Dystrophic Epidermolysis Bullosa Research Association of America - DEBRA
staff@debra.org
www.debra.org/ 
Other Contact Information
40 Rector Street
Suite 1403
New York,
NY 10006
887-88-DEBRA (Voice - Toll-free, Patient Information)
212-868-1573 (Voice)
212-513-4099 (FAX)
Description
The Dystrophic Epidermolysis Bullosa Research Association of America (DEBRA) was formed in 1979 as a self-help group for persons suffering from epidermolysis bullosa (EB), a group of inherited skin disorders characterized by the formation of blisters after mild trauma. Staff provide professional and emotional guidance, raise funds for research, and help administer public and professional education. DEBRA of America and its sister organizations in Australia, England, New Zealand, and Israel are dedicated to improving public and professional understanding and awareness of EB.
Print Resources
Booklets describing the disease and the Association are available. Serial publication: DEBRA Newsletter, twice yearly--news on Association activities and research results.
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