This Raynauds Awareness Month, Dani shares her story and advocates for research. She was diagnosed with scleroderma in 2016—after noticing the classic signs of Raynaud's phenomenon. “Time has made me...
Read More
As we share our February edition of eNews, it's been nearly a month since we lost SRF Board Member and dear friend Bob Saget. In this edition, SRF Chairman of...
Read More
SRF Board member Bob Saget always went above and beyond to help raise awareness about scleroderma and be an advocate for research to find a cure. His decades-long commitment to...
Read More
If you missed our most recent webinar, don't worry—you can now watch it online. Learn more about GI involvement in systemic sclerosis in a webinar presented by SRF-funded researcher Dr....
Read More
We remain overwhelmed by the outpouring of involvement and support from people across the world who are putting their talent and treasure towards the SRF, finding their own personal ways…
Saget’s commitment to building awareness of the disease will continue through support of family, friends, and fans San Francisco, CA (January 13, 2022) – The Scleroderma Research Foundation (SRF)—the country’s...
Read More
It is with a very heavy heart that we mourn the loss of our dear friend and Board member, Bob Saget. Bob was a champion for scleroderma patients everywhere dating...
Read More
Scleroderma Research Foundation board member Bob Saget remembers his sister on her birthday: "Today would have been my sister Gay's 75th birthday. She lost her life to scleroderma when she...
Read More
Want to learn more about how research can help scleroderma patients with gastrointestinal complications? SRF-funded researcher Dr. Zsuzsanna McMahan, Assistant Professor of Medicine in the Division of Rheumatology at Johns...
Read More
As we start 2022, thank you for inspiring all of us at the SRF to remain laser-focused on our mission—finding a cure for scleroderma. And thanks to the support of our…
