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˜•

Focusing On The Positives

Went to my follow-up appointment yesterday with the endocrinologist after my full body scan. I dunno, I guess it was mostly good news, but it wasn’t the “all clear” that of course anyone would prefer to hear. πŸ˜• But honestly, the chances of a doctor saying something like that are probably pretty slim anyway – since the last thing they probably wanna seem like they’re doing is handing out “guarantees” when it comes to something with such serious potential consequences.

The Negative: The scan did show a few tiny areas that lit up, meaning there’s some remaining thyroid cells there – as they had absorbed the iodine radiation and blew their cover during the scan. πŸ”¬πŸ‘¨πŸ»β€βš•οΈΒ Also, there’s no way to determine if those thyroid cells have cancerous cells in them as well… it just confirms that thyroid cells are there, and that we’ll need to periodically keep an eye on them. πŸ˜’

The Positive: The tiny bits that lit up were where they should be, where my thyroid used to be, meaning that none of those cells had migrated to any other locations where they could cause different kinds of trouble. The radiation that made those cells visible to the scan also serves to continue killing and shrinking those cells, so even over the next month or so they should continue to decrease in their already small size.

You can think of the surgery in the same way as someone trying to carve a hunk of fat off the edge of a steak before grilling it. Someone like me, I’d want to get as much of that fat cut off as possible – but at the same time you don’t wanna accidentally cut away good, non-fat, steak meat. 😏 Same thing with my surgery. The surgeon tries to cut away all of the thyroid, but not at the expense of accidentally cutting away non-thyroid meat. 😳 I guess it’s not terribly uncommon for tiny bits to be left behind because of that logic.

It won’t be for quite a while, but next year I’ll have to have an ultrasound of that area, to see if those cells appear to have grown. And since thyroids don’t grow back, I’ll assume that would be a bad thing. So at least the next “next step” isn’t stopping my meds and getting dosed with radiation again. ☒️🀒☒️ That tells me that while there is reason for concern and monitoring, it’s not of the “oh shit” variety where one of the most extreme measures is the first measure taken.

So, like I said, I guess overall it was a good result. I mean, there’s plenty of ways where it obviously could have been worse, but it’s still shitty that my first radiation didn’t kill offΒ all of the thyroid cells – because there’s no way that this won’t be something that floats around in my thoughts more than I’d like it to. πŸ˜’ I guess all my other recent lab numbers are good though, and I still feel like I’m gaining back more energy with each day that passes, so there’s that as well. I just wish that was the only thing that was going on with my neck.

So, yeah… πŸ€·πŸ»β€β™‚οΈ

Something Like That

This heatwave that we’re currently going through… it’s a pretty good way to explain how I’ve been feeling over the past few days. Just go outside, walk around your property for about 15 minutes, then stand there a while… and that’s basically how I’ve been feeling each day all day. Again, not bitching, just trying to describe it in a way that people can understand.

Thankfully I’m almost half way through the process, so at least there’s a light at the end of the tunnel that I can look forward to. No matter what results I get, at least I can get back on my thyroid meds after the scan has been completed. It makes me feel bad for folks who have suffered with thyroid issues all of their lives, because the constant nausea, overheating, and dizziness… it’s no joke. Not thrilled that it has been made crystal clear that this will indeed be a medication that I’ll be taking for the rest of my life though.

I’m a cheap-ass, so I usually wouldn’t do this, but last night I turned the thermostat all the way down to 68 when I went to bed. I knew I’d be sleeping at least part way into the day and the house would heat up quickly, but despite it staying that cool in the house – I woke up early and completely drenched in sweat again. (Also… gross.) That’s why I mention how far along I am in the process… because if I didn’t know that there was an end to this, it would be some scary shit.

I’ve been drinking a lot more water, so the muscle spasms and dehydration hopefully won’t become an issue. It’s pretty shitty though, that the insurance industry has decided that this is an acceptable thing for patients to go through while preparing for their second radiation dosage. The alternative way, staying on your meds and just getting two injections before the scan… that costs several thousand dollars, so I guess you can’t blame them for trying to find somewhere to cut costs in what has likely been a very expensive surgery.

Again though, knowing that this is a temporary thing for me, it really makes me feel for those folks who don’t have insurance at all, and even for the people that do but have a chronic condition that still isn’t covered by their plan for whatever reason. As with most things like this, it’s something that we don’t think much about until it starts to affect us personally. So, yeah… still feeling super awful… and I feel like it’s continuing to slowly get worse, but I’ll be good as long I just keep reminding myself…

“It’s only temporary. It’s the lack of meds, not anything more scary. You’ll have more answers soon. Just (n) more days and this will all be over. Consider yourself blessed that you’ve made it this far. Plenty of other people have it worse than you, and it’s not temporary for them. Yeah, it sucks… but don’t be a pussy. It’s only temporary.” etc…

I’m trying to stay positive. I need to stay positive.

Checking Off Boxes

Typical “workers comp, beginning of the month, get my scripts filled” day today. Three different calls to the pharmacy, issues with my information in the computer, problems with certain ones not being approved… same bullshit as usual, except due to the incorrect information in their system I even had to stop in myself, with receipts and printouts and crap from last month. The folks that work there are great. It’s never the people there that I have a problem with… and after my visit we think everything is now updated, correct, and in process of being authorized – so maybe sometime today I’ll actually be able to pick them up.

I had to be out today anyway, so stopping in to get all this stuff sorted out wasn’t a big deal. I mean, I actually feel kinda bad for them – with how much of a pain in the ass “my case” is for them each month. It makes me wonder if any pharmacies have ever decided that certain customers’ situations were just too much work, too many calls, and too big of a PITA – and just told them to take their business elsewhere. ‘Cuz I can see how they could feel that way about me, if they weren’t such understanding and helpful folks.

But at my other stops, along with having several vials of blood drawn, we’ve started getting a lot more things set in stone. I’ve now got dates (if not exact times, yet) for the next blood draw, the administration of the radiation dose, how long I’ll need to stay away from people (which included rearranging another unrelated doctor appointment), when the full scan at FMC will be, and then the followup with my main thyroid doctor after all of the results are back and interpreted.

It’s surreal… how this is such a “big deal mind fuck” thing for me as I’m going through it, yet I’m just one of many. There are enough people needing this kind of treatment that once a week, every week, it’s radioactive “dosing day” for thyroid patients at FMC. But for whatever reason, even as you’re out in town, seeing other people doing whatever… it’s easy to feel like you’re the only person going through this shit, while actually we probably pass by people each day who are going through the same thing or worse. Working in nuclear medicine, giving the doses… I can see how that job could start feeling pretty heavy after a short while.

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.

Trying To Not Read In To This

I got a message two days ago from the doctor’s office that is handling my thyroid cancer treatment. My next session with the radioactive iodine treatment, which should be my final session (if everything goes well), was scheduled to start near the end of July… but they now actually want to schedule that as soon as possible. 😐 They asked me to call in yesterday so we could start making a plan, but to be honest the message had me a little too shook… πŸ˜₯ and since I was actually having a decent day yesterday, I didn’t wanna risk nuking that by bringing all of my thoughts back to the “unknown” about what’s remaining inside me, if anything.

That’s also why I took advantage of the day yesterday to get caught up with some things around the house, because I know that this next step is gonna be a bit of a nightmare. 😣 I have to completely stop taking my thyroid meds for a couple of weeks, and they were clear about how it could have drastic physical and mental side effects. (Also part of the reason that I stopped the Paxil, so I didn’t have one crap thing on top of another.)Β Then once the thyroid medication is completely out of my system, that’s when I’ll go to the hospital for the radioactive pill and another full body scan about a week later. πŸ˜•

Confession… I didn’t call them back today either. 😞 Instead, what I’m going to do is just go into the office tomorrow and talk to them in person. To be sure that I understand the details of the plan, to be sure that everything is scheduled properly… and also to see if I can catch some kind of vibe by the way that they speak with me about it. 🧐 Like I said, I’m trying to not assume that something has gotten worse just because they want to start things sooner. 😳 It could be as simple as being easier on their schedule, and just better for me (or anyone) to do all of this “second phase” stuff sooner rather than later anyway.

So yeah, that’s the next thing on the radar… movin’ in fast. 😟 And lemme tell ya’ something. πŸ˜’ Uncertainty, when it comes to something like this… it’s a special kind of slow, drawn-out torture. I’m ready though. I was doing good at keeping it out of my thoughts up until now – but whether I got that call a couple days ago, or whether we stuck to the original end-of-July starting point… either way the anxiety was gonna come. So I agree… let’s get this shit started. 🀨

Unrelated: I just updated my Windows 10 and all of my emojis now have thick black outlines. πŸ€”πŸ€·πŸ»β€β™‚οΈ

Good? I Guess? Maybe?

Got the fastest call-back from a doctor today about those knee x-rays. I was thinking I wouldn’t hear anything ’til the start of next week, but nope… scans are back, and there’s nothing abnormal that can be seen in the x-rays. πŸ˜πŸ˜’ Of course that doesn’t mean there’s nothing wrong… I mean, it could mean that, but it could also mean that it’s going to take an MRI to actually see the problem. But as I was warned, they said that they can set me up with some physical therapy appointments.

I told her that I felt like I have been on a slight upward path, and that I was gonna see how things go through the weekend – then if it doesn’t seem like it’s getting significantly better I’ll probably call (or stop) in on Monday and get that scheduled. Not looking forward to that idea, but it’s better than continuing to hobble around and possibly make whatever-the-problem-is worse. πŸ˜• And then, of course, if a full round of PT doesn’t work, then we can ask for that MRI. Cripes… fecking MRIs… πŸ™„

In unrelated news… I have a tractor in my back yard. 😳 Lawn d00d sent a couple of his guys over late this afternoon to drop it off and size up how they’re gonna go about things tomorrow. I’m assuming tomorrow… unless it keeps raining, which is what chased them away today. The line of bushes have grown a surprising amount since we originally made plans, so I don’t know if he’ll end up plucking them with the claw on the front of this tractor or if they’ll just have to go down the line with a chainsaw, getting them one by one. πŸ€·πŸ»β€β™‚οΈ Either way works for me, so hopefully they don’t stress on it too much if I’m not awake or not here. πŸ™‚