Sitting in the waiting room, I realised I had more in common with the nurses handing out the chemo than the patients receiving it.
It’s a weird feeling, being the youngest person in the room, not just once, but again and again. In the waiting rooms. In the infusion chairs. In the scan corridors. And when I say youngest, I don’t mean by a few years. I mean often by decades. Enough that people do double-takes. Enough that you start to wonder if you’re in the wrong place, or if maybe they are.
When the average doesn’t match your reality
Bowel cancer is still seen by many as an “older person’s cancer,” and that attitude trickles down into everything, from awareness campaigns to waiting room magazines. So when you’re diagnosed young, and suddenly you’re deep in the world of oncology wards, you stick out. Not in a way that makes people point and whisper. But in the way that makes you feel quietly other.
You see couples in their 70s, shuffling in together. You overhear conversations about grandchildren and retirement homes. Then there’s you, maybe still working, dating, thinking about having kids, or just trying to pay rent. You’re in a totally different phase of life, but you’re fighting the same disease. Sometimes even harder.
Younger doesn’t mean stronger
There’s this sneaky little expectation that if you’re young, you’ll handle it better. You’ll bounce back faster. You’ll be more resilient. And sure, maybe your organs are in better shape. But that doesn’t make it emotionally easier.
If anything, it’s lonelier. Because you can be surrounded by people all day, other patients, nurses, doctors, volunteers and still feel completely alone in your experience. Your life was supposed to be about starting things. Building things. Living. Instead, you’re navigating scan results, treatment plans, and grief. And that disconnect can mess with your head more than the chemo itself.
Too old for the AYA lounge, too young for the pensioner jokes
There’s a weird middle ground that many young adult cancer patients fall into. Old enough to legally be adults, but too young to be treated like the “average” oncology patient. If you’re in your late 20s, 30s or even early 40s, you’re often too old for the adolescent and young adult (AYA) cancer resources, but too young to feel seen or heard in the mainstream cancer world. It’s not a fun limbo.
Even when you access support groups, it’s rare to find people your age. You join Facebook groups hoping to connect and end up scrolling past endless posts about mobility scooters and grandchildren. There’s nothing wrong with that, it’s just not your world.
More in common with the staff than the patients
One of the strangest parts of being young in an oncology ward is realising that the people sticking needles in your arm, setting up your IV, and reading your obs are about your age and you relate to them more than the people sitting beside you in the treatment chairs.
I’ve had casual chats with nurses about Netflix, holidays, and weekend plans, and then turned to the patient next to me who wants to talk about hip replacements or how the vegetables with their Sunday roast weren’t boiled long enough. You start to feel like a weird hybrid, old enough to be in this system, but young enough to not quite belong.
Sometimes, I see it in the way staff speak to me too. The more experienced nurses are often lovely, but there’s a generational difference. It’s the younger staff, the ones still doing their post-grad or just out of uni, who tend to “get” it. They speak to you like a friend of a friend, not a patient. That connection matters more than people realise.
It’s not just about age, it’s about stage of life
The thing is, being young with cancer isn’t just about numbers. It’s about where you are in life. When your friends are having babies and planning weddings and you’re losing your hair and dealing with chemo farts, it hits differently. When you’re meant to be chasing career goals or hikking through South America, and instead you’re trying to figure out if you’ll still be alive for next year’s footy season, that’s a different level of emotional whiplash.
And sometimes, it’s hard to even talk about. Because you don’t want to make older patients feel like their lives matter less. They don’t. Every life matters. But there’s something deeply unfair about being diagnosed with something life-threatening before you’ve even had a chance to fully live. That grief doesn’t always have a place in the oncology ward. But it should.
Finding connection outside the ward
If you’re reading this and feeling that same isolation, you’re not alone. It might feel like it, especially in hospital settings where you’re the outlier. But there’s a growing community of young patients out there, and more support than there used to be.
Bowel Cancer Australia’s Never Too Young initiative is pushing hard to make young-onset patients more visible. They’ve got online support groups, peer-to-peer networks, and even education programs for GPs to help fight the “you’re too young” dismissal many of us have heard. It’s not perfect, but it’s something.
You can also connect through social media, not the curated influencer type, but the raw, real posts where people talk about fear, fatigue, and dark humour. That’s where you’ll find your people. People who understand what it’s like to have a stoma and a Spotify Wrapped. To get bloods done before brunch. To cry in the car because someone your age just died from the same thing you’re still fighting.
Final thought
Being the youngest person in the oncology ward doesn’t make you stronger. It doesn’t mean you’ll handle it better. And it sure as hell doesn’t make it easier. But you’re not the only one walking this path. And even if you feel like you don’t belong in that chair, you deserve to be seen, supported, and treated with the same respect and compassion as anyone else in the room.
You might feel alone in the room. But you’re not alone in this experience.
Message from the author:
Thank you so much for reading. I truly hope you found this blog helpful. If there’s anything you’d like to see covered in a future blog, or if you have thoughts or questions about what you’ve read, please feel free to comment below or send me a message. I also hope you take a moment to explore the rest of my page. There’s plenty of additional information for bowel cancer patients, caregivers, and anyone wanting to learn more.
Disclaimer:
I do my best to keep the information here up to date and relevant, all while navigating my own cancer journey. Just a gentle reminder: I’m not a healthcare professional, I’m a cancer patient sharing what I’ve learned along the way. Everything shared here is general information and may not be right for everyone. This is not medical advice, and you should always consult your healthcare team before making any changes that could impact your treatment.


You write so well Jake! The insights you provide are going to make someone else’s journey that bit easier to navigate or at the very least Will be a shoulder. You are relatable and you’re bringing up topics and issues that someone might not be able to just put their finger on how they are feeling.
I hope you’re writing helps your own journey as I’m positive it will be helping others.
Thinking of you both with love and sending waves of strength, hope they have a butterfly effect 🦋
Thank you so much for this, your words really touched me. I hope I can keep doing justice to what you’re describing. Your kindness and strength mean a lot. Sending love and gentle waves of encouragement right back