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.
Tuesday, November 24, 2009
Just a quick note to let everyone know that Magnus went in for his surgery as scheduled. The team said that they will NOT be calling with any updates. We will be heading to the waiting room at around 1 p.m., as they told us that that was the absolute earliest we could expect them to be done, but it could be significantly later when we hear anything. They said they have wireless there and I'm bringing my laptop, so I'll do my best to update the blog as quickly as possible when we hear.