I might be Autistic: Exploring and accepting my autism

I was sitting in the front seat of my then-boyfriend’s car when he looked over at me and said, “Sometimes I think you might be autistic.” I said, “I could be.” I did not know then that the fact that I did not deny a label that was meant to dehumanize me was further proof that I was most likely autistic.

I did not realize he was looking for an out in the relationship, because when I don’t want to be in a relationship anymore, I simply tell the person I don’t want to be with them anymore.

I do not recommend that. It’s how I got my second stalker. Another time, I was in the neighborhood store when a neighbor looked at my face and said, “You look like S” (S is my disabled half sister from a different mother). Then she asked if I felt bad when people said I looked like S. I said I did not. I did not realize that she was indirectly signaling that I, too, was wrong in the brain for being okay with being associated with a disabled person.

You might be reading this and thinking, “How did she not pick up on these social cues?” or “How did she not know she was autistic?” There are a few reasons for my misunderstanding these situations, but I think the main reason is that I walked at 7 months old, talked at 1, and could read and write by 2.

In the Caribbean in the 80s, that’s all that mattered, and my sensory processing issues were written off as willfulness. The status quo was to yell children into submission, so I learned to mask at an early age. It wasn’t till now, at nearly 40 years after a lot of heartache and complete breakdown of most of my relationships, that I am finally ready to admit that I might be autistic and explore my autism.

This is my journey.

Honestly, I am not entirely certain how I made it this far in life without significant difficulty. I think I was just lucky. For the most part, I had an accepting and supportive family. I was very lucky that I also had mostly accepting teachers. As I progressed to adulthood, these once-supportive people grew less supportive with each passing year.

Directness and honesty are cute in children, but you’re expected to be socialized out of that by adulthood. I was not. When added to the intersectionality of being a black woman from the global South, it’s easy to see that I was destined to have the crisis that I now face.

Luckily for me, I found the online community of #ActuallyAutistics who are revolutionizing how autism is viewed. With their help, I am slowly figuring out how to exist in a world that does not want me.

Autistic Adults are redefining what it means to be autistic. They’re explaining autisitic traits, pushing for acceptance and support instead of punishment and correction. Slowly, they’re normalizing neurodivergence and pushing past the stereotypes that autistic people are violent, antisocial weirdos who lack empathy.

If it were not for these people working tirelessly to raise awareness while battling their own demons, online trolls and bigots, I would have killed myself last year because I was tired of being called controlling, mean, and heartless without any explanation or examples.

I knew there was something I was not getting. Without these autistic activists breaking it down, I would never understand. I was ready to peace out of this social contract that I did not sign up for and did not understand. I was ready to leave this world because it was all too hard and made no sense.

Even now, knowing all that I know and being sure that I am most likely autistic it is hard for me to claim this openly. There are a few reasons for this. The first being that it is near impossible for me to be officially diagnosed because of my age, ethnicity, and where I live.

The second is that I am still wrapping my head around the idea that self-diagnosis is as valid as professional diagnosis. This is because I have come across too many people who self-diagnosed as neurodivergent in order to excuse and continue harmful behavior.

The third and maybe biggest reason is that I know my family will not likely believe me and use the fact to further ostracize me. If a few people can push the narrative that I am faking asthma to get attention, how will they ever believe that with all my academic excellence I have been autistic this whole time?

The final reason is that as a Black woman, I know if I admit it openly online it will lead to a new brand of harassment.

I never learned the social skills that are required for allistics adults to accept each other.

Already, I do not feel safe online. I have had a few instances of people using things I posted online to destroy my relationships offline. I do not feel safe in my home where my disabilities are often used against me. I am excluded from family activities because accommodating me is seen as a burden as well as my aforementioned unsubstantiated controlling nature, meanness, and “how I talk.”

Mind you that these same people who could not be bothered to include me in their fun times know exactly where to find me when they need help.

I do not feel safe in workplaces because coworkers have repeatedly used my allergies and sensory issues against me. Also, it is hard for me to interact with adults in workplaces because I never learned the social lies, I mean social skills, that are needed for allistic adults to accept each other.

I find I come to work one day and people have a problem with me, no one can say what the problem is, but it’s accepted that something is wrong with me and they slowly push me out of the job.

In the beginning of this journey, I thought that if I could say I am autistic that they might be forced to accept me as I am. Recent experiences have led me to believe that I am wrong.

Last year I was a part of what I assumed to be a like-minded community of Left-leaning makeup lovers. I really enjoyed the space, and it was so supportive. I felt seen, heard, and nourished. That feeling did not last. Autistic people tend to see patterns that allistics have not noticed. I started to notice patterns that made me uncomfortable.

At the time, I was using phrases such as “the way my brain works” or my “brain doesn’t work like this” as a disclaimer when I explained things. Even though I did not fully know then that I was autistic, I knew that when you point out patterns and remember small details people think you are creepy and don’t want to be friends with you.

I also didn’t realize that people (usually privileged white folks) were out there self-diagnosing as autistic or adhd, and then entire communities would accommodate them by allowing them to be assholes with no accountability. I was so naive. I also believed that when people said they were committed to anti-racist work and not centering on whiteness, that it meant that they would listen to Black women.

Eventually, I pointed out the “wrong” pattern and offended rural white America, and that was that. I didn’t feel safe there because I was not sure what I could say without being labelled as the mean Black woman again.

I saw a group of people who had gone out of their way to excuse the racist, misogynistic, general assholery of a self-diagnosed autistic, trans, nonbinary person simply put me in the box of mean Black person at the first disagreement. I was blind-sided. When I tried to discuss the disagreement in terms of my possible autism so that we could find a way forward, it was not even acknowledged.

So many Black femme autistics are erased out of existence because of the intersectionality of race and gender oppression. I felt destined to be another statistic of the gifted child who fizzled out because society would not accept them. I felt that if I self-diagnosed as autistic, I would not be accepted; instead, it would lead to unwelcome scrutiny. I was not ready to openly admit that I might be autisitic and deal with the consequences of that admission.

At the same time, my life offline was also collapsing. My fibromyalgia medication no longer worked, and the new medication made my brain feel scrambled. Coming off the medication made my brain feel even more scrambled. My endometriosis was flaring like never before.

I was losing days to pain so severe I often did not know where I was. The pandemic made it very difficult to get access to medical care. The people that I reached out to for help were either unable or unwilling to help. I did not want to be alive. I was afraid to talk because I did not know what would make people angry. At times, I physically could not talk.

In those darkest days, I could not bear to look at a screen or hold my phone. Every noise was too loud, every texture too rough. The realization that I would never have the social skills to be accepted by “normal” people broke me. I lay for days topless in my room. I don’t know how I survived. My mind and body were equally broken. I would have gone to the mental hospital, but it was so loud there that I knew I would not survive.

Instead, I lay in bed with my soft blanket to comfort me; and sometimes my godson. The little nugget that hated shirts, heat, and bottles as much as I do gave me reason to go on. I stayed alive because of the kids.

I did not want them to have to deal with the trauma of my death. On the day of my grandmother’s 80th birthday party when all my little cousins were hiding from the family in my room, I knew I had made the right decision.

Slowly, I dipped my toes back into society both online and in person. When I came back, I found that I was no longer welcomed. I had gone too far by ‘going away’ for a few months. Those months when I did not know if or how I would heal had offended some. They did not care that I had nothing left to give and needed time away. I suspect it was just the excuse they needed to finally cut me out of their lives for good.

It was as if I reached the critical mass of adulthood where my peers would no longer accept my social ineptitude and refusal to conform.

I was in my late 30s, childless, and single. However, I did not hate children or claim to not want children. Neither was I obsessed with having a child or being in a relationship for that matter.

I did not claim any sexuality. I still don’t understand why that confuses people. I still don’t know what people mean when they say I am controlling. I do not know what they mean when they complain about “the way I talk to people.” I try not to worry about it or the folks who cut me out of their lives.

I try to hold on to the few people who stood by me through it all. Those who patiently waited for me to be strong enough to talk again. Those who listen when I share that I might be autistic. Those who do not judge me for taking time off to heal. Those who accept me as I am. I am thankful for these people. I am thankful for the autistic activists being their authentic selves online. Their work gives me courage to face the truth that I might be autistic.

I know that my journey is only going to get more difficult. I also know that I will be okay. I am committed to finding support. I am committed to figuring out how to not just survive, but thrive. I am encouraged by the progress we have made no matter how small.

I may not be ready to be my full self in public right now. I may not have the courage I need just yet. I know that one day when these wounds that hurt so much right now will heal.

Then I will be able to look into the world and proudly say, “Hi, I’m Mo, and I am autistic.”

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17 Responses

  1. And it is happenings of a nature such as these which create a level pain, frustration, anger, that results in having an attitude of, Neurotypical culture/society is a sadistic evil empire which fully deserves to be, which must be, torn down and destroyed without mercy.

  2. “Even though I did not fully know then that I was autistic, I knew that when you point out patterns and remember small details people think you are creepy and don’t want to be friends with you.”

    True, true words. For me, the pattern-seeing can also mean that we know what will happen next, what cycles are repeating, whether something is likely to be a lie, even what will be said at times, making us all the more uncanny and unwanted by many.

  3. I’ve wondered why that pattern-awareness bothers some people so much. Maybe it makes them feel overly self-conscious, analyzed, scrutinized? And in our judgement-intensive society, maybe people automatically assume that, if we perceive the patterns they are playing out, we are also judging them?

    1. From my own observations, I’d say it’s partly that, and partly that we’re seeing their lives so clearly when they can’t, or when they don’t want us, aren’t ready for that, and whatnot.

  4. Hi, Mo. Thank you for writing. I wish you all the time, all the love little cousins bring, and all the acceptance from fellow pattern-recognizers whose brains are similarly wired!

  5. My parents don’t believe in the soft sciences. Even though my father is a medical doctor, he thinks that autism is just an excuse to engage in deviant behavior. As a child, my parents used “tough love” to break me of “bad habits” like self stimming. “Tough love” is just a polite way of saying that they used to beat the crap out of me.

    While I appreciate the idea that you want to be loved and accepted by your parents, the reality is that we are the people that we are. Our parents may or may not be accepting and if they’re not, then shame on them. Our lives go on and we owe it to ourselves to live the best possible lives that we can regardless of what our parents think.

    I am now 61 years old. While I used to care what people thought of me, I’ve gotten the point where I really don’t care what they think so long as I am accorded my rights under the Americans with Disabilities Act. If someone doesn’t like me, that’s on them. People don’t have to like me to treat me with dignity and respect. I have filed one lawsuit and two civil rights complaints against people who have violated my rights. I recently came close to filing an EEOC (Equal Employment Opportunity Commission) complaint but stopped after my building administrator and my union dealt with a hostile work environment complaint.

    I am done being a metaphorical punching bag. I will not tolerate harassment or bullying. I will not be the butt of stupid and mean spirited jokes nor will I accept insults that are given under the guise of free speech. I will stand up for myself because the alternative is to be a door mat who enables bullying by doing nothing. To paraphrase and appropriate Helen Reddy’s feminist battle cry, I am autistic, hear me roar!

  6. Self-diagnosis is not as valid as professional diagnosis, the only people who say are the fakers who have over took the autistic community and have push us out because they know if they tried to get a professional diagnosis they would rightfully be told that they don’t.

    If you think you have autism you owe your self to try as hard as you can to get a professional diagnosis, not just to make sure you have autism but because you may not that but one of many neurological conditions

    Nothing wrong thinking you have autism as a first step, every thing and bigoted in just saying are self-diagnosed at the first step and calling it a day.

    1. Interesting how the only takeaway you have is her self-diagnosis while completely ignoring the real socioeconomic challenges she described with getting diagnosed.

      Case in point, she discusses how sharing one’s autism neurotype online as a Black woman invites foolishness and here you are, self-appointed autism gatekeeper.

    2. G, you are completely ignoring the hurdles she so eloquently described. The idea that those who haven’t been diagnosed are “faking” is so offensive, it makes me wonder why you are bothering to read an article about autism at all.

    3. Self diagnosis if valid.
      And no less valid then professional one.

      It looks like the author is very unlucky with people in their life.
      There are good people out there.
      I was directed here from a face book group which helped me a lot.
      If not already a member, maybe try if it is to your liking?


    4. Amazing how you didn’t EVEN consider the barriers many have to actually being assessed let alone Get a diagnosis . Fantastic way to show just how privileged you are . Plus you assume the diagnosis criteria itself is a good one – it isn’t as it was created by Neuronormative professionals who didn’t consider nor have any respect for the Autistic experience.
      Self diagnosis IS VALID

  7. Thank you for sharing your story. I am so sorry that you’ve been so isolated and misunderstood for your whole life. Life is tough and unforgiving. Socialization is so easy for some and a struggle for so many others. I am happy that you have found a community of pioneers changing the narrative and smoothing out the wrinkles of understanding for people. People are rigid and intolerant, especially for things that they don’t understand.

    Embrace your new community and remember that you are not tied to the family you were born in to. You can create a family of your own, full of people who don’t take it personally when you need to take a step back to care for yourself.


  8. I really enjoyed reading this. I also found it validating, being in a similar position, trying to reconcile the hardships of being different and realizing that there might be a name for the reasons you are cast out by society. Reading and finding information that can be identified with, that explains some of those difficult experiences. Realizing those experiences revolve around being mistreated, just for being different, and people not knowing how to tell you.

    The challenge is mutual, though, I mean, apparently! When people are concentrated into groups, every group and their respective idiosyncracies can be broken down into social mechanisms that are used to navigate interpersonal relations within the group. However, we tend to overlook this and subjugate those that differ, because their idiosyncracies are offensive to the group. The concept of “normal” is just a statistical measurement, and a “normal” can be found in any group, we’ve just failed to understand that being different from the majority doesn’t make you bad or disabled. It all just makes me wonder if an inability to get along stems from perceptions of superiority and prejudice, motivated by an over-reliance on statistical inferences? Emerging research and the influence it has on shifting perspectives seems to suggest so.

  9. Re: “It all just makes me wonder if an inability to get along stems from perceptions of superiority and prejudice, motivated by an over-reliance on statistical inferences?”
    Here at 07:07 in the morning I’m not able to offer any source documentation though from my lived experience of over half a century I’m going to say that you are definitely on the right track.

  10. I am not autistic but my husband is and he hasn’t yet gotten a formal diagnosis. He has had similar barriers to that, and we do suspect it is because he’s a person of color. And I am a white woman… gender does hinder it; we’ve been told I’m confusing ‘marital problems,’ despite my accomplishments, rational intelligence, love and support of my husband, and the fact we’ve had years of individual and couples therapy…. 🙄. I’m here, hoping to truly understand him and myself and this article—in so many ways—is a wonderful, honest and helpful resource in that journey. Thank you. I should mention I am and have been formally diagnosed with ADHD and PTSD, from years of trauma outside of our relationship, but also years of misunderstanding with traumatizing effects. But those, in my eyes, are definitively overcomeable (is that a word? I’m a writer & editor; I should know this, but it works here so I shall now call it a word!). It is resolvable in acknowledging where these behaviors and feelings come from, instead of assuming the worst. Being informed leads to massive understanding in this case. Again, thank you so much.

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