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 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,...
On January 24, 2026, our Florida and Puerto Rico Chapter successfully hosted Scleroderma Insights, its first in-person scleroderma educational event in...
In the scleroderma community, support groups are more than just a gathering – they are lifelines. They offer connection, understanding, and shared strength....
En la comunidad de esclerodermia, los grupos de apoyo son más que un simple encuentro: son un salvavidas. Ofrecen conexión, comprensión...
