Nov 17, 2022
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...Topics: Living with Sarcoidosis/ Patient Voices/ Take Action
Oct 25, 2022
“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 community.” Calvin Harris FSR Patient...Topics: Living with Sarcoidosis/ News/ Other/ Patient Voices/ Research/ Take Action
Oct 20, 2022
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...Topics: Living with Sarcoidosis/ Research/ Take Action
