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Make a donation and help fund research for a cure. Featuring cocktails, hors d’oeuvres, auction, and dinner. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). Attend the 2024 debra of america benefit on october 25, 2025 at southern exchange ballrooms in atlanta, ga 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).
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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). 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. For more information or if you have any questions, feel free to contact us at
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.
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