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Items tagged with: PwME


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News Release 26-May-2026:

"Mayo Clinic study details set of options family medicine physicians may consider to treat ME/CFS and long covid"

eurekalert.org/news-releases/1…

Paper:
annfammed.org/content/annalsfm…

#MEcfs #LongCovid @longcovid #PwME #ME #MyalgicE
@mecfs




Emerge Australia:
Communiqué: Fatigue isn't the same as post-exertional malaise (PEM)

"PEM is real. It is serious. And it must not be made worse by misunderstanding."

Signed by researchers, clinicians and advocates.
emerge.org.au/wp-content/uploa…

#PEM #MEcfs #CFS #PwME @mecfs


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As part of ME Awareness week, ME Research UK will consider research progress, and challenges faced, when working to understand key symptoms of ME/CFS.

Today, the focus is on Post-exertional malaise (PEM), the cardinal feature of ME/CFS.

Read more: bit.ly/42bpC2D

#pem #mecfs #cfs #pwme @mecfs


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From ME Awareness Week.
tinyurl.com/MEAW2026

The experience of cognitive dysfunction, ‘brain fog’, cannot be equated to the occasional forgetfulness and lapses in concentration experienced by healthy individuals.

How does 'brain fog' impact your daily life?👇

#mecfs #cfs #pwme #brainfog @mecfs


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This week, ME Awareness week 2026, ME Research UK are considering research progress, and challenges faced, when working to understand key symptoms of ME/CFS.

Today, the focus is on Brain fog (also known as cognitive dysfunction): bit.ly/42bpC2D

#brainfog #mecfs #cfs #pwme @mecfs


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From ME Awareness Week.
tinyurl.com/MEAW2026

Fatigue in ME/CFS is not just tiredness, it is a persistent symptom that is not adequately relieved by rest and significantly impacts activities of daily living.

How does fatigue impact your daily life?👇

#mecfs #cfs #fatigue #pwme @mecfs


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Credit to themsbloke. A high-energy video that might require pacing!

He has multiple sclerosis himself rather than ME/CFS.

Note that the F word is used.

#MEcfs #PwME #MyalgicEncephalomyelitis #ME #MyalgicE
@mecfs



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For ME Awareness week 2026, ME Research UK has considered research progress, and challenges faced, relating to key symptoms of ME/CFS.

Today, the focus is on fatigue: bit.ly/42bpC2D

#mecfs #cfs #fatigue #pwme @mecfs


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From ME Awareness Week.
tinyurl.com/MEAW2026

Unrefreshing sleep is a common issue in ME/CFS, where a full night's sleep, doesn't leave one rested. There can also be other changes in sleep quality/quantity/patterns.

How does sleep dysfunction impact your daily life?👇

#mecfs #cfs #pwme @mecfs


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As part of ME Awareness week 2026, ME Research UK have put together a series of articles considering research progress, and challenges faced, when working to understand key symptoms of ME/CFS.

Today, the focus is on sleep difficulties: bit.ly/42bpC2D

#mecfs #pwme #cfs @mecfs


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From ME Research UK:

Whilst symptoms and comorbidities of ME/CFS are debilitating, the disease can be isolating due to factors such as disbelief from others and lack of accommodation. tinyurl.com/MEAW2026

How has ME/CFS impacted you?👇

#mecfs #pwme @mecfs


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From @meresearchuk

This week, for ME Awareness week 2026, ME Research UK has published a series of articles discussing the progress made, & challenges faced when investigating key symptoms of ME/CFS, a disease which affects over 400,000 people in the UK. Read more: bit.ly/42bpC2D
#pwme #mecfs @mecfs


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ME Research UK:

Highlights of the International ME/CFS Conference 2026 included a presentation on the results from the DecodeME study and discussion of next steps, and a presentation on whole-body positron emission tomography (PET) scans for ME/CFS.

Read more: tinyurl.com/2crj6zd6

#mecfs #pwme @mecfs


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Image is extract from new US study that sounds interesting (but I don't understand)

Association of Coronary Vasomotor Disorders and ME/CFS in Patients Undergoing Invasive Cardiopulmonary Exercise Testing

academic.oup.com/ajrccm/articl…

Invasive Cardiopulmonary Exercise Testing allows more interesting data to be collected than ordinary exercise testing.

#MEcfs #PwME #ME #MyalgicE
@mecfs



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Dr Amolak Bansal & I

I knew I wouldn't be able for whole Dublin event so only arrived at end of Q&A session but all feedback I've heard about his talks has been positive.I enjoyed chat I had with others

@IrishMECFSAssociation meetings left: Sat in Galway & Sun in Sligo.

#MEcfs #PwME #ME #MyalgicE
@mecfs



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I was fortunate to experience a nice family #BlueSunday2026 #TeaPartyForME2026 celebration yesterday in aid of the Irish ME/CFS Association @IrishMECFSAssociation

idonate.ie/fundraiser/BlueSund…

Thanks to my mum for all the work she put in organising it and to everyone who attended. 👍👏

#MEcfs #PwME #CFS #BlueSunday @mecfs


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Delighted to get this coverage in the Sunday World, one of the newspapers with the largest readership in Ireland

#MEcfs #PwME
@mecfs



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Thanks to my mum for getting everything ready for our family
#TeaPartyForME2026 on #BlueSunday2026 (on Sunday).

We’re doing it in aid of the Irish ME/CFS Association @IrishMECFSAssociation
idonate.ie/fundraiser/BlueSund…
but other worthy charities are available (see:
the-slow-lane.com/donation-pag… )

#MEcfs #CFS #PwME #BlueSunday @mecfs


Hope to see some of you at the Dublin meeting tomorrow. I don’t have the energy for the whole event so I will lie in the back of our car till part way through the Q&A section to be around for chat section. Do come over and say hello if you are there. 👋
#MEcfs #PwME @mecfs



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90-second local TV news (in New Mexico) segment on recent study looking at memorial messages for 500 people with ME/CFS

Universal links:
msn.com/en-us/health/medical/s…
or
youtube.com/watch?v=7T91vSdfL5…

This link won't work for many people:
koat.com/article/study-says-ch…

#MEcfs #PwME #CFS @mecfs


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UK government press release: "Thousands of ME/CFS patients to benefit from first genomics study: People with chronic fatigue syndrome, also known as ME, to benefit from world-first genomics study"

gov.uk/government/news/thousan…

#MEcfs #PwME #CFS @mecfs


I had a stressful dream last night, maybe appropriate for May 12! In the dream, I have a new or stand-in GP [family physician] and I am trying to persuade them to sign a disability form. They are smirking away, not very sympathetic. So I have to list my symptoms and losses over the years.

#MEcfs #May12 #May12th #WorldMEday #pwme @mecfs

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