In 1997, after several months of dealing with confusing symptoms, I was diagnosed with sarcoidosis in my lungs and lymph nodes. The surgeon who completed the biopsy suggested I not bother to research the disease, as it would scare me. On my way home from the hospital, I stopped at the library to start learningLearn More The post A Rare Type with a Rare Disease appeared first on Foundation for Sarcoidosis Research.| Foundation for Sarcoidosis Research
It is with deep sadness that we share the passing of our dear friend and longtime volunteer, Bob Gross. For many years, Bob was a dedicated FSR Patient Navigator, always offering his time to ensure those newly diagnosed with sarcoidosis or diagnosed with a new manifestation had someone to connect with and receive much neededLearn More The post In Memory of Bob Gross appeared first on Foundation for Sarcoidosis Research.| Foundation for Sarcoidosis Research
The Foundation for Sarcoidosis Research (FSR) is proud to celebrate a major milestone for the FSR Sarc Fighter Podcast, which has officially surpassed 100,000 downloads since its launch in 2020. Hosted by John Carlin, member of the FSR Board of Directors and sarcoidosis patient and advocate, the FSR Sarc Fighter Podcast is the first podcast dedicatedLearn More The post FSR Sarc Fighter Podcast Surpasses 100,000 Downloads appeared first on Foundation for Sarcoidosis Research.| Foundation for Sarcoidosis Research