This page will have updates and photos regarding his condition etc. This also aided in providing information on how others could assist us in the costs incurred during his fetal surgery, bed rest and delivery. Now it's a centralized location that everyone can stay up-to-date on his development and health. He was given a huge step-up in life by undergoing the fetal surgery but he does have and always will have Spina Bifida. He will do great things with his life and we ALL will be here to watch him do it!! Adam John Luke is a feisty, strong willed, determined two year old little boy with beautiful brown eyes and blonde hair. Adam's form of Spina Bifida is called myelomeningocele in which the spinal cord and nerves develop outside of the body and are contained in a fluid-filled sac that is visible outside of the back area. To provide Adam with the best odds in his favor, we flew up to Philadelphia and underwent fetal surgery at Children's Hopsital of Philadelphia at the 26th week of his gestatation to close his spinal cord opening. He was later delivered via C-section at 37 weeks gestation on October 18, 2011. Adam's hind brain herniation reversed because of the fetal surgery closure and he has not required a shunt to be placed into his brain to reduce hydrocephalus. Although Adam does show stress incontinence with his bowel and bladder, he has been fortunate to not require catheterization to empty his bladder. Adam has weakness/paralysis from his ankles down and his left hip dislocates but he doesn't let it stop him. He wears Ankle Foot Orthotics (AFOs) and a month ago began using Twister Cables to help keep his feet straight when walking. He walks with a posterior walker in sprints and is growing stronger daily. We have hopes that he will be independently walking with his walker soon. His orthopedic foresees him being able to walk with arm crutches by preK or sooner. Adam has defied odds, proven medical professionals wrong and surpassed many expectations & I am truly blessed to have received this gift from God.