Jacqueline, NSW

Name: Jacqueline Gillespie

NET Type:

  • Small Bowel
“To take control of the things I could control, and let go of the things I can’t control. . . I think I am more balanced in my life now, which is better for my overall health.”
- Jacqueline Gillespie

Jacqueline, 62 years old and diagnosed with a NET.

For Jacqueline and her partner Meg, her diagnosis came as a surprise and led to some life-changing decisions about her work-life balance.

“I was diagnosed with neuroendocrine cancer, which was a big shock to our world… and I did keep working for some time. But, I came to the conclusion that the stress of the job… wasn’t good for my overall well-being… And so the challenge is to find other things to keep you stimulated.”

Like others living with NETs, her symptoms of heart palpitations, breathlessness, and tiredness could easily have been dismissed for other causes such as a heart condition, asthma, or menopause.

“There was never any kind of thing found, there was no conclusion to those episodes. . . so when I think about symptoms to diagnosis, it was probably about 7 years.”

A doctor ordered a scan to examine her bloated abdomen, discovering the tumour. An important thing for Jacqueline and Meg was educating themselves about it and trying to understand what it was all about.

Meg reflects on the stress around the time of diagnosis.

“It had been highlighted that something wasn’t quite right… It was quite overwhelming. What Jacq did really well was to educate herself, and get a sense of the prognosis and what the treatments could be. Through that process, we could have open conversations.”

Finding NECA provided Jacqueline and Meg with the support they needed.

“My oncologist put me onto NECA, which is an amazing support organisation that helps patients understand the cancer… and navigate the medical system. It’s really getting yourself educated so you can manage yourself and others.”

 

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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.