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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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2014
(61)
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June
(41)
- Home
- It's official
- ???
- You guys are still here?
- Womp womp
- Ugh, probably not today
- Fingers crossed
- Closer to home
- Out of the ICU
- What day is it?
- Day 10
- Day 9
- Day 8
- Corner turned
- Good day
- Quiet afternoon
- In surgery now
- Bumped
- Surgery day again
- Plication is on
- Day 4 post-op
- Some progress
- Blurgh
- New plan
- Morning update
- Much better day
- Feisty
- Long night
- Post-op Day 1
- Steps forward, steps back
- Morning update
- Sleeping
- They're finally done!
- Another update
- OR update
- Still waiting
- So now we wait
- First case tomorrow
- The preparations begin
- 10-11!
- Cath day again
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June
(41)
If I could find a quick way to escape my job tomorrow and drive down there to hang with you and Magnus, I would. I will do my best at scheming. In the meantime, know that there's a huge swell of collective support out here in the cybersphere, rooting for you and Magnus to get the green light and fly the coop soon!
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