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...
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...
On February 28, we join the global community in recognizing Rare Disease Day, a time to raise awareness and advocate for...
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...
On October 12 and 13, Lorraine Biaggi, executive director of the National Scleroderma Foundation Florida and Puerto Rico Chapter, and Monica...
