In 2010 when Jamie was only 32 years old, with a 6-month-old baby at home and the world at her feet, she was diagnosed with a mid-gut neuroendocrine tumour (NET).
Jamie, diagnosed
2010
The Senate laid out clear recommendations to improve care
for NET patients. The government is yet to respond.
Our role is vital to the lives and outcomes of those impacted by neuroendocrine cancer.
Our vision is clear: to assist patients and carers, lobby for new treatments and investigations, raise awareness among the medical community and public about NETs, and support Australian research in neuroendocrine cancers. To achieve this, we’ve developed a National Action Plan for nationwide improvement in neuroendocrine cancer care and research.
Supporting your journey when you need it the most.
To improve the care and experience of patients across Australia suffering from Neuroendocrine Tumour (NET), an Optimal Care Pathway (OCP) is now available to ensure NET patients receive the right care, at the right time, in the right place.
NeuroEndocrine Cancer Australia is the only non-for-profit medical charity providing support to Australians living with neuroendocrine cancers.
We are governed by the following five pillars:
These pillars have been created to give neuroendocrine cancer patients, their families and friends, a voice in the community and access to the care and treatment that they deserve.
NeuroEndocrine Cancer Australia Support Service
Contact our NET Nurses
Our NET Nurses are here to help support you from diagnosis to treatment, and living well with NETs.
