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FSR Updates

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.

Toolkits

White Papers

Annual Updates

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FSR Blog

two older women holding their hands near their chest in yoga psoe

Balancing Act: Fitness, Chronic Illness, and Your Mental Health

May 16, 2017

Pictures from the Nashville KISS 5K!

May 4, 2017
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VIDEO: Hershey Patient Conference

May 2, 2017
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April might be ending…

April 30, 2017

..but our fight isn’t over. It may be the end of Sarcoidosis Awareness Month, but unfortunately patients and their loved ones will continue toLearn More

Team KISS’s Top Fundraisers

April 27, 2017

A First Responder’s Story

April 25, 2017
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Taking Steps Towards A Cure

April 21, 2017
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FSR Ambassador at Senate Press Conference

April 17, 2017
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Couple’s 5K Grabs Local Media Attention

April 17, 2017

Perry and Melissa Enyedi are an Ontario couple hosting an independent K.I.S.S. walk in Brantford, ON this Saturday. While sarcoidosis is a rare disease,Learn More

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VIDEO: Sarcoidosis Treatment and Future of Research

April 12, 2017
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