#pwme

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hbrpgm

@hbrpgm@adalta.social

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hbrpgm

@hbrpgm@adalta.social

adalta.social

@hbrpgm@adalta.social · Feb 25, 2026

📺 https://peer.adalta.social/w/kqRH8K2ZTgjShFoaNHUR1g 🔗 [🇩🇪🇺🇸🇫🇷](https://p4u.xyz/ID_5UF0567O/1) 🔗 [ℹ️](https://anzmes.org.nz/wp-content/uploads/2025/07/Hospital-Care-Plan-for-Severe-Very-Severe-ME_CFS-and-long-COVID-1.pdf") La publication d'un plan de soins spécialisé marque un tournant dans la prise en charge de ces pathologies invalidantes. #longcovid #mecfs #pwme #cfs #severeme

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Tom Kindlon

@tomkindlon@disabled.social

95% of posts on # MyalgicEncephalomyelitis , # LongCovid or # chronicillness . With ME/CFS 37 years, severely affected 31 years. Health has deteriorated post Covid (March 2022).  Irish ME/CFS Association* trustee 28 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

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Tom Kindlon

@tomkindlon@disabled.social

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@tomkindlon@disabled.social · Feb 02, 2026

Living with #MECFS All of these things can be out of reach, or close to, for some #MyalgicEncephalomyelitis patients. Some will be able to attain some of these things at certain points during their illness. From Lu Baker Art https://instagram.com/lubakerart (repeat) #CFS #PwME #ChronicFatigueSyndrome @mecfs@fedigroups.social

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