JOIN US FOR OUR 3RD ANNUAL DIGITAL SHOW
NOVEMBER 20TH, 2022
The evening will feature incredible stories of individuals with EB and their families along with celebrity friends and EB doctors. 
​Click below to watch this year's show:

WATCH NOW

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OUR STORY

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

About eb

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

OUR MODEL

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

Financials

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

SALIM: DYSTROPHIC EB

CLARA: EB SIMPLEX

RYAN: JUNCTIONAL EB

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