our family counts on the MDA, my son has Becker's Muscular Dystrophy, he has a medical team of his own and we see many of his doctors through our local MDA clinic. Every summer he is treated to the MDA summer camp at no charge, which he loves and calls the best week of his life each time.
Many things are coming about in trying to find a cure for these muscular diseases, it's getting closer all the time.
If you can, please make a donation, every bit helps fund the clinics, pays for life altering equipment to help those affected, and brings us closer to cures and treatments.
Answer by pinkdena at 7:11 PM on Sep. 5, 2010
Answer by victoriamom2007 at 10:57 PM on Sep. 5, 2010
Answer by sstepph at 5:18 PM on Sep. 6, 2010
Answer by Ashlynnsmommy07 at 1:22 AM on Sep. 10, 2010
Answer by mekarevell at 2:08 PM on Oct. 19, 2010
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