@tomkindlon@disabled.social
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tomkindlon

@tomkindlon@disabled.social

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness.

With ME/CFS 35 years, severely affected 29 years. Health has deteriorated post Covid (March 2022).

Irish ME/CFS Association* trustee 26 years. 26 publications in peer-reviewed journals.

MEpedia entry which has links to my social media accounts (among other things): https://me-pedia.org/wiki/Tom_Kindlon #ChronicFatigueSyndrome #MECFS #PwME #fedi22 *IrishMECFSAssociation@mastodon.ie

This profile is from a federated server and may be incomplete. Browse more on the original instance.

tomkindlon, to cfs
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tomkindlon, to mecfs
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BBC Chronic fatigue syndrome: Protestors call for specialist ME services

https://www.bbc.com/news/uk-northern-ireland-69000501

Article about a demonstration for specialist ME services in Northern Ireland. Interviews with Joan McParland, founder of Hope 4 ME and Fibo NI, Rosie Pigeon and Rebecca Logan

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tomkindlon, to mecfs
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Post-Exertional Mayonnaise ME and the cult-like nature of psychologisation

https://youtu.be/qxQmMopanY0

Description from @s4me update:

“Podcast interview with Eliza Charley. Highly informed and very well articulated discussion of the experiences of medical, societal and self-gaslighting in the context of medically-induced stigma”

@mecfs

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Recording of 13-minute presentation to recent BACME conference
https://youtu.be/UnZ7L905y6M?si=-JnilaSdhzwG-VnC

Features:
Claire Dransfield, Research Manager, Action for ME
Prof Chris Ponting Principal Investigator, DecodeME @cgatist.bsky.social

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1/

tomkindlon,
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2/

Includes findings from the questionnaire part of the study showing thousands of pwME report that pacing is helpful, CBT is not helpful & GET causes harm. Chris Ponting also highlighted the valuable contribution of partnership with patients.

#MyalgicEncephalomyelitis #ChronicFatigueSyndrome
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