FSR is consistently working to ensure that researchers and physicians have plentiful opportunity to get involved in the world of sarcoidosis research. One such way is our recent $1M investment in our new Clinical and Research Fellowship Program. We also recently give...
FSR was excited to partner with NBC Chicago to shine a spotlight on sarcoidosis this month. As you all know, April is Sarcoidosis Awareness Month. Check out the video linked below to see a segment featuring sarc warrior Kristin and Dr. Daniel Culver of the Cleveland...
This April, we’re doing everything we can to ensure that the world know about sarcoidosis. Our theme for this year’s campaign is #SarcoidStories, in an effort to raise awareness with the general public about the ups and downs in the daily lives of sarcoidosis...
American Lung Association, CHEST Foundation and Foundation for Sarcoidosis Research are joining forces to raise awareness of sarcoidosis! Our new campaign homepage offers patients tools and resources they need to learn more about the disease and spread the word to...
April is Sarcoidosis Awareness Month! While here at FSR we spend 365 days a year spreading awareness, we’re excited each April to partner with other organizations to help get the word out to a larger audience. Each year, we partner with the American Thoracic...
New Sarcoidosis Advocate Zach Kerr FSR is thrilled to announce a partnership with professional football player Zach Kerr who plays as a defensive lineman for the Denver Broncos of the National Football League. Zach has been personally affected by sarcoidosis. His...
This April, we’re teaming up with the American Lung Association and the CHEST Foundation for our annual awareness campaign surrounding Sarcoidosis Awareness Month. Our theme for the campaign this year is #SarcoidStories, in an effort to raise awareness with the...
We’re excited to unveil the new design for the 2018 Team KISS 5K shirt! Team KISS shirts are included with all Team KISS event registrations through the links below. Please note that only official Team KISS walk registrations through our website guarantee you a...
It’s Rare Disease Day! Each year, Rare Disease Day falls on the last day of February. This is a day for the rare disease community to come together and celebrate what we have in common as well as what makes us all, well….rare! We hope to raise awareness...
