Find a Cure. End EB.
Imagine your skin being as fragile as a butterfly’s wings.
Imagine every movement you make causing your skin to shear off your body.
Imagine cures and treatments being almost within grasp.
 
Welcome to the Jackson Gabriel Silver Foundation (“JGSF”). We fund scientific research with the goal of curing and treating Epidermolysis Bullosa (“EB”), a group of devastating, painful, disfiguring and currently incurable blistering disorders that affect children from birth.

Tremendously encouraging and viable research is ongoing to treat and cure EB. Given that EB affects fewer than 25,000 people in the United States, advancing this research relies on the generosity of individuals and corporations.

Curing a rare disease is always a race against the clock. Curing EB is a race against a clock moving at warp speed. The more funds we can raise, the more research we can fund and the more lives we can save. With your help, children with EB can grow up to live full and pain-free lives.
      Find a Cure. End EB.
 
Epidermolysis Bullosa (“EB”) is a group of devastating, painful, disfiguring and currently incurable blistering disorders that affect children from birth.
Treatment for Epidermolysis Bullosa | What Is Epidermolysis Bullosa? | EB Research | EB Cure | EB Treatment | Dystrophic Epidermolysis Bullosa | Junctional Epidermolysis Bullosa | EB Pictures | Recessive Dystrophic Epidermolysis Bullosa |