Dear all
Some of you group may be interested in joining the International Palliative Care Family-carer Research Collaboration. Please see the attached flyer. I have also set out some references on carers and palliative care that one of our members has kindly sent
Mc Veigh C, Reid J, Hudson P, Larkin P, Porter S, Marley AM. The experiences of palliative care health service provision for people with non-malignant respiratory disease and their caregivers: an all-Ireland study. J Adv Nurs. 2014 Mar;70(3):687-97.
Gadoud A, Macleod U, Kane E, Ansell P, Johnson M. A palliative care approach for people with advanced heart failure: recognition of need, transitions in care, and effect on patients, family carers, and clinicians. The Lancet. 2014 Feb;383:S50.
Bentley B, O’Connor M, Breen LJ, Kane R. Feasibility, acceptability and potential effectiveness of dignity therapy for family carers of people with motor neuron disease. BMC Palliative Care. 2014;13(12).
Giesbrecht M, Wolse F, Crooks VA, Stajduhar K. Identifying socio-environmental factors that facilitate resilience among Canadian palliative family caregivers: A qualitative case study. Palliat Support Care. 2013 Nov 11:1-11,
O’Brien MR, Preston H. Family carer perspectives of acute hospital care following a diagnosis of motor neuron disease: a qualitative secondary analysis. BMJ Support Palliat Care. 2014. Online first.
Funk LM, Stajduhar KI, Outcalt L. What family caregivers learn when providing care at the end of life: A qualitative secondary analysis of multiple datasets. Palliat Support Care. 2014 Feb 13:1-9.
Sampson C, Finlay I, Byrne A, Snow V, Nelson A. The practice of palliative care from the perspective of patients and carers. BMJ Support Palliat Care. 2014.
Mary
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