Perfect Storm

Three things:

  • I didn’t get my nap today, so I’ve been awake since 3a… and it is currently 11p.
  • Despite that, I still made it in town to meet up with my friends for dinner.
  • I had a good time… but my shoulder is fuuuuuuuuuuuuuuucked. 😏🤷🏻‍♂️🤦🏻‍♂️

Note, this isn’t a complaining post, even though it’ll sound like it. ‘Cuz my shoulder is frozen in the “up” position, but thankfully isn’t throwing a fit anymore. 🙄 Good lord, I haven’t had it shake this much in a long time. I’ve also got that familiar tilt of the head to the left. 🤕 Yeah, tomorrow is going to royally suck.

This was one of those “price of entry” situations I’ve mentioned before. Where a combination of normally trivial things combine to flip the switch, even though it was something I wanted to do. 🤷🏻‍♂️ Not quite enough sleep, sitting up against the wall in an uncomfortable booth, not being able to fidget around as needed, loads of noisy people all around, using “social energy” I didn’t really have, an unfamiliar place, and then going from the warm to the cold as we finally gave up our seats and took it outside to finish talking. 😏

But it was Jim, Adam, and Brad, and we all went to The Pink Cricket. Haven’t stepped inside that place since I was barely a teenager, when me and my cousin Jim went in because they had a new (at the time) Ms Pacman machine. Ironically, they still have three arcade machines, and they’re all vintage. 🤓👍🏻 Adam is a bit of a foodie, so I was happy to go there – since us getting together these days technically qualifies as “an event.”

The only time we weren’t talking was when we were cramming food in our mouths, but at a little over an hour my shoulder really started twitching. 😳 We had finished eating and were just taking up space, so I asked if they’d mind going outside so I could move around a bit. Well, we ended up standing outside for another 45 minutes, and all the little triggers came together and I ended up putting on a pretty good show. 🤕😏 Just meaning that my shoulder wouldn’t stop, and it’s probably the worst that they’ve seen it.

We covered a lot of topics but of course eventually it turned to my shoulder, then workers comp stuff, then all of our various aches and pains that we now bitch about… 😏 typical fare for four d00ds who are approaching “old fart” territory a little quicker than we’d like. But they had to drop off Brad before Adam could head back to Columbus, and then Jim up to Marion, so we broke it up and headed out around 10:30p.

Fun fact… I started this entry around 11p when I got home, but I’ve had to take so many breaks that it’s now after midnight. 😳 That’s the stuff that people don’t see. Spending an hour leaning against the space heater, typing a couple sentences here and there, and doing my best to make the “ugh” go away. 🤷🏻‍♂️ At least my shoulder’s down and my head’s back in a normal position now. But yeah, still glad that I went.

(But ask me tomorrow when I wake up. 😏 It’s time for bed.)

Tired of This Shit

I’m not sure how this month’s appointment with the WC doctors is gonna go. 😕 I think I’m actually seeing Dr Walter this time, when it was the new guy that I had the in-depth discussion with about the state of my treatment last month. Regardless, since the WC insurer is coming at me with the shenanigans again, the conversation will have to revolve around that rather than the stuff that I started bringing up last month.

I’ve got to be careful, because it almost feels like a “trap” that WC could use against me, but this month I have to start discussing possible alternatives for the meds that I’m taking right now. Because if they are somehow able to weasel out of paying for what I’m currently taking, the cost of two of those medications would simply be too much for me to continue taking them long term. 🙁 That’s where the “trap” part comes in.

When I start discussing more affordable potential alternatives for the meds I’m currently taking, I want it to be clear with my doctors and in my records that I have no desire or intention to make any changes now… and that the research and discussion is really just to act as my parachute if I get pushed out of the plane. But I can see where my fear of being forced to pay for my own meds, which has made me research cheaper (but likely less effective) alternatives, means that I now know that there are cheaper alternatives, so they’ll probably think that they have the right to force me to change to them – despite my preference to keep taking the ones that I’ve been taking. 😏 Heh… I know, that sounds a bit convoluted, but it basically make sense, no?

But until I’m able to discuss this with them, I know that I’m just taking barely-educated shots in the dark when it comes to what might or might not be suitable replacements. 🎯😎 I mean, even though I know that Lyrica has very specific actions – at its most basic level I know that it is considered an anti-seizure / anti-convulsant medication… so that’s where I start looking. 🤓📚 And now I have four or five medications that I think could be good replacements… but for all I know, even though they’re anti-seizure, they may have totally different actions – and ones that aren’t even close to being applicable to my situation. 😒

So for now that’s all I can really do… look for “close” meds and make sure there are more positive side effects than negative. Then I’ll just hope that I’m actually on to something, and that information can be put in my back pocket until it is needed. Between now and then I just have to figure out how to condense all of this crap down into a tolerable three to four minutes. 😳⏱👨🏻‍⚕️ Gotta impress the importance of this on him, while also not rambling so much that my point gets lost in the noise. I’m better at that than you’d think, actually… it just doesn’t seem that way here because I know I can go on and on about something and it doesn’t matter, since hardly anyone reads this blog anyway. 😏🤷🏻‍♂️