Jaxon was born Sept. 05 2014 @25weeks. He weighed 1"14oz. He was born with a very common but severe chronic lung disease. He needs constant assistance from a high flow camula to breath normally. As well as hypertension and coronary artery disease. Hes our little SuperMan. Jaxon was due Dec. 18th and is making miracles happen everyday but for now and the years to come will need constant support and medical attention. The long hours and constant back in forth have taken its toll on our family in everyway possible. The fiancial burden has overwhelmed us like we could have never imagined and were still in the early stages of our baby boys journey. Jaxon has sufficient medical coverage for most of his needs but certain vitamins special dietary needs and breathing equipment etc... Unfortunately falls upon us. We are reaching out to our family, friends and community for any kind of financial support they can help us with. Jaxon is still in the NICU at Winnie Palmer Hospital in Orlando Florida and at this time we are beginning the discharge process to have him home we hope by the end of January 2015. Thank you for anything and everything you can spare to help us out getting baby Jaxon home and happy with his Mom and Dad. God bless.