Peyton's Project came about when our middle son was diagnosed with Duchenne Muscular Dystrophy (DMD). We were told there was NO CURE, NO TREATMENT and it’s 100% TERMINAL. We realized quickly that we wanted to turn this negative into a positive and help make a difference in not only our son’s life but also the lives of other DMD children. These kids deserve a chance to enjoy life like their siblings, friends and peers.
We are closer to slowing the progression DMD than in the history of this disease and it’s because of you that we can continue to fight the good fight and find hope where there once was none.