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DonateWith help from supporters like you, Debra of America continues to provide programs and services to people with Epidermolysis Bullosa and their families, and to support EB research.Thank You. |
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The mounting cost of bandages is most often not covered by an EB family's health insurance. |  |
89.4¢ of every dollar donated goes directly to EB patients, families, and research. |
Connect With Others
By connecting with others who's lives have been affected by EB you have the opportunity to gain strength, become better informed and offer much needed support to others who's lives are similarly affected. Debra offers many opportunities for families to connect with each other as well as with medical professionals, researchers and other health care providers in both formal and informal settings. Together we can conquer this disease.
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Become a fan of Debra on Facebook and connect with families, organizations, communities
and individuals who are looking for a cure.
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Partners & Sponsors
Any contribution, large or small, helps
EB patients and families and makes
continued research possible.
DebRA's 2012
Patient Care Conference
Countdown to a Cure
Patient Care Conference
Countdown to a Cure
July 30, 2012 - August 2, 2012
Register Now
What is EB? helps teachers and students
understand the issues facing children with
dystrophic EB in the classroom.
of every dollar donated goes to EB
patients, families, and research.
