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Become a Sarcoidosis Advocate in Your Hometown!

Become a Sarcoidosis Advocate in Your Hometown!

Rare disease patients find out soon after a diagnosis that they’ll have to learn advocate for themselves- in the doctors office, to insurance companies, and even to the government. Unfortunately, rare diseases are still often overlooked in legislation, even though...
FSR Staff Presents at International Sarcoidosis Conference

FSR Staff Presents at International Sarcoidosis Conference

Three FSR team members presented at the World Association of Sarcoidosis and Other Granulomatous Disorders (WASOG) Annual Meeting in Crete, Greece this month. The conference was an annual meeting between the leading experts in sarcoidosis research and clinical care...
Penn Medicine’s Sarcoidosis App Now on Android!

Penn Medicine’s Sarcoidosis App Now on Android!

We received a great deal of feedback asking when the app would be available on android devices. It has always been our goal to have the app available to everyone to give equal access to these sarcoidosis resources, as well as to help sarcoidosis researchers obtain the...