National Scleroderma Foundation

Our Mission The National Scleroderma Foundation’s mission is to advance medical research, promote disease awareness, and provide support and education to people with scleroderma, their families and support networks. Our vision is to be a relentless force in finding a cure and improving the lives of people affected by scleroderma.
Find Your Best Path

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.
Find What You Need

One of the most challenging things about scleroderma is that it presents differently in each person. Find the right resources for you.
Find Support

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.
Find Resources

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.
Find a Scleroderma Center

Find the right specialists to make up your team. Locate designated scleroderma centers, specialists, clinical trials, studies, and get help navigating the healthcare system.
Connect Locally The Foundation can connect you with others living with scleroderma through our nationwide network of chapters, in addition to more than 100 support groups.
HOPE Line The National Scleroderma Foundation’s HOPE Line (800-722.HOPE/4673) is a free service offering support for people living with scleroderma, caregivers, families and the public. Anyone can contact the HOPE Line during the hours of (8:30am-5pm ET) to speak with a team member. Callers can leave a voicemail after hours. All inquiries will receive a response within 2 business days. You can also email us at support@scleroderma.org
Get Involved Find a Walk Near You Stepping Out to Cure Scleroderma walks give you a way to get involved and help advance the mission.
Join a Walk
Learn More about Scleroderma Learn about scleroderma, the facts, the latest research, and treatments through our Fact Sheet.
Fact Sheets
Support the Mission The need is great, and the path forward is challenging. You can help make a difference in the lives of people with scleroderma today by supporting our mission.
Donate Now
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Featured News Read the latest news and information from the Foundation.
April 29, 2026 Foundation Celebrates 2026 Scleroderma Research Grant Awardees

The National Scleroderma Foundation is proud to announce the 2026 Scleroderma Research Grant Award recipients. To date, the National…
April 27, 2026 Setting the Stage for Progress: Inaugural Patient Advocacy Summit

The National Scleroderma Foundation brought together stakeholders from the scleroderma community this weekend in Bethesda, including people living with scleroderma, researchers,…
April 20, 2026 Things to Do in Baltimore

If you’re joining us in Baltimore this July, take some time to explore everything Charm City has to offer….
April 15, 2026 Welcome Back, Robert Riggs

That National Scleroderma Foundation is pleased to welcome Robert Riggs back to the Foundation as the new Vice President…
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Join Us for a Foundation Event Upcoming Events

Events

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Today

  • Yoga for Scleroderma Support Group

    Virtual Event

    Join Brooke to enjoy a chair yoga class with an emphasis on joint mobility and range of motion. When: Wednesday, May 13, 2026, 6:30pm ET This is a live class and we don't record it, so turn your video on and ask your questions. All the practices are GERD friendly and have options so you […]

  • Newly Diagnosed Scleroderma Support Group

    Newly Diagnosed Scleroderma Support Group
    Virtual Event

    Individuals newly diagnosed as having scleroderma face an overwhelming number of questions about how it will affect their lives. Participation in a support group is one way to obtain information and receive support from others. This group will help navigate these questions and support newly diagnosed individuals. Click here to register in advance. A meeting […]

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Join Us for a Foundation Event Upcoming Events
September 16, 2025, 7:00 p.m. ET Bereavement Support Group
September 16, 2025, 7:00 p.m. ET Morphea/Localized Scleroderma Support Group
September 17, 2025, 6:30 p.m. CT West Metro Support Group (MN)
September 18, 2025, 6:00 p.m. ET Central North Carolina SSc Support Group
Research Initiatives

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.

Research Funded by the Foundation