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, January 15, 2008
The waiting game...
Wyatt had a nice day today. We are waiting to hear the plan. I talked to many of Wyatt's doctors today. Dr. Leften-Gref would like to wait about two more weeks for the swallow study and neurosurgery suggested that we wait for Wyatt's organs to heal more. Wyatt's soft spot on his head is still soft, but it's swollen and a little more firmer. So it sounds like we will be waiting for Wyatt to become healthier and stronger. I had a great day with him! Wyatt's nurse, Brandon was FANSTATIC!!! She stayed in his room for most of the day and tended to all his needs. She really cared about his comfort and we appreciate that soooooo much!!! I sent out an e-mail to our family and friends about visiting him while we are not there. If you like for me to send you the e-mail, just let me know.
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1 comment:
Wyatt is so cute! I'm so glad he's doing well. If you need to talk or have any questions, CHERUBS is here for you.
Dawn
CHERUBS - The Association of Congenital Diaphragmatic Hernia Research, Awareness and Support
Over 2000 CDH families and 150 CDH medical professionals, working together since 1995
http://www.cdhsupport.org
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