Has anyone had their email inviting them to have a second go at the activity quesionnaire that we did the first version of 2 weeks ago?
I've been looking for the first time at the patient information that was linked from the first version and wasn't, at the time I did the questionnaire, available.
That their GP, primary care practitioner will have misdiagnosed them with depression, anxiety, 'we all get a few aches and pains, there's nothing medically wrong', burnout, and offered antidepressants, told them to buy some vitamins, told them to try to get more exercise, go to the gym, try...
Thank you for continuing the conversation constructively. I'm sorry if my reaction seemed dismissive.
Give him time. It's possible, especially if some researchers and clinicians with experience of ME/CFS like Todd Davenport continue to challenge the effort preference thing. He may come to his...
Thanks, @Braganca. I hope you're right.
The problem I see with moving on from the problems with the Walitt Nath study's conclusions is that they are not going away. If they are allowed to be the key people at NIH deciding on ongoing studies funded by NIH some awful dross will continue to be...
Crossposted with Ravi's latest post.
Are people 'harping on' about the intramural study? I'm a bit out of touch with what's happening. If so, which people?
ME organisations and individuals are and have been for decades pushing for more funding. I don't think it's either/or.
The BPS people...
I don't think that's a good reason for stopping funding such research. There's so much more that could be sensibly explored, including replication of small promising studies that were too small to stand on their own.
I certainly agree that their own intramural studies led by Walitt and Nath are a failure and should be discontinued. They have shown themselves unfit to research this area because of prejudices about 'effort preference' and worse.
But does Nath also have any say over the amount or direction of...
@cassava7 I'm so sorry to hear you are continuing to have such a difficult time. I wonder whether this post is of any use to you and your doctors:
https://www.s4me.info/threads/gastroparesis.3476/page-2#post-535089
@MelbME are you likely to test a comparison group between intravenous delivery of saline etc and the equivalent quantity of the same solution orally? Is there something specific about bypassing the stomach and going straight to the bloodstream?
Good. He had definitely gone rogue some time ago. I could never understand why Karl Morten thought he was a fit and proper person as a research colleague.
Unbelievable. An NHS 6 week program at a tennis club for pwLC to learn to play tennis while also getting lifestyle advice.
This from an NHS that is falling apart from lack of funding and clinicians and they waste money on this.
The world's gone mad.
The 16th Invest in ME Research International ME Conference 2024
28 June 2024
Wellcome Genome Campus, UK
#IIMEC16
Advancing Understanding of ME: Bridging Research and Clinical Treatment
https://www.investinme.org/IIMEC16.shtml
Programme
IIMEC16 CONFERENCE AGENDA - 28 JUNE 2024
The...
To lighten the tone, a BBC article today:
Glue pizza and eat rocks: Google AI search errors go viral
Quote:
Google's new artificial intelligence (AI) search feature is facing criticism for providing erratic, inaccurate answers.
Its experimental "AI Overviews" tool has told some users...
I think their crafty way of getting around all the medical ethics and science issues is that they call what they do 'training' not 'treatment'. That puts them in the category more like personal trainers, so not needing any recognised qualfications or evidence.
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