The National Scleroderma Foundation is delighted to be participating in the Rare Disease Week and Rare Disease Day activities organized by...
The National Scleroderma Foundation is very excited to introduce Chrissy Geimann to the team. Chrissy joined the Foundation in early 2026,...
As we step into a new year, we are excited that 2026 will be a celebration of our “Beacons of Hope.”...
The National Scleroderma Foundation is very excited to share that one of the key pieces of legislation we have been supporting this year...
Health behavioral scientist offers evidence-based cognitive strategies for living well with scleroderma. Many people with scleroderma use the term “brain fog”...
The National Scleroderma Foundation is gearing up for a busy year for our community’s legislative advocates. There are several federal health...
Stepping Out Takes a Walk on the Wild Side Several chapter Stepping Out to Cure Scleroderma events have found a...
A look back at a year of growth with Vice President of Community Engagement Ashley Pruett The National Scleroderma Foundation spent...
The Foundation is a proud member of The Ensuring Access through Collaborative Health (EACH) and Patient Inclusion Council (PIC), otherwise known...
