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  3. I, personally, don't think the author goes hard enough on the guy (and the industry he's in) selling "think positively" as a treatment for #MECFS

I, personally, don't think the author goes hard enough on the guy (and the industry he's in) selling "think positively" as a treatment for #MECFS

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mecfsneisvoidlongcovidpwme
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  • thesunnyone@eldritch.cafeT This user is from outside of this forum
    thesunnyone@eldritch.cafeT This user is from outside of this forum
    thesunnyone@eldritch.cafe
    wrote last edited by
    #1

    I, personally, don't think the author goes hard enough on the guy (and the industry he's in) selling "think positively" as a treatment for #MECFS

    Especially considering she admits that the "brain retraining" took about as long to work as *not* doing that (ie, a placebo), and the guy she paid for that placebo was an engineer, not a medical professional.

    But still an ok read of what ME/CFS can be like.

    Original post I saw this:

    https://mastodon.ie/@swoonie/116130323587022897

    Article without the "accept all cookies or pay for a subscription" wall:

    https://www.removepaywall.com/search?url=https://www.theguardian.com/society/2026/feb/24/my-maddening-battle-with-chronic-fatigue-syndrome-on-my-worst-days-it-feels-almost-demonic

    #NEISvoid #LongCovid #pwME

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