I thought I would repost this to highlight again some of the many varied symptoms that can be found in #MyalgicEncephalomyelitis/#ChronicFatigueSyndrome

Particularly relevant when similarities with the #LongCovid presentation in some people are being missed

@mecfs
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome @longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 #LC #Covidlonghaulers #PostCovidSyndrome #longhaulers #COVIDBrain #NeuroPASC

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"Reimagining You: Finding identity, meaning, and purpose when life doesn’t look the way it used to"

https://onelifelivedwell.substack.com/p/reimagining-you

Blog post by a sympathetic and knowledgeable occupational therapist who specialises in ME/CFS and long Covid.

@longcovid
#LongCovid #PASC #PwLC #postcovid #postcovid19 @mecfs
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #chronicillness #ChronicIllnesses #Spoonies #Spoonie #ChronicallyIll #Fibromyalgia #Fibro #FMS #FM #POTS @pots

#FollowFriday If you are interested in the current research of #MEcfs #CFS etc. follow @tomkindlon and @IrishMECFSAssociation for news and informations.

Fresh and new are the groups for these topics: @mecfs and @longcovid

How to use #groups in the Fediverse: https://fedi.tips/how-to-use-groups-on-the-fediverse/

#LongCovid #Covid #health #healthResearch #corona

How to use discussion groups on Mastodon and the Fediverse | Fedi.Tips – An Unofficial Guide to Mastodon and the Fediverse

An unofficial guide to using Mastodon and the Fediverse

RenderATL 2026 - CfP Watch

A collection of open Call for Papers for (aspiring) speakers.

DevBcn 2026 - CfP Watch

A collection of open Call for Papers for (aspiring) speakers.

Interesting new research from Sweden:

Low Vasopressin In Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

https://www.endocrinepractice.org/article/S1530-891X(25)01349-7/fulltext

Vasopressin or antidiuretic hormone helps the body hold on to fluid

#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome @mecfs

New article by Action for ME's CEO.

Briefly discusses DecodeME, LOCOME before arguing that ME/CFS research is underfunded in the UK & calls for more funding & the creation of a Strategic Research Hub for ME

https://www.lbc.co.uk/article/treatment-chronic-fatigue-myalgic-encephalomyelitis-opinion-5HjdQ46_2/

@mecfs
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome

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Blog post about using props (like pillows, bolsters, and wedges) to help promote relaxation, by a sympathetic and knowledgeable occupational therapist who focuses on ME/CFS and long Covid.

https://onelifelivedwell.substack.com/p/repose-the-new-relaxation

@longcovid
#LongCovid #PASC #PwLC #postcovid #MEcfs #chronicillness #Spoonie @mecfs
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #PosturalOrthostaticTachycardiaSyndrome #POTS @pots

New:

Extract from: "Journal Publishes Confusing Section on “Enduring Symptoms” by David Tuller which mainly focuses on critiquing the discussion between 2 UK biopsychosocial proponents

https://virology.ws/2025/12/31/trial-by-error-journal-publishes-confusing-section-on-enduring-symptoms

@mecfs
#MEcfs #CFS #PwME #MyalgicEncephalomyelitis #ChronicFatigueSyndrome

ME Research UK:

Concluding our review of ME Research UK's charity year

Informing - https://tinyurl.com/fdke3pya
Influencing - https://tinyurl.com/vdupvzcz

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME @mecfs