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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

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Neurosarcoidosis Meeting at Washington University in St. Louis

July 8, 2015

At this meeting, experts who have significant experience with managing neurosarcoidosis will gather to share their latest observations, then participate in a planning retreatLearn More

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Foundation for Sarcoidosis Research joins elite group of medical research foundations

May 14, 2015

FSR is proud to announce our membership acceptance into the elite group of medical research foundations represented by Faster Cures TRAIN. These selected TRAINLearn More

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We are speaking at the DIA 51st Annual Meeting

May 12, 2015

The Foundation for Sarcoidosis Research’s Executive Director Ginger Spitzer is speaking at the 51st Annual DIA 2015 Meeting. She will be speaking about theLearn More

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Join the conversation at the National Heart, Lung and Blood Institute!

May 6, 2015

The National Heart, Lung and Blood Institute is gathering ideas for the most compelling scientific priorities in the four NHLBI Strategic Goals to address overLearn More

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Meet-the-Experts

May 4, 2015

Join us! For the 9th Annual American Thoracic Society Public Advisory Roundtable (PAR) FREE patient/family forum. SATURDAY MAY 16, 2015 from 10:00 a.m. to 2:00 p.m. SheratonLearn More

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Seek Answers Inspire Results -Rick’s Story

April 30, 2015
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The Foundation for Sarcoidosis Research will be attending Rare Disease Week on Capitol Hill

February 18, 2015

Global nonprofit Foundation for Sarcoidosis Research announced today that it will be attending the upcoming Rare Disease Week on Capitol Hill from February 23Learn More

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Learn how you can change the face of sarcoidosis research

February 18, 2015

The Foundation for Sarcoidosis Research announced they are entering their second year with FSR Sarcoidosis Patient Registry. The FSR Sarcoidosis Patient Registry was established inLearn More

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Sarcoidosis Week at ATS

February 3, 2015

Current Progress in Sarcoidosis Research Attend the webinar Feb 10th at 2pm EST We have partnered with the American Thoracic Society for their SarcoidosisLearn More

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Q&A Session from Meet the Experts in San Diego

June 12, 2014

Thank you for all that attended out Meet the Experts event in San Diego at the American Thoracic Society conference. For those of youLearn More

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