Kaydens Medical Expenses

Kayden Lane was born with cleidocranial dysplasia…A rare genetic diseases affecting one in one million people. On top of this diagnosis he has micrognathia. These together affect his ability to eat and breathe. Because this disease is so rare doctors aren’t sure why his body is doing some of the things it’s doing, such as storing carbon dioxide instead of releasing it. You can call our little champ a “medical mystery.” He’s going on 30+ days in neonatal intensive care unit in Chicago, IL with no idea as to when he’ll be home. We try to stay with him as often as possible but bills and all the back and forth is going to start to add up. Anything helps. Even just a prayer or a share.