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Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america. Featuring cocktails, hors d’oeuvres, auction, and dinner. Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services.
JOHNGY'S BEAT: Debra McMichael at Blizzard Brawl 2021
Make a donation and help fund research for a cure. Attend the 2024 debra of america benefit on october 25, 2025 at southern exchange ballrooms in atlanta, ga Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb).
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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. 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). 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).
