@pathfinder@beige.party avatar

pathfinder

@pathfinder@beige.party

58 years old, ish (Yes, I'm sticking with this lie, because it still remains my only chance for immortality) Autistic and British. Into philosophy and spiritualism and pretty much anything that might explain the meaning of life, up to and including that it might really be 42.
Male, he/him

#ActuallyAutistic
#Autism
#Neurodiversity

This profile is from a federated server and may be incomplete. Browse more on the original instance.

ashleyspencer, to random
@ashleyspencer@autistics.life avatar

Me and my little husky plush went to the store to get snacks and other stuff.

I made myself leave because I haven’t gone anywhere in a few weeks. Only open the door to put out the trash.

Brought the plushie along on my lap for moral support.

pathfinder,
@pathfinder@beige.party avatar

@ashleyspencer
Hopefully the first of many trips out. It does the mind and soul good. 😀

Tim_McTuffty, to actuallyautistic
@Tim_McTuffty@beige.party avatar

Diary of an ASD Squirrel. Day 198 , Monday 13/05/2024

Up early for some reason beyond this simple squirrels reasoning.
Tidied up after herself, did my chores & went for a walk in the warm early summer sunshine !

I cannot seem to find the impetus to get stuff done, I work best to a deadline & the only person pushing me at the moment is me, which would be fine but I have minimal motivation levels at the moment.

I’m wondering from day to day like a leaf blowing in the breeze, no direction, no purpose.
At least the days are warm now & a lot sunnier, saving energy is easier , my lone mission to drag our energy bills down is less onerous in the summer.

Final Thoughts.

I suspect that I am going through a depressive episode, I hope I come through to the other side soon.

Thank you to all those who are helping me on this journey, in a myriad different ways. I am thankful to each & every one of you! 🫂 🫶🐿️🖖

@actuallyautistic

pathfinder,
@pathfinder@beige.party avatar
LehtoriTuomo, to actuallyautistic
@LehtoriTuomo@mementomori.social avatar

Sitting in the bus after a day at work. Feeling tired. The meeting that ended the day dragged on and I stopped even trying to follow the discussion. I haven't listened to music in a bus in ages but now I find myself thinking that maybe I should buy a set of noise-canceling headphones.

The bus is hissing loudly, there are conversations that I can't hear which somehow makes them even more annoying. On top of all I'm sitting under a loudspeaker that plays the stop signal in a very loud tone. Shit, it rang again and startled me. Why does it have to be that loud?

Fortunately I'm not too far from home but still.

@actuallyautistic

pathfinder,
@pathfinder@beige.party avatar

@LehtoriTuomo @actuallyautistic
Until I started wearing earphones and earplugs regularly. I didn't even begin to realise how much of my, I can normally cope, was actually, I can spend energy I don't have ignoring the fact that I'm not really coping and how stressed out by that fact I am.

ashleyspencer, to random
@ashleyspencer@autistics.life avatar

I’m exhausted from a long hard day of doing nothing.

pathfinder,
@pathfinder@beige.party avatar

@ashleyspencer
Or finally allowing yourself to feel how exhausted you already were, it's difficult to tell. 😀

mariyadelano, to actuallyadhd
@mariyadelano@hachyderm.io avatar

Question for fellow @actuallyautistic and @actuallyadhd neurodivergent folks:

How do you explain your ideas to neurotypicals?

I constantly struggle because my brain has made connections that are not obvious to others, and when I try to guide them through my thinking I confuse them with details or by skipping explanations that seem obvious to me but completely surprising to anyone else.

Frameworks, links, anything is appreciated!

pathfinder,
@pathfinder@beige.party avatar

@mariyadelano @actuallyautistic @actuallyadhd
It strikes me that you are expecting people to think. Most people don't like doing that. They much prefer to have a conclusion, followed by what ever proofs are required to satisfy that conclusion.

lifewithtrees, to actuallyadhd
@lifewithtrees@mstdn.social avatar

“What do you want to do 5 years from now?”

🤔

😬

🤯

I am having a difficult time visioning 5 years from now, what I want to do and then how to get there.

Some of this is due to the chaos of the last few years, but I also think it could be a challenge due to

Also I am 42 so midlife stuff?

That all said, how do you vision 5 years from now?

@actuallyadhd @actuallyautistic

pathfinder,
@pathfinder@beige.party avatar

@lifewithtrees @actuallyadhd @actuallyautistic
I never think about where I will be, or what I will be doing in x years time. Either my mind doesn't work that way, or I've always recognised the futility of it. Looking back 5 years, could you have imagined where you are now?

Uair, to actuallyautistic
@Uair@autistics.life avatar

@actuallyautistic

How are you with animals?

I tend to throw off the wrong vibe for people, but get along with even the iffy animals. Dogs that don't like most people warm to me.

Just wondering how much of that is autism and how much me. My dad hates animals.

pathfinder,
@pathfinder@beige.party avatar

@Uair @actuallyautistic
I'm really good with animals and most animals take to me. Except horses, they really hate me.
Most of us far prefer animals to people, because they are what they are. I suspect the reverse may be true too.

dyani, to actuallyautistic
@dyani@social.coop avatar

Yesterday was my 1 year AuDHD anniversary!

1 year since the most life-changing realization ever. My resting heart rate dropped by ~10 points after I figured it out.

Knowing this about myself has given me so much peace & confidence. It's given me even more compassion for myself and others. I advocate for my needs now, and I have better boundaries.

Every day I marvel at how amazing we ND folks are, and how much we bring to the world.

I so appreciate this community!

@actuallyautistic

pathfinder,
@pathfinder@beige.party avatar

@dyani @actuallyautistic
🎉🎉 ❤️

Susan60, to actuallyautistic
@Susan60@aus.social avatar

I’ve always been a “coper”, constantly trying to find ways to manage, to do what “needs” to be done etc, except for those periods when I was burnt out. I remember when feeling overwhelmed years ago, a counsellor helped me to see that it was possible to achieve everything that I needed to do over the next few days, as a single mum, students, part time worker. Which was great in the short term…

We got home from several days in Sydney yesterday. Monday & Tuesday we went out after spending the weekend with family, but kept it low key. Today I was supposed to head out for a counselling appointment, treating myself to a tram trip to a lovely neighbourhood & a cafe lunch afterwards. Instead she’s going to send me a link for an online session. And I might have a nap afterwards. I’m learning. Slowly.
@actuallyautistic

pathfinder,
@pathfinder@beige.party avatar

@Susan60 @actuallyautistic
Just keep pushing, pushing, pushing. The mantra of so many of us. Getting out of that habit, really is a work in progress. Any step in the right direction is huge 😀

pathfinder,
@pathfinder@beige.party avatar

@Susan60 @actuallyautistic
In so many ways, the same.

ashleyspencer, to ADHD
@ashleyspencer@autistics.life avatar

Lately the ADHD has taken over.

I’ve been unable to work, can’t clean, not getting anything done. Always too burned out to function.

But today I got the hyperfocus part of ADHD.

Mostly it’s like, I’m incapable of functioning.

I’ve gone weeks unable to function. I can drink 2 energy drinks and still barely function.

Today I woke up full of energy and in hyperfocus hyper speed work mode, so I just rolled with it. Tomorrow I could be nonfunctional again. It’s so unpredictable 🙃

pathfinder,
@pathfinder@beige.party avatar

@ashleyspencer
Sounds unpleasant. I thought your meds had settled you down?

pathfinder, to actuallyadhd
@pathfinder@beige.party avatar

@actuallyautistic
@actuallyadhd

After joining a post by Niamh Garvey (hopefully a successful link to it below) about whether she had adhd as well as autism, I have spent the last couple of days contemplating this idea for myself as well.

I am still not entirely convinced, but I am beginning to suspect that I might well be in this situation as well. After watching a number of YouTube videos from those with both autism and adhd and reading up on adhd, I can see a number of things that point on that direction certainly, although I'm not entirely convinced.

I have always been aware of the near overwhelming urge to either interrupt people, because there is something I want to say and if I don't then, then I know there is a more than a reasonable chance that I will forget what it was. I also have a tendency to want to finish people's sentences. Both of these things though I have taught myself to resist. Even though I feel a great deal of discomfort doing so. I am also more than aware that I can forget what I was saying, or thinking, halfway through a sentence. That digging through the trash to find the package with the instructions on, that I only just threw away after reading, is not uncommon. As is failing completely to understand or remember the instructions someone just gave me.

But then, my short term (working) memory is basically non-existent. But, I'm also aware that this is a fairly common problem for autistics and even before I realised I was autistic, I built up systems to help myself deal with this. As well as with my general forgetfulness. Lists, memory aids, even making the route out of my flat a trip hazard to make sure I don't forget to take something with me. Also, I live alone and essentially there is a place for everything and everything has its place. Not foolproof and I have lost things in a very small flat that I still haven't found. But generally speaking effective.

I struggle to start tasks, especially tasks that I have no real interest, or desire to do. Being interested in something has always been my main motivator. But eventually, I can normally force myself and work my way through things, especially if I know they are necessary. Knowing I have this problem is also why I hate leaving things to the last moment. I know that I am more than capable of doing that if I allow myself, but also that the stress from doing so is nearly overwhelming, even if it can be motivational. As is the stress of clutter. Not the organised clutter that is my flat, where I know where everything is, as in somewhere in that pile over there, but the clutter that builds up eventually and begins to feel as if it is out of control.

Novelty is a factor in my life. Or, boredom, rather. Because sooner, although far more likely later, I will grow bored with routines, or things like safe foods, and need to change them. Many of my interests also seem to suffer from a similar threshold. A certain point where I lose interest and no longer feel any need to maintain them, even though this might make me feel guilty about giving up on them. In fact, I hate boredom and I have always needed a certain amount of new things to watch, or discover and to be actively doing stuff, if only in my head. And whilst I have never thought of myself as being particularly spontaneous or impulsive. I am, within certain limits of self-control. There is a rationality that often has to be appeased that gives me a sense of control. I have also taken stupid risks and great risks. But rarely beyond what I knew was necessary, or to my mind, at least, controlled to a point.

I can be easily distracted, by random thoughts or by, (well obviously not squirrels, I mean who would be? but, oh, oh, there's a butterfly) things. But not always to the point that I'm not at least marginally still aware of what I should be paying attention to. Letting myself wander whilst maintaining at least a marginal awareness is an old trick of mine. I have always been a fidgeter, but that's also how I maintained concentration. Feeling the overwhelming need to move, has always seemed to me to be anxiety driven, or is the way I focus and think. In fact, movement for me has always been as much about settling and regulating myself, as it has been compulsive.

As I said, there are certain things that seem to fit, even if they also seem to have been effected and possibly modified by my autism. I would love to hear your thoughts.

https://beige.party/@niamhgarvey@mastodon.ie/112390279791932822#

Cassandra, to random
@Cassandra@autistics.life avatar

Could somebody explain to me, briefly, what Book did to Burnham? I missed season 4 and don't know if it’s something I would find inexcusable or if I should be team love conquers all.

pathfinder,
@pathfinder@beige.party avatar

@Cassandra
It's worth watching because it's a wee bit complicated. But, essentially, he went behind her and star fleets back to try and avenge the death of his planet, even though it was not the way she was going in solving the issue.

pathfinder,
@pathfinder@beige.party avatar

@Cassandra
Her's was the more logical, his the more emotive. Somewhat obviously, I preferred her's. But, that's just me. 😀

pathfinder, to Autism
@pathfinder@beige.party avatar

@actuallyautistic

Much to my shock I realised that I could be autistic when I was 53, roughly 7 years ago. And it was a shock, even though I suspect a very small, well hidden and very much ignored part of me, might have suspected. No one told me about it, or suggested that it might be the case. I did not see myself in relatives, the way so many of us do. I just happened to come across an autism test online and for no particular reason, took it.

It was that, that started me on my path to realising and finally accepting the truth that I was autistic. But, looking back, I sometimes find it hard to understand how I didn't know earlier. So much of my life now, just screams autism at me. But even ignoring the horribly ableist and medieval view I had of what autism was, the main reason why I didn't was probably because I could mask, both from myself and others, so well.

It was, I realise now, a life lived in denial. A denial of how much things bothered me, how much effort I had to put into things. Even a denial of the things I knew I couldn't do. Because this is the thing about appearing to mask so well, for so long. It is, in a sense, a lie. I couldn't mask well, if at all. Not all the time. Not in all situations or circumstances. There were things I just couldn't cope with, or even begin to deal with. But the trick was, that I either knew about them, or learnt the hard way about them and then I could manage my life to avoid them. Because they were things I could live without, without affecting how I appeared to be coping. Things that didn't affect the way I lived, even if they did affect my sense of worth. Because, how broken did you have to be, not to be able to go to crowded events, like a sports match, or a concert? Or to be able to deal with the socialising of a large gathering, or a family event, without having to hide in the kitchen, or forever outside, or break down in a toilet?

It was all part of how I masked myself from myself. The internal masking, as I like to call it. If I couldn't cope, then I was broken. If I couldn't stand something, then I was too picky, or sensitive, or I simply needed to learn to ignore it. And somehow I did learn. I learnt how to cope with noise and smell and visual overwhelm. I learnt to not let things bother me. To a point at least. There was always a step too far, when I couldn't, or didn't have the energy any more to maintain it. And this did take energy, a lot of it. Something I've only realising now that I don't have the energy to spare to even try it. Or the ability to, in many respects now that I know what I was trying so desperately to hide from.

Because when the truth is known, it's far harder to deny it. It's far harder to live the life where appearing to cope, is as good as coping. Where blaming yourself, is easier than seeing others faults. Where ignoring the pain, makes the pain go away. It's hard to see the mask as a benefit and always a good thing, rather than the shield and tool it always was.


pathfinder,
@pathfinder@beige.party avatar

@TheBreadmonkey @actuallyautistic
Discovering something like this about yourself is not easy, it's not even painless. It tends to make us look back and reframe our entire lives. Often that can feel like grieving all the "what might have been's", or it makes us angry, even bitter at times, when we see how avoidable so much was. If only we had known, or others had even tried to "see" us as we were.
But, this also gives us access to so much more. To a community and its knowledge and experience. We are no long alone. We can truly begin to understand what being us, is and not only how to express that, but nurture it. We can learn how to shield ourselves and take care of ourselves and to live so much better.

pathfinder,
@pathfinder@beige.party avatar

@Susan60 @actuallyautistic
More fine, than not. I still feel like I've had a very lucky life, especially compared to so many others. But, I can't help feeling a bit miffed sometimes, when I realise just how much bloody effort I had to put in, just putting one foot in front of another through life.

(Please note that as I'm British, for a bit miffed, please read, incandescently angry 😅)

pathfinder,
@pathfinder@beige.party avatar

@TheBreadmonkey @actuallyautistic
You're on the path we've all been on and feeling what we've all felt. Nothing to apologise for. The beginning of the path is rocky to say the least. May I suggest you follow the actuallyautistic hashtag and group, it's for you as for anyone else who thinks they may be or has self-diagnosed, like me, or been officially diagnosed. Even if it turns out that you're not autistic (and personally I wouldn't entirely trust the diagnostic process to give you that answer) you may still learn things that help you to make sense of things, or simply make your life better.

pathfinder,
@pathfinder@beige.party avatar

@everyday_human @actuallyautistic
The test I took pointed me in a direction. After that, it was a shit ton of reading and soul-searching and taking and retaking tests. After a certain point, reason doesn't allow you to ignore it any more. True acceptance took a little longer. 😀

pathfinder,
@pathfinder@beige.party avatar
pathfinder,
@pathfinder@beige.party avatar

@Susan60 @actuallyautistic
Whether we know, or don't yet realise, the path's pretty rocky and not looking to get any smoother any time soon.

pathfinder,
@pathfinder@beige.party avatar

@Tooden @Susan60 @actuallyautistic
The UK is currently walking down a particularly obvious and obnoxious road. In part, at least, it's why I have no particular desire to get officially diagnosed.

pathfinder,
@pathfinder@beige.party avatar

@Tooden @Susan60 @actuallyautistic
In the UK they've simply followed the time-honoured practice of reducing the number of assessors and therefore making the waiting lists impossibly long. Unless you have the ability to go private. It's the good old, if there aren't so many being diagnosed, there isn't a problem.

pathfinder,
@pathfinder@beige.party avatar

@danimo @actuallyautistic
There does seem to be a never ending supply of things to realise and see anew.

pathfinder, to random
@pathfinder@beige.party avatar

There is also problems with the diagnostic process itself, that make so many of us distrust it.
That it's still geared towards children and demands parental reports from adults who may not have them anymore, or who may not be in touch with them for good reason.
That it's still weighted towards male, white and cis. Sometimes to the point that it's almost impossible for anyone else to get fairly assessed.
With the need to get referred by a gp, who is probably even more out of date than the assessors.

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