Scott has decided to take the Leap for Lily in honour of our nephew Fletcher who lives with mito. Seeing the affects this has on him have been heartbreaking but it doesn't stop him from doing anything he wants to do! he is our little superhero!

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.