Epidermolysis Bullosa (EB) Information & Support
About
DEBRA provides a range of services intended to enhance quality of life for the Epidermolysis Bullosa (EB) community, whether they are members of DEBRA or not. Support includes information, advice, practical, financial, emotional support and advocacy. Becoming a member offers opportunities to connect with others living with EB, attend specialist events and contribute to raising awareness and enhancing expertise in EB.
About DEBRA
DEBRA is the national charity that funds research and healthcare to support individuals and families affected by Epidermolysis Bullosa (EB) – a painful genetic skin blistering condition which, in the worst cases, can be fatal.
Good to know
User Cost/Charge Information
Membership is free if you have EB or are a relative, primary carer or partner of someone with EB.
You can also become a member if you work with EB patients or specialise in EB as a healthcare professional or researcher. For membership enquiries please email: membership@debra.org.uk
Find out more
DEBRA
Email
debra@debra.org.uk
Website
https://www.debra.org.uk/
Location
DEBRA
8-10 Bridge Road
Farnborough
Hampshire
GU14 OHS