Every day in the UK a child is born who will develop mitochondrial disease. This genetic condition has limited treatments and no cure. It is life limiting and can be debilitating. Those living with it face enormous challenges and it has taken too many lives.The Lily foundation want to change this and offer hope to families across the UK by offering support and funding important research.I'm running 26.2 miles for them so please donate if you can and help me, help them make a difference. My friends Ben and Sophie Thomson, recently and tragically had to say goodbye to thier beautiful Boy Albie, I'm doing this in memory of Albie, in support of Ben and Soph, and for all those families effected by these cruel conditions.