If noone has ever heard of CDH it stands for Congenital Diaphragmatic Hernia. This is a birth defect that ca be treatable but is more times than not fatal to the infants born with it. I am writing this strictly because recently my life has ben affected by CDH. A very close friend new that her daughter would be born with CDH, they would take her directly from the womb to a Children's hospital where they would perform surgery to try and prevent further damage and to fix what had already been done. due to the difficulties from two surgeries her 17 day old daughter lost her fight with CDH. The website of Breath of Hope Inc. is www.breathofhopeinc.com for those who would like to help support research on this and find out more about it. I feel it is very important to shatre this with everyone I can as it was a deeply saddened time for my friend and her family after spending 17v days at the hospital with her daughter to only get to hold her once as she lay in her arms and took her last breath, mty friends life was changed forever. Shatring this story with millions could possibly change the future of this defect and hopefully help support finding a better way to change it!
