Are ME/CFS Patient Organizations “Militant”?

Author:

Blease CharlotteORCID,Geraghty Keith J.

Funder

Fulbright Ireland

Irish Research Council (IE)-Marie Sklodowska Curie Global Fellowship

ME Association

Publisher

Springer Science and Business Media LLC

Subject

Health Policy,Health(social science)

Reference53 articles.

1. #ME Action 2016. Progress in ME/CFS patient advocacy: Overcoming the militant meme & why we must keep evolving. #ME Action, February 24. http://www.meaction.net/2016/02/24/progress-in-mecfs-patient-advocacy-overcoming-the-militant-meme-why-we-must-keep-evolving/.Accessed October 20, 2017.

2. Åsbring, P., and A.L. Närvänen. 2002. Women’s experiences of stigma in relation to chronic fatigue syndrome and fibromyalgia. Qualitative Health Research 12(2): 148–160.

3. Blease, C., H. Carel, and K. Geraghty. 2017. Epistemic injustice in healthcare encounters: Evidence from chronic fatigue syndrome. Journal of Medical Ethics 43: 549–557.

4. Blease, C., J.M. Kelley, and M. Trachsel. 2018. Informed consent in psychotherapy: Implications of evidence-based practice. Journal of Contemporary Psychotherapy 48(2): 69–78.

5. Blease, C., S.O. Lilienfeld, and J.M. Kelley. 2016. Evidence-based practice and psychological treatments: the imperatives of informed consent. Frontiers in psychology, 7, 1170.

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