National Scleroderma Foundation CEO, Mary J. Wheatley, IOM, CAE, joined the global scleroderma community at the 9th Systemic Sclerosis Patient World...
More than 1,000 clinicians and researchers joined together for the 9th Systemic Sclerosis World Congress. Organized by the World Scleroderma Foundation, the event runs parallel with the...
The National Scleroderma Foundation and our network for patient advocates are preparing for our next Virtual Hill Days meetings. Scleroderma advocates...
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...
