Free educational summit brings together nationally recognized specialists, healthcare professionals, patients, and care partners to improve sarcoidosis care across the region The Foundation for Sarcoidosis Research (FSR), the leading international organization...
Lessons from a rude awakening Everyone suffering from sarcoidosis has a unique story to tell. There is nothing cookie-cutter about how the disease presents itself, how it is diagnosed, how it is treated and how the course of the disease will run. So, here’s my...
The Foundation for Sarcoidosis Research (FSR) is proud to share our implementation of a Patient Stakeholder Reviewer Panel into our grant review cycles. This is a review process that brings the patient voice directly into evaluation of research proposals. It gives...
From July 15–17, 2026, Porto, Portugal hosted clinicians, researchers, and patient advocates from around the globe for the 2026 Congress of the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG). The Foundation for Sarcoidosis Research (FSR)...
