Alastair Miller is lead author of this frustrating new piece in the BMJ: “Patients with severe ME/CFS need hope & expert multidisciplinary care”
https://www.bmj.com/content/389/bmj.r977
It mentions recovery.Here’s my post showing the real evidence that he again ignores:
https://www.s4me.info/threads/dr-alastair-millers-misleading-claims-about-effectiveness-of-the-english-nhs-rehab-me-cfs-clinics-royal-society-of-medicine-webinar-in-sept-20.17120/#post-292167
#MEcfs #PwME
https://www.bmj.com/content/389/bmj.r977
It mentions recovery.Here’s my post showing the real evidence that he again ignores:
https://www.s4me.info/threads/dr-alastair-millers-misleading-claims-about-effectiveness-of-the-english-nhs-rehab-me-cfs-clinics-royal-society-of-medicine-webinar-in-sept-20.17120/#post-292167
#MEcfs #PwME
Comments
As one person said on my Facebook page:
“Those authors are utterly deluded. Sorry, fed up with being polite. This type of advice means the end of hope for us. Perpetuation of the same ineffective nonsense that hasn't and doesn't help”
#MyalgicEncephalomyelitis #MyalgicE
Thanks to Suzy Evans for getting a response in early to this drivel
https://www.bmj.com/content/389/bmj.r977
Plenty of other points can be raised. Ideally include some references to strengthen your points.
#MEcfs #PwME
https://bsky.app/profile/kacheston.bsky.social/post/3lp7xmbumz22o
we need effective physiological treatments, not more bullshit psychological blame