Welcome to the SRF Scleroderma Patient Forum. 

A FREE online event for people living with scleroderma and those who care about them.

Missed the forum? You can still watch the sessions! Sign up for our email list, and you'll be notified when they're on YouTube, or keep your eyes on our YouTube channel!

Learn about scleroderma and connect with experts at the SRF Scleroderma Patient Forum.

The Scleroderma Patient Forum (SPF) is an annual online forum hosted by the Scleroderma Research Foundation that anyone can attend for FREE. This year, the SPF was hosted on Thursday, June 11th, at 9:00 am PDT/12:00 pm EDT as part of our efforts for Scleroderma Awareness Month.

The day included educational sessions on symptom management, new developments in research, and your role in finding a cure for scleroderma:

• Informative sessions presented by leaders in the field of scleroderma research and medicine

• Live Q&A following each presentation

• Opportunities to win exciting prizes to mark the forum's 5th anniversary

Register Now

Interested in becoming a sponsor for future events? Contact Gloria Blecha, Vice President of Programs and Operations, at gloria@sclerodermaresearch.org

We have a bold vision for a world without scleroderma.

The mission of the Scleroderma Research Foundation (SRF) is to fund and facilitate the most promising, highest quality research aimed at improved therapies and, ultimately, a cure for scleroderma. We have become the largest nonprofit investor in scleroderma research in the United States and a global leader in the field.

Until this disease is eradicated, we are dedicated to providing education, raising awareness, and sharing the most up-to-date information that the scleroderma community needs.

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