This picture was taken on Friday, 9 days post op.
That thing on her head is called CPAP and she hates it almost as much as the ventilator. It's still helping her breathe a lot.
A lot of people have asked us when we'll be going home. The truth is, I have absolutely no idea. We don't know when her next surgery is going to be. They are starting to lead us to believe it will be a few more months. We don't know if they are going to keep her here as long as she's in heart failure. If so, we'll probably be here awhile still.