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.
Still here, still alive and still kicking on less than 3 hours of sleep in 24. I l-o-v-e my job some days.
CHD Awareness - talking about insurance today (health, that is), and trying to find other families that have been deemed "uninsurable."
Labels: CHD Awareness
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