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.

Our good friends Mark and Ruth have three daughters Maya, Ivy and Willow.  Ivy is now eleven years old and she was diagnosed with Mitochondrial Disease when she was only ten months old.  Please read Ivy's story, here is the link.

http://www.thelilyfoundation.org.uk/about-us-2/your-stories/11+ivy-gage/

Over the years we have seen how incredibly supportive The Lily Foundation has been to them and we're so pleased to have this opportunity to contribute to this amazing charity.  For more information about the Lily Foundation, here is the link.

http://www.thelilyfoundation.org.uk/

Thank you very much for your support!

The J Team (Johnny, Jonathan, JD)  Part III/VII