Abstract
Background
Meaningful patient and public involvement (PPI) is increasingly recognised as an important component of health research. However, relatively few publications describe patient involvement from the first-person perspective of a patient partner or patient leader. This commentary reflects on my experience as a patient leader in the COMFORT Nursing Programme, a research programme developing person-centred approaches to symptom management for people living with advanced kidney disease and their informal caregivers.Main body
I reflect on my experiences as a person living with kidney failure, an informal caregiver, and Chair of the Danish Kidney Association while working alongside researchers in the COMFORT Nursing Programme. I describe what motivated my involvement, how an equal partnership was developed, and how my lived experience, patient-leadership role and wider contact with patients and informal caregivers contributed to the research. My involvement included reviewing study materials and language, contributing to research discussions and priorities, supporting recruitment of patient partners, and participating in dissemination. I also reflect on the time and commitment required for intensive patient involvement, the challenges posed by fluctuating health, and the need for research teams to accommodate different preferences and capacities for participation.Conclusion
My experience illustrates that patient leadership can extend beyond sharing personal experiences to contributing to research priorities, methods, communication and dissemination. Patients and informal caregivers can bring forms of expertise that complement clinical and research knowledge. Meaningful involvement should therefore provide genuine opportunities to influence research while remaining flexible enough to accommodate individual needs, health circumstances and preferred levels of participation.