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.
Friday, November 5, 2010
We dropped Magnus off in the cath lab a little before 9, and still haven't heard anything back. They said they'd call if they were going to do any interventions, so I guess we're hoping to hear from them soon.