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.”

 

Share this article

More patients diagnosed with Small Bowel

Denise, NSW

  • Small Bowel
When the histopathology returned six days post-surgery, everything made sense. A slow-growing cancer: Carcinoid, or Neuroendocrine Tumour, a term only just coming into use at that time. My feelings? Overwhelmingly, relief. Validated after two and a half years of being dismissed. Some anger, too, but mostly relief to finally have a diagnosis I could understand and act on.

Nat, SA

  • Small Bowel
Before I was diagnosed, I had ongoing medical issues including bowel obstructions and endometriosis, which made it easy to dismiss my symptoms. But I started experiencing rashes across my chest, hot flushes, shortness of breath and heart palpitations. Something did not feel right.

Allison, WA

  • 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.”

Our NET Nurses are here to help support you from diagnosis to treatment, and living well with NETs.

Free and confidential, our NET nurses are available Monday – Friday, 9am – 5pm (AEDT).