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Happy holidaze

27 Dec

12:58 am

I do sort of feel like I’ve been in a daze this season, mainly because of everything that’s been going on. The other day, I posted something and then deleted it, worried that it was too revealing about my father. And, I’m glad I did; this isn’t a blog about him.

I haven’t felt much like blogging recently; not sure why, it just feels like overexposure. I’ve also been working a ton and going-going-going with my brothers, getting my dad situated in a nursing facility–simply put, we think he has dementia, and it is *probably* not going to get better. I mean, we can hope it’s related to a transient, post-operative effect (he recently had surgery; the reason he had surgery, though, was because of his “dementia” thinking, which I see so clearly now)–but, he’s been in decline for like, at least three years, it just wasn’t presenting itself as memory loss, per se. Anyway, it’s been draining; there is no rule book, which is bizarre since so many people go through this!

In light of everything that’s come to a head this year–started menopause, put my dog to sleep, watched my dad literally go from, ‘Oh, Dad’s just being Dad’ in August, to, ‘Holy shit, there is something really very wrong here’ in November–I do feel grateful. I mean, I’m still here, for one. I’m still sane, still working (uber-grateful for this), still breathing, still loving, still content with most everything that comes my way.

Everything that has happened this year that could have definitely been given a strictly negative spin has actually led to something better. I lost my job–but I needed to leave anyway, and ended up finding something better, for the most part. I had to put my dog down–but she needed to Rest, and we were just holding onto a creature who was in unbearable pain. I went into menopause–but I feel SO much better, overall, than I did in perimenopause, and, I’m no longer on the birth control pill, which, I would say is much worse than hormone therapy (today’s bioidentical versions). What else? Oh, so yeah, my dad sort of “went into” dementia–but, considering that these past three years have been a long, crazy lead-up to what we’ve all just realized is actually cognitive decline, at least my dad is safe now. Even Covid has had many silver linings–one could say that Covid allowed nature to come back, people to take stock and be more mindful, mRNA vaccines to have their day probably faster than they would have had.

Anyway, it’s been a long few months. I had a GREAT Christmas, though; yes, we got together, and no, I don’t feel guilty about it (though, there are some people in places where Covid is still raging who would blame me and my friends for spreading the virus)–we are not a hot spot, and the people I hang out with are like me in that, no one really socializes! I am not worried that anyone in the group last night had Covid or has been exposed recently; there were three younger people (someone’s kids in their 20s) who had flown in, but, only two were recent arrivals and everyone has to take a Covid test before being allowed to enter the airport.

Tomorrow, we’re going on a boat trip–a big, twin-hulled catamaran, which should be awesome! I have never stepped foot on a boat like that, so I am looking forward to the experience. Speaking of which, I’ve had some down time to actually remember and cherish some old trips and friends lately–to mind come volunteer trips to Haiti, to Ecuador; a self-styled yoga retreat to Nosara, Costa Rica; years ago, a solo trip to Turkey; years before that, one to Greece; a year abroad in Paris; many exploratory trips all over the mainland through recent years. Ahh, the memories; I am proud of the trips I’ve taken of late, and really, truly can’t wait to be able to travel again…

I hope my dad can entertain himself with his own memories; it’s painful, wondering what he is thinking about right now, you know? I know he has some great memories, so…that’s a small consolation.

Oh, and we got another doggay! He is the most ridiculous dog ever–his cuddle factor is so high, he’s almost TOO cuddly! I do miss my girl so very much–and our boy–but…life goes on. It’s nice to have a little buddy to care about, to walk, to have sleep all over you (we are not letting him on the bed; he will never, ever leave if we do…).

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!

Still here, plugging away

24 Oct

9:39 pm

I just wanted to jump on here and say, hi! I am still here, just plugging away at two jobs (when it rains, it pours; but, I’ll take the deluge after being unemployed for five months after I was furloughed from my job, thanks to Covid). Essentially, I have been working 12-hour days since the start of the month, which has left little time for anything else (especially fun stuff like my blog!).

In any case, I had been having this weird leg muscle and joint pain the last time I blogged, and I had gone to the doctor to seek some answers–and all the tests came back normal and/or negative.

As it turns out, I went off the generic and onto a (much more expensive) brand name estradiol patch and lo and behold, MOST of my leg *muscle* pain went away within a day, or days. I’ve been on it for a week now, and while my joints (hip/groin/lower back, ankles, feet, fingers) still (sort of) hurt, I swear, my legs started feeling better within a day of taking the new medication. Could it be? Well, yeah, it must be, right? I recently read a story about semi-shady pharma manufacturing plants in India and how, the FDA-sanctioned regulatory checks at drug-making plants there leave a lot to be desired in that they let shit slip through the cracks. I have had a similar experience with a generic birth control pill in that I had all the side effects, but the second I went back on my name brand drug, they went away.

Correlation does not equal causation, but, I am like, 99% sure that the DAY AFTER I changed patches, my leg muscles started to feel normal again. That continues to today, where I have gone for a couple jogs this week and have not felt debilitating pain for days after my workout, where I am able to just get up and go for walk and not feel like I ran a marathon. Fingers crossed, it keeps getting better. I will pay the price if it means that I don’t have crazy leg pain! (I will add, with every generic or brand name switch, it has felt like I’ve changed medications and am starting over, so, that kind of sucks)

Today, I got to go for a walk in the morning and a soak/swim in the afternoon–and, it felt like a long-lost luxury. Add to that coffee and the tropical natural world? Cloud freaking nine, people.

On that note, I have missed touching base with this community and my “old” DDG self (am I still her? is she still here?). I hope I find more time soon so that I’ll be able to just ponder and enjoy and be grateful because, well, I miss that and I need that.

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!

Exhale, and believe

7 Sep

3:01 pm

That’s my mantra these days. Exhale, and believe.

Exhale, sure. Calm down. But, believe? In what? Well, that things will change. That, um, I will change. That I will have the courage to just let things be if they’re not working for me anymore. That I will have the courage to just let my thoughts go if they’re causing me more harm than good.

This past week turned out better that I imagined it would, considering that I landed two contract jobs, which means I’ll have at least part-time work through the end of the year. (My “dream job” got back to me, too, requesting an interview, but…I am not sure what’s going to transpire with that, so, I’m just waiting and seeing.) All the work I am doing now came from networking with my existing contacts, not cold calls, as it were. So, that’s a big lesson right there, which is, eff Indeed! (haha)

I am slowly getting over putting our sweet girl down coming up on a month this Wednesday. We’ve thought about fostering a dog (or two) since we’ve now got the time *and* have to be in the same place (now that I am working again, I need to be settled; plus, the only place we would want to travel would be the West, in an RV, and um, it’s kind of literally Hell there right now). It’d be a shame, in my opinion, to not give love when you are able to give love; there are plenty of dogs in need at the local shelter–just like our girl and our boy needed our love, those many years ago. We’ll see…

I’ve sort of been on autopilot the past few weeks, sometimes wanting to give up this blog, sometimes wanting to write more on it; just plugging, getting back into work mode (man, my brain is slow after five months on furlough–haha). It’s been great, though, to redirect my attention to something else, anything else, but trying to work on my book (hashtag fail) and staring at my belly button.

I don’t know if my new hormone therapy is working or not, really; there aren’t any hard and fast rules when it comes to “what is supposed to happen in menopause” and I am not sure if I can expect 100% “back to normal.” However, I know what I want, and I don’t feel what I want yet. Unfortunately, even though I’ve been going through this crap for three years, I probably won’t see the light at the end of the very hot tunnel until the end of this year, considering how long you have to take your regimen to see if it’s working (three months) before you can request a change or upgrade (if that’s even possible, I don’t know). The wait is not as much of a problem as the fact that this has been going on for three years, and it has been really trying, and I just want to feel like myself again. The uncertainty factor has been the most irritating part of this process–you just don’t know how you’re going to feel or when it’s going to feel better.

Today marks three years plus one day that Hurricane Irma hit. Our lives were forever changed. A part of me really misses that time; amidst the chaos there was excitement, and promise–of something new. We lived that “new” and are now back to where we started. Except, there’s a pandemic now and no one can do anything–which, actually, kind of sucks more than the aftermath of a hurricane, mostly because, the aftermath and rebuilding had/has a finite end! Anyway, I wonder, what’s next? What’s going to be new? I am so jones’ing for something new again, aren’t you?

So, I come back to my mantra: exhale–what will be, will be; let the planning go for now–and believe–things will change, they will not be this way forever. Exhale, and believe.

Another day…

11 Aug

11:53 am

…and, I am simply grateful!

Our beloved doggay has lived to see another day–in fact, she’s sleeping peacefully (?) in “her spot” in front of the door, and has only been between there and one of her beds since 3 am (when I finally stopped eating mac and cheese, used my slow-breathing technique–in for 5 seconds, hold for 10, out for 5–to cool down, and went back to bed to fall asleep). She actually stayed down for four hours, according to my boo, who got up at 7 to let her out.

(Btw, the bonus of being up at 3 in the morning is that I get to see Venus rise. If you haven’t seen Venus right now, rising above the northeastern horizon in the pre-dawn hour, you are in for a treat: it is shockingly bright, beaming from the sky like another moon, and huge. It’s a HUGE spot in the sky. I saw a shooting star–the Perseid meteor shower is going down right now–and noticed how high Mars was in the sky compared to the moon, rising later and later every night. Finally, I was also able to watch my girl doze, her head slightly illuminated in the waning moonlight, thinking, gosh, she is sweet. Fierce. And still here.)

Granted, all this sleeping on her part has been made possible ONLY by the trazadone we dosed her with around 9 pm last night. I have to accept the fact that she will likely exist in what I believe to be a drug induced-haze from here on out (maybe erroneously; I just hate having to med her up so much), but, it’s SO much better to sleep from 3 to 9 than to have her waking me up every hour on the hour, yelping for help to get up to switch beds.

So, she lives to see another day. And, I am grateful.

On another note, as I am inundated again with daily COVID news, I have to wonder: Have my aching, burning joints and body parts (entire feet, not just ankles) and frequent headaches been caused by COVID? Like, is this my experience with it? I am not going to get any tests (I don’t see the point in either an antibody or virus test, right now), so I guess I shouldn’t bother myself wondering, but… It’s been weeks, actually, since I’ve had joint pain, and I’ve had these headaches (usually in the mornings, but not always) on a somewhat regular basis. I never get headaches, so, they make me go, hmm/wtf, ouch, this hurts!

I don’t know. The symptoms seem so varied now, considering the descriptions of more and more COVID survivors; I guess I’ll just assume that my chikungunya (the mosquito-borne viral infection I got six summers ago) has resurged because my immunity was affected by lack of sleep, or stress, or heartache (my doggie!); and, hope that I am not infected with the coronavirus.

More like my dog

8 Jul

1:14 pm

During these dogs days of summer–I can’t believe we’re well into July; it’s been a steamy one here, too–I’ve been watching my dog a lot. And, man, I wish I could be more like my dog. She is fierce, endlessly patient with herself and her limitations; she is never mean, always loving, and keeps trying and trying, adjusting to every new normal as if it’s no big thang. If it’s sunny, she’s resting peacefully in her spot outside in front of the door; if it’s raining, she wants to be out there, too, getting wet and inhaling the breezes, more alive than ever as she stands guard against enemy dogs who might try to take advantage of the dark wet night’s cover. She never, ever complains; when she is unhappy or depressed about her condition, she gives a nod that she wants to be left alone, and then sleeps it off. Oh, boy, I wish I could be more like my best girl!

Me, on the other hand, I am not patient; I try to take my transitions in stride, but, usually, I let them get the better of me. This past week has been hard, with my hormones not quite right–major heat, constant heart palpitations, anger. The other night, my night heat got the better of me: after about 1.5 hours of sleep, I was jolted awake by some freaking intense heat, burning up head to toe. I turned the a/c down, cranked the fan up, and decreased the temperature setting on my chiliPAD (it’s been a lifesaver these past few years; Google it!). I rushed out to the kitchen, literally gave myself a bath at the kitchen sink, and overheard myself whisper-screaming, This is a living hell; this is truly a living hell. (One more week, then an off-week, and then I start the estrogen patch–we’ll see if it helps.)

My dog just rolls with it at night, which is her worst time, too (panting like crazy, hurting from the day). When I get up at night, she just looks at me like, what? I pet her, smell her ears and feel her fur, and it all just makes me feel better. She helps me get through the nights, which are “dark, and full of terrors”–she’s my best friend, mainly in that she knows more about my nights than anyone can or would want to know. And, still, she loves me!

I am trying to just embrace the days and live free. I’m still off Facebook–and it feels great. I got off in April, didn’t go back on until June, and then went on two more times last night and this morning…which was an excellent reminder that I’m so much better off without it, at least right now in my life. I can’t speak to Twitter or the ‘gram or any other social sties, as I have never been a big user of these platforms.

I do miss certain things about Facebook–I miss my “on this day” feed, which is kind of like a journal that reminds me of the cool things I’ve done on this day in years past; I miss my groups; and I miss certain people, mainly those people with whom I don’t have typical friendships (like, folks I met while volunteering abroad, locals who live in those communities). Most of the other posts fill me with a sense of, this virtual reality is not only not real, but it is designed to keep people stuck in it, wasting time, wasting their actual, in-real-life energy! Increasingly, I see it as a tool to remind me of MY life, but not as a way to actually interact with others. Only took me a decade to figure this out!

I had a job interview yesterday, and I think it went well. The huge plus of job searching as a remote employee looking for remote work is that…everyone is now open to it, if not at least initially. I have been working remote for a long time, years and years; every time I interview for a job, though, it feels like a piece that requires explanation and justification. Not now! And that’s a wonderful relief–it’ll allow everyone to finally focus on the job, not the logistics or politics, you know? We’ll see; it’s one of those jobs that will require a long interview process (at least two more people and then a panel video interview with, I’m guessing, three to six more people), but, it will be worth it if I do land the gig!

It’s a beautiful day here, so I am trying to embrace the wonder; the past few days, I was just angry all day (thanks, hormones), and I took it with me–on my walk, around my boo, maybe even toward my best girl. Today, I’m just trying to be more like my dog: patient, taking it as it comes, and accepting all of things, good, bad, and in between.

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…

Insomnia is a mental illness

8 Jun

11:40 am

And, actually, it IS! According to Medscape:

The DSM-5 defines insomnia as dissatisfaction with sleep quantity or quality, associated with one (or more) of the following symptoms: Difficulty initiating sleep. Difficulty maintaining sleep, characterized by frequent awakenings or problems returning to sleep after awakenings. Early-morning awakening with inability to return to sleep.

What I mean, however, is that insomnia causes mental illness (and that is part of its definition, too, in the DSM). For me, personally, that means anxiety, depression, and relatively speaking, “suicidal” thinking (i.e., what’s the point, everything sucks). I had one of my nights the night before last, and it took almost the entire day for me to rebound, to feel like myself again–to come out of the depths and to be able to think positively.

Honestly, it feels WAY too much like a night of blackout drinking and the next-day hangover from blackout drinking: you’re in and out of sleep, you’re having nightmares, you’re angry–oh, boy, does insomnia make me irrationally angry–and you’re delusional. It truly is horrifying, doubly so because it is like a replay of one of the MILLIONS of blackout-drunk/next-day hangovers I’ve had over the course of my drinking career (which gratefully ended when I started this blog eight years ago). It really does feel like I’m hungover the next day, too: intense anxiety, forcing myself to get out of bed, depression, this sense of darkness around my world and goals, the inability to think clearly, the list goes on and on.

Usually, I experience nights of insomnia caused by perimenopause–sometimes, I can’t fall asleep because I am burning up or otherwise wired wide awake; usually, I wake up after three or four hours sleep and can’t fall back to sleep. This time, however, it was because my stomach was cramping all night long (I have been toying with going on the keto diet; however, I am definitely crossing eggroll-in-a-bowl off my list of things that I can eat–LOL). I had some crazy nightmares, too: one was, the brother who wrote me off (after a bad blackout verbal assault!) was attacked by Trump supporters; the other was, our house, with floor-to ceiling windows looking out onto the ocean, was being flooded by HUGE waves that we could see come crashing down on our roof…and inside was a friend who ghosted me in 2017 (she just stopped emailing and texting, after 11 years of friendship, and I have never learned why). God, it was a dark night!

The next day, yesterday, I gave myself what turned out to be a gift: I went to our local Humane Society and spent the morning walking dogs! It felt really good to get out of my head, outside myself, and just help others, even if those others were fur-balls! Later in the evening, I went alone to our closest beach and took a sunset soak. It gave me the chance to remember how many times volunteering my time, helping others, actually saved me from myself. Getting outside myself has been what has saved me more than once from depression, anxiety, and everything that comes with too much self-focus.

It’s Monday, and while the protests are still going on and the COVID is still going on, I have to get on with my life. Which means, rebooting my (professional) writing portfolio and starting to send out ye olde resume. I don’t necessarily believe I won’t get my job back, but…it’s good to consider the possibility that I won’t.

I am eight weeks Facebook-free today, and I feel pretty much great about that. I do miss my actual friends’ posts, and I know that I am missing out on some events and “in the know” activities; however, for the most part, I believe I am not missing anything and I feel better about myself, calmer about the pace and progress of my days. I keep thinking of a few friends especially, wondering how they’re doing; otherwise, most people are simply not on my radar in that way (and, I would venture that most of anyone’s friends on Facebook are not really their friends, per se, people whose lives they’re actually interested in keeping up with). Anyway, I will keep going with it; I might not deactivate as I said I would, but I’ll probably stay off for a while longer, at least. The benefits are just too good!

Our dog is hanging in there; it was a bit sad to walk such fiesty pups at the Humane yesterday and come home to our “old” girl, barely able to hobble around for a few minutes outside. On the bright side, she IS still able to get herself up and down, and she IS still able to walk outside to pee–all good, right? I have come to accept her aging, the process of her aging, a wee bit more with every passing day. It’s part of life; I just wish it wasn’t part of HER life–haha.

Blessings, all, for a good week. Stay strong (or not); either way, you got this.

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