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.
Sunday, March 7, 2010
Just got a chance to talk to one of the docs, and it looks like Magnus is on track to go home Tuesday or Wednesday! Basically he just needs to continue to do OK and to show them that he can eat well. He said the only two things that might slow him down at this point were a fever or collecting fluid around the lungs, and he said that both of these are unlikely.