That National Scleroderma Foundation is pleased to welcome Robert Riggs back to the Foundation as the new Vice President of Philanthropy....
In a recent interview, Kate Bogner shared her story with striking honesty and strength, offering a perspective shaped not just by...
Scleroderma advocates from across the country spent Wednesday and Thursday speaking with legislative offices about the critical legislative priorities of the...
The National Scleroderma Foundation’s Florida & Puerto Rico Chapter, in partnership with Mayo Clinic Jacksonville, will host Scleroderma Insights: Advancing Knowledge,...
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 excited to introduce Dionna Bartos as our new Director of Education. Dionna first joined the Foundation...
Q: Do you have any advice regarding how people can/should go about getting a proclamation from their local areas for Scleroderma...