symptoms

Physiotherapy. 2018 Mar;104(1):129-135. doi: 10.1016/j.physio.2017.07.005. Epub 2017 Aug 4. Symptoms of chronic fatigue syndrome/myalgic encephalopathy are not determined by activity pacing when measured by the chronic pain coping inventory. Thompson DP1, Antcliff D2, Woby SR3...

These last few days I’ve taken to my bed, not feeling bad but just so very very tired and sleepy. I’m not normally sleepy, and although I’m often fatigued and without energy reserves I would not say I normally feel tired. I did have a busy week before this and it could theoretically just be...

Paywalled at https://onlinelibrary.wiley.com/doi/full/10.1111/jsr.12689

http://www.journal-of-cardiology.com/article/S0914-5087(18)30058-3/fulltext#.WrzVHiFZs-E.twitter

https://www.ncbi.nlm.nih.gov/pubmed/29562557

Caroline C. Kingdon, Erinna W. Bowman, Hayley Curran, Luis Nacul, Eliana M. Lacerda https://link.springer.com/article/10.1007%2Fs41669-018-0071-6

https://www.medscape.com/viewarticle/893766 See also this thread about Dr. Bateman's Summary of Clinicians' Summit March 2-3, 2018

I’m currently crashing and I’m just curious about how you would describe your crashes/flares/PEM/bust phases? What does it feel like? (Bearing in mind I won’t be able to read long answers ;)) To me it feels like the top of my spine is inflamed and also the area which is likely my spleen. Light...

Extending blue badge scheme to include non-physical Just listened to a discussion on this on the Jeremy Vine show. ie now https://www.bbc.co.uk/radio/player/bbc_radio_two it will be available to listen to on iplayer later. The last caller had Chronic Fatigue Syndrome, Fibro.

http://www.mdpi.com/2411-5150/2/1/2 Restricted Spatial Windows of Visibility in Myalgic Encephalomyelitis (ME) Nadia S. Ahmed, Irene Gottlob, Frank A. Proudlock and Claire V. Hutchinson * Department of Neuroscience, Psychology and Behaviour, College of Life Sciences, University of Leicester...

One for those who enjoy being wound up by this stuff. The main example they discuss is fibro, not ME, but that's unlikely to reduce your outrage. It is interesting that this sociologist is unquestioningly buying into the assumption that those with contested illness are not really ill at all...

I've seen the word air hunger used with respect to me/cfs, and I'm wondering how to tell if that's what I have. It feels difficult to get enough air, as if I'm taking half a breath instead of a whole one. I don't have mucus. It feels sore and tiring if I expand my lungs all the way. I feel like...

A test of the adaptive network explanation of functional disorders using a machine learning analysis of symptoms Author Information: Melidis C, Denham SL, Hyland ME. University of Plymouth Abstract The classification and etiology of functional disorders is controversial. Evidence supports both...

Perhaps some of you remember the study Housebound versus non housebound patients with myalgic encephalomyelitis and chronic fatigue syndrome from last year by Tricia Pendergrast, Abigail Brown, Madison Sunnquist, Rachel Janice, Julia L. Newton, Elin Bolle Strand and Leonard A. Jason...

I found this report from 2013 which I think is pretty good and accurate (I'm only skimmed thro it though). It is more than the title would suggest. It's a shame that it would seem nothing resulted from it...