I am a Congenital Diaphragmatic Hernia (CDH) baby. My diaphragm developed with a hole in it and my organs were misplaced in my chest cavity. The organs pushed on my lungs, causing one lung to be very small. I was born on October 9, 2007 at Johns Hopkins. Now it is three years later: I am saying a bunch of words, I still receive foods through a g-tube and am on oxygen while I sleep. I can't walk yet, but believe I can out scoot anyone! Here is the story of my amazing and patient recovery.
Sunday, November 11, 2007
Wyatt eats for the first time!
Yum Yum!! says Wyatt after eating 13 cc's of breast milk every four hours through his NG tube (feeding tube that goes through his nose). At first he did not like it and spit the milk up. I don't think I would like food going down my nose either!!Then the nurses decided to vent his feeding tube and now he seems to keep most of it down. His stomach is probably smaller than normal since it grew in his chest cavity. The surgeons said that his organs are probably not in the proper places in his abdomen, so his stomach will have to adjust to food. Wyatt looked so comfortable today and his stats were great. I noticed that his respiratory rate is much lower along with his heart rate. He is not breathing as hard which is a great thing!! Wyatt also enjoyed having a visitors other than his parents. My neighbors, Heather and Janice were so sweet to visit, and my parents were able to hold him for the first time!
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