Problem: Cancer patients commonly feel unsupported when transitioning from active treatment to surveillance and follow-up care.
Objective: The aim of this project is to establish a patient passport. This Passport is the patient’s personal document and is introduced and explained to them at diagnoses. They are encouraged to bring it with them to each hospital visit so that they can update their information at that time. They can use it as a place to store their information during their treatment and as a place to refer back to for treatment details, advice post operatively or on the side effects of treatment and when treatment ends, it can contain the agreed plan for follow up surveillance. It is hoped that this will support patients to take ownership of their follow up care and surveillance
Implementation status: Pilot initiative