Epidermolysis Bullosa (EB) is a rare and painful genetic condition which causes the skin to blister. I have several family members who suffer with this, luckily they have it mildly and it mostly just affects their hands and feet. Even so, it has changed the way they live their life daily and restricted them from doing certain things. I want to raise awareness and money for the people who have been affected by EB in any way.

DEBRA UK has faced one of its toughest years in its history, but with your help they have been able to continue to provide vital services to the EB Community. Please help support my challenge so that an EB diagnosis doesn't have to mean a lifetime of pain and no one has to face EB alone.£126 could provide someone with EB access to vital community support and membership services - really making a difference to people's quality of life. #FightEBDEBRA are the only charity supporting the EB Community through grants to help members get access to food supplies, assisting with other financial issues, securing dressing supplies and supporting mental health and wellbeing. We have been able to adapt our services to help combat key issues of loneliness and anxiety, through new virtual support groups run by our crucial Support Team.