A Spinal Muscular Atrophy diagnoses turns your world in another direction. When we heard the words for the first time, we had no idea what SMA was. We left the doctors office that day in August, frightened, devastated and lost. Since that day in 2008 ,we have found so much comfort, support, and knowledge from so many other families with SMA. The Spinal Muscular Atrophy family is very close and always one that you can lean on. We are all here for one another, to share ideas, fears and most of all HOPE!!! Our charity focuses on both medical research and helping families with the financial burden that SMA places on a family. If you are interested in learning more about what we do, please visit the Unite 4 Peyton foundation page or contact us.