Team Kaden his fight to beat CDH

Team Kaden his fight to beat CDH This is Kaden Jayce. Kaden was born with CDH. What is CDH? Congenital Diaphragmatic Hernia (CDH) This is the the Journey of Kaden Jayce Mosley. each year).

At 22 weeks Kaden was diagnosed with CDH. Congenital Diaphragmatic Hernia (CDH) occurs when the diaphragm fails to form or to close totally and an opening allows abdominal organs into the chest cavity. This inhibits lung growth. CDH occurs in approximately 1 in every 2,500 births (1,600 cases in the U.S. The diaphragm is formed in the first trimester of pregnancy and controls the lungs' ability to inhale and exhale. The cause of CDH is not yet known. CDH is different in each child, but overall little is known about it. In fact until Kaden was diagnosed with it I had never heard of it before. Since that time I have learned what a devastating issue it can be for families who have a child who has CDH. Many of these children live very short lives, others have life long medical issues. As his memaw I want to share his journey in hopes that others learn about CDH, by raising awareness more research can be done, and maybe one day we can find a cure our at least increase the odds for these sweet little CHERUBS.

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