Knowledge Hub
Knowledge Hub
Free, evidence-based resources for patients, families and health professionals navigating neuroendocrine cancer in Aotearoa New Zealand. Written in plain language, reviewed by clinicians.
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NECNZ founder and former CEO shares her NETs story
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Dave's NET story, part 2 – reflections fifteen years on from diagnosis, on living well with neuroendocrine cancer.
Dave's NET story, part 1 – how a diagnosis of adenocarcinoma with unknown primary led him to a neuroendocrine tumour answer.
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Bryan documents his NETs journey from an unexpected diagnosis
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Jenny's story – small intestinal NETs running in her family, and the path to genetic testing and ongoing care.
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Lynette shares her experience of a malignant carcinoid tumour – diagnosis, treatment, and life beyond it.
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Chris's NET cancer experience has created more upsides to his life than downsides
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Peter self-funded a treatment that we're now campaigning for
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Suzanne shares her experience of pulmonary neuroendocrine carcinoma – diagnosis, treatment, and what she would tell anyone newly diagnosed.
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Malcolm's story – living with a pancreatic neuroendocrine tumour and liver secondaries, told in his own words.
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