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, March 5, 2010
Still moving slowly
When I got to the hospital around 6 a.m., they had started the spontaneous breathing trial and he was doing fine, but then the attending physician showed up and I guess she was mad because they had started the trial without her being here. So, even though he was doing fine, they turned the vent back on. They just turned it down again a little while ago, but it's still on, just at a lower setting. Magnus is sleeping and seems pretty comfortable, so I'm just sitting here catching up on some work and waiting, waiting, waiting...