Speaking of which, since our last post Karsie has been doing quite well. She is handling the 2 hours on 1 hour off feeding well. She didn't have anymore spitups today, which is great. At least her stomach is getting a chance to digest and get hungry for an hour. She needs to know what that feels like (my humble opinion). I am very excited about her doing so well breast feeding for one very big reason. Once she is handling the condensed feeding on 1/2 hour on 2 1/2 hours off, they will try to get her to feed orally. I figure since she is doing so well already and getting much more than her hour's worth in one feed, once she is hungry and used to having a lot to digest, she will do okay on her oral feeding. At least that's what it seems. I'm not sure what would keep her in the NICU after she is feeding completely by mouth, so here's hoping.
Michelle also told me that they took her down on her O2 flow today to 200mL. That's just a tad lower than the 1/4 L. The only reason it's staying on at this point is by our request. We really want to give Karsie the best chance at feeding smoothly, and since she's just a click away from being off the nasal cannula anyway we figure what's the harm at this point?
I got in touch with another mom with an omphalocele baby today. She has commented on our blog before, so if you get a chance to read her blog (I hope she's okay with me saying this) go to Baylee and Blair's website. It is so very similar to our story and it was nice to be able to talk to her about some of the things we can expect with Karsie during her first year. Little Blair is just about 1 1/2 years old and has just had the surgery to close up her stomach, so she will need lots of prayer, but she is doing very well. Their family still needs lots of prayer for the two girls (and the mom), but it's wonderful to see the progress made.
Well, I guess I've blabbed enough. We'll probably put up another post tonight for an update (unless there isn't any news, which is very probable), but for now, take care.
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