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 7, 2014
Well, we're here at the hospital. So far, Magnus has been having a great time charming the nurses and playing with the toys Child Life brought him. Apparently the first case in the cath lab started late, so I'm assuming that means we'll start late, too. In about half an hour, they're going to place his IV, so they just put some numbing cream on him. The last few times he's had IVs or blood draws, he's been very stoic about it, so hopefully that will still be the case.