Photo of the sunrise over the Sahara Desert taken in Morocco August 2024.
I spent today in Cardiff at the National Neurodiversity Show. I listened to and talked with neurodivergent people about their life experiences and advice: some were selling books, inclusive technology, diagnostic services, or neuroinclusive organisations.
The quote above, “You’re not broken, you’re just orbiting differently,” from @beaconwithin, was particularly inspirational. It made me think about a favourite topic to teach Year 5: Earth and Space.
Every person on this planet is taking the same orbit around the sun, though our orbits are different.
The Speed: Some are fast like Mercury's 88 days; some are like poor neurodivergent Pluto's 248 years.
The Rotation: Some planets rotate quickly, like Jupiter’s 10 hours, whereas some are slower like retrograde Venus's 243 days.
The Tilt: Some are tilted at 97°, Uranus, and some are near 0.03°, Mercury.
Stay with me here! In those orbits, we have satellites of our own: emotional intensity, executive function, sensory sensitivity, rituals and routines, interests, and sense of self.
Some "satellites" orbit closer, while some orbit further away. These characteristics create that spiky profile which acts as our solar system. That system may be one of Autism, ADHD, Dyslexia, Dyspraxia, Tourette’s, Down Syndrome, and so forth. We have got to accept our own journey so we can advocate for ourselves.
My own orbit has recently taken me beyond the path I was on. Sadly, tomorrow, 01/05/26, my contract officially ends. Unless I get a phone call or email in the next five hours, I will join the orbit occupied by 70% of the autistic population in the UK. This is an actual figure quoted by the National Autistic Society: Unemployment.
I don’t know what the next path my orbit will take. Hopefully, I’ll get a job bringing money soon. Am I scared? Yes. Am I hopeful better things await? Absolutely.
I am not broken. Watch this space.
Shearwater Lake April 2025- sitting on the bench, waiting for an elusive Kingfisher.
Below- The cliffs near Combe Martin, Devon- the highest cliffs on rhe southwest coast path- taken 06/07/20- 2 days after the UK came out of lock-down! I was straight to the coast!
Sunset on 11/07/20- Hartland Quay- Devon.
Below: Sunset over one of my favourite local walks- Crooks Peak in the Mendips. You don't need to travel to the next county over to find a gorgeous sunset!
Some of you may notice that the blog sequence has skipped from 6 to 8. I have chosen to keep Blog Post 7 hidden away for now. While the "Authentic Voice" is vital, the "Strategic Voice" knows when to wait for the right conditions to share certain stories.
However, the conclusion of that untold story remains the same: we need role models who are allowed to be active, to participate, and to show that being autistic is not a flaw. It's not a piece of paper. It is a gift. My battle to stay in the classroom might be officially over, but my work as an advocate (the catalyst) is only just beginning.
The Restless Vista
One of my greatest pleasures in life is hiking. I can spend hours walking, getting lost in the rhythm of nature. My favourite hikes always involve an Edge or a Peak: heading to the end of a cliff to stare out at the sea, or climbing to the top of a hill where the vista stretches out beneath you.
If there are waves crashing against the shore or a sunset casting that changing orange glow over the landscape, that is where you will find me. During the pandemic in 2020-21, when restrictions were lifted, I managed to complete 91% of the South West Coast Path. Just not in one go.
Despite my love for these places, I cannot sit still for long. Last weekend, I was on a short Sunday afternoon walk around Shearwater Lake with my dad. As we sat on a bench, a realisation hit me: I just wanted to keep walking. I needed to keep moving.
My dad wanted to stay put, take in the lake, and perhaps catch a glimpse of a kingfisher. Now, I have seen that lake many times. It is beautiful. The woods are calming. I enjoy the walk. But have I ever seen a kingfisher? No. Because to see a kingfisher, you have to be still. You have to wait.
My family has faced this dilemma for 31 years, keep moving because I am restless, or stay put. Yet, I can sit for minutes (I wouldn’t say hours!) at a time staring at a sunset or a clifftop. I need to watch the whole sunset, see it through to its conclusion, and watch the landscape change colour.
I realised this isn't a lack of patience. It is a need for stimulation and a need for "Newness."
When I am moving, my brain is occupied by the changing environment. If I sit still in a place that isn't providing a complete narrative (like a sunset finishing its cycle), my other thoughts catch up with me. The Parallel Circuit in my mind becomes overloaded with internal data.
Watching a sunset or waves crashing is a dynamic, high-stimulation event. Waiting for a kingfisher is a static, low-stimulation event. For my restless mind, the walk itself becomes the Catalyst. It provides the kinesthetic input I need to keep my brain running smoothly.The dopamine hit. Yes, seeing a kingfisher would be an amazing dopamine hit. But is it worth 15 mins of restlessness? It is the compromise between a mind that needs constant stimulation and a soul that needs peace and rest.
Picture taken from the hill at my cousins wedding in June 2025
And suits, do not even get me started. I look pretty smart in one, but on a hot summer day, a suit is a sensory straightjacket. It is an absolute nightmare for thermal regulation. Can I please just wear a cotton shirt and jeans? It is not about being underdressed: it is about keeping the engine block cool enough to function. (I do look pretty smart though :))
Received an invitation to a wedding after-party today. I am obviously excited for them and will be RSVPing "yes." Between my sister’s wedding another big day next year, my calendar is looking at three major parties. My series circuit mind is already going into overdrive just looking at the dates.
At these high-voltage events, I usually prefer finding a quiet corner rather than mingling or dancing. Once the loud music starts and the small talk begins, my internal equilibrium shifts. I am very lucky to have two large families on both my parents' sides who have always understood my quirkiness and social awkwardness. Growing up, most weekends were spent between grandparents’ houses spending a lot of time with my 15 cousins. In adulthood, these close relationships, like most of my social relationships, have drifted away to perhaps seeing them once a year only at weddings and funerals.
I remember a wedding about ten years ago, before my diagnosis. I spent most of the evening in my hotel room, preferring the solitude to the booming music and jubilant dancing. At another more recent wedding, I remember needing time out so I walked up and sat on a hill overlooking the mingling. I needed to recharge my chemical battery and thermally regulate. The "heat" of the social interaction was simply too high, and the hill was the only place where my system could find its baseline again.
The University Loop and the "Odd" Label
It makes me think back to my university days, when I was often the first to leave the nightclubs after tagging along in an effort to feel social. I remember thinking then, before my diagnosis, why I could not stand these events. Why must I mess up socially and become isolated from the crowd, which every other nineteen-year-old studying for a degree is doing? We were all intelligent people, but my brain always told me to flee and find peace.
I vividly remember being introduced to a bunch of my ex’s friends who were in the year above me. Having to pretend to be social, only to hear someone whisper, "He's a bit odd, isn't he?" It caused an immediate panic and I had to flee. Anyway, I know my family will never judge me, and I know they understand why I need to have peace: they have known me for 31 years! But I still feel haunted from the past. It is hard to shut down the Vigilance Mode when the environment is loud, even when you are surrounded by people who love you.
The 10 PM Pizza: A Strategic Withdrawal
Then there is the tradition of serving food like pizza at 10 PM. Christ. By that time, my HD-mind has usually spiked so high from the noise and voices that my mind has just turned to jelly.
Expecting to process the sensory input of a crowded room and the complexity of late-night food is a big ask. It is safe to say I won’t be staying for the pizza! Leaving early isn’t about being rude: it is a strategic withdrawal to prevent a total system crash. Masking feels like a protective coating, but eventually, the coating wears thin. Finding that hill or that quiet hotel room isn't "fleeing": it is essential maintenance.
August 2025. Flying over Miami, Florida, en-route from Heathrow to Cancun. I was upgraded to business class, which was pure luxury, but even there I needed my head pressed against the plane wall to anchor myself. Luxury or not, the window seat remains a non-negotiable requirement for me. It is not just about the beauty of the world beneath. It is about that vital physical contact. Leaning my head firmly against the cabin wall provides the proprioceptive grounding my brain needs to feel steady at 35,000 feet.
Below- Somewhere over the Alps- taken enroute on a family holiday to Italy April 2015. The ice fields of Greenland taken July 2018 en route to Las Vegas
One question that keeps popping up in job applications lately is whether I consider myself disabled and if I need any reasonable adjustments for the interview. Personally, I do not view autism alone as a disability. It is more of a fundamental difference in how the mind processes information. I have noticed that some forms are starting to separate "disability" from "neurodivergence" now. When that second option is available, I always tick it. If it is just the one box, I feel obliged to tick it but then clarify in the "other" section that I am diagnosed with an Autistic Spectrum Condition. I use ASC rather than ASD because I find the term "disorder" disheartening.
I have started asking for three specific reasonable adjustments in the interview box to ensure my parallel circuit does not blow a fuse.
1. Access to Questions in Advance
I ask for the interview questions, or at least the key themes, at least 24 hours in advance. This allows for scripting so I am not taken aback by sudden questions. Without this, I tend to either waffle on as my brain tries to process every bottom-up detail at once, or I suddenly go completely quiet while I wait for the data to download.
2. The Swivel Factor: Vestibular and Proprioceptive Seeking
I request a swivel chair or an office chair rather than a rigid, fixed-back chair. I need that freedom for movement and stimming. It actually surprised me when someone recently pointed out that I simply do not sit still. When I am in a rigid chair, I swing back all the time.
It turns out this is called vestibular and proprioceptive seeking. Essentially, my brain is looking for sensory input to understand where my body is in space. It explains so much about my life, including why I always need the window seat on a plane. It isn't just about the beauty of the world beneath, it is about having those additional surfaces to rest and lean against. My brain needs that physical pressure to feel grounded.
It made me look back at comments from my students when I was teaching. They noticed it too. I was always swinging on a lab stool or sitting cross-legged, even if it was a bit of a "bad example" for health and safety! I think that is why my favourite classrooms when I was at school were science and art rooms. Those stools were just more comfortable for my brain. My tutor was an art teacher, and despite my lack of skill in drawing, I always felt comfortable in that classroom. I think the stools had a lot to do with it.
Even at my last teaching school, there was a wheely office chair in the lab. I never used it in favour of a lab stool because I was worried I would just wheel around all day and break it. I also didn't want to encourage bad habits for the kids! Turns out I did this anyway with the stools! Whoops- sorry if you have taken over my classes recently!
3. Fiddling and Sensory Needs
The third adjustment is being allowed a fiddle toy or something to keep my hands busy. I have recently realised that I always fiddle with something. In social scenarios, I tear the labels off bottles or fiddle with candles and flowers. I fiddle with my sleeves or my phone.
This sensory seeking shows up at home too. When I am in the home office, I sit with my feet on the wall. I have actually peeled away quite a lot of the wallpaper in the process. When I sit on the sofa reading, I need to stretch out with my feet above me on the back of the sofa. I do sit in some very odd positions. Sorry, Dad!
All of this is stuff I will be discussing with my GP when I get referred for an ADHD assessment. It certainly gets my mind thinking about how these quirks are actually my brain's way of trying to regulate its own chemistry all this time!