Cody is a 13 year old with so much humour, wit and heart. We are fundraising for The Little Miss Hannah Foundation. Cody was born with a rare genetic disorder Gaucher's Disease. Up until two years ago we were told he had type 1. Our worst nightmare came to reality and we were told he had Gaucher's Disease Type 3,no treatment and no cure!! He suffers with epilepsy,ataxia,tremor and has lost his ability to walk independently. This race is for us to bring awareness to this horrible life limiting and life threatening disease. He faces every day with hope and a smile. He is a fighter!!! He plans on walking across the finish line!!! Help us raise money for this amazing foundation.