Irish ME/CFS Association
irishmecfsassoc.bsky.social
Irish ME/CFS Association
@irishmecfsassoc.bsky.social
Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association

NB: Posts should not be considered advice

Registered Charity Number 20100254
CHY 22039

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME. Some #LongCovid items also
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‪A second pack has now sold out. We also only have one pack left for one set; 2 packs left for another set; and 4 packs left for 2 other sets.‬

‪#MEcfs #MyalgicE‬ #MEcfs #PwME #CFS
November 25, 2025 at 6:12 PM
Reposted by Irish ME/CFS Association
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Trial by Error by David Tuller Another Exercise Trial with Clinically Insignificant Findings

virology.ws/2025/11/21/t...

Screenshot from latest Science for ME weekly update

#LongCovid #PASC
November 25, 2025 at 1:39 AM
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67 comments have now been posted in reply to this on FB.
A lot of them are not specific to Ireland (some are specific to the UK) so may be of interest to others in the same or a similar situation elsewhere:
www.facebook.com/TomKindlonME...
Tom Kindlon's ME CFS & related page: News, Research and more
A woman (from Ireland) has asked me the following question and has given me permission to share it to see what comments come in. -- Hi I am wondering if I could get some advice regarding a doctors...
www.facebook.com
November 23, 2025 at 10:55 PM
Can you let us know who this is please? Feel free to private message us if you prefer. Thank you very much.
November 23, 2025 at 10:47 PM
Reposted by Irish ME/CFS Association
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I’ve heard people with ME say they react badly to monosodium glutamate (MSG)

#MSG
November 22, 2025 at 3:49 PM
Reposted by Irish ME/CFS Association
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"Glutamate, which is found in high levels in processed foods & also occurs naturally in some foods like tomatoes and mushrooms, is the most abundant excitatory neurotransmitter in the nervous system, where it is known to play a role in mediating pain."

#migraines #headaches
November 22, 2025 at 3:39 PM