Giving Him the Finger

I had a breakthrough in accepting myself on Sunday. Forgiving myself for everything I didn’t know before my mother died (my mother didn’t want me to know I was disabled because she thought that I was too smart for what was then called “the special classes.” I don’t know. Maybe I would have been happier. My teachers would have seen how smart I was and I probably could have taught myself better than they could. Special Education is actually more about room to stretch out than it is the curriculum being different. Special Ed understands meltdown, burnout, demand avoidance, lack of executive function, going selectively mute when you’re overwhelmed, and everything my other teachers wouldn’t have understood because they didn’t study being neurodivergent for a living.

I have trouble with transitions. I absolutely hated school after first grade, and it’s not that there weren’t genuinely good moments. It’s that in every school I attended, there were only five minutes between each bell. That’s not enough time for an AuDHD person to adjust to the next thing. It is EXACTLY like being at a party and needing to go to the bathroom just to recharge.

Also, five minutes is not enough time for a person with floppy muscles and depth perception issues to be able to run fast enough to be on time. I have been punished for my disability many times, which is how I found myself in the nurse’s office because a teacher was pissed at me for being a couple of minutes late every day and I knew it……. so I was hauling ass and I fell down two flights of steps.

Because I am low needs, I am trying to speak for the ones who can’t. You can’t imagine how brilliant most autistic people are if you take the time to get to know their brains rather than focusing on what they cannot do. It bothers me that people treat those with autism in which they can’t social mask like children. It’s one thing to have a childlike brain. It is starting how many people think all high needs people have problems with intelligence and not communication. It’s what bothered me so much about the “Autism Speaks” ad where a mother talks about one night in which she thought about putting her daughter in the back seat and killing them both. If her problem is limited to communication and not intelligence, what do you think it does to a person to sit with that knowledge for years on end? People think they’re talking behind our backs because in their minds “autistic” is shorthand for “stupid” and not different.

I would bet there are many more AuDHD people than me out there, but would never want to get tested because of how autistic people are treated.

  • Because Autism Spectrum Disorder means that your brain processes information differently, people at the lower needs end are told things like “you don’t look autistic.” “Everyone’s a little bit autistic.”
  • I am going to bet that those people have never experienced demand avoidance down to not being able to make demands of *themselves,* much less being able to communicate when other people make demands of them. If someone makes a demand of me, I have to white knuckle my way through it if I’m on a deadline, because I have problems with, again, transitions. I like to know what people need from me plenty in advance, because I know at first my body will say, “no. Not doing it.” Autism makes it where when someone makes a demand of you, you go into fight or flight (meltdown). It’s not because we don’t want to do things for other people AT ALL. It’s transitioning from one thing to another. We all wish that part of it would go away, because it’s the biggest reason even low needs people have trouble taking care of themselves. It’s not laziness, it’s not an unwillingness to do anything. It’s that our brains are shutting down because we cannot handle overload.
  • I realize that I have anxiety and I go through cycles. Sometimes, I want to stay home and chill because I’d rather spend time with myself, either writing or reading/watching something to spark my own creativity. This is problematic in two ways, and neither one of them have anything to do with me.
    • Sometimes, I’m on a down and I’d rather isolate than interact because I’m more likely to go into a meltdown from feeling overwhelmed. Recharging also means getting away from my own writing, navel gazing. I have learned that many, many autistic people are like this (the isolating part, not the blogging part) because too much activity in a room is overwhelming to an enormous degree. If you are low needs, that seems incredibly odd and they’re weirded out by it. People can clearly see that in high needs autism, but they cannot see that low needs does not mean less distress. We are just capable of social masking because we can recognize when we’re making you uncomfortable and adjust constantly, knowing you won’t adjust toward us. I am sure that you cannot say this about an autistic kid’s parents or siblings most of the time, but I’ll say it again….. NO ONE KNOWS what to do with autistic kids after they graduate from high school.
  • There has never been an apology to me by a boss when they have miscommunicated with me. It’s “how can you be so stupid/airheaded/flaky?” Why are you “not living up to your full potential?” Because you don’t have the skills to communicate with a neurodivergent person nor any empathy for those disabilities. It is always on the neurodivergent person to pick up what a neurotypical person is putting down when they literally can’t. Especially in an office, where everyone and their dog has a PhD in bullshit. If you don’t, you’re a problem child quickly….. mostly because since most bosses don’t know how to work with neurodivergent people, they don’t know how to get their message across in the way that they meant it because the chasm is *wide.* Bosses do not like to hear the truth most of the time. Very few will let you speak truth to power. Therefore, if I acknowledge a problem in their logic during a meeting, it doesn’t matter that I didn’t pick up on the social cue. I wasn’t focusing on them at all, but the matter at hand. I also want to contribute to the discussion in a major way because I’ve had bosses talk to me privately and steal my ideas.
    • It really, really matters whether your boss can hear criticism or not when you’re autistic, because you are literally trying to help with your different pattern recognition and it is seen as threatening, particularly to men. The first boss I ever thought really had my back was at Marylhurst, when in a meeting with Google I laid a truthbomb on the table and he saw what dog I was walking immediately. I was so touched when he said, “I think we should get back to what Leslie was saying, because I’m going to need an answer on that.”
      • I’d spent so many years thinking my words and opinions didn’t matter, so it made my year.
      • He actually did that twice. Dana thanked him for hiring me and he said, “Leslie is worth every penny.”
  • These are the things I remember when it all goes to shit later because literally no one understands me after a while.
  • I am one of those people who needs iron structure every single day like clockwork, and also angry when I feel micromanaged. There has to be a middle ground, and there is. But it’s more work than it would be for a neurotypical employee because what you say is not what we hear and vice versa. It’s why when I need to relax, I watch cartoons.
  • If you react to us realizing the pendulum has swung too far with negative attention….. “oh, look who FINALLY decided to show up FOR ONCE,” we’ll never show up to anything ever again. It’s easier to watch family friendly and kids’ shows so that you can study shows that present big ideas to little kids. Avatar: The Last Airbender comes to mind………… It’s almost as if it’s a hidden layer that’s gold when you find it.
  • Here’s what I mean about good writing where you least expect to find it…… Rigby says “tonight, let’s do something REALLY scary.” Pops says, “we could go to bed early and be alone with our thoughts.” It was at that moment I realized Pops had given me nightmares. 😉 It was a truth I, and most people with mental heath issues/processing disorders need to be able to voice. That’s part of the problem. Not being able to completely take care of ourselves makes us bad at communicating our needs as well. That makes society doubly difficult.

There is nothing scarier than being alone with your thoughts when you’re disabled. The system is not built for you, especially when you’re low needs and “seem normal,” You walk around all day, every day, feeling worthless and useless because we cannot accept that we have disabilities. It’s easier to believe everyone else….. you’re either slow on the uptake or a judgmental dickhead.

When you think of us as “stupid,” it comes across in a sugary sweet voice that no one needs. That voice is the shortest and quickest path to driving me up the wall. If I have to ask for information again because I didn’t catch it the first time, it’s downhill from there. That’s why I prefer working through e-mail. I do not like conversations at all regarding work because I do not want there to be anything missing in the conversation that I can’t go back and read. It’s what keeps me from having to ask “stupid questions.”

We don’t need your pity, but we do need your advocacy. Thank God the neurodivergent community found programming, because starting when I was a senior in high school, being a programmer meant getting rich. Not necessarily working at a company, but joining a small company that has venture capitalist money on a project in which you really know to the core of your being that it will succeed.

But that has backfired in a lot of ways because when programmers are sitting around together, they’re all tracking the same way and they get shit done faster than you can imagine. Therefore, the perception is that you’re either a savant at something, or you belong in special ed. There is no middle ground, because we’ve made it that way. Social masking has made it where we’re choosing not to take up room not to rock the boat.

Has it worked yet?

And now I realize I haven’t explained the title. In accepting my disability, I could laugh about it. In accepting his disability, Zac could laugh about it. He said “if you think I’m adorable, it probably has something to do with your depth perception issues.” I said, “I’m wondering if I should give you the finger you don’t have.” He said that was VERY well played. Because I realized something. That I can joke about it with Zac in a way I won’t let anyone else in the world get away with. EVER.

That’s because he’s not punching down, and neither am I.