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.
Wednesday, June 1, 2011
Iggy just called up and they're finished in the cath lab. We're going to meet up with the head cath Dr. in about 15 minutes to discuss how things went and where we go from here. I may not be able to update for a while, though, because hopefully after that we'll get to go to recovery and see Magnus.