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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

Shot of a happy senior couple cooking a healthy meal together at home

Healthy Eating Habits: Heart and Lungs

August 15, 2018

Developing healthy eating habits while dealing with sarcoidosis can be hard. Here are some diet tips to help keep your heart and lungs healthy.

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Will You Help Us Find a Cure for Sarcoidosis?

August 8, 2018

FSR strives to bring patients the most up-to-date information about sarcoidosis, but we can’t do that without you. Besides being a rare disease, affectingLearn More

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3 Tips for Coping When You’re Chronically Ill

July 23, 2018
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FSR Hosts Clinical Studies Network Meeting in Chicago

July 9, 2018

The members of the FSR Clinical Studies Network met on June 29th in Chicago, Illinois to determine and plan the next CSN Core StudyLearn More

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The Role of Functional Medicine in Chronic Illness

June 30, 2018
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Become a Sarcoidosis Advocate in Your Hometown!

June 21, 2018

Rare disease patients find out soon after a diagnosis that they’ll have to learn advocate for themselves- in the doctors office, to insurance companies,Learn More

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Find Your Community: Connecting with Other Chronic Illness Warriors

June 21, 2018
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FSR Staff Presents at International Sarcoidosis Conference

June 11, 2018

Three FSR team members presented at the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG) Annual Meeting in Crete, Greece this month. TheLearn More

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Penn Medicine’s Sarcoidosis App Now on Android!

June 10, 2018
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Educating the Public with RareInsights

June 5, 2018

Our partners at NORD recently launched a new initiative called RareInsights: RareInsights™ is a NORD® initiative to help expand public knowledge of rare diseases and translate that knowledge intoLearn More

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