11/26/2019 and Beyond: Aftermath
Although I had been discharged, that wasn’t the end of the recovery process. As previously noted, I had to stay on the nimodipine for another three weeks, which meant waking up every four hours to take two gigantic pills. I’ve never had so many alarms set on my phone in my life. (The tone I chose for these alarms was the “Barking Dog” sound, because that was the least jolting one I could find. After 20 years of having dogs around, you get used to all the barking.) Annoyingly, my “hip flask” refused to adhere to the same schedule as my medication, so in between the times when my phone was barking at me, I had to get up at odd hours to empty that thing out. As a result I didn’t get more than two or three consecutive hours of sleep for nearly a month, and I doubt my wife did either.
Continue reading “The Event, Part 6”
Monday 11/11/2019 – Saturday 11/16/2019: ICU
I was in the ICU for a total of nine days while they kept my blood pressure very tightly controlled and checked me daily for vasospasms. (They got a concerning doppler reading one time, so off I went with Substitute Charlee for another CT scan; it did show vasospasms were occurring, but I remained asymptomatic, and scanned clean the next day.) My cousins and a few friends continued to drop by to keep me company, which was nice, and I had a series of terrific ICU nurses to take care of me. After a few days in ICU they decided to take out my IV and put in a subclavian PICC line, so they could administer medications and draw blood without having to stick me all the time. That was a relief, although the process of getting it put in was far from fun. Once the PICC line was there I mostly forgot about it; funny what you can get used to when you have to, and when the alternative is multiple jabs with sharp pointy objects.
Continue reading “The Event, Part 4”