Throughout the month of August, legislators will be back in their home districts during Congress’ Summer Recess. This allows advocates a chance to meet with their representatives without having to travel to Capitol Hill. For those affected by rare diseases...
Back in 2016, FSR began our Sarcoidosis Disease Model program with a Request For Applications for research projects that looked for a viable disease model for sarcoidosis. In the years since, we’ve awarded $1,050,000 towards multiple promising projects through a...
FSR awarded an additional $300,000 towards our Sarcoidosis Disease Model program.This recent award brings FSR’s total investment in finding a viable disease model for sarcoidosis to $1,050,000 to date.A major limiting factor in discovering new insights into the...
If you have been with living with sarcoidosis for any amount of time, you know that this nasty disease will often kick you in the teeth and leave you frustrated just about every day. As a fellow sarcoidosis sufferer for about the last five years, I know that I wrestle...
