Some of you may already know that my lovely nephew, George, suffers with Epidermolysis Bullosa (EB). EB is the name for a group of rare, inherited skin disorders that cause the skin to blister and peel from even the slightest touch. This causes painful, open wounds, and can affect the internal organs. In the worst cases, EB can be fatal in infancy and, where it isn't, can still be significantly life-limiting. There is currently no cure. 

This video here is a great representation of what it's like to live with EB: https://youtu.be/bwuzaZPR9P0. 

DEBRA is the national charity supporting those directly affected by, and working with, Epidermolysis Bullosa (EB) – a potentially fatal skin condition that causes constant pain due to unstoppable internal and external blistering. DEBRA provides lifelong care and support to the entire EB community.Together we #FightEB and together we will beat EB.

I know that George wouldn't be the happy little boy he is today without the help of DEBRA, and your donation can help others like him. Just £115 can provide 6 months worth of support to someone suffering from EB. Please give generously and I'll repay your kindness with regular updates and a slew of sweaty photos of yours truly.