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, March 3, 2010
We just got the call: they're done and everything went well! They were able to do it without putting him on the bypass machine, too (more on that later). Gotta run...