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, April 16, 2008
In Surgery
Wyatt's G-J surgery just started. It's a little different this time. Instead of putting him to sleep through an IV, he was given gas. We were able to be with him during this process and tried to keep him calm. Also, his Anesthesiologist, Dr. Swartz was his doctor from the PICU while on ECMO, so she knows him very well and I feel good about that! The doctor who is doing the procedure is a radiologist who will insert the new tube through his intestine using an x-ray and the existing hole. Wyatt will be intubated during the process and hopefully will be extubated in the operating room. His recovery will be in the PICU on the 7th floor and then hopefully we can go home!!! Keep those prayers coming. Oh... and Wyatt wanted to come to the hospital and let everyone know it!!.... because his wound from ECMO on his neck is becoming irritated. A stitch is coming through and it's becoming red and puffy. His surgeon, Dr. Chandler was paged and she sent the wound nurse to look at it after he went to sleep. She said, it should be ok and that the stitch is dissoluble and Wyatt's body is trying to reject it. It's always something!!
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