Mel, WA

Name: Mel Taylor

NET Type:

  • Pancreatic
“They found a tumour about the size of a tennis ball on my pancreas… It’s a shame that it takes a diagnosis like this to change the way people live their life.”
- Mel Taylor

Mel Taylor, a 49-year-old artist was diagnosed with a pancreatic neuroendocrine tumor in 2017.

Mel was initially diagnosed with epilepsy, narcolepsy, menopause, IBS, GERD/GORD, and mental health issues. Her symptoms included fatigue and anxiety which remained unexplained. The discovery of a tennis ball-sized tumor on her pancreas marked a turning point, but living 600 km away from a capital city presented challenges in accessing specialized care.

“I had a doctor say to me, ‘I don’t really know what’s going on. Let’s just ‘wait and see.’ If I had done that, I may have been in a very different position than I am now.” 

Her children, daughter Ellie and her son, witnessed their mother’s ordeal, with Ellie visiting her in the intensive care unit and being exposed to the reality of cancer from a young age.

Since her diagnosis Mel has found solace in art, creating a series reflecting on life with neuroendocrine cancer. Describing her journey as “the absolute worst time” but also the best, Mel acknowledges the transformative impact NETs has had on her art.

Additional solace has been found in the support offered by NeuroEndocrine Cancer Australia (NECA) and its support groups. NECA has guided Mel, offering invaluable support and helped to reinforce the importance of trusting her instincts in seeking medical advice.

“NECA has made a huge difference… you can’t always just trust what medics say.”

Finally receiving a proper diagnosis has brought relief and a plan for Mel.

“Now we can get it under control.” 

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More patients diagnosed with Pancreatic

Jo, QLD

  • Pancreatic
In that moment, everything just crumbled. One minute, I was thinking I’d be home in a day or two. The next, I was being told I had stage-four, inoperable cancer.

Terri, VIC

  • Pancreatic
I know that if there was more understanding of the disease and its effects my experience wouldn’t have been so isolating. The lack of knowledge within the medical profession was really shocking to me, as was the lack of information and support offered after diagnosis.

Chris, VIC

  • Pancreatic
Looking back over the last few years the symptoms were always there but life gets in the way and you dismiss them. To say I was in shock was an understatement. I was numb. I’m 42 years old with 2 children and a wife and family, I can’t get cancer.

Hamish, WA

  • Pancreatic
The diagnosis of a PNET has changed the way I look at life, and I am extremely grateful for the cutting edge research the oncologists bring to the table when treating the disease.

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.