Our son Magnus was born November 19, 2009 with a serious congenital heart defect, HLHS. I set up this blog to keep our family and friends updated on his condition, and to connect with other families dealing with HLHS.
Thursday, March 4, 2010
6 a.m.
...is the new ETA for Magnus's extubation. He's still doing fine and making progress, they just want to get a little more fluid off him before they extubate. I'm spending the night at home, and plan to be back at the hospital for 6.
Thinking of you. Good to hear Magnus is making progress. Sweet dreams. Hope you're all home together very soon.
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