As most of you may know my son Finn was born with a very rare genetic disorder. Thanks to the constant drive and determination of The Lily Foundation we now have a diagnosis for Finn. Whilst it wont dramatically change his life, it will allow us to keep pushing the boundaries of the medical professional to see what improvements can be made in the future.

The Lily Foundation was founded in Lily's memory, having lost her battle to Mitochondrial Disease at just eight months old. The charity aims to give hope, answers and support to the many other children and families that face the challenges of this disease today. Did you know every twenty minutes a child is born who will develop Mitochondrial Disease by the age of 16! There is no cure for this disease which is for many, debilitating and life limiting.

Please stand with us and fight Mitochondrial Disease and fight for hope.

Please support our 2017 London Marathon Team and together we will make a difference.

Kieran & Gareth