Oh the Disabilities...
"There are some advantages to being in a wheelchair... you get to have cute boys push you around." - Jean Scott (My E.A)
I've never quoted someone I actually know personally on this blog so far, but I thought this one was too funny to pass up. It was a comment made to me when my Educational Assistant met my boyfriend Marc. She is right that my disability can give me the upper hand in some situations. As far as being noticed, I generally receive a lot more attention from others due to my obvious differences, which makes a great platform to speak about my faith. For some reason I have yet to fully understand, people admire me and are inspired by me. Perhaps they wonder how I can be so upbeat with my disability, but it's easy to understand how a person surrounded by loving friends and family and respected by peers would feel pretty cheerful most of the time. No, my disability isn't that bad. In some ways, I've learned to see it as a blessing. There are, however, some downsides to being disabled as well.
Yesterday my mother took me in to have a conference to determine whether I could qualify for disability pay when I turn 18 this November. We are currently receiving about $100 monthly from the government to help pay for medications and other inconveniences which are a part of having cereberal palsy. However, it turns out that I don't qualify to receive anything once I am officially an adult. My wise parents have saved up $5,300 to go towards my education in a savings bond which I can't access except for educational purposes. However, they consider this an asset, something I can use towards myself. Since I have assets of over $5,000, I don't qualify to receive a dime, even though this money can't be used to cover the costs of my disability in any way. Now I know I shouldn't complain, since my parents don't have trouble bringing in enough to support our family, but I know that I do eat a larger hole out of my dad's wallet what with vitamins, chiropractors, osteopaths, orthodics, and frequent drives to appointments and school. Other disabled kids I know qualify for $800 a month, as long as they don't get a job, at which point the coverage ends.
Maybe I'm just angry that I had to be taken out of school just to be told I didn't get a dime, but something about this doesn't seem quite fair.