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"Recommended ME/CFS resources for medical educators" from ME/CFS Medical Education Campaign UK https://mecfsmeded.files.wordpress.com/2023/04/mecfs-learning-resources.pdf A collection of papers, articles & audiovisual material

Our guide to developing training on ME/CFS for undergrad medical students has been updated! https://mecfs-med-ed.org/medical-educators/

Oops, thanks. I have now edited that in. :thumbup:

Lunch & Learn – Virtual Event July 20 @ 11:30 am - 1:30 pm MDT Free Registration page: https://batemanhornecenter.org/event/lunch-learn-virtual-event-46/ 1:30 PM ET/6:30 PM in Great Britain & Ireland Find the time in your time zone here...

#MEACTION GEORGIA SUPPORT CALL July 20 https://www.meaction.net/event/meaction-georgia/2023-07-20/ People from around the world are welcome 1:00 pm - 2:00 pm EDT/6 PM in Great Britain & Ireland Find the time in your time zone here...

Tuesday, July 18 free-professionally-facilitated online support group https://batemanhornecenter.org/event/online-support-group-51/ 3 PM ET/8 PM in Great Britain & Ireland Find the time in your time zone here...

Well in this case it relates to the level of bias and how important it is. In some scenarios, not having a truly socio-economically balanced cohort could mean there was a large level of distrust about the findings. However I'm not sure where possible biomarkers and the like were being...

As I understand it, the proposal was to get research done on the cheap by using existing data. Future studies could use a different methodology.

From listening to the accents of callers to the helpline for the association I help run over the last 25 years, I can tell that people from lower socio economic groups/more deprived backgrounds are less likely to call. Similar things can be seen from their addresses from people who enquired. My...

The perfect can be the enemy of the good. My guess is many ME/CFS studies do not have a truly representative sample of the population. Certainly I imagine that's the case in many US ME/CFS studies. I think publishing data on the results from tests that had been paid for (esp. if you had other...

Bateman Horne Center Tuesday, July 11 online support group Topic: Helpful Technology https://batemanhornecenter.org/event/online-support-group-50/ 3 PM ET/8 PM in Great Britain & Ireland Find the time in your time zone here...

ME Research UK e-newsletter - June 2023 (29 June 2023) https://www.meresearch.org.uk/e-newsletter This is the correct link for ME Research UK e-newsletter - June 2023 (29 June 2023) https://www.meresearch.org.uk/e-newsletter-june-2023/

Long covid: nearly half of doctors affected can no longer work full time, finds survey https://www.bmj.com/content/382/bmj.p1529

What different characteristics would people with ME/CFS who had paid for a test have over those who did not? I could understand that possibly being an issue with a large population study but most ME/CFS studies use convenience samples and it's unclear to me what the different characteristics...

EXCLUSIVE: Former tennis starlet Tanysha Dissanayake on the heartache of being forced to retire aged 21 due to long Covid as the Brit admits she is too 'jealous' to watch Wimbledon this year Tanysha Dissanayake had seemed set to be one of the stars of British tennis Dissanayake shared a locker...

Saturday, July 15 caregiver support call (for caregivers of people with me (mylagic encephalomeylitis), long covid and associated conditions) https://www.meaction.net/event/me-caregiver-support-call/2023-07-15/ 3:30 PM EDT/8:30 PM in Great Britain & Ireland Find the time in your time zone...

As you know, the 6-minute walking distances in the PACE Trial in the four trial arms all “increased” but still remained low.

I wonder whether the numbers could be obtained using a freedom of information request?

Thanks very much to those who wrote. It was great to get this out of them: It's a pity they didn't give the raw numbers but still useful.

I found the last item via this short video which doesn’t go into much detail itself