Brad, VIC

Name: Brad McKenzie

NET Type:

  • Small Bowel
“I went and got the diagnosis alone. Probably not a good idea. You hear the first words, ‘You’ve got cancer’ and then you don’t hear another word after that.”
- Brad McKenzie

Brad, diagnosed with neuroendocrine cancer.

Brad shares his journey with neuroendocrine cancer, explaining that some symptoms he had been exhibiting since 2009, were signs of cancer. Initially misdiagnosed due to symptoms resembling a heart condition, the NET tumour was discovered during an unrelated investigation.   

Fortunately for me,” Brad explains, “we found the metastasised cancer to the liver when the primary cancer in my bowel caused a bowel obstruction.

 Reflecting on his experience, he emphasizes the importance of not ignoring symptoms, as early detection could have altered his situation significantly. 

You need to pay a bit of attention to your body,” he advises. 

Brad candidly discusses his struggle with the lack of control over his condition, noting, 

Everybody’s cancer behaves differently, so you’re never quite sure whether it is going to pop up somewhere else.” 

He highlights the importance of holistic health, both physically and mentally, and shares the value of seeking counseling to understand mortality and manage stress. He advises newly diagnosed patients to connect with Neuroendocrine Cancer Australia (NECA) for immediate support and resources, stressing,  

Getting the right information and educating those that don’t (know) should be priority one.”

Brad also talks about his treatment routine, where he receives injections every 28 days, and the adaptability it requires, such as his wife being trained to administer the injections providing more flexibility in their lives.  

He appreciates the support from the Neuroendocrine Cancer community, including practical advice and emotional support through the NECA Facebook groups. By sharing his story, Brad hopes to provide guidance and support to others facing similar challenges, emphasising the importance of community and understanding in coping with cancer. 

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More patients diagnosed with Small Bowel

Allison, W.A.

  • Small Bowel
This experience has made me a firm believer in screening, early diagnosis, and specialist NET care. I feel incredibly lucky — and grateful — that my NET was found at such an early, treatable stage.

Patricia, NSW

  • Small Bowel
There’s such little awareness about this cancer, even among medical professionals. I’ve had GPs say to me, “I’ve never seen a neuroendocrine cancer patient in my life.” And I tell them, “You probably have — you just didn’t diagnose them.”

Bronwyn, NSW

  • Small Bowel
I encourage everyone to share their story—on the NeuroEndocrine Cancer Australia website and within their own communities—so that NETs is recognised and diagnosed earlier. I also encourage fundraising for NeuroEndocrine Cancer Australia if possible.

Chris, WA

  • Small Bowel
I have worked in healthcare my entire life I had never heard of NETs until my diagnosis and I’m pretty sure none of the doctors I had seen in the lead up to diagnosis knew about it either.

Walk, run, or ride this March4NETs!

For its third year, March4NETs will run throughout March 2026.

Get involved and support the 31,000 Australians living with neuroendocrine cancer.