It has been almost 10 years since we lost our Em to mitochondrial disease. Never a day goes by where she is not in our thoughts and hearts.

This fundraising page has been set up to raise a further £10,000 for the Lily Foundation, in remembrance of Emily and our continued support of the charity.

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.