Rambling Elaboration

Yesterday’s entry was admittedly pretty bleak… but not all of yesterday was completely full of suck, so I figured I should come back in here and sprinkle a little bit of that “good” around – even though I know it won’t really do much to balance out the tone of the blog lately or overall. πŸ€·πŸ»β€β™‚οΈπŸ˜•

Knowing that soon I’ll be runnin’ completely without my thyroid meds, there were a few things inside and outside of the house that I wanted to get to… just in case the next several weeks are as “challenging” as I’m expecting them to be. 😟 The inside stuff was whatever… but the outside stuff, that’s the kind of stuff that kicks my ass even when I’m at my relative best these days. It also didn’t help that it was still 87 degrees in the late afternoon, when I finally went outside, since “waiting for the heat to die down” wasn’t really gonna work unless I intended to do my yard work in the dark.

When they took out my line of bushes, they plucked about a 1/3 of them, and the remaining 2/3 were cut off at the base – as close to the ground as possible. I told Jason that I had plenty of poison spray when they were doing it, and he suggested that after they were done I should probably go out and hit all the remaining “nubs” in the ground, to discourage them from trying to make a comeback – and to hopefully make them brittle enough that anything still above ground will eventually just start breaking off. So, that was mini-project number one, and luckily I didn’t need my cane nor did I have any neighbors eyeballing me as I worked.

I still had juice left in the sprayer when I was done, so I started hitting weeds along the fence, under a bunch of the evergreen bushes, all over the empty-but-weedy spot (where a big bush used to be) beside the garage, and then all around the AC unit just to make sure nothing considers growing up around it. I was sweating balls at this point. Actually, I was sweating balls within the first 10 minutes of being outside… but yeah, it was time for a break in the cool air inside.

It felt nice, but when it became obvious that I wasn’t gonna stop sweating, I sucked it up and went back outside. I’ve got a couple different sprays for spiders, wasps, bees, and ants – so I treated all the areas that needed it. 😷 Front porch got most of the spider attention, back porch had the bees, and then I sprayed what amounts to an “ant barrier” at the bottom and lowers sides of all of the doors that go outside or into the garage. (They’re a fan of Maven’s messy eating habits, usually leaving bits of cat food on the floor for them to sniff out and come after.)Β Bugs don’t really count as “critters” I suppose, but I still hate to be an exterminator. πŸ˜• But when they won’t stay outside, or try to take over certain areas when they do, they’ve gotta go.

Don’t you love how I can take “Sprayed some poison on the bush stumps and weeds, then killed some bugs” and turn it into a multi-paragraph blog entry? This time it’s intended… to make it sound as time-consuming and exhausting as it actually was. πŸ˜“ I ended up sweating so much that the mosquito repellent finally quit working, but I had done everything that I wanted – so it was time for a shower, and to stop friggin’ sweating.

Throughout the process, I learned that I have another mutant ability. πŸ™„ I can work outside for a little less than an hour, come inside into the cold air conditioning, take a shower to get all the stink, grass, and stray poison mist off of me… but I can continue sweating for a full two hours after everything was done and I should have been good. πŸ€¦πŸ»β€β™‚οΈ I’m guessing it’s a thyroid thing that I just hadn’t discovered yet, since I’m usually too gimpy to work that much outside. But yeah… cool shower, cold air, and two more hours of sitting here with a towel to keep drying myself off.

It’s fine though… because as much as this all might sound like bitching, it felt good to accomplish so many things when there were so many other things trying to mentally or physically discourage me from doing so. Until I started to not be able to do a lot of things, I didn’t realize how important that it could be to be able to do something with purpose. So even though this stuff is probably most people’s typical weekend, it’s my little thing to grab hold of and feel good about. πŸ€·πŸ»β€β™‚οΈ

And, obviously, I have to take what I get when it comes to stuff like that these days.

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Hands Off The Controls: Autopilot Has Been Engaged

I didn’t get to sleep until almost 6am this morning, and I had posted a somewhat moody blog entry about an hour before that… but I went ahead and deleted it when I woke up, deciding that I should wait until I had a little more sleep, time, and information under my belt before commenting on the stuff I was commenting on.

It was just really bad timing last night… first, forgetting to drag the trash buggy out to the road, so I ended up doing that around 3:00am. And of course since I was out there, I grabbed whatever was in the mailbox from the past couple of days. And the letter on top had to be from my WC attorneys, letting me know that my mandatory “independent” WC exam has been rescheduled. That was the appointment where I got up at dawn to drive to the NW side of Columbus, with my bum knee at the time, and they cancelled on me about five minutes away from their office. 🀨 Yeah, so that’s now rescheduled near the end of the July.

It had actually slipped my mind, since my brain has been in a state of constant anxiousness regarding my lengthy but (hopefully) finalΒ thyroid cancer treatment beginning. So with that and other other crappy stuff on my mind, having had to deal with the kitten situation yesterday, and then just not being able to sleep because of all of it – seeing that envelope pushed me past sad, mad, frustrated, nervous, or whatever… eventually to just numb. 😐 It’s happened before… I’ve simply “felt” to the point of no longer being able to feel. πŸ€·πŸ»β€β™‚οΈπŸ˜• And I don’t know… with the way I’ve been, numb is probably better.

I’ll let my attorneys know that the appointment is just days before I’m due to begin the radiation part of my treatment, so we’ll see if WC still demands that I show up – or if they’ll decide to wait until it’s over and I’m at what they’d consider my “normal” physical self. The latter would give a more accurate representation of how my disability and meds affect me, but who knows what they really want.

The last handful of entries should give you a good idea of where I’m at and where things are heading. I don’t know how much time I’m going to be spending online in the near future, and there’s a good chance that I’m going to be even more difficult to reach than usual. I apologize that I’m probably going to come off as more inconsiderate than typical… but I can’t really do anything for anyone, I can’t see how my presence right now could possibly be a good thing… so I might end up in my bubble for a while. 😐 If anything significant happens though, good or bad, I’ll make sure I at least make a small post – just to keep the people who still care in the loop. Try not to worry about me though. Whatever happens next is all out of our hands.

I’m The Right Wrong Person

Being a critter person is awesome, but man can it also be really rough at times. 😟 Maven’s fine… in fact, she’s hogging my recliner right now, zonked out and oblivious to the activities of my day. Unfortunately though, one of my friends has a cat that had a litter of kittens… and well, sometimes everything doesn’t go like you want it to, like youΒ thinkΒ it will, or how you know that it should. πŸ˜₯Β I hate even thinking about it, let alone typing it out and making it feel even more real, but the sad fact is that two of them didn’t make it.

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She lives in an apartment complex, so she doesn’t have anywhere that she could bury them (which she obviously wanted to do) so I guess I was the first person that popped into her mind, when it came to somewhere that the two little ones could rest peacefully and undisturbed. 😞 She’s devastated about it… just like I would be if I was in her shoes… so despite the miserable heat and already feeling run down – I got dressed, went ahead and picked them up, and brought them back here with me.

It’s the least I could do… I mean, there’s no way to make someone feel better when something like that happens… so helping make it a little easier for them and sharing in their pain, those are about the only things a person can do. πŸ₯Ί The older I get though, the less I’m able to absorb this kind of sadness. The curse of being a critter person… you can’t just turn it off and on, and with each critter that you lose (or experience losing with someone else) you end up feeling it that much more each time it happens. πŸ˜₯

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With the tone of this entry, I’m sure you’re looking at the pictures of the double rainbows and wondering what the hell they have to do with anything. 🧐 Well, that’s what I got to see during the last ten minutes of the ride back home. I know that they’re “just rainbows” but in that moment it made me smile, thinking that maybe Mom, God, and all of the other “critter people” were up there recognizing this sad moment, giving me something so brilliant and peaceful to literally follow home, where the little guys will be staying. 😊😒

Unfortunately… Nope

This will be a lengthy entry.Β Β πŸ€”Β  Although, I suppose that’s typical for me and the blog… 😏

A few days after going to my full dose of Paxil, one in the morning and one at night, the side effects that I hoped would go away were actually getting much worse. 😳 So over the past couple of days I’ve weaned myself back off… and today was the first day I started feeling close to my normal “normal.” 😟

The biggest problem was the tremors. Any time I would yawn, which was a lot,Β probably due to the new med… every time I would yawn, my left shoulder and arm would start shaking uncontrollably – sometimes lasting up to 30 seconds before it would calm. 😧 And then it started doing it with my other shoulder as well, to where eventually when I yawned (and even when I wasn’t) I’d honestly compare the tremors to what you would see in a person with Parkinson’sΒ disease. πŸ˜₯ I suppose it makes sense, as the disease is related to dopamine problems and that’s often something that psych meds mess around with as well.

The daily waking up in a near panic attack… that didn’t stop either. And when on the full dose, taking the morning dose was no longer relieving the anxiety when I took it. So, it was waking up with severe anxiety, taking the pill (along with my others) that was supposed to help with anxiety, only to have it then stay around all day. 😣 Awesome. πŸ™„ That was reason enough for me to reconsider if I wanted to continue taking it… and I really did want to give it a chance, to wait out the side effects to see if they’d pass. But you have to remember, after my work injury, the main thing that my doctor and I had to work on for a long time was getting my left shoulder with the nerve damage to stop randomly shaking.

So not only was the new med increasing my anxiety, but it had brought back the uncontrollable shaking in my left shoulder, which always leads to much more pain by the end of each day. πŸ˜’πŸ€¦πŸ»β€β™‚οΈ So I hope most people would understand why I wasn’t willing to “just keep hoping it’ll pass” while possibly risking it getting worse or even becoming permanent again.

It’s disappointing, but again I’m experiencing the “Ahhh” of just losing all of those awful and scary side effects, and returning to my “normal” self… which now feels like a relief – hopefullyΒ returning just to “how I was” a couple of weeks ago. πŸ™‚Β (The tremors weren’t gone today, but they’ve lessened quite a bit.) And with my thyroid doctor calling today and wanting to accelerate the next step with that issue, I just don’t think I’d be able to do it while essentially fighting against the side effects of the Paxil. The next step with my thyroid stuff is gonna be difficult enough as it is. πŸ€•

More on that when I know more. (Although I’m gonna try to squeeze in a subjectively more positive entry between this one and that one.) But in the mean time, I’m still wondering if sometimes it’s in the doctor’s plans, or at least something that they know can happen – where a medication that is supposed to help makes you feel so awful that when you stop taking it, you actually feel happier and more relieved just to be back to how you were. πŸ‘¨πŸ»β€βš•οΈπŸ€¨ Because boy, that’s been the trend with me, the few times I’ve been prescribed something by a shrink. 😏

  • Just to cover my ass, I’m not saying with any type of certainty that the Paxil definitely caused all of the symptoms that I was experiencing while taking it. It’s possible that all of the things that I considered “side effects” were completely unrelated… this is just my account of how things went while I was taking it.

Adjustment

At my most recent shrink appointment, he prescribed Paxil and Lamictal. He spooked me with the Lamictal though, so I haven’t started taking it yet. Serious talk about the possibility of a rash that could mean something very bad. 😳 So it’s a difficult medication to “sell” when someone already has high anxiety. But the Paxil, the first week (which is now done) I was to take only one in the morning. Now, I’m supposed to take one in the morning and one at night. I’m hoping that will help the problem that I’ve noticed all this week.

I’m also going to start the Lamictal tonight as well. I just never like starting two new meds at the exact same time, because then whether I experience a benefit or a side effect, you can’t know which one was the cause… although I suppose sometimes you don’t get the benefit or side effect unless you’re taking both of them. 🧐

This past week, even though I usually slept well, every time that I’d wake up the next day I would have instant severe anxiety already happening. 😣πŸ˜₯ Now, it’s not like this is the first time that this has happened… and I know it sounds bad to describe it this way, but sometimes when anxiety is so bad, it’s just the disappointment of waking up that triggers it. 😐 Oof, yeah, that sounds way worse than I intend it to. But yeah, it was random before, but it’s been a constant since I’ve started taking the Paxil in the morning. So hopefully now that I’ll be taking an evening dose as well, maybe that’ll change how I wake up.

That’s the one positive though… as long as I take it immediately upon waking up in a near panic attack, the feeling actually goes away relatively quickly. πŸ€·πŸ»β€β™‚οΈπŸ™‚ So I’m still hoping this will be something good, and it’s just a matter of getting on the right dosage. And yeah, it’s probably a little weird that I’m just putting this all out here for anyone to read – but it’s not like I’ve tried to keep the “twitchy” side of me a secret. 😏 And I really do know the majority of the things that have triggered it (and keep triggering it) so it’s not like I’m staggering around in the dark, unable to see the boogeyman.

It’s not a permanent solution, because it’s not a good solution, but part of me getting my head straight is by cutting myself off from people for a while. 😞 As I’ve described it before, my empathy is like a horrible super power that I’ve got… and when I know so many people that are going through so many awful things, I absorb the feelings that they’re experiencing regarding many of those things. 😣 Add that on top of my medical stuff, my workers comp stuff, my disability, etc… and unfortunately the easiest way to reduce anxiety is by avoiding the sources (and even potential sources) other than my own. πŸ₯Ί Then (I’m hoping) once I’m in a better place, I’ll be better able to function like a “normal” human and bring myself back into the fold. I don’t know if it’s a good plan, but it’s a plan…

EDIT:Β  Jesus… maybe I’m not quite ready to risk this Lamictal. 😯 I shouldn’t have googled.Β 

My Selfish “Good” Day

I had a lucky day yesterday, where my knee decided it would cooperate with me, so I was actually able to pick back up on some of the tasks that had the brakes slammed on them when my knee originally went out. It happens when I have sudden problems with my back as well… those things around that house that you just assume you’ll be able to get to tomorrow or the next day, once your knee or lower back goes screwy, those are the messes and tasks that you’ll have to just look at for the next days or weeks… until the pain hopefully goes away enough to finish those things up.

So I was finally able to bring up the laundry from the basement, as well as do another couple of loads. (And let me tell you, I now understand how the basement stairs were a big “nope” for my Aunt C when she reached an older age.) Got that all folded, hung, and put away. And then I finished up the grooming of the cat… at least as good enough as I care to get it… and then also picked up all the big globs of fur, ran the vacuum over the two rugs that I was using in the bathroom to catch it all, and then went over the carpet in the living room and hallway to catch the rest of the stray hair.

I did a few more small things, essential things, and with each thing I did I could feel my knee reminding me to take it easy… and I really did. Being careful with each step or turn, making sure I didn’t move it in any wonky ways that could derail the rest of my meager plans for it for the day. Like, I didn’t even try to put all my junk back on my bookshelves in the bedroom, although after my appointment today I might take a stool in there and attempt it. Yeah, that’s another reason why I didn’t mind “risking” yesterday’s actions, since I knew that “back/knee guy” was already on the agenda for today.

It was such a relief to be able to do those few things, but it still left me feeling guilty. My knee has been screwed for about a month now, which has also screwed my neck and shoulder more than usual, which has kept my anxiety at shitty high levels… and it’s kept me from being able to do so much. So when “good knee day” was gifted to me, knowing that it would likely be a limited resource, out of all the things I could have done – I did choose “work around the house as best / long as I can” over other things. 😟

I had to… because I already feel ineffective enough on most days, so having to sit here with most of my clothes clean, but in the basement… and with two big ass rugs in my bathroom, covered with an obscene amount of cat fur… along with going out to fetch my trash buggy, empty the litter box, and even just finally putting my groceries away and standing there to do the dishes. If I would have not gotten that stuff done yesterday, and woke up with a fucked knee today, which I did, all of that stuff would have been even more heavy on my mind.

So I ghosted almost everyone, doing what I needed to do for my brain to be a little more at ease during this whole “doctor / workers comp BS week” and the time immediately after. Still gotta get it through my head that I need to not fuck things up around the house (and not immediately clean it up or undo it or whatever) since there’s a pretty good chance that the next day could bring me some new surprise that physically stops me from doing so. I’m not old old yet, but the things affecting me… I may as well be. 😐 I need to start figuring out how to think about life in that way. Making use of, in all ways, the good days – and not just counting on each following day to be the same or better.

That’s why my anxiety messes with my head when people count on me or rely on me… because I can’t even count or rely on myself half of the time. So, kudos to all those people who are dealing with daily pain, disability, anxiety, depression, etc… but who still manage to carry on with their lives and not let it tie them in knots like it does me. I keep hoping it’s just a matter of getting used to it. But again, it makes me think of my Aunt C, who was in horrible shape and probably hurt in more ways than any of us ever knew… yet all the way up through her final days, she still lived her life without complaint, fought against the pain to play the organ at church each Sunday, and probably lots of other stuff that only she knows.

So whether it’s my neck, shoulder, thyroid, back, knee, or whatever’s next… I hope that I can eventually at least be like her, and just accept things as “how they’re gonna be” once doctors have determined that yes, this is just how it’s gonna be. I still haven’t gotten past the “Nope, I’m not that old, I shouldn’t feel like this.” phase – as made obvious by all the appointments just this week, and my decade-plus long battle with workers comp – but maybe it’s time to try and start accepting and adjusting, rather than fighting. πŸ€·πŸ»β€β™‚οΈ Meh… I dunno… but my appointment is soon, so I better get off here or I’ll just keep rambling… wish me luck.

Bad At Feeling Bad

Saw my workers comp doctor on Thursday, discussed the additional pain in my neck and shoulder from relying on my cane (for my unrelated knee pain) this past month, but mostly discussed the upcoming WC mandated “review” – and he’s just as frustrated by what they’re trying to do as I am. πŸ˜’ Then I finally went back in to my prescribing shrink after taking a couple months’ break to get used to my new WC doc meds… and ended up spending an entire hour with him.

Granted, when you talk to a counselor you usually get an hour, but typically the pill shrink just wants to get you in and out of there, prescribing what he feels is appropriate based on the counselors notes and maybe a few followup questions. He talked to me about so many different possible meds, I have to admit that I don’t even know which ones he ended up calling in for me. I guarantee you that I’m going to be doing a lot of googling before I start taking anything… especially considering the other meds I’m already taking, and that in about a month I’ll have to stop taking my thyroid meds to prep for the next radiation pill treatment.

Meh… I’m not gonna get into all that. But I’m gonna try what he thinks I should, as long as I don’t find anything concerning that he maybe didn’t consider. πŸ€·πŸ»β€β™‚οΈ But for the past hour or so, I’ve been waking up and psyching myself up for the trip into the pharmacy. Three different doctors, multiple prescriptions, many new, some to be covered by WC, but still might not be, and then others meant to go through my regular insurance. 😣 For some reason they can’t mark it in their system, which meds go through which insurance, nor can I count on some of them being approved anyway, so this’ll be a fucking process today. 😠

I know. 😐 This is just what people have to do. The medical / workers comp / insurance programs in the US are shit, nobodyΒ does it without jumping through hoops, dealing with delays and irritation… but I’m still gonna bitch about it. 😏 And sure, whether it’s WC or traditional insurance… once, maybe twice, do what you have to do to verify that “Yeah he’s broken. Yeah he needs those meds.”Β (I get it… fraud prevention) but then just cover the shit plz. πŸ€• Go through that sort of bullshit long enough and you can totally understand why people, as they get older and feel more broken, just can’t or don’t want to have constant adversarial engagements with the whole system – and just stop bothering with some of it. 😒 Especially when the doctor’s hands are tied and they can’t even prescribe you the meds that could actually make you feel better – whether due to WC guidelines, insurance not covering it, or it simply being too cost prohibitive. 😠 Man it fucking pisses me off…

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I’m just bad at feeling bad when a)Β I’m denied treatments that could make me feel better, and b) people are still fighting to take the things away from me that merely keep my pain tolerable. πŸ˜–

Oh, and my insurance company… they keep leaving messages, saying that they want to schedule an in-home visit from a doctor that can evaluate me and give me his or her opinions as well. πŸ™„ Yeah, um, no. You’re insurance. Just be insurance. Get my health info from my records like a normal company… and don’t expect me to invite you into my house with another handful of hidden hoops behind your back. 🀨 Okay, I guess I’ve dragged my feet long enough, and should get in town and see what kind of luck I have with all this shit.