FSR has spent 20 years serving sarcoidosis patients and their families, as well as the healthcare providers and researchers who dedicate their careers to fighting sarcoidosis. In response to the inequitable treatment of Black individuals in America, we want to...
FSR has made the decision to transition our in-person Patient Education Summits to be Virtual Summits. This decision was made due to the ongoing challenges of the COVID-19 pandemic in order to be proactive about the health and comfort of our community. While we are...
As part of FSR’s 20th Anniversary, we’re profiling some of the people who make everything we do at FSR possible, including our co-founders, Board of Directors, and staff. First up, meet our co-founders, the Wilsons! Andrea Wilson is a sarcoidosis warrior...
Sarcoidosis patients are used to talking about their physical complications, since both the disease and its treatments can cause so many physical symptoms. Chest pain, aching joints, debilitating fatigue, shortness of breath, or whatever else your most recent flare-up...
