NEWS

On 23 February 2022, DEBRA International had a webinar on the Pregnancy, Childbirth and Aftercare in epidermolysis bullosa...

DEBRA International was delighted to support DEBRA Indonesia team in holding the EB Awareness Month October 2021. In October 2021, EB...

DEBRA International is delighted to announce the First Art exhibition for EB children in Egypt and worldwide in cooperation with Yasmin...

On the 16 December 2021, the UN General Assembly has formally adopted the UN Resolution on Addressing the Challenges of Persons Living...

We are delighted to announce the publication of the "Physiotherapy for epidermolysis bullosa: clinical practice guidelines" in the...

Sesión virtual para pacientes y familias dedicada al proyecto sobre EB de Rare Commons

Take the survey in English: https://survey.sfu.ac.at/EB2021/?q=E_Qnr Take the online survey in German: https://survey.sfu.ac.at/EB2021/?q...

Rare Commons es un proyecto de investigación del Hospital Sant Joan de Déu de Barcelona que se centra en el estudio biomédico de las...

With 28th February 2021 marking Rare Disease Day, DEBRA Brasil and Illumina have joined forces to launch a pioneering and high impact...

DEBRA International is delighted to welcome DEBRA Belarus as one of its newest member groups. The Republican Public Association for Aid...

In 2019, DEBRA International was delighted to be able to support its member group, DEBRA BiH with a grant for their project to create and...

DEBRA International, through its EB Without Borders programme, was delighted to support the DEBRA Pakistan team in holding their first EB...

DEBRA International is delighted to welcome the Yasmin El Samra Foundation - DEBRA Egypt as one of its newest member groups. My name is...

Every CPG published is the result of 18-24 months of hard work and dedication by a volunteer panel of clinical and patient experts.

The "Supporting sexuality for people living with EB: clinical practice guidelines" have been published!