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Living and coping with Parkinson's disease: perceptions of informal carers.

Living and coping with Parkinson's disease: perceptions of informal carers.

http://www.wikidata.org/entity/Q37800758

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Adaptation and psychometric evaluation of the Preparedness for Caregiving Scale, Caregiver Competence Scale and Rewards of Caregiving Scale in a sample of Swedish family members of patients with life-threatening illness.Understanding the barriers to identifying carers of people with advanced illness in primary care: triangulating three data sources Understanding the Burden on Caregivers of People with Parkinson's: A Scoping Review of the Literature The challenges of uncertainty and interprofessional collaboration in palliative care for non-cancer patients in the community: a systematic review of views from patients, carers and health-care professionals More than what the eye can see: the emotional journey and experience of powerlessness of integrated care service users and their carers Good-quality social care for people with Parkinson's disease: a qualitative study Personal identity and the role of 'carer' among relatives and friends of people with multiple sclerosis Reaching Those Most in Need - A Call to Action for Advanced Parkinson's Disease.Learning to live with Parkinson's disease in the family unit: an interpretative phenomenological analysis of well-being.The Level of Knowledge of Parkinson's Disease among Nonprofessional Caregivers in a Movement Disorders Center in Turkey Using meta-ethnography to understand the emotional impact of caring for people with increasing cognitive impairment.Palliative care for Parkinson's disease: has the time come?Palliative Care and Parkinson's Disease: Caregiver Perspectives.Nursing Research in Parkinson's Disease From 2006 to 2015.Core elements to understand and improve coping with Parkinson's disease in patients and family carers: A focus group study.Integrating Patient Concerns into Parkinson's Disease Management.Palliative care for Parkinson's disease: a summary of the evidence and future directions.Caregiver Burden in Parkinson Disease: A Critical Review of Recent Literature.Family caregivers' views on coordination of care in Huntington's disease: a qualitative study.Female Parkinson's disease caregivers have much anxiety and depressive symptom.Service user perspectives on palliative care education for health and social care professionals supporting people with learning disabilities.Living with breathlessness: a survey of caregivers of breathless patients with lung cancer or heart failure.Symptom prevalence, severity and palliative care needs assessment using the Palliative Outcome Scale: a cross-sectional study of patients with Parkinson's disease and related neurological conditions.Palliative care for patients with Parkinson's disease: study protocol for a mixed methods study.The Importance of Connection to Others in QoL in MSA and PSP.The self-management balancing act of spousal care partners in the case of Parkinson's disease.High Burden and Depression Among Late-Stage Idiopathic Parkinson Disease and Progressive Supranuclear Palsy Caregivers.Predicting psychological distress of informal carers of individuals with major depression or bipolar disorder.Validity, Reliability, and Insights from Applying the McGill Quality of Life Questionnaire to People Living with Parkinson's Disease (MQoL-PD).Health and Social Service Access Among Family Caregivers of People with Parkinson's Disease.Adapting psychotherapy for older patients with Parkinson's disease.Experiences of caring for a family member with Parkinson's disease: a meta-synthesis.Quality of life and burden in caregivers for patients with Parkinson's disease: concepts, assessment and related factors.What impacts on the stress symptoms of Parkinson's carers? Results from the Parkinson's UK Members' Survey.Palliative care for Parkinson's disease: Patient and carer's perspectives explored through qualitative interview.Cognitive Behavior Therapy for Anxiety in Parkinson's Disease: Outcomes for Patients and Caregivers.Development of a toolkit to enhance care processes for people with a long-term neurological condition: a qualitative descriptive study.The experience of being diagnosed with Parkinson's disease

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P2860

Living and coping with Parkinson's disease: perceptions of informal carers.

http://www.wikidata.org/entity/Q37800758

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 15 October 2010

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Living and coping with Parkinson's disease: perceptions of informal carers.

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Living and coping with Parkinson's disease: perceptions of informal carers.

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type

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Living and coping with Parkinson's disease: perceptions of informal carers.

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Living and coping with Parkinson's disease: perceptions of informal carers.

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Living and coping with Parkinson's disease: perceptions of informal carers.

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Living and coping with Parkinson's disease: perceptions of informal carers.

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Palliative Medicine

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Living and coping with Parkinson's disease: perceptions of informal carers

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Barbara Cochrane

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Dorry McLaughlin

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Felicity Hasson

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Helen Chambers

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Marian McLaughlin

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Mary Waldron

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P2860

Parkinson's disease: clinical features and diagnosis

Living with a person who has Parkinson's disease: the spouse's perspective by stage of disease. Parkinson's Study Group.

[The situation of people suffering from Parkinson's disease and their relatives in the mirror of literature - an overview].

Cognitive behavioural therapy (CBT) for carers of patients with Parkinson's disease: a preliminary randomised controlled trial.

Health outcomes of bereavement.

Pessimism and optimism as early warning signs for compromised health for caregivers of patients with Parkinson's disease.

Reduced life-space of non-professional caregivers to Parkinson's disease patients with increased disease duration.

Palliative care and support for people with neurodegenerative conditions and their carers.

Caregiver-burden in parkinson's disease is closely associated with psychiatric symptoms, falls, and disability.

Parkinson disease at the end of life: caregiver perspectives.

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177-182

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scholarly article

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10.1177/0269216310385604

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2

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25

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George Kernohan

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2010-10-15T00:00:00Z

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Parkinson's disease