95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness.
With ME/CFS 37 years, severe ME 31 years.
@IrishMECFSAssoc trustee 29 years
26 publications in peer-reviewed journals
Social media: https://me-pedia.org/wiki/Tom_Kindlon
Tom Kindlon
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I am so proud to be associated with those living with very severe #ME. You are the most courageous, determined and intelligent people ever. So few know anything about what you are facing, or how the UK State lines up to attack you through NHS 'standard operating procedures'.
Update due justice4me.uk
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"findings suggest that microvascular impairment may represent a persistent feature of PCS rather than a change attributable to physical deconditioning, with objective endothelial and perfusion abnormalities documented months after infection"
#postcovid19 #PostCovidSyndrome
Campaigning for ME (Myalgic Encephalomyelitis) to be medically managed safely, to protect families from permanent disability or death from neglect of the illness.
A woman with ME discusses the effect the illness has had on her a bit in this programme
www.tg4.ie/en/player/ca...
#MEcfs #PwME #Gaeilge #AsGaeilge #spéirgorm #speirghorm
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If no rain is expected, I do go out to the back garden.
