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Make a donation and help fund research for a cure. Dell children's medical center 4900 mueller blvd austin, tx 78723 in partnership with university of texas at austin For more information or if you have any questions, feel free to contact us at
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Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). Saturday, october 4, 2025 where Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services.
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). 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 Learn more about our work. Please contact debra of america's national office with further questions or concerns
At present, there is no specific treatment for eb Current therapy is directed toward the prevention of skin trauma, prevention of infection, and the treatment of complications.
