Last year, the SRF’s Cure Crew—a grassroots group of volunteers—raised more than $157k for scleroderma research! Thank you SO MUCH to everyone who helped make a difference. Here’s just two…
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Today wouldn’t be complete without honoring the memory of another person—January 9th is also the birthday of Gay Saget, Bob’s sister who lost her battle with scleroderma in 1994. This video is...
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The Scleroderma Research Foundation (SRF) reflects on one year after losing longtime supporter and board member, Bob Saget, and looks ahead to continuing his legacy in 2023. For more than…
Learn how your donation helps SRF-funded researchers like Dr. Torok (University of Pittsburgh) push the envelope on cutting-edge studies like the juvenile scleroderma project—all to find a cure. Will you help...
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Information about scleroderma and why we need research is coming to broadcast TV! The Scleroderma Research Foundation will be featured on Behind the Mystery, airing on The Balancing Act on…
Don't miss the last SRF eNews of 2022! In this special holiday edition, learn more about an exciting new awareness project we're working on, meet our new Director of Philanthropy,...
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Thinking back to her early symptoms, Kierra (dx 2020) remembers how “simple things like walking became a chore. My body felt like it was breaking down and I couldn't figure...
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Last week during the American College of Rheumatology Conference in Philadelphia, the SRF hosted two meetings to convene Principal Investigators and Research Coordinators from all 17 institutions participating in the…
Thanks to our many friends & supporters, we’ve made real progress for those living with scleroderma. But there’s more work to do to find a cure—and research is the key. When…
It’s been 26 years since the release of “For Hope”—the first and only movie to tell a family’s story of living with scleroderma, directed and executive produced by SRF Board…
