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.

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Join Us for a Foundation Event Upcoming Events
  • Yoga for Scleroderma Support Group

    Virtual Event

    Kathy Randolph leads a reclining series to release your legs, hips, back, shoulders, and neck, perfect at bedtime. If you have GERD, get your inclined plane ready, that's your wedge pillow or blankets or your already elevated bed. The class ends with the Sleep Breath Relaxation, good for going to sleep and even better for […]

    Free
  • 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 […]

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.