Abstract Background Caregivers of Amyotrophic Lateral Sclerosis (ALS) patients experience
varying psychological responses following the patient's death, including sadness …

Living with a person with amyotrophic lateral sclerosis (ALS) is a complex and difficult
experience. Most research involves only the primary caregiver and uses a quantitative …

Up to 50% of patients with amyotrophic lateral sclerosis (ALS) show mild to moderate
cognitive-behavioural change alongside their progressive functional impairment. This study …

Objective: The aim of this study was to illuminate experiences of finding meaning in life
among spouses of people with amyotrophic lateral sclerosis. Method: Thirteen interviews …

Informal caregivers provide the major part of care for persons with amyotrophic lateral
sclerosis (ALS), a terminal neurodegenerative disease. Apart from providing care, informal …

Multidimensional socio-medical care with an early integration of palliative principles is
strongly recommended in amyotrophic lateral sclerosis (ALS), but provided inconsistently …

Objective: To analyze the quality of life (QoL) and frequency of depression in primary
caregivers of patients with amyotrophic lateral sclerosis (ALS) in two neighboring European …

Background: Amyotrophic lateral sclerosis (ALS) causes distress in caregivers. The present
study aims to examine the association between coping strategies and psychological distress …

Objective: Amyotrophic lateral sclerosis (ALS) affects the life of the family caregiver as well
as the patient. This study aimed to determine the care burden and related factors among …

Our objective was to determine which factors contribute to depression symptoms or
increased burden in caregivers of amyotrophic lateral sclerosis (ALS) patients. The five …