The New England Chapter recently hosted a special Patient Education Event at Dr. Jonathan Garlick’s lab at Tufts University, giving patients...
The countdown has begun to the 2026 National Scleroderma Conference in Baltimore, Maryland. While the entire Mid-Atlantic Chapter is very excited...
National Scleroderma Foundation recognizes 2025 Pre-Doctoral Fellowship Awardees The National Scleroderma Foundation’s Pre-Doctoral Summer Fellowship Award Program is a demonstration of...
Scleroderma researchers from around the world convened at the 19th International Workshop on Scleroderma Research this week at St. John’s College...
At the opening ceremony of the 19th International Workshop on Scleroderma Research, Dr. John Varga was honored with the 2025 Edith...
The National Scleroderma Foundation, the leading patient advocacy organization serving people living with scleroderma in the United States, announced today that...
The National Scleroderma Foundation’s mission is powered by the volunteers who commit themselves every day to improving the lives of people...
We’re proud to introduce a new Teen Scleroderma Support Group for young people living with scleroderma! Designed specifically for ages 13...
When Shirley was diagnosed with scleroderma at just 29 years old, she had no idea how much her life was about...
