I'm pleased to announce that the view from the peak of Mighty Mt. Sinai is pretty much the same as it was 2 yeas ago. My point being that it all seems very familiar. Same rooms (too hot), same nurses (the BEST), same food (don't ask).
Personally, I feel much better at this point than I did 2 years ago. But the symptoms and sensations are all familiar. And just as unpleasant. You don't want to know.
Surgery took place as scheduled on Tuesday morning, Feb. 17. It was long and complicated, I'm told, and they put me into the ICU that night to keep a close watch.
I was then moved to a "Step-down" ward for my second night, and finally into my room on Thursday. Lots of moving about. Just what I wanted.
Since then it's been I-V's, blood thinners, laxatives, Tylenol, vitals tests, blood tests. And a CT scan. Also midnight wake-ups to take my pills, 5am wake-ups, to take my pills, and just random wake-ups "Hi Mr. Miller. How you doing? Want some pills?" Glurg
Through all this, Sharon has been my rock, reminding me to eat or drink, making me get up and walk, and reading me a story (no, really!) before she leaves for the night. Thanks, Love. I know you're tired. We can go home soon and see the cats. I love you.
As for going home, the surgeon suggested this weekend, Sunday or Monday. I suggested I didn't think very much of either choice, but she's holding the keys, so I went for Sunday. We'll see.
That's all for now, because I'm sitting on the edge of my bed, about to fall over, and my head refuses to tell my fingers where to do their walking.
See you soon.
Pat