“She was an anomaly for the scleroderma world,” says Olivia Muñoz Mulkin of her mother, Maria “Missy” Cavazos. This Mother’s Day, as we celebrate the strength and love of mothers…
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Collaboration is critical to making research progress. That's why the SRF co-sponsored a recent workshop with the National Institutes of Health (NIH) & other nonprofit organizations to discuss scientific advances in immunotherapies and...
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The SRF's recent Annual Science Workshop brought together researchers from across the country for innovative collaboration. Held this year on April 12 & 13, the workshop serves as the cornerstone...
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Registration is now open for "Collaborating for a Cure," the SRF Patient Forum on June 3rd, a free virtual event for those affected by scleroderma. Also, join us in celebrating...
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Register now for "Collaborating for a Cure," the SRF Patient Forum, on June 3rd! 📋 You're invited to a FREE virtual forum for people living with #scleroderma and those who care...
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Here at the Scleroderma Research Foundation, research is at the center of all we do to find a cure—and that's only possible because of the dedicated support of our community....
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Do you have tips and tricks for living with scleroderma? Find out how you can share your innovative life hacks for managing scleroderma by submitting a short video to be...
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SRF-funded researcher Dr. Howard Chang shares a breakthrough discovery he & his collaborators made, shedding light on why women are more likely than men to develop autoimmune diseases like #scleroderma,...
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In this month's eNews, read about Dr. Howard Chang's groundbreaking new study exploring why women are more likely to develop autoimmune conditions. We're also featuring patient stories, including Dee's experiences...
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Nearly 90% of those with scleroderma have Raynaud’s symptoms. This is why Raynaud’s can be a “red flag” that helps lead to diagnosis and treatment of scleroderma. And for Aneila, dx…
