This is Part I of a special issue of Health Promotion and Chronic Disease Prevention in Canada, titled Social prescribing in Canada: An emerging approach to health and well-being.
Editors for this special issue are Kate Mulligan, Kiffer G. Card, and Sandra Allison. It includes an editorial statement, evidence synthesis, original qualitative research, commentary, and an at-a-glance article.
Dr. Jennifer Rayner, the Alliance's Director of Research and Policy, presented this at the 2024 Alliance Conference: Co-Designing the Future of Primary Health Care, as part of the Governance stream. It's an overview of the key things board directors at Alliance-member organizations need to know about sociodemographic (SD) data collection, including:
Patients from equity-deserving populations, such as those who are from racialized communities, the 2SLGBTQI+ community, who are refugees or immigrants, and/or who have a disability, may experience a unique set of challenges accessing virtual models of care.
This resource is also available in English.
Cette la note d’information à été publié par le Centre de collaboration national des déterminants de la santé. Elle este une partie de leur série « Ce qui détermine la santé »
This practice brief is part of the Determining Health series of online resources from the National Collaborating Centre for Determinants of Health (NCCDH).
This article highlights the integrated work of the East Toronto Health Partners and their high-priority communities. It describes how they built a community-embedded learning health system in which patient partners are included in each step of the research cycle, from idea generation to dissemination.