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Walt Disney World Half Marathon January 2010
The Race for Christopher November 6th marks exactly one year since Michael and I received the news of our son Christopher’s devastating diagnosis. While much of the shock has abated since then, the heartbreak continues until a treatment or cure can be found. On that day last November, we were told that our seemingly perfectly healthy 2-year-old boy had Duchenne muscular dystrophy, a fatal genetic disorder. The doctors told us that Christopher would probably lose the ability to walk by age 10 to 12, the use of his arms by his late teens, and would not likely survive his twenties. There is currently no cure. Duchenne affects approximately one in every 3,500 boys and is a progressive disease that slowly causes complete loss of muscle function. Although Duchenne is a genetic disorder, approximately 35% of cases occur because of a random spontaneous mutation. Duchenne can affect any family. There is hope. For the first time in the history of this disease, there are clinical trials underway for treatments that have the potential to dramatically slow its progression. These treatments may change Duchenne into a disease that can be managed over a lifetime, much like diabetes is today. And there are many other research initiatives underway, all pursuing promising advances. However, research takes a long time, is extremely expensive and is often delayed due to lack of funding. We need your help. Your donation, large or small, will fund research and help researchers in their quest to turn good ideas into viable treatments and cures. Together, we can change the outcome for Christopher and thousands of boys like him. If you think this page contains objectionable content, please inform the system administrator. | |||||||||||||||||||||||||||||||||
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