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.
Wednesday, September 3, 2008
A good day...
I am sitting by Wyatt's bedside now and he finally fell asleep after being awake since 6am!! He doesn't want to miss anything! I worked today and Benji stayed by Wyatt's bedside and I arrived after work with Chloe to do the kid switch-a-roo and for the night shift. My kids are great! Chloe is so happy to drive an hour to Hopkins, spend 30 min visiting her brother, and then drive an hour home. She is only two and stays in such a good mood during these long car rides. Today Wyatt had his head CT scan, ultrasound, and a new g-tube. We were also moved from the IMC to down the hall (a room across from the nurses station). Tomorrow we will have a consult with the pulmonary docs to see how we can get some of his fluid out of his lungs. I heard the "H" word today... but I am not saying it aloud until it actually happens:) He is up to 35ml of Elacare.. just a few short of his goal and seems to be tolerating it nicely.
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