Where to Start
More than 300,000 Americans live with some type of scleroderma. Today, the face of scleroderma includes people of all ages, genders, and backgrounds. Scleroderma can affect young parents, children, grandparents, and teenagers. Thanks to the passion and dedication of countless volunteers, scientists, and supporters, we’re advancing our mission faster than ever.
One of the most challenging things about scleroderma is that it presents differently in each person. Find the right resources for you.
Share and learn from others, at different places in their journey, through ‘Living with Scleroderma Groups’ for adults, children, and those who care for them.
No matter what type of scleroderma or where you or your child are on your journey, the Scleroderma Foundation can help you find your best path.
National Scleroderma Foundation CEO, Mary J. Wheatley, IOM, CAE, recently reviewed key mission metrics with Foundation stakeholders. Watch this…
We’re excited to meet with you in-person or virtually for the 2023 National Scleroderma Conference! We’re busy working behind…
On Monday, Jan. 16, the National Scleroderma Foundation joins the rest of nation in honoring the life of Dr….
I hope you had a wonderful holiday season and are having a good start to 2023. We have lots…
The Foundation’s peer-reviewed research grant program is a leader in scleroderma research. Learn more about how this program accelerates the search for better treatments, and ultimately, a cure.