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
The OR called the waiting room around noon to say that everything was going fine. We just took a tour of the ICU where he'll go after surgery and briefly met our nurse and social worker.