My Story

DEBRA charity 

My son Milo was born with epidermolysis bullosa simplex in 2021. The disease has no cure, is rare, complicated and causes much pain and suffering for those who have the condition. EB causes blistering of the skin with very little friction due to it been so fragile and spreads around the body causing extreme discomfort. 

Debra charity means a lot to me and my family. They help support family's and people with the condition while finding new medicines and treatments to battle pain management while doing vital research to help find a cure.

I'm blessed to have such a strong and supportive family in my life, and we do everything we can to support Milo with his condition. Milo battles EB daily and we understand the hardships/difficulties and mental toll it can take on the individual and caregivers. 

I will try to raise as much as I can for DEBRA. All funds go to towards research and making improvements in the lives affected by EB. My goal is to try an archive 1750 pounds. Every little helps 

Thank you for spending the time to read and for your generosity.