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Make a donation and help fund research for a cure. Brittany daniel, brooke shields, debra jo rupp, jackie debatin, jessica simpson, laura prepon, mila kunis, tanya roberts Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.

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Debra of america is part of debra international, a worldwide network of national groups working on behalf of all people living with epidermolysis bullosa (eb).

Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services. When there seems to be no way out, there's debra of america, a lifeline for thousands of families living with “the worst disease you’ve never heard of,” epidermolysis bullosa (eb). Learn about debra of america's team working to raise eb awareness, and provide eb support to patients and families affected by epidermolysis bullosa (eb). Founded in 1980, debra of america is dedicated to improving the quality of life of all people impacted by epidermolysis bullosa (eb) in the u.s

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