Debra Paget's

Debra of america is a non-profit organization providing free programs & eb support services to those living with epidermolysis bullosa. 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. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at 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). Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services. 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.

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). With your support, debra of america provides free programs and services that ease the unrelenting physical, emotional, and financial burdens of eb. 833-debraus (833-332-7287) our team is here to support you with any questions or.

Oct 25, 2025attend the 2024 debra of america benefit on october 25, 2025 at southern exchange ballrooms in atlanta, ga.