About Me
A quick summary
I was diagnosed with stage 4 bowel cancer at 31. It started with subtle symptoms, an itchy bum and going to the toilet more often, nothing that screamed cancer. But a colonoscopy in 2022 found a large tumour in my bowel, and scans revealed two suspicious spots on my liver.
After recovering from bowel surgery, scans confirmed that those two liver lesions had increased to fourteen within six weeks. A liver resection was off the table, so I started aggressive chemo. I did 12 full rounds of FOLFOXIRI + bevacizumab, followed by two micro-ablations. Scans in March 2023 showed no active cancer. I kept going with maintenance chemo, 48 rounds total, before being forced to take a break in late 2024 and that’s where we’re at now.
Since my diagnosis, I’ve made it my mission to raise awareness. I run Grinding Chemo on social media, I’ve been on TV and podcasts, spoken at national and local events, and even published a children’s book to help families talk about cancer.
I’m still here. I’m still going. And I’ll keep speaking up, because no one should be told they’re “too young” for cancer.
My Cancer Story
Prior to Diagnosis
I’ve always seen myself as a pretty average Aussie bloke. I grew up in regional WA, Harvey as a kid, then Exmouth from age 14. Sun, surf, fishing, and whale sharks. After school, I became a chef, but the split shifts and pay weren’t for me, so I headed offshore.
I worked on deck out of Dampier for nearly a decade. The 4-weeks-on, 4-weeks-off life was intense, but it gave me the chance to travel, through Europe, Southeast Asia, Mongolia, the Pacific Islands. The most life-changing trip, though, was to the US, where I met my wife on a Contiki tour.
Eventually, we settled in Perth. That move probably saved my life, though I didn’t know it at the time.
The Diagnosis
In August 2022, I was 33 and living what felt like a normal life. I was at work one day, scrolling Reddit, when I came across a post: “I’m going to the toilet 4 – 5 times a day, is that normal?” The comments mostly said: See a doctor.
That hit me. I’d been doing the same. I also had an itchy bum. I’d been putting off going to the doctor, figuring I’d wait until something was “really” wrong. (Terrible idea, by the way.)
When I got home, I saw my GP. I told him about the itch, and before I could even mention the toilet stuff, he said he was referring me for a colonoscopy. I thought he was overreacting.
Two weeks later, I went in. I watched other people come and go from the theatre, quick procedures, then sandwiches and home. Mine wasn’t quick. When I woke up, they were taking bloods.
Then the doctor came in and told me they’d found a large tumour, 30cm up my colon, so big they couldn’t even get the camera past it. I was stunned. But my brain kicked straight into fix-it mode: Okay. What’s next?
What came next was a CT scan, a referral to a colorectal surgeon, and the scariest phrase I’d heard yet: “It’d be best if your wife came with you.”
That’s when it really hit.
When she picked me up, I managed to hold it together until we walked outside. Then I broke. I told her I probably had cancer. She barely blinked, just said, “Right. What do we do now?”
The Rollercoaster Begins
On 9th September 2022, I had surgery to remove the tumour, a lower anterior resection. There was a 50/50 chance I’d need an ileostomy, but thanks to an incredible surgeon, I avoided it.
Six days in hospital. Walking within 24 hours. Then home for six weeks to recover and prepare for a planned liver resection, because scans had shown two suspicious lesions.
But just before that surgery, we got new scans. The two lesions had increased yo 14.
Surgery was off the table. We had to hit it with chemo, and fast.
Chemo, Round After Round
I started FOLFOXIRI plus bevacizumab in October 2022. It’s one of the strongest regimens they throw at bowel cancer. Six hours in the chair, then home with a chemo pump for 46 hours. Every two weeks.
My worst days weren’t in the chair, they were the Friday, Saturday and Sunday after. The drugs were still in my body, but the meds that softened the side effects had worn off.
After 12 rounds, scans showed a miracle: the 14 liver lesions were back to two, and shrinking. That opened the door to micro ablation, they burned the remaining ones from the inside out.
In March 2023, I got the words every patient hopes for: no active cancer on scans.
Not remission. Not cured. But a kind of peace in the storm.
The Ongoing Grind
I stayed on maintenance chemo, round after round, 48 in total, before finally taking a break in October 2024. Somewhere along the way, I shifted to three-weekly cycles. Not as intense, but still bloody relentless.
In January 2024, I made a successful claim on my life insurance. And while that claim was a huge financial relief, taking massive pressure off me and my wife, the process was confronting in ways I didn’t expect.
To be approved, I had to provide letters from both my oncologist and GP confirming that I likely had less than two years to live.
It’s hard to describe what that feels like, reading that sentence in black and white. Seeing your own life expectancy written in a report. Even when you already know, it still hits different.
The Stuff No One Talks About
Chemo wrecks your body. I’ve had neuropathy, reflux, chest pain, fatigue so bad I’ve slept through entire days. I had a mouth infection that meant removing three wisdom teeth, and a perianal abscess that made it painful to sit, stand, walk, or lie down. Honestly, that abscess was worse than chemo.
Mentally, the hardest part wasn’t treatment. It was making the phone calls. Telling my mum and dad I had cancer. Telling my best mate, I had to text him because I couldn’t say the words again.
And I made the mistake of looking up survival stats. Stage 4 bowel cancer. Five-year survival rate? 14%. That number crushed me for two straight days. Then I decided, fine. I’m going to do everything I can to be part of that 14%.
Support, Privilege, and Perspective
I’ve had incredible support. My wife has been by my side from day one. My friends, family, employers, all amazing.
And I’m aware that’s a privilege. Not everyone gets that. I’ve met people who’ve had to keep working through chemo. People who’ve been misdiagnosed, delayed, dismissed.
I’ve also had the safety net of insurance, sick leave, and a GoFundMe that helped with the out-of-pocket costs. Without that? I honestly don’t know how we would’ve coped.
Why I Speak Up
Since the start, I’ve documented my story on social media, mainly TikTok, under Grinding Chemo. I’ve had strangers message me to say they booked a colonoscopy or finally saw a GP because of something I shared. That makes every post worth it.
I’ve spoken at Bowel Cancer Australia’s Never Too Young: Call on Canberra events in 2023 and 2024. I’ve appeared in multiple TV and newspaper stories, guested on podcasts, and recently gave a presentation at my local Rotary Club.
I also published a children’s book, Hope Avenue, to help parents talk to kids about cancer, because these conversations matter.
This isn’t about sympathy. It’s about awareness. Advocacy. Action.
Don’t Wait. Don’t Settle.
If you’re young and something feels off, get it checked.
If your GP dismisses you, get a second opinion. Don’t wait. Don’t assume. Bowel cancer doesn’t care how old you are.
And if you’re in the fight already, I see you. You’re not alone.
I’m still here. I’m still going. And I’ll keep going, for me, for my wife, and for everyone who deserves a better chance at catching this early.
i'D LOVE TO HEAR FROM YOU
This blog isn’t just about my story, it’s about building a community where we can share, learn, and inspire one another.
Got questions, ideas, or suggestions for what I should write about next? Perhaps you’d like to share your own story? I’d love to hear from you and explore ways we can create something meaningful together.
Let’s keep the conversation flowing
