Updated COVID Guidance from the National Scleroderma Foundation Medical and Scientific Advisory Board As the designation of COVID as a global...
On Rare Disease Day, February 28, the National Scleroderma Foundation will join the global rare disease movement to spread awareness about...
The Scleroderma Foundation evolves into the National Scleroderma Foundation to help those affected by scleroderma find their best path and live...
The sudden loss of Bob Saget on Sunday, January 9, 2022, is a terrible loss for his family and the entire...
“You could be the person who finds the cure!” — Debra Lurvey did not let her diagnosis of systemic scleroderma change...
Annual research funding increases to $2.723 million — On the occasion of World Scleroderma Day, June 29, the National Scleroderma Foundation...
2021 marks 40% increase in submissions — The National Scleroderma Foundation announces an increase of its peer-reviewed scientific research funding to...
A Virtual Conference for Parents & Guardians — The 2021 Kids Get Scleroderma, Too! conference (KGS2) took place as a one-day,...
