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May is Myalgic Encephalomyelitis (M.E.) Awareness Month.

You can help by sharing and/or liking this image.

Day 5

#MEcfs #CFS #MyalgicE #MyalgicEncephalomyelitis #chronicfatiguesyndrome

@mecfs

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May is Myalgic Encephalomyelitis (ME) Awareness Month.

You can help by sharing and/or liking this 102-second video. "What is ME/CFS?" (excerpt from LEFT OUT, reproduced with kind permission from UpNorth Film, Norway)

https://youtu.be/bXAdsrk0FZw

#MEcfs #CFS #MyalgicEncephalomyelitis

Day 5

@mecfs

What is ME/CFS? (excerpt from LEFT OUT, reproduced with kind permission from UpNorth Film, Norway)

YouTube

Hi there,

I just wanted to surface a Reddit post here on the fediverse. A very severe/extreme ME/CFS sufferer is currently in a precarious situation and needing financial support.

Her name is Ali and you can read more about her situation on Reddit here:

https://www.reddit.com/r/cfs/comments/1t11zip/fundraiser_for_ali_veryextremely_severe_me/

Thanks.

#MECFS #MyalgicEncephalomyelitis #CFS #MyalgicE #ChronicIllness #ChronicFatigue #ChronicFatigueSyndrome #spoonie #spoonies

Given all talk re: Post Exertional Malaise/Post Exertional Symptom Exacerbation in #LongCovid:

Here is "Symptoms made worse due to physical or cognitive exertion" in #MyalgicEncephalomyelitis & #ChronicFatigueSyndrome

Also shows all the range of ME/#CFS symptoms

From: "Assessment of Post-Exertional Malaise (PEM) in Patients with ME and CFS: A Patient-Driven Survey" (2019) by a Leonard A. Jason team
https://pmc.ncbi.nlm.nih.gov/articles/PMC6468435/pdf/diagnostics-09-00026.pdf

#MECFS @mecfs @longcovid

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‪May is Myalgic Encephalomyelitis (M.E.) Awareness Month.‬

‪You can help by sharing and/or liking this image.‬

‪Day 3‬

#MyalgicE‬ ‪#MyalgicEncephalomyelitis
#mecfs
@mecfs

3/

May is #MyalgicEncephalomyelitis (ME) Awareness Month

You can help by liking +/or sharing this video

(9 minutes) This is ME (2020) "A short film exploring 'Spoon Theory' told through the eyes of a young woman struggling with ME/CFS"
https://vimeo.com/338532785

Day 3

#mecfs #PwME

@mecfs

This is ME (2020)

A short film exploring 'Spoon Theory' told through the eyes of a young woman struggling with ME/Chronic Fatigue Syndrome ** Follow Pickup_Films on Twitter…

Vimeo

The Mansion - a short story

https://discuss.tchncs.de/post/59502423

The Mansion - a short story - tchncs

Lemmy

Latest news article from View from the Trenches of Myalgic Encephalomyelitis covers a variety of topics:

- ME Global Chronicle (MEGC) No. 56
- Hillary Johnson’s latest articles
- Loss of advocate David Black
- Dr. Groysman
- David Tuller - Last Berkeley Fund Raiser
- Nasal spray to treat cognition issues
-Hummingbirds’ Foundation for ME Website Update
#MyalgicEncephalomyelitis #longcovid

https://colleensteckelmeiccinfo.substack.com/p/news-2026-may-1

News: 2026 May 1

This, that…and some other stuff

View from the Trenches of Myalgic Encephalomyelitis

Perth folks, I can't find a shareable source of info but I got an email from AusME saying they now have collection points in WA for their research biobank. General details here:
https://emerge.org.au/ausme/

#MyalgicEncephalomyelitis #LongCovid

AusME Registry & Biobank – Emerge Australia