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, March 18, 2008
Wear Turquoise on March 31st
It's CDH Awareness Day on March 31st and my friend Vicki made Wyatt this cool bib that says that I am a Johns Hopkins CDH and ECMO Survivor... it's so nice, that I don't want him to spit up on it!! She also made me a T-shirt and sent an iron-on for Chloe. Thank you Jack's mom!!
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Wyatt cannot possibly look any happier....well, at least no more than Mommy and Daddy!!! Great pictures Gina...I think of all of you everyday and thank you for my CDH ribbon...I have it on my jacket and it reminds me everytime I look at it how heroic these babies are and the struggles that their families have had to face.
Make sure you take lots of pictures after the *bunny* visits!!!!!
Hugs and love,
Karen :)
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