A Fantasy Author's Adventures in Fiction & Life

Tag: communication

My most delayed thing after long covid in 2022 was planning to travel. Navigating with autism and ADHD alone can be overstimulating, tiring and frustrating. But with a Fibro diagnosis, I now have to plan not only for autistic sensory needs and ADHD challenges, but for low physical energy, high risk of chronic fatigue and pain. So whether you’re travelling as or with an autistic person, ADHD person, or someone prone to fatigue and pain, I’ll attempt to unpack the factors I think you need to consider to minimise stress, fatigue and pain and to maximise comfort on your trip.

Sensory Challenges

Road Works, Construction & Obstructions

As navigator and driver, for me navigating unknown roads with roadworks is like navigating with one eye blindfolded and someone poking me repeatedly in the arm. My brain processes a row of cones, construction workers in their fluro clothes, trucks and other equipment as ‘big mass of stuff.’ I don’t want to look at ‘big mass of stuff’ because its overstimulating. So if the entrance to the venue, or my turn is next to or beside, behind or otherwise close to ‘big mass of stuff’… I struggle to process said venue/ turn’s existence.

I will miss the turn, because I’m so busy juggling not being overstimulated with not crashing into traffic moving at a different speed and direction, that I have zero processing power to perceive the second road. I’ll walk right past the entrance because I don’t see an entrance, just ‘shit ton of visual info, brain is jamming, look away!’

Obstruction Management Tip 1: Reduce Stimulation & Pressure

To locate the venue when roadworks, construction sites or other obstructions are present, I suggest navigating as near as you can by car. Then park the car. Now you don’t have to worry about crashing, so you can consult your phone and compare it to reality under less pressure. If you have to turn back into traffic and drive further; that’s fine. Its better than crashing. Its also better than a verbal argument with your navigator because you’re visually overstimulated and stressed.

Obstruction Management Tip 2: Reduce Stimulation & Pressure With Help

If your brain is already jammed with sensory overload, or fogged by covid, fibromyalgia or other condition, and you can’t connect your phone’s navigation directions to geographical reality… ask someone on the street. Or a customer service person in a shop.

Sometimes our brains fail us (I’ve navigated with moderate brain fog, moderate fatigue and severe ADHD and could barely navigate a supermarket, let alone New Zealand.) Don’t be hard on yourself, don’t persevere if your brain will not co-operate or is otherwise being an arse. Just ask someone else when its clear reality, your map and brain are not co-operating. This will save time, frustration and spare you the exhaustion of doing something very draining, because you’re attempting it while cognitively and or physically impaired.

For advice on minimising visual overstimulation at home, see this post.

Do You Have the Right Travel Companion?

To the able bodied, neurotypycal reader, if you’re travelling with someone who struggles with navigation/ overtimulation, and you struggle to be patient with that; I suggest don’t travel together. There are too many factors with the potential to cause tension, stress and frustration on both sides. If you don’t understand and or can’t be patient with the other person’s struggles; you’re likely making a challenging situation worse.

To the neurodivergent/ disabled reader, if you suspect your travel companion(s) do not understand why navigation is so difficult/ frustrating/ stressful for you; can you manage better on your own? I often travel solo, so I KNOW its more work. But depending how much strain travelling with a companion puts on you, is it ultimately less stressful/ less exhausting to travel solo? (You could just meet them at your destination.)

Navigation Communication Challenge: Noise

If you’re travelling with an autistic person, please bear in mind that we can hear you, and the conversation next to and behind us, and birds chirping and traffic and car horns and- If you are travelling with an ADHD person, they may be listening to you, then that song they love pumping out the window of a passing car, or something funny the person behind them said.

Communication Tip: Seek Quiet

For autism, be prepared to step into a quiet laneway, shop or somewhere less noisy, so the autistic person you’re speaking to is processing what you, and no one else is saying. We can’t receive the message ‘lets go into that museum’ when its competing with ‘(insert lyrics),’ ‘Mum I want an icecream!’, ‘Hi Steve!’ Bang, thud thud, DRILLL! from the construction site.

So to give an autistic (or ADHD) person the best chance to hear what you’re saying about where to go next; say it somewhere quiet. Turn off the radio. Ask the back seat passengers to stop speaking when a passenger is giving the driver directions.

Minimising noise makes audio directions or suggestions easier to access and respond to. It also saves you having to repeat yourself umpteen times every time you want to say, ‘I need to go to the toilet first.’

Sensory Overload

City’s are fun. They have buildings from many eras, and people from all over the world moving through their streets. They’re also busy, noisy and jam packed with visual information. I love walking city streets, listening to foreign accents, and taking photos of historic buildings. But as an AuDHD person; I NEED balance in my site seeing. I DO NOT WANT to site see in a busy, crowded, noisy city multiple days in a row. There comes a point where every hour I get tireder, more overloaded and more easily frustrated. Where city site seeing has become a tiring struggle to process ‘big wall of sound and visual info overload’.

Site Seeing V.S. Sensory Need Balance Tip

My favourite way to let my overstimulated brain and tense body relax, is to punctuate loud, crowded city site seeing with quieter, peaceful breaks. For example, spend 30 mins or more wandering a state library. Spend an afternoon at the zoo, or a morning wandering the city’s botanic gardens. I love gardens and animals, and tend to visit at least either in every city. I find it makes for calmer, more relaxed, more enjoyable travel.

View through grubby windscreen of a bend lined with protective metal fence, right pointing arrows, pretty gum trees and green slopes down to pale blue and cloudy horizon.

Avoiding ADHD Time-Fail Tax

Last year I navigated New Zealand’s North Island with moderate brain fog, moderate fatigue and severe (undiagnosed and unmedicated) ADHD. My biggest learning was; do NOT book morning anything unless staying within a 15 minute drive of that activity. I was one hours drive away from one activity, gave myself two hours to get there and still missed it. My ADHD got distracted, and missed a turn. Then I lost track of time, and drove 20 minutes beyond the turn before realising I’d missed it.

ADHD Booking & Time Tips

  1. Use a Physical Calendar, with days of the week and dates labelled to write bookings on manually. (Days and dates DO NOT correlate in my brain and a device offers too many distractions. So I have an A4 weekly calendar notepad and its a huge help to my school holiday and travel planning.)

2. Dates: double check the month, year and 24 hour timing when you book. (Yes, I did drag my family to the air port 12 hours early to see me off the first time I flew to England. Better 12 hours early than 12 hours late!)

3. Timezones: check your device for local time before you plan your next step. Especially before you go buy food at an airport. (Yes, they may refer to flight number but not destination when changing your gate just before boarding. And not page you to the new gate when you don’t board on time).

Tours and Accomodation Tips

Morning Activities: Only book a morning anything, which doesn’t allow for mis-navigating the countryside, if you’re staying a SHORT distance from the morning activity.

Extra Time: If your drive is theoretically 30 minutes, give yourself AT LEAST one hour to get there. (To allow for factors you forgot to consider that could delay you, like traffic, road works, finding a car park etc.)

If there’s one thing you really want to do/ see, plan your trip so if there doesn’t end up being time for it today; you’ve got time tomorrow. Flexibility was essential to my last solo, unmedicated ADHD trip!

Low Spoons Travel (Pain/ Fatigue/ Chronic Illness)

I’ve just come back from a road trip with my mum. I put my back out on day one, just before we got in the car. Constant back pain quickly became fatigue. It mean difficulty getting in and out of the car and difficulty walking. It meant I burnt through energy quickly, and got tired and frustrated swiftly. These latter are things I have to be aware of all the time, because I have fibromyalgia, and that (permanently) predisposes me to brain fog, fatigue and chronic pain.

Low Energy Management; Snacks

Normally we try to cut back on snacks because we’re eating too much period, or too many calories. This DOES NOT apply to me when I travel. On my recent 9 day road trip, I didn’t just need breakfast, lunch and dinner. I either needed a substantial breakfast, lunch, afternoon tea and dinner, or breakfast, morning tea, lunch and dinner. Any one big physical activity, like an hour long walk, needed to be followed by eating and drinking. I might not notice I was hungry, but a meal made me feel better. Food and drink as fuel run out faster for me when I travel.

Low Energy; Pace Yourself

Even when my back recovered on my road trip, I still had to pace myself. If the slope was steep, or there were too many stairs, or I walked for longer than an hour, a flare of burning back pain and or fatigue (due to fibro) were likely. (When I say fatigue, my feet/ legs/ lower back feel A LOT heavier than usual, like I have to peel my feet off the ground and actively fight gravity to take each step).

Low Energy; Rest Breaks

What if I wanted to spend two hours walking around the botanic gardens/ nature trail/ city centre? This happened in Adelaide recently. I was able to walk for several hours; mostly because in the middle we sat at a cafe for a good forty minutes. I sat in a chair with proper back support and sunk into it, letting my body recharge. (And used this as the snack and drink recharge mentioned above). After that sit down; I could keep walking.

Another option when travelling solo for me is that with my seat adjusted to support my back sufficiently, sitting in the car driving helps me physically recharge.

Low Energy; Mobility Aids

The thing about invisible illnesses is you can’t see the bastards. Vision impaired people can get glasses, and hearing impaired people can get hearing aids. But do people with fatigue or chronic pain need mobility aids?

This is a conversation I didn’t have with my doctor, not when diagnosed with long covid, or fibromyalgia. But with back pain from putting my back out, my mother, having her own back issues, knew I wasn’t able to walk. So she did some research, and found that walking polls can provide physical support, while also helping a person build their core body muscles. (This article is aimed at hikers, but consider how more even distribution of your weight and the strain of making it walk can aid low energy movement.)

My mum bought me walking polls in Adelaide, which I used on nature trails. I found them especially helpful to reduce the strain on my body and my proneness to pain and fatigue when walking uphill, and up or downstairs. They were also great for longer walks, where I wanted to go further, but was tired and or fatigued.

So if you’re prone to chronic pain or fatigue, I suggest discussing mobility aids with your GP.

Yes, this blog title is intentionally provocative. With RFK Junior spouting all sorts of nonsense about autism, as an autistic person, I’d like to counter that with how some of my autistic traits make my life BETTER. I want to share with you how certain autistic approaches to speaking, communicating, logic and decision making, facing and dealing with the darker sides of reality, and appreciating the good stuff in life could, if you’re prepared to shift your perspective, help you do any of above more effectively. Autism isn’t a disease, its a difference and difference is an opportunity to learn.

Content Warning: suicide and rape are mentioned in relation to why its important to talk about unpleasant things under ‘Society Says You Can’t Say That, I say Say It.’

Value People For Who They Are

Some neurotypical person: You have to look people in the eye when you speak to them.

Me: why?

Them: because people will think you’re not listening, or your suspicious or maybe unstrustworthy.

Me: And that’s my problem? People making utterly unfounded assumptions about me, that have nothing to do with me personally? People not bothering to get to know me or bothering to judge me for who I am?

I wouldn’t do that to someone else. As an autistic person, I tend to miss cues in real time social situations (and my ADHD gets distracted), and I need to process in peace and quiet on my own. So the only thing I assume about other people is; there’s loads of things I don’t know or understand about them. I think that’s the golden rule to understanding people, yes, even someone you’ve been close to for years. If you don’t get their behaviour; assume you’re missing something.

Learn Before You Judge Someone

As an autistic person, whether I’m looking at students to judge their needs and how to support them, or at a fictional character, I don’t think anything until I’ve noticed and connected multiple things about that person/ character. If someone is upset, and another person is not expressing concern for them or doing anything to help, but is standing still, anxiously fidgeting and avoiding eye contact with the upset person; I’ll conclude they care. They just don’t know how to help or respond. Whereas another person might only see them not responding and assume they don’t care. One cue isn’t enough to go on, even if you ARE neurotypical.

So my first autistic lesson on people is; don’t make assumptions. Seek more information. Give people the benefit of the doubt. And instead of only looking for what you expect to see, notice what’s actually there. Don’t disregard someone because they didn’t do the thing you expected. Credit them for the helpful/ constructive thing they did do. (Unless they’re a politician, in which case I advise a healthy dose of skepticism for every side of politics, and trust what they actually do ten times more than anything any politician ‘claims’ they will do.)

Communicate When Your Expectations Aren’t Met

While we’re on expectations, if you aren’t happy with someone’s response, don’t expect them to just know you want them to respond a certain way, regardless of the context of the situation. None of of us grew up in the same house or have identical lived experiences, even if we did grow up with the same era/ culture/ religion.

Your neurotypical style of communication is DIFFERENT to my autistic, ADHD style communication. Making assumptions based on your experience is the fast lane to misunderstanding me, and anyone who differs from you in ways you didn’t realise. So be straight and honest with people, to ensure everyone in the conversation IS on the same page.

Value Logic and Questions

Autistic people can get ourselves into trouble for not respecting social hierarchies or for ‘answering back.’ There’s a very good reason for this; I don’t respect social hierarchies because I don’t see the point of them. I ask questions because I don’t understand and I want to understand. Or because I’m challenging someone who didn’t bother asking any questions, who just accepted something, which is why I think what they think is bullshit.

Age & Rank Alone Don’t Matter to Me

An example of both is ‘respect your elders.’ Problems with this include; age does not necessarily equal wisdom, life experience or knowledge. Age certainly doesn’t make anyone right by default. There are times as a teacher when a child says something that challenges my thinking. Where they change my mind about how we as a class or their group will do something. Because they asked a question, gave a good reason for their request, and I hadn’t thought of that and respected their reason.

I don’t care how old or rich you are, how many degrees you have or any privilege you claim. I don’t care for rank, whether its big boss in a workplace or Prime Minister. Its the knowledge and understanding you bring to any given situation that I value. Its your wisdom. Whether you’re treating people decently and resources appropriately. Its whether or not yours is the best solution to the problem, on the basis of evidence, reason and logic.

When the far right are on the rise, and having a field day in America, I don’t think I need to explain why the above is SO important.
If you’re an adult who feels threatened when kids ask you questions, or when they argue and give superior reasons to yours; this isn’t about your ego. Its not about your authority. Its about having the humility, the good grace and the sense to make use of the best logic, reasons and evidence in the room, to make the best decision for all parties effected.

So I urge you, don’t just make decisions based on what you feel. Evaluate the logic and all the reasons of the situation, like an autistic person. Seek the biggest, fullest picture, to best decide what to do with it.

There is No ‘Normal or ‘Abnormal’ Person

A lot of autistic people get bullied as kids/ teens for being different. A lot of neurotypical people approach communication assuming neurotypical norms are THE communication norm, thinking everyone should; make eye contact, greet people by name, ask how people are and so on. None of those communication styles is ‘normal’ to me. Just because you and lots of people you know do it that way doesn’t mean everyone else does. There are cultures where for certain people to make eye contact with others is disrespectful and rude. But we were assuming ‘white’ culture is the ‘norm’, weren’t we?

And when you assume your white, neurotypical, able bodied, cis gender, heterosexual ways are the norm, some people assume anything that doesn’t meet those expectations, anything ‘unfamiliar’ or ‘different’ is necessarily bad and wrong.

The Downside of Calling Humans ‘Normal’

‘They are not like me, and I am normal, therefore they are a freak/ bad/ wrong’ seems to underly every form of discrimination there is. It covers racism and sexism to homophobia, transphobia and ableism. When we get to white supremacy and ableism, the narrative becomes ‘my culture/ race/ body is better than yours, therefore I have value and you do not. My life matters. Your’s doesn’t.’

So I think that for any ally of any marginalised group, a great thing to take from autistic attitudes is not viewing yourself as ‘normal.’ And not viewing anyone unlike you as ‘abnormal.’

I was raised the way I was, you were raised the way you were. My brain is wired in certain ways, your brain is wired differently. There is no ‘normal’ and ‘abnormal’. There’s how we were taught we are supposed to live, ways we were taught some people live, and ways of living we weren’t taught about. All that means is there are different ways of living.

If we think of it as ‘people live differently’ as opposed to, ‘some people are normal and others are freaks,’ its becomes harder to alienate any human from their rights.

You Don’t Need Permission To Speak

A thing I often forgot to do as both a young autistic person who is inclined to do what they think makes sense, and as ADHD distraction prone, is to ask people how they are. You’re ‘supposed’ to do this. Its ‘good manners’. But the thing that really gets me about this is when I’m over half an hour into a conversation before I think to ask ‘how are you?’, and the person responds with something they really wanted to tell me. And I think, ‘Why did you wait 30 minutes for me to invite you to share that? If it matters to you; it matters to me. Why not just tell me?’

Somewhere along the way, I think many neuropytical people fell into the habit of only sharing their special news or saying how they’re going when someone asks them first. I suspect this is why there’s ‘never a good time’ to tell people bad news. Because people never ask, ‘What’s terribly wrong with you today?’ And they don’t expect or hint its ok to say shitty stuff. And with people feeling they don’t have ‘permission’ or an ‘invitation,’ or a ‘right time,’ I wonder if a lot of crap that needs saying doesn’t get said, or gets said late, by which point the relationship is falling apart.

Just Tell Us Your News!

I think that when people meet or catch up, it should go more like autistic or ADHD conversations. Where it may begin with ‘hi’, and the next point is, ‘I really wanted to tell you about x, because its so interesting/ exiting/ it matters to me and you matter to me, so I want you to know.’ We don’t literally say all this of course, but the ‘info dump’ of many of things neurodiverse people rattle off to each other when they haven’t seen each other for a while, like me and my mum when we catch up, is often this.

I think its a good thing. With neither party feeling the need for ‘permission,’ or ‘invitations;’ everyone shares what matters to them. Then we can ask for more details if we want them. No one feels unheard. No one feels ignored or like they don’t matter. There’s no room for misunderstandings, because everything either party wanted to say has been said.

True, it can still be tricky to broach for example potential sources of tension in relationships, but like all the good stuff, that still comes under ‘it matters to me so I told you.’ There’s no waiting for ‘right times’ that don’t come. No letting it sit on your chest and fester. I suggest; get everything said, communicated and know what’s going on with each other.

Make Personal Connections With What the Other Person Said

I know, controversial! Because when autistic people do this, some neurotypical people cry, “You made it about you! It was supposed to be about them! You’re supposed to give them their moment!”

So I’m supposed to let them stand on a pedestal saying some great or terrible thing that happened to them and say merely, ‘That’s great’ or, ‘O no. That’s terrible.’ That sounds like their ‘moment’ means being the centre of attention, while everyone else superficially engages with what they have to say. I don’t see the point of that. Superficial responses don’t signal ‘you are not alone.’ They don’t signal, ‘I get you.’ They have no capacity to deepen a relationship.

The Value of Sharing Personal Connections

If I’m sharing something important to me with you; its probably because I want to connect with you. I want to see that you understand.

If you’re sharing something bad with me, and I can make a deep personal connection to what you said; I am showing you that I get it. When my connection doesn’t quite fit; I’m showing you I don’t quite get it. If all I say is, ‘I’m sorry that happened to you,’ all I’m displaying is a very basic grasp of what you’re saying. And I’m leaving you standing on your own, little better off than you were before you opened your mouth.

Sometimes there’s isn’t anything we can constructively do to help people with their problems. But we can do more than just be there for them. We can show them; ‘not only am I here, I have stood where you stand and I get it. You are not alone.’ It matters for people to know that. So I say, go ahead and connect to the time when you think felt that way, or had to make a similar choice.

Abolish Taboo Conversation Topics

Suicide & The Need to Talk

According to Suicide Prevention Australia, Suicide is the leading cause of death among 15 to 25yos in my country, but we’re ‘not supposed to talk about it.’ Taboos like that seem to be part of neurotypilcal social expectations. The idea that some things are ‘too dark,’ or ‘not nice enough’ to discuss.

Suicide Australia also say 7 million Australians (roughly one quarter of our population) have been impacted by suicide. That’s 7 million people who would be left feeling isolated, with no one to talk to about their feelings or experiences, if we don’t talk about it because ‘its not nice’. In this case silence threatens people’s wellbeing.

There are things that NEED saying. Things people need to get off their chests and to inform their loved ones about. Then you can deepen your relationships by working through it together, or get the help or support you need etc. For the sake of our health, our wellbeing and our planet; we NEED to talk, directly, about unpleasant shit. Sure, maybe everyone can’t do it as bluntly and logically as some of us autistic people, but when it matters; give it a shot!

How Can We Deal With It, If We Won’t Even Discus it?

The other big reason we NEED to talk about unpleasant shit is things like; I think RFK Junior is a eugenicist (there’s a good explanation of how his antivaxxer stance promotes ‘soft eugenics’ from Science Based Medicine in this article). If we don’t admit what he is, or what he’s trying to do; we won’t stop him doing it. If we don’t call it ‘climate catastrophe,’ we’ll sit and watch the world burn.

And if we aren’t supposed to say ‘not nice things’ like ‘that person sexually abused me,’ if everyone in unused to hearing that, despite that according to the Australian Institute of Health and Welfare 26.1% of Australian women have been sexually abused… we get a culture where people don’t talk about sexual abuse. They don’t hear it.

Then they don’t know how to respond. They don’t know how to accept that something like that happened to someone they know. They don’t know how to respond to the fact that they, like 20% of those women, know the offender. And they sure as hell don’t know how to support victims of sexual or family violence.

The direct statements of an autistic person calling out something as immoral, with no neurotypical filtering to sound ‘nice,’ might make some people uncomfortable. But our lack of giving a shit about what we ‘can’ or ‘can’t,’ say, or whatever makes neurotypical people squeamish about calling out reality; that positions autistic people like Gretna Thunberg to tackle climate change.

We need more non-autistic people standing up and saying how and why something is wrong and that it SHOULD NOT BE HAPPENING.

Get Comfortable With Your Own Discomfort

Austistic people are used to not being comfortable. Many of us frequently feel like we ‘don’t fit’ and like we blunder through social situations. We’re used to being in environments like classrooms or shopping centres where the amount of STUFF on shelves, walls, the NOISE of so many PEOPLE screams at us, and is TOO MUCH. (Minimisation tips in this post.)

Discomfort is normal to autistic people. Its not pleasant, but it does have an advantage. Sometimes I feel like neurotypical expectations have raised people to be fragile. To have sensitive ears that hurt when you say things like ‘genocide’ or ‘rape’. But anyone who struggles to even listen to those words is completely useless when it comes to stopping the horror that’s the actuality of genocide and rape culture. Raising people to ‘dance on egg shells’, ‘beat round bushes’, and ‘don’t say that, it’s not nice,’ is raising a generation of people too gutless to confront abuse, exploitation, corruption or genocide.

Cut The Minimising Platitudes

Here we come across a plethora of sayings that aim to silence dissent and preserve the status quo. ‘Don’t rock the boat,’ ‘don’t make waves,’ ‘don’t upset the apple cart.’ Never mind that the ‘boat’ allowed white supremacy, sexism, misogyny, ableism, homophobia and transphobia to thrive for centuries. That its still deeply tainted.

And then we’re onto other sayings, ‘calm down,’ ‘chill,’ ‘it can’t be that bad.’ These allow people to disconnect from reality and deny how bad any given situation is. They seem aimed at ensuring people feel comfortable, even as the world burns around us, because we were too complacent to do enough about climate change, soon enough.

Speak Up & Protest!

When it comes to what’s wrong with the world, autistic people like Gretna Thunberg may be the voice you don’t want to listen to. You’re conscience sayng ‘this is wrong and we have to act.’ Again, this is not about YOU. Its about Palestinians being starved to death in Gaza by a regime that’s come full circle, from fleeing fascism to embracing it to annihilate Palestinians. Its about all the disabled people RFK Junior wants to stick in ‘wellness’ camps.

The autistic strength when shit gets fucked is we don’t put our personal feelings about shit being fucked first. We’re not shocked at finding ourselves outside our comfort zone (we pretty much live there already). And I think our struggle to sometimes understand emotions, and the ease we tend to have with logic, inclines us to put our logical understanding that shit is fucked and action MUST be taken to unfuck it first.

Our blunt calls to do so bypass neurotypical uncertainty because something pushed them outside their comfort zone. They bypass the neurotypical tendency to flinch from the truth, not call things what they are, delay, delay, delay; until things get WORSE. So SPEAK UP (like we do)!

Disclaimer

(Yes, I acknowledge not all neurotypical people are the same. Nor are all autistic people. But the general patterns I see with a lot of neurotypical people when it comes to stubbornly refusing to abandon the illusion of their comfort zone, to face shit being fucked and get off their backsides and DO ANYTHING for our planet, democracy, Palestine etc, CONCERNS me.)

Sharing the Good Stuff

Having raised some heavy shit, I’d like to end with an autistic approach to life that can make the good parts better. My mum likes travelling with me. She says seeing my enthusiasm makes site seeing more enjoyable. I’ve never cared if people view my displays of enthusiasm as ‘child like’ or ‘over the top’ or whatever. If I LOVE something, than I LOVE it. I’m not going to tone it down because ‘maybe someone will judge me.’

When the emotion is enthusiasm, I don’t think I’ve seen someone judge me badly. As an adult, people either smile, or they don’t click with whatever I’m responding to and they move on. And by not giving a shit either way, I get to fully feel and express my excitement at seeing something beautiful, or new. Heck, I’ll pause part way down the street to stare up at possums at night, or to smile at birds by day.

Smell Those Roses

All of us are so busy with our own lives, we often don’t even notice things. I once went to the supermarket wearing fluffy rainbow slippers because I forgot I had them on under my flared jeans. A group of teens had a chuckle when they noticed and smiled at me. No one else noticed a thing. I think ‘other people’ care far less about any one person than that one person thinks. I think most people care far too much about what other people might think of them. And I’ve never had any intention of letting fear of others opinions get in the way of having fun.

I don’t know strangers. Therefore I don’t care what they think. (Though them agreeing with me does score them points ;). Expressing my autistic enthusiasm for life lets me enjoy it fully, and it makes other people either notice what I’m noticing, or notice my enjoyment. Either one tends to make them smile.

In a world with TONNES OF SHIT going on, its important to smell those roses, smile at screeching rainbow lorikeets zooming past your head, stare at pretty sunsets etc. Let yourself fully enjoy life, and rather than people judging you, you may see them enjoying it with you.

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Related Reading

Writing Neurodiverse and Disabled Characters

Oh, I’m Also Actually Autistic (Identifying which of my traits are autistic).

Manging My Neurodiversity (Communication, processing and mental health strategies).

Minimising Visual Overload (for autistic & ADHD comfort)

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