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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After two years of virtual meetings, the SRF's Science Workshop returned as an in-person event! This past weekend, over 50 clinicians and scientists gathered in San Francisco to discuss innovations in scleroderma...
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Today would have been Bob Saget's 66th birthday. It still seems unimaginable that we would lose him so soon, and all of us at the SRF miss him more than...
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SAN FRANCISCO (May 9, 2022) – The Scleroderma Research Foundation (SRF) will host its inaugural Virtual Patient Forum, Collaborating for a Cure, on Wednesday, June 1, 2022, to kick off...
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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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Jennifer was diagnosed with scleroderma in 2018—years after seeking help. “I started having Raynaud's attacks in 2013 along with other weird things like red blotches all over my face, later...
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Kick off Scleroderma Awareness Month by attending the SRF’s Collaborating For a Cure, our inaugural Virtual Patient Forum! On June 1st, we’ll be hosting our first ever half-day Virtual Patient Forum for all those…
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, we are deeply saddened to learn of the passing of Gilbert Gottfried. He was a good friend of late SRF Board Member Bob Saget, and so he also became…
