this heart broken

the story of Zoe Marie

This is the journey through our daughter’s Congenital Heart Defect and eventual heart transplant. When you “decide” to go down the transplant route as it is called there are certain things you find out after you sign on the dotted line.

Archive for August, 2006

Pssst! I’m going home tomorrow!!!

Thursday, August 31st, 2006

It’s true, me and the pink elephant are bustin’ out of Children’s on Friday evening. This could possibly slip to Saturday, but I’m crossing my fingers for tomorrow…
Zoe

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Day 20

Wednesday, August 30th, 2006

I finally got the laptop to log onto the wireless connection in our room so I should be able to post more frequent updates.
We’re starting the process towards going home. As exciting as that is it feels overwhelming at the same time. Going home this time makes last time seem like a cake […]

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This Ain’t Kansas

Thursday, August 24th, 2006

Well, on the 20th Zoe got released from ICU and sent down to the recovery floor. This means a nice room (with our own bathroom) but also that one of us has to be with her around the clock. It’s been a hectic four days…hence the lack of updates.
First, they discovered the first […]

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Scrubs Outside the Box

Wednesday, August 23rd, 2006

I know I need to provide an update on Zoe (she’s doing really great!), but I was inspired by an episode of Scrubs to step outside the box.
I remember the night we received the call from the transplant coordinator at Children’s Hospital… I was holding Zoe, Jenny was sitting in the crimson Puff Chair, […]

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No More Tube….at least until Monday

Friday, August 18th, 2006

Zoe got her breathing tube out this morning! She did really well overnight and so they took it out about 9:15 this morning. The amazing thing was that she wasn’t agitated at all before they got it out…she just got a little mad when they were taking the tape off her cheeks. […]

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Well, Jenny and I were so happy to see Zoe’s chest closed up, we forgot to post the good news yesterday afternoon. With all that went on today, we were a little sidetracked.
I have a picture of her from today, but I’m not quite sure if it’s suitable for the masses. If you […]

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Please help us mourn Alanah

Thursday, August 17th, 2006

I’ve thought about how to write this post, but I can’t really think where to start or end. I think the best thing to do is announce the sad reality, and let my emotions drive the bus. Last night, another family in the Cardiac ICU lost their 3 month old baby Alanah in […]

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Chest Closure Today

Wednesday, August 16th, 2006

Well, there is another lucky family getting a heart today, so we were moved back till approximately 3 for Zoe’s chest closure. However, the surgery scheduled for 1:30 PM was pushed back, so we’re moving up again!
I have to admit I was skeptical when Dr. Boucek told us we’d be able to close her […]

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Day 6

Tuesday, August 15th, 2006

It was a bizarre day today; up and then down. She’s still doing fantastic and the surgeon decided the plan will be to close her chest tomorrow at 1:30. Good stuff. As you read in the previous post, we were waiting to hear if Noah has the chickenpox. When we first thought […]

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Day 5

Monday, August 14th, 2006

More progress today…..During rounds this morning Dr. Permut (the other cardiac surgeon) further reduced her chest opening with tape……yes, you heard me. He crossed tape over the dressing on her opening to bring the sides closer together. I thought a “duct tape fixes everything” joke would have been appropriate. She also had […]

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