Scleroderma Research Foundation board member Bob Saget remembers his sister on her birthday: "Today would have been my sister Gay's 75th birthday. She lost her life to scleroderma when she...
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Want to learn more about how research can help scleroderma patients with gastrointestinal complications? SRF-funded researcher Dr. Zsuzsanna McMahan, Assistant Professor of Medicine in the Division of Rheumatology at Johns...
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As we start 2022, thank you for inspiring all of us at the SRF to remain laser-focused on our mission—finding a cure for scleroderma. And thanks to the support of our…
It's time for the last eNews of 2021, our December edition. We share the highlights of the year—only possible because of our dedicated supporters—and share research updates and more. And,...
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The SRF launched the CONQUER Registry in 2018 through a collaborative effort with the largest scleroderma centers in the U.S. The goal of this registry is the enrollment of thousands...
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Sophie Anne and her family are filled with hope, and they inspire us every single day to stay laser-focused on finding a cure. With your support, together we can make...
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Prompting conversations about scleroderma that help to raise awareness about the disease and increase funds for research has been a life-long commitment for Will Whitehurst. "I believe so strongly in...
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It’s that time—the November edition of eNews is now available to read online! Make sure you didn’t miss out on any of the highlights from this month, like advances in...
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Doing good comes in many different forms, and David Hinman’s story represents one such way. David's mother, Kathryn Daub Hinman, was diagnosed with scleroderma in the late 1970s. He recalls...
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This holiday season, we're reflecting with gratitude on the many ways we’ve been able to accelerate the pace of scleroderma research. This is all because of people like YOU. Thanks...
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