NEWS
DEBRA UK completes its largest ever EB patient insight study
ERN Skin meeting held in Paris attended by DEBRA representatives from Ireland, Croatia, and Belgium
DEBRA Chile holds 2nd Research Day for EB patients and families
DEBRA Croatia celebrates Rare Disease Day
DEBRA Ireland launches an EB Expert Panel to help shape its support and research priorities
In memoriam: Lisa Brains
Maria Korosta's letter to us all
In memoriam: Catina Bernardis
DEBRA Germany introduces a new video on EB wound care
Remembering Prof Jouni Uitto
Sesión virtual para pacientes y familias dedicada al proyecto sobre EB de Rare Commons
Take part in an international research study on burden and resources in EB - online survey
Únete a Rare Commons para compartir tus experiencias y ayudar a mejorar el conocimiento de la EB
People with EB in Brazil have the opportunity to access genetic sequencing tests free of charge
We welcome DEBRA Belarus as one of our three new member groups
DEBRA Bosnia and Herzegovina launches picture book, Butterfly Boy
We welcome the Yasmin El Samra Foundation - DEBRA Egypt as one of our three new member groups