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.
Sunday, June 28, 2009
Feeling better...
Wyatt is feeling a little better. It has been one full week since he has been home from the hospital and today is the first day he has not had any pain medication!! He seemed happy most of the day except if he wanted to take a nap. His stereo strips on his incision are falling off and it seems like it is healing nicely. I gave him a bird bath today (since we can not get the incision wet) and cleaned his g-tube really good. Good news... it looks like March 31st could possibly be declared National Diaphragmatic Hernia Day- Read Sofia's blog for more information!! Unfortunately someone has written some really bad stuff about March 31st being declared as CDH Awareness- check it out here . If you want to see how the CDH community is fighting back... just read the comments. I feel really sorry for the author Peregrin Wood. How could anyone be againist CDH awareness. Little research is done and half of all babies die from it. It happens in 1 in every 2,500 births a year and is just as common Spina Bifida and Cystic Fibrosis. Who would be againist creating more awareness??? only good would come of it by creating awareness.
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