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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.

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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).

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