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.
More than 1,000 clinicians and researchers joined together for the 9th Systemic Sclerosis World Congress. Organized by the World Scleroderma Foundation, the event runs…
The National Scleroderma Foundation and our network for patient advocates are preparing for our next Virtual Hill Days meetings….
The National Scleroderma Foundation is excited to introduce Dionna Bartos as our new Director of Education. Dionna first joined…
Events
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Central NC Scleroderma Support Group
Virtual EventGuest: Dr. Ankoor Shah, Director, Duke Scleroderma Center Learn about the newest treatments and research available for scleroderma. Use this link to register and ask questions. https://us02web.zoom.us/meeting/register/RbpMm7_5RkORyZgmnVL8ug
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Texoma Scleroderma Support Group
Virtual EventFor more information, please email dcharlton@scleroderma.org Use this link to register in advance: Meeting Registration - Zoom
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Global Webinar: Advances in Scleroderma Research
Zoom Meeting link available after registrationVirtual EventAdvances in Scleroderma Research - Global Webinar A series of virtual meetings open to the global community of scleroderma investigators. A CD57+ CD8 T Cell Subset Links Cytotoxic T Cell Function to Fibrotic Lung Disease in Systemic Sclerosis - Takanori Sasaki, MD, PhD, Keio University Arginase-1–Derived Ornithine Drives Collagen Synthesis in Lung Fibrosis - Mallar […]
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St. Louis Support Group
Virtual EventThe St. Louis Scleroderma Support Group serves the Heartland Chapter and meets virtually on the 3rd Saturday of odd-numbered months. For more information, please email support@scleroderma.org.
