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@adelinej@thecanadian.social cover
@adelinej@thecanadian.social avatar

adelinej

@[email protected]

Franco-Canadienne au Canada depuis +20 ans. FSL teacher to adults, 2nd Y. Diploma Egyptology, Manchester. English is my 2nd language, I make mistakes. Very late realization being autistic at 49 and ADHD. Learning to deal with ableism because I’m invisible. Breast cancer behind me, 2024. Toot mainly in English.

Pour me lire en français [email protected]

elle/she

Pls read the pinned posts

I don’t always follow back, not enough energy. I have many interests.

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

murdoc , to actuallyautistic
@murdoc@autistics.life avatar

I suspect I already know the answer but I'd like to know: does anyone else struggle with resisting the urge to "feed the trolls"? When someone posts something that seems innocuous but is factually incorrect, so you decide to help out, and before you know it you are attacked and bullied and wishing you never spoke up and just want to crawl back into your shell and say to hell with the world?

I wish I wouldn't do that. Yesterday I was called a "Karen" for my comment. Like wtf?
Talking with other ND people is such a relief because they usually appreciate it. But OTOH I think that it has emboldened me, making me more susceptible to this problem. I guess I need to sharpen my skills at recognizing trolls. Is this a DEP issue?

@actuallyautistic

adelinej ,
@adelinej@thecanadian.social avatar

@murdoc @actuallyautistic I’m getting better at this, but it’s hard especially when I read stupid and ignorant things especially about autism, not especially from trolls.

Usually, I’m good to detect them because when I began many years ago to use Internet I quickly learned the “don’t feed the trolls“ and I learned how to detect them. There also now keyboards warriors and sealioning, this is a more advanced way of trolling I guess.

olena , to actuallyautistic
@olena@mementomori.social avatar

Fellow , , and other folks, do you relate to that stereotype that we always choose the smallest spoon?
I couldn’t relate to it because no, I won’t eat soup with the smallest spoon.

Because choosing the right spoon is more complex than just size.

For my soup, the spoon should be deep and with proper proportions to keep the perfect balance, so I need to do less deeps in order to finish my bowl and spill less soup doing so(and yes, I prefer eating liquid food from bowls and not plates because it helps to maintain the temperature, lets grab it more efficiently and spill less if accidentally moving the bowl or the table) - which is quite important taking to consideration the usual autistic dyspraxia. It also has to be right to touch(not rough), without sharp edges. I hate too small or too shallow spoons for soup because using those means I would get tired of the process of eating way before I finish it.

On the other hand, for all the yoghurts and other packed desserts I find even a teaspoon to be too big, so I buy coffee spoons, and I use them for eating everything that comes in those small plastic/foil containers - because it’s just the right size in proportion and because it’s easier to reach each corner.

But, for the desserts that come in a glass, I have cocktail spoons, because there should always be a certain distance between my hand on the spoon and the glass, and it should be able to reach to the bottom and not sink inside.

Any spoon should, of course, have a right balance, touch, shape and edges.

Though, all of these things with a spoon are nothing compared to the forks!
My family ridicules me for my quest for finding The Right Fork.
The fork should not just be correctly balanced, nice to touch and with smooth edges, oh no, for a fork what’s actually important is the teeth! They should be long, but not too broad and not too narrow, not too thick and not too thin, and spaced correctly, and with sharp enough tips, but not sides, rather roundish than flat, and just curved at a right angle so my wrist doesn’t go in an uncomfortable position whether I’m trying to pick something or to hold something while cutting. Ah, and the side should be just right to be able to cut my food, but not my mouth. And, of course, almost everything that’s not liquid gets eaten by the fork.

Ah, and also I have fruit forks. Those tiny ones. Because I have a habit of making a fruit plate daily(cut a few fruits in thin slices), and eating them with a fruit fork allows me to not have juicy hands afterwards :). These have to be as little as possible without making my fingers tough the food, and also sharp enough.

So nooo, I don’t relate to ‘always chose the smallest spoon’, but can’t say I don’t care about the cutlery either

@actuallyautistic

adelinej ,
@adelinej@thecanadian.social avatar

@olena @actuallyautistic I had no idea about this stereotype. I choose the spoon depending on the use.

18+ marenf , to actuallyautistic German
@marenf@autistics.life avatar


Hi, I'm looking for some advice on the following:
Most behavioral therapists will recommend to depressive people to create a daily schedule and be as active as possible.
On the other hand, my experience is that being autistic, I take this kind of advice too literally and stress myself out as a result. However, if I do less, I keep beating myself up for not doing more.
Can anyone relate? Any advice on how to find a balance as a depressed autistic?
Thanks in advance!

@actuallyautistic

18+ adelinej ,
@adelinej@thecanadian.social avatar

@Cattz @marenf @actuallyautistic

Same for me. Since I learned about autistic burnout it makes a huge difference.

I'm not saying of course that we can't have depressions, I had 2, and from my experience it was caused probably because of an intense autistic burntout.

StarkRG , to actuallyautistic
@StarkRG@myside-yourside.net avatar

I learned a new allistic phrase this week. "Do you drink tea very often?" apparently means "should the tea be easily accessible instead of at the back of a hard-to-reach cabinet?" I can kinda see the connection there, but I don't understand why allistics can't just ask the question they're actually asking.

@actuallyautistic

adelinej ,
@adelinej@thecanadian.social avatar

@CynAq 🤦🏻‍♀️ Why not asking this directly!? (rhetorical question)

@StarkRG @actuallyautistic

PossiblyAutistic , to actuallyautistic

"thinking aloud" and infodumping are not the same thing, right? Or are they? How is thinking aloud with someone else called? In my experience, that's a specifically neurodivergent thing ... @actuallyautistic

adelinej ,
@adelinej@thecanadian.social avatar

@PossiblyAutistic @actuallyautistic For me thinking aloud helps me to process find an answer and/or a solution, while info dumping is when I share something already processed.

pathfinder , to actuallyautistic
@pathfinder@beige.party avatar

@actuallyautistic

Like many autistics, I struggle with change suddenly being thrust upon me. It can and will upset me and put me on the back foot. Potentially ruining that day and, indeed, quite a few to come, as I struggle to get back into the structure of my days and a sense of balance, emotionally and mentally. This is because that sort of change, in a very real way, is imposed in that moment. It's beyond my control and the ramifications of it, even if it is only a very small change, can dash like dominoes all my carefully prepared plans and options and whatever preparation I may have already made.

Change, in and of itself, though, I don't have a problem with. And that's because I expect it. For me, the potential for change is inevitable. And this is because I live entirely in the now. The past is the memory and understanding of what went on that I have now. Which is subject to change as my understanding and perception of it changes. The future is merely the potential of what may happen and is not carved in stone. I am aware that there are events and situations that I have to prepare for, presents to be bought, for example, preparations to be made. But the future is only ever a potential and never a certainty.

This expectation of uncertainty is also why I think I can be better at dealing with change than many others. I don't cling to what I think the future should, or even will, be. If I can sense that the potential for changes are coming, then I will begin to prepare for them, just as I prepare for them not happening. Sometimes, of course, changes can be so huge, like suddenly going into lockdown, that it can take me some time to get any traction on that preparation and get my head around what needs to be done. But, it doesn't mean that I can't get my head around the fact that things have changed and that I have to deal with it.

So, for me, the upset of sudden change has never been about change as such. It has always been about the jarring impact of its sudden introduction. Change I don't have a problem with, as long as I have time to prepare and an ability, as much as possible, to control how it affects me.


adelinej ,
@adelinej@thecanadian.social avatar

@pathfinder @actuallyautistic I’m wondering how much my ADHD part helps me dealing with change because I can manage it pretty well.

vger , to actuallyadhd
@vger@fidget.place avatar

@actuallyadhd @actuallyaudhd

When I refer to my autism, I like to say "I am autistic". Now, I also have ADHD and would like to treat it like that as well. But "I am ADHD" sounds way off to me. Is there something similar for ADHD?

adelinej ,
@adelinej@thecanadian.social avatar

@vger @actuallyadhd @actuallyaudhd

I guess it's also a personal choice? I know it sounds weird to say I'm ADHD, but I have seen it used the same way as some people say I have autism instead of I am autistic.

I'm autistic and ADHD and I tend to say I'm AuDH, it easier for me this way. 😄

26pglt , to actuallyautistic
@26pglt@mastodon.au avatar

These findings are unsurprising but it’s important to see them spelled out.

In research publications around , medicalised language is used most commonly in older studies & those that frame differences as deficits & seek to identify biological correlates to observed behaviour. Language that frames differences in terms of is more likely to be used in studies that are more recent, that include autistic adults & that consider topics identified as important by autistic people. Language used is likely influenced by the conventions of different academic journals.

@actuallyautistic

https://www.liebertpub.com/doi/10.1089/aut.2023.0030?utm_campaign=AUT+FP+July+12%2C+2024&utm_content=Article3&utm_term=&utm_medium=email&utm_source=Adestra

adelinej ,
@adelinej@thecanadian.social avatar

@26pglt @actuallyautistic About the cultural difference in language. I’m experiencing it daily here interacting in English or in French (with my other account) with autistic people. It makes it difficult for me and challenging at the same time, because often it illustrates the gap between my own journey and learning in English with the own journey and learning of the person I’m speaking to in French. I’m guessing that I’ve also a bicultural autistic identity not knowing always how to interact. 😄

Susan60 , to actuallyautistic
@Susan60@aus.social avatar

Someone sent this to me a while back & I’ve only just got around to looking at it. (ADHD) Rang a lot of bells, & is no doubt another factor is late diagnosis.
@actuallyautistic

https://poweredbylove.ca/2017/11/21/atypical-autism-traits/comment-page-1/#comments

adelinej ,
@adelinej@thecanadian.social avatar

@Susan60 @ClipHead @actuallyautistic I learned to say that I am a different normal. 😁

chevalier26 , to actuallyautistic
@chevalier26@mastodon.social avatar

@actuallyautistic Just found out that NT people have REAL habits that happen basically on autopilot. This is news to me.

What most NT people think of as a "habit" I think of as a "task," even if it is a part of my routine. For example, brushing and flossing my teeth is a part of my daily routine, but I have to make myself think about each action separately. I wouldn't call them habits because I literally remind myself to do them every night. It isn't automatic.

adelinej ,
@adelinej@thecanadian.social avatar

@chevalier26 @actuallyautistic I have learned recently the difference between routine and habit thanks to this link. (I’m AuDHD)

https://www.shimmer.care/blog/habit-vs-routine

adelinej ,
@adelinej@thecanadian.social avatar

@Susan60 @chevalier26 @actuallyautistic I know so little about my ADHD. My therapist (who is ADHD) explained to me that impulsivity is not only physical, that I don’t have, but also verbal that I have. I had no idea!

Sadly I can’t listen podcasts, it’s impossible for me to focus on.

chevalier26 , to actuallyautistic
@chevalier26@mastodon.social avatar

@actuallyautistic Wish more YouTubers and content creators added a toggle to their videos that could switch off background music. Idk about y'all, but so many videos have added music that is unnecessary, distracting, and overstimulating.

I have seen videos on YouTube where the closed captions settings have been programmed with a separate audio track with no commentary, so I know it can be done! Would probably be so helpful for so many people!

adelinej ,
@adelinej@thecanadian.social avatar

@matty For me its because auditory processing disorder. It’s very hard for me to understand when there is a background music, whatever kind.

@actuallyautistic @chevalier26

adelinej , to random
@adelinej@thecanadian.social avatar

I have just watched the 1st episode of A Kind of Spark thanks to @PetitPas

It’s a Irish British American Canadian series. In Canada I’m watching it on CBC Gem, in the UK it seems to be on the CBBC channel, for the others countries I don’t know.

I like it because the 3 autistic sisters are played by autistic actors, use of the words autistic, masking, meltdown. etc. Shows sensory overload, etc., ignorance and bias.

To watch it in Canada https://gem.cbc.ca/a-kind-of-spark

adelinej OP ,
@adelinej@thecanadian.social avatar
adelinej OP ,
@adelinej@thecanadian.social avatar

If you have an autistic loved one, please watch the show mentioned in the first toot if you can.

If you are autistic, please tell me what you think of it. I know that it won’t talk to all of us, but I’m seeing so much of myself in the series even I have learned only at 49 that I was autistic.

I know that the show is not perfect but for me it’s the first time that I’ve seen such an accurate representation of our experiences and suffering.

@actuallyautistic

dave , to actuallyautistic
@dave@autisticnomad.social avatar

@actuallyautistic Saw this at the pharmacy and picked it up... curious to see what it says.

adelinej ,
@adelinej@thecanadian.social avatar

@dave @actuallyautistic I’m curious about the “treatments”.

wakehamAMR , to random
@wakehamAMR@mastodon.social avatar

Trying to make sense of my identity and personal history in reference to my late dx of ASD is, exhausting.

My assessment is coming up in early May. Early indications suggest being medicated will be life changing.

Anyone know of any decent adult support groups?

adelinej ,
@adelinej@thecanadian.social avatar

@wakehamAMR It’s a good suggestion. Welcome to the community. 😊

adelinej ,
@adelinej@thecanadian.social avatar

@wakehamAMR I forgot to mention the @actuallyautistic , not sure if you are aware of it.

adelinej , to actuallyautistic
@adelinej@thecanadian.social avatar

I have a question for AUTISTIC parents homeschooling their children.

Do you have any neurodivergent affirming ressources about PDA and homeschooling of teenagers?

It's for an autistic friend, she lives in France (I'm in Canada), she's homeschooling her 3 children for years now and she's struggling a with her 12 years old boy. Thank you.

@actuallyautistic

18+ adelinej , to actuallyautistic
@adelinej@thecanadian.social avatar

Please dear @actuallyautistic sign the petition below and boost!

Here is a link through Google Translation (I know sorry) to have the petition page in English. It’s about a movie to be broadcast on April 12 (!) on national French tv: “Thou shalt not kill”, it’s about the murder of an autistic child by her mother. More about it:

https://www.change.org/p/pas-de-diffusion-du-film-tu-ne-tueras-point-sur-france-2?recruiter=39730646&recruited_by_id=6ec56820-4a90-0130-fb7e-00221964dac8&fbclid=IwAR0K76beFgf-n6G9egu2urJQocDcEABbtOUhohltH6gELVeUAOYuWnpf4uQ

To see the original post in French

https://neurodifferent.me/@Autistrain/112084706324625722

18+ adelinej OP ,
@adelinej@thecanadian.social avatar

@actuallyautistic I’m sorry I don’t know why but the Google translate link above has been automatically changed and it shows only the original page in French 😩

Sci_Fi_FanGirl , to actuallyautistic German
@Sci_Fi_FanGirl@hessen.social avatar

Dear fellow @actuallyautistic people,

Can you relate? Sometimes there are upcoming events and I know they'll overwhelm me completely. I'd like to avoid them, but sometimes I don't dare to ask because I don't want to be the person that always asks for a special treatment (German: Extrawurst). I'll complain all the way, but I don't opt out.

I know I have to work on this. It's not about a solution.

Is it internalized ableism? Camouflaging? People pleasing? Insufficient coping at the event?

adelinej ,
@adelinej@thecanadian.social avatar

@Sci_Fi_FanGirl @actuallyautistic Ableism and masking in my opinion.

And I don’t force myself anymore. I asked if accommodations are possible and it’s always no, so now I stay home.

adelinej ,
@adelinej@thecanadian.social avatar

@Sci_Fi_FanGirl @actuallyautistic

Being able to attend remotely for example as I don’t drive, but everyone assumes that I do, or that I can walk 10 minutes to go at the bus stop, and the bus network in my town is awful since the pandemic or that I have friends who can drive me. And, it feels safer to stay home as I just had a breast cancer and so little people masks.

I made the choice of loneliness trying to protect myself from the ableism of the society with 0 support from it.

adelinej ,
@adelinej@thecanadian.social avatar

@aevole What do you think would help you to accept? I know it’s a hard question. 😊

@Sci_Fi_FanGirl @actuallyautistic

ratcatcher , to actuallyautistic
@ratcatcher@c.im avatar

Periodic reminder that the @actuallyautistic group and hashtag are intended for discussion BETWEEN AND AMONGST people who are autistic (diagnosed or self-diagnosed) or think they may be.

If you are not autistic, by all means read what is posted, but please respect this as an autistic space and do not post here.

There are plenty of other groups and hashtags under which more general discussion of can take place and can include professionals, academics, non-autistic parents of autistic children and those with a general interest in the subject.

But the second - often overlooked - issue is this:

My fellow autists - when someone who is clearly not themselves autistic does post to the group, PLEASE, PLEASE do not engage. I know it's hard, but ultimately it just subverts, dilutes and prolongs discussions which can rapidly become unhelpful and adversarial.

adelinej ,
@adelinej@thecanadian.social avatar

@ratcatcher @actuallyautistic

I plead guilty 😔 but I'm working on it. And yes it's hard to not engage with these "I'm not autistic but I know better than you".

I'm always wondering if they do the same with a wheelchair user or someone legally blind? Do they tell what they should do/react/live etc.

It's a rethorical question, it's just a vent. Thank you for this periodic needed reminder!

tine_schreibt , to actuallyautistic
@tine_schreibt@literatur.social avatar
adelinej ,
@adelinej@thecanadian.social avatar

@tine_schreibt @actuallyautistic I guess as an autistic my first answer to this question would be “I’m me”, or "I’m the sum of all the experiences I went through. I’m in constant evolution and since I know that I’m autistic, I know now why I try to adapt and to fit in a world not made for me, why it is exhausting to live a world in which I feel constantly assaulted by noise, light, smell, social expectations and rules, etc." If you are autistic you know what I mean.

Autistrain , to actuallyautistic
@Autistrain@neurodifferent.me avatar

I'm asking my fellow for books on Autism. If you have suggestions, I'm happy to hear about them!

@actuallyautistic @neurodiversity

adelinej ,
@adelinej@thecanadian.social avatar

@Autistrain @actuallyautistic @neurodiversity

“Since starting That Au-Some Book Club in 2019, our group has grown to over 10,000 members and has released several recommendation lists.

Our book lists are crowd-sourced by members of the book club, and Autistic opinions are prioritized in our decision making process.

While we have yet to find a perfect book on autism, all of the books we recommend have been discussed and chosen with care.”

https://notanautismmom.com/bookclub/

clouddweller , to actuallyautistic
@clouddweller@raccoon.place avatar

@actuallyautistic what is your relationship to cannabis?

adelinej ,
@adelinej@thecanadian.social avatar

@clouddweller @actuallyautistic I feel better since I stopped using it for my osteoarthritis. It was a very, very low dose of THC but the psychiatrist, whom suggested autism to me, warned me that it could worsen anxiety for some of us. It was indeed the case for me.

adelinej ,
@adelinej@thecanadian.social avatar

@dyani @clouddweller @actuallyautistic You are not, someone else in the thread mentioned it too. 😊

JeremyMallin , (edited ) to actuallyautistic
@JeremyMallin@autistics.life avatar

I wonder… before the Internet, how did most Autistics do special interests and research rabbit holes? Hang out in libraries? But lots of books? 🤔

Thinking back, I guess I used to look for television documentaries and public broadcasting type stuff. It definitely wasn't as helpful as Internet.


@actuallyautistic

adelinej ,
@adelinej@thecanadian.social avatar

@ashleyspencer Same for me with the little card drawers (but you are younger than me 😁).

Public and school libraries were my favourite place to search and read a lot about many things.

@JeremyMallin @actuallyautistic

anomalon , to random
@anomalon@neurodifferent.me avatar

Pattern brain:
Why the rush to a new hashtag when has been in use for ten years and is understood across every platform in use now?

Rude brain:
Why did all the cool kids get up and decide to sit at a new lunch table when the poor weird kid who was raised in a cult sat down with them?

Pattern brain: Shut up

Rude brain: I'm doing your job now.

adelinej ,
@adelinej@thecanadian.social avatar

@FrightenedRat @CynAq @anomalon @autistic[email protected] @actuallyautistic

When I read the AA tag for the 1st time I had no idea what it meant so I looked online. I understand the wish to have a new # because of the gatekeeping aspect but I have seen several new ones today + groups and it’s confusing.

As mentioned in the initial post of this thread the # is used everywhere online since 10 years, so I will continue, for myself, to explain its meaning to people wondering about it. 😊

adelinej , to random
@adelinej@thecanadian.social avatar

(if you are not autistic please don’t comment, read and learn. Yes, I’m fed up to read allistic comments in thread asking input from autistics. And don’t waste your time and mine by trying to argue with me about that I will simply block you)

Why did you choose to identify yourself as , , being on the spectrum, etc. ? Usually from what I read it’s a generational word and/or a cultural one as our is international and this is too often forgotten

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