Severe and Very Severe Myalgic Encephalopathy/Chronic Fatigue Syndrome ME/CFS in Norway: Symptom Burden and Access to Care

There is a striking lack of systematic knowledge regarding the symptom burden, capacity for activities of daily living, and supportive measures for the most severely ill ME/CFS patients. The present study seeks to address this through a national, Internet-based survey targeting patients with severe...

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Detalles Bibliográficos
Autores principales: Sommerfelt, Kristian, Schei, Trude, Angelsen, Arild
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963221/
https://www.ncbi.nlm.nih.gov/pubmed/36836022
http://dx.doi.org/10.3390/jcm12041487

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963221/
https://www.ncbi.nlm.nih.gov/pubmed/36836022
http://dx.doi.org/10.3390/jcm12041487

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