Masking: hiding your neurodivergence and its costs
You learned to hide parts of yourself for good reasons. You deserve places where you can put the mask down and simply be you.
By the numbers
What research shows about masking so far.
Research
Wellbeing
What is masking?
Hiding parts of yourself to fit in or stay safe.
Masking means hiding parts of yourself, on purpose or without noticing, to avoid being judged or hurt. Researchers also call it “camouflaging.” It can mean hiding natural ways of moving, talking or reacting, and copying others instead.
Not everyone knows they are masking. For many people it started so early that it just feels like “how I am in public.”
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In research, autistic adults described “hiding behind what I want people to see.” This can mean holding in stims, keeping quiet about a deep interest, or hiding how much noise hurts.
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This means using clever workarounds so struggles don’t show. People described rehearsing conversations, using scripts, and studying how others behave.
Compensating can look like coping well from the outside, while taking huge effort on the inside.
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Researchers call this “assimilation”: trying to fit in with the group, even when it feels uncomfortable. People described copying others’ expressions, phrases and style.
Masking is wider than autism
ADHD, tics, learning differences, and every gender.
Most research on masking has been about autistic people. But studies show people with ADHD and other neurodivergent people mask too. Many parts of masking, like copying others and feeling exhausted, are shared across different kinds of brains.
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Some parts of masking seem more specific to autistic people, like hiding stims and hiding distress from noise or lights.
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In a study of adults aged 30 to 90, people with ADHD masked more than people without ADHD or autism. Young adults with ADHD also say masking depends on the setting.
It might look like
- Over-preparing so no one sees you lose track
- Sitting very still while your body wants to move
- Staying up late to catch up in secret
- Using jokes to cover forgetting
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Some people with Tourette’s or other tic conditions can hold back tics for a short time. It takes effort, can be distracting, and tics often can’t be stopped completely.
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People with dyslexia and other neurodivergent people took part in masking research too, and also described masking and its costs.
It might look like
- Avoiding reading out loud
- Making excuses not to write in front of others
- Pretending to have read something
- Taking work home to finish slowly in private
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Masking can make autism harder to spot in girls. But boys and men mask too, and so do nonbinary people.
Researchers warn against calling masking a “female” trait. That idea can make it harder for men, nonbinary people and anyone who doesn’t fit a stereotype to be recognized.
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People who face stigma for more than one part of who they are may feel they have to mask more, or in different ways. Researchers say this needs much more study.
What masking can look like
Everyday examples people describe.
Masking looks different for everyone. Here are some things people describe. Noticing them is not a diagnosis. It is simply a way to understand yourself better.
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People describe
- Asking lots of questions to keep the focus off themselves
- Copying others’ phrases, laughs or expressions
- Forcing eye contact
- Rehearsing conversations beforehand
- Using prepared “scripts” for small talk
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People describe
- Hiding stims or fidgeting
- Holding back tics
- Keeping a calm face when overwhelmed
- Sitting still when you need to move
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Some autistic people hide how much sounds, lights or textures hurt, so they don’t seem “difficult.”
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Many people hold back from talking about the things they love, for fear of being called “weird” or “too much.”
Some people describe having a “repertoire of roles” for different places: one way at work, another with friends, another at home.
Why people mask
Safety, belonging, jobs, and not always a free choice.
People mask for real reasons. In research, autistic adults said they masked to make friends, avoid bullying, and get jobs and qualifications. One person said they were sure no one would hire them if they didn’t mask in interviews.
Researchers see masking as a response to stigma: negative ideas about people who are different. Because of this, masking is often not a free choice. It can feel like the only safe option.
Reasons people give
- Keeping a job or getting through school
- Making friends and being accepted
- Not wanting to be a burden
- Staying safe from bullying or rejection
What masking can cost
Exhaustion, losing yourself, and missed support.
Masking can make everyday life feel exhausting and stressful. Many people need time alone afterwards to recover and feel like themselves again.
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In one study, exhaustion was by far the most common result of masking. Some people also felt intense anxiety and stress once a social event was over.
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People across different kinds of brains said masking made them feel disconnected from their true self, and that others didn’t know the “real them.” This can feel lonely, even around people.
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A large study of autistic adults found more masking was linked with more anxiety, social anxiety and low mood. The link was there for people of all genders.
Masking for a long time can also add to autistic burnout: deep exhaustion, losing skills you used to have, and being less able to handle sensory input.
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Masking can lead to a late or missed diagnosis, because others don’t see what you’re going through.
Children and teens who mask
For parents, caregivers and teachers.
Children can learn to mask too. Autistic girls, for example, may copy how other children behave and play, or stay quiet when things are hard. Boys can mask as well.
Masking often grows over time, in response to negative reactions to being different. Researchers say it is important to understand when and why it starts.
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Masking uses a lot of energy, and many people need time alone afterwards to “reset.” If a child seems fine at school but is very tired, upset or withdrawn at home, masking may be one reason worth exploring.
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Ideas
- Build quiet time into the after-school routine
- Celebrate their interests, however unusual
- Let them stim and move freely at home
- Share what you notice with the school, kindly and calmly
- Tell them often that who they are is welcome
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What helps
- Allow movement and fidget tools
- Check in privately, not in front of the class
- Notice quiet students as well as loud ones
- Offer a calm space for breaks
- Take parents’ and caregivers’ reports from home seriously
Unmasking gently, at your own pace
Small, safe steps toward being more yourself.
Unmasking doesn’t mean dropping every coping strategy overnight, or being fully open everywhere. Research shows masking depends on the setting. It is okay to mask in some places and relax in others.
Seeing the good in how your brain works may matter a lot. In one large study, people who saw benefits in their ADHD or autism reported better quality of life.
Small steps to try
- Notice: when and where do you mask the most? What does it cost you?
- Start at home: let yourself stim, move or rest without hiding.
- Find one safe person and share a small truth, like “Loud places wear me out.”
- Drop one small mask in a low-risk place, like wearing headphones in a café.
- Plan recovery time after days when you need to mask a lot.
- Connect with other neurodivergent people who “get it.”
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After years of masking, some people aren’t sure which parts are “really me.” That is a normal result of masking, not a sign something is wrong with you.
Gentle ways to explore
- Ask yourself: “Do I want this, or do I think I should want it?”
- Notice what you enjoy when no one is watching
- Notice which clothes, sounds and places feel good
- Try writing or drawing about your day
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Some places don’t feel safe to unmask, and that is not your fault. Researchers say masking is often an “illusion of choice,” shaped by stigma. Changing that is everyone’s job, not only yours.
How others can help
Friends, family and coworkers can make it safe to unmask.
Masking grows where differences are judged. It eases where people feel accepted. The people around a neurodivergent person can make a big difference.
Helpful things to say
- “Do what you need to feel comfortable.”
- “I like hearing about this. Tell me more.”
- “We can leave whenever you’ve had enough.”
- “You don’t have to explain.”
Things to avoid saying
- “But you seemed fine!”
- “Everyone has to fit in sometimes.”
- “Just stop fidgeting.”
- “You don’t look autistic.”
Things you can do
- Ask what helps, rather than guessing
- Don’t point out stims or tics
- Keep what someone shares private, unless they say it’s okay to tell
- Offer quiet spaces and breaks at events
In research, some autistic adults said having their masking pointed out could feel like being “outed” without their consent. Let people share on their own terms.
How community helps
Being with people who “get it.”
Many neurodivergent people say finding others like them changed their lives. Being around people who understand means less masking, more laughter and less explaining.
Places to start
- CHADD local chapters for people with ADHD
- Groups led by autistic people, such as those connected to the Autistic Self Advocacy Network (ASAN)
- Interest-based clubs, like gaming, art, nature or coding
- Online neurodivergent communities
When and where to get help
Signs it’s time to reach out, and where to go.
Reach out to a clinical provider or therapist if
- Anxiety or low mood is making daily life hard
- You are losing skills you used to have, or feel burned out for months
- You feel you have lost who you are
- You wonder if you might be neurodivergent and want an assessment
Look for a therapist who understands neurodiversity, respects how you communicate, and doesn’t try to make you “act normal.” See Finding a therapist who fits.
The 988 Suicide & Crisis Lifeline is free, confidential and open 24/7 by call, text or chat.
Outside the U.S., findahelpline.com lists free, confidential helplines by country. If someone is in danger, call your local emergency number.
📝 Worksheets for this guide
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Sources
- Hull, Petrides, Allison, Smith, Baron-Cohen, Lai & Mandy (peer-reviewed) (2017). “Putting on My Best Normal”: Social Camouflaging in Adults with Autism Spectrum Conditions (Journal of Autism and Developmental Disorders)
- Miller, Rees & Pearson (peer-reviewed) (2021). “Masking Is Life”: Experiences of Masking in Autistic and Nonautistic Adults (Autism in Adulthood)
- Pearson & Rose (peer-reviewed) (2021). A Conceptual Analysis of Autistic Masking: Understanding the Narrative of Stigma and the Illusion of Choice (Autism in Adulthood)
- van der Putten, Mol, Groenman, Radhoe, Torenvliet, van Rentergem & Geurts (peer-reviewed) (2024). Is camouflaging unique for autism? A comparison of camouflaging between adults with autism and ADHD (Autism Research)
- Wurth, Fuermaier, Strand & Thorell (peer-reviewed) (2025). Diagnosis acceptance, masking, and perceived benefits and challenges in adults with ADHD and ASD: associations with quality of life (Frontiers in Psychiatry)
- Hull, Levy, Lai, Petrides, Baron-Cohen, Allison, Smith & Mandy (peer-reviewed) (2021). Is social camouflaging associated with anxiety and depression in autistic adults? (Molecular Autism 12: 13)
- Raymaker, Teo, Steckler et al. (peer-reviewed) (2020). “Having All of Your Internal Resources Exhausted Beyond Measure and Being Left with No Clean-Up Crew”: Defining Autistic Burnout (Autism in Adulthood)
- NHS (UK National Health Service). Signs of autism
- NHS (UK National Health Service). Signs of autism in adults
- Centers for Disease Control and Prevention (CDC). About Tourette Syndrome
- Centers for Disease Control and Prevention (CDC). Information about Tourette Syndrome for Educators
- CHADD (Children and Adults with Attention-Deficit/Hyperactivity Disorder). Find a Local CHADD (Affiliate Locator)
- Autistic Self Advocacy Network (ASAN). About ASAN
- 988 Suicide & Crisis Lifeline. 988 Suicide & Crisis Lifeline
- Substance Abuse and Mental Health Services Administration (SAMHSA). 988 Suicide & Crisis Lifeline
- Find A Helpline (ThroughLine). Find A Helpline
This guide is for education and self-care. It is not a diagnosis or a substitute for professional care. Please talk to a counselor or clinical provider about your health. Reviewed October 2026.

