o cope with their condition and accommodate their needs quite sufficiently. They go out carefully planned, non-peak hours because they do realize that others have rights to see a movie or dine in peace.Researching this paper has had a profound impact on me. I really feel for the sufferers of this senseless disease. Sometimes we take things for granted, like the simple act of walking undisturbed, and unnoticed down the street. People with TS are constantly gawked at. They are very misunderstood. People who do not know about the disease can be down right cruel. The next time I see someone walking and ticcing, I will not stare. Instead, I will know what is wrong with that person and I know that they cannot control their disease and did not ask for it. In conclusion, I end with the words of Jason Valencia, a Tourette sufferer.“Differences” Who are you to judgeBecause I’m not the same as youSome actions and some words I say,I do not voluntarily do.Who are you to make me cry?Because you think odd of what you see?Have you never given a second thoughtTo take a deeper look at me?If you look beyond my physical traitsAnd see the person inside,You’ll see how tough my struggle isFighting something I am not able to hide.Maybe I spit. Maybe I swear,Or constantly tap my hand.How do I explain these things to you,When I myself don’t understand?Yes, it hurts me deep insideWhen I hear the taunting words you say.And you, my friend, may need me nearWhen you get judged one day.Understand that I’m not crazyI’m not trying to make you mad.Understand I have unique problemsThat I’ll probably always have.I don’t expect you to treat me Differently, nor cut me lots of slack,The only thing I ask of you is Please— Don’t turn your back.1993, age 17...
