They tried having me get up a little yesterday evening. I got up and got my legs hanging off the side of the bed and then I felt really nauseous and had to lay back down again. I slept horribly last night. Someone came in at least once every hour to do something to me and there were so many noises going on - toilets flushing, doors closing, machines beeping. I also couldn't find a comfortable position for my back and neck... One nurse came in a around 4 in the morning and said "good morning" and turned the overhead light on! He had come in to draw some blood for lab work and I asked if he could just use my port so he checked with my nurse and found out that they could, so he left the stuff to have her do it.
Both surgeons came in to on check on me in the morning and they both said that things went really well during the surgey and that I was looking really good. I asked my main surgeon if they could take out the IV line going into my neck but she said not yet in case they need to give me more blood. Iwas able to get up in the morning and transfer to a chair to sit in for a while. It felt good to be in a different position. I then had all different sorts of therapists come in and talk to me about different things. One of them was a respiratory therapist who brought a small breathing machine that he taught me to use to help strengthen my lungs after the surgery. He had me do it a few times and then said I needed to try and do it 10 times an hour while I am awake. Then he said he wanted me to cough as hard as I could. I didn't want to because I knew it would kill me. I finally did though and since I still have a bit of a cold, it was a loud, horrible sounding cough that made me have to cough a few more times. He said that that was good because it would help prevent pneumonia in my lungs.
The nurses in the morning asked if I wanted to clean up a little in the bathroom today, but I didn't feel like I was up for it yet. They did bring stuff to me so I could brush my teeth though.
For lunch I was able to eat chicken broth, jello and some Italian shaved ice. I then got up and walked a little down the hallway. The physical therapist walked with me and she helped me put my shoes on to walk in. Apparently my feet are pretty swollen because she had to loosen up the laces a ton before they would fit on. I was pretty tired again most of the day, but the swelling has gone down some. My parents stopped by with some flowers in the morning and then DH spent a good chunk of the rest of the day with me. One of my neighbors stopped by and chatted with us for a while which was really nice. Dinner was some beef broth with jello and more shaved ice. The beef broth tasted totally salty so I complained and they brought me some more chicken broth instead.
We had thought about bringing the kids by to see me but decided to wait until Friday. Instead he left a little earlier so the kids could talk to me and see me through Skype. I think that MJ especially is having a hard time with me being gone.
The hardest and most painful part for me is just getting up and down because of the stomach muscles that are used. I still have the epidural in for my pain meds and because of that I have a catheter in my bladder and an oxygen tube in my nose. I also have to keep a blood oxygen sensor on the pointer finger of my left hand (which makes it difficult to type).
You are amazing that you are able to document everything so well while being in a hospital bed hooked up to so many things! I am impressed! I am also really hoping you are home with your family for Christmas. Stephanie, I am so inspired by the way your have faced this trial with courage and optimism. I'm sure you don't feel like that all the time, but I can't help but be amazed by the strong woman you are. I will pray for a speedy recovery, that you will not be in great discomfort, and that you will be able to enjoy Christmas with your family. I'll be thinking of you.
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