Facebook Page: Super Noah Facebook Page VIDEO: Watch My Story
“If everyone could give just $1, we can change the course of this families life” -The McClures
Four month old Noah Jacob Walker was born on January 27th, 2018. “Super Noah” as his family affectionately calls him was born with Down Syndrome, Atrioventricular Canal (Heart) Defect, Multicystic Kidney Disease, Pulmonary Hypertension and Obstructive Sleep Apnea. He stole his parents’ hearts as well as many of his Instagram followers with his adorable personality and courageous attitude. At three months old, he underwent heart surgery to repair large hole in his heart. Doctors informed his parents that a second heart surgery would be necessary in two months in order to repair another hole located in his pulmonary valve. This repair will assist Noah with his breathing and overall quality of life. Noah’s parents are doing their best to provide all the necessities that he needs. They recently had him fitted for a cranial doc to repair the shape of his head which is due to his condition. This cranial doc also known as a “helmet” would cost them $2,200 and it is not covered by his medical insurance because it is considered cosmetic. Noah also requires 24-hour care that his parents cannot provide due to physical and financial limitations. Noah’s medical insurance provider has denied coverage for a home nurse which surprised the doctors. Noah’s dad has closed his moving company and sold the assets to have the time and money necessary to care for Noah. His mom is trying to balance her small business while still trying her best to be there for Noah. It is extremely difficult to earn a living when you are in a hospital by your child’s bedside for weeks at a time. His mother's name is Yamileth Johnson and his father's name is Daniel Walker.