CAMDEN
Retrun to 22q StoriesYou are here
Camden, 4-month-old son of Michael and Rachael of central IL, was born with a rare chromosome defect known as 22q11 or DiGeorge Syndrome like many others here. Camden spent the first 6 weeks of his life at the Children’s Hospital at OSF in Peoria to determine the severity of his condition which includes a hole in his heart; also, he is unable to be fed by mouth because he aspirates so a feeding tube was surgically inserted in his stomach through which he gets his formula. Camden will undergo another surgery in October to correct his hypospadias. He is a happy little guy that never complains much and smiles a lot. He has the support of a great loving family and group of friends.
Latest News
Growing with Grace
Hi! My name is Gracie Chavez, I’m 25 years old, and I have 22q11.2 Deletion. Also, I have 5 siblings and I'm the youngest. I’m a dog mom and an aunt. I own a floral business, and I need to mention I'm a Lego lover!I became an intern because I...
Upcoming Event
Special Education Advocacy Training: Virtual
Do you have a child or student with 22q11.2 deletion syndrome? Do you want to gain insight into how these students learn best and identify stregnths and weaknesses that come with this diagnosis? We invite you to become an expert with us! Starting...