I’ll let you decide which title you prefer once you’ve had a read (and I promise it’ll be quick. Look, just five minutes! A record for me, considering that whenever I say “I’ll be quick, I promise…” it usually spells the kiss of death to any desired brevity of prose).
Some of the content in this post is about dementia and degenerative disease and may be triggering for some. [Reading time: 5 mins]
Anyway…
Life hasn’t been easy lately. I know I’m not the only one, but god, I’m tired. REALLY tired.
Middle age, midlife, “your 50s”, the golden years… whatever you call it, no one prepares you for it. Or at least, no one prepared us Gen X-ers for it. (Are we preparing Gen Z-ers enough? I’ll let you ponder that while you read.)
I will admit that, at times, midlife SUCKS.
I’ve had a lot going on this year. Our family has had a lot going on this year. I thought that by talking [writing] about it, it might give me some perspective. So this is going to come from the heart I guess, it’ll be a bit random and maybe not that structured, and I’ll just write. You may well be going through the same kind of shit, and I’m so sorry if that’s the case. It may be different kinds of shit to mine, but it’s still shite, isn’t it?
Here goes.
So, going back to my point about not being prepared, and to quote John Lennon: nobody told me there’d be days like these. In our youth, we (hopefully, in a stable and loving family environment) get help and guidance when navigating our childhood and teens and how to become an adult, but in terms of getting older… the fact that so many things change – and the way they change – can come as a massive and (often) unwelcome shock.
No one is there to give us guidance on “how” to age. No one tells you what to expect or how to cope. You start to wonder how many more things can go wrong/be shit/annoy you/hurt you.
Rather than waffle on with long paragraphs for each “thing”, I thought I’d just summarise the year I’ve had so far (worse than some people’s perhaps, but likely not as bad as others):
There may well be more things, but I can’t think of them right now. I think you can probably tell how challenging 2024 has been so far, however.
So that’s my summary of this year to date. Anyone who’s had similar experiences – now or in the past – can, I’m sure, relate to how tough this stuff can be. Tough and tiring. The ageing (and required care) of my parents and my own health divebombing are what’s contributed most to my exhaustion; I never really noticed my own ageing till now.
It will take time to adjust to this new life, rather: this new chapter of my life. It is a HUGE gear change. The way I think about so many things is forever changing and I honestly don’t feel like the same person I was 10 years ago, maybe even 5 years ago (or pre-pandemic, shall we say).
I’m now acutely aware of my own mortality, having to cope with being unable to cook, clean or even work during my bouts of sciatica. Sitting at a desk was intensely painful, despite me having a very expensive ergonomic office chair, so my output plummeted. I couldn’t find comfortable positions in bed to lie in so my sleep was erratic at best. Self-care, what’s that? All I want is to be pain-free.
And of course, perimenopause continues to be fun and games. On the one hand, we are talking about menopause so much more which is amazing, and it’s good for the younger generation (and all men!) to have a greater understanding of menopause. But on the other hand… oh god, we know so much more. So many books to read, so many discussions to have with friends, so many health adjustments or remedies to consider, so much battling with doctors, so much confusion over the endless symptoms and what to do about them.
Nevertheless, I’d rather live in a more-informed world than a less-informed one… knowledge is power, as they say.
This is the worst bit for me, and something I’ve only touched on in previous posts or other platforms. My dad is now in advanced stage dementia, and I honestly can’t describe quite how that feels. I’m not, in fact, going to describe my feelings or talk about his condition in any detail, because 1. I don’t actually want to share my honest, true feelings, and 2. I guess I’m doing it out of respect for the wonderful man I once knew.
It’s not because I’m in denial about the whole thing – quite the opposite, in fact. It’s just that my feelings may come across as cold-hearted, unkind, too pragmatic or just downright blunt. We essentially lost our father a long time ago… I now understand when they say that dementia is “the long goodbye”. It’s a hard thing to explain but I’m sure there are people who know (sadly) what I’m getting at.
So if you’re going through/went through something similar (and my trigger warning didn’t put you off reading), then do know that I get exactly how tough it is. The physical side of tending to them and everything/everyone around them. The emotional side of everything that’s happening. The financial side and just how eye-wateringly expensive round-the-clock care is.
It is DRAINING. Not just where dementia and Alzheimer’s are concerned, but for anyone coping with – or caring for someone with – any sort of degenerative disease.
I said it before, but I’ll say it again… nobody told me there’d be days like these. I see you, I really do.
✷ ✷ ✷ ✷ ✷
I have no “quick fixes” to offer. I can’t give any sound advice because I’m finding everything hard to cope with myself. But sometimes it’s good to get it off your chest, it’s good to start discussions (head to the comments and sound off if you wish), and where the positive side of the internet is concerned, sometimes it’s a case of reading a post like this and just realising you’re not alone.
As I mentioned before, I’m sorry if you too are going through a shitty time, whatever form it may be taking. I have to remind myself – for want of a less cheesy quote – that “this too shall pass”. To look at the positive side of things, my five months (and counting) of physio treatment has “mended” my body back to about 85% pain-free, and I can finally exercise again. I AM feeling better, albeit slowly.
We are falling into a better routine with the care for my parents. Rather than myself and my family being responsible for 90% of the care they require, we’re now responsible for about 20% of what they need, and the professionals take care of the rest.
I don’t know quite HOW I could have been more prepared for this shift in life circumstances, because I’m still wrapping my head around it all.
So, back to my opening line: I’ll stick with It’s All A Bit Shit, Isn’t It?. Because I still don’t know how to cope. I guess the answer to that is simply, “Take one day at a time” – and that’s all any of us can do.
Thanks for reading,
For more information and support on Alzheimer’s disease and dementia, please visit the Alzheimer’s Society. It’s a fantastic resource.
Linking up to… Monday: Inspire Me Monday, My Glittery Heart, On Mondays We Link Up || Tuesday: Turning Heads Tuesday, Confident Twosday, Happy Now Blog Link Up || Wednesday: WowOnWednesday || Friday: Fancy Friday, On the Edge
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