• 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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Collage of a photo of 2 doctors holding folders, and the covers of 3 clinical practice guidelines for EB

31.03.2014

Five things you need to know about EB clinical practice guidelines

DEBRA International is very focused on the development of clinical practice guidelines for EB but what are they and how do they help? Read more

Screenshot of the homepage of the EB Handbook

31.03.2014

A guiding handbook for people living with EB

Colleagues from the EB House Austria in Salzburg have developed a valuable online resource for those affected by EB.Read more

Screenshot of DEBRA Iran's website

12.03.2014

A focus on DEBRA Iran: No EB patient should be left alone

This time, the highly committed Iranian doctor Amir Barzgar gave us valuable insights into DEBRA Iran.Read more

Research assistant Emma Batten giving information at a stand (The Royal Holloway University of London), which is decorated with DEBRA UK logo and posters

03.03.2014

The limelight on research for Rare Disease Day

On Rare Disease Day, DEBRA International Research Manager Dr. Clare Robinson took part in some activities to highlight the importance of EB researchRead more

Yellow tube of Diacerein cream

13.02.2014

Promising cream for butterfly children (EBS) receives "orphan designation" status

A clinical pilot study showed that the Diacerein cream resulted in better stability of the skin and reduced the formation of blistersRead more