, ugh!), and while there are disabilities that many people want a cure for (and rightfully so), I don’t like to see “finding a cure” as the biggest topic in a disability community or message board. It just reeks of ableism – it’s always the disabled person who has to change, and not the community around them, right? And when your community (I’m speaking specifically about the Muscular Dystrophy Association) is ALL about finding a cure and pitying you, you just want that attitude to go away.

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Responses

  1. This is so true. Great piece. How about we “fix” minds and hearts.

    • SO true! Thanks for the comment ;)

  2. I totally agree! Those “cure” campaigns bug the sh*t out of me.


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