
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…
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…
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…
Thanks to our many friends & supporters, we’ve made real progress for those living with scleroderma. But there’s more work to do to find a cure—and research is the key. When…
We’re so grateful to SRF Board Member Regina Hall for representing us at the Cantor Fitzgerald Charity Day this year! Every year, since 9/11/2001, Cantor Fitzgerald commemorates the 658 employees…
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…
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…