The latest...
8 years ago
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.
Hoping for no chest tubes soon! Go, Magnus!
ReplyDeleteWow, that's great news!
ReplyDeleteI remember it took Josh longer than I expected for him to smile again...it really worried me, but other moms I talked to said the same. So don't let that get you down, even though it's tough seeing them unhappy. It seems like it's the norm for them to go several days with out any signs of their old self. But believe me, it won't be long before he's amazing you with his new found energy (and weight gain etc. etc.:)!
Glad to hear of progress! Yay!
ReplyDeleteYes! Go, Magnus!
ReplyDeleteThanks for all of the updates in the midst of all this action, Jen, and I'm glad things are continuing to go well.
ReplyDeleteyay magnus!
ReplyDeleteChest tubes are really, really hard. It should be a lot easier for him when they're out. Go Magnus!
ReplyDeleteGlad to hear this! I will report back to everyone at Weetacon on this exciting development!! Yay!!!
ReplyDeleteWay to go Magnus!! Thank you for taking the time away to update us, Jen. Looking forward to more good news soon!
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