Inadvertent supports in undiagnosed autism

Diagnosed as autistic at the age of 51, I still feel like an outsider in the autistic community. Not because of internalised ableism. Not because I don’t believe I’m autistic. But because I don’t see me in other late diagnosed autistic women.

Now, don’t get me wrong. I know that autism is different for every autistic person. But what if…

What if my adoptive parents inadvertently gave me supports, because of their social, cultural and aspirational expectations?

In context, my adoptive father was born in 1917. My adoptive mother was born in 1920.  He was born into a large family, already entrenched in Australia. She was born into a large family who had migrated from Scotland to Australia in the early 1910s.

They grew up during the roaring 1920s and the Great Depression. He went to war in World War II. She was a nurse caring for soldiers sent back from the Papua New Guinea and Coral Sea fronts. He had malaria. She was his nurse.

They married in 1942, and had a son, Warren, in 1947. So their child-raising experience was from the late 1940s, in a world reeling, some countries still on rations, the 1950s and the 1960s. The social expectations on young men and women were very different, compared to what they experienced growing up, to parenting their own son.

Warren, their son, died in a car accident in 1967. They adopted me five years later, as a baby, in 1972.

Here we have a couple, still grieving their son, and maybe determined not to make the same mistakes, to do better. Their idea of a well-behaved young lady was shaped by what they experienced, themselves, as children, and in bringing up Warren. The 1920s, the 1950s and the 1970s, all coming together in that home at that time. Coming together at that time and centred on an autistic girl, in a time when autism was barely recognised in boys, let alone girls.

I have a strong suspicion, a hypothesis, if you will, that their ideas about what a young lady needed to know were actually inadvertent supports for their autistic daughter.

From the age of about 4 to 13, I attended ballet classes, speech and drama classes, piano lessons and singing lessons.

Were 1970s speech and drama classes and singing a good substitute for the speech pathology of today?

Were 1970s ballet classes and piano a good substitute for the occupational and physical therapy of today?

Did their expectation of raising a young lady with grace, poise and refinement actually help their undiagnosed autistic daughter with social skills, communication, coordination and emotional expression?

ChatGPT’s perspective

Engaging in activities like ballet, speech and drama, piano, and singing could have provided valuable benefits to girls with undiagnosed autism across different time periods, including the 1800s to the 1990s. Here’s how:

Structured Routine: The structured nature of these activities could have provided a sense of predictability and routine, which can be comforting and beneficial for individuals with autism who often thrive in structured environments.

Sensory Integration: Many autistic individuals experience sensory sensitivities or differences. Activities like ballet and music can help with sensory integration, providing opportunities to explore and manage sensory inputs in a controlled setting.

Social Skills Development: While the social expectations may have varied depending on the time period, engaging in group activities like ballet or drama would have still provided opportunities for social interaction, turn-taking, following instructions, and working collaboratively—all of which are important social skills.

Emotional Expression: Creative activities such as singing, piano, and drama allow for emotional expression in a safe and supportive environment. This can be especially beneficial for individuals with autism who may struggle with verbal communication or expressing emotions.

Self-Confidence: Mastery of skills in these activities can boost self-esteem and confidence, providing a sense of accomplishment and identity outside of potential social challenges.

While these activities might not have been specifically tailored for autism support, their inherent structure, sensory components, social interactions, and emotional outlets could have indeed provided meaningful support and development for girls with undiagnosed autism during those times.

I would also add competing in the local eisteddfod – in speech and drama, singing and piano – for several years as a self-esteem and confidence booster.

So despite all the difficulties my adoptive parents had, and the intergenerational issues we had, did they accidentally, inadvertently, do the best things possible at the time for the daughter that they didn’t know was autistic?

If so, way back in the 1800s, or even earlier, in English society, did the social mores of the time, for boys and girls, inadvertently give support to people with autistic brains, even though we didn’t know about autism back then?

Is modern society making it harder to be autistic than ever before?

Autism and the white rabbit

Alice in Wonderland, by Lewis Carroll, is a marvellous, classic tale, rich with imagery and allegory.

In a University of Illinois blog, Manas Godha wrote:

Symbolism of Time: The White Rabbit’s obsession with time is a prominent symbol in the story. As he constantly checks his pocket watch and exclaims, “I’m late, I’m late, for a very important date!”, he embodies the concept of time slipping away and the pressure of keeping up with societal expectations. The White Rabbit’s anxiety-ridden behavior reflects Carroll’s commentary on the fast-paced, time-centric nature of the modern world and the pressure to conform to rigid schedules and deadlines.

https://manasgodha.web.illinois.edu/2023/04/18/hopping-into-symbolism-decoding-the-white-rabbit-in-alice-in-wonderland/

If you consider autism, and masking, the pressure of keeping up with social expectations, we autistics could be a bit like the rabbit. The rabbit could be a very good depiction of autism, don’t you think?

Why am I thinking of the white rabbit? Because I had another revelation about my ingrained masking, thanks to… laundry pegs.

Bringing in laundry from the line the other day, I commented to myself that I had used matching pegs on an item. That’s when the mental avalanche started.

  • I’ve used matching pegs, and I didn’t notice
  • I’ve always avoided my wish to have order and matching things with the thought in mind that I couldn’t be obsessive, couldn’t be “too much”, because I wouldn’t fit in.
  • This even saw me wondering, all my life,  if I had an addictive or compulsive  personality.
  • That extended to deliberately NOT having matching pegs on an article when hanging it out on the line

That inner voice had another mic drop moment with that.

A lifetime spent deliberately limiting myself, depriving myself of things I itched to do, all coming back to me. Limited because, even though undiagnosed, I struggled socially until I learned to mask; such as not matching pegs on the laundry.

Not getting into trains, because that’s not cool, not accepted.

Not getting into planes and helicopters and ships, and Janes’ military catalogues … gosh,  so many things in 52 years of life that I have denied myself in order to fit in.

You might think that grief would be a response to this, but no, not today. It wasn’t grief, but victory that I had “caught” another masking trait in the act.

Today, instead, I had the images in my head of a girl, who looks a lot like Alice, chasing the rabbit to catch it and, jumping, diving, pouncing on that rabbit. saying, “Gotcha, you little wretch,  you’re not gonna do that again!”

I’ve said it before,  and no doubt I’ll say it many, many more times – why isn’t there an exhaustive list of all autistic traits and characteristics? This business of discovering it bit by bit is, well, not optimal.