Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research—A Research Model

Most of the research about Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has focused on ambulant patients who are able to attend clinics. It is estimated that 25% of people with ME/CFS are severely, or very severely, affected and are housebound or bedbound; some require tube feeding. D...

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Bibliographic Details
Main Author: Helen Baxter
Format: Article
Language:English
Published: MDPI AG 2022-07-01
Series:Healthcare
Subjects:
Online Access:https://www.mdpi.com/2227-9032/10/7/1278