Assessment of major gaps from the perspective of patients, patient advocates and NET health care professionals.
Due to the increasing incidence and prevalence of neuroendocrine tumors (NETs), there is a need to assess any gaps in awareness and care. A survey was undertaken in 2017 to identify perceived unmet needs from the perspectives of patients/families, patient advocates and health care professionals (HCPs). The survey consisted of 33–37 questions (depending on type of respondent) across four areas: information, care, treatments and research.
Recent News
Neuroendocrine Cancer Support
Natter Local and Virtual Support Groups ➡️ https://www.neuroendocrinecancer.org.uk/supporting-you/local-support-groups/ NCUK Online Community ➡️ https://www.neuroendocrinecancer.org.uk/supporting-you/our-online-community/ Living with Neuroendocrine Cancer ➡️...
Neuroendocrine Cancer of the Testes
April is Testicular Cancer Awareness month! Neuroendocrine Cancer of the Testes accounts for less than 1% of all testicular tumours and can be divided into 3 subtypes: Primary Testicular Neuroendocrine Cancer (approximately 76%) Secondary Neuroendocrine Cancer of...
Neuroendocrine Cancer patient journey within a Local Hospital
📽️ Watch Philippa Hand and Anna Koziel discuss the Neuroendocrine Cancer patient journey within a Local Hospital - the London North West University Healthcare NHS Trust experience here ➡️ https://vimeo.com/475986568