'Brain fog': the people struggling to think clearly months after Covid...
Does psychosomatic illness exist? We all know that ME/CFS is NOT psychosomatic. And we know that a lot of studies into psychosomatic stuff (like...
This thread has been split from Concerns about craniocervical instability surgery in ME/CFS ....I know you have a lot of pull on here @Jonathan...
Moderator note: This post has been copied and following posts moved from this thread: Epidemiological and clinical factors associated with...
Threads about articles and people's experiences with LDN have been merged into this single thread. Medscape: Low-dose Naltrexone Explored as...
Moderator note: This post has been copied and following posts moved from this thread: Concerns about craniocervical instability surgery in...
I’ve decided to take a closer look at the evidence for chronic Lyme disease. I’ve chosen to skip issues relating to the persistence of the...
Threads have been merged Fatigue as presence of sensation or absence? This is another one of those posts where I try to describe some highly...
Moderator note: This post has been copied and subsequent posts moved from this thread: Concerns about craniocervical instability surgery in...
I’m after some information about scales which measure severity of disease in ME/CFS, in terms of functional impairment (mild vs severe). There...
I would like to use this thread for a discussion on the effects of a lack of blinding in randomized trials, something that frequently comes up in...
Does anyone know of research into sensory sensitivities in ME? (I know MERUK have something in motion, but is there anything already published?)...
Moderator note: This post and the next two have been copied, and subsequent posts moved from this thread: JAMA -"Advances in understanding the...
All Having skimmed over contents over the past week, I can't see substantive difference between gulf war syndrome sufferers and being a pwME. I...
Thought it might be helpful to have a thread on the use of this scale. The HADS is often used in research into ME/CFS because it was, as is said,...
(This isn't really "news" but I didn't know where else to put this thread.) Firstly let me clarify that I am not talking about the bogus...
This post and others on the thread have been copied or moved from this thread on MEAction Research Summary 2019 One example: The ME Action...
I’m wondering if anyone is aware of any appropriate mouse models of ME/CFS? I’m familiar with the Japanese model of putting the mice/rats in a...
I decided to start this thread based on the latest findings of the Whole Genome Sequencing webinar from SolveCFS. During the seminar a slide was...
Has anyone had their complement levels tested? Is a low C3 relevant??? My C4 has come back at the bottom of the normal range, and my C3 is below...
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