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Items tagged with: PwME
Well, not the happiest intro but I’l cut/paste this here while I still remember then add a proper intro spoons allowing..⬇️
Please #boost and share to other platforms spoons allowing.
Seems I’m desperate enough to go to the media for help. Yes, the trapped woman in the article below is me.
My story: thecanary.co/global/world-anal…
More info on how to help:: buymeacoffee.com/halcionandon/…
I’ve tried every level of government and they simply won’t help. Please ask people if they have a spare room or somewhere to go. Maybe you have somewhere?
Is anybody a #DisabilityAdvocate? #SocialWorker? Need help.
Please don’t give me contacts for domestic violence orgs. They don’t help disabled people with housing & only offer counselling. Also, that list of disability advocates going around for #Melbourne #Australia (where I am) is outdated - there aren’t any in my catchment. So I’m looking for volunteers with some background.
Thanks for reading
#PwME #LongCovid #MECFS #Hypothyroidism #ChronicIllness #Neisvoid #NacissisticAbuse ##Housing #Dysautonomia #SocialWork #MedMastodon #PWLC #MutualAid
#HumanRights #Press
@mecfs @chronicillness @neisvoid
@disability @disabilityjustice @socialwork @dyssupport
@mutualaid
(If I’ve broken any rules in posting this, please let me know.)
[Thread]New article "Safer Hospital Care for Severe ME".
worldmealliance.org/2024/08/sa…
Of course many of the tips are relevant to patients of all severities.
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME #SevereME @severeme @mecfs
1/
Safer Hospital Care for Severe ME - #SevereMEDay 2024 - World ME Alliance
Severe ME Day, held on the 8th of August each year, is a significant occasion for the World ME Alliance and the global community affected by Myalgic Encephalomyelitis (ME).World ME Alliance
New Leicester (UK) #MEcfs & #PostCovid study that is recruiting
Investigating the impact of ME/CFS & #LongCOVID on visual perception & sustained attention using Pupil Frequency Tagging & EEG
dougiebarrett.github.io/Lab/pa…
ME Research UK-funded
Not a biopsychosocial study
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME