March 15th - I've made it through what I thought must be the worst of it. I am still breathing AND they can find the Doppler flow (both arterial and venous)
I was basking in the fuzziness of drugs and enjoying a diet of nothing. You heard me right, for 24 hours, I wasn't allowed anything my mouth. I enjoyed the odd sponge dipped in water.
Yum.
At 8 am, I was allowed to have juice and tea. I drank the juice the tea looked really awful.
At noon, I was allowed to have juice and tea. I drank the juice, the tea, again, looked awful.
At dinner time, you guessed it! I was allowed juice and tea!
The worst part has been the caffeine free diet. The nurses came in and asked me my pain level and I really could bear up the pain from the surgery, but I couldn't handle the pain in my head. I'm not sure that I'm going back to coffee ever again.
In the afternoon, the physio came in with 2 nurses and gave me the orders, to get out of bed. I thought they have *got* to be kidding. But, they weren't. So they taught me to draw my knees up and roll onto my side. I was literally gasping for air it was so painful. When I got rolled over, I used my arms on the bed railing to pull my upper body up, while letting my feet go to the floor.
It hit me all so hard, instantly I was sick to my stomach, I had broken out in a sweat and was
incredibly hot. One nurse got the emesis basin, while one nurse ran out. I was trying to breathe through it--but the nausea was intense. The nurse came back in the room with a syringe and she put the drug into the IV butterfly in my leg. Instantly, the nausea subsided. From the sitting position, I was asked to stand. So I did.
I knew this would be painful. But I don't think that words can describe how intense the pain was.
A couple hours later - the nurse came in to say it is time to take the catheter out and I about lost it. That means, having to get in and out of bed on my own, probably every hour. Remember, all I am having is fluids.
So, they took the catheter and I began getting out of bed. The first time was excruciating, but each time after that, it got easier and easier.
Sometime on Wednesday night or Thursday morning, they were checking me every 2 hours--and we made the decision to stop the "big drugs" and transfer me over to the medication I'd be taking at home for pain. Good decision or not, I hate feeling high and not being able to focus.
As I woke into Thursday morning, the pain level was tolerable....as long as I didn't move. Moving was a whole other story!
Thursday morning, it was decided that I'd be going home in the morning. As long as I did a walk around the ward and I accomplished that by Thursday afternoon.
Friday I woke feeling like a completely different person. I was clear in my head. Kent arrived to take me home and after a shower, and getting dressed I could see that I was completely able to go home.
Kent wheeled me down to the discharge lounge while he went to get the car. The drive home was excruciating. I felt every bump ... this city has incredibly bumpy roads!
Once home, I set up home in my recliner in the living room. It felt like I had had a very long day and it was only 11 am. Fortunately for me, I have round the clock nursing care in the form of Kent and Pippin.