They told us when she went in that we would probably be in the ICU for about 4-7 days depending on how things went. This picture to the left was her after the surgery. She was pretty much out of it and on pain meds the first day. The epidural cracked during surgery so they had to take that out and give it to her based on her pain. The first night was a tough one as she kept waking up and feeling like she was going to throw up.
This is a picture of her the first night. This was taken right after one of her episodes. The nurses were great in helping my husband and I. Thankfully my husbands mom came and stayed with the other three kids at home the first night. So we could both be there for her.
Day Two
Wednesday was the surgery, Thursday was the day the therapy dogs came. As you can tell she is still kind of out of it, but before she went in she was hoping to see the therapy dogs. So, with the nurses help we got her in a chair for when they came around. My sister, Kristyn, flew in from Texas (with the help of one of my neighbors, which I will be forever grateful). She is a nurse, so it was great having her here. Since she was able to get out of the bed, with help, they decided that we should try and get her to go to the bathroom on her own. With the chest tube, this became quite difficult, but needed to get her out of there. When the therapy dogs came around she was "excited", and by excited I mean woke up, to see them. It was great because we needed her to start moving her arm, because she didn't want to and it was becoming stiff. So we made her reach out to touch the dog. As you can tell in this picture she really just wants to use her good arm. She was not too happy about trying the other. I understand, but this program was a great help! This was part of the Child Life program, which I will blog about another time and put the link on here. It is a great program and without it I think it would take children longer to recover.
Kiley enjoyed having the siblings with her during her stay. Later on that day she started sitting up more and watched a movie with her brother and sisters. Here is a picture of them in the room enjoying time together.
It was nice, but Kiley got use to watching a lot of TV. It was helpful, because when she was watching the focus was on the TV, not on the pain. So, night times were really hard. Looking back I might of just turned on the TV to help with the pain, but she did get some good sleep in between the pain and nausea. But, that usually came at night when all had settled down.
Day Three
They wanted to get her up and walking more, she had really only gotten out of bed to go to the bathroom, which like I said was hard enough because of the chest tube. It was stuck in her chest through her side and if she moved when they took her to the bathroom it was tons of pain. So on day three all the drainage had come out and they took the chest tube out. After they did that she was a new woman! They got her up and decided to go for a walk with her siblings to the activities room. There was also an ice cream social for all the kids and musicians playing for them. It was an incentive to get a move on. So here is a picture of our nurse, Heather, walking Kiley down the hall. I will post more pictures of the actual events in my Child Life post. She walked all the way down to the play room and they had the Wii set up. This was great because she and her twin played the drums on the Rock Band game and we made her try and use her hurt arm, but of course she mostly used her good one, but it was good to try it out. It got a smile on her face.
That night she slept a lot better and we were told that she would go home the next day! We had no idea she would recover so quickly. We attribute it to all the prayers that people were praying for her all over the world, as well as, the determination herself to GET OUT OF THERE! Our God was faithful in watching out for her, our verse for this whole experience is Ephesians 3:20-21 "Now to him who is able to do immeasurably more than all we ask or imagine, according to his power that is at work within us, to Him be glory in the church and in Christ Jesus throughout all generations, for ever and ever! Amen."Day Four-Going Home
She enjoyed one last arts and crafts project from Child Life and then we got ready to go home.
1 comment:
I also have shone's. You have a brave little daughter! I had a coarctation at the age of two. I also had the surgery on my side, not open heart - but then 35 years later I needed open heart surgery. I wrote about it hear; http://shonessyndrome.org/
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