Category: FSR Events
The importance of finding your sarcoidosis community
Why is finding your community important? After a diagnosis that changes your life, you need people who understand the journey you are about to embark on and find strength and support from others. After getting my sarcoidosis diagnosis I felt alone, I have family,...FSR Inaugural Sarcoidosis Crystal Awards Gala to Honor Exceptional Individuals in the World of Sarcoidosis
The Foundation for Sarcoidosis Research (FSR), the leading international nonprofit organization dedicated to finding a cure and improving care for sarcoidosis patients, announces FSR’s Inaugural Sarcoidosis Crystal Awards Gala: Celebrating Connections, Collaboration,...FSR to Hold Third Annual Global Virtual Patient Summit: Unveiling Possibilities
FSR is proud to bring together sarcoidosis patients, caregivers, and family and friends at the Third Annual Global Virtual Patient Summit: Unveiling Possibilities. This summit is the world’s largest virtual sarcoidosis patient event. This year’s summit...FSR Sarcoidosis Support Group
FSR Sarcoidosis Support Group In response to feedback received in 2021 and a growing need to support patients where they are, FSR has launched an online peer-led support group for people living with sarcoidosis. While 2024 will bring additional, more localized...Save the Date for our Virtual Patient Education Summit – June 12-13th!
Click here to register now! Join us for this year’s Virtual Patient Education Summit, June 12-13, 2021! Our summits in September and November of 2020 were incredibly successful. This year we will be offering a unique two-day experience on a fun, interactive...Steroids and Sarcoidosis Town Hall Virtual Meeting
Please join John Carlin, FSR Patient Advocate and host of the Sarc Fighter podcast, on Tuesday, April 27, at 11:00AM CST as he moderates this panel discussion on sarcoidosis and steroids.