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. Learn about epidermolysis bullosa (eb), a rare genetic disorder, its symptoms, treatments, and personal stories from the eb community at debra of america.

For more information or if you have any questions, feel free to contact us at: Staff@debra. org phone: 833-debraus (833-332-7287) our team is here to support you with any questions or … Get to know the dedicated team behind debra of america, working tirelessly to support individuals and families affected by epidermolysis bullosa (eb). 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). Your support is more than a donation â€it's a lifeline. With your support, debra of america provides free programs and services that ease the unrelenting physical, emotional, and financial burdens of eb …

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). Your support is more than a donation â€it's a lifeline. With your support, debra of america provides free programs and services that ease the unrelenting physical, emotional, and financial burdens of eb … Explore our mentorship programs, eb nurse educator program, new family advocate program, debra care conference & additional support services.

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