Steffens Scleroderma Foundation

Our Story

The Steffens Scleroderma Foundation was established in memory of Ann Elizabeth Steffens, a dedicated advocate for those affected by scleroderma. With the generous support of her mother, Helen Polenz, the foundation aims to make a significant impact in the lives of patients and their families.

Impact

By actively supporting research and new treatment developments, the foundation has contributed to advancements that allow individuals to experience extended remission from scleroderma.

Why Donate?

Your contributions are vital for providing hope and support to those affected by rare diseases, enabling ongoing research and educational initiatives.

Get Involved

Join the fight against scleroderma and Degos disease. Your donation, whether in cryptocurrency or cash, can help transform lives and advance critical research. Together, we can make a difference!