On Sept. 4, 2006, Madeline "Sadie" entered the world with a congenital heart defect known as TGA. This blog began as a way to chronicle Sadie's struggles and triumphs, her sister Katie’s adjustments and our reactions. But it turned into something else - a way to reconnect, to spread CHD awareness and to vent about parenting, work and daily life. Now that I've started blogging, I can't seem to stop - I enjoy writing here, and it keeps me slightly more sane. Slightly.
I thought I'd throw a few photos up now that we're back home!
The PICU room Sadie was in for over two weeks.
Sadie, post surgery (9/17/06. Surgery was 9/15.)
First time I held Sadie, on the day her vent was removed (9/21). Katie's showing her the picture she made for her that day.
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