EB is a group of devastating, painful, disfiguring and currently incurable blistering disorders that affect children from birth. Find a Cure. End EB. Learn more about how you can have an impact at www.jgsf.org.
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.
JGSF funds 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.
Within the foreseeable future, and even sooner with your support, children with EB can grow up to live full and pain-free lives. Find a Cure. End EB.
JGSF was founded by Alex and Jamie Silver in 2010, with the goal of finding a cure for their son, Jackson, and all other children who suffer from this terrible disease.
JGSF is a 501(c)3 established in 2010. All contributions are tax-deductible.