Carly now weighs 6.1 pounds. All of the nurses that have cared for her all comment on how huge she looks compared to when they last saw her. As you can see from the picture above, she is totally off oxygen now and is breathing room air beautifully! Her hematocrit was low yesterday, so they gave her a blood transfusion last night so she'd be all prepped and ready for surgery today. In the "take down" surgery they will be removing her jejunostomy and connecting her remaining small intestine to her large intestine so she'll be able to finally start pooping out of her bottom like a big girl.
We came across this hat in the NICU that says "Gastroschisis Baby - Some Assembly Required" that I thought was the most adorable thing ever. Carly's little body has taken quite a bit of "assembly" but we have been so amazed at how well she has progressed and how wonderfully she is doing. Prayers most definitely are being answered.
Carly has started to bottle feed and I've been able to feed her several times. They only give her 5mL in the bottle, which is only about a teaspoon, but she is doing so great with it. After her surgery, they won't feed her any breast milk for about a week to give her intestines a chance to heal, but then they'll start her feedings back up again.
Carly's current feeding plan.
Favorite quote this week:
"Always remember that your present situation is not your final destination. The best is yet to come."
Life rules.