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#MyalgicEncephalomyelitis
Tom Kindlon
TomKindlon
New: “Post-Covid syndrome, Myalgic Encephalomyelitis, and the recurring pseudoscience of mass hysteria” (July 27) by Prof Brian Hugheshttps://thesciencebit.net/2020/07/27/post-covid-syndrome-myalgic-encephalomyelitis-and-the-recurring-p
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Tom Kindlon
TomKindlon
Press Release from NICE about its new draft #MECFS guidelines that are out for consultationhttps://www.meresearch.org.uk/nice-guideline-update-press-release/“The draft guideline also highlights the importance of ensuring that people remai
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Karen
hopeforMEyet
I've avoided Twitter since October after becoming bedbound, but needs must Since Paul Garner is keen to promote positive thinking as a cure for ME, I'd like to remind
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Tom Kindlon
TomKindlon
[Thread]“Re: Management of post-acute #covid19 in primary care - A warning to #PostCovid sufferers and their clinicians” by @ozfish (who has #MEcfs for 30 years)https://www.bmj.com/content/370/bmj.m3026/rr-7#LongCovid #LongHaulers #Scep
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Brad Hoffman
brad_with_a_mal
The hidden COVID tidal wave you dont see on the graphsEvery day I come across one graph or another showing the numbers of new cases, rolling cases, hospitalizations, and/or deaths
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Craig
MECFS5
@MattHancock if a test becomes available for #CFSME would our government be willing to accept it as diagnosis. Those people should then be assisted to claim benefits. I've spent half
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Ivana Fulli
DrFulli
#LongCOVID19 thread.Even only #chronicSmellingLoss #Anosmia can be devastating emotionally:Affected people loose any enjoyment in domains like food, ignore bad smelling warnings of many hazards, can become anxieux about body odours
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