Tired of This Shit

I’m not sure how this month’s appointment with the WC doctors is gonna go. πŸ˜• 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. πŸ™ 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 nowΒ 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. πŸ€“πŸ“š 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. πŸ˜’

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. πŸ˜³β±πŸ‘¨πŸ»β€βš•οΈ 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. πŸ˜πŸ€·πŸ»β€β™‚οΈ

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Inescapable

My brain and body have definitely been on pause today. Thursday night into Friday afternoon was a rough chunk of time… going over to say goodbye to my friend Christina with a ton of family around, then a couple hours sleep before heading to the hospital at 6.5a for the radioactive iodine treatment, and shortly after I got backΒ home I learned that Christina was gone. πŸ˜”

We knew it was coming, and we were all there the night before because we honestly thought it would happen that evening – but she held on for one more day. It was so nice to be around all the family, many of whom I hadn’t seen in a good while, and I even met her biological dad… who was a really kewl old d00d. We all tried to keep the vibe as positive as possible for each other, but of course it was still really sad. I wasn’t even going to go over, feeling like it wasn’t my place, but Bri reminded me that I’m just as good as family – and that of course I was welcome and wanted there.

Meh… I don’t really wanna talk about that anymore. My thing at the hospital took over two hours, although most of that was pre-treatment lab work, having three pages of precautions read to me, and of course the signing of all sorts of documents. Once they opened the lead-lined container and used tongs to get the pill out to hand it to me, it was literally a minute until they were shuffling me to the door. They really want you to just gtfo once you’ve got the radioactive vibe.

The lady that did it all, you could tell that she was used to it… because even before the pill was in the area, she would still do things like asking me to place my ID on the tray table so she could grab it, rather than me handing it directly to her and risking actually touching her. And boy, once that pill was out and in my hand, she backed across the room until I took it – and as she guided me to the quickest way out of the building she reminded me to stay at least six feet away from her. Good stuff, eh?

I didn’t have any nausea or sickness as side effects, but it did make me have a funny taste in my mouth… and I unintentionally fell asleep that afternoon from about 4p until midnight – but that was as much from the lack of sleep the night before as it was the medication. I have to stay on this low iodine diet for a few more days, I’m supposed to not be around kids or pregnant people at all for a week, and six feet away from anyone else… and poor Maven, when she wants to sit on me or lay next to me, I have to put her down on the floor at the base of the recliner – but I make her a little nest in the blanket and share the space heater with her, so she’s okay as long as she’s close to me. She hasn’t left my side since I got home… pretty sure she senses the “bleh” I’m giving off.

Just hoping I don’t irradiate her too much until it’s out of my system.

Unrelated to Adulting

Okay, now that I’ve got all that other shit out of my brain for the moment… now I can write about the other stuff from the past week or so. Let me start off by talking about a new toy that I couldn’t resist. 😊 It was only $80 shipped, which isn’t too bad… and considerably less than what the original (with disk drive) would have cost new. It’s called The C64 Mini, and while it’s not an official Commodore product, it’s essentially an entire C64 emulated on a teeny board, in a teeny replica of the original “breadbin” style Commodore 64.Β πŸ˜ƒ And before you ask, no… the keyboard doesn’t actually work… but you can plug a USB keyboard into it and use it as an actual computer – and the company intends to come out with a full-sized, completely working replica soon. 😁

I’ve yet to even power the thing on, because I’m waiting for a spell when I’ll be able to do nothing but mess with the thing… which will include upgrading the firmware to allow me to load any program from a flash drive, and loading it up with all of my favorites from when I was a kid. It does have 64 licensed games built in, but most people are like me and get it so they’ll have the closest thing to an actual C64 – but with HDMI output – for the best looking Commodore 8-bit computer ever. 😊

I suppose everyone has a “thing” from their generation that they loved when they were younger, and therefore want to have again once they’re old. 😏 Classic video games and Commodore computing are definitely my thing, the same way that HAM radio is Dad’s thing… and like me, he’s still got a few toys as well that he plays with to this day.Β πŸ€“ I’m even learning how to take a C64 disk image, open it on a Windows 10 laptop, add or remove C64 programs as I see fit, and then export the new C64 disk image for use on this thing. 😯 That’s how it is with me though… give me something I’m genuinely passionate about, and my brain will start absorbing everything that it needs to know about it.

Okay, gotta keep this entry short-ish. 🀨 Maven is almost completely done with her home-grooming, which means my bathroom and living room carpet areΒ covered with poofed hair for now. 😟 I’m lucky that she’s so cooperative though. In fact, for the most part she loves the process. Bri came for a visit right before Halloween, not only to hang out (she drew the face on the pumpkin and I carved it upΒ πŸŽƒπŸ˜) but to also distract from her mom’s deteriorating health. She’s actually had a couple of good days, so it was nice to see her have a little more energy. However, my friend Greg, his mother passed away this past week. 😒 She was having a rough time, so it’s one of those deals where you’re almost relieved.

Cassi came down to spend the night on one of her days off. Her life is so hectic, between all of the hours that she’s been putting in lately and then having her, her mom, and her (very opinionated) 17 year-old sister all there at her house, making noise at each other. 😏 So coming here, even if half of her time is spent sleeping… it really is like a teeny mental vacation for her.Β πŸ™‚ Plus she helped me out with some chores, including the whole de-flea-ing process with the sprays and the carpet powder, etc. (Plus the most important and helpful thing… getting Maven to swallow that damn Capstar flea killin’ pill.)

As we sat in the living room watching the new “Charmed” show, we also each had our notebooks and were fastidiously jotting down the things that we intend to work on in the next few days. It’s strange how just having her here “working” in the same way that I was, how it helps to settle my brain and let me get down to business without getting as easily distracted by Twitter, Facebook, or YouTube. 😡

So there ya go… just so you don’t think my entire existence is grumping and bitching. 😐 There’s always some good sprinkled in there – and even when it isn’t “good” in general, I’m thankful that I have the right kind of friends to help me through those times, and vice versa.Β πŸ™‚Β Okay, carry on…

But It’ll Be Fun

Feeling pretty miserable today. 😞 Christina’s cancer fund-raiser is this evening, but I just can’t make myself go. They’re doing it as a “bar crawl” since she used to be a bartender, and therefore has a ton of friends/acquaintances that would be likely to come out in that fashion… but me, with my twitchy social anxiety and introversion, it’s just not my scene anymore.

I feel bad, because I’d really like to be able to go and show my support, but there’s not really anything that I can do about it. I sent a message to Chelsea a bit ago, explaining why I wouldn’t be there, and I think she’ll understand for the most part. The shirts they had made for the event… it marks the third “cancer support” t-shirt that I’ve bought this summer in regards to a friend who’s fighting that battle, and that’s three shirts too many. (And that’s only my cancer-fightin’ friends who are doing that sort of fund raising.)

But like I told her, I’m not doing very good at accepting “bad” these days, and when there’s an option of being reminded of that “bad” vs. hopefully just being able to avoid the thought of that “bad” altogether and acting like it’s not real… heh… well, I think you know which option my brain chooses for me. I mean, I know they’re gonna have fun and that it will be hopeful, goofy, optimistic, etc… but right now everything just feels too heavy and I can’t be there. (And yet here I am, still feeling “bleh” about it since my brain won’t let me go. πŸ˜’ It can be frustrating being me sometimes.)