1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Join the National PR Campaign for ME: Power to the Patient (P2tP)
Have you had enough of all the neglect and abuse of ME/CFS patients? Gabby Klein says now is the time for a National PR Campaign for ME/CFS to impress a change. Join the Patient Revolution to restore power to ME patients ...
Discuss the article on the Forums.

(from 2006) CBT for Relatively Active and for Passive CFS patients

Discussion in 'Latest ME/CFS Research' started by Dolphin, Jul 31, 2010.

  1. Dolphin

    Dolphin Senior Member

    Messages:
    6,865
    Likes:
    6,131
    This is not new but I don't think has been highlighted much in CFS circles. I thought I would post it as CBT studies involving Gijs Bleijenberg and his team are often quoted to claim that CBT is an evidence-based therapy for CFS.

    However, compliance generally isn't measured and I'm not convinced that most patients are actually following the program which the authors claim is the way to treat CFS.

    In particular, I think the percentage of "relatively passive" CFS patients who would follow this program can't be particularly high:
    ETA: people shouldn't feel they have to read it all. It's not that exciting.

    -----------

    ==========
    Treatment manuals:

     

See more popular forum discussions.

Share This Page