Stay up-to-date on FSR’s latest activities and learn about the ways that FSR is driving progress and accelerating research towards a cure.
FSR launched the Ignore No More: ACTe Now! Campaign (Advance Clinical Trials for Equity in Sarcoidosis) to address the underrepresentation of Black Americans in clinical trials. As part of the campaign, FSR conducted the first of its kind, IRB-approved national patient survey for Black Americans to better understand the challenges and experiences Black Americans with sarcoidosis face as it pertains to clinical trials and their disease journeys. FSR also conducted a Key Opinion Leaders Thought Workshop (KOL) and Patient Focus Group to explore the findings in greater depth and to identify recommendations for how to improve clinical trial access and overall care of Black sarcoidosis patients.
Some recommendations that emerged include building a blueprint for clinical trial design that increases access and supports diversity, clinical trial navigation and support specifically targeted for Black patients, and educational toolkits to better educate patients and physicians about trial opportunities and engagement. Though this campaign was specific to Black Americans with sarcoidosis the learnings are relevant to improving access to clinical trials for all Black Americans.
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FSR’s Women of Color Committee
Foundation for Sarcoidosis Research is seeking applicants for our first Women of Color Committee. African Americans in the U.S. have been the group mostLearn More
COVID-19 Vaccine and Sarcoidosis: a survey of vaccination rate, tolerance and barriers
Authors: Arindam Singha, MD1; Tricha Shivas, MBe2 ; Elliot D. Crouser, MD1 Since it was declared a global pandemic in March of 2020,Learn More
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 NovemberLearn More
Why Sarcoidosis Awareness Month Matters
As the nation’s leading nonprofit organization dedicated to sarcoidosis, we believe in the power of community and that game-changing results in sarcoidosis research can be made when we workLearn More
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.
FSR Welcomes New Members to its Board of Directors
CHICAGO, Feb. 24, 2021 /PRNewswire/ — The Foundation for Sarcoidosis Research (FSR), the leading international nonprofit organization dedicated to finding a cure for sarcoidosis andLearn More
Becoming an FSR Patient Navigator: Stories of Resilience and a Desire to Make a Difference
You are not alone. The journey of sarcoidosis feels lonely sometimes. After months or even years of misdiagnoses, difficulties of excusing yourself from eventsLearn More
February Cardiac Sarcoidosis Webinars
Friday, February 19, 2021 West Coast Cardiac Sarcoidosis with Stanford 5-6PM CST (3-4PM PST, 4-5PM MT, 6-7PM EST) Join Doctors Matthew Baker and Ronald WittelesLearn More
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