When Mike Hart talks about his family, there’s a mix of pride and pain in his voice. Mary Lynn, his younger...
We’re excited to announce that registration for the 2025 National Scleroderma Conference is now open. This year’s conference will be held...
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....
Are you hoping to close this year with a charitable gift that supports the scleroderma community and reduces your taxes? Read...
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...
