Wednesday in the Pediatric Intensive Care Unit was, I hoped, going to be slightly different than Tuesday. After spending all Tuesday lying flat on my back, I was looking forward to being able to sit up. Unfortunately, that didn't happen till much later.
At about 8am, Dr. Ling poked in and asked me how I was doing. After answering a few of his questions, his nurse came in and removed my bandages. It bothered me that I was still unable to see what my wound looked like or even how big the incision was. Breakfast consisted of strawberry flavored gelatin which I carefully spooned in to my mouth (most of it ended up in my bed). My parents arrived at my room just after Dr. Ling left.
I figured out that if I held my breath long enough, the machine that was monitoring various things on my body would begin to beep and flash causing the nurses to come and ask if I was having trouble breathing. I would answer no and they would look at the machine and then leave. Also, if I flicked my fingers rapidly on the heart rate sensor that was attached to my other hand, I could reach a heart rate of 99 beats per minute. This also drove the nurses crazy.
Later I turned my attention to the TV which our good friend Fred had fixed the night before. Since there was no quality programming, I left it on at the “New Parents” channel, in Spanish. When my Dad came back and heard the TV yammering in a foreign language, he asked if it would be bettering Korean (our satellite radio has a Korean talk station an it really annoys my Dad.). We both laughed at his comment and I said Spanish was just great. About noon, the nurse finally came in and raised the bed 30 degrees. Finally! I could see more than just foam ceiling panels!
After a lunch of jello, (this time it was orange!) I smiled as visitors came and chatted with me. My Dad brought my computer so I could write this blog as it happened, but if you read my first post, you would know that it is pretty difficult to charge a computer with a printer cable. A friend of ours, Jenifer, came and brought us a HUGE bag of snacks and drinks for us to eat. The Story’s care group compiled all of this so we wouldn’t starve on hospital food. Unfortunately, I wasn’t allowed to eat solid foods L.
At about 4pm, Mrs. White showed up with Jacob. Being one of my best friends, it was great to see Jacob. He told me all that had happened at school while I was gone for the last two days. Being missing for only two days, ther really wasn’t much going on. We sat in the room and watched SpongeBob while our parents chatted.
After eating a solid lasagna dinner (and keeping it down), they cranked the bed all the way up to about 80 degrees, comfortable sitting level. The nurses did some final vital signs and unplugged a couple of cords from the machines. I was ready to be transported.
The transporters arrived in mini ambulance. It was about the size of an oversized golf cart. (Okay, maybe I’m going a little far…) No, It was just to nurses that pushed my bed to the Oncology Unit (Cancer Unit). Why the Cancer ward? Cleanliness. When the doctors have been playing inside your nerves, you are pretty susceptible to bacteria. So I got a sweet room for the night.
So hopefully, this indepth enough for your certain people.
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Travis