Any time you’re in a conversation with patients with chronic illness, the topic of alternative treatment is bound to come up. For people who live with constant pain, fatigue, and other burdens of being ill, it may seem to make sense to turn to these kinds of...
Rare disease patients find out soon after a diagnosis that they’ll have to learn advocate for themselves- in the doctors office, to insurance companies, and even to the government. Unfortunately, rare diseases are still often overlooked in legislation, even though...
Written by Margot Hahn Communications Intern At FSR, we aim to find avenues that connect sarcoidosis patients across the United States and abroad. People living with sarcoidosis are no stranger to the degree of unknown information about the disease and its effects....
Three FSR team members presented at the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG) Annual Meeting in Crete, Greece this month. The conference was an annual meeting between the leading experts in sarcoidosis research and clinical care...