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.
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,...
The National Scleroderma Foundation is thrilled to announce the Indu Sapra, MD Memorial Research Grant. Thanks to a generous $5 Million commitment...
This Volunteer Appreciation Month, we want to extend our deepest thanks to all of our incredible volunteers who make a difference...
When Mike Hart talks about his family, there’s a mix of pride and pain in his voice. Mary Lynn, his younger...
The National Scleroderma Foundation is excited to announce its 2025 Scleroderma Research Grant awardees. The National Scleroderma Foundation fosters development of...
On February 28, we join the global community in recognizing Rare Disease Day, a time to raise awareness and advocate for...
The National Scleroderma Foundation’s senior director of mission delivery, Kate Anastasia, and member of our patient advisory board, Nikhil Bhat, recently...
Join us for the first #TealTalk of 2025! Join us for our virtual discussion on Zoom: Advocating for the Scleroderma Community in 2025....
