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Abstract Background. The aim of this study was to clarify the pathophysiology of functional dyspepsia (FD), a highly prevalent gastrointestinal syndrome, and its relationship with the better understood syndrome of gastroparesis. Methods. Adult patients with chronic upper gastrointestinal...

Great work

Sorry to hear that, hope you'll improve again soon. Health always comes first.

They defined long COVID as symptoms lasting 3 months or longer after the initialSARS-CoV-2 infection that were not previously present.

Table 2 shows that they tested for 'Fatigue with PEM lasting >14h' and that 35% of the persistent cases had this compared to 0% of the stable controls.

Ok thanks for letting me know. Might try again later.

It's too buggy for me. Had multiple times where it crashed when I tried to save changes. It's also so slow that editing takes 5-10x more time to do than in other programs.

'You will contribute to the social scientific study of illness recovery stories posted to YouTube, developing conceptually innovative and politically vital research.' Weird. This almost sounds like a joke.

Is it my computer/internet or is MEpedia really slow to load?

Thanks I'll try to add some references and improve the text if energy permits. It would be good to have an example of a bad ME/CFS image and a good ME/CFS image clearly next to each other. Perhaps also a section on severe ME and a section that explains core ME/CFS symptoms such as PEM, POTS...

https://thesciencebit.net/category/me-cfs/

These sources might also be useful: How to Report with Accuracy and Sensitivity on Contested Illnesses - The Open Notebook Journalists_-How-to-Report-on-ME_CFS.pdf (meaction.net)

Perhaps we should just try it then. If I understand correctly, MEpedia automatically stores older version so if we want to restore something from it we can always go back to copy it.

All sound good to me. Depends a bit on the other MEpedia editors: will they revert big changes for example if we replace the current with the draft I posted above?

I agree, it should best be rather short and refer to other more respectable sources that provide more info. I've quickly written something down based on the info that was already on the page and other ME/CFS factsheets and guidelines. ME/CFS Myalgic encephalomyelitis (ME), sometimes referred to...

Here's the link: https://me-pedia.org/wiki/Primer_for_journalists What is the best way to approach this? The text doesn't seem very wrong or inaccurate but mostly chaotic: some arguments are repeated in multiple subheadings etc.

Short summary: They searched for RCT, removed those that were high risk of bias according to the Cochrane Risk of Bias tool 2 (RoB2) and converted all baseline fatigue scores of ME/CFS patients into a scale of 0 to 100 point. 60 RCTs with 7088 patients with ME/CFS were included in their...

Great to hear it is ongoing. Thanks for working on this.

I think that would be the correct way to do this experiment. I believe the authors' significance testing is somewhat misleading as it only takes into account the variability (in the measured behavioural response) of the mice, not the variability (in IgG) of human participants. In the...

In the Netherlands they are planning to do a platform trials study for Long Covid. This is mentioned in the study led by Prof. dr. Anske van der Bom but unfortunately not many details are given. https://www.zonmw.nl/nl/artikel/nieuw-netwerk-brengt-samenhang-onderzoek-naar-post-covid