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The sarcoidosis community needs your help to put an end to this disease. When you participate, advocate, and donate, you advance the fight to find the cure and lead us toward a world without sarcoidosis.
patients are helping researchers find a cure for sarcoidosis through the FSR Patient Registry
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FSR Appoints Two New Members, Calvin Harris Jr., CPA and Joel D. Rosen, Esq., to Board of Directors
The Foundation for Sarcoidosis Research (FSR) is pleased to announce the appointment of Calvin Harris Jr., CPA and Joel D. Rosen, Esq. to the FSR Board of Directors. "We are thrilled to welcome Calvin and Joel to the FSR Board of Directors," said Dr. Louise Perkins,...
FSR Releases White Paper and Hosts Congressional Briefing on Advancing Clinical Trial Equity for Black Patients with Sarcoidosis
Foundation for Sarcoidosis Research (FSR), the leading international organization dedicated to elevating research, raising awareness and providing support for individuals affected by sarcoidosis, is proud to announce the release of the Ignore No More Campaign on...
aTyr Spotlight: Accelerating Sarcoidosis Research and Supporting the Sarcoidosis Community
Recently, we asked our dedicated and generous Sarcoidosis Awareness Campaign Gold Level Sponsor, aTyr Pharma, Inc., to share more about their passion for raising awareness and improving the lives of those impacted by sarcoidosis. Check out how they are accelerating...
FSR Team Member Runs in Boston Marathon for Rare Disease Awareness
Rebecca Epstein, Senior Research Manager for Foundation for Sarcoidosis Research, participated in the 2023 Boston Marathon on April 17, 2023, running with the National Organization for Rare Disorders (NORD) team. This year's marathon also commemorated the 10th...