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, September 22, 2009
To my blog readers... you are the best!! Thank you for all the kind comments you have left over the past two years. It really is truly helpful and supportive. Some of you are family, friends, and even people I never met before. I couldn't ask for a better support network. I learn so much from what you have to say!! by the way... I also enjoy reading your blogs about your CDH kids and learn so much from them:)
Subscribe to:
Post Comments (Atom)
1 comment:
Ditto! I love reading Wyatt's updates and learn so much from him as well.
Post a Comment