Jordan C.’s passion for scleroderma research is deeply personal—his sister was diagnosed with juvenile diffuse systemic scleroderma. Wanting to make a difference, Jordan turned to what he knows best: music....
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On August 25, Ally’s Allies held their 3rd Annual Golfing for a Cure—and it was their biggest yet! With 160 golfers participating, the event raised over $25,000 to support scleroderma...
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After her scleroderma diagnosis in 2006, Tracy had to step away from her career—but not from her drive to make a difference. “I couldn’t work a traditional job anymore, but...
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On June 30th, all four Grove Wine Bar & Kitchen locations in Austin, Texas, celebrated Scleroderma Awareness Month by donating 10% of their net sales to support the SRF's research...
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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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