It's only a few days until #RareDiseaseDay2023 on 28th February. We're taking a patient centered approach, this means understanding their journey so we can better understand how we can help to improve it by closing the gaps in education.
Hear from Christo as he describes in his own words what it’s like to live with epidermolysis bullosa, and his perspective as a patient.
Visit our focused learning center for more information on the education we provide here.
Address:
Web M D Global, Kent House
14-17 Market Place
London
W1W 8AJ
United Kingdom