In this weeks episode we talk to one family who is on a mission to find a cure for their boy Michael.  He was diagnosed a hereditary spastic paraplegia type 50, otherwise known as SPG50. Children afflicted with this genetic disorder present with a variety of symptoms, including global developmental delay, microcephaly, seizures, malformation of the brain, and hypotonia. What would it take to find a cure for your childs rare disease?  I talk to Terry, Michaels father and we speak about the process for raising money, hiring a team and what this entails.  Would you give up a good chunk of your life, your money, and even your career to find a cure for your child?  What if the cure never comes?