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My bad and all that, I was busy yesterday and didn't bother to look beyond the abstract, even though I knew the percentage reported would be questionable. Any percentage a review on this subject reported would be questionable, simply because pretty much all the studies are flawed and the...

I am certainly not an expert in this, but my understanding is that the NICE Guidelines are only suggestions, not mandatory requirements. That is why they are called 'guidelines', and they have 'recommendations'. My understanding was that doctors are free to deviate from guidelines if they...

Latest petition update: 1 October 2024 Enough is Enough Thanks to our supporters Thank you so much to all have signed and shared the petition link. Thanks to Fatigatio e.V. Bundesverband ME/CFS in Germany for adding their support to this campaign. We now have 77 organisations, including most...

Looking at the data, there was a bit of a trend to the creatine group having slightly better results than the placebo group in terms of fatigue and time to exhaustion. But the small sample size and the small differences means that nothing much was statistically significant. e.g...

The abstract says that creatine supplementation increased tissue creatine levels and that people taking creatine had less symptoms over time. But it doesn't say that the reduction in symptoms in the people with creatine supplementation was more than in the people without creatine supplementation.

Thanks for the analysis @ME/CFS Skeptic and @EndME. I was conscious when I posted that I was giving it a bit of a free pass, partly due to it reporting conclusions aligned with my belief that a significant part of Long Covid is ME/CFS. Looks as though the analysis in the paper should have been...

Although that statistic is often used in information about ME/CFS, it is based on scant evidence. The time since onset seems to have a big impact on chances of recovery - recovery seems to be common up to 2 years, and is still happening up to 3 years. If someone is taking heavy duty drugs that...

I don't know what the +- is, SD? But it doesn't look as though even all the people who didn't drop out experienced a benefit in fitness. Peak work rate +16 +-20 W suggests that some people had a decline in peak work rate VO2 peak +1.55 +-2.4 mL/kg/min suggests that some people had a decline...

Unfortunately, small sample sizes - only 8 PASC. And with the data coming from samples from seven publications, there could be problems with the selection of the people contributing the samples. I've got to say that it is impressive that there is a database that can offer this sheer quantity of...

Useful review paper out: The persistence of [ME/CFS] after SARS-CoV-2 infection: A systematic review and meta-analysis, 2024, Dehlia et al Finding that 51% of people with Long Covid in the included studies meet ME/CFS criteria

From the abstract, it looks like a useful paper for advocacy. Very good conclusion. Of course, who knows if it is 50%, and I expect there were all sorts of problems with selection differences.... but it's good to be able to back up a statement of 'a significant proportion of people with...

We have had a complaint that this thread is becoming very hard to follow and the moderators agree. Please remember that the topic of this thread is 'Maeve Boothby O'Neill - her life, death and inquest' Before posting, consider if your post would be better on another thread. For example: This...

Thanks for writing about your ME/CFS and recovery @siobhanfirestone. Sorry the mods didn't see your question about where to put the thread. The treatments section is fine, we will just expand your title to include the full name of the drug. (If ever anyone wants to ask about where to post a...

I read the story a while back, and I agree. Well written and easy to read. From memory, Lily reports having chronic EBV, with periodic flares of substantiated active EBV disease, but also with ME/CFS. I meant to go back and read it again not focussed on the story but instead on the symptoms...

New abstract (paragraphs added by me for improved readability) The only change from version 1 in the abstract is the use of ME/CFS as the disease name. There's just this bit that I think still needs more work They say that ME/CFS status had a significant effect on only one trait, and then...

Yes, I agree. Dr Kane speaks very well, she manages to come across as both likeable and authoritative. But yes, she, and by extension we, are very vulnerable to how Kane's use of an unevidenced potentially harmful treatment on children is seen. I hope Dr Kane will have the insight to see this...

(Finland) Social and health services used by persons with chronic fatigue syndrome (Myalgic encephalomyelitis/Chronic fatigue syndrome), 2024, Rentola

(Finland) Social and health services used by persons with chronic fatigue syndrome (Myalgic encephalomyelitis/Chronic fatigue syndrome), 2024, Rentola I assume this is the result.

For one shocking moment I read that as Wessely being directly involved in the e-learning, but the screenshots don't suggest that, it's just(!) that he's on the Board of NHS England. Yes, re David Strain - I hope he brings in lots of support for that development work. He might find it helpful...