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.
Wednesday, March 3, 2010
They're done!
We just got the call: they're done and everything went well! They were able to do it without putting him on the bypass machine, too (more on that later). Gotta run...
Thank goodness. Can't wait to hear more details and to get your up close and personal report on how he's doing. Thanks for the update. Now we can breathe a little easier.
Time to do a happy dance! I'm elated at the good news. So glad this major step is behind you and even better that he didn't need the bypass machine. SMILE! Go Magnus!
Great to hear!! (Understatement.) We love you guys!
ReplyDeleteThank goodness. Can't wait to hear more details and to get your up close and personal report on how he's doing. Thanks for the update. Now we can breathe a little easier.
ReplyDeleteWay to go Magnus! I can't wait to hear about the surgery, Jen. No bypass? This oughta be good!
ReplyDeleteYAY!!! So, so glad to hear!
ReplyDeleteYay!! Go Magnus!
ReplyDeleteGood to hear!!! He's gonna recover in no time:) I'll bet he looks pinker!
ReplyDeleteHow wonderful what today's doctors can accomplish. Best wishes to Magnus and his family.
ReplyDeleteTime to do a happy dance! I'm elated at the good news. So glad this major step is behind you and even better that he didn't need the bypass machine. SMILE! Go Magnus!
ReplyDeleteWhew! We expected no less. You've got yourselves one tough little guy! Onward and upward!
ReplyDeleteNancy
just learned about mister Magnus via my friend Clare-- sending you energy and am very happy to hear your great news! go Magnus, go!!
ReplyDeleteJulia in GA
Great news! Way to go Magnus!
ReplyDeleteRachel B