I Remember When I Started Masking My Autistic Traits (The Cookie Story)

I’m a late diagnosed Autistic woman. This is about the first time I remember noticing that I was different and started learning to mask my Autistic traits.

I was really young, like maybe 6? I don’t remember where I was, or who I was with but I was at someone’s house with a group of people. It might have been a potluck.

I was watching the other kids, when a girl went up to an adult and left with a cookie. It was one of those hard oatmeal cookies you get at the store. I wanted a cookie too, so I went up to them and asked for one.

This is the first time someone gave me what I ominously call “The Look”.

I felt like I had done something wrong. Their reaction was not what I was expecting and I was confused.

I did get my cookie and went back to observing the other kids. I started to notice when they asked for things, their voices had a different inflection and intonation. They also added a lot of pleases and thank-you’s (e.g. “Can I pleEEease have a cookie?”). My voice was flat and fast; straightforward – “Can I have a cookie.”.

It was after that I started practicing speaking. Under my breath I would repeat phrases again and again with different inflections, intonations, trying to make my voice sound less “flat”. I wanted my voice to fit in.

This was also something people noticed, because I was walking around whispering to myself all the time. If I got a positive reaction, I would repeat it back to myself to memorise the tone. If I got a negative one, I would carefully listen to other people speaking and start practicing it again. Over time, I learned how to make my voice sound more “normal”? But sometimes my tone still came out completely wrong and people would misunderstand what I meant.

Now that I’m working on unmasking, I don’t worry about my voice so much. If something comes out in the wrong tone, I say so and laugh.

(P.S. I find it hilarious that I was just sitting watching everyone. Knowing what to look for now, I was so obviously autistic. I did play with other kids, but I didn’t know how to join in without being explicitly invited to.)

Unmasking Adventures: Stimming at The Self-Checkout

Since I got diagnosed a year ago, I’ve been working on unmasking my delightful Autistic self. A big part of that for me is stimming freely. Whether I’m excited, nervous, happy, or just vibing; I stim. It’s simply how I regulate my nervous system.

People sometimes assume a lot when they see me stimming in public. I’ve had complete strangers come up to me and tell me to breath when I’m just doing my thing.

A month ago I was using the self checkout and it took me a hot second to scan my lip balm. I was just vibin’, doing my finger-flicking and nail rubbing stims.

The employee managing the self-checkouts instantly materialised and told me how to scan it. Which is totally fine! But then they started guiding me through scanning everything.

“Just turn it that way a little more, here let me- oh there you got it!”

I was done scanning and went to do the rest of the buttons. This person stood watching over my shoulder and started coaching me on what buttons to push! They reacted if I pushed one they didn’t tell me to “Oh wait, oh okay, you sure?”

I wanted to get the hell outa there so I said I didn’t have a membership card.

“Oh, wait wait wait! Here (pushing the back button); Isn’t that your mom? Maybe she has a card you can use.” Then they went over to my mom, got her card from her and scanned it for me.

Maybe they were just a really friendly, helpful person? Yeah they certainly could be, but I was the only one they interacted with like this. I wasn’t struggling and I’ve used this checkout dozens of times.

This behaviour isn’t helpful to me. It’s the opposite! It’s overwhelming and stresses me out. I don’t always have the words to communicate “Thanks, but I’m good now” or “Thanks I’ll ask for help if I need it” which is frustrating.

These kinds of interactions leave me feeling conflicted. I understand they are trying to me helpful and kind, but I don’t like that the assumption that I need help. Plus, their tone of voice and the way they went about it felt kind of infantilising (and maybe a tab ableist?).

Please don’t automatically assume I need assistance simply because I’m stimming; just ask me!