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.
Friday, March 5, 2010
Still on
I called in to the hospital about a half hour ago, and they said that Magnus had a good night, and that the plan is still to do a spontaneous breathing trial around 6 or 6:30, and if that goes well, to extubate around 7.
Sounds good! Thanks for keeping us posted.
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