- 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
- Understanding Epidermolysis Bullosa (EB) | debra of America
Learn about Epidermolysis Bullosa (EB), a rare genetic disorder, its symptoms, treatments, and personal stories from the EB community at debra of America
- Supporting the EB Community Since 1980 | debra of America
Get to know the dedicated team behind debra of America, working tirelessly to support individuals and families affected by 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
- DEBRA International | debra of America
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
- Patient and Caregiver Support Programs for EB - DEBRA
Explore our Mentorship programs, EB Nurse Educator Program, New Family Advocate Program, debra Care Conference additional support services
- 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)
- 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
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