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debra debra of America is a non-profit organization providing free programs EB support services to those living with Epidermolysis Bullosa Make a donation and help fund research for a cure
DEBRA International | 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)
Donate to Epidermolysis Bullosa Research Support - DEBRA 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)
Understanding Epidermolysis Bullosa (EB) | debra of America For more information or if you have any questions, feel free to contact us at: Email: staff@debra org Phone: 833-debraUS (833-332-7287) Our team is here to support you with any questions or concerns regarding EB diagnosis, treatment, and ongoing care
What We Do - debra of America 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
En Español | debra of America 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