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...
The reality show was supposed to be entertainment. Instead, it was a mirror. By Donna R. Dinkin Recently, I binge-watched 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...
As the only national patient advocacy organization in the US, the National Scleroderma Foundation is honored to represent more than 300,000...
This November, our Upper Great Lakes Chapter is inviting you to take part in a special Gratitude Challenge. The goal is...
