DEBRA Ireland's mission is to fund the development of treatments and cures for all forms of Epidermolysis Bullosa, and meanwhile to do all in its power to alleviate the suffering caused by EB.
Donate now

DEBRA International


DEBRA Ireland is a member of DEBRA International, a worldwide network of patient support groups whose collective goal is to help people with Epidermolysis Bullosa (EB). The first DEBRA group was founded in the UK by a group of parents whose children were affected by Epidermolysis Bullosa (EB). The original aims of the charity were to stimulate knowledge of, and interest in, EB for the benefit of those with the condition and their families and to fund medical research into EB. From these humble origins DEBRA has grown significantly with DEBRA groups now having been established in about 40 countries around the world. DEBRA International is an umbrella group whose members are the national associations representing people with EB in their countries. All member groups are autonomous, choosing to work together on matters of common interest. Europe, North America and Australasia are well represented amongst the member groups and there is a growing membership in Central and South America, Asia and, to a lesser extent, Africa.

For further information on DEBRA International you can visit their site at www.DEBRA-international.org

DEBRA International
Am Heumarkt 27/3, 1030 Vienna, Austria
office@DEBRA-international.org
T: +43 1 876 40 30-0  F: +43 1 876 40 30-30