Tag Archives: menopause

Life, in a few words

13 Apr

5:19 pm

It’s mid-working day on a Tuesday, and all I have to say is, I am tired. Like, I know I work from home, but…I feel kind of burnt out. To be sure, I am grateful, which is why and how I keep going, day in and day out; but I’m tired, too. It’s made keeping up with this blog difficult, actually, even though all I need to do is take 20 minutes and jot a post. So, I am finally doing that now…

In a nutshell, my dad was officially diagnosed with mild-to-moderate dementia/Alzheimer’s disease–and um, yeah, if you’re sort of going, well, what does that mean, I am rolling my eyes and thinking the same thing. Life! Why can’t you be who I want you to be! Haha.

The truth is, that’s about as close as we’re going to get, in terms of closure to our questions about the why and how of his recent descent into bizarre thinking and behaving. (And, it’s about the same with getting any definite answers when it comes to menopause: well, your serum levels say this, but…you might feel this, or that; this drug may, or may not, take away some, or all, of your symptoms to some, uh, variable degree…) Insert head-crashing-on-table emoji!

Through a lot of sweat and tears (and PTSD-like anticipatory dread of his phone calls to us and our ever-repetitive answers back to him), we’ve somehow managed (all remotely, with the help of our soon-to-be ex-step-mom and the nursing staff) to get him to stay at the nursing home since December; and get him back and forth for an MRI and then, to see a neurologist, who did an EEG and came back with an official diagnosis (they found evidence of dementia on the scan, which puts *us* at ease, mostly; I think my dad has already forgotten about the entire appointment).

What else? Well, we’ve gotten him through a messy divorce involving cleaning up his dumpster fire of a financial life and applying for Medicaid. One day soon, we’ll have to go back to our home town to “transfer” him (kicking and screaming, I’m sure) to a new facility that takes Medicaid as well as clean out his (our) farm house in order to list it for sale sometime in the late summer or early fall. He’s lived there since 1979, and it’s where I grew up; needless to say, it’s the end of an era, *his* era, but he won’t be around to see what happens to the place that he loved so fiercely that he never left. (My mom bolted us out of there in 1988 after she divorced him; and we only went back to the farm to visit him, once in a while, over the years.)

What have I taken away from this experience? Hmm. Well, I can say for sure that neither my brothers nor myself is in any way interested in buying the farm (he cannot gift it to us on Medicaid) for any kind of old time’s or sentimental sake. Going through this process has made me glad I don’t have kids of my own and clued me in further as to why I never did. And, I am seriously thinking of hitting up a lawyer and having some sort of living will written that explicitly instructs my partner on what to do if I develop dementia.

I’m not sure if I care enough about my dad to look on the bright side; he wasn’t a good father, he didn’t care about his kids when we got older (he cared about himself), and I’ve literally spent my entire adult life trying to build my own wealth because he one, never cared to do so for us when he was younger and two, spent (like, beyond spent) any and all retirement savings he had doing stupid shit. We aren’t jones’ing to visit him in the nursing home; the only time I’ve seen him is on a video doctor’s appointment a few months ago, and he treated me like I was a “little woman.”

I feel bad for him, I do; I feel guilty about not caring that much, even guiltier about letting it go and living my life. But, I have to; my brothers and I have to let go and live our lives. We get to be happy…even though what he’s going through really sucks. No one can live it for him, unfortunately.

That’s mainly what’s been happening here. I am still cranking out 1.5 jobs, wrangling two new mutts (the one needs some serious training–we seem to have finally housetrained her; now we’re working on getting her to not go cray-cray pulling and barking when she sees another dog or human on the walk–and they both need to be treated for heartworm, which the one is getting and the other will get in a few weeks), and managing my post-menopausal stuff (things have gotten better, but it’s up and down; I think that being athletic and sober has really helped my symptoms not be all that bad, relatively speaking). I am still really happy and grateful…and looking forward to life post-vaccine (gulp: we got the Janssen jab a week ago, so…haha, I am just waiting for that two-week mark to come and go without um, a blood clot!?).

On that note, I am being eaten alive and sweating to death; seems the weather has turned to zero breeze and 90% humidity overnight, and the mossies are out in full force, nibbling at my ankles and feet. Hope all are well and I write more soon!

Stay strong, and stay sober. You got this.

In with a bang?

21 Feb

12:20 pm

Is that an expression? I think it’s actually, out with a bang, but considering how much of a whirlwind the first seven weeks of 2021 have been, I don’t think it really matters…

I’ll dive right in, how’s that? I have to say, while this year has had a lot of good stuff, which I’ll get to later, it’s been sort of a shit show on one end. I feel less in control of life than I have ever felt–mainly due to my dad having dementia, believing he is being “held hostage” by us, his three kids, in the skilled nursing facility (aka, nursing home) where he is at right now. I think I have a newfound understanding of anxiety! I mean, I have always reacted to certain things or thoughts with anxious behavior, but I have never felt what I guess some people describe as “anxiety,” which is, I wake up every morning with this feeling of uncertainty, like an elevator is dropping in my belly, like there is no solution to how to stop the rock that is going to be careening downhill at me that day.

I have missed writing, and I’m sorry that I have not this year; I just feel like all I’ve been doing, all year long so far, is triaging the dad situation on the weeknights and weekends with my brothers: getting him to a nursing home, getting him to stay there, getting him on much-overdue meds; delving into his crumbling life, which is, managing his assets to get him through his divorce in order to apply for Medicaid in order to find him a “home” for after he is (soon to be) discharged from the nursing home. (He’s there for hip rehab from a hip reconstruction surgery that he had to have because he drove at night without breaks, crashing his car into a tree and crushing his hip; he refused to stay at the first rehab back in September, and ultimately, he was in and out of ERs until early December–it was a mess!)

Um, I have felt mostly guilt and anxiety over this, but, past few weeks, as we talk more with him and the staff–well, I am starting to feel less guilty. It really is what it is, and there is nothing we can do to change or fix it for him. His short-term memory issue does not seem to be getting better, in that, he does not remember from one minute or block of time to the next; practically, that means he doesn’t remember the conversation that we had with him yesterday, let alone yelling at us for telling him that we are moving ahead with the divorce in spite of his objections. Where his mind is at is, I was served papers and OK, I am in agreement with getting divorced. In reality, our step-mom filed in May 2020; he was unable and/or unwilling, mentally, to respond by the deadline last July; so, we have managed the work of organizing his assets, hiring an attorney to represent “him,” negotiating the settlement proposal with all parties excluding him, and finally, beginning to list his assets for sale as part of the fulfillment of his end of the deal. It’s just one example of the loops we’ve found ourselves to be stuck in when trying to reason with him.

In fact, there is no “reasoning” with him anymore, even though he is quite lucid. Which means, when the time comes to “put him somewhere,” he is going to go kicking and screaming, literally. And, just getting to the point where we are all somehow OK with that–that’s caused and causing me anxiety. However, the facts don’t lie: he has dementia-thinking (which, goes FAR BEYOND memory loss and goes way back, before his accident). Like everything, it’s a process, and, well, many others have been down this road. This, too, shall pass.

Anyhoo… Other than that, life is pretty OK! Working a ton–my new job continues to kick my butt; but, at least I am down to only one gig–and spending a lot of time training our two new foster dogs. The second one, a girl, is a handful, but she is getting better and better at being someone’s dog. We had to sort of housetrain her when she got here; we’re working on getting her to not bark at our landlady; soon, I hope she can just chill inside, not in her crate, when I leave the house.

This weekend, I started on new glaucoma drops (yeah, man, wtf? I am 46 years old, and the doc said that I have mild in one eye, mild to moderate in the other!), and they suck. They give me anxiety! It is strange and I thought I was imagining it, but no, turns out, thanks to good old Google, that timolol is notorious for its systemic side effects. I am sensitive, sure, but these drops make me feel really out of sorts. We’ll see; I mean, there are other options, so, of course, I am gonna have to advocate for myself.

And, I have to say, the menopause stuff (yeah, man, am I just a fast ager? Haha) is finally seeming to iron itself out. My hormone therapy still does need some tweaking, but, after, um, almost a full year, at least I am beginning to see what might be ME and not a side effect (or vice versa); and, importantly, what works for ME and not what every article on the Internet says “should” be the right dose or effect! All this said, my night heat is much better (not gone, but better), my insomnia has much improved (knock wood!?), and the “other stuff” is super-slowly getting better. Thank GAWDess. The worst thing about this has been, ya don’t know what to expect so everything feels permanent and catastrophic. I would tell my early 40s self, and anyone out there who would listen, this is NOT true; it will change, and it will get better.

Whew.

In any case, I remain ever-grateful, still, for my sobriety, for the lessons learned. No matter how many ups and downs the days take me on, I still have that overwhelmingly sense of, I am one of the lucky ones, I got out. No matter how “bad” things seem, I am still sober–and that is everything good. That is literally everything. That is glitter and unicorns and an endless Mardi Gras parade.

A painful truth vs a beautiful lie

21 Nov

9:23 pm

One day last week–sorry, it’s been SO LONG since I’ve posted a blog; I’ve been buried under work, the kind that makes me not want to read or write for “fun” after the day is over–I came across someone’s meme on Facebook that read: You hate me (haha; only on the ‘book can you feel assaulted and insulted after three words of a half-read meme) because you are a beautiful lie and I am a painful truth.

Ouch. And, huh.

Well, for one, I don’t hate this person (or anyone, for that matter!) and I really haven’t been thinking about it all that much–her life, I guess, and how it’s turned out these past oh, 30 years since she got pregnant at 16 and dropped out of high school (and went on to build a nice life and family, btw)–but, now that you mention it; yeah, it’s kind of true. Not the hating anyone part, but the difference between beautiful lies and painful truths *on social media*.

The sad (to me) reality is, we don’t ever tell or talk about our painful truths. I mean, not really. Not ever, really. And, I guess that’s the challenge of authentic living–how to talk about your painful truths without scaring people away. I am still figuring that one out, but, I will say, social media turns that battle even more uphill because of what it encourages, which are glossy, doctored misrepresentations of a life. It’s not real!

I think I might just need to take a break from Facebook again…

Speaking of real, things are still pretty real here. It’s been quite the trip these past four months/three effing years (haha), trying to “balance my hormones.” After years of dealing with the most disturbing symptoms of perimenopause (which, after going on some Facebook groups, mine have not been bad at all, compared to what some other women go through), nothing really scares me about it anymore. However, I have kind of resigned myself to the fact that, it’s just going to take trial and error, time, and hopefully, not becoming an exhausted lunatic before either *I* get my “hormones balanced” once and for all, or, they balance themselves out over time.

The insomnia comes hard the majority of nights, and I usually don’t get more than three hours in a row–it truly sucks, but there is beauty in those wee morning hours. I see new constellations now–a reminder that a whole season has passed since I was sitting on the floor next to my dying dog, trying to comfort her as she freaked out all night. I find solace in knowing that the light I see is ancient, some of it from sources that have long since burned out; that that light will be here LONG after I am gone. There is immense beauty in getting a momentary glimpse of what is really here, which is so much bigger than me, and my life, and my dog’s much shorter life. I don’t know.

On a different note, today marks ONE year since we flew back here–a place that we lived for many years, left for about two, and then came back to last year (we moved back into the same house, with our old furniture even!?). It’s been a strange year, actually, and not just because of the Covid. It’s been a year of, well, painful truths, honestly. Good truths, but still painful ones. I feel like the vast majority of people we called friends here have either moved on physically/literally or just aren’t really friends anymore. Maybe they weren’t to begin with? I feel like I have aged two decades in two years and am really done with passive aggressive behavior.

Good also came: I was forced out of a job by the Covid but ended up finding well, a better job. I am slowly but surely getting over putting our dog to rest (sweet girl!) and becoming ready to love a new furry best friend again. I would never in a lifetime have volunteered to make the turkey, but–this year, I feel safe enough in my own skin and um, cooking abilities, to have put that into motion! I am heading up the Thanksgiving turkey and stuffing-making! What? Yup! Add a key lime pie to the mix (I swapped desserts for drinking when I first got sober), and we’re going to be very good to go next week. (we are doing a small thing, just a few close friends who practice safe Covid’ing)

Yeah, so, that’s it, in a nutshell. I mean, lots more on the parents front–aging sucks; mental health disorders left untreated over the course of a lifetime suck even more!–but I will save that for another Saturday night. 🙂

Happy sober weekend, all!

Sunday afternoon ramblings

4 Oct

2:53 pm

As I wrote about recently, over the past few weeks (going on a month now, actually), I’ve had terrible leg pain. I thought I had some terrible disease (of course, I did), so I went to the doctor–a first in that, this doc took me seriously and ran every blood test possible for a complaint like, “my legs hurt”–and, well…nothing is wrong. No Covid, no infectious disease, no autoimmune disease, blood panel good, muscles fine. I also got a blood test done for both my estrogen and progesterone levels, and for where I am at in the process of both menopause and taking estradiol via the patch, those came back normal, too.

SO, I have to conclude that it’s something to do with the estradiol patch (which, btw, is only one method of transdermal application; there are also creams, gels, sprays, probably others). And, that kind of really sucks since, I don’t know if another via-the-skin application will work for me. I am going to keep riding it out and see what happens.

So, that’s one reason I’ve been quiet on my blog, I’m just trying to take care of myself–mentally, it’s really hard for me to accept pain and not being able to work out because of pain. I usually just push through pain, but my muscles seem to take days to recover from even the slightest workout, so I have been obeying my body’s commands. It’s not easy not knowing either; and, I’ll never know unless I take the time to go off everything, let my body readjust, and then, go back on things one at a time. The patch is working for my night heat and insomnia, though, which is glorious!? Still, if I can’t live WITH the medication, then…it’d have to be a dealbreaker.

I am well, and my doctors took me very seriously–so, a huge win. Plus, it appears that I never got Covid, which is a relief as well.

I’ve been working full-time and will start working a new remote contract gig this week, putting me at full-time-plus for the next few months, so…that’s been great! It’s a relief to have work, sure, but even more of a relief to not have to job and gig search for a while.

Another thing that’s been going on is that my dad has gotten himself into some physical trouble (think: crashing cars and breaking bones) due to well, untreated bipolar disorder (in my opinion). Long story short, he’s doing fine but he’s still up to his tricks, so to speak. Lesson learned on my part: he will never change until and unless he takes medication; he will never admit anything is wrong; and, importantly, there is nothing I can do for him. I have thought of telling him, I refuse to talk to you until you get meds, but, I don’t quite get how an “intervention” or “ultimatum” would truly work or be beneficial for a mental health disorder like his. He doesn’t believe–refuses to believe–that there is anything wrong. How can you force him to consider an ultimatum that doesn’t really mesh with his version of reality? I don’t know.

On that note, I am going to exhale–my mantra these days–and go for a walk. I can do that at least; it’s funny how much of an “athlete” I am: I have already acclimated to this new level of pain and have found ways around it. I will never stop working out! (maybe that’s what got me here to begin with? lol)

Thank you, one and all, for still being part of my life. This blog-o-sphere is truly one of my favorite places to be on a Sunday afternoon…

A challenging few weeks

22 Sep

11:10 am

I just wanted to check in to say, hi, howdy, hope all is well with everyone!

In brief, I have been suffering…from pain, like, full body pain. I’ve gone from being an athlete who stands at her desk most of the day, walks the dog (well, with no more dog, I walk myself), AND goes for a jog or swim/soak every day. SURE, that’s a lot, and I do have probably above-average aches and pains. BUT, since last week, the symptoms of achey joints and malaise that I wrote about all the way back in late July–and have only kept getting worse since then–took a turn for the much worse!

Last Tuesday was the last day I could jog–or walk–without pain. I also had some weird neurological stuff going on Friday through Sunday, but thankfully, that’s gone. (I had headache; cognitive difficulties; changes to vision, hearing; anxiety–um, happily, living through many years of active alcoholism and ridiculous hangovers prepped me well to endure feeling like I was losing my mind for a few days!) It is scary and it sucks! I have been trying to not take anything (no pain meds, no CBD) and see how I feel, but every day, I wake up feeling a burning ache in my entire leg muscles, lower back, and joint pain pretty much everywhere.

I thought it was that my old chikungunya infection (from 2014; it comes back now and then, with mild symptoms) had resurfaced, but, that usually doesn’t last for more than a few days; and, this leg muscle pain is definitely not how that feels. I have a hunch/obsession that this is all due to the estrogen patch–strangely, the same week I put my first patch on is the week that these pains started. But, I don’t know. I mean, how can one know? Maybe THIS is menopause and I need more estrogen (higher patch dose). Maybe this is the patch side effects–and I just need to give it more time? I’ve been on it for about 10 weeks, and the pain has just increasingly gotten worse. I don’t know.

I am starting what I would call my “diagnostic odyssey” on Wednesday by going to see a general doctor to rule out some of the obvious–Covid, Lyme’s, maybe some common sources of bacterial or viral arthritis, possibly some common autoimmune diseases, like, RA and lupus. Does anyone have any ideas or suggestions? I am SO new to this menopause and hormone replacement stuff that any ideas would be welcome. All I know is, this cannot be my life for the next 40 or (hopefully) 50 years.

Otherwise, things are going pretty well! I’ve been working steadily since the start of this month, and while I haven’t gotten paid yet (gotta love contracting and/or freelancing!), it’s coming. As for the Covid, we’ve re-opened a little bit here, with restos at limited capacity, some establishments open; bars are still closed, and there might be a universal mask order put in place soon (meaning, masks all the time, everywhere). I have been too busy and in too much pain to really do much in the outside world the past week, but, that’s what I’ve heard/read is going on.

I hope everyone is doing well. I have to say, after joining a few menopause Facebook groups, you guys a refreshingly SANE bunch–so, thank you for being part of my world!

Days go by

25 Jul

5:05 pm

Days go by, and I keep plugging away.

There’s my job search, which is going well. I’ve got a great lead on a great company/gig, and I have what I believe might be my final round of interviews on Monday. I am trying to not overthink it, as in, wonder all sorts of things about the industry, full-time vs. freelance, my own emotional and/or mental investment… However, here and now, in the midst of a pandemic where over half of my own organization was furloughed; where jobs in THAT space are few and far between; where a TON of people are without work and I should be thrilled that this job even exists, let alone that I have the potential opportunity to be offered said job–I am trying to not overthink it, keep an open mind, and focus on the task at hand.

Which is definitely being helped by me being off Facebook! I actually went on last night–and, of course, I got sucked in for a whole hour, from 2 to 3 am! The good news is, I didn’t really obsess about anything or anyone’s posts; I didn’t let much affect me–that felt good; it felt good because I was able to check my groups (which I miss), read a few people’s updates (I miss keeping up with some friends’ lives, more regularly that I would in person), and then…log off. I will probably continue to go on periodically, but I don’t have a desire to get hooked in on a daily basis.

Speaking of my 3 am bed time, um…yeah. I am trying, but it’s hard for me to get to sleep before 3–especially when I don’t have to go to work the next day. I mean, I have always been a night owl, but I actually want to see if I am waking up after three hours (so, 6 am) every night because I went to bed too late and it’s sunny as shit by then or because, well, menopause.

I started on the estrogen patch this week, so, I’ve been off the birth control pill for two weeks. I have to admit, I think I’m actually having daytime hot flashes/flushes now, and I never had those before on the pill. Hmm…maybe it’ll just take a while for the patch to start working? Or, maybe I’m just hot (it is really hot here right now; 90 degrees in the shade, lawd knows how humid)? Maybe I need a higher dose? Who knows? (I’ve stopped trying to figure it out…because, well, menopause! WHO KNOWS what’s going on? I don’t, and I majored in physiology!?)

Maybe I’m hot because I am taking care of our dog all day long? It’s like a crossfit workout, taking care of her! My girl hasn’t been able to walk for oh, three days now. Her hind legs are just so tired–atrophied , crossing each other (it’s like, her left hind has lost all tension). She’s struggling. We spend a lot of time helping her get up, walk across the room and outside, go for walks on the harness. I say, it’s a crossfit workout, taking care of her, what with the bending and kneeling and lifting. She’s been pooping on her bed for months now, but recently started losing control of her bladder, SO…lots of wiping and washing and drying, spraying and folding and moving and tucking in… I love her, but we’re all getting tired.

I was thinking of how much of a higher power she was to me when I was getting sober. I’ve written about it on my blog before, how she and our other dog (RIP, sweet boy) were my higher powers. He taught a newly sober me how to love others; she taught me how to love myself. That’s all I can say. They were such a huge part of my early years here, on island; such a huge part of my sobriety–I know, I know, they’re “just dogs,” but, to me, for me, they were so much more than that; they helped me more than most humans could have helped me. I just can’t imagine life without her, her not having life–it’s too hard to contemplate. She wants to live, and until she lets me know otherwise…?

What else? I swear, my chikungunya is back. It usually resurfaces to a degree when either I am infected with another virus (the flu, for example) or my immunity is low (when I work out too hard, for instance). Past few days, I’ve felt achey all over, especially in my ankles and wrists and fingers, and like, have had this familiar internal burning feeling in these areas; just blah–“chikungunya-y.” I hate to say it, but, maybe I’ve contracted the COVID? Hopefully not. I’ve been reading about the chronic nature of COVID for some patients, and it reminds me of the way chikungunya virus can hide out for a long time in some people (apparently, me; I got it in 2014, and I still have symptoms once in a while). Yipes. No, thanks!

On that note, I’ll sign off.

Letting the days go by, let the water hold me down/into the blue again, after the money’s gone/once in a lifetime…

On dust clouds and mid-life

24 Jun

12:29 pm

So, we live in the vicinity of the Godzilla dust cloud from the Sahara, and um, it is making things almost hilariously apocalyptic. As if we didn’t have enough to deal with, considering the pandemic, the BLM protests/riots, and now, one of the worst dust seasons (it is a seasonal thing) in history! I tried jogging the other day and felt like I just had to stop after two miles, I was so…heavy all over. Yesterday, we went to the beach and I almost fell asleep in my chair; this dust makes me tired, which seems like a really strange reaction to me. Sure, I can feel it in my lungs, a tight burning when I breathe; in my eyes, which burn; it gives me a headache; but, falling-asleep-tired? Stranger things have happened, and at this point, I have become sort of used to taking things as they come, in stride, and moving along.

I thought about whether I wanted to write this post, about my mid-life transition, and I am posting a truncated version of what I wrote yesterday. Yes, I want to share, but eh, not in THAT much detail.

Suffice it to say, I was finally able to follow up with my gynecologist and get all that woman stuff taken care of, including blood work to test my hormone levels. As I suspected–things changed this year, and I sort of knew, somehow, in my body/mind that things had changed–I am now menopausal (versus perimenopausal). At the ripe old age of just-turned-46. Haha. It’s all good, and I knew it was coming early for me. Actually, I feel better than I have in almost two years. My night heat (I guess my version of hot flashes will have been this intense burning up at night along with dry chills) has improved and I don’t have insomnia nearly as often as I used to.

The past two or three months, as the night heat has gotten better, I’ve found myself letting go of caring about making it better or controlling it or just worrying about it. It sucks, but I have found ways to cope (cooling showers, deep breathing–yeah, that really does work). Maybe it’s partly a sense of relief and hope–this shit actually DOES get better. When you’re going through it, and can’t find a damn thing online that matches what you’re experiencing, there isn’t a light at the end of the tunnel.

In general, I feel like I care less about everything, am more willing to just let things go, to stop trying to control everything. Maybe it’s the series of events this year that has made me go, you know, you just cannot control everything/anything, and your reaction–and chain reaction to your reaction–is key to staying sane, at least for me (I don’t have clinical depression or anxiety, so I am not talking about people for whom it’s not as easy as “think positive”). I mean, maybe it’s what our move back to the island taught me recently–there is only so much you have control of here, and so much you can care about or try to change. Maybe it’s the changing nature of our friendships; when you “go home again,” they have changed, and you have to change your expectations (otherwise, you’re just going to be irritated all the time by expectations being not met!).

Mabye it’s the coronavirus, these protests, the fact that I was furloughed from my job. I don’t know, but I am holding on less and less to the idea that I have control or even should care–and that has done wonders for my mood! I am focusing more on the life in front of me, on the “now,” mostly because I don’t have a clear view of the past or the future anymore–I am forgetting/letting go of the past, and the future is way too uncertain to make any predictions.

On the “menopause” (in quotes, because there is no rule book) front, I think I’m relieved to have finally gotten some “answers” (my hormone tests came back showing much different readouts than last year). I am no longer in this limbo, in a way, searching for information, for some kind of absolute truth–it does not exist, and frankly, most of the information out there is conflicting. I chose a gynecologist who seems current in her knowledge and is very pro-treatment/hormone therapy. Others might choose to not take hormones. Both are OK.

The maddening search has ended, mainly because I am through the worst of it (I guess?) but also because I just gave up trying to find what I was looking for, which was my experience! I literally found zero information on my version of “hot flashes,” which are that I burn up at night, have dry chills, but as far as I know, have never had the kind of hot flash that you think of when you think of menopause (drenched in sweat, red, panicky) during the day; I have never had that kind of hot flash, actually…unless it was so slight that I didn’t distinguish it from just being hot.

Anyway, the point is that, it’s gotten better, and as it’s gotten better, I’ve started to care less and hold onto EVERYTHING less, to let things roll off me more–in all aspects of my life, it seems.

I went through a period of mourning, years ago, actually, for my fertility, for my youth; I came to the, gasp, “shocking” realization that I am going to age and die, like everyone else! (Actually, I am glad I had to confront this early on, and not wait until my 50s.) The thing that still makes me a bit sad is that I never shared this experience with anyone. For the most part, I kept it to myself. Sure, my boo knows every detail–thank Goddess, he is cool about it all and offered as much advice and support as he could. However, I’ve never told my mom (a different post, but she would just make it worse), rarely talked about it with close girlfriends, never revealed the emotional aspects to my gynecologist (she was too busy and not interested in that angle). No one seemed to care–moreso, I didn’t want to talk about it myself, actually. I just wanted it to pass so that I could move on with my life.

Yet, it was a HUGE part of the past few years and in some ways, all-consuming: What is happening to my body, why am I burning up every night, will I ever feel normal again?

I’m just glad I’m through it, knock wood. Glad my only symptoms are/were mild, relatively speaking. If there is more to come, I can keep on keepin’ on; no one is going to die, as a hilarious coworker of mine used to say in the face of the extreme–and ridiculous–concern over the building of the company’s website pages. Haha.

I have to say, being an active alcoholic for at least a decade has definitely made my tolerance for pain much higher than the average woman’s! I mean, pfft, a little burning up at night, chills, and waking up after four hours is NOTHING compared to being blackout drunk for 12 hours and then hungover for another 48 (and all the mental anguish, the suicidal thinking, that ensues). NOTHING can be worse than that except maybe paranoid delusions or drug-induced psychosis, in my opinion. So, another silver lining to having been a drunk!

On a different note: I am still off social media–since mid-April–and it feels great. It’s really working for me; literally, it’s doing wonders for my sense of calm, peace of mind, ability to focus on what I need to do, which is stay focused on a job search. And, as for our pup, she is still fighting; she doesn’t have much control anymore over her hind legs, but she is a fighter and has a strong will to live. She has always been a happy dog, a dog who loves life; so, when she lets me know that her pain (so to speak; I think she is more numb back there than in pain) is greater than her will to live, then we’ll think about next steps.

Happy week, all! Thanks for reading this post…

Making assumptions

9 Jun

12:20 pm

You know how everything in years past came back to drinking and getting sober?  Well, these days, everything seems to be coming back to perimenopause–and you know what?  I am no longer going to be afraid or apologetic writing about it on this blog.  It’s a HUGE reality for me, for women in general, I have to think; and that means it occupies a lot of headspace and takes its toll in many areas of one’s life!?

Perimenopause.  Menopause.  Getting older.  Women’s bodies.  HORMONES.  Of course, I GET it, I get why people are afraid to talk about it!  Women’s issues are taboo, women’s bodies are not our own; we’re not supposed to talk about them lest we start asking questions and become, oh, I don’t know, advocates for our own health!  Really, I get why everyone, women included, are afraid to broach the subject in public forums.

What I don’t get is why they won’t talk about it even in private!?  I mean, do women have THAT far to go that even women themselves won’t talk about it, as if it’s something to loathe, be afraid of, be ashamed by?  You know, it’s not just my own gynecologists, who have brushed me off or implied that I should just get over it, get on with it; it’s my women friends who have gone through it or are going through it, and they either don’t want to talk about it with me/at all, or they try to pass it off as something that isn’t, well, kind of, sort of horrible.

I mean, you are fucking breaking out into a cold sweat before my eyes, and you’re still smiling as if it doesn’t bother you?  I get being positive and all that, but what about being real?

Beyond the physical changes, it means you’re getting old–and, I refuse to believe that I am the only woman who primarily associates this (at least at first, until I get a grip on getting older), with losing my sexuality and losing my youth and all that that entails in our culture!?  I really wish that were the case, actually; I am used to my own paranoia, and it’d be great to know that I am, indeed, the only one who feels this way.  BUT, I really, truly doubt it.

See, I refuse to hide the fact that this is driving me a bit crazy and angry and mad and frustrated and sad; that I’ve wondered if this night heat is THE THING that is worth starting drinking again over (it would be much easier to pass through the three to five hours of night heat if I was drunk); that I’ve always known that the pill offers relief but that it’s SO FAR from matching what is usually happening in a woman’s body that it might well be partly causing my lack of optimism and sometimes-paranoia.

Lately, I feel like I have become a bit paranoid.  For example, I wonder if my coworkers don’t like me, or are annoyed by me.  I am chalking it up to things beyond my control, and to politics–I don’t truly believe that my work is not good.  At home, I have been wondering if my love no longer likes me as a person–again, or course, I truly don’t believe that, and I know that he’s going through some tough transitions now, as am I…

I don’t want to make assumptions anymore, though, about what people want to hear about or talk about–if you’re still reading, that means you do want to hear about this and I’m glad!  I partly attribute this sometimes-paranoia to my hermetic lifestyle–making assumptions involves getting inside your head and not coming out for reality checks, which is usually helped by interacting with friends who normalize your tendency toward outlier (extreme, probably unhealthy) thinking and behavior.  I need more friends.  I need, in a word, to get out more!

I won’t assume that you, my awesome readers, don’t want to hear about my thoughts on perimenopause.  I won’t assume that my man doesn’t like or love me because he told me not to step in horseshit yesterday on our hike (haha–it sounds funny now).  I won’t assume that my coworkers don’t like me because one or two of them have personal issues and are using my writing to play politics in the workplace.

Onward, toward clarity and optimism, I hope.

(I have to say, my burning up at night has gotten a lot better after starting a new pill, with higher dose estrogen, and after making it through the first 10 hellish days on the pack.  I hope that it just keeps getting better from here on out.  I do turn 45 this week–a part of me realizes how young I am, while another part just wants this phase to be over with!)

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