The world's largest conference on Epidermolysis Bullosa (EB), connecting thousands of experts in research, healthcare professionals, clinical management, and the EB Community.
For over 40 years DEBRA International has been helping patients affected by the genetic skin blistering condition epidermolysis bullosa (EB). It's the world's leading EB Patient Support and Advocacy Network on a mission to improve the lives of those living with EB.
Every year DEBRA International hosts its annual congress in one of the member countries. In 2021 the congress will be organised by DEBRA Russia.
* Parents of EB patients (children), and EB patients (18+)
Healthcare professionals
Patients organisations
DEBRA groups
Patients*
DEBRA groups
Healthcare professionals
Patients organisations
* Parents of EB patients (children), and EB patients (18+)
First ever Online Congress on EB
Due to the current pandemic situation worldwide, DEBRA International Congress 2021 will be held online for the first time in history.
By using an online event platform, we will be able to reach a higher number of attendees, making the event even more accessible for patients from different countries for the first time.
Online possibilities
Live Stream on Stages
Scheduling 1-on-1 meetings with other participants