Kayla Mae Olmstead

Kayla was born with Left-sided Congenital Diaphragmatic Hernia (LCDH). When she was born she was in the NICU for a total of 55 days. She reherniated two years later, had her repair surgery in May 2011 and spent 11 days in hospital recovering. She is a tough little girl and we are truly blessed to have her here.

I'm Growing, I'm Growing!

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But we...

Posted by Kathryn Olmstead / 7:48 AM /
still got to go home!!! Yay!!! Dr said to keep her on small meals, keep away from fatty foods... problem is K doesn't like much else.. :) But we'll do it just to keep her from barfing!!!

So here's what we think triggered her barf the night before-
she shoveled it in!! didn't eat it all, but more than K usually eats on a healthy day!


We did have a great last day though....
snuggled with "curious george" 


played with Charlie- she LOVES Charlie!! <3

and Charlie LOVES her too!! <3

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1 comments:

Danielle said...

I am so glad you are finally home! I hope the days ahead go smoothly without much stress.
Take care,
Danielle

May 24, 2011 at 12:35 PM

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