A very close family member of mine has been severally affected by the Mitochondrial disease, in its most extreme form. There is no cure for this disease which is for many, debilitating and life limiting. She is a strong, amazing inspiration to us all.

Please stand with us and fight Mitochondrial Disease and fight for hope!!!! xxx

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!