I've lived for more than 30 years with ME/CFS symptoms that have sometimes kept me bedbound or homebound for months but also were sometimes mild enough for me to work full time for several months in a row. So I am not at all surprised by the finding that people with long COVID sometimes think they're better and then are very much not.
https://www.ucsf.edu/news/2023/08/425961/long-covid-symptoms-can-emerge-months-after-infection
I think the big issue with GET, is that it sounds SO appealing, so it can be hard to turn it down
Having a medical professional tell you its possible to get over ME if you just exercise in the right ways, is somewhat the sirens call of chronic illness
Some days life happens and I have to layer #PEM upon #PEM until I'm just a big pain lasagne, a mess of ground meat and dizzy sauce and flat pasta #mecfs #MyalgicEncephomyelitis #pwmecfs #pwme #PacingIsForRichPeople
#PEM #pacingisforrichpeople #mecfs #myalgicencephomyelitis #pwmecfs #pwme
I have just donated to David Tuller.
I only get to read some of what he writes these days but it’s reassuring to know he's keeping a close eye on the output from those from the biopsychosocial viewpoint who have caused so many problems over the years
Donate link: https://bit.ly/40kHhkY
@mecfs @cfs @longcovid #MyalgicEncephalomyelitis #myalgice #pwme #PwMEs #pwmecfs #pwlc #LongCovid #PostCovid #PostCovid19 #cfs #cfsme #CFIDS #PostViralIllness #PostViralSyndrome
#MyalgicEncephalomyelitis #myalgice #pwme #pwmes #pwmecfs #pwlc #LongCovid #PostCovid #PostCovid19 #cfs #cfsme #cfids #PostViralIllness #postviralsyndrome
One month to go
#May12 #May12th #MyalgicEncephalomyelitis #mecfs #cfs #cfsme #pwme #pwMECFS @mecfs @cfs #ChronicFatigueSyndrome
#may12 #may12th #myalgicencephalomyelitis #mecfs #cfs #cfsme #pwme #pwmecfs #ChronicFatigueSyndrome