Jun 27, 2017
The Foundation for Sarcoidosis Research prioritizes the long-term care of sarcoidosis patients and supports healthcare legislation that acknowledges and protects the needs of our community. As such, we feel compelled to voice our concern when pending legislation could...Topics: News
Jun 21, 2017
The Foundation for Sarcoidosis Research is sharing this urgent call to action from the National Organization for Rare Disorders (NORD): WE NEED YOU to call, email, tweet, and message your Senators… Urge them to stand up for the millions of children and adults...Topics: News/ Take Action
Jun 19, 2017
Summer officially starts June 20th! It’s time for backyard barbecues, time with friends and family, and some fun in the sun. There’s no better time to join Team KISS! This summer, sarc warriors and their families are getting together to raise awareness and...Topics: Living with Sarcoidosis/ Team KISS
Jun 14, 2017
Here at FSR, part of our mission is to bring educational experiences and knowledgeable physicians to as many patients as possible. That’s why we’re proud to be hosting a record of seven patient conferences all across the country this year. We know it’s difficult for...Topics: Online Educational Content
