Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews

Background: Family caregivers of people with Motor Neurone Disease/Amyotrophic Lateral Sclerosis, an incurable, mostly rapidly fatal neurodegenerative disease, face many challenges. Although there is considerable research on caregiver burden in Motor Neurone Disease/Amyotrophic Lateral Sclerosis, th...

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Veröffentlicht in:Palliative medicine 2015-09, Vol.29 (8), p.737-745
Hauptverfasser: Weisser, Fabia B, Bristowe, Katherine, Jackson, Diana
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Sprache:eng
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