Owen was diagnosed with Congentital Hyperinsulinism at birth. He is a thriving, energetic, smart, ambitious three year old. At birth Owen's blood sugar level was a life threatening 21. He spent 3.5 weeks in the NICCU and was then flown to the Children's Hospital of Philadelphia where they are one of the only hospitals who specialize in Hyperinsulinism. As parents we were scared and devastated for our first born child to have sever health issues at birth, but hearing he had any disease with no known cure was heart wrenching. We are very thankful that Owen's form of Hyperinsulinism is managed by medicine, his Hyperinsulinsim was caught at birth so he did not suffer any brain damage or other side effects from low blood sugar, and he is believed to be outgrowing it!! We are doing this to help fund research for Congentital Hyperinsulinism, we do not want any other families to hear the words No Cure. We give all the glory to God for healing our Owen, and sending us the right doctors and research teams. We know his healing may not be right when we want it, but we are patiently waiting for His time!