For more information or if you have any questions, feel free to contact us at Saturday, october 4, 2025 where 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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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.
