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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

Living with ILD: A Sarcoidosis Patient Perspective

September 15, 2021

My journey with Interstitial Lung Disease (ILD) started about 15 years ago, although I did not know it at the time, nor did theLearn More

older male doctor speaking to younger female doctor

Update on Coronavirus, COVID-19

August 30, 2021

COVID-19 Vaccine Boosters for Immunocompromised Patients

August 23, 2021

Sarcoidosis does not automatically indicate an immunocompromised diagnosis. FSR cannot determine or provide recommendations for your individual immunocompromised status. Please consult your physician forLearn More

Introducing the FSR Patient Speakers’ Bureau

July 19, 2021

We are thrilled to announce the formation of our new FSR Patient Speakers’ Bureau!   This bureau consists of 14 experienced and trained sarcoidosisLearn More

FSR-MNK Sarcoidosis Research Fellow Awarded for 2021-2023

June 4, 2021

The Foundation for Sarcoidosis Research (FSR) is pleased to announce the Foundation for Sarcoidosis Research Fellowship Grant for 2021-2023 is being awarded to Dr.Learn More

FSR Welcomes Three New Members to its Board of Directors

May 25, 2021

The Foundation for Sarcoidosis Research (FSR), the leading international nonprofit organization dedicated to finding a cure for sarcoidosis and improving care for sarcoidosis patients,Learn More

FSR’s Women of Color Committee

May 20, 2021

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

May 5, 2021

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!

April 20, 2021

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

April 14, 2021

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

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