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Moderator note: This video was taken down and a new one has gone up, details are in this thread https://www.s4me.info/threads/updated-what-is-me-video.13534/ New Video (7 mins) : What is ME? Experts provide a brief overview of symptoms, severity, problems with exercise, guidelines and pacing...

From an email from them. Our “Advances in ME/CFS Research and Clinical Care” Webinar Series features presentations by researchers who contributed articles to a special ME/CFS issue of the journal Frontiers in Pediatrics. Published over 2018 – 2019, the issue includes 24 peer-reviewed articles...

This Thursday 24th October: Autumn conference, with guest speaker Professor Brian Hughes from 2:30pm All welcome, or watch the livestream on Sheffield ME And Fibromyalgia Group's Facebook page: https://www.facebook.com/SheffieldMEandFibromyalgiaGroup/ Prof Brian Hughes is Professor of...

https://www.eventbrite.co.uk/e/me-uk-research-ethics-public-health-journalist-dr-david-tuller-guests-tickets-75779964915 eta: good date for it! can't wait for the fireworks.:emoji_boom:

Here's their website: http://aaemconference.com/fall/index.php Details of speakers here: http://aaemconference.com/livestream.php Includes speakers on diverse topics including biomedical, diagnosis, treatment, theories etc about CFS, EDS, MCAS, MCS, GWI mold, toxins... Speakers include...

eta:

https://www.youtube.com/playlist?list=PLl4AfLZNZEQPiRL9zpis8LtfaHBEMy4jS vvv The individual talks from the OMF-sponsored Third Annual Community Symposium on the Molecular Basis of ME/CFS at Stanford University are now available as individual talks .... ...(Transcripts will be made available at...

Recent podcast on the subject of drug-resistant infections. 1 Hour. I recommend it if you have the juice for it.

Gene mutation IDO2 Every ME/CFS patient has this mutation. Biochemists and Geneticists say IDO2 is not necessary, it doesn't have a function. Clearly not true as every patient has this mutation. We have hypothesis: No details yet but called 'Metabolic trap'. We are trying to prove...

http://voicesfromtheshadowsfilm.co.uk/2018/dialogues-for-a-neglected-illness-a-new-mecfs-project-awarded-wellcome-funding/

Merged thread I wasn't sure where to post this. I haven't watched it, so I have no idea what it's like.

From a Solve email DR. KENNETH J. FRIEDMAN KICKS OFF “ADVANCES IN ME/CFS RESEARCH AND CLINICAL CARE” WEBINAR SERIES! In our upcoming research webinar series, we’re taking a closer look at some of the topics covered in the special issue of Frontiers in Pediatrics devoted to ME/CFS. Solve M.E...

full details here: https://www.lshtm.ac.uk/newsevents/events/lshtm-120-keynote-lecture-alumni-frontline-innovation now on Youtube: oh the irony

Saw this on TV by chance. Found it on the internet.

Ron Davis discusses his research at Stanford – interview with Llewellyn King, ME/CFS Alert

Half the research spending for ME in a 10 year period in the UK went on the widely discredited £5M PACE trial [1]. The trial is taught in textbooks [2] and universities [3] as an example of how not to conduct a clinical trial. Over 100 experts and 80 charities want an independent review [4] and...

Why does Hanson now think that it's a virus? I thought the researchers had moved away from that idea. Anyone who was there or has watched the talk (I can't) - @Michiel Tack @Wilhelmina Jenkins @Ben H - did she say why she thinks it's a virus? I'm confused because I thought that OMF were...