If you are in Austin, TX, you can support scleroderma research by going out to eat! Stop by any of the four Grove Wine Bar locations on Tuesday, June 28th...
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On a warm Texas evening this February, friends, and family gathered to play casino games, bet on silent auction items, and win raffle prizes at the 12th Annual Bet on...
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Long-time SRF Cure Crew members and scleroderma advocates, the Connors-McBride and Zini family, continued their seven-year tradition of producing a comedy show called "Best Medicine" to raise funds for a...
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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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Participating in research is crucial to finding a cure for scleroderma. SRF Cure Crew member Melissa talks about just this in a new 23andMe blog post. She participated in 23andMe's...
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The SRF Cure Crew members have always been an important voice for scleroderma awareness. They have raised substantial funds for the SRF’s research, even during the pandemic. We celebrate and…
Scleroderma advocates don’t stop during a pandemic—they adapt. The Connors-McBride and Zini family demonstrated just that. They transformed Best Medicine (usually a live comedy show) into a virtual experience, raising...
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