Overdue For One Of These

Had my monthly WC doctor visit today. Good timing for two reason… first, because it looks like we’re gonna get our first measurable snow tonight (possibility of 2 to 3 inches) and second, because my shoulder was bad this morning. 😣 Most of the time when I have my appointments with him, I’m in my typical / average condition. Not good, but not too bad. But luckily, every now and then, my shoulder has one of its little fits while I’m in the office so he can see in real-time what I deal with a lot of days. Of course I never want to hurt, but it’s like when you take your car to the repair shop and it just won’t “make that noise” for the guy… yeah… my shoulder was making all kinds of “noise” for the doctor today.

It kinda doesn’t matter though… πŸ˜• and that sucks. πŸ˜’ I mean, my treatment is based on my condition, and he already knows that’s part of my condition – so seeing it happening “live” isn’t gonna change anything about it. It’s hard to describe the frustration of just wanting to “feel okay” while also knowing that there really isn’t anything that can make that happen. 😐 (And yeah, I know, I’m far from the only person that feels that way.) I’m gonna have to ask him at my next appointment, how much WC is affecting what he’s able to do for me. Lord knows they look for any reason to fight even paying for the meds that I’m on now, so I could see where he might know that some options would just be “off the table” from the start.

Meh… gotta try to not dwell on that stuff. πŸ™πŸ» But that’s why I’m a little more twitchy than usual once a month. Every time my WC appointment comes around, it just brings up all the frustration that I go through, for treatment that just makes things tolerable, and the fun waiting and wondering if / when my pharmacy will be given approval for each of my meds, etc, only to do it all over again a month later. πŸ€¦πŸ»β€β™‚οΈ It’s just a shitty cycle that it seems I’m gonna be stuck in forever.

But like I told the doctor today… yeah, I might have times where I bitch about this stuff more than usual, but I also know that things could be a lot worse. I see the other people as they walk into the office… or, sometimes, as they’re rolled by in a wheelchair. 😟 I know that while my disability is definitely full of suck, there’s a lot of folks that have it a lot worse than me – so I try to keep my perspective. (But it doesn’t stop me from thinking that there’s got to be something out there that could still help me more.)

So, yeah, I haven’t done one of these rants for a little while… so there it is. πŸ˜πŸ€·πŸ»β€β™‚οΈ Honestly, if you took my doctor appointment off of today’s schedule, everything was about the same as any other day – a random mix of good, bad, frustrating, okay, painful, tolerable, etc. πŸ™„ It just happened that today, the worst of the tremors happened at the most influential time. So despite several paragraphs of complaining, I’m fine… just thinking out loud and getting shit off my chest like usual. πŸ™‚πŸ‘πŸ»Β It’s all good…

A Little of This, A Little of That

The past several days have been kind of mundane, but I suppose that could be considered a good thing. I did make it out to see Bri on Sunday, and Ariel and the girls were also there when I first got there, so it was nice to get to see all of them in one pop like that. πŸ™‚ Bryson’s growing like a weed, and man is he a happy baby… always giggling and smiling at his mama, and for whatever reason he thought I was particularly funny and worth staring / laughing at for most of the time that I was there too. πŸ™„πŸ˜

Once the week started, everything’s just been kinda meh. Tending to bills, various paperwork, doctor calls, dealing with insurance, dropping off medical release forms at my attorneys’ office, etc. πŸ˜’ I could have just mailed those back to them, but because I let my mail sit for over a week before realizing that their correspondence was in one of those envelopes, I didn’t wanna cause any further delay – so taking the forms directly to them was the quickest option. πŸ€·πŸ»β€β™‚οΈπŸ™‚Β (I wanna do whatever I can to help them help me.)

The bills from the hospital didn’t end up being as bad as I was fearing. Six envelopes arrived from them within a day of each other, all having the same appearance as their typical “amount due” mail… 😟 so I just cringed and put them off to the side for a while, not quite ready to start writing checks. But when I opened them the other night, each one was just a form letter that let me know that because I have a fixed income, their financial assistance program covered the difference between what everything cost and what my insurance actually paid. πŸ˜―πŸ˜ƒΒ Nice to have something go my way, particularly right now.

Then today I had to go to pick up some soda, so I decided to go out to Meijer – where I could also grab a bag of dirt, some grass seed, and a couple bags of pebble-type stone. 🀨 The lawn guys kinda “over-whacked” some weed areas, like around my light post and the clothesline poles out back – so the next time we’re gonna have a few days of rain, I’m gonna try to cover those areas. πŸ€” Nobody was working in their garden department to help me get the bags over to my cart, but luckily I was able to just slide them over from the stack and onto the underneath rack of my buggy. πŸ˜₯ Getting them into my trunk, however… that required creative use of my right arm and right leg.Β (And that crap can stay in my trunk until I’m ready to use it, thankyouverymuch.)

Oh, the pebble stones… that’s for out by my mailbox. When it rains a little more than average, that area turns to slop – and not only does it make it slick for the mailman, but their vehicle also then continues to wear away that spot each time they drive through it. πŸ˜• I put sand there a couple of years ago, but it’s just time for me to try something else. I’m gonna wait until it’s wet for that as well, when I’ll drive my car out to the end of the driveway and just spill the new gravel directly out of the trunk instead of effing with the heavy bags.

But that’s been the tone of the first half of the week… just thinking about or working on “meh” stuff and getting it out of the way. πŸ€·πŸ»β€β™‚οΈπŸ˜ Some good, some bad, but most just “whatever.” I’ve been sleeping in the recliner, and that’s actually helped when it comes to getting sleep and waking up in a little better condition, but I’m starting to miss my comfy bed. πŸ˜΄πŸ’­πŸ›οΈΒ  Β (Well, it’s comfy as I’m going to sleep, at least… heh)

One more night in the chair and then my bed gets another shot. This all makes me sound so old… πŸ˜πŸ€•πŸ‘΄πŸ»
Oh… and my friend had her pacemaker installed yesterday, they had her in and out of surgery before noon, and she was back in her room and texting with me like normal by the early afternoon. πŸ˜ŒπŸ™πŸ» We’re fortunate to live in a time where there’s such a thing as “minor” heart surgery like that. I’ve got a short list of things that I wish we had cures or fixes for though, that’s for sure… but overall we’re lucky with what’s available to us when it comes to procedures and treatments for a whole lot of stuff. πŸ₯πŸ‘©πŸ»β€βš•οΈπŸ‘¨πŸ»β€βš•οΈ

Medically Deferred Deportation?

I’m gonna try to do a mental reset tomorrow, and get all this workers comp stuff out of my head until a hearing is scheduled and things are closer to being in motion in that regard. I did what I needed to do in so far as writing a response to claims in the report, so I can’t let the frustration and annoyance linger when there’s nothing else that I can do.

Plus I’m watching Rachel Maddow right now, and she’s covering the topic of people who are in the United States who have been receiving some sort of deferred deportation due to medical conditions that they have, for which they are receiving treatment within the United States. Apparently there are still plans in place which will remove that protection from at least some of the people who are getting life-saving treatment here. Treatment that they wouldn’t be able to get if they were sent out of the country… so that helps to put my problems into context.

Yeah, all of the stuff I’m going through is a giant pain in the ass, and there are significant implications to my future medical care that will be decided based on these current reports I’ve been talking about… and yeah, it’s really working my anxiety. But it’s nothing like what those people are facing. I can’t even imagine being previously allowed to stay in the country because you’re getting life-saving treatment, only to be told that nope – you have to leave the country within the next 30 days, which essentially sentences some of those people to death. It must be nearly impossible to process that news.

So yeah, what I’m dealing with feels unfair, unjust, and uncalled for… and I know how awful just that makes me feel – but man, how does your mind react when you find out that the country is kicking you out, and sorry about your luck when it comes to your medical treatment. Ugh…

And this isn’t even meant to be a political post. I don’t know how these “medically deferred deportation” people got here… whether they have visas, whether they were brought illegally as kids, whether they were originally granted entrance because they were seeking medical care and the administration changed its mind… because it kind of doesn’t matter. What matters is one moment they’re legally allowed to be here and get their treatment, and the next moment someone has decided that that particular program is no longer going to be allowed, at least in some circumstances, and they just have to go.

When you’re upset about your own shit, sometimes you forget how bad other people’s shit can be. πŸ˜•

You Never Get Used To It

(Oh yeah… this is quite a rambling one.Β  Strap in…)

While I was off of my thyroid meds, losing energy with each day that passed, preparing to have my second cancer scan done, as you may remember – I still had to drive over an hour up to NW Columbus, to go to the “Independent Medical Evaluation” initiated at the request of my former employer’s WC insurer. πŸ˜’πŸ€’ For those who haven’t been through it, it’s essentially one of the methods that can be used to try to get medication or treatments disallowed from a claim, based off of a report from a doctor (like in this instance) who has seen you as little as one single time. 🀨 That almost always sets up an Industrial Commission hearing, where (in my case) that report will be compared against the records of my own doctor, who has been treating me consistently for this work injury and disability for well over a decade. 😯

Of course my thoughts were more focused on the upcoming cancer scan at that point, so I went up, had my exam, went back home, and then mostly forgot about it while I dealt with my other medical concerns. But upon collecting my mail from the box a couple of days ago – I saw that enough time had passed for that doctor to have generated his report, which is easily 30-40 pages (if not more), and have copies sent to me, my attorneys, and my own doctor. I waited a few days to open it, because I knew there would be nothing good about it, nor would there be anything that I could do about that fact. 😟 It might as well have been labeled “Envelope Full of Frustration” but I finally made myself open and read it all yesterday.

I’m going to sugar-coat the shit out of this as I continue. πŸ™„πŸ˜ For my second pass through this thick report, I grabbed a yellow highlighter and began to mark and number the areas where more info was needed. 🧐 Whether it was adding context, pointing out inconsistencies, noting conflicting statements within the same report, or bringing attention to things that were implied, inferred, or assumption… I ended up with 48 different sections that required a response. And, unfortunately, there were several things that were simply false. Absolutely false. But still written in this report as if it were fact. 😠 I’m not saying that this doctor just pulled some things straight out of his ass, but it’s a shame how many “inaccuracies” were made by someone that shouldΒ have the presumption of being knowledgeable and accurate, especially given the duty that he’s performing and the way it could affect the future of anyone that he evaluates.

So now my copy of that doctor’s report has 48 highlighted areas, to go along with a numbered “rebuttal report” that I created to address each of those problem areas. So when I give it to my attorneys, they’ll be able to read my comments right along with the numbered and highlighted areas on the original report. πŸ€“ And despite having another doctor appointment at 11am this morning, I was up until after 2am last night… because correcting or clarifying (what I believe to be) inaccurate things in that report is really the only thing that I can do right now when it comes to “defending myself” or possibly helping my attorneys with their argument points. πŸ€·πŸ»β€β™‚οΈπŸ˜ž But yeah, once I started, the areas that needed my attention just kept coming, and I wasn’t going to stop and go to sleep until I had addressed everything that I felt needed it.

Of course my doctor will write a rebuttal report… something that he’s done many times before, to the point where he’s often repeating himself – because the facts are the facts, and they don’t change over time. But when there’s a hearing, it’s just expected that the doctor of record will submit a report, so he’s unfortunately stuck in this situation just like I am. πŸ˜• Thankfully, my doctor is awesome. And like me, he’s not a fan of having his words twisted, his knowledge and methods belittled… and he’s definitely not a fan of any claims, implications, or “facts” that seem to be based on little-to-no actual evidence. So not only will he write a truthful and accurate rebuttal based on all of the medical evidence, but it also serves as a way for him to “defend” himself – which is the same feeling that I have, and why I wrote my index of rebuttal points. 🀨

I have a ton of other things that I would like to say about the doctor’s report, but it’s in my best interest to just stop at this point. I’ve covered the basics, and you’re more than welcome to imagine the non-sugar-coated version… but even if you did that, there’d still be some things that would legitimately shock you. So now I can only hope that my rebuttal points will be helpful and useful to whichever attorney ends up representing me at the actual hearing. πŸ‘¨πŸ»β€πŸ’ΌπŸ‘©πŸ»β€πŸ’ΌπŸ—’οΈπŸ‘¨πŸ»β€βš–οΈΒ (And I’ve always felt the “commission” folks do seem to care as well.)

But the law firm that represents me is great, and we’ve (knock on wood) got a great track record from the beginning through today… so I know that they’ll have already picked apart many of the same things that I’m bringing attention to, but there still might be something that I say here or there that will contribute to the arguments that they use on the day of the hearing. πŸ€·πŸ»β€β™‚οΈ And at the very least, having more information “straight from the horse’s mouth” will be beneficial in general, since we usually only have about a half hour to sit and quickly discuss the case before the hearing starts.

It would be hard for anyone to find the words to accurately express the feeling and level of frustration that comes along with this situation. πŸ™‡πŸ»β€β™€οΈ To have decisions being made by other people, about things that will dramatically affect your future, knowing that “the truth” is the only weapon that you have… it’s such a helpless feeling, especially when you’re already feeling pretty damn helpless most of the time, due to the disability and pain that this whole thing is about in the first place. 😒 So other than the info I’ll be giving my attorneys, it comes down to sitting, waiting, and hoping… and there’s nothing relaxing or reassuring about that. 😞

Any good luck or positive juju that you want to mentally send my way is greatly appreciated. πŸ€žπŸ»πŸ™‚πŸ™πŸ»

Sweet Corn Festival

A few months ago, when I was still looking at the then-upcoming schedule of medical stuff, it looked like everything would be wrapped up well before this year’s SCF in Millersport. It’s tradition that me, Jim, Adam, and sometimes Brad will meet up for at least one of the days there to walk around, catch up, and see how many former classmates or teachers we can spot. But Jim messaged me yesterday to let me know where and when he’d be there… and it wasn’t until then that I realized that this week was already festival week. 😯⌚

The surprise is from bouncing back a little more slowly than I originally anticipated, so as my mind has been on all that stuff, I guess it just snuck up on me. I’ve got every intention of going… and in fact, I’m pretty sure I’ll be able to handle it much better than last year. 😬🀞🏻 Last year, I hadn’t had my surgery yet, so my energy levels were all over the place, and I was also stuck using my cane at the time. πŸ‘¨πŸ»β€πŸ¦― I can’t remember if it was for my back or for my knee, but I do remember that I only had enough oomph to make a single meandering “pass” with them from the ride area through to the food booths a bit past the covered bridge area. πŸ˜•

I was trying to “mind over matter” myself through the evening, but it just wasn’t happening. I feel kinda bad about how I was, because I know that my friends were concerned about me – and seeing me struggle to just walk around probably ended up being somewhat of a buzzkill for the rest of their evening. 😟 I think I was there for an hour at most before I realized that I was gonna have to call it a night, so it was nice that they walked me all the way back to where I parked so we could get in as much time as possible. There were a lot more unknowns at that point in time.

Since then I’ve had my thyroid removed, been dosed with radioactive iodine twice, been to doctors and a chiropractor for my back, learned of some new damage in my neck… but when it comes to the thyroid stuff, most of that ended up going about as well as it could, and the new “neck stuff” isn’t something that’s an urgent or immediate issue – so this year’s Sweet Corn Festival meet-up should be a heck of a lot better for all of us than the last one. πŸ™‚πŸ€·πŸ»β€β™‚οΈ I suppose anyone with visible health problems feel the same way… for certain moments in time you wanna act like nothing’s wrong, you don’t wanna let your friends or family see how bad it can get, ‘cuz you don’t want them worrying about you – whether the worry is justified or not. You want your “normal thing” to be that normal thing.

Meh… I’m just thinking out loud here. πŸ˜’ I’m obviously still not 100%, so I think I’m talking about it to keep myself motivated and optimistic. πŸ€” I did fix my sleep last night, something that actually surprised me, so I (hopefully) know what I need to do to not screw up my sleep or energy the day before we’re supposed to meet up. (Man, am I trying to jinx myself lately or what? 😏)Β I’m just really looking forward to the possibility of having a normal day with my friends at our old stomping grounds, with the thoughts of all my current “other stuff” being pushed from my brain as we have a good time being reminiscing old farts, eating overpriced crappy-but-awesome fair food, and maybe seeing some other old fart friends in the process. πŸ€·πŸ»β€β™‚οΈπŸ™‚

Roll With The Changes

So I tried the Impossible Whopper on my way home from my workers comp doctor appointment today. It’s strange… I don’t know exactly what to say about it. πŸ€” It was different than a normal Whopper, which you’d assume, but not in a way that made it any worse or any better than the traditional kind. πŸ€·πŸ»β€β™‚οΈ I suppose the only thing that I’d have even noticed, if someone had just brought it to me and let me think it was a regular Whopper, was that it was a little dry / less greasy.

But by the time the cheese, lettuce, mayo, ketchup, etc is added – it’s honestly hard to notice any difference. And if it is legitimately more healthy (or at least less un-healthy)… something which I never bothered to Google… then yeah, I’d probably always order it over the “normal meat” Whopper. I think White Castle has the same kind of “fake meat” in a version of their sliders, so I might have to give those a try sometime as well. I’ve got no problem reducing my meat consumption as long as it tastes basically the same and isn’t detrimental to my health. πŸ„πŸ€ πŸ€·πŸ»β€β™‚οΈ

As for my appointment today, again I suppose that I just took for granted that it wouldn’t be much different than any of my other visits with the workers comp doctor. But since it was with his PA (also a “real” doctor, of course) there was a set of “fresh eyes” on all my info. πŸ‘¨πŸ»β€βš•οΈπŸ”Ž He actually did that because the first time I saw him, many months ago, when I was originally going to be moved mostly to his schedule, I wrote a summary letter for the past decade and said I’d appreciate hearing if anything jumped out at him which may not have been something that me and my original doctor had been addressing.

Be careful what you ask for, though… 😏 It’s nothing bad bad, but having new xrays and scans of the area from fairly recently – he took a good long look at them in comparison to the ones from before / recently after my original surgery, as well as whatever few that have been done between then and now. πŸ‘¨πŸ»β€βš•οΈπŸ’» It’s nothing that I’ll have to address any time soon, but as always expected… after over a decade of three of my vertebrae being fused, the one above it is just showing signs of eventually needing attention as well. πŸ˜• Nothing horrible, nothing urgent… and since it’s something that I was already aware of as an eventual and likely possibility, having him remark about it honestly just rattled me because it hasn’t been one of the things on my mindΒ lately… not because it’s an “Oh no, a new surprise thing” thing.

But I like this doctor… I mean, time will tell if I like him as much as Dr Walter… but he talked with me a long time today, despite knowing that I’m still somewhat radioactive, and in detail that let me know he’s aware (or at least assumes) that I’m able to understand more than the average patient. πŸ€“Β I think he’s even older than Dr Walter, so I’m not sure why he’s got a PA position there. It could be he does his “real” doctor-in’ on all the other days when he’s not at this particular office. πŸ€·πŸ»β€β™‚οΈ But yeah, it’s fine… and if anything, I still think the “fresh eyes” are good… especially since he might end up having to write some reports that explain how my original work injury / surgery is what has caused this newer potential issue – because you can bet your ass that I’m going to do everything that I can to get it included into my current claim for wheneverΒ I might have to start doing things that involve it. 🀨

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.