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, May 21, 2015
We're hanging out with Magnus in the recovery room. He's still fairly groggy from the anesthesia, but generally seems OK. He has to lie completely flat for 4 hours after the procedure to prevent bleeding where they put the catheter in. The goal is to get up and walk at 7:30 p.m.