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doctors

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BMJ Opinion: The Illusion of Evidence Based Medicine, 2022, Jureidini and McHenry (and some doctors' opinions)

https://www.bmj.com/content/376/bmj.o702 Evidence based medicine has been corrupted by corporate interests, failed regulation, and...

Thread by: DigitalDrifter, Apr 4, 2022, 14 replies, in forum: General ME/CFS news
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Why doctors over estimate their skills

A Tweet that I thought interesting [MEDIA]

Thread by: Keela Too, Dec 1, 2021, 6 replies, in forum: General Advocacy Discussions
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Why Doctors Like Me Need To Read Chronic Illness Memoirs - An essay

This brilliant essay from Electric Lit is a gem. It's affirming, easy to read, longish and mentions ME & Jen Brea. WARNING - I fell in love with...

Thread by: Helene, Sep 23, 2021, 3 replies, in forum: General disability topics and advocacy
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An Audit of UK Hospital Doctors’ Knowledge and Experience of Myalgic Encephalomyelitis, 2021, Hng, Geraghty & Pheby

Abstract Background and Objectives: There is some evidence that knowledge and understanding of ME among doctors is limited. Consequently, an audit...

Thread by: Sly Saint, Aug 27, 2021, 1 replies, in forum: General ME/CFS news
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Survey: what explanations GPs use for conditions that have no agreed biomedical cause and the impact of those explanations on social support & stigma.

[MEDIA]

Thread by: Sly Saint, Aug 2, 2021, 7 replies, in forum: General ME/CFS news
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Blog: Royal College of Physicians: "Doctors believe in ME", Nina Muirhead

"In a follow up to her 2019 blog post, Dr Nina Muirhead discusses a recent surge in clinical interest in myalgic encephalomyelitis/chronic fatigue...

Thread by: Andy, Jul 15, 2021, 2 replies, in forum: General ME/CFS news
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The disabled doctors not believed by their colleagues

(Not sure whether I've posted this before) 19 April People often feel nervous when they visit a doctor with some fearing their symptoms may not...

Thread by: MeSci, Apr 26, 2021, 11 replies, in forum: Other psychosomatic news and research
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Correcting inaccuracies in consultant letter [UK]

I'm under a rheumatologist at the moment, who's actually quite helpful. The last correspondence I got from him after a telephone review...

Thread by: InitialConditions, Mar 22, 2021, 5 replies, in forum: General clinical care
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Australia – ME/CFS doctor/clinic in SE NSW?

Any recommendations for a good doctor/clinic in the SE corner of NSW (Monaro region), for a newly diagnosed patient in that area? Thanks.

Thread by: Sean, Jan 28, 2021, 2 replies, in forum: Other clinics and doctors
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UK: Dr Sarah Myhill

[MEDIA] [MEDIA] [MEDIA] Dr Sarah Myhill is one of the leading doctors to stand up against the prevailing orthodoxy that ME is ‘all in the...

Thread by: Arnie Pye, Oct 5, 2020, 27 replies, in forum: UK clinics and doctors
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BMJ Rapid Response: Dr Nina Muirhead

I hope this link works? Re: Long covid: doctors must assess and investigate patients properly | The BMJ Long covid: doctors must assess and...

Thread by: EducateME, Dec 10, 2020, 13 replies, in forum: General ME/CFS news
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Persistent symptoms after Covid-19: qualitative study of 114 long Covid patients and draft quality criteria for services, 2020, Greenhalgh et al.

[MEDIA] Preprint paper here: Persistent symptoms after Covid-19: qualitative study of 114 long Covid patients and draft quality criteria for...

Thread by: Dx Revision Watch, Oct 14, 2020, 35 replies, in forum: Long Covid research
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Duties of a doctor

I am starting a thread on the 'Duties of a Doctor', which in the UK has replaced the Hippocratic Oath (as far as I am aware for graduating...

Thread by: Simbindi, Sep 20, 2020, 4 replies, in forum: General Advocacy Discussions
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BMJ letter from LongCovid doctors.

https://www.bmj.com/content/370/bmj.m3565 It's basically a manifesto for care and research.

Thread by: obeat, Sep 15, 2020, 149 replies, in forum: Long Covid news
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Improving teaching about medically unexplained symptoms for newly qualified doctors in the UK - Yon et al 2017

Improving teaching about medically unexplained symptoms for newly qualified doctors in the UK: findings from a questionnaire survey and expert...

Thread by: Sly Saint, Aug 20, 2020, 10 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
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Call for doctors to clearly declare any funding from industry

In Baroness Julia Cumberlege report on the pelvic mesh etc scandal, calls for doctors to have to clearly declare any funding from industry. If...

Thread by: Daisymay, Jul 9, 2020, 7 replies, in forum: Other health news and research
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Allen Frances tweets about CFS

[MEDIA] [MEDIA] He seems to totally get it. Amazing. Yet another sign the public perception of ME/CFS is improving.

Thread by: strategist, Jul 7, 2020, 7 replies, in forum: General ME/CFS news
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Looking for feedback on my letter to local doctors

I’m writing a letter to local doctors in the hopes some can be convinced to complete this new medscape CME on ME/CFS diagnosis and treatment...

Thread by: jonathan_h, Jun 7, 2020, 11 replies, in forum: Advocacy Projects and Campaigns
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UK: ME/CFS CPD module from Study PRN and supporting podcasts

Nina Muirhead has created this free Continuous Professional Development module for health professionals in the UK. For those interested, it's...

Thread by: Andy, May 11, 2020, 32 replies, in forum: Training courses
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Survey: Doctors' Knowledge and Understanding of Myalgic Encephalomyelitis, UK, 2018, Hng

Originally intended to be published in a journal, Dr Hng has decided instead to release this into the public domain. Introduction It has long...

Thread by: Andy, May 1, 2020, 16 replies, in forum: General ME/CFS news

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