Sandi, NSW

Name: Sandi Smyth

NET Type:

  • Small Bowel
“Being told you have an incurable cancer is a big moment to process… My symptoms were quite acute and they had a very sudden onset. Abdominal pain, cramping, vomiting, sweating.”
- Sandi Smyth

Sandy, a 74-year-old was diagnosed with grade two, stage four neuroendocrine cancer in 2022.

“My mum is an inspiration in literal terms. She’s constantly pushed boundaries that she’s found herself up against through her entire life.”

Sandy’s symptoms, including acute abdominal pain, cramping, vomiting, and sweating, prompted quick medical attention. Despite normal test results, a gastroenterologist’s determination led to the discovery of the unsettling truth through imaging. Sandy recalls the life-altering moment, stating,

“Being told that you have an incurable cancer is a big moment to process and then integrate into how you approach and manage your life. Basically from that point on, well… how do I live with that?”

The emotional toll on Sandy’s family is evident, with her son, Jake expressing the difficulty of witnessing Sandy’s vulnerability and the uncertainty of the future.

“There’s a real torture to having that sort of dam hanging over you for such a long time.”

Amid the shock of a diagnosis, Sandy and her family found support in Neuroendocrine Cancer Australia (NECA). Describing NECA as “an organization that punches well above its weight,” Sandy highlights the commitment and advocacy of the individuals at NECA.

“There is a value and an incredible worth and wealth of information that can provide support. So yeah, NECA has been phenomenal.”

Jake concludes with gratitude for his mother’s guidance through life and since her diagnosis, stating,

“This is difficult. This is hard. None of us have had to do this before. Go and show us how to get it done, mum. Go show us how to do this well, and she has, she really has. She’s mapping onto all of us an appropriate way to live life in the midst of a very, very difficult place. And it’s something I’m really grateful for.” 

Sandy’s journey stands as a testament to courage, family unity, and the transformative role of organisations like NECA in providing crucial support for those facing neuroendocrine 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.