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...
The Foundation for Sarcoidosis Research announced they are entering their second year with FSR Sarcoidosis Patient Registry. The FSR Sarcoidosis Patient Registry was established in collaboration with National Institutes of Health (NIH) to provide critical data for...
