- 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
- 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
Learn about Epidermolysis Bullosa (EB), a rare genetic disorder, its symptoms, treatments, and personal stories from the EB community at debra of America
- 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
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
- Wound Care Assistance - Epidermolysis Bullosa (EB) - DEBRA
Get free wound care supplies through debra of America's Wound Care Distribution Program, providing support for those with Epidermolysis Bullosa (EB)
- Dystrophic EB | debra of America
No one should face Dystrophic EB alone debra of America offers free programs, personalized support, and trusted online resources to help individuals and families navigate life with EB
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