Those who take on the global industry that traps research behind paywalls are heroes, not thieves. After my cancer diagnosis this year, I was offered a choice of treatments. I wanted to make an informed decision. This meant reading scientific papers. Had I not used...
Neuroendocrine Cancer Awareness: Bournemouth patient Carolyn Evans and Brighton patient Brian Rubin Neuroendocrine Tumours (NETs) are relatively rare cancers and originate from cells that have the ability to make hormones and can be found anywhere in the body....
This is our amazing NET Patient Foundation ambassador Craig Speirs. Craig is a 39 year old married father of two and he wants to share his brave and honest story with you. Please watch, listen and share ❤️ #FACESOFNETS...
Saturday 8th February 2020 – 7pm til late Live Music, Food, Silent Auction, Charity Prize Balloons & Grand Draw! [npfButton size=“small” text=”Click here to find out more”...
An exciting opportunity has arisen for a registered nurse to join our core staff at the Neuroendocrine Cancer UK (formerly NET Patient Foundation). [npfButton size=“small” text=”Click here to find out”...
‘I feel like I’m sitting on a time bomb’ – Kath reveals how incurable cancer affected her life. A woman with incurable cancer has spoken of how the disease has affected her life. Kath Lewis was diagnosed with neuroendocrine cancer in June 2015, just six weeks before...
