Unfortunately I don't have the energy to put together some info for the mega this week, hopefully I can pull together something for next week though. As always, we ask that in order to participate in the weekly megathread, one self-identifies as some form of disabled, which is broadly defined in the community sidebar:

"Disability" is an umbrella term which encompasses physical disabilities, emotional/psychiatric disabilities, neurodivergence, intellectual/developmental disabilities, sensory disabilities, invisible disabilities, and more. You do not have to have an official diagnosis to consider yourself disabled.

Mask up, love one another, and stay alive for one more week.

  • Luna [she/her, null/void]M
    ·
    29 minutes ago

    Re: fine motor function. I've been really busy lately, extremely exhausted, and I can barely do anything involving fine motor. I'm struggling to type this right now, I type fast and am used to having to backspace, but this is taking me so much longer to type right now. Literally every couple of words. Was really bad today when I kept messing up and bumping the trackpad of my computer while taking notes. It would move the cursor to a different spot and then mess up other sections of the notes, which I had to take time to fix.

    Sorry for venting yet again, it's just frustrating, because I don't feel like there's much I can really do to help with the problem. I won't do this again this week, I promise catgirl-sorry

    Anyway, should really post something positive at least. I'm somehow managing my really large load of coursework right now, although it's probably why my spoons are as depleted as they are.

  • x87_floatingpoint [he/him, it/its]
    ·
    34 minutes ago

    Can anyone tell me about air filters? No energy to go look for information catgirl-flop

    Heard they can provide some protection from the COVID in an indoors space? How effective is that? I will probably move back to my family soon, they go outside a lot more often and I worry about catching COVID from them.

    How big is the air filter? Do you just put it in a corner of the room or what? Are they noisy?

  • Blockocheese [any]
    ·
    4 hours ago

    A lot of my hobbies are more popular with older people and it does hurt my heart a little when I see that they can do them more often and for longer periods of time than I can :/

    For some reason after I wrote the ":/" the first suggested word in my phone was "gangstalking" lmao

  • peripateticpeasant [none/use name]
    ·
    11 hours ago

    Both sides of my family have history of disabilities. Some have neurodivergence, some psychiatric and many physical.

    So it is almost insane to me when I encounter people with no disability or anything. Not even a single allergy.

    I do wonder how much is generational trauma, colonization and the fast transition to industrial capitalism (we come from a place that rapidly transitioned within a few decades). I wonder how all that factors in all this.

  • belligerentkitten [they/them, it/its]
    ·
    12 hours ago

    i did thing. i feel just enough strength to do more thing. things are important. i am proud of myself.

    it really sucks when ur disabled but if u don't get on with the things then eventually it will be catastrophic so u just gotta do the things, but also be careful not to push urself in such a way that it makes u worse. i even went to a series of classes on pacing that were offered by the health service a few years ago and i put it into practice best i can. but there's just something about like the material conditions of life, and how sometimes there is no chance to rest.

  • TheSpectreOfGay [he/him, she/her]
    ·
    18 hours ago

    i would really like to get an autism diagnosis, because it feels like it's the root cause of a lot of my social issues, and i would really like support for dealing with that. and it might help towards getting disability aid ig but my doc said i should qualify without it

    but the wait time for adult diagnosis is a year catgirl-flop

    • ReadFanon [any, any]
      ·
      edit-2
      13 hours ago

      I've been trialling a drop-in peer support space run via the game Webfishing. I'm auDHD and I reasonably knowledgeable about the ins-and-outs of autism and late diagnosis.

      You're welcome to join the ping list for when I notify people of the upcoming drop-in peer support space so you can chat with me or whoever else is in there, if you're interested.

      Currently I've only really been promoting it on the neurodiverse comm so the autistic power levels of the server are off the charts leslie-shining

      • TheSpectreOfGay [he/him, she/her]
        ·
        4 hours ago

        oh sure i'd appreciate it, can't promise i'll attend but i'd like to be pinged if i feel up to it. thanks for the offer!

        • ReadFanon [any, any]
          ·
          3 hours ago

          Don't sweat it, there's no participation requirements or anything. Just come in if the server is live and you feel up for it.

          Welcome to the ping list!

  • Ivysaur [she/her]M
    ·
    18 hours ago

    Really feeling the call of the abyss lately. How can I have hope for anything when we can't clear the very simple bar of pandemic mitigation? I'm so tired.

  • ReadFanon [any, any]
    ·
    1 day ago

    Unfortunately I don't have the energy to put together some info for the mega this week

    If you want I've just uploaded the audiobook version of Exile and Pride Disability, Queerness, and Liberation by Eli Clare to TankieTube and there's a PDF copy of the book available here. I haven't read it yet but it looks interesting.

    Here's the publisher's synopsis:

    First published in 1999, the groundbreaking Exile and Pride is essential to the history and future of disability politics. Eli Clare's revelatory writing about his experiences as a white disabled genderqueer activist/writer established him as one of the leading writers on the intersections of queerness and disability and permanently changed the landscape of disability politics and queer liberation. With a poet's devotion to truth and an activist's demand for justice, Clare deftly unspools the multiple histories from which our ever-evolving sense of self unfolds. His essays weave together memoir, history, and political thinking to explore meanings and experiences of home: home as place, community, bodies, identity, and activism. Here readers will find an intersectional framework for understanding how we actually live with the daily hydraulics of oppression, power, and resistance. At the root of Clare's exploration of environmental destruction and capitalism, sexuality and institutional violence, gender and the body politic, is a call for social justice movements that are truly accessible to everyone. With heart and hammer, Exile and Pride pries open a window onto a world where our whole selves, in all their complexity, can be realized, loved, and embraced.

    If you like the sound of it, you're welcome to copy this along with the links into the body of your post as a substitute for other content. If you do I'll delete this comment so it's not clogging up the mega unnecessarily.

  • Luna [she/her, null/void]M
    ·
    1 day ago

    I hate being reminded of the fact that I can't perform fine motor functions. I've gotten used to it when journaling, even though I can't really read my handwriting, but I was trying to do a lab today and just kept fumbling and messing up the setup. I couldn't help but constantly apologize to my lab partners almost constantly, and once they finished with their portions they had to help with mine, and I essentially had to step back and do other parts of the lab work. Ugh catgirl-flop

    Too autistic for the autistics strikes again sadness-abysmal

    • hexbee [she/her]
      ·
      1 day ago

      Bless you, I find it's hard to not put myself down when I'm not able to do things that seem so simple for those around me

  • ReadFanon [any, any]
    ·
    edit-2
    1 day ago

    I think you commented in the old mega right on the buzzer @HexaSnoot@hexbear.net. Bringing it over here to answer:

    (About Maslow's) It's individualistic and a cooptation of better concepts and it's just gross but your run of the mill therapist who just scraped by to get their qualification is almost certainly going to like it.

    What are those better concepts?

    Power isn't given, it's something that is taken.

    This is particularly endemic in how privileged people talk about "giving people a voice". Please stfu.

    Lol Everything onwards from this really helps me understand more about power dynamics. Thank you.

    People tend to graduate from Maslow's Hierarchy (though far too few) on to things like Bronfenbrenner's Ecological Systems Theory:

    Show

    While that one is better and it doesn't fall trap to hyperindividualistic nonsense, I think this one falls into a different trap: "the net that catches everything catches nothing". I could talk about the arrows but there's no fucking point. Either point them somewhere useful or if you can't do that then your diagram is designed incorrectly or you are being patronising of your audience.

    I'm partial to the Dahlgren and Whitehead model, despite its flaws:

    Show

    It's simple enough to grasp without requiring an hour long lecture first. It provides key information without listing every goddamn detail (Is the chronosystem in Bronfenbrenner really necessary?? Do you genuinely need to represent the flow of time, that the things in the present come from the moment that directly preceded them and so on? [Is it too late to do a coconut tree joke? Would that be in poor taste now?] Do you really need to tell people that time affects everything? Why did you feel the need to call it a chronosystem - was "time" or "history" too simple? Would a two-sided arrow with the downwards poiting one labeled as "past" and the one pointing to the surface layer labeled as "present" be too simple and intuitive to grasp? What, did you run out of space to talk about the flow of ideas and neuronal networks and the thermohaline conveyor and intra-religious conflict fuelled by schisms?)

    The problems with this one are there too - it's explicitly depoliticised, the green part is okay but it's not really very cogent but it's more like a scattershot of things that Dahlgren and Whitehead tried to list 10 factors for but they only managed to phone in 8 before calling it good; agricultural production factors matter yet manufacturing production factors are absent (tell me you're living in a so-called "post-industrial" country without telling me), the centre doesn't show it in this one but other ones are revised to have a family to make it less individualistic and yet in doing so it either ignores intrafamiliar factors or it just kinda shoehorns them it "There - a family. Now you fill in the blanks!" and it either centres the nuclear family (Can you tell which countries this is made for and which type of country it was made in yet?) or they put grandma in so she can be in the nice picture as well before they shuffle her back off to the nursing home.

    • robot_dog_with_gun [they/them]
      ·
      22 hours ago

      iirc maslow stole from indigenous people and the more direct descriptions of those original ideas seemed better as well.

      • ReadFanon [any, any]
        ·
        21 hours ago

        Not me, in the previous comment chain with the locked mega that you didn't see that led to this comment:

        But that's my style of conversation tbh and I'd feel pretty comfortable discussing the topic [of Maslow's Hierarchy]. It might be a different for others though, and maybe approaching it from a place of learning would suit them better, for example, than taking the approach of musing from a postcolonial critical perspective of Maslow's work would, you know what I mean? I can't tell you what an "authentic" way (cursed term) is for you but I'd encourage you to approach this sort of discussion in a way that feels right to you.

  • AdmiralDoohickey@lemmygrad.ml
    ·
    1 day ago

    I talked with some union people at my workplace, and I asked them if they plan to resist the full return to office that is coming. I shit you not, they welcomed the news (they were clueless) because "we will communicate and work better" [sic].

    They only really care about their higher wages and people like me can fuck off and die I guess. I don't know why I expected solidarity from neurotypicals. It's shit like this that completely discourages me from organizing

    • hexbee [she/her]
      ·
      1 day ago

      I'm sorry you're going through that comrade

      I feel quite discouraged from organising as well :c

  • DisabledAceSocialist [comrade/them]
    ·
    1 day ago

    Well, I got a couple of messages of support last week about the behaviour of my therapist so I thought I'd give you all an update. I mentioned how I'm going through a benefit appeal, and also having mental health therapy for depression and anxiety, and this therapist is worse than useless but I don't dare to quit because the DWP (benefit assessors) will use it against me, they've done it before, used me not having treatment for a condition as an excuse to stop my benefits. Anyway, I mentioned how I'm struggling to keep going to the therapy appointments because they are so useless and stressful and I have a lot of other medical appointments to keep up with too (oncologist, endocrinologist, stroke clinic, ophthalmologist, physiotherapist, neurologist, etc) so having this weekly useless therapy appointment is just an extra stress and waste of time. I mentioned this to my therapist and she got offended and told me to just quit therapy if I don't want to go. When I explained that the DWP will use that as an excuse to permanently stop my benefits and I'll end up homeless and permanently destitute, she didn't care at all and said "benefits aren't a good enough reason to have therapy."
    Well anyway the update is that I missed an appointment with her and I've been feeling more unwell than usual this past week as a treatment I was given by the neurologist has worn off now, so the therapist agreed that this month we can just have one appointment instead of the usual 4 and see how that goes. I just really want her to let me have one a month until January, when the therapy comes to a natural end. That way I've completed the 6 month course of therapy rather than quitting halfway through and the DWP won't be able to use it against me. I really hope she doesn't expect me to have the full 8 sessions that are left after that. I hate this therapy so much, it's absolute crap. She's such a crappy therapist she can't even think of things to do in the sessions and tries to make me think of things to do. I once told her I was interested in trying meditation so now 20-25 minutes of each session are her doing a rubbish mediation where she talks complete nonsense while I have my eyes closed. Then she gets out crayons and tells me to draw pictures of whatever I'm feeling. Then she gets out a diagram of a human and tells me to colour in whatever parts of my body hurt that day. The end! How is this meant to help me? My problems are that I'm ill from cancer and the effects of it's treatment, I'm learning to walk again and adjusting to becoming partially sighted after having a stroke, and I'm living in poverty, always fighting benefit appeals and struggling to get enough to eat and keep a roof over my head. No therapy will fix this but this excuse for therapy is particularly bad. And I can't quit or it will be a big strike against me in my benefit claim. People are meant to have a free choice about whether to accept medical treatment or not but there is no free choice when you'll be made destitute, homeless and starving in retaliation for refusing the treatment. And this shitty therapist refuses to understand how badly I need a roof over my head and food. Someone here recommended I talk to her about Maslow's hierarchy of needs to try to get her to understand, I will do that at the next appointment and see what she says. I'll let you all know how that goes.

    • Belly_Beanis [he/him]
      ·
      1 day ago

      God that sounds fucking awful. I've had my share of shitty therapists, but I don't think I've ever encountered someone this awful. Where I'm at now is a clinic that focuses on intersectional problems, so that's why probably why they're better at helping me with my physical disabilities. My current psychiatrist didn't even hesitate to write recommendations to Social Security.

      Honestly it sounds like your therapist should just get the fuck out or learn to do self-crit (as much as liberals can lmao) because nothing you've requested is unreasonable. I'm guessing she hasn't even brought up Cognitive Behavioral Therapy?

      • DisabledAceSocialist [comrade/them]
        ·
        1 day ago

        I don't think she does this, and it wasn't on offer from the NHS. 5 years prior to this I was given DBT on the NHS from a different therapist, who was even worse than this one. The DBT therapist just made me write lists of why I shouldn't feel depressed or anxious and why I shouldn't commit suicide, and look at those lists whenever I felt bad, to make me feel better. That was the entire therapy! And she admitted that she wasn't even qualified yet. I've totally given up on therapy actually helping me, it's all shit. I'm only toughing it out because of my benefit claim.