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
  • Coalition of Skin Diseases Hill Day

    Advocacy

    The Coalition of Skin Diseases is hosting its annual Hill Day visit in Washington, D.C. in May. The National Scleroderma Foundation is a proud member of the Coalition of Skin […]

  • BIPOC Support Group

    Virtual Event

    The facilitators of BIPOC (Black, Indigenous, and People of Color) Virtual Support Group invite you to join their upcoming Zoom support group meeting. Register in advance for this meeting: https://us02web.zoom.us/meeting/register/3q7RtYIIS5Oq6KbUSu6cIA After registering, you will receive a confirmation email containing information about joining the meeting.

  • ILD in Systemic Sclerosis: Understanding Progression and Treatment Options

    Virtual Event

    Please join us for The Lungs in Scleroderma (ILD) webinar! Francesco Boin, MD, professor medicine, director of the division of rheumatology and director of the Kao Multispecialty Scleroderma Program at Cedars-Sinai Medical Center, will lead the discussion. This webinar is sponsored by Boehringer Ingelheim. Please note there has been a schedule change for this event. […]

  • Bereavement Support Group

    Bereavement Support Group
    Zoom
    Virtual Event

    If you have lost a loved one to scleroderma, you may find support and solace in speaking with others who are grieving. Our monthly bereavement support group will be on the third Tuesday of every month from 7:00-8:30 p.m. ET. Click here to register in advance for this meeting. After registering, you will receive a […]

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.