“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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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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Found a creative way to manage Raynaud's flare-ups? Got advice for how to stay organized while juggling doctor's appointments? Or discovered some other way to make your life easier while...
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Earlier this month, the Scleroderma Research Foundation hosted an international group of investigators to learn more about CONQUEST, our groundbreaking platform clinical trial, at the Systemic World Congress Meeting in...
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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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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…
