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Living With Spina Bifida

Robert M. Hensel
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I grew up with a birth defect known as spina bifida, a disability that affects my sense of balance, causing me to walk with a limp. Not only does it affect the function of the legs, but it also has an impact on the kidneys, causing them to deteriorate.

           The disability has had its ups and downs. As a young child, I can remember the way other children would look at me and stare because of the way that I walked. There were many times that my schoolmates would laugh at me and call me names simply because of their lack of understanding of why I was a little different, especially back in the mid-seventies and early-eighties. Children then were just unwilling to take the time to learn why one of their classmates might walk, speak or seem noticeably different from themselves. Now that I am an adult, I have noticed that the stares and names have begun to fade, and judgments that once were negative have begun to turn toward acceptance.

           The signing of the ADA has played a great part in breaking down some of those barriers that, as a child, left me to fight a war that seemed to have no end. Now I look beyond what I can't do and focus on what I can. I have learned that limitations open doors that have been closed, showing other ways to meet our needs. I have always looked at life as a challenge, grasping each obstacle with open arms. There is nothing in this world that comes easy. I must stand tall and look forward, to be ever so ready for what still lies ahead.

           People often feel sorry for those who were born with some type of disability. But their compassion is misplaced. Yes, I may not be able to run as fast or perform certain tasks, but my disability gives me a better look at life and all that's around me. I want to be seen not as a disability but as a person who has, and will continue to, bloom.

           So I decided to become a advocate on behalf of disabled Americans, to fight for our rights that for so long have been ignored. I feel that it only takes one powerful voice to change the minds of many nations, and as long as I have a mouth to use and a mind to think I will continue to work to bring peace upon the disabled community.



About the Author (click here) © 2001 Robert M. Hensel, all rights reserved
 appears here by permission



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