“In July 2019, I started to notice my fingers becoming puffy, and suddenly, I couldn’t remove my wedding ring easily,” Vaneeta (dx 2020) remembers. "I had an annual physical and...
Read More
After her scleroderma diagnosis in 2006, Tracy had to step away from her career—but not from her drive to make a difference. “I couldn’t work a traditional job anymore, but...
Read More
For Sydney N. (dx 2020), making an impact with the SRF Cure Crew is integral to her personal mission. “Being a part of the Cure Crew is a badge of...
Read More
Big news for scleroderma research: NIH Strategic Plan highlights autoimmune diseases 🔬 We are encouraged by the recent publication of the NIH‑Wide Strategic Plan for Autoimmune Disease Research for 2026–2030....
Read More
Right now, you have the power to fund critical scleroderma research by donating to the SRF Research Challenge. 🔬 When you give, you can help uncover new therapies, fund cutting-edge...
Read More
Registration opens soon for a special ILD-focused webinar, taking place on Tuesday, September 16, 2025, at 9:00 AM PT / 12:00 PM ET. Led by Dr. Toby Maher, Professor of...
Read More
On July 18, Strike Out Scleroderma Day returned to T-Mobile Park, bringing members of the scleroderma community together for a day of scleroderma awareness and baseball. Over 30 members of...
Read More
🎥 Watch Kimberly (dx 2008) share why she believes that funding research is key to finding a cure. Join her in supporting the SRF Research Challenge by donating today. At...
Read More
"My mother had a personality that could capture an entire room, and an infectious laugh and charm people were drawn to," says Cecilia D., of her mother, Lynda (dx 1988)....
Read More
Launched at EULAR during Scleroderma Awareness Month, Scleroderma Forum is a new educational website developed by the University of Leeds that is dedicated to the dissemination of the latest developments...
Read More
