JaimeS
Senior Member
- Messages
- 3,408
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- Silicon Valley, CA
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Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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If Morris and Maes are cited there's no way I will contribute to this.. They're still thinking this a retrovirus!
I don't think it's fair to object to a source due to the name of the researcher. Rather it should be the quality of the piece of research which counts. People can have bizarre theories, but still produce proper research on that or other topics.I'm having a hard enough time with Myhill and De Meirleir being cited!
I feel it would be unprofessional to comment on them, at least at this point, as it would end of being quite provoking. If you look at the history of Morris he is a highly dubious person. I will try and find some sources that can say it better than I can. But I may need some time as I don't want to go off half cocked.
In the meantime I would suggest finding his history of what he did to this forum. I'm not sure I know where to look but will try. This guy has serious problems and there are few people I would feel comfortable saying that.
I've confused Morris and Moss-Morris before too.
....wait, are you thinking of Moss-Morris? He's part of the biopsychosocial crowd. You wouldn't be the first:
Rona Moss-Morris is a woman, and I think that the Prof Morris I was referring to was a Richard Morris... it can get confusing!
Phew. I've been following this thread and trying to work out who the heck Morris was (conclusion: a Bee Gee. Oh, hang on, that's Maurice ....)
I find their research into ME disappointing.
LOL![]()
Quite right. Though some might say "Seen worse".
TragedyI find their research into ME disappointing