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.
Monday, June 9, 2014
Apparently everything is going "fine" and they "might be starting to wrap up soon." (All our information is relayed through the waiting room staff, so we don't get to ask for more details).