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 27, 2009
Just called the hospital, and they're getting ready to close his chest right now. The nurse said she thought it would be done in the next half hour or so. She said he had a really good night and his blood pressure and heart rate are still looking good. I have a few errands that desperately need to be run this morning, but plan to get over to the hospital as soon as I can to see him!