This blog is about the journey of our son Micah and his battle with lymphatic malformation (sometimes called cystic hygroma). He is the light of our lives!
Tuesday, August 30, 2011
Home!
We got home yesterday about 4pm.
We go back Thursday, LOL. So goes the life. He's going to the OR to get his stitches out, get his drain replaced and get an airway scope.
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