EB Research Partnership

OUR STORY

Epidermolysis Bullosa (EB) is a rare and life-threatening genetic skin disorder that affects children from birth.

We're building a faster path to heal EB. Our innovative model puts speed in the system to find cures quickly.

Committed to financial responsibility. With the highest charity ratings, we ensure your dollars make an impact.

LIFE WITH EB
Click on the photos to read each child's story.

SALIM: DYSTROPHIC EB

CLARA: EB SIMPLEX

RYAN: JUNCTIONAL EB