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The Ambitions for Palliative and End of Life Care seeks to help transform end of life care across the country. A research team from The Open University set out to explore how people make sense of and use this document in their practice.
Erica Borgstrom and Jon Rainford share how you can help bereaved neurodivergent children with some guidance and advice.
You or someone else you know may be experiencing grief as a widow or widower and finding a way to cope through loss. In this article, Hazel Carter, who cared for her husband through motor neurone disease to the end of his life, describes her experience of grief and becoming a widow and about her thought-provoking insight into her journey from care giver to a self-published author.
What is it like supporting someone who knows they have a life-limiting diagnosis? You might think it is depressing or incredibly difficult. While it can be hard, there is still scope for joy and love. In this article, Hazel Carter shares her experience of what it was like after her husband, Alan, was diagnosed with motor neurone disease (MND).
Death is part of life and is something we all need to face; not only our own death, but the deaths of those around us. Many of us are unprepared for this major event in our lives.
Have you ever considered how the location and spaces in end-of-life care impact on a carer’s experience? Let's look at how attention to detail can make a huge difference.
Death is part of life and is something we all need to face, not only our own death but the deaths of those around us. Yet many of us are unprepared for this major event in our lives.
Patient preference in end-of-life conversations can depend on multiple factors; this article and animation offer guidance for health and social care professionals.