My beautiful daughter Sophie suffers from mitochondrial disease which means she has very little energy and struggles with everyday activities that you and I may take for granted. Sophie is a real inspiration and has an amazingly positive attitude and sunny nature.

Please take a look at the Lily Foundation website to understand the condition and learn about all the research that is being funded to try and improve the lives of children and young adults and the support that is provided for many families .

Please donate as generously as you can.

THANK YOU !!!!!

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.