The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study

From symptom onset to a diagnosis of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND): Experiences of people with ALS/MND and family carers – a qualitative study

(2011) Mary R. O'Brien et al.   Amyotrophic Lateral Sclerosis

Meeting the needs of family carers: an evaluation of three home-based palliative care services in Australia

(2010) Kristina Thomas et al.   PALLIATIVE MEDICINE

Part 1: Home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998-2008)

(2010) KI Stajduhar et al.   PALLIATIVE MEDICINE

‘All in the same boat’? Patient and carer attitudes to peer support and social comparison in Motor Neurone Disease (MND)

(2010) Louise Locock et al.   SOCIAL SCIENCE & MEDICINE

Development of the Motor Neuron Disease Carer Questionnaire

(2009) Carole Mockford et al.   Amyotrophic Lateral Sclerosis

How common is depression among ALS caregivers? A longitudinal study

(2009) Judith G. Rabkin et al.   Amyotrophic Lateral Sclerosis

Informal carers of older family members: how they manage and what support they receive from respite care

(2009) Sirpa Salin et al.   JOURNAL OF CLINICAL NURSING

How people with motor neurone disease talk about living with their illness: a narrative study

(2008) Janice Brown et al.   JOURNAL OF ADVANCED NURSING

Satisfaction with services among people with progressive neurological illnesses and their carers in Australia

(2008) Marita P. McCabe et al.   Nursing & Health Sciences