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Make a donation and help fund research for a cure. Learn more about our work. 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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For more information or if you have any questions, feel free to contact us at 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 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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Its mission is to help patients, families, and doctors in countries where there is no debra structure to support them and to assist new groups to form and develop.

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