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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)
- 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
- 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
- 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
- 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
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
- Donate to Epidermolysis Bullosa Research Support - DEBRA
Make a donation to debra of America and support our mission to improve the lives of those with Epidermolysis Bullosa (EB) Employer matching Tax-deductible
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