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, September 2, 2009
News Flash: Wyatt likes to EAT!!
As you may already know, Wyatt depends totally on g-tube feeds and just eats for enjoyment. He NEVER tolerated anything close to his mouth since bottle feeds were stopped at 5 weeks old due to the vocal cord paralysis. We try every day to feed him and our nurse Susan has him loving ice coffee from Starbucks, Ben and Jerry's ice cream, chocolate pudding, anything expensive, yummy, and bad for you:))) We love our nurse Susan because it worked!!! Wyatt is starting to love to eat. He looks forward to dinner time because that's when he gets a container of Yo Baby yogurt to eat by himself and make a complete mess and we are happy about that:)) Dinner has now turned into something enjoyable. For the past two years, Benji and I ate dinner in shifts while one person tended to Wyatt the other eats with Chloe. We originally all start out at the dinner table, but Wyatt always wants to do something different since he wasn't enjoying it. Now he loves it!! We all sit, take our time, and talk. A pleasant change:))
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4 comments:
Yay!!!!!!!!!!!!!!
Go Wyatt!!
What a huge hurdle to conquer. Yeah for family dinners. How exciting. Go Wyatt!! Let mommy feed you all the yummy foods, veggies can come later. :)
YAY Wyatt!!!
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