Dedication, commitment, and lifelong love–the Kosmach family embodies it all. Since 1995, they have poured their hearts into fundraising for scleroderma research in memory of their beloved mother, Joan Kosmach....
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This year, Beth L. and Lisa D. brought the second annual Picklepalooza to life, hitting the courts for a cause close to their hearts. Beth, a Cure Crew champion with...
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This November, Jess M. (dx 2011) hosted her third annual fundraiser for the Scleroderma Research Foundation through her knife sharpening business. For every sale she made from Nov-15, she donated...
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Earlier this month, Cure Crew member Molly S. dedicated the proceeds from her annual 2-night concert, "Dumb Diseases", to the SRF. For the past two years, she has held this...
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Long-time SRF Cure Crew members and scleroderma advocates, the Connors-Zini family, recently hosted the 9th Annual Best Medicine Comedy Show on October 24th in conjunction with Live Snakes Comedy, carrying on...
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At this time, we are fondly remembering our dear friend Sandy Kosmach Ribich, a devoted advocate and longtime supporter of the SRF's mission to end scleroderma. Sandy, who passed away...
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On August 28, Ally's Allies hosted the second annual "Golfing for a Cure" event benefiting the Scleroderma Research Foundation. SRF Cure Crew member Ally W. was diagnosed with scleroderma in...
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“My father was the strongest man I knew, and I miss him every single day,” says Samantha C. of her father, Louis P. (dx 1990), who passed away in 2021....
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"I never imagined I would be grateful for my diagnosis, but it has helped me understand myself better and given new meaning to my life,” says Nafisa Z. (dx 2020)....
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Give a big round of applause to the SRF Cure Crew—in 2023 alone, they raised more than $158,000 for research! The Cure Crew is a grassroots group of volunteers that...
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