Welcome to the Patient Voices Network! Everyone must complete an orientation in order to participate in engagement opportunities. The orientation will cover everything patient partners on Vancouver Island need to know to be a PVN member and answer any questions they may have.
Patient and family partners should not be a check box on research proposals! They need to be involved right from the start. I know patient and family partners are doing their part by providing their knowledge to researchers from their lived experience. It’s a win-win for us to work together through PVN to make sure our input drives improvements.