All sessions from our 5th annual Forum are now available to watch, whether you missed the event or just want to revisit a presentation that stuck with you. Visit our...
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A recent editorial in BioCentury by author Steve Usdin shines a light on a serious new threat to the very foundation of American science. At issue is a proposed Office...
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Check out the latest research updates from the wider community from this month. While we didn't fund these projects, we're encouraged to see a continued focus on understanding scleroderma. Fewer...
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This year's Annual Science Workshop—which took place on May 8 & 9, 2026— was an intense two-day collaborative research event that serves as a cornerstone of our Research Program. 🔬...
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June is here—and so is Scleroderma Awareness Month. We’re asking you to say it with us: #SayScleroderma. 📣 Scleroderma is complicated, often invisible, and still widely unknown. This leads to...
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"I choose to #SayScleroderma because the initial isolation and despair I felt upon diagnosis is something I want others to avoid," Ronna B. (dx 2022) says. This Scleroderma Awareness Month,...
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Your Scleroderma Questions, Answered is a monthly Q&A column featuring responses from the SRF’s Chief Medical Officer, Dr. Gregory Gordon, who shares guidance grounded in decades of clinical expertise. In this...
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"My story with Scleroderma has been a silent one," says Carmen (dx 2014). "I have always been very active and it was very difficult to notice my symptoms until they...
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"When I first received my diagnosis, I made a commitment to be involved in research, advocacy, and awareness," says Charles (dx 2025). And this Scleroderma Awareness Month, he meant it....
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"Research is the key to not only finding a cure but to improving treatments and quality of life for those living with scleroderma," says Alex P. (dx 2022), pictured above...
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