The Voiceless Minority

It falls again. It's been a while since I've written because I'm back in school, and that comes with the Fall and along with another great American past time, that being NFL. The National Football League is one of the most talked-about things in American life. Sports, in general, play a significant role in American culture. The sports phenomena units people that frequently have very little in common. There is a spirit about competition in the sports arena that is hard to find anywhere else. However, usually, one group of individuals who are not associated with sports or at least disability in sports doesn't come to mind simultaneously in most people's minds. The disabled are not that different from anyone else, though, when it comes to their love of sports.        Anyone who knows me will tell you that I am an avid New York Giants fan, and I often yell at the T.V. when they screw up (which happens to be a lot this season). I am also a die-ha...

       As human beings, we have an inherent desire to achieve independence, and it is only through social contracts in societal constraints that we enter into communities with others. This is a very simplistic way to put human beings’ desire for independence into words. However, it often right that this desire often comes with conflict relating to society and everyday constraints. Some groups face different conditions. Like for example, the restrictions placed on the disabled community are more prominent.         When it comes to disability, I have a unique perspective. I’m a twenty-seven-year-old male who relies on others for most of my physical needs to be met. When I say that I rely on personal care, I include such tasks as showering, eating, dressing, and even moving from a supine position in bed to a functional upright position in my wheelchair. Those in the aide care profession are crucial to my life,...

       Hi guys. This blog will go a little off format. I know this blog is designed to talk about disability issues, and this one will cover a few personal details as you all seem to have responded well to the last blog, where I told a little bit of my personal story. That gave me the idea for this one.         A new school year is about to begin. My baby sister is finally growing up! She moved into college dorms this weekend, and that hit me interestingly. I know it's not a very good description, but it's the best way I can describe it. I have two Bachelor's degrees, and I'm working on my third. People think that's so impressive and amazing, but I look at this little seventeen-year-old genius (yes, I said seventeen), and I wonder, what am I doing with my life? She is already certified with 90 hours of preschool assistance that translates into some certificate in Maryland. Sorry, Kim. I don't remember all the d...

  “On the one hand, she was viscerally aware of what polio had done to her body and of the day-to-day realities of living with a disability. But she was also aware of what she called “a gentleman’s agreement” at home and at school to pretend that her disability didn’t exist.”         This is a quote from chapter 1 of Fred Pelka’s book  What We Have Done: An Oral History of the Disability Rights Movements.  This particular quote is a part of the Childhood chapter, and he’s introducing Corbett O’ Toole. In the pages following this quote, Corbett O’ Toole’s interview describes a fundamental problem still relevant in society today--that of identity.         As we progress from childhood into adulthood, we struggle to find our identity. We strive to no longer be perceived as so-and-so’s child but rather our independent person. This is no different, no matter your race, religion, sexual orienta...

So it’s been a while since I’ve written. I can’t say precisely why, but recently I’ve gotten inspiration back. I’m reading a great book by Fred Pelka, the first global history of the Disability Rights Movement that is actually told by people there. It is called  What We Have Done: An Oral History of the Disability Rights Movement . This book does a great job of two things: teaching someone who is disabled more about their movement because, sadly, I am not well informed, and secondly, backing it up with scholarly research. However, it’s this book and recent conversations that have caused me to write this blog.         There are several perceptions of disability but one perception of disability that irritates the disability community and me in particular. Fred Pelka has the medical model of disability. Rather than using this technical term, I refer to it as the “need to fix what is not broken.” Often in my life, I have encountered both person...

  On July 26, 1990, a quiet minority found their voice. President George Herbert Walker Bush would sign into law the most comprehensive disability rights legislation to date 1 . However, the Americans with Disabilities Act was just the culmination of a silent minority struggle to be heard.  This struggle is not often recognized. Since this blog is designed to empower people with disabilities and educate others, it would be inappropriate not to examine the Disability Rights Movement's history. For a group to have a powerful voice, they must understand their roots. In terms of the disability rights movement, it is important to examine the key figures involved and critical events and milestones within the training and the movement's goals up until the present day. The term disability is defined as "lack of adequate power, strength, or physical or mental ability; incapacity"  2 Initially, the term eugenics was coined by Sir Francis Galton in 1883 in his book  Ess...

Disabled and can’t work? Call xxx-xxx-and-we-will-get-the money-you-deserve-at-no-fee-unless-we-win-your-case. I saw this ad for a law firm that will remain nameless late last night as I was browsing my Cable, and it raised an interesting question in my mind. Are these ads another way to perpetuate stereotypes of disability? I was not convinced one way or another until this morning I saw one of those ads that claimed the following: “Does your child has a birth injury?” And then listed several, including my disability. The ad went on to say that the disabilities entitled the persons concerned to large sums of money. Then they guaranteed that they would help advocate for that money. After seeing both of these ads, it raised a profoundly disturbing question. Why do we perceive disability as so weak? This goes back to my terminology debates. In my opinion, but quite simply, I believe we perceive disability as a weakness rather than an obstacle. This is by the way we address it.  ...