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.
Monday, June 9, 2014
We're waiting for Magnus to wake up enough that his breathing tube can be removed. He's taking his time. He's having some issues with low blood pressure and his fingers & toes are cold & purple although his overall oxygen saturations are in the 90s. Despite all that, the atmosphere in here is pretty calm. The doctors are visiting less frequently and that's a good thing.