Mable Mythbusters: Autism

Disability

Last updated

27 Mar 2024

Reading time

4 min read

Share

As a late-identified autistic woman, who spent the first 35 years not knowing she was autistic, I know all too well some of the myths about autism and autistic people. It’s my mission to ensure that the next generation, and those who have grown up unsupported, do not miss out on the support they need to live well and achieve their goals.

Knowledge is power. The more we know, the more we can provide informed and tailored support that enables people to live empowered lives.

There are still many myths surrounding autism. It’s important we bust those myths to help spread awareness, and advocate for autism acceptance and inclusion.

Myth: Autism only affects children

Fact: Autistic children become autistic adults. Autism is not a disease. It is a neurotype that comes with specific strengths and challenges. Each autistic person has a unique brain and therefore individualised needs. As the saying goes, “if you’ve met one person with autism, you’ve met one person”. This means, don’t generalise, get to know the individual and throw biases in the bin. Many people, like me, get diagnosed as an adult.

Myth: Autistic adults don’t need as much support as children

Fact: Have you noticed how many services there are for autistic children? It’s as if autistic adults don’t exist. Newsflash: we do.

Being an adult comes with its challenges for everyone. So, it’s logical that autistic adults are going to need support to navigate the initial transition into adulthood and other life stages in addition to various day-to-day supports.

We need a lot more allied health and other professionals to fill this gap in services. We also need general awareness to increase so that autistic adults can not only get the professional support they need, but also the social, community, and family support they need.

Myth: All autistic people have intellectual disability and are non-speaking

Fact: Autism and intellectual disability are two separate conditions. Being non-speaking is not required to get an autism diagnosis. In fact, lots of autistic people can speak well and many are public speakers who have done TED talks.

Myth: Autism is more common in boys and men

Fact: Autism is not gender specific. The stereotypes portrayed in the media, on TV, and in movies have perpetuated this stereotype. It’s so widespread that even some health professionals will reinforce this stereotype, meaning girls, women and non-binary people can struggle to get a diagnosis.

Myth: Autism has become an epidemic

Fact: With greater awareness comes more diagnosis of people who have been missed by the system, namely, girls, women, non-binary people, people living in rural and regional areas, people from non-white cultural backgrounds and older people.

We are in catch-up mode, that’s all.

Information is power and thanks to the autistic community being visible on social media, the Internet and TV, awareness of the diversity among the autistic population has increased.

Also, let’s be clear that the definition of ‘epidemic’ refers to a disease, usually an infectious disease. Autism is not a disease. You can’t catch autism. The media has a significant role to play here in resisting the urge to create click-baity headlines using the words ‘epidemic’ and ‘autism’ in the same sentence, and it needs to stop. It is factually incorrect and isn’t helping anyone at all.

If you overhear someone saying false statements about autism, sharing the facts can be a great help. When more people join in, it creates a positive ripple effect that can lead to better outcomes for autistic individuals in all aspects of life including health, wellbeing, employment, social, community acceptance, and inclusion.

Thank you for reading and for being an ally.

Kory Sherland (she/her) is a freelance writer and the founder of Autie Talk: an employment coaching service to neurodivergent teens and adults. Autie Talk also offers neuro-affirming practices training to employers and service providers through team training and online professional development programs. 

You might be interested in

NDIS reforms announced: What we know so far
We know recent news about NDIS reforms might feel heavy. For many of you, your participants, and your loved ones, hearing about potential service caps or changes to funding for social and community participation is deeply stressful. We want to start by saying: we hear you, and we are here for you. Our commitment to you remains unchanged While the government works through these changes, we want you to know Mable's business model is not changing. Our platform continues to be a place where you can find and book independent support workers who best meet your needs or those of your clients. While we may make a few small technical updates behind the scenes, your ability to use Mable remains exactly as it is today. We're your partner and advocate During this transition, we're dedicated to supporting safe, transparent connections. We are actively advocating for person-centred approaches to care that respect your choice and control, and we'll keep helping our community understand what these r
Disabled mums are the quiet supermums
As the water trickled over the rocks and my kids explored the bush, their laughter mingling with birdsong, I sat quietly on the wooden seat, taking it all in. The peace, the joy - but also something else. My eyes welled up just as my independent support worker glanced at me. She slipped an arm around me and gave a gentle squeeze. I didn't need to explain what I was feeling but she already knew. That feeling is something that I think every parent living with a disability needs to hear and embrace. A different kind of angst Mum - and dad - guilt is almost synonymous with parenting these days. We worry we're not doing enough, not being enough; that there's never enough time, money, or energy. But when you're parenting with disability, that feeling cuts deeper. It's the sting when you can't do something for, or with, your kids. Like driving them to a birthday party, kicking a soccer ball in the backyard. It's crying quietly in the kitchen when disability and parenthood all feels too much.
Independent Thoughts: Melissa and Simone
Independent Thoughts digs deeper into what it really means to live on your terms, sharing insights into life for people with disability and older Australians. We invite guests with lived experience to share their perspectives in an open dialogue. From casual chats to asking some of life's biggest questions, Independent Thoughts covers it all. Independent Thoughts is an invitation to join us as we challenge the status quo, shatter stereotypes, and redefine independence – one open-hearted conversation at a time. In this episode, we meet Simone, who manages support for her dad, Con, through Mable. She speaks with host and Clinical Psychologist, Melissa Levi . Finding the right support Dogs, flowers and a veggie garden. These are three things that bring Con joy, according to his daughter, Simone. But as he got older, it became physically harder for him to stay connected to the parts of life he loved. When Con and Simone felt it was time to begin looking for help at home, it was import