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A Rare Type with a Rare Disease

A Rare Type with a Rare Disease

Oct 29, 2025

In 1997, after several months of dealing with confusing symptoms, I was diagnosed with sarcoidosis in my lungs and lymph nodes. The surgeon who completed the biopsy suggested I not bother to research the disease, as it would scare me. On my way home from the hospital,...

Topics: Patient Voices

In Memory of Bob Gross

In Memory of Bob Gross

Oct 3, 2025

It is with deep sadness that we share the passing of our dear friend and longtime volunteer, Bob Gross. For many years, Bob was a dedicated FSR Patient Navigator, always offering his time to ensure those newly diagnosed with sarcoidosis or diagnosed with a new...

Topics: Other/ Patient Voices

FSR Attends WASOG 2025 International Conference

FSR Attends WASOG 2025 International Conference

Sep 1, 2025

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...

Topics: News/ Research

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