Global nonprofit Foundation for Sarcoidosis Research announced today that it will be attending the upcoming Rare Disease Week on Capitol Hill from February 23 -27. They will be joining the Rare Disease Legislative Advocates to learn about how they can advocate for...
February 28th is Rare Disease Day! We partnered with our online Inspire community to conduct a survey to help better understand the quality of life for our patients. Here are some interesting...
FSR is pleased to support the research of Dr. Caroline Broos by awarding her the American Thoracic Society Abstract Scholarship during the ATS Conference in May 2013. We are grateful for Caroline’s research and confident her work will help promote the need for other...
We know you want answers — come meet the experts who have them!! At this Meet the Experts session, you’ll have an opportunity to discuss the latest in research, clinical trials, and clinical care with experts on many different lung disorders on Saturday, May 18...
$500,000 Donation to FSR ensures research investment and establishes The Marvin And Harlene Wool Giving Society! We are pleased announce that FSR was recently granted a $500,000 gift from Marvin and Harlene Wool who are dedicated advancing sarcoidosis research. Their...
FOR IMMEDIATE RELEASE Contact: info@stopsarcoidosis.org The Foundation for Sarcoidosis Research Hosts K.I.S.S. Chicago 2013 CHICAGO (November 6, 2012) — The Foundation for Sarcoidosis Research (FSR) is hosting its major benefit, K.I.S.S. (Kick in to Stop Sarcoidosis)...
