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FSR Receives 2025 RareVoice Award for Federal Advocacy

FSR Receives 2025 RareVoice Award for Federal Advocacy

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...
FSR Attends WASOG 2025 International Conference

FSR Attends WASOG 2025 International Conference

Members of the FSR team joined over 300 global experts, clinicians, researchers, and advocates for four days of learning, collaboration, and engagement at the World Association for Sarcoidosis and Other Granulomatous Disorders (WASOG) 2025 Conference in Ottawa, Canada...
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