With Scleroderma Awareness Month just a week away, the National Scleroderma Foundation is incredibly excited to share some news with you—we’re...
Advocates from the National Scleroderma Foundation traveled to Washington, D.C. this past weekend to participate in Hill Day 2026 hosted by...
The National Scleroderma Foundation brought together stakeholders from the scleroderma community this weekend in Bethesda, including people living with scleroderma, researchers, clinicians, industry...
If you’re joining us in Baltimore this July, take some time to explore everything Charm City has to offer. From waterfront...
That National Scleroderma Foundation is pleased to welcome Robert Riggs back to the Foundation as the new Vice President of Philanthropy....
Scleroderma advocates from across the country spent Wednesday and Thursday speaking with legislative offices about the critical legislative priorities of the...
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...
