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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). La pagina de internet de debra provee pacientes, cuidadores y profesionales de salud con la información mas reciente sobre eb, mientras ofrece un lugar donde la comunidad de eb puede. Make a donation and help fund research for a cure.
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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). 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).
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