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.

This is a charity close to our hearts as my beautiful step daughter Maddy suffers with Mitochondrial and as a result of this cruel disease is severely sight impaired. She is such a brave little girl and despite everything she endures, Maddy always has a smile on her face and is an inspiration to us all.

I have signed up to run/walk/cycle 200km by 22nd September - her Daddy's birthday! Ultimately I will keep on going until 22nd September and clock up as many miles as I can!

Please support me and raise money for the wonderful Lily Foundation. Every little helps and I truly appreciate any donation. 

Thank you xx