The Making of a Myth: Unreliable Data on Access to Palliative Care in Canada

Jocelyn Downie, Georgia Lloyd-Smith

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Assisted death is now the subject of conversation in the media, in public meetings, and around kitchen tables across the country. A frequent part of many conversations about assisted death law reform is access to quality palliative care in Canada. Throughout the literature and other forms of media, the claim is made that only 16-30% of Canadians have access to palliative care (or, its derivative, 70% are without access). The “16-30%” claim has been widely accepted as a fact. But is it, in fact, true? We are driven to the conclusion that the oft-repeated claim that only 16-30% of Canadians have access to palliative care should be retired. It is based on a misrepresentation of outdated data and it ignores the provision of palliative care outside of the acute care hospital setting.

    Original languageCanadian English
    JournalArticles, Book Chapters, & Popular Press
    Publication statusPublished - Jan. 1 2014

    Keywords

    • Canada
    • Palliative Care
    • Assisted Dying
    • Empirical Data
    • Law Reform

    Disciplines

    • Health Law and Policy
    • Law

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