… but this is 2020. Just you wait.
No, really, it is! Or at least, it was last year — Congress passed a bill designating September 2019 as such! It seems even these days, it’s possible for the parties to agree that Brain Aneurysms Are Bad. Of course, in September of 2019, I was still a couple of months away from being forced to pay attention to such things … 🤷♂️
In 2020 I guess it has only been designated as such in a few states, but you can read more about National Brain Aneurysm Awareness Month here.Continue reading “September is National Brain Aneurysm Awareness Month”
As I’m sure most readers are aware, I also run The Oceanside Animals blog (formerly Dennis’s Diary of Destruction). Proving the truth of the admonition never to work with children or animals, because they will steal all the scenes in which they appear, their blog has always been much more popular than this one, but every once in awhile, they share their fame with me. This week, I got to tag along with them on their Sunday Awards and Meme Show, when they were given the Liebster Award and I got tagged for it as well. Naturally most of the space in the post is devoted to Charlee, Chaplin, and Lulu, but I got to answer a few questions too. The show is reproduced here in its entirety with the kind permission of their agent.
So this week (Thursday, specifically) marks six months since The Event, when an undetected 3mm aneurysm at the base of my brain ruptured on November 7, 2019, causing a serious subarachnoid hemorrhage (SAH) and putting me in the hospital for about two weeks, most of that time in ICU. After being released, I spent the next couple of months recovering at home and returned to work on January 2, 2020. Also in January, my wife and I started going to our local dance studio again, and I resumed exercising and most of my other normal activities, at least until California shut down due to the coronavirus about six weeks ago.
So I was talking this week with my parents, who remember the polio epidemics of the 40s and 50s. Each summer the virus would flare up in different cities and regions. When there were outbreaks in a particular locality, movie theaters and bowling alleys would shut down, and swimming pools and beaches would be closed. It seems to me the present situation is not unlike a polio outbreak where the air is a swimming pool, the entire country is a movie theater.
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.
Saturday 11/16/2019 – Monday 11/18/2019: Telemetry
Once I was well enough to leave ICU, the hospital transferred me to the “step-down unit”, also called Telemetry. (If you never heard of a unit called “Telemetry”, you’re not the only one.) I was moved by wheelchair on Saturday evening, schlepping most of my stuff—my blanket and pillow from home, the get well cards I had accumulated, the posters made by our friends’ daughter, pictures of the animals, and, of course, Substitute Charlee—on my lap. The rest of the stuff was transported in a bag by a courier, A.K.A. my wife.
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.