FSR’s progress in research, patient support, advocacy, and clinical care is transforming the lives of people affected by sarcoidosis. Your support has made groundbreaking new initiatives possible—including the Insurance and Disability Support Patient Referral Network, legislative advocacy through the bipartisan Congressional Sarcoidosis Caucus, and the FSR Sarcoidosis Clinical Data Registry involving at least 2,000 patients across 13 U.S. clinical sites. As FSR looks toward 2027, continued financial support is essential to sustain this momentum, advance research, improve access to care, and ultimately find a cure.
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