“Raynaud’s has never really sidelined me. I just roll with whatever my body serves up as best I can," says Julia P. (dx 2011). "Despite all that I have been...
Read More
In response to a recent powerful op-ed describing the consequences of the anti-vaccine movement, we invite the community to stand up for vaccines and the science that promotes lifelong health. In the...
Read More
We hear it all the time: clear information and expert insight can make a real difference in managing scleroderma. The SRF Scleroderma Patient Forum is designed with that goal in...
Read More
Earlier this week, in recognition of Raynaud’s Awareness Month, the SRF hosted a webinar on Raynaud’s and digital ulcers featuring Dr. Tracy Frech (Vanderbilt University)—and the full session recording is...
Read More
“I was diagnosed with scleroderma at 17 years old, which means I’ve lived more than half my life navigating this disease,” Kim (dx 2003) says. Her journey began at a...
Read More
The SRF joins the global scleroderma community in celebrating the life of Maureen Worron-Sauvé, a cherished leader, tireless advocate, and inspirational champion for everyone affected by this disease. For more than a decade, the SRF had the...
Read More
Read about what we achieved in 2025, register for our upcoming Raynaud's webinar, and more! Read Now
Read More
“I was diagnosed with lupus in 2003, and I attributed all these weird things happening to me to my lupus,” Yvette T. (dx 2016) says. For years, symptoms like Raynaud’s,...
Read More
February is here, and we’re turning up the volume for #RaynaudsAwarenessMonth and #RareDiseaseDay. 📣 There are 6,000+ rare diseases, and scleroderma is one of them. For those living with this...
Read More
From symptoms to treatment to day-to-day concerns, your scleroderma questions matter. "Ask a Doctor" is a new Q&A column featuring responses from the SRF’s Chief Medical Officer, Dr. Gregory Gordon,...
Read More
