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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Join Us in Ann Arbor, Michigan!
Join us to learn from expert physicians about different sarcoidosis manifestations, treatment options, and the latest advancements in research. Alongside fellow patients and lovedLearn More
The June JAMR Memorial Ride was a Success!
Every year in June, the friends and family of the late Jerry Mac Grimes (1946-2014) get together for the June JAMR, a motorcycle rideLearn More
FSR Signs Support for DIA and ODTC
The Foundation for Sarcoidosis Research recently signed two petitions to show our support for important polices that directly impact many sarcoidosis patients. FSR makesLearn More
Rare Disease Research Consortium Announces Ambitious Goals
FSR is excited to share some breaking news from the world of rare disease research that could have a huge impact on the futureLearn More
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