
DEBRA UK wants to fund you to help create a world where no one suffers with epidermolysis bullosa (EB). This painful and life-limiting condition affects many major organs of the body, including skin, eyes, kidneys, gastrointestinal and urinary tracts, causing painful blistering, scarring and increased risk of skin cancer. We fund research on all of the four genetic types of EB and encourage applications from researchers working on EBS where there is an unmet need.
See below full information on our research strategy, funding criteria and application deadlines. To apply for our funding, please download our application form, complete and submit by email to research@debra.org.uk.
You can also sign up to our researchers database to be kept informed of future research funding and other opportunities.
If you wish to discuss your proposed research area in advance of submission, please contact Dr Sagair Hussain, Director of Research: Sagair.Hussain@debra.org.uk.
DEBRA UK wants to fund you to help create a world where no one suffers with epidermolysis bullosa (EB). This painful and life-limiting condition affects many major organs of the body, including skin, eyes, kidneys, gastrointestinal and urinary tracts, causing painful blistering, scarring and increased risk of skin cancer. We fund research on all of the four genetic types of EB and encourage applications from researchers working on EBS where there is an unmet need.
Download our research strategy
Our research funding is awarded through a rigorous process including experts by experience and scientific experts and is supported through our membership of the AMRC.
Applicants may also choose to attend our Applications Clinic to involve people living with EB in the design of their application.
Our key criteria will be:
We also co-fund research with other charity partners.