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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