Collaborating for a Cure The SRF Patient Forum

Thank you for an incredible

“Collaborating for a Cure”

held on Monday, June 3, 2024

 

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

 

Watch the Scleroderma Research Foundation Patient Forum, “Collaborating for a Cure”

In this Scleroderma Research Foundation Patient Forum video Dr. Shah reviews symptomatic management of systemic sclerosis without medication including Raynaud’s Phenomenon, digital ulcers, GI symptoms, joint pain, contractures, and fatigue.

The Scleroderma Research Foundation Patient Forum, “Collaborating for a Cure,” is a yearly online, half-day forum with new information about scleroderma and research that anyone can attend for FREE. Learn about advances in treatments, disease management, clinical trials, and more.

The forum features educational sessions on scleroderma symptom management, new developments in scleroderma 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

  • Interactive games and activities to win prizes

Watch the Past Scleroderma Research Foundation Patient Forums on YouTube

The SRF Forum, Scleroderma Awareness Month, and YOU

Because of our singular focus on understanding scleroderma, the SRF has the most up-to-date and relevant information about scleroderma complications, treatments, and related research. Everyone should have access to this information. That’s why we created the SRF Patient Forum as a part of our efforts for Scleroderma Awareness Month—so that you’re armed with the most relevant facts about scleroderma, all while the search for a cure continues.

Spread the word by sharing what you’ve learned or your story, using #SayScleroderma on social media during Scleroderma Awareness month and beyond.

Learn More about Raising Awareness

Thank you to our generous industry partners for sponsoring the 2024 SRF Patient Forum.

Interested in becoming a sponsor for 2025?

For more information contact Kate Ceredona, Director of Philanthropy, at kate@sclerodermaresearch.org