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.
October 5, 2026 Dr. Jacobe to Join Duke Health in December

Heidi Jacobe, MD, MSCS, will serve as chair of the Department of Dermatology at Duke Health beginning in December….
September 1, 2026 Two CAR-T Clinical Trials Paused: An Update

National Scleroderma Foundation leadership is aware of the pause in two CAR-T clinical development programs and is closely following…
August 16, 2026 Remembering Dr. Thomas A. Medsger Jr. 

The National Scleroderma Foundation joins the scleroderma community in mourning the passing of Dr. Thomas A. Medsger Jr., a…
August 5, 2026 A New Chapter: Lisa’s Journey with Scleroderma and Lung Transplantation

For more than 20 years, Lisa dedicated her career to helping children learn and grow. A Tampa-area teacher, wife,…
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Join Us for a Foundation Event Upcoming Events

Events

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Today

  • North Shore Support Group

    North Shore Support Group
    Virtual Event

    The North Shore support group meets on the 2nd Wednesday of each month (except for July and August) from 11am-1pm ET. Please register here: https://us02web.zoom.us/meeting/register/hF0UQ2O6TpejTioM142I6Q Please email northshoresg@sclerodermavolunteer.org with any questions.

  • Yoga for Scleroderma Support Group

    Virtual Event

    The Yoga for Scleroderma Support Group will meet on October 14 from 6:30pm to 7:30pm PT. The Yoga Therapy for Digestive Health-Seated Class P(68) session will be taught by Kathy Randolph, C-IAYT. Click here to register. Questions? Email: YogaSG@sclerodermavolunteer.org  

  • 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. The Newly Diagnosed Support Group meets on the […]

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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