The Voiceless Minority

Yesterday was 4/29/3013, just another day for most, but for a select group of people, that day meant the world to them. When we are children, we often let our imaginations run wild. We sometimes play games where genies grant us wishes from a lamp; in fact, Aladdin's popular Disney movie is based around this concept. However, life is a different struggle for those with terminal diseases. Those with terminal illnesses often do not get the same experiences as the rest of us. When they should be going to a high school football game, homecoming, or a prom, they can often be found, instead, in hospital rooms, battling for their lives. One organization decided to change that. One Kid's Wish They say that if you put your mind to it, you can do anything you want. For Christopher Greicius, there were many obstacles in his way, but he had a great imagination. Every day, the 7-year-old dreamed of being a police officer. His wish was only granted for one day, but it would help inspire a...

According to my friends, I am a twenty-six-year-old male who is funny, charming, and intelligent. Apart from these traits, I do have one that makes me stand out from the crowd. I have a disability. It is known as cerebral palsy. This is not a life-threatening disability, but it does limit my movements and other activities in my life. I am currently going for a master’s degree in education and hold two bachelor’s degrees, one in history and one in the theater. By many people’s standards, I would be considered well on my way. However, there are still obstacles I must overcome. As I’ve stated before, in 1990, a piece of legislation was introduced known as the Americans with Disabilities Act. This Act attempted to eliminate as many barriers to inclusion in society for people with disabilities as possible. It specifically focused on five areas, which included making it easier for people to seek public education, making it easier for people to get into public buildings, improving communi...

Today, as I was preparing to write my next post for this blog, I was bouncing around with my head topics. I thought my next blog would be about the social security problem (i.e., How social security is designed to keep individuals with disabilities on it, rather than intended as an incentive to assist them in better their lives.) While this is an important issue and one that I will discuss later, I came across an article that I feel is my duty as a blogger for disability rights.  An article by a lady named Sunny Taylor titled  The Right Not to Work: Power and Disability . In the article, Miss Taylor indicates that she is an individual who has arthrogryposis multiplex congenital. According to Web MD 1 , "Arthrogryposis is a general or descriptive term for the development of nonprogressive contractures affecting one or more areas of the body. A contracture is a condition in which a joint becomes permanently fixed in a bent (flexed) or straightened (extended) position, com...