06 December 2025

Ouch!

 

Ouch

If you were sitting in a waiting room and someone walked in and smacked you in the head with a cardboard box, what would you expect to happen?

If I’d hit you, I know what I would do. If I were the one carrying the box, I’d apologise—profusely. Even if I hadn’t seen you. Even if I hadn’t meant it. It would still be my mistake. My responsibility. The onus on me to put it right, and not do it again. 



That’s why it feels so bizarre that, as a disabled person, when somebody hits me in the face with whatever they’re saying, 
I’m the one expected to apologise for being hurt. I’m told I shouldn’t have been sitting there. I shouldn’t have come on that particular day. I shouldn’t be in the waiting room at all—almost as if disabled people are supposed to warn the world of our presence before entering a building.

On a personal level, you can imagine how upsetting this would be if it happened once. But it doesn’t. It happens so often that the bump from the cardboard box is becoming quite painful. I find myself making more and more excuses not to be in any room anywhere—not because of one dramatic incident, but because I’m exhausted from being hit in the head and then told it’s somehow my fault.

On an organisational level, I genuinely don’t understand why a policy can’t be put in place to stop people knocking me in the face in the first place. If customers or patients were being regularly inconvenienced—or literally struck—surely it’s up to the organisation to make a change. Yet whether it’s parking bays, accessible entrances, safe walkways, or waiting rooms, the burden is consistently placed on the disabled person to complain afterharm has happened. Only then—maybe—is something reviewed.

This is against compliance - which is anticipatory - furthermore, it’s unfair.

Most of the time, reasonable adjustments aren’t made because no one at senior level has thought about them - or had disability equality training. Safe public spaces are assumed, and potential harm as a small operational detail, not something worth planning properly. But planning safe routes for staff to move through day in, day out, year after year is a management responsibility. It requires an impact assessment. It requires someone to think, “Could the way we work harm someone? Could this exclude someone? Could this be done better?”

I’ve noticed that many organisations have quietly stopped doing the very impact assessments that meaningfully include disabled people at all. The result? They hit you in the head first, wait for the complaint, and then consider changing the practice.

But here’s the sticking point: the complaint itself. I’m tired—angry, even—about having to complain in the first place. I retired in the hope of finally escaping the relentless expectation that I should fix the ableist systems I move in. And, worse, I should expect being hit. As an individual I was never responsible for educating every organisation I encounter. And frankly, I’m worn down by having to say, over and over again: can you please stop hitting me?

This isn’t a matter of personal sensitivity. It’s a matter of education, compliance, justice, and basic equality. No one should be behind you with a box. And in this analogy—and in real life—organisations should make sure their practice isn’t ableist. The fact that something wasn’t intentional doesn’t remove the responsibility to apologise. And it certainly doesn’t justify blaming me for simply existing in the space.

The aim needs to be to avoid hitting people in the first place—not to tell disabled people it’s our job to get out of the way.


03 December 2025

International day of Disabled People

 


Celebrating Disabled People’s Creativity, Experience and Voices on the International Day of Disabled People


Pools and Prejudice: Death in the Shallows

On this International Day of Disabled People, there’s no better time to celebrate stories that challenge expectations, confront prejudice, and centre disabled lives with honesty and strength. That’s why I wrote Pools and Prejudice: Death in the Shallows— I hoped to balance tension, wit, and social commentary with rare precision.


If you’re looking for a book that will both grip you and make you think differently about the world, Pools and Prejudice: Death in the Shallows is exactly that. Today, we celebrate disabled creativity, disabled resilience, disabled truth-telling. 


I wanted the plot to shine a light on the realities of disabled people navigating a world that often refuses to see us clearly. 


The story follows Meg whose experiences of exclusion, institutional failure and everyday ableism are woven through a mystery that unfolds in and around a local swimming pool—a community space that becomes a microcosm of society’s attitudes towards disabled people.

I refused to soften the truth, and avoided speaking in metaphors or inspirational clichés. Instead, to give readers a narrative grounded in lived experience and disability equality: flawed systems, hidden hierarchies, the exhausting bureaucracy disabled people face, and the emotional resilience required simply to exist within them. And also hoped to capture the warmth, humour, friendship, and the small acts of solidarity that keep people going. 





Readers say: 


“Characters bring texture, complexity and humanity, each revealing different sides of disability, trust and belonging.

Pools and Prejudice is more than a mystery; it’s a challenge to look deeper—beneath the surface of institutions, beneath polite conversations, and beneath assumptions about what disabled lives should look like. It’s bold, unapologetic storytelling from a disabled writer who understands that representation is not a luxury but a necessity.”


On days like today, when the world pauses to recognise disabled people, their rights and their contributions, it reminds us why authentic stories matter. They expose injustice. They provoke conversation. They forge connection. And, importantly, they carve space for disabled people to be protagonists in their own narratives—complex, fierce, and fully realised.


Furthermore in order to respect Disabled People’s Identity and highlight Stereotypes, I was careful not to counter the negative stereotypes imposed on disabled people with equally toxic positive ones.


https://www.amazon.co.uk/dp/B0DLBHGBLX