“I was diagnosed with lupus in 2003, and I attributed all these weird things happening to me to my lupus,” Yvette T. (dx 2016) says. For years, symptoms like Raynaud’s,...
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February is here, and we’re turning up the volume for #RaynaudsAwarenessMonth and #RareDiseaseDay. 📣 There are 6,000+ rare diseases, and scleroderma is one of them. For those living with this...
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From symptoms to treatment to day-to-day concerns, your scleroderma questions matter. "Ask a Doctor" is a new Q&A column featuring responses from the SRF’s Chief Medical Officer, Dr. Gregory Gordon,...
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For decades, scientists have worked to understand one of the immune system’s most complex players: regulatory T cells (Tregs). Long recognized for their potential to restore immune balance, Tregs have...
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Read about what we achieved in 2025, register for our upcoming Raynaud's webinar, and more! Read Now
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There’s no one way to be part of the Cure Crew, but there is one thing we know—you all make a difference. In 2025, this global community of volunteers took action...
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CONQUEST is a platform clinical trial designed by the SRF to accelerate the development of potential new treatments for scleroderma. With 142 sites across 24 countries, CONQUEST is bringing together...
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For people living with rare diseases, recognizing early signs and symptoms is critical. In scleroderma, Raynaud’s phenomenon is often one of those first warning signs. That’s why February—Raynaud’s Awareness Month, with Rare...
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Created by the SRF in 2018, CONQUER is a first-of-its-kind registry and biosample repository collecting real-world data from people living with scleroderma over time. By intentionally enrolling participants with various...
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This month, we hold two extraordinary people especially close in our hearts: Bob Saget and his sister, Gay. January 9th marks both Gay’s birthday and four years since we, and...
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