Autistic Burnout: Ignoring Special Interest and rest needs will Slowly Destroy You

okt 8, 2025

How My Autistic Burnout Unfolded

 

My autistic burnout didn’t strike like lightning. It built itself layer upon layer across my entire life, like the infamous boiled frog metaphor: the water grows warmer and warmer until you don’t even realize you’re being cooked alive.

For me, “normal life” meant constantly pushing myself to the very edge, mentally and physically, then labeling the exhaustion as laziness. If I had trouble completing routine tasks, the conclusion was always the same: I’m weak. I need to push harder.

What most people don’t realize is that for an AuDHD brain, everything that isn’t driven by intrinsic motivation costs one hundred times more energy. ADHD comes with a broken reward system for routine or boring tasks. There’s no natural dopamine hit for doing laundry, replying to emails, or cooking dinner. Every action has to be done manually, step by step, as if wading through syrup. “Just do it” doesn’t exist. Each task is a negotiation between brain and body: Move your arm. Now your hand. Now pick this up.

And yet, the inner critic whispered: But everyone else does it. How hard can it be? You’re just lazy. Try harder.

So I did. I forced myself through life.

Childhood and Adolescence

As a child, I struggled deeply with fitting in. I was the “weird kid,” always slightly off from what was expected. But by my teenage years, I cracked the social code. I became adaptable, even popular, wearing the mask so well that nobody suspected how hard it was.

But behind the mask, I began experiencing panic attacks at sixteen. I ignored the signs. I thought it was just part of life. I kept pushing, kept adapting, kept pretending.

When you live this way—masking, forcing, never resting—something eventually breaks.

Motherhood: The Steepening Slope

Becoming a mother made everything heavier. The hill I’d been climbing suddenly turned into a vertical wall. Sleepless nights, breastfeeding, the endless cries of “mama” every day, all while trying to maintain a career, a household, and a relationship.

Add in the invisible labor: doctor’s appointments, school meetings, birthdays, playdates, shopping, cooking, cleaning, and remembering every tiny detail of family life.

It’s a choreography of a thousand moving parts—and I refused to drop a single ball. Delegating cost even more energy than doing it myself. So I carried it all.

And then came the breaking point.

The Final Straw: A Crashed Hard Drive

One day, our hard drive failed. Years of personal photos vanished. Birthdays, vacations, ordinary moments of joy—erased. To make matters worse, an entire wedding shoot for a client was on that same drive. We managed to recover most of the client’s photos from memory cards, but our own images were gone.

It might sound trivial, but for me, it was the straw that broke the camel’s back. As I write this, I still feel the sting. Those memories were irreplaceable, and losing them ripped something open inside me.

I shattered.

Eight Months of Collapse

Every morning, I woke with violent heart palpitations, as if an electric current jolted me awake. My body shook with adrenaline. I curled into a ball under the blanket until my heartbeat calmed.

I survived only by functioning on the bare minimum. I took my kids to school on sheer willpower, then came home and collapsed on the couch under a blanket, paralyzed by exhaustion. Eight months passed like this.

Cooking, cleaning, even making myself a drink were impossible. Some days I lay frozen, unable to gather the energy to feed myself. My life shrank to survival mode: keep the kids alive. That was it.

The doctor called it “probably depression” or “just burnout” and told me to rest. But what does rest mean when you’ve already abandoned everything except bare survival? Even resting was too much. My recovery stalled. Two steps forward, one step back.

The Diagnosis Journey

I entered the diagnostic process, which dragged on for nearly three years. First they suspected ADHD. Then autism. Then “maybe just one, maybe both, maybe neither.”

Finally, the conclusion arrived: ADHD, Autism, and Anxiety. Along with one truth I already knew in my bones: I was in the depths of autistic burnout.

The Forgotten Lifeline: Special Interests

Looking back, I can see it clearly: a huge piece of my collapse came from starving my special interest.

Before kids, my life was built around creation. Career, art, content, sports, and rest balanced each other. I had space to breathe.

But with children, that space vanished. All my time and energy poured into family logistics. Creativity, art, and content creation became luxuries I no longer allowed myself. The cruel irony is that the very things that recharge me were the first things I abandoned. How could I sit down to draw, write, or create when there were still groceries to buy, dinners to cook, forms to fill out?

My perfectionism wouldn’t allow it. So I kept going, drained dry, until nothing was left.

And this is the cruel cycle: without art, I lost my lifeline. Without rest, my brain had no time to form ideas. Without ideas, there was no creation. Without creation, there was no self-expression. And without self-expression, I lost myself.

Something in me withered. The piece of me that makes me me: gone.

Recovery: Art as Medicine

The turning point came with my diagnosis. With words to describe my brain, we could finally restructure our household, hire help, and carve out breathing room.

And when I returned to art, I returned to myself. Creativity is not indulgence—it is survival. My AuDHD brain thrives on hyperfocus, structure, and the deep dive into special interests. It’s both my strength and my vulnerability. But only when I feed it the fuel it needs: creation.

Now I treat my art the way others treat medication. It is non-negotiable. It is medicine.

What Happens When You Finally Make Space

The difference is night and day. When I carve out space to create, the ideas pour in. My brain sparks like a nuclear core. Hyperfocus takes over—I lose track of time, forget to eat or sleep, and surrender to pure creation.

And those moments? They’re not indulgence. They’re survival.

This is the cruelty of burnout for neurodivergent parents, especially mothers: the first things sacrificed are the very activities that keep us alive. Self-care, creativity, joy—they’re the first to go. And the cost is devastating.

The Message: Claim Your Space

If you are neurodivergent and see yourself in my story, hear this:

Your special interest is not optional. It’s not “just a hobby.” It is your oxygen, your compass, your lifeline.

Claim the space. Demand the time. Fight for the hours that seem impossible to carve out. Because without it, you risk losing yourself too.

I lost myself when I abandoned art. Through art, I found myself again.

And that is the quiet truth of recovery: sometimes survival looks like picking up a pen, a brush, a camera, or a keyboard—and letting your whole self breathe again.

Body Picking & Jaw Clenching: A Neurodivergent Struggle

okt 1, 2025

When people hear about “bad habits” like biting your lips or picking at your fingers, they imagine it’s something you can simply stop. A matter of willpower. But for those of us who are neurodivergent, living with ADHD, autism, or sensory processing disorder, these aren’t habits. They’re survival strategies. They’re called stims.

What Stimming Really Is

Stimming, or self-stimulatory behavior, is a form of self-regulation. It’s the body’s way of calming an overwhelmed nervous system or maintaining focus in a chaotic world. For some people, stims are harmless, like bouncing a leg or twirling hair. But for many of us, they turn into body-focused repetitive behaviors (BFRBs), where our own skin becomes the outlet.

My Personal Reality

For me, this has meant decades of bloody fingers, shredded cuticles, and raw lips. I bite, pull, and pick until the skin breaks, often without realizing it until it hurts. Add jaw clenching and tensing around my eyes, and I end up with headaches, tension, and even worn-down teeth. It’s not pretty, and it’s not optional. Stress, sensory overload, or even deep concentration will trigger it.

I once walked around with bandages on every finger, hiding the damage from myself and others. I tried the usual “cures”: bitter nail polish, snapping elastics on my wrist, even sheer force of will. None of it worked—because the root cause was never “bad behavior.” It was my nervous system crying out for regulation.

Why Neurodivergent Brains Do This

Research into sensory processing disorder (SPD) explains why so many autistic and ADHD people stim. Our brains process stimuli differently: louder, brighter, more intense. Stimming releases that pressure. For some, it’s repetitive movement. For others, it’s skin picking, biting, or clenching. What looks destructive is actually an attempt to survive sensory and emotional overload.

Finding What Helps

My turning point came with something as small as a fidget ring. I was skeptical. After thirty years of bleeding fingers, how could a piece of jewelry fix it? But it worked. The repetitive motion my brain craved finally had a safe outlet. For the first time in decades, my lips and fingers healed.

That’s the key: not punishment, not shame, not “just stop”, but replacing harmful stims with ones that meet the same need without leaving scars. For some, that might be fidget jewelry. For others, textured fabrics, putty, or movement. It’s about trial and error, and about giving ourselves permission to stim safely.

The Bigger Picture

Stimming is often misunderstood, even within neurodivergent spaces. Not every autistic or ADHD person experiences it the same way. Some stim outwardly, others inwardly. Some destroy their skin; others don’t. The spectrum is wide. But for those who live this reality, know this: you’re not broken. You’re adapting.

Final Thoughts

Body picking and jaw clenching aren’t quirks I can laugh off, they’re part of my neurodivergent wiring. They’ve caused pain, scars, and frustration, but they’ve also taught me resilience. I’ve learned that my body isn’t the enemy. My nervous system is simply looking for balance.

If you struggle with BFRBs, you’re not weak. You don’t lack discipline. Your brain is wired differently, and that’s okay. With understanding, compassion, and the right tools, healing is possible—sometimes one fidget at a time.

Autism, ADHD and Energy: Why Rest Is Survival, Not Laziness.

sep 24, 2025

If you live with Autism or ADHD, you already know your brain doesn’t run like everyone else’s. It processes more data, faster, with fewer filters, and that comes with a cost. What looks like “doing nothing” from the outside is often an exhausted brain trying to recover from a heavy cognitive load.


Understanding this energy cycle can help replace shame with acceptance. Rest isn’t weakness. For autistic and ADHD brains, rest is survival.

 

 

The Brain That Sees Everything

An ADHD/Autism hybrid brain, for some, can be wired to observe details most people filter out. Every sound, smell, expression, or subtle change in environment gets noticed and processed. On top of that, the brain makes endless associations, mapping connections at lightning speed.

The result? A mind that operates like a supercomputer, but one that burns through energy far quicker than most.

Why Energy Runs Out So Fast

Many neurodivergent people describe their energy system as “all or nothing.” Full throttle, then collapse. There’s rarely a middle ground.

Even joyful experiences can be draining:

  • A family birthday
  • A day at the pool
  • Meeting a celebrity hero
  • A concert or festival
  • A Themeparc
  • The gym

These moments are amazing, but they also involve sensory input, social interaction, and nonstop processing. The aftermath can feel like a physical hangover, not because the event was bad, but because the brain spent all its reserves.

The exhaustion can go so far as to the point where I’m unable to get myself a glass of water or get up for my book. That’s not laziness. That’s energy bankruptcy. When the tank is dry, even the smallest action feels impossible. The cost of “just get up” can be days of recovery. My body isn’t dramatic — it’s depleted.

 

 

Rest Is Not Laziness

From the outside, recovery can appear to be “doing nothing.” But inside, the autistic/ADHD brain is still hard at work:

  • Mapping experiences
  • Sorting through emotions
  • Filing sensory data
  • Making sense of patterns

This invisible labor explains why rest doesn’t always mean sleep. Sometimes it’s sitting in silence, letting the brain untangle its own complexity.

 

 

The Cost of Overdrafting Energy

 

When reserves are gone, even small actions feel impossible. Choosing not to get up for water isn’t laziness, it’s energy bankruptcy. The body prioritizes survival.

Pushing through this state often means borrowing energy from tomorrow, leading to multi-day crashes. Recognizing this cycle is the first step toward protecting long-term well-being.

 

 

Reframing Rest: The Lioness Analogy

 

Think of a lioness. She isn’t lazy when she rests. She’s conserving energy for when it matters most: The hunt.

The same is true for autistic and ADHD brains. Rest is what allows us to show up fully when it counts. Without it, the tank stays empty.

 

Powerful and demanding

 

Living with Autism and ADHD means living with a brain that is both powerful and demanding. It processes more, feels more, and burns energy faster than most.

That’s not a weakness. It’s different. And with that difference comes a truth worth repeating: rest isn’t optional; it’s essential.

Autism, ADHD: When Empathy Becomes Absorption

sep 17, 2025

When people talk about autism, they often repeat the stereotype of the “cold, unempathetic” person. But that couldn’t be further from my experience. As someone with both autism and ADHD, empathy is not something I lack; it’s something I drown in.

Feeling emotions as if they’re mine

I remember being in the hospital as a child for a minor procedure. Next to me was a younger child who cried a lot. Every time they cried, I didn’t just hear it; I felt it. Their fear, pain, and sadness landed in my own body as if I was experiencing it too. It confused me for years. I thought that’s how everyone felt emotions.

As I grew older, I realized this was a pattern. If someone cried, I cried. If someone fell and hurt themselves, I felt the sting in my own head. If someone radiated joy, I was high on it too. Later, I wrote a blog post about it (back in 2019) when I thought I was “just” an empath. Now I know this goes deeper—it’s connected to how autism and ADHD shape my brain.

What the science says

Research has shown that autistic people don’t lack empathy—our empathy often just functions differently. Some studies describe this as “emotional contagion”: the automatic process of mirroring and absorbing another person’s emotional state. Combine that with ADHD’s heightened sensitivity and impulsivity, and you get a brain that reacts instantly and intensely to other people’s feelings.

For me, this means I don’t just understand someone’s emotions—I become them. Neurologically, my boundaries blur. My nervous system doesn’t filter: what’s yours feels like mine.

The double-edged sword

On one hand, this hyper-empathy is a strength. It allows me to connect, to comfort, to notice when something is “off” even if someone hides it. It’s also tied to my ability to “cold read”—analyzing micro-expressions, tone, and posture until I know what someone isn’t saying.

But it’s also a weight. When emotions are huge, I can lose myself in them completely. If someone else is angry, I feel it burn through me. If someone else is anxious, my own chest tightens. And that leaves me drained.

Learning to set boundaries

The difference today is that I understand what’s happening. I know when a feeling comes from me and when it belongs to someone else. That doesn’t stop me from feeling it—but it allows me to draw a line. “This isn’t mine. I don’t need to carry it.”

It’s not easy. It takes conscious energy every single day. But naming it helps. And it prevents me from collapsing under the emotional weight of others.

Why this matters

Autistic empathy doesn’t always look like the stereotype. Some people on the spectrum may indeed struggle to recognize or express empathy in the expected way. But others—like me—experience it in overdrive. Both versions exist, and both are valid; both belong under the autism and ADHD spectrum.

So if you’re reading this and think: “That’s me, too”—know that you’re not broken, you’re not “too sensitive,” and you’re not alone. This is simply one of the many ways neurodivergent brains connect to the world.

A note of compassion

When people lash out in their own overwhelm, it’s not fair—but often, it’s not malicious either. They’re drowning, too. Holding that perspective helps me stay calm. I remind myself: their emotions are theirs, mine are mine. That boundary is survival.

And when it’s joy, excitement, laughter? Let yourself get carried away. Ride the wave. Just maybe… think twice before you act on every impulse in that moment. (I’ve learned that the hard way.)

Unmasking, Social Scripts, Eye Contact & the Villain Era of Self-Preservation

sep 10, 2025

Unmasking, Social Scripts, Eye Contact & the Villain Era of Self-Preservation

, “Wow, but you make such good eye contact, you can’t be autistic!”
 …Sure, Sharon. Because what you don’t see is the silent dance happening in my head: 2…3…4 look away. Smile. Nod. Back to eyes. Don’t stare too long. Don’t look at the mouth. Did they just frown? Was that sarcasm? Keep the rhythm.

For neurodivergent people, social interaction isn’t just “natural.” It’s an algorithm.

The Choreography of Eye Contact

Every conversation is a balancing act. Too much eye contact? Intense. Too little? Cold. Too long at someone’s mouth? Flirty. Too distracted? Disconnected. It’s exhausting. What looks like “instinct” for others, I run like software in the background of my brain, while simultaneously analyzing tone, microexpressions, body language, and context.

It’s not just about eyes. It’s about decoding, predicting, and managing connections in real-time.

The Energy Cost

People often think “social battery” means you get tired gradually. For me, it feels more like an implosion. The download of information keeps running long after the conversation ends. Sometimes, an hour later, I’ll suddenly get a flash: oh… that was sarcasm. Or: wait, were they upset?

Masking, forcing myself to keep the choreography perfect, multiplies the cost. It leaves me drained, second-guessing, and sometimes spiraling into self-doubt.

 When Masking Breaks

Here’s the paradox: the only times eye contact feels easy are when I’m deeply interested. Then the mask falls away, and I slip into hyperfocus. The result? Either intense, unblinking eye contact that makes others squirm, or none at all, because I’m lost in words. Cue the “verbal diarrhea.” Both confuse people. Both are authentic.

The Misreads

My focus on facial details can backfire. Sometimes I get mistaken for flirting when I’m simply overanalyzing expressions. Other times, genuine flirting goes right over my head because I logged it as “friendly.” These misfires aren’t carelessness; they’re the brain juggling too many layers of input at once.

And honestly?
 “I’m probably not flirting, it’s just the ’tism.”

What feels like deep interest and focus to me can easily be read as romantic or suggestive. Long, unbroken eye contact. Fixating on someone’s smile. Mirroring their expressions. To me, it’s data collection, connection, or genuine enthusiasm. To the other person, it can look like an attraction.

On the flip side, when someone really is flirting with me, I often don’t notice, because I’m too busy running my inner choreography: keep the rhythm, decode tone, manage my own body language. By the time I realize, the moment has usually passed.

This double-bind is something many neurodivergent people recognize: being misunderstood socially, even when your intention is simply connection, not seduction.

Learning to Unmask

The truth? I actually like people. I enjoy connection, deep conversations, and shared laughter. But to survive socially, I’ve often over “masked” suppressing quirks, running the full choreography, and pushing myself past my own limits.

Now, I’m learning to loosen my grip. Sometimes I’ll hold eye contact too long. Sometimes I’ll avoid it. Sometimes I’ll ask 101 clarifying questions. Sometimes I’ll choose silence and headphones instead of small talk. If masking takes too much energy, I will think: Adapting or explaining myself is too much work, please just judge me if you must. 

And that’s okay. Because the people who truly matter, the ones I want close, don’t need the mask. They accept the quirks, the glitches, the intensity.

Tips (short & simple):

  • Notice your own limits. When you’re masking too hard, pause.

     

  • Let go of “perfect” eye contact. Authentic beats choreography.

     

  • Protect your energy: you don’t owe everyone full access to you.

     

  • Remember: unmasking filters out the wrong people and draws in the right ones.

     

villain era

Unmasking sometimes feels like my villain era, like I’m being mean by not accommodating others to be more palatable, but honestly? Unmasking is freedom. If that makes me “strange” in the eyes of some… so be it.

My energy, my rules.