21/09/2026
Head and Neck Cancer patients deserve the right care at the right time regardless of where you live.
We know from speaking to you that far too many people are facing unacceptable delays, from waiting weeks for a GP or dentist to spot the signs (if you can even get an appointment), to sitting on an NHS waiting list while a tumour grows, to being sent from department to department after treatment ends, trying to find someone who understands what "late effects" really means. It's not the fault of the amazing oncologists and other professionals who are working tirelessly to support head and neck cancer patients, it's the system that needs to change. H&NC care needs to be joined up, and properly funded.
We've heard from patients who've waited months for surgery, and others who, years after finishing treatment, are still fighting to access something as basic as free dentistry or a prosthetic they desperately need to eat, speak, or simply feel like themselves again.
We know these aren't small inconveniences. Every delay, before treatment and long after it, has a real, lasting impact on a person's chances and their quality of life.
As Professor RenΓ© Leemans, Chair of the Make Sense Campaign, puts it: "Right Care at the Right Time means looking across the whole head and neck cancer pathway. From awareness and earlier diagnosis to referral and specialist care, we all have a role to play in reducing avoidable delays and helping people with head and neck cancer access the care they need, when they need it."
We believe that care shouldn't depend on your postcode, not at diagnosis, not during treatment, and not in the months and years that follow, when so many patients are still quietly living with the late-effects nobody warned them about.
This Head and Neck Cancer Awareness Week, 21β26 September 2026, we're proud to stand alongside voices from across Europe, united by one shared ambition:
Helping more people get the right care, at the right time, wherever they live, and for as long as they need it.