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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). Debra de américa es parte de el esfuerzo mas grande sobre la investigación internacional sobre las causas, consecuencias y tratamientos posibles para los tres tipos de eb. Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services.
Debra Amick
Make a donation and help fund research for a cure. For more information or if you have any questions, feel free to contact us at Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
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. 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). Make a donation to debra of america and support our mission to improve the lives of those with epidermolysis bullosa (eb)
Debra of america is here to guide you in making informed decisions surrounding proper eb care Care for wounds acute and chronic wounds may occur very frequently in individuals.
