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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.

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FSR Blog

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6 Tips for Talking About Sarcoidosis With Loved Ones

August 16, 2017
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Can Tracking Fitness Help Sarcoidosis Patients?

August 8, 2017
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FDA’s Patient Engagement Advisory Council Plans First Public Forum

August 7, 2017
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The Stages of Pulmonary Sarcoidosis- What Do They Really Mean?

July 21, 2017
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Rough Roads: Cycling with Sarcoidosis

July 20, 2017

The Long Road to Diagnosis

July 10, 2017

Allison Hawley- like so many other sarcoidosis patients- has had a tough time getting a diagnosis. Her journey has been filled with misdiagnoses, complicatedLearn More

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Protecting Patients: How the Proposed Healthcare Act Could Affect You

June 27, 2017
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Take Action: AHCA Will Remove Key Protections for Pre-Existing Conditions

June 21, 2017

The Foundation for Sarcoidosis Research is sharing this urgent call to action from the National Organization for Rare Disorders (NORD): WE NEED YOU to call, email,Learn More

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Join Team KISS This Summer!

June 19, 2017

Summer officially starts June 20th! It’s time for backyard barbecues, time with friends and family, and some fun in the sun. There’s no betterLearn More

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VIDEO: ATS Meet the Experts 2017

June 14, 2017
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