tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

Read the latest (US) National Institute of Neurological Disorders and Stroke [NINDS] Director’s Message from Dr. Walter Koroshetz: Advancing Research on ME/CFS.

https://www.ninds.nih.gov/news-events/directors-messages/all-directors-messages/advancing-research-mecfs

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

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon,
@tomkindlon@disabled.social avatar
tomkindlon,
@tomkindlon@disabled.social avatar

3/
Different diagnostic criteria available for ME/CFS with a concise history of timelines.

From:
#MyalgicEncephalomyelitis / #ChronicFatigueSyndrome: the biology of a neglected disease

Free:
https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1386607/full

#MEcfs #CFS #PwME
@mecfs

tomkindlon,
@tomkindlon@disabled.social avatar

4/
Infectious pathogens thought to promote the development of ME/CFS including viruses, bacteria, fungi, and parasites

From:
#MyalgicEncephalomyelitis / #ChronicFatigueSyndrome: the biology of a neglected disease

Free:
https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1386607/full

#MEcfs #CFS #PwME
@mecfs

ahimsa_pdx, to mecfs
@ahimsa_pdx@disabled.social avatar

Here's the News in Brief summary from the Science for ME forum, for week starting May 27:

https://www.s4me.info/threads/news-in-brief-may-2024.38393/#post-535789

This summary includes news articles, videos, research, advocacy, coming events, and more.

@mecfs @longcovid

#MEcfs #LongCovid #ChronicIllness #MyalgicEncephalomyelitis #Science4ME

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

ME Research UK

Part 2 highlights from the 1st International Conference on Clinical and Scientific Advances in ME/CFS and Long COVID, including-

  • History of ME/CFS

  • Clinical assessment of ME/CFS and

  • Immune and metabolic abnormalities

Read: https://www.meresearch.org.uk/1st-international-conference-on-clinical-and-scientific-advances-in-me-cfs-and-long-covid-lisbon-highlights-part-2/

@mecfs

duna, to longcovid
@duna@hachyderm.io avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

🧵
The Untapped Power of “We Don't Know”: Epistemological Humility in the Era of #COVID19

https://journals.sagepub.com/doi/10.1177/23743735241252475

"There are several arguments for how saying “We don’t know” might benefit patients.

@longcovid
#LongCovid #PwLC #PostCovidSyndrome #LC #PASC #postcovid @chronicillness
@spoonies #chronicillness #spoonie @mecfs
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME
1/

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

"Tin Foil Hat Territory? The Gupta Program, the Lightning Process and the BPS [biopsychosocial] in and ME: How brain retraining therapies intersect with the biopsychosocial model"

https://longcovidadvocacy.substack.com/p/tin-foil-hat-territory-the-gupta

Hashtags:
@longcovid

@mecfs

tomkindlon,
@tomkindlon@disabled.social avatar

4/

"We need to be vigilant and educated to spot this charlatanry. We need therapeutic treatments that actually work and stop gaslighting those with post-acute viral disease."

@LongCovidAdvoc @longcovid @mecfs

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

Responding to a BBC programme, Dr Edzard Ernst highlights data showing many are harmed by the Lighting Process and the lack of evidence for claims made.

He concludes: "Does anyone think that LP or its promoters are remotely serious?"

https://edzardernst.com/2024/05/almost-anyone-can-recover-from-long-covid-just-pay-a-lot-of-money-for-the-lightning-process-no-please-dont-i-was-joking/

@longcovid

@mecfs

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

🧵
The Norwegian Broadcaster NRK has an article about the survey from the European ME Alliance (EMEA) which included 11 000 people from 44 countries. 74% answered they have little to no health care.

Google translation:
https://www-nrk-no.translate.goog/sorlandet/3-av-4-svarte-at-de-fikk-lite-eller-ingen-stotte.-anja-vil-vaere-en-inspirasjon-for-andre-med-me-1.16838776?_x_tr_sl=no&_x_tr_tl=en&_x_tr_hl=en-US&_x_tr_pto=wapp

@mecfs

1/

tomkindlon,
@tomkindlon@disabled.social avatar

2/

One of the authors of the survey and deputy for the Norwegian ME Association Trude Schei calls for more knowledge among GPs and to not push ME patients into treatments with no documented effect.

Despite the results from the survey, paediatrician and ME researcher Maria Pedersen claims CBT has good effect as treatment for ME.

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

tomkindlon,
@tomkindlon@disabled.social avatar

3/
The article also discusses 22-year-old Anja Vesterhus who has lived with ME for 12 years and wants to help others by sharing on Instagram.

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

halcionandon, to chronicillness
@halcionandon@disabled.social avatar

Unsure how common this is in other affecting cognition, but when you have the writing errors you’re almost guaranteed to make are:

  1. Double the same word
    or
  2. Exclude it altogether
    Or do both!

So frustrating & the sicker you are the worse it gets. You simply can’t see mistakes! Other problems too ofc but I’ve found this is the most common error made by

I did both when composing this!

I miss my old brain!
😩

@mecfs @longcovid @chronicillness

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

New sympathetic editorial:

Medical students highlight the importance of medical education, kindness, compassion & belief when learning about patients with #MyalgicEncephalomyelitis / #ChronicFatigueSyndrome

Free:
https://journals.sagepub.com/doi/full/10.1177/14782715241255977

#MEcfs #CFS #PwME @mecfs

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

(UK)
"Government funders of research in ME/CFS, academic researchers and persons or representatives of persons/groups with lived experience of ME/CFS came together to develop a Researcher Toolkit"

https://www.cso.scot.nhs.uk/toolkit-now-available-to-help-me-cfs-researchers/

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

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

MEAction : Celebrating An Impactful Campaign

https://www.meaction.net/2024/05/17/teachmetreatme-celebrating-an-impactful-campaign/

"Over the past several months, clinicians and medical students across the U.S. have attended presentations, roundtables and conferences to learn about ME/CFS – and how to take the Mayo Clinic Proceedings Continuing Medical Education course on ME/CFS."

@mecfs

1/

tomkindlon,
@tomkindlon@disabled.social avatar

2/

In the UK, #MEAction UK advocates pulled off a wonderful Postcard to Doctors Campaign encouraging medication professionals to take a CPD module on ME"

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

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar

NHS England Launches New E-learning Module on ME/CFS - ME Association article

https://meassociation.org.uk/2024/05/nhs-england-launches-new-e-learning-module-on-me-cfs

MEA's article includes a summary of the content of the module which covers definition, causes, symptoms, management & links to ME organisations.

Discussion thread:
https://www.s4me.info/threads/me-association-nhs-england-launches-new-e-learning-module-on-me-cfs.38610/

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

1/

tomkindlon, to mecfs
@tomkindlon@disabled.social avatar
tomkindlon,
@tomkindlon@disabled.social avatar

2/

Full paper has now been published:

The German Multicenter Registry for ME/CFS (MECFS-R)

https://www.mdpi.com/2077-0383/13/11/3168
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME
@mecfs @mecfs_de

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