Amazon has announced that they are discontinuing AmazonSmile on February 20, 2023. To everyone who prioritized the SRF while you shopped, thank you. You’ve helped us accelerate the pace of…
Do you live with scleroderma and have digital ulcers? You’re invited to complete a survey launched the World Scleroderma Foundation ad hoc GI Committee—led by SRF-funded investigator Dr. Zsuzsanna McMahan,…
Calling all scleroderma advocates—February is Rare Disease Awareness Month and Raynaud’s Awareness Month! The SRF stands with the rare disease community because being rare does not mean being alone. And…
As we start the new year, join us in welcoming the newest member of the team! Meet Kate Ceredona, our Director of Philanthropy. Kate is a development professional with over…
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…