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Mental Health

What Autism Really Looks Like: My Personal Experience

It’s Autism Awareness Month—a time to celebrate neurodiversity, challenge misconceptions, and share real stories about what living with autism actually looks like. Autism comes with a lot of stereotypes: rocking back and forth, not making eye contact, or being “weird.” But the truth is so much more complex. Autism is a lived experience, and for me, it’s not always visible.

Sensory Overwhelm

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For me, sensory overwhelm shows up in a lot of ways. I’m highly sensitive to lights, sounds, smells, textures, and crowded places. I try to avoid situations that might cause too much overwhelm. But when I’m already experiencing these sensitivities, it’s difficult to manage. Sensory overwhelm causes me headaches, irritability, sweating, and dizziness. It feels nearly unbearable to escape those symptoms.

Irritability and Emotional Reactions

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Irritability is always there, just waiting to be triggered. I tend to get angry easily. When things don’t go my way or there are disruptions to my routine, the irritability intensifies and can boil over into rage. The reaction itself can become a full-blown meltdown: I’ll cry, scream, lash out irrationally, and sometimes even hit myself just to feel grounded. It’s an explosion of emotions guided by the ever-present irritability I carry.

The worst part is that I can’t seem to control it. I try stimming to soothe myself, taking deep breaths to calm my nerves, or splashing cold water on my face. But no matter what I do, I often can’t get through it with composure.

Reading People Too Deeply

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One aspect of autism that isn’t talked about is how it sharpens perception. I notice the smallest details about people. I recognize their energy, tone, mood, and behavior. Truthfully, I read people like a book. Perhaps it’s because I’m always in my head, silently observing a person or the situation to understand my environment. Reading people has always come naturally to me, and while this helps me feel deep connection, it also means carrying a lot of emotional information—which can be incredibly exhausting.

Overexplaining and the Need to Be Understood

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I spend a lot of time explaining myself. I think it’s because I’ve spent most of my life feeling misunderstood. People rarely seem to really get me. I may come across as quiet, shy, or aloof at times, but there’s a lot more to me than meets the eye. I’ve always felt overlooked because of the way I come across.

When I’m speaking, most of the time nobody fully listens. In one-on-one conversations, where listening is unavoidable, I feel the need to overexplain myself. I’ve struggled with communication all my life. I often stumble over my words and feel like I’m in the spotlight—I have to communicate clearly, or I’ll look foolish. Whenever someone says, “What’d you say?” I feel rejection. I repeat myself, go deeper, and provide more context. It’s exhausting. And it all stems from people not understanding my neurodivergent brain.

Social Burnout and Recovery

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Socializing can be wonderful, but it can also be incredibly draining. I get tired quickly, and if I push past my limits, I completely shut down. Social situations are a mental mind game. I have to prepare ahead of time: what I could say, who I’ll encounter, and how I’ll exit if needed. My brain never relaxes around groups of people. I constantly overthink: Do they want to talk to me? Do they like me? Do they want nothing to do with me? I’m running a marathon I never signed up for.

Recovery time is necessary. It’s where I rest, recharge, and reconnect with myself again.

Meltdowns and the Invisible Struggle

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Sometimes, my meltdowns aren’t always visible or look like what other people expect. Often, they involve tears, rage, panic, or anxiety—but other times, it’s an internal spiral that no one can see. My meltdowns feel like a storm inside me. The fog is so thick I can’t see clearly, thunder roars inside my bones, lightning strikes my nerves, and the rain feels like tiny needles pricking me from the inside out. In those moments, I never know if there will be a sunny day again. Autism doesn’t always look obvious. And just because I seem “fine” doesn’t mean I’m okay.

Autism is Not a Stereotype

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This is what autism looks like for me. Not a stereotype. Not a label. A lived experience.

What assumptions have you made about autism that might not reflect the real experience?

“Autism is not a tragedy. Ignorance is the tragedy.” — Trisha Van Berkel

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4 Comments

  • Liz

    I am only starting to understand autism in under the last couple of years. And from reading a couple of books (which 2nd book I am still reading) and a couple of websites I feel like what I have read feels like me.
    I have just started counselling not long ago again. Going back to a counsellor I seen before. I am going on a few things. But sensory issues is mainly the reason I went back after another meltdown I had. But this one I didn’t see coming and scared me the most.
    She thinks I may have a trait of autism.
    Although what I read feels so much like me, I do have trauma from childhood. I am an introvert all my life. And I discovered in 2018 I am a HSP which explained a lot.

    The last time someone said to me I may have autism was when I was in my early or mid 20s, a lady who had autism herself. Which I didn’t know she had autism until she came out with it after saying she thought I may have autism. But I didn’t have a clue about autism then. I am 50 now.

    Whether I will one day see about having an assessment, I don’t know. Because I do have stuff I have forgotten from childhood and so scared of opening Pandora’s box so to speak. But also I have fear just the idea of approaching my doctor’s about it.

    I am in early stages of counselling and I plan to have quite a few sessions. So, maybe I will feel more braver about approaching doctor. But here in the UK there are long waits to be assessed so I hear.

    • Embrace The Unseen

      I can completely relate.

      I’m a HSP as well, and when I learned of the term RSD (Rejection Sensitivity Dysphoria) it was like looking my name up in the dictionary. This is a common trait for people with ADHD…and autism I later learned.

      I honestly did a self-diagnosis of autism. The assessments are still designed with men in mind and women are incredibly overlooked. The tests are pricey and I don’t need someone to confirm what I already know about myself.

      It’s great that you’re seeing a counselor. I need to get on that and see one myself. My therapist left the group I was with, and I haven’t found one since.

      Thank you for your thoughtful comments. Please feel free to share and comment any time you’d like.

      I feel like we’re two like-minded souls.

      • Liz

        I have been reading quite a few of your posts since discovering you after you came to my blog.

        I haven’t heard of Rejection Sensitivity Dysphoria before. So, hearing this on your blog was where I first heard this. I will read more of that later another day

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