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.
Tuesday, November 20, 2007
Eating more...
My sister is a gifted writer and she recently added a comment on the blog that was very touching. She said, "Wyatt, I really enjoy your blog. My past time is to start at the bottom and scroll up. It is proof of the miracle God performed on you. Given your strong fight for life, I can only imagine what you will be when you grow up." Wyatt is making a difference in this world already and we are so proud of him. Wyatt's feeds are now increased to 22 ml per hour. When we reach 28 ml per hour, he will reach his maximum feeds... we are almost there. He also had a CT scan of his head today and we will receive the report tomorrow. His daily head measurements have not changed and he is not having seizures... all good signs! Wyatt still has fluid, but is getting suctioned less. Because he is weaned off his narcotics, he his much more alert, so to keep him busy, we hold him, put him in his bouncy seat, and a swing. He loves looking around. I want to say thank you to my good friend from college, Laura came to visit Wyatt over the weekend.
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment