Ensuring the Voice of the Very Severely Affected Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patient Is Heard in Research—A Research Model...
Hi All, I have just had a request from the Department of Health & Social Care policy team for a citation supporting the often cited statistic...
Abstract Persons living with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) vary widely in terms of the severity of their illness....
I am looking for the paper that shows that 25% ofME patients are housebound or bed bound. Thanks!
The 25% ME Group: The Crushing Physical Burden of ME by Simon Lawrence of the 25% ME Group for those with severe ME on 14/08/2018...
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