Next thing I knew, I was opening my eyes in ICU. Before I could even blink they were plugging me into machines and hooking me up to a breathing treatment. Then one nurse started asking stupid questions, like what year is it and crap like that. I was trying to answer these stupid questions and the other nurse was barking the “breath” order at me, with my breathing treatment tubes sticking out of my face and all the while I haven’t even come around enough to know if I am alive. Thank you God! That continued to play through my mind, as they worked at getting everything done they needed to do.
My Best Friend |
What the? |
I Hate You! |
After completing all tests and blood work, I was in stable condition. That was when they introduced me to what they called “My New Best Friend” a breathing apparatus. I have not, nor will I ever call this contraption any kind of friend! It sits right next to me all day long, and as much as I hate it, I use it all day long!
Thursday January 10, 2013 started out as a good strong day with everything positive. I could have gotten sprung from ICU, but there were no available beds in the hospital due to the flu going around. On the plus side, I didn't have to share a room with anyone that might be sick. I also ended up with some the most painful muscle spasms on my right shoulder blade and under my armpit that would bring tears to my eyes. Of course this happens after they turn off my morphine pump and start me on Vicodin so I could go home. They can’t send you home on morphine, so I had to make the switch.
We did come to discover, that if I would NOT use my newly traumatized arm to push myself up off the bed or the chair, it would not go into excruciating and painful spasms! So that bettered my day, as well as a quick call from my best friend Valerie and the love of my life at my side!
As everyone knows, you can never get any rest in the hospital. Vitals at the top of every hour, medications…never all at once, and the breathing treatment every four hours, who has time to sleep?
Friday January 11, 2013 I was finally moved to a regular room. Now missing my privacy a bit, just hoping that some with the flu does not get the bed next to mine. My surgeon, Dr. Vigneswaran came to check on me, and I filled him in on the loss of blood from my chest tube. After looking at it briefly, he put on some gloves, pushed a few times in a few places that could have made anyone scream! My hero again, distracting me from this painfully obvious situation I was in, by mushing my face into his side. My glasses almost became a permanent fixture on my face, but we pried them loose before it was too late. The Dr. was barking breathing orders at me, and announced he was going to pull my chest tube! It was over quickly and I could begin to compose myself again. He said that my tube was leaking because I did not have enough skin fat to hold it more securely in place.
That was already enough action for me that day; I was falling asleep before my honey was even ready to leave. He texted me when he was home safely and I must have sleep texted him back because neither of us knows what the heck it says. LOL!
Everyone at the hospital was outstanding from beginning to end. I cannot say enough about the wonderful care I feel I have received from University of Chicago Hospital. All the Doctors, nurses and other employees have been a shining example of team work and played a crucial role in my surgery and recovery.
~Romans 8:28
And we know that God causes everything to work together for the good of those who love God and are called according to his purpose for them.
I tried to get this blog posted on 1/17/12, but ended up in the ER! I will try to get that blog on in the next couple of days.
Another fun filled day downtown tomorrow, stay tuned.
You are amazing Shirley. Love you and praying each day gets easier. Love Annie, Pete, Elijah, Amaria and Charlie
ReplyDeleteWow you are amazingly tough. Keep getting better. Your friend Ray.
ReplyDelete