Out for a supercharged walking therapy session.

My first direct contact with FSR was my attendance at a patient conference in Hersey, PA, 2015. It was at this conference that I met the wonderful; folks involved with the foundation. Heard explanations of the disease by world-renowned expert doctors and researchers and met other patients like myself. I learned I was not alone in this world, maybe it was a small group but not alone. Since then I have attended numerous fundraising events, conferences and workshops learning and understanding much about the world of sarcoidosis. With FSR’s help I sought out second opinions from experienced doctors resulting in an improved treatment plan, which lead to improvement in my condition. We are very fortunate to have this foundation and its dedicated professionals advocating on behalf of the sarcoidosis community. Please join us today with your support.