Kit’s story
by his mum, Micaella
My son was diagnosed with Junctional Epidermolysis Bullosa (JEB) when he was a newborn. When I gave birth, he had no skin on his hands and feet. At first, it did not sink in for me.
When the doctor came and explained what my son’s condition was, it made my heart break. But I told myself, I need to fight so that my son will fight also.
I hope that one day they find a cure for my baby’s condition and for all that have this painful disease.
