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.
Thursday, May 21, 2015
Recovery
We're hanging out with Magnus in the recovery room. He's still fairly groggy from the anesthesia, but generally seems OK. He has to lie completely flat for 4 hours after the procedure to prevent bleeding where they put the catheter in. The goal is to get up and walk at 7:30 p.m.
Good luck with the “lying flat bit,” but I guess he’s got the hang of it by now.
ReplyDeleteThinking of you all.
ReplyDeleteHe's really grown since I last saw a picture of him. Taking on a resemblance of certain parents.
ReplyDeleteSorry, the news is not as good as it could be.
Good luck!
Cory G.