• Help people with EB

    Your support of DEBRA International or a national EB group enables us to provide the best quality of life for families and individuals affected by EB.

Donation Account: IBAN AT65 6000 0005 1004 5254, BIC BAWAATWW, DEBRA International, Am Heumarkt 27/1, 1030 Vienna

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Welcome to DEBRA International

DEBRA International is a worldwide network of national groups working on behalf of those affected by the genetic skin blistering condition Epidermolysis Bullosa (EB).

Our vision is to ensure that people living with EB have access to the best quality support and medical care, while also driving the development of effective treatments and cures for EB.

In this section you will find information about the association DEBRA International, its history, vision and goals, and how to join this umbrella organisation as a national EB support group. Over 50 groups worldwide are already part of this network. See also the various services member groups are offered.

EB without borders is a key initiative of DEBRA International. 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.

If you are interested in supporting DEBRA International or EB patients nationally, you will find options to do so in the Donate / Support section.

Please don't hesitate to contact us if you have any questions or suggestions.