There is no more helpless feeling than to have your child diagnosed with a condition you've never even heard of and that many in the medical community know little or nothing about. Our daughter Lindy was a competitive gymnast who developed RSD three years ago (March 2002) and has been on crutches ever since. We wish so much that we had known about the Foundation back then. It has been such a source of hope for us, along with providing valid scientific information about this life altering disease. Our hope lies with future research.
We are grateful to all those responsible for the countless hours devoted to the projects and services provided by the Foundation. If we all work together, we can ease the pain of everyone around the world who suffers from RSD.
-Kathy, Steve and Eric Snyder
In Honor of Lindy Snyder (Pictured)