“Ten years ago, I heard a word that would quietly change the course of my life: sarcoidosis. At the time, I had no idea how much that single word would teach me—about patience, uncertainty, suffering, resilience, and the deep importance of living mindfully in...
Often described as a “snowflake disease,” sarcoidosis can affect every patient differently, making it difficult to diagnose, treat, and even recognize. This April, the Foundation for Sarcoidosis Research (FSR) is leading Sarcoidosis Awareness Month with its 2026...
The Foundation for Sarcoidosis Research (FSR) has been named a 2025 RareVoice Awards recipient by EveryLife Foundation for Rare Diseases, earning national recognition for Federal Advocacy by a Patient or Organization. The award honors FSR’s leadership in securing a...
The Foundation for Sarcoidosis Research (FSR) has awarded four grants in the amount of $100,000 each to Dr. Christen Vagts from the University of Illinois at Chicago, Dr. Chieh-Yu Lin from Washington University School of Medicine in St. Louis – both Members of the FSR...
