Tucker Scott born August 1st 2013 was diagnosed shortly after birth with HLH. A serious rare condition treated with chemotherapy,steroids and in most cases a bone marrow transplant. Baby Tucker has been in the hospital since he was born battling this terrible disease that his insurance will not cover. Baby Tucker was then recently transferred to Cincinnati Children's Hospital because they were more qualified for the care of this condition. Upon arrival of Cincinnati baby Tucker did not improve and conditions seemed to escalte and doctors were saying he was fighting off an infection. Unfortunately the infection attacked his brain liver and kidneys and Tuckers parents Jason and Leeann had to make a difficult decision. The doctors and Tuckers parents ultimately decided that nature taking its course was best. I regret and am deeply saddened to say that on August 30 2013 Baby Tucker passed. We are asking for any donations to help with medical costs and memorial arrangement. We are also hoping after you read this that you will spread the awareness for this terrible disease that claims the life of young and old. Most people are turned away when they have this cause its not easily diagnosed. The research on this disease is not federally funded so the treatment options are limited.