Our mission is to stop sarcoidosis — join us.
The sarcoidosis community needs your help to put an end to this disease. When you participate, advocate, and donate, you advance the fight to find the cure and lead us toward a world without sarcoidosis.
patients are helping researchers find a cure for sarcoidosis through the FSR Patient Registry
dollars in funding awarded through FSR grant programs.
dollars raised by supporters for sarcoidosis awareness!
I Am One: Using My Voice to Bring Awareness to Sarcoidosis
Darlene Anita Scott is a writer and visual artist living with sarcoidosis. She applied to become an FSR Global Sarcoidosis Clinic Alliance (GSCA) Community Outreach Leader and is dedicated to sharing her sarcoidosis story with the public to raise awareness and help...
The Foundation for Sarcoidosis Research (FSR) awards $50,000 in support of cardiac sarcoidosis
The Foundation for Sarcoidosis Research (FSR) is pleased to award Dr. Nabeel Hamzeh, Professor of Internal Medicine - Pulmonary, Critical Care and Occupational Medicine at The University of Iowa, funding for cardiac sarcoidosis research in the amount of $50,000. Dr....
Blog: Addressing Healthcare Issues that Disproportionately Affect Black Americans
“My hope is that this campaign will greatly increase awareness of sarcoidosis and encourage Black patients to participate in clinical trials. That will ultimately improve our lives and benefit everyone in the sarcoidosis...
The Importance of the FSR Patient Registry
If you have sarcoidosis, you MUST join the Foundation for Sarcoidosis Research (FSR) Patient Registry. With less than 200,000 of us diagnosed each year, we are the sources of data needed to advance sarcoidosis research. FSR created the Patient Registry to share...