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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.

  • DisabledAceSocialist [comrade/them]@hexbear.net
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    3 days ago

    It’s great being able to get out and go to shops and things again, but nobody is wearing masks and multiple people literally cough and splutter all over me. They don’t even turn their heads away or cover their mouths. Just disgusting.

    Oh and I have a lovely new thing to worry about. I’ve always heard that if i win my benefits case they will check the previous 6 months of my bank accounts. But now I’ve seen threads from disabled people on other sites saying they checked their accounts right from the start of the claim! The disability charity Scope told me it’s OK that some people put money in my paypal account because they said it’s a gift, but I’m not so sure, it might look suspicious, from multiple random people.

    It’s infuriating that so many people think living on disability benefits is the easy choice. Constant assessments, having your payments stopped for no reason, having to beg for food, bank checks and constant worry you’ll be told you’ve done something wrong. Not to mention the endless threats from the government to make it more difficult to claim and to lower payments. What a way to live. All for the crime of getting too sick to work.

    • un_mask_me [any]@hexbear.netOPM
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      3 days ago

      People have learned nothing from the pandemic, and kind of seemed to have regressed in caring at all about illness. It’s good to be able to get out of the house, though, even when it can cause anxiety with other people thrown into the mix.

      I hope the payments aren’t used against you for your benefit appeal. It’s ludicrous to enforce such awful circumstances on the disabled for the sake of capital. What are you supposed to do when they don’t even provide you with the means to eat while this appeal process is in motion? Just ludicrous. I hope you get the benefits soon and this unnecessary stress is put behind you quickly.

  • Keld [he/him, any]@hexbear.net
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    3 days ago

    The food bank gave me 30 parsnips. They gave me some nice stuff too. But they also gave me 30 parsnips. What do I do with 30 parsnips

    Edit: I’m gonna make hasselback parsnips.

  • DragonBallZinn [he/him, they/them]@hexbear.net
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    3 days ago

    Neurotypicals: “You are autistic, this means you can sometimes say out-of-pocket, insensitive things because you cannot hope to know any better.”

    Also neurotypicals: “Hey by the way! I will randomly make comments on your appearance, and how you remind me of this famous unattractive person you never asked for! I know you can’t help it, but I figured you need to be reminded of your insecurities. Just in case you forgot! Wait, why are you mad at me?”

    Sure, and I’M the one who can’t understand social cues….and I’m taking this “advice” from people who never keep their unasked for opinions or commentary to themselves.

    • Salah [ey/em]@hexbear.net
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      3 days ago

      Neurotypical people use their judgy comments more strategically (although accidents happen for anyone). They say them when they are insecure, feel threatened or for some other reason want to make someone else feel bad about themselves. This is also why they get more offended when a neurodivergent person says something that the NT person perceives as judgy. The NT person assumes that the ND person intentionally wants them to feel bad because they project their own behavioural reasoning onto others.

    • gingerbrat [she/her]@hexbear.netM
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      4 days ago

      To me, it always feels like what they’re actually saying is “Don’t tell the truth to someone, just be judgy when you talk about or to them.” I share your anger, it’s frustrating how insensitive some people are doggirl-growl

    • un_mask_me [any]@hexbear.netOPM
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      3 days ago

      Feels like a lot of NTs make themselves feel better by punching down this way. Almost as if by othering those around them they gain a sense of power and control.

  • un_mask_me [any]@hexbear.netOPM
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    3 days ago

    Pet sitting this weekend has reminded me of how much love and affection animals can give. I wish it was feasible for everyone to adopt pets. My legs are numb from this cat in my lap and I couldn’t feel much more content at their warmth and little motor purr. I’d feel jealous, but I can’t provide for a pet like their owners and I’m just glad they’re so well loved and properly cared for. I’d spoil this fluff if I had them, too.

  • Veggie_Deluxe [any, comrade/them]@hexbear.net
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    4 days ago

    I am trying to get back into making music, got around to uploading this little dungeon synth track i did a little while back. I’ve been trying to get back into things i was passionate about before life got considerably worse and ive been tinkering with music and trying to get my Mandarin back up to fluent levels. I gotta Keep pushing forward<3 Vile Humors - Miasma

    • un_mask_me [any]@hexbear.netOPM
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      3 days ago

      This is awesome, ty for sharing! Very dungeon boss vibes, I had fun listening to it. I hope you continue to keep making music, you have a talent for it <3

    • gingerbrat [she/her]@hexbear.netM
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      4 days ago

      I had no idea Baroque Dungeon Synth was a thing in music, so I was surprised to listen to your little piece of art! I enjoyed it, so thank you for sharing. I also hope you can find the time (and passion) to continue pursuing this hobby of yours. It was fun listening to something that was completely new to me meow-hug

  • HexaSnoot [none/use name]@hexbear.net
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    4 days ago

    I just posted a question that is partly about my disabilities and mostly about what I’m proud of. Just watched Frankenstein 2025 last night and it has me rethinking what I can be proud of.

    • un_mask_me [any]@hexbear.netOPM
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      3 days ago

      I just watched it too! Visually very cool. I think I’m proud of how far I’ve come as a person, and being able to find a bit of joy in each day. It’s honestly inspiring to me to meet and talk to people of all walks of life and abilities. Everyone has such interesting and varied experiences, I wish I could talk to and meet more people, if only to hear their thoughts and stories.

      Appreciate you sharing, sorry I missed the original post.

      • HexaSnoot [none/use name]@hexbear.net
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        3 days ago

        Guillermo del Toro is amazing and I aim to watch every last movie of his. Finding joy can be hard with certain disabilities and mental states, so congrats. I love people even though I’m socially anxious, I hope for the same in knowing people and their wisdom, experiences, and how they deal with and enjoy life.

        You’ve got nothing to feel sorry about.

  • Keld [he/him, any]@hexbear.net
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    6 days ago

    Now having permission from Gingerbrat to post my whining. Please ignore this if you don’t want to hear about my work woes.

    I was called a slur by a person visiting a patient after I brought them coffee from the staff lounge. They were frustrated and lashed out and I get that, and I need thicker skin, but I’m still offended given that I had literally no involvement with their treatment. I just saw people sitting around and asked who wanted coffee or tea and smuggled it out and my reward was slurs thrown my way.

    • un_mask_me [any]@hexbear.netOPM
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      5 days ago

      It sucks to have someone take out their emotional stuff on you, but that doesn’t excuse using a slur. It shouldn’t have happened and it’s perfectly okay to feel upset at the interaction. You were just trying to help, and that should be appreciated.

    • gingerbrat [she/her]@hexbear.netM
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      6 days ago

      I love that I’m getting the “Mom said I could” treatment for this comment i-cant

      This is really rude, but sadly not atypical. I’m sorry that instead of a thank you, you got insulted. You deserve better, especially since you were being kind to them cuddle

      • Keld [he/him, any]@hexbear.net
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        4 days ago

        Now if people don’t like the post it’s your fault instead doggirl-smart

        I’ve been subject to some abuse before, but always because I was directly involved in care. Getting it for doing someone a favor was new.

    • gingerbrat [she/her]@hexbear.netM
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      6 days ago

      No, it is not insensitive. Work is stressful and can be very unpleasant, so it’s just as legitimate as complaining about never finding work (which is also immensely stressful and unpleasant).

  • mononoke@lemmy.sdf.org
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    7 days ago

    COVID has made a real doomer out of me. As usual, the people taking it seriously now will be the ones to pick up the mess caused by the hubris of those who think they’re built different, your “comrades” included. Silence = death.

    • gingerbrat [she/her]@hexbear.netM
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      6 days ago

      It’s almost impossible to stay optimistic when you look at the state of covid treatment - generally speaking. It’s becoming harder and harder to get new vaccination shots where I live, masks are getting more expensive, and even if you manage to get a mask and a shot, people will treat you like you’re infectious when you walk into any place with a mask on. It’s disturbing how quickly the covid denial swept through all branches of society.

      Please don’t give up hope yet, though I know it’s hard, I’m sure there’s some sort of silver lining at the end of the tunnel cuddle

      • mononoke@lemmy.sdf.org
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        6 days ago

        I feel compelled to push back wherever I see complacency about all of this madness, but I can feel it taking its toll. It was Sankara who said we don’t get the luxury of being tired of explaining…but I am very, very tired.

        • gingerbrat [she/her]@hexbear.netM
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          6 days ago

          Maybe we shouldn’t treat tiredness as a luxury. I mean, I get what Sankara was saying, but it’s not like you can stay up on your feet forever. We all need breaks, so becoming and being tired is a foregone conclusion. Maybe what we need is shifts in explaining. You can’t do it all on your own, you know?

  • un_mask_me [any]@hexbear.netOPM
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    7 days ago

    I hope you know you’re not alone and that others out here care about your well being. Much love to all my disabled comrades <3

  • Keld [he/him, any]@hexbear.net
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    15 days ago

    Eating yummy broccoli. No one at the food bank wanted their broccoli so I got 7 heads of broccoli. People at the food bank are such picky eaters I swear.

        • un_mask_me [any]@hexbear.netOPM
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          14 days ago

          A handful is usually all you need! I don’t normally eat broccoli raw, but when I do I definitely notice a difference. Same with cauliflower; but when I cook it first it doesn’t mess with my stomach as much. I think it removes some of the things that can cause distress, if I’m remembering correctly. A lot of that depends on the individual, though. Sometimes our bodies just don’t like what we try to feed them, especially when meds and illnesses come into play.

          • DisabledAceSocialist [comrade/them]@hexbear.net
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            14 days ago

            The problem is I’ve been diagnosed with a folate deficiency and the folic acid supplements aggravate my bladder terribly. I thought I would get extra folate by eating extra veg but the gastric symptoms it gives me are too bad. My tingling and pins and needles are getting worse and I’m really scared about it because it seems there’s nothing i can do, and the GP is so useless, she just tells me to take the folic acid anyway.

            • un_mask_me [any]@hexbear.netOPM
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              13 days ago

              Oh I wasn’t suggesting that you should try it that way, I guess I was just over-sharing, sorry. I’m sorry the pins and needles are getting worse and that your GP isn’t helping at all. You’d think they’d have a shot or something they could give you that wouldn’t mess with your stomach. I hope you can get some proper care soon.

            • gingerbrat [she/her]@hexbear.netM
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              14 days ago

              Could it be that the folate is doing something to the fibroids? And out of curiosity (don’t answer if you don’t want to share) what type of disturbances do you experience?

              • DisabledAceSocialist [comrade/them]@hexbear.net
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                14 days ago

                I’ve had IBS for ages, although it was quite recent that I realised that a lot of vegetables were aggravating it. Wind and loose stools being the main symptoms of that, and caused by many different veggies. And the veggies that don’t trigger the IBS trigger migraines and bladder irritation. The only ones I can eat without any bother are potatoes, carrots and spinach, although apparently spinach can cause kidney stones so I’m hesitant to eat it more than twice a week. It’s just an awful way to live, I would love to be vegan and eat lots of vegetables, I wanted to do Dr Joel Fuhrman’s Eat to Live diet but it’s out of the question.

                I don’t think the folate is doing anything to the fibroids, according to google, unmetabolised folic acid gets into your bladder and irritates it, so that’s probably the issue with that.