Saget’s commitment to building awareness of the disease will continue through support of family, friends, and fans San Francisco, CA (January 13, 2022) – The Scleroderma Research Foundation (SRF)—the country’s...
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Kheesa’s scleroderma symptoms started in 2005. She received her diagnosis two years later, after the birth of her first child. Now she's a mother of two. “They are the achievement...
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Scleroderma research isn't one size fits all–each investigator approaches it from a specific angle. For Dr. Zsuzsanna McMahan of the Johns Hopkins University School of Medicine, this means focusing her...
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Lack of awareness about scleroderma causes delays in treatment or misdiagnosis. This must end. At the SRF, we are committed to shining a spotlight on this disease. Patients like David…
