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...
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...
The Upper Great Lakes Chapter’s annual holiday cookbook has become a joyful tradition – and the chapter is inviting the entire...
This November, our Upper Great Lakes Chapter is inviting you to take part in a special Gratitude Challenge. The goal is...
Help demonstrate the strength of our community and speak up for policies that will improve the lives of people living with...
National Scleroderma Foundation recognizes 2025 Pre-Doctoral Fellowship Awardees The National Scleroderma Foundation’s Pre-Doctoral Summer Fellowship Award Program is a demonstration of...
The National Scleroderma Foundation, the leading patient advocacy organization serving people living with scleroderma in the United States, announced today that...
