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Make a donation and help fund research for a cure. 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 unirse sobre la linea. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.
DEBRA MESSING at Impact of Will & Grace 25 Years Later at Paley Museum in New York 06/05/2023
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 For more information or if you have any questions, feel free to contact us at Learn more about our work.
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