Scleroderma Voice is the home for feature stories about people living with scleroderma, the latest in scleroderma research, and what is happening around the National Scleroderma Foundation.
Stepping Out Takes a Walk on the Wild Side Several chapter Stepping Out to Cure Scleroderma events have found a...
The reality show was supposed to be entertainment. Instead, it was a mirror. By Donna R. Dinkin Recently, I binge-watched a...
A look back at a year of growth with Vice President of Community Engagement Ashley Pruett The National Scleroderma Foundation spent...
As the only national patient advocacy organization in the US, the National Scleroderma Foundation is honored to represent more than 300,000...
The countdown has begun to the 2026 National Scleroderma Conference in Baltimore, Maryland. While the entire Mid-Atlantic Chapter is very excited...
The National Scleroderma Foundation’s mission is powered by the volunteers who commit themselves every day to improving the lives of people...
When Shirley was diagnosed with scleroderma at just 29 years old, she had no idea how much her life was about...
This Scleroderma Awareness Month, we’re proud to share Stories of Strength – real-life journeys from individuals living with scleroderma and the...
2023 Established Investigator Awardee Explores Ways to Measure Changes in Patients Skin Over Time Project Summary Provided by: Andreea Bujor, MD,...
