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…
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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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Congratulations are in order: SRF-investigator Ami Shah, MD, MHS, of Johns Hopkins University has been awarded the Henry Kunkel Early Career Investigator Award at the ongoing American College of Rheumatology...
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It's Rheumatic Disease Awareness Month and we're sharing stories of people like Kimberly (@strong_selflove). Despite being diagnosed with scleroderma at age 8, Kimberly went on to become an accomplished violinist....
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During Rheumatic Disease Awareness Month, we're sharing stores of people like Sunny (@therealsunnysidhu), diagnosed with scleroderma at age 13. Sunny was a promising, young athlete who dreamed of becoming a...
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Fresh off the press—Regina Hall representing the Scleroderma Research Foundation as our Ambassador for CFC Charity Day! Every year since 9/11/2001, Cantor Fitzgerald commemorates their 658 employees who were lost…
Throughout September, Rheumatic Disease Awareness Month, we're sharing stories of people living with scleroderma. Having an active scleroderma community is a powerful resource. Dinah knows that better than anyone else....
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September is Rheumatic Disease Awareness Month, and we're taking part by sharing stories of people living with scleroderma. Rumbie (@sclerodancer) has always had a passion for dance and started her...
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The challenges of the past months haven't stopped SRF from focusing on funding scleroderma research. They haven't stopped Melissa, either, as she heads back to school. Melissa received her scleroderma...
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