Filling the gap in service provision. Partners as family carers to people with Parkinson's disease: A Scandinavian perspective.
Ellen Gabrielsen HjelleHelle Rønn-SmidtAnita HaahrSilje Bjørnsen HaavaagDorthe SørensenMaría Victoria Navarta-SánchezMari Carmen PortilloLine Kildal BragstadPublished in: Chronic illness (2023)
A recommendation for practice is recognition of the complex roles of partners to people with PD and reaching out to both regularly to determine needs. This may enhance the collaboration between partner carers, people with PD and healthcare providers, ensure sustainability of the system and optimise living with PD in the family.