The wonderful Sophie has recently been diagnosed with a mitochondrial disease after a year of numerous hospital appointments and investigations. The Lily Foundation has been of tremendous support to her family through this difficult time and I want to help make a difference to Sophie and all the others effected by this disease. Everyday in the UK a child is born who will develop mito, no treatment no cure. This needs to change. Together we can make a difference and hopefully one day find a cure for this debilitating disease. Please donate as much as you can. Thank You