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The Art of Difference by LoveArtPix

From chaos to change: living, learning, and leading with a late autism and ADHD diagnosis    This piece forms another chapter of our Neurotribe…

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From chaos to change: living, learning, and leading with a late autism and ADHD diagnosis
 
 

This piece forms another chapter of our Neurotribe work – The Art of Difference series – sharing space with extraordinary neurodivergent creatives and changemakers. Each story in this series celebrates the many ways neurodiversity shapes perspective, creativity, and purpose. If you’re an artist, poet, or writer with lived neurodivergent experience, share your work here.
In this one, artist and founder of LoveArtPix reflects on life, art, and leadership after a late autism and ADHD diagnosis – and how naming difference can become a catalyst for change.

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I was 41 when I finally had words for the way my brain works. Autism. ADHD. Late, yes – but not too late to change everything. That diagnosis reframed my past, eased my self‑judgment, and gave me new direction for the future. It’s why my work as LoveArtPix is more than art on walls or social media platforms; it’s a language, a map, and, when needed, a megaphone.

I’m a self‑taught, award‑winning artist from Manchester with no formal qualifications – just relentless curiosity, graft, and a vision I won’t let go of. I’ve learned that when your difference finally has a name, your voice gets clearer. Mine did. My art did. My purpose definitely did.

The diagnosis that changed my lens

 

A late diagnosis can be a complicated mix of relief and grief. Relief, because your history finally makes sense: the overwhelm, the hyperfocus, the sensory storms, the social burnouts. Grief, because there’s a collection of misunderstood years and missed support. For me, it wasn’t about becoming someone new; it was about understanding who I’d always been – and choosing to meet that person with honesty.

That honesty is everything. It’s what I bring into my practice, my collaborations, and the communities I serve. It’s why I speak publicly about my experiences of being autistic and ADHD as an adult – and why I share openly how art became my language during and after my diagnosis: a way to turn overload into visual narratives that move conversations forward.

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Art as a first language and a loudspeaker

 

I’ve been creative in different ways throughout my life, but after my diagnosis, art became the bridge from chaos to connection. In my debut exhibition in 2025, I made a deliberate choice to centre neurodivergent creativity – not just my own, but a wider community of ND voices, collaborating across poetry, music, tattoo art, and more, from ages 11–63. I finished every piece digitally in Picsart before printing onto glass; it was the first UK exhibition where every work was made in that medium – accessible, contemporary, and unapologetically different.

At my gallery space in Spinningfields, Manchester, I’ve leaned into that same purpose: exhibit the truth, invite the conversation, and use the work to make inclusion feel tangible – not theoretical.

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From awareness to action: prisons, schools, public spaces

 

Art has led me to launch hands‑on initiatives well beyond the gallery:

  • HMP Manchester (Strangeways): a pioneering NEAF course that empowers neurodivergent prisoners to explore identity and emotion through art – helping with rehabilitation, reducing stigma, building agency, and bringing humanity into a system that often overlooks difference. This strand of work led to a humbling moment: an invitation to His Majesty The King’s Garden Party for those working in Education and Skills – recognition not just of me, but of the message itself: inclusion must be lived, not just said.

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  • Schools and education: creative projects that give young people tools to express themselves, understand neurodiversity, and see their differences as strengths.

Public exhibitions, school workshops, prison education – different settings, same mission: make the world more responsive to minds like mine.

“Autism: The Gift in the Curse” – the documentary

For three years, I’ve been working with the Eklectics Production team on a documentary that pulls back the curtain on my late diagnosis and the role art plays in survival and change. It’s raw, it’s honest, and it’s scary at times – but necessary. Autism: The Gift in the Curse is set to release later in 2026. It’s about the power of finally understanding yourself, and the ripple effect when one person refuses to hide.

No formal qualifications. Self‑taught. So why has it worked?

People often ask how I’ve managed to do all this without the “right” credentials. My answer is simple: vision, consistency, and raw honesty. I say the thing. I create the art. I show up again. Is that what society is hungry for right now – a kind of unfiltered truth we can build from? Maybe that’s why it resonates. Or maybe it’s that when you stop masking, your work finally speaks in your real voice. Either way, the story isn’t about perfection or pedigree. It’s about persistence.

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Disorder – or mismatch?

 

Medically, autism is classed as a disorder. I don’t experience it that way. What I experience is a mismatch between how society is designed and how my brain processes the world. If we built the world differently, a lot of “symptoms” would simply be differences.

We didn’t label wheelchair users as the problem; we built ramps. Where are the ramps for neurodivergent people?

What I’m committed to next

 
  • Keep sharing my journey – messy, moving, real – so others feel seen, and so outdated systems feel pressured to change.

  • Grow the education and prison work, because transformation shows up fastest when people are given tools to express and understand themselves.

  • Use exhibitions and public art to put neurodiversity in front of the wider public, so awareness becomes action.

  • Release the documentary and keep the conversation going beyond the screen – into classrooms, boardrooms, and communities.

I believe in the power of one person with a clear purpose, but I don’t believe change is a solo act. My art began as a survival skill; it’s become a tool for social change. If my late diagnosis gave me anything, it was permission to be fully myself – and to build ramps where none existed.

If you’re reading this and seeing your own story in mine, you’re not alone. Let’s keep building – truthfully, practically, and together.

You can find more about LoveArtPix on their website and Instagram – definitely worth following their journey!

 

Article via Neurotribe

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