It was like deja vu, having to rush in to the hospital with her wearing basically pajamas and not knowing what was wrong with our baby. I cried a lot for a few hours. Then eventually they said she was doing well enough that she could go straight to a room on the regular unit, and not have to go to the ICU. So that afternoon we went up to the regular floor and they took her off oxygen since she seemed to be doing better. They also let me start nursing her which definitely made me and her feel better. This was about 2pm and she hadn't eaten since 7am that morning -- she had only had the IV since about 9:15am. I think when we got to the regular room and they took her off oxygen and I was able to feed her I calmed down a ton and just prepared to stay. Wesley went home and let our dog out and got us some clothes and toiletries.
What was cool (if you can call anything about that situation cool) is that the floor we were on at the hospital is the same floor she'll be going to after her surgery to recover. It's the "neurological" floor they called it. She will have the same nurses and a similar room. It was really good to know that. I have to say, I HATE going to the hospital with Lucy, but I cannot say enough good things about Children's at Egleston and their doctors and nurses. They are so supportive and so perfect to work with kids and their parents. One nurse hugged me in the E.R. and all the other doctors and nurses make sure to ask if you understand everything that's going on and they know it's frightening and they just try to make it better. Like letting me hold Lucy while they transported us everywhere instead of just making her lay alone on the bed.
The only test they were waiting on was the EEG, which I guess can't be done on the weekends unless it's an extreme emergency. So we knew it would be Monday before we could have that done, but we were hoping we could come home and then go back to do it outpatient. But the doctors said they wanted to keep her in the hospital through Monday just to be sure nothing happened again since they said if it was going to happen again, the greatest chance would be within 24-48 hours after the original incident. So we were stuck there until Monday afternoon. But I have to thank our friends Drew and Diane (and little Anna!), and Jeri, and Sarah and Jarrett for coming to visit us. It definitely made things easier and just less boring and overwhelming. I'm sure visiting a hospital on the weekend isn't their idea of a fun thing, so we really appreciate it.
Lucy slept great both nights and the only thing that bothered her was this hard splint on one arm to keep the I.V. in and the fact that the nurses and doctors were always in and out at odd times checking her out and getting her vitals. Wesley went home both nights to sleep since there was only one pull-out couch bed in the room. (I'm guessing this will be what happens when she is recovering from her surgery, too.)
So the end of the story is that we just don't know what happened. Nothing showed up -- everything was normal. They are making her wear an apnea monitor for about 2 weeks 24 hours a day (except for bathtime) and then for about a week just when she's napping/sleeping/in the car seat. It's just a band that goes around her chest that has electrodes in it that measure her heart rate and her breathing. It's really annoying because it has to be plugged in as much as possible so wherever we go, even from room to room, I have to carry the big pack around and all the wires, etc. The wires are always getting tangled up in her legs, too! But it gives me some peace of mind knowing that God forbid, if something should happen in the next few weeks, the monitor would let us know immediately. I'm hoping nothing will happen and nothing will show up!
They also made us take an infant CPR class yesterday before going home. It was really good for Wesley and I to learn about how to do CPR on Lucy should we ever need to. It just gives me confidence that we at least know what we're doing but I hope we never need to use it!
So we're back at home and just enjoying all that means ... our own beds and homecooked food and only a few wires attached instead of lots of wires. I'll be glad when we can take the monitor off, too!
Another good thing is that we thought we didn't know her blood type, but while we were there I asked about it again and they looked in her records from her previous hospital visit and the blood type was there: O+! So now we know and we can find people to donate since neither Wesley or I are a match (B+ and A+ respectively). But we know Lucy's Gigi is a match and we have lots of O- volunteers, too, which is a blood type she can receive.
So, you know, just another eventful weekend in the Fielding household! Looking forward to this weekend and all it's boringness! :)
Lucy in the hospital -- everyone remarked on how happy she was and how friendly she seemed to be. :) Our little sunshine.
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Wires: the fall's hottest baby accessory.
Gosh, that's more like a big scare! I'm so glad that ya'll are home now, and Lucy is doing so well! We had to take the infant CPR too, which made me really nervous! Hopefully there will be no need to use it!
ReplyDeleteI'm so glad to hear that she's ok! No facebook = no updates on Lucy!
ReplyDeleteOops! Forgot I was signed in as Jacob. Well, we're both glad Lucy's home :)
ReplyDeleteErin,
ReplyDeleteI really don't even have any words. I just love you guys. All three of you and I am so glad that Lucy is home safe and sound. So many people are praying for her. Us included. She really is a little sunshine isn't she?
Kelsey