nilchance: original art from a vintage print; art of a woman being struck by lightning (on my meds)
Laughing Lady ([personal profile] nilchance) wrote2008-05-28 08:55 am
Entry tags:

(no subject)

My thoughts on disability rights, let me show you them.



Recent Denial Rates for Disability Applications, provided by Disability Blogger

California - In California, 55.5 percent are denied.
Texas - In Texas, 61.5 percent are denied.
Pennsylvania - In pennsylvania 55.1 percent are denied.
Wisconsin - 62.6 percent denied.
Washington - 58.9 percent denied.
Virginia - 61.6 percent denied.
Massachusetts - 54.7 percent denied.
Maryland - 66 percent denied.
Michigan- 64.1 percent denied.
Minnesota - 57.6 percent denied.
Mississippi - 72.8 percent denied.
Missouri - 66.8 percent denied.
Nevada - 50.4 percent denied.
New Jersey - 50 percent denied.
New Mexico - 59.6 percent denied.
New York - 61.9 percent denied.
North Carolina - 67.2 percent denied.
Ohio - 71.1 percent denied.
Oklahoma - 66.1 percent denied.
Oregon - 66.3 percent denied.
Arizona - 53.4 percent denied.
Arkansas - 63.2 percent denied.
Colorado - 73.7 percent denied.
Florida - In Florida, 64.9 percent are denied.
Georgia - 71.8 percent denied.
Illinois - 61.2 percent denied.
Indiana - 67.8 percent denied.
Kansas - 67.3 percent denied.
Kentucky - 67.7 percent denied.
Louisiana - 68.8 percent denied.
Tennessee - 74.3 percent denied.
Alabama - 70.6 percent denied.
Connecticut - 62.2 percent denied.
Utah - 69.8 percent denied.


These are the people who could afford to apply for disability. Who went months without income to qualify, yet scrounged up the cash to pay a lawyer. These are the people who scraped through for groceries, pills, doctors visits, wheelchairs, chemotherapy, child care.

These are the people who filled out humiliating forms that required them to state over and over again that they had nothing to contribute to society. That they couldn't work. That they were broken and needed help. These are the people who went in front of county boards to say to them, "I can't."

These are the people who went through that and were refused.

The media pushes the idea that everyone is trying to cheat the system. That people file for disability for acne and broken fingernails. And there is that minority; I work in disability services, and I've seen people try to claim services on false grounds. But in trying to get rid of the dishonest minority (which is estimated at the MOST as 5% of all cases), the government is screwing more than half of the people who apply.

I look at that and think, that could be me. That might still be me. I'm textbook fibro in my mid-20s, when most patients are diagnosed in their 40s-50s. I have chronic daily headache. I suspect that I have CFS/ME. There are times when I miss 2-3 days of work a week. I work in disability services, I'm lucky that way, but still I've had my boss request medical records and second-guess my doctors. I've had a supervisor suggest in an official context that I need therapy.

I'm one of the lucky ones. I don't have cancer. I can work. I'm not in a wheelchair yet. I have an invisible condition that was verified by a doctor. I'm not bipolar or schizophrenic. I don't pay rent. I have insurance. I don't have kids. I'm so goddamn lucky in this economy. And I could still slip. Anyone could. Being able-bodied is a temporary condition.

Confession: my mom is on disability. She has advanced MS and bipolar disorder. She was granted full service-connected status as a veteran, and disability benefits as well. She's one of the minority from Illinois who won her case. And she is goddamn miserable to be retired. She's a brilliant woman trapped in a failing body. She's running out of books to read and movies to watch. She's 54 and she feels like she's already considered dead. And the government still has watchdogs overlooking her case and those like hers, making sure that the person is still disabled, making sure that they're not cheating.

Only one presidential candidate has a public policy on disability. (Obama, for the record.) McCain's policy is 'don't get disabled.' Returning wounded veterans are being asked to return their signing bonus. The people above went to the government to ask for the disability benefits that they funded with their paychecks through years of service, through working, and the government said simply, 'fuck you, you're faking it.'

I'm afraid for our country. I'm afraid for myself.

[identity profile] atypia.livejournal.com 2008-05-29 04:53 am (UTC)(link)
I'm incredibly lucky. I've been on Disability Support Pension for coming up to eight years. It's a bitch to get on.

The forms break my heart. It is so hard to focus on every single thing I can't do. After the first few years I learnt that I need to focus on the good things in my time. Surround myself with people who understand that I need cheering up, to focus on my abilities and not my disabilities. And it's not like the forms are the basics, either. They're so thorough and horrible. And it's not just the form I need to fill out, it's going to the doctor and having them ask me all the questions and assessing exactly what I can't do and to what extent I can't.

I love my GP. I travel to the other side of the city to see her when it's time for my forms to be filled out. She knows how to fill them out properly, with the ridiculous details. And she doesn't ask me too many questions. She knows the answers, then asks me for clarification on things if she needs to.

It's just so fucking horrible.

But I'm so lucky. I got my application turned down initially, but appealed and got it approved. There's no lawyers or anything involved here, doctors make the decisions. Our system makes SENSE.

Heaps of medications are on the PBS (pharmaceutical benefits scheme) here, so they are heavily subsided for absolutely everyone. Since I'm on a pension, I get any meds on the PBS for only $5.80 each (or something like that), even if I'm on a high dose.

Same thing with xrays, ultrasounds, blood tests - they're covered by medicare and don't cost me anything. And when I first got sick, I had so many fucking ultrasounds, xrays, blood tests and so on. There were lots of things that cost my parents a lot of money, and then there was the huge guilt for that. Them spending all their money on endoscopies and crazy doctors and acupuncturists and naturopaths and chiros and and and and and.

I fucking hate the whole thing. I HATE IT.

[identity profile] atypia.livejournal.com 2008-05-29 04:58 am (UTC)(link)
Oh, and lets not dwell on my ex-boyfriend's mother, who when I was going out with him told me that she didn't want her tax dollars wasted on me, that I wasn't really sick, I was faking, I was a liar, I was a "drain on [her] resources".

I've been told I couldn't possibly be sick because my hair was too shiny.

I was told at school that I needed to put on weight (I lost 5kg when I first got sick, which put me in the anorexic bmi range). I was super skinny, looked almost green because I was so sick all the time, and missing tonnes of school. And this guy, who wasn't even my teacher, called me into his office as I was walking past to tell me that he knew I was ill and that I needed to gain some weight. Can you fucking believe that?! I felt so conspicuous, having this strange man commenting on my body when I had no control over my body as it was.

Ugh. I have throw so many people out of my life because of shit like that.

[identity profile] atypia.livejournal.com 2008-05-29 04:59 am (UTC)(link)
The forms break my heart. It is so hard to focus on every single thing I can't do. After the first few years I learnt that I need to focus on the good things in my time.

I meant "learnt that I need to focus on the good things in my LIFE".