Sep 1, 2026
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...Topics: Clinician Engagement/ FSR Events/ Living with Sarcoidosis/ News
Aug 11, 2026
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...Topics: News/ Patient Voices/ Research/ Take Action
Aug 4, 2026
The Foundation for Sarcoidosis Research (FSR) has awarded $700,000 in grant funding to four awardees through its Early Career Fellowship and Established Investigator grant funding opportunities. The 2026 Established Investigator Grant has been awarded to Dr. Laura...Topics: News/ Research
Jul 14, 2026
The Foundation for Sarcoidosis Research (FSR), the leading international organization dedicated to finding a cure for sarcoidosis and improving care for those living with the disease, has announced a new partnership with Patient Advocate Foundation, the nation’s most...Topics: Awareness/ Living with Sarcoidosis/ News
Jun 1, 2026
In May 2026, the FSR team came together in Orlando, Florida for the 2026 American Thoracic Society (ATS) International Conference. ATS is a major professional gathering that brings health care professionals, industry representatives, nonprofit organizations, and...Topics: Advocacy/ Awareness/ Clinician Engagement/ News/ Research
Apr 23, 2026
Through the long-standing collaboration between Foundation for Sarcoidosis Research (FSR) and the American Thoracic Society (ATS), FSR and ATS are pleased to announce that John Matthew “Matt” Craig, PhD, has joined ATS staff as Senior Vice President, Translational...Topics: News
Apr 20, 2026
The American Academy of Dermatology (AAD) 2026 Annual Meeting in Denver in March 2026 was an important moment for the sarcoidosis community, especially for people living with skin (cutaneous) sarcoidosis. This year’s meeting featured more than 275 sessions covering...Topics: Awareness/ News/ Research
Feb 24, 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...Topics: Advocacy/ News
Jan 21, 2026
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...Topics: Community Partners/ News/ Research
Jan 16, 2026
The Foundation for Sarcoidosis Research (FSR) proudly announces the addition of seven new institutions to its growing FSR Global Sarcoidosis Clinic Alliance (FSR-GSCA): University of Chicago Medicine, Houston Methodist Hospital, Hospital Clínic de Barcelona (the first...Topics: Clinician Engagement/ Community Partners/ News
