Project Scleroderma, a longtime partner organization of the SRF that raises scleroderma awareness globally, recently premiered their new documentary created with the team at New Pace Productions. It’s called Run…
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The SRF mourns the loss of former board member Daniel Morton, who passed away last month. He joined the board of the SRF in the early ’90s, after reading a…
Today is #WorldSclerodermaDay, a day created to tell people what it means to have scleroderma and recognize those who live with it. Join us today as we #SayScleroderma so that…
Once again in June, Grove Wine Bar will join the Scleroderma Research Foundation’s campaign, #SayScleroderma, for Scleroderma Awareness Month. Over 400 employees will wear T-Shirts branded with the Grove, SRF,...
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A huge thank you to Jeff Ross for his dedication as a longtime supporter of the SRF and scleroderma advocate. As a close friend of SRF Board Member Bob Saget,...
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A big thank you to Jodie Sweetin for playing for the SRF on Name that Tune—we recently received a stunning gift of $10,000 in prize money after she won against...
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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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It's National Volunteer Week and we want to say thank you to the SRF’s incredible Cure Crew, a grassroots volunteer community of scleroderma patients, friends, and families. You make a huge impact...
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When Maggie was diagnosed with scleroderma in 2019, she didn’t know anyone else with this disease. Her mom remembered that her neighbor had a niece, Erin, who had been living...
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Today is National Doctor’s Day, and we want to offer huge thanks to every doctor in the U.S. and around the globe for their dedication and compassion in serving the…
