User perspectives on a psychosocial blended support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: a qualitative study

BACKGROUND: Partners are often the main caregivers in the care for patients with amyotrophic lateral sclerosis (ALS) and progressive muscular atrophy (PMA). Providing care during the progressive and fatal disease course of these patients is challenging and many caregivers experience feelings of dist...

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Detalles Bibliográficos
Autores principales: de Wit, Jessica, Vervoort, Sigrid C. J. M., van Eerden, Eefke, van den Berg, Leonard H., Visser-Meily, Johanna M. A., Beelen, Anita, Schröder, Carin D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570885/
https://www.ncbi.nlm.nih.gov/pubmed/31202270
http://dx.doi.org/10.1186/s40359-019-0308-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570885/
https://www.ncbi.nlm.nih.gov/pubmed/31202270
http://dx.doi.org/10.1186/s40359-019-0308-x

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