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.
Saturday, February 9, 2008
No more oxygen!!
I never thought this day would arrive, but it did.... Wyatt is off oxygen and is doing just fine!!! When Wyatt was born, we would not have survived with out oxygen. He endured ECMO, ocillator, ventalator, CPAP, Oxygen, and now... NOTHING!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! One less tube. Well, it looks like we have a plan. We will be seeing our surgeon, Dr. Abduallah in two weeks in clinic and then possible G-tube surgery. The G-tube surgery is scheduled, just in case we do it. It looks like he will get a G-tube and this will get him home faster!! Today, I worked, so my Dad spent the day with Wyatt, then after work, I played with Chloe until bedtime, put her to bed, and then went to the hospital to play with Wyatt, and then came home to blog... just call me supermom!!! No, actually my mom is supermom--- she watches Chloe, cleans my house, spends time with Wyatt, made dinner for us tonight, does our laundry, and she even works full time (actually more than 40 hrs a week)!!! She is supermom!!
Subscribe to:
Post Comments (Atom)
1 comment:
Gina and Gina's Mom,
Like I've said before, it's genetic! You are both super! And you have a super strong son and grandson! I pray not just for Wyatt but for the strength of the women who are loving and supporting him and the families around him.
PatV.
Post a Comment