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.
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....
Día de los Muertos, or Day of the Dead, is a treasured tradition in the Latino community that celebrates the lives...
Dr. Natalie Saini, National Scleroderma Foundation 2023 Established Investigator Awardee, is a co-author of groundbreaking research exploring the connection between systemic...
The Fall Edition of Scleroderma Voice is Here! This season’s magazine brings inspiring stories and updates from across the scleroderma community....
The Summer Fellowship Award Program is designed to recognize PhD students conducting research related to scleroderma. The program encourages and fosters the next...
For many in the scleroderma community, Cos and Ronni Shulman Mallozzi are household names. Together they served the scleroderma community for...
Upper Great Lakes Chapter Executive Director Randy Slikkers knows a thing or two about bee colonies and their hives. Randy is...
