Pace Yourself, Dummy

Felt like I had a little more energy than usual yesterday, so I trimmed my hobo beard here in the living room (with a trimmer that allegedly catches all the trimmed hairs) but then of course I still wanted to vacuum up whatever it didn’t get. Turned it on, but the vacuum wasn’t sucking, and then it just shut itself off. 😒 Awesome. Didn’t realize how many filters were inside this thing, but they had become clogged with the flea dust that I spread and vacuumed up a couple weeks ago. 🤷🏻‍♂️🔧 So I had it in pieces, took out and washed all the filters, and that was it for me.

Not that I had anything that I needed to do after that, since the filters needed to dry overnight anyway before I could even try it again… but yeah, went from “okay” to completely whupped without any warning. Took a shower to see if that would jump-start things, but nope… just made me ready for bed. 😏 And yeah, I was thinking about how I’d be missing the meteor shower, but there were enough passing clouds that I didn’t feel too crappy about not having the oomph to stay awake and set up the camera to do things properly. 🔭🧐 Looks like it might end up even more cloudy tonight, but we’ll see.

But yeah, as I was starting to fear as the time got closer – just a few days of being back on my thyroid meds hasn’t quite done the trick yet. I’m noticing a difference, so that’s good, but I just have to be patient and stop trying to do more than I should. I mean, taking apart the vacuum wasn’t even physically difficult… but yeah, I just gotta keep taking it easy for a while. That’s what I did today, and the most I plan to do tonight or tomorrow is maybe that time-lapse video and then getting through the current stack of mail. 🙂🍰 No physical stuff, even though I’ve got a basket-and-a-half of somewhat radioactive clothes that I will need to get to sooner than later. (But it’s out of the way and not hurting anybody, so meh…)

Only real obligation tomorrow is my workers comp appointment, which is typically just in and out unless we get chatty… but it’s my doctor’s assistant that will be seeing me tomorrow, so other than letting him know how run down I’ve been for the last month and why, it’s just gonna be getting those meds on track. I’m barely out of the window where I’m technically supposed to be avoiding people for extended periods of time anyway, so I’ll make sure to let everyone in the office know that when I get there, which should also help to keep this visit short and to the point.

And whether this jinxes me or not, I like that I haven’t gotten a call from my thyroid doctor’s office on either of the business days since I had the scan done. 🤔 Different, unfortunately, from one of my friends who has been having some heart testing done – and she got one of those “Let’s go ahead and get you in here as soon as possible…” calls, which always makes your stomach drop. 😳😟 Can’t dwell though… all this shit is in the doctors’ and God’s hands, and we all just have to hope for the best. 🙏🏻

Advertisements

I Have My Reasons

Still hangin’ in there, still waiting through this process… 😟 of which the next step will be Monday, when I’ll get (what should be) my final lab work done before they decide if my levels are where they need to be for the radiation dose the following week. 💉😬📉 I’m more anxious about the test than I am the dose later, simply because there’s a chance my levels won’t be right – which would mean going even longer without taking my thyroid meds, until they are. 😐 Without elaborating, I really, really don’t want to have to do this a day longer than I absolutely have to.

Unless it’s unavoidable I’m pretty much just staying at home and trying not to move around too much, to keep from throwing everything even more out of whack. I can’t fake my way through feeling okay right now, so staying at home lets me feel how I feel, protects me from anything that might make it worse, and protects others from having to see me like this, acting how I actually feel. 🥺 My “game face” is out of order. (I haven’t even been on Facebook for days and days, and the last time was to just let everyone know I was okay. I really hate how this has been affecting my interactions (or lack thereof) with friends and family.)

And I don’t blame people for being concerned, or not knowing how to react, when the topic is cancer and there’s still more “unknown” than “you’ll be fine” at the moment. But this current craptacular phase of “bleh” isn’t (likely) caused by anything cancer related, but is actually due to not being able to take the thyroid meds that I need. But to everyone else, I’m sure it looks and feels as if cancer is kicking my ass, which leads to all sorts of difficult and crappy emotions.

Toni and Shannon invited me out for a bonfire last night, and in my heart I wanted to go… but I wouldn’t have been able to conceal how I felt, physically or mentally, and I honestly didn’t want to be a buzzkill on their evening – which is what I likely would have been. 😒 If it turns out that the doctors weren’t able to remove all of the cancer, or if it has spread or changed or anything… that’s when I’d be more willing to let people feel bad for me, to treat me differently, etc. I do feel like hell right now, but I would feel like it would come across as “crying wolf” – since even though I know why I’m sick, that’s not how everyone else is gonna see it. I reassure people that I’ll let them know if there comes a time when they truly should be concerned or worried for me, so I hope they know I mean that.

Meh… anyway… see what I mean about my mood? The same way I ramble about it on here now and then, I just didn’t wanna end up doing that to them last night. (Or to anyone, really…) Instead, thanks to Shannon texting me again this morning to let me know, they all had a good evening. Sharing lots of happy memories and stories about Mom, while still commenting on how it doesn’t seem real, how it doesn’t seem fair, and how as we all get older – how it’s getting harder to escape all of this type of bleh. Having me there, in my condition, certainly wouldn’t have helped to change that opinion.

But with any luck I’ll get to be one of those surprise cases in the future, where we’ll all be sitting around together, upset at whatever injustices we’re seeing or experiencing, but then someone will be able to say “But hey, you had cancer and you’re still here and fine now… so there’s always hope…” 🙂🤷🏻‍♂️🙏🏻

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.

Bubble Doesn’t Always Work

It’s been a rough, rough week… but I’m not even gonna talk about all of it. I don’t want to take the chance of spreading more negative emotions just because it helps me to get things off my chest. Going to bed early tonight. Hoping for a reset of my body and mind. Glad I made it through the week… sadly, the same can’t be said for one of my old friends from school. He was a couple grades ahead of me, so I was actually closer to his little brother. Definitely one of those things where nobody even saw it coming. But yeah, I’m tired of this week… so the sooner I get to sleep, the sooner it will be over and I can try to start fresh.

Happy (late) birthday, Dad…  trying to get good enough where I can visit soon. Sorry… that’s all I can say. 😞