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EDIT: I’ve had a few messages and a phone call from family and friends asking how I am as a result of this blog post. Let me say that I’m talking about filmmaking, not my day job which I thoroughly enjoy.

There was a time when I couldn’t switch my brain off from filmmaking. A shot would catch my eye on a walk and I’d be reverse-engineering the lighting before I’d finished crossing the road. A line of dialogue would land wrong in something I was watching and I’d be rewriting it in my head, half paying attention to whatever I was actually meant to be doing. It wasn’t a job I was working towards. It was just how my brain worked, all the time, whether I wanted it to or not.

I’m not sure exactly when that stopped. That’s part of what makes this hard to write about. There’s no single morning I can point to and say “that’s the day it left.” It was more of a slow leak than a puncture. One day I looked up and the tank was just… lower than I remembered, and I genuinely couldn’t tell you which mile it happened on.

I want to be honest about this, because I think a lot of people carry some version of it quietly, and the quiet is the worst part.




It’s Not One Thing. That’s What Makes It Hard.

If I could point to a single cause, this would almost be an easier post to write. A bad experience, a project that fell apart, a person who knocked the wind out of me. Something with an edge to it, a villain, a clean narrative.

It’s not that. It’s everything, a little bit, all at once.

It’s the back injury and the bone spurs that mean a full day on set, on my feet, lugging kit, isn’t the straightforward thing it used to be. It’s the fatigue that comes with managing a chronic illness I’ll be carrying for the rest of my life, even in remission, even on a “good” day. It’s running front of house at the Tower Theatre, which I genuinely love, but which also takes a great deal of the same creative and organisational energy that filmmaking demands — there’s only so much of that particular fuel in the tank on any given week, and theatre has, fairly, been getting most of it. It’s the writing projects, the wiki work, the music, Sadie’s care, the general business of staying upright. Filmmaking didn’t get pushed out by one thing. It got quietly outcompeted by a dozen things, none of which were its fault, and none of which I particularly regret choosing in the moment.

And then there’s the industry itself, which I won’t pretend hasn’t played its part. The gap between the dream version of filmmaking — the one I had in my head as a younger man, scripts and sets and a clear path forward — and the actual mechanics of trying to make anything happen as an independent creator with limited time and limited budget, is a genuinely difficult gap to keep staring across. I’ve written things I’m proud of. Story bibles, scripts formatted properly, projects with real bones to them. And then they sit there, because the next step requires a kind of relentless self-promotion and networking energy that I simply don’t have spare most weeks. That’s not the industry’s fault either, particularly. It’s just true.

So: a mixture. Health, time, energy, the industry, life. All of it, a little bit, pulling in the same direction.

The Guilt Bit (You Knew There’d Be a Guilt Bit)

Here’s the part I find hardest to admit. There’s a specific kind of guilt that comes with losing interest in the thing you always said was your dream. Other people remember you talking about it. They ask how the latest script is going, with genuine warmth, and you have to decide in that moment whether to give the easy answer or the true one.

The easy answer is “yeah, ticking along.” The true answer is closer to “I haven’t opened that file in three months and I’m not entirely sure why, and when I think about opening it I feel something closer to tired than excited, and I don’t know what to do with that feeling.”

I don’t think losing passion for something makes it less real that you once loved it, or that you might love it again. But it took me a long time to separate “I’m not currently excited about this” from “I’ve failed at the thing that mattered most to me,” and I’m still not sure I’ve fully managed it. Those two sentences feel identical at 11pm. They are not, in fact, the same sentence.

What I’m Not Going to Do

I’m not going to wrap this up with a neat resolution, because I don’t have one. This isn’t the part of the post where I tell you I rediscovered my spark on a long walk and everything’s back to how it was. That would be a nicer ending. It would also not be true, and I promised myself a while ago that this blog is the place I tell the truth rather than the highlight reel.

What I will say is that I don’t think the passion is gone. I think it’s buried under quite a lot of other, currently louder things — pain, fatigue, caring responsibilities, a job I love that takes more than it gives back some weeks, and an industry that asks for energy I don’t reliably have. I don’t think that’s the same as it being dead. Dead feels permanent. This feels more like a fire that’s gone quiet under the ash, still warm somewhere underneath, waiting for slightly better conditions than the ones I’m currently in.

I don’t know when those conditions arrive. Maybe when the back settles into something more manageable. Maybe when there’s a stretch of life that isn’t quite so determined to throw things at me, on the evidence of my last blog post, which — if you’ve read it — you’ll know is a fairly long list. Maybe it just happens gradually, the way it left, and I won’t notice the exact day it comes back either.

For now, I’m trying to let that be okay. Trying not to force a passion that isn’t currently there, because forcing it has never once worked and has only ever made me feel worse about both the not-wanting-to and the guilt about the not-wanting-to. Trying to trust that the bit of me that used to rewrite dialogue on the walk home is still in there somewhere, just resting.

If You’re In This Too

If any of this sounds familiar — if there’s a version of you that used to light up about something and currently just feels tired when you think about it — I don’t have a fix for you. I’m not sure there is one, or at least not a fast one. But I don’t think you’ve failed, and I don’t think it’s gone for good. I think you’re just carrying a lot, and the thing that needs the most energy is, unfairly, often the first thing that gets quietly put down when the energy runs low.

I’d genuinely like to know if this resonates. Has your relationship with a dream changed shape over the years? Did it come back? What did that look like? Drop it in the comments — I think there’s more comfort in knowing this is common than there is in pretending it isn’t happening at all.


Gary is a designer, developer, theatre manager, songwriter, and — somewhere under the ash — a filmmaker, based in Kent.

Let me paint you a picture.

It’s morning. I’m sitting on the edge of the bed, sock in hand, preparing for what has become the daily ritual that most accurately summarises my relationship with my own body. My foot needs to reach the sock. The sock is approximately thirty centimetres away. This should not be a problem. It is, nonetheless, a significant problem.

What follows can only be described as a man attempting to kickstart a motorbike with his foot while simultaneously being electrocuted. There is lunging. There is twisting. There is a level of grim determination usually reserved for people attempting Everest. Eventually — eventually — the sock goes on. Victory.

This is my life now. And honestly? It’s the funniest part of my morning, right up until it isn’t.



I’ve been thinking lately about the accumulation of it all. The full inventory of what my body has put me through over the years, laid out plainly. Not for sympathy — I’m not built that way — but because I think there’s something worth saying about how you carry it. How you keep going. How you find the dark laugh in it when the alternative is just sitting with it, and sitting with it is no fun at all.

So here it is. The full list. Don’t say I didn’t warn you.

In 2012 I had surgery for pectus excavatum — a congenital chest wall deformity where the breastbone sinks inward, asymmetrically in my case. The surgery to correct it is called the Ravitch procedure, and it is not, to put it mildly, a minor operation. My surgeon broke ten ribs and my sternum, repositioned everything, and held it all together with titanium bars. I was out of action for a year. A full year. I joke that I’m part robot now, which is true. That was the opening act.

Then there are the knees. Brittle cartilage, both of them, a gift I’m fairly confident I earned by jumping twelve to fifteen feet off Cleethorpes Pier onto the sand in my younger and considerably more stupid days. At the time it felt brilliant. My knees have been filing a formal complaint about it ever since.

Then, in 2019, came the diagnosis nobody wants: stage 4 SMZL — Splenic Marginal Zone Lymphoma. Cancer. I’ll let that land for a second. Six months of chemotherapy followed, ending in March 2020. Two weeks later, the country went into lockdown. I’d like to say the timing was darkly poetic. It was, in fact, just dark. The world shutting down precisely as I emerged from the other side of chemo — when you’re supposed to start rebuilding, seeing people, feeling human again — is something I don’t talk about much. But it happened, and it cost something.

It cost more than I realised at the time. Because my immune system had taken such a battering from the chemo, I had to shield for the entire first year of lockdown. I did not leave the four walls of my home for twelve months, other than a couple of hospital follow-up appointments. Twelve months. No fresh air, no wandering, no pub, no people. Just the walls, the silence, and a body I was still learning to live in after everything it had been through. I don’t say this to make anyone feel sorry for me. I say it because it happened, and it shaped things, and pretending otherwise would be dishonest.

The cancer is currently in remission. The less good news is that it’s incurable — I’ll carry it for the rest of my life, managing it, monitoring it, living alongside it like an uninvited lodger who won’t leave but has at least learned to keep the noise down. I’ve made my peace with it. You have to.

In February 2024, I tore a muscle in my back hauling ten-stone beer barrels at work. The tear itself was bad enough. What followed was worse: bone spurs developing along my spine, my body attempting to repair itself and making a fairly poor job of it. Now I live with constant pain. Some days it’s manageable — background noise, a dull ache I’ve learned to work around. Other days I can barely stand. The socks, as you now know, are every day regardless.

Four months later, in June 2024, I was diagnosed with type 2 diabetes. Of course I was. At this point my body was clearly just working through a list.

And then there’s the ADHD. Not yet officially confirmed, but we’re heading there — the pieces fit too well to pretend otherwise. Here’s the thing about having ADHD when you also have a back injury that’s stripped most of the hyperactivity out of you: the H has largely gone quiet. My body isn’t bouncing off walls anymore. My brain, however, absolutely is. It will pick a song — usually, inexplicably, a McFly song — and play it on a loop for weeks. When I wake up. When I go to sleep. In my dreams, sometimes. Full production. No fade out. No mercy. Thank fuck I like McFly, genuinely, because I think a Coldplay phase would finish me off entirely.


And then there’s Sadie.

My wife lives with her own long-term chronic health conditions — I won’t share the details here because they’re hers to share, not mine — but what I will say is that managing my own health while also being her carer is something I carry with a lot of love and, occasionally, a lot of weight. I have a Carers Card. An actual, official Carers Card. I am, technically, a registered carer. If you’d told me that ten years ago I’d have laughed. Now I carry it in my wallet and feel, if anything, quietly proud of it. We look after each other. That’s what it comes down to.


So. Did I do something very bad in a past life? Statistically, it’s starting to feel that way. Titanium ribs. Lymphoma. Knees that haven’t forgiven me for a pier jump in my twenties. A back staging a slow mutiny. Diabetes. ADHD. A wife I love deeply and care for practically, every day.

The thing is, I don’t say any of this from a place of despair. I say it from a place of — I don’t know, exhausted honesty? There’s a version of this post where I wrap it up neatly with something about resilience and perspective and silver linings. But that would be a bit dishonest, and I’m not really in the business of performing okayness at the moment.

What I am in the business of is getting through the day. Doing the work I love. Looking after Sadie. And spending time with Reggie — our three-legged cat, adopted at the end of April, who has brought more light into this house than I can properly explain. He gets around better on three legs than I currently do on two, which says something, though I’m not entirely sure what. He also likes to help me write. Daily. Usually by walking across the keyboard at a critical moment and contributing a paragraph of his own — ggggggggggggg, typically, or perhaps xxxxxcccc if he’s feeling creative. I’ve learned to save regularly. He has not learned to care.

And talking about it. Because I think a lot of people are carrying their own version of this list — the accumulation of things, the ways their body has let them down or surprised them or just refused to cooperate — and not saying much about it. So consider this me saying something.

What’s on your list? Drop it in the comments. I’d genuinely love to know I’m not the only one having a one-sided argument with my own spine every morning.


*Gary is a designer, developer, theatre FOH Manager, and occasional filmmaker songwriter based in Dover, Kent. He puts his socks on every day. It takes a while.*