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.
Monday, March 31, 2008
Happy CDH Awareness Day!
Today was CDH Awareness Day. Jack's mom hosted a blood drive in honor of Jack in Frederick. After work I traveled to Frederick to give blood. As Vicki and I donated blood, we were saying that our little boys endured so much compared to this. They are tough little fighters that gave everything they had to survive. Wow!! we are so proud of them. Baby Sofia and Baby Ned's blog has two great CDH Awareness Day stories. The above photo is a picture of the CDH moms. Jack's mom and Andrew's mom are standing next to me. Andrew was born at Hopkins after Wyatt and Jack at 32 weeks with CDH and survived for just a couple of days. We are always thinking about Baby Andrew and their family.
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2 comments:
Hi Gina. It was so great to see you today. I can't wait for the boys to meet soon!
Love
Vic
Hi Gina...
Wyatt continues to look happier and happier...and Chloe has truly taken on the "big sister" role and looks to be doing a marvelous job!!!
I proudly wear my CDH ribbon...thank you so much for thinking of me.
Always in my thoughts and heart...
Karen :)
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