A few years ago our friend's daughter was diagnosed with Leigh's Disease. Leigh’s disease is a form of rare, inherited neurometabolic disorder that affects a person’s central nervous system. The disorder is progressive and starts in infancy between the ages of three months and two years. On rare occasion, Leigh’s disease can occur in either adolescents or adults. While there is no cure for this disease, there are different therapies and wholistic approaches that insurance companies won't cover. A group of high school friends got together to hold fund raisers in 2011 and 2012. These events were extremely successful and we'd like to keep that ball rolling. Please help us raise additional funds to help Diana continue with a quality of life that every little girl deserves.