For Amy G., creating soft sculpture animals isn’t just an art form—it’s a way to connect and give back. Her whimsical collectible bears have found homes around the world, and...
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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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"I've learned that I'm absolutely a fighter,” says Tiffany S. (dx 1989). "Scleroderma has shown me how resilient I am." "I've never known a life other than fighting and living...
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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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This #NationalVolunteerWeek, we're sending a heartfelt shoutout to the amazing Cure Crew of the Scleroderma Research Foundation! 🙌 This grassroots volunteer community of scleroderma patients, friends, and families dedicate their time and...
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This past January, Carl Mayer hosted a special version of his #15dollargameshow on Instagram Live in memory of his long-time friend, Bob Saget—raising more than $3,100 for scleroderma research! Over 400 viewers…
Last year, the SRF’s Cure Crew—a grassroots group of volunteers—raised more than $157k for scleroderma research! Thank you SO MUCH to everyone who helped make a difference. Here’s just two…
Information about scleroderma and why we need research is coming to broadcast TV! The Scleroderma Research Foundation will be featured on Behind the Mystery, airing on The Balancing Act on…
We're extending a big thank you to the 100+ golfers who participate in the inaugural Elfus Sports Management Foundation Charity Golf Tournament and helped raise over $10,000 for the SRF! And so...
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For Teri, living with scleroderma means not only managing physical challenges but also lack of control she feels while doing so. “Scleroderma is part of my conscious mind every day,”...
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