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!

Lilypie Fourth Birthday tickers
Lilypie Third Birthday tickers Lilypie Pregnancy tickers

New Website Question- please read previous post for more info.

Posted by Kathryn Olmstead / 5:58 PM /
If you would like your website left OUT of the website CDH Family- please email me at olmstead161@gmail.com.
Also if you could please put www.cdhfamily.com on your blog rolls...a lot of your followers don't necessarily follow Kayla's.
PLEASE SEND ME PICS OF YOUR LITTLE ONE THAT YOU WOULD WANT ON THIS WEBSITE- you can do before and after like I did- or just a pic of your little one that you like angels and all.

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