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6 years ago
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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.
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CHD Friends
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Facebook Updates9 years ago
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Whatever happened to 3620 Clifton Avenue?10 years ago
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Mother of the Year11 years ago
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Day Six post Fontan12 years ago
Good things
HLHS links
Blog Archive
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2010
(86)
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March
(29)
- Post-Glenn
- Life at home
- Going home!
- Bloodwork looks good!
- Waiting to hear
- So far, so good
- 48 hours
- Testing, testing
- Morning update
- Progress report
- Up and down
- Exit strategy, take two
- Low sats
- Update
- Exit strategy
- Tubes are out!
- The plan
- Destroyer of lines
- Extubated!
- Still moving slowly
- Still on
- 6 a.m.
- Still waiting
- More of the same
- Roadbump Number One
- They're done!
- Good omens
- It's on!
- Appointment day
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March
(29)
Oh Jen, I'm so happy for all of you and so glad to hear that Magnus is feeling good. Wish we could be there to hold him and give him a big hug and kiss.
ReplyDeleteI'm with grandma - I wish I could be there to welcome you all home! I am so so so happy for you and Iggy and especially Magnus!! Way to go, Magnus the Mighty!
ReplyDeleteWoohoo!
ReplyDeleteExcellent!
ReplyDeleteNancy
Yay! Best Saturday morning news ever!
ReplyDeleteOh I just read the comments and realized I said "feeling good." My perfectionist side would like to correct that to "feeling well."
ReplyDeleteCan't wait to see him on Skype. Send videos whenever you can. We live for those.