Image text: @agnieszkasshoes: “Part of what makes small talk so utterly debilitating for many of us who are neurodivergent is that having to smile and lie in answer to questions like, “how are you?” is exhausting to do even once, and society makes us do it countless times a day.”

@LuckyHarmsGG: “It’s not just the lie, it’s the energy it takes to suppress the impulse to answer honestly, analyze whether the other person wants the truth, realize they almost certainly don’t, and then have to make the DECISION to lie, every single time. Over and over. Decision fatigue is real”

@agnieszkasshoes: “Yes! The constant calculations are utterly exhausting - and all under the pressure of knowing that if you get it “wrong” you will be judged for it!”

My addition: For me, in addition to this, more specifically it’s the energy to pull up that info and analyze how I am. Like I don’t know the answer to that question and that’s why it’s so annoying. Now I need to analyze my day, decide what parts mean what to me and weigh the average basically, and then decide if that’s appropriate to share/if the person really wants to hear the truth of that, then pull up my files of pre-prepared phrases for the question that fits most closely with the truth since not answering truthfully is close to impossible for me.

https://www.instagram.com/p/CvPSP-2xU4h/?igshid=MzRlODBiNWFlZA==

  • octoperson
    link
    fedilink
    English
    arrow-up
    7
    ·
    edit-2
    1 year ago

    Sometimes. Generally no. Not without the work I outlined above.

    As I understand it, people usually have an innate sense of affect - their general energy level, and valence - how positive or negative they feel. More specific emotions are basically narratives - I feel X because Y and that’s called Z. Well I can sense my affect, but my sense of valence is pretty murky most of the time. So coming up with those narratives is hard work, and I rarely have much confidence in them.

    (Oh, and please don’t take this as a general guide to ‘what autism is like’ because, 1) I’m not diagnosed, and 2) ND experience is very diverse)

    • Blóðbók@slrpnk.net
      link
      fedilink
      English
      arrow-up
      4
      ·
      1 year ago

      Your descriptions reflects my experience quite accurately (and I am diagnosed, AuDD). I usually try to be vague on purpose when answering how I am, or give non-answers (such as “I [simply] am”).