Monday, October 26, 2009
It's in the genes
Tuesday, September 22, 2009
Happy 1st Birthday!
Here are a couple of videos of her birthday cupcake. Please forgive the awful singing or mute your computer for the beginning of the first one. :) I split it into 2 parts so that it wouldn't get rejected.
Tuesday, February 3, 2009
We're Back!
Sunday, November 16, 2008
Day 57 - No Tubes!

Tuesday, October 28, 2008
Day 38 - Bad Daddy
Monday, October 13, 2008
Day 23 - Room With A View
Thursday, October 9, 2008
Day 19 - Big Girl Bed
She weighed in today at 2 lbs. 12 oz. and is getting 18ml with each feeding. 23ml is her max so if she gets to that point and is still tolerating her feedings well then they will remove her PICC Line and go only on her food. That could happen within the next few days. Oh yeah, she also graduated to a bigger pacifier which apparently she loves even though it is almost the same size as her face.
Oh, and Ryan wanted to say "Happy Halloween" to everyone too.
Saturday, October 4, 2008
Day 14 - Caption This!
Thursday, October 2, 2008
Day 12 - Ready for the Road
Wednesday, October 1, 2008
Day 11 - Say Cheese
I took a quick screen capture of Ryan's toes sitting on the end of my finger. As you can see, all five of them fit right there.
While I was visiting I was able to hold her for the first time. The nurse snapped a quick video of it for me.Thursday, September 25, 2008
Day 5 - Blue Light Special
Ryan got an upgrade today. The light that they've been using to help her with her jaundice got switched out for a newer, more high tech LED version. That's why the video looks kinda blue and her color looks a little odd.
She's doing great on the Bubble CPAP and is still getting antibiotics but they think that will only last a couple more days since all of her blood work is coming back good. Tomorrow she'll have a brain scan done which is a normal part of the routine in the NICU. Hopefully those results will come back normal. There's never a shortage of tests with potentially scary results but so far she's passed with flying colors so that takes some of the edge off.
On a lighter note, here are some observations from the NICU staff...
- She likes her pacifier
- She hates having her diaper changed
- According to the nurse, you can tell how feisty a baby is by how many pacifiers are in their bed. Ryan already has two in there so if my math is correct, she should have around 40 by the time she comes home.
- And finally, here is a comparison of a regular newborn diaper and the diapers Ryan is wearing right now.
Wednesday, September 24, 2008
Day 4 - Look Ma, No Chest Tube
Tuesday, September 23, 2008
Day 3 - Meet your Mommy
They didn't take the breathing tube out today but they will tomorrow if she does okay overnight. Apparently preemies can get a little too comfortable and forget to breathe so right now the tube is just adding a breath in if she skips one. The technology is amazing. She's mostly breathing on her own though and she's getting no supplemental oxygen, just what you'd get with normal room air. She's also off the dopamine which they had been using to regulate her blood pressure. Once she's breathing okay their attention turns to the heart to make sure that the Ductus Arteriosis closes off. If it doesn't, they will give her medication to try and get it to close. If that doesn't work they have to do surgery to clip it and tie it off . Her doctor said that hers is very small right now so she hopes it will take care of itself. Oh, and sorry Nanna Jones, no red hair under that hat...
Monday, September 22, 2008
Day 2 - Size


