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I am relying mainly on the comments above (thank you) and the authors’ conclusion, but the paper seems to be saying that looking at the blood metabolomics in the way that has been done to date, by a variety of researchers, has basically drawn a blank. That also means, if I've understood this...

Seriously, how do you dig out this information, let alone grapple with it? It is so complex/mind-numbing, yet also so important. Thanks for your continuing vigilance and work.

I’d like to add my thanks and congratulations + DX. This is an incredible achievement especially since some people at WHO clearly wanted ME/CFS to be included under bodily distress syndrome, which surely would’ve been very bad news for patients. I realised early on that I would never master the...

7,500 people have now signed up to support the study. Thanks, everyone. Still time to join in - closes end of Tuesday 21st, just over 48 hours from now.

In case the tweet isn’t showing for anyone, the signup total is now just over 6000. That’s pretty impressive. Getting close to 10,000 would be awesome.

Questionnaire conundrum Good discussion on the merits and pitfalls of optional questionnaires I would add to that extensive experience/results from non-profit marketing, which shows that giving people more choices/options reduces response rate - effectively people are more likely to be put...

Thanks for the blog post likes and thanks for sparing my blushes by not pointing out that I had used a picture of DNA from a parallel universe. The DNA helix spirals with a clockwise (right-hand) twist, not anticlockwise (as a researcher pointed out to me). It's now correct in the first post...

I expect many people here have already signed up, but if you like the blog, please share widely. I think the figure is approaching 5k sign-ups. With 2 weeks to go, we could get 10k. Thanks

Sign up! Your support could help win funding for a game-changing ME/CFS study January 8, 2020 Simon McGrath Comments 0 Comment Researchers and patients are about to submit an application to the UK’s two big medical research funders for a 20,000-patient genetic study. The team want people...

Thanks, and thanks for the helpful questioning of this estimate of the patient community. In terms of estimating the patient community, the key question is probably "how big is the 'silent group' that is linked to the patient community but not counted by likes of either of the two main...

If the UK patient community is 40,000 people, what does that mean for recruitment to the GWAS? In marketing terms, including non-profit marketing, getting 50% of any audience to do anything is a very tall order. Assume we can persuade 14,000 people with ME (40% of the UK patient community with...

My estimate of the size of the UK patient community - feedback appreciated The UK online patient community, loosely defined, might be 35,000 people, with perhaps another 5000 beyond that who can be reached through ME/CFS groups and charity member mailings. So 40,000 people with ME in total. (I...

Some comparisons with the GLAD study, which I think illustrate why reaching the target will be so hard, at least recruiting in the UK: Key numbers 1 in 3 people have ever had anxiety or depression, so the GLAD study needs to recruit less than 1% of its target audience. In marketing terms, this...

Happy Christmas and thanks to @Chris Ponting,@Andy, Sonya Chowdhury and all members of the Public Patient Involvement Group who have been putting in epic amounts of work to try to make this project happen. Above all, thanks to all the above for engaging with the patient community in a real and...

You came across a smart and thoughtful, as usual. You raised important issues, and as you can see from Andy‘s reply, the project, particularly the PPI group, has spent time thinking about just these things. I have tried to engage With ICC-only supporters but got absolutely nowhere. Still, I...

From the website (for referennce): Recruitment Plan for the ME/CFS Biomedical Partnership We will need saliva samples from at least 20,000 people with ME/CFS for the genome wide association study to look at whether some of the reasons that people get ME/CFS are genetic. You can find out more...

I think Koroshetz is referring to something rather different. The key point is that here are people who meet the criteria for me/cfs, appear to have me/cfs, but deep exclusionary diagnosis during a week-long in-patient admission at what is probably the best diagnostic facility in the world (the...

Read the transcript: mostly the NINDS council report implementation seems to me to be based on a lot of good things, but none of them is game-changing. Even so, a few things that came up caught my eye: 1. Funding, including possible set-aside funding 2. A new biobank of mecfs samples...

Not an answer for ME/CFS, but here's an example of (non-nanoneedle) bioimpedance being used to measure changes in cells for studying the effect of candidate drugs in fibrotic disease. https://pubs.acs.org/doi/full/10.1021/acssensors.7b00442?src=recsys# Crucially, the study identified what was...

Janet Dafoe has posted a very helpful note from Ron Davis on PR explaining in much more detail the status of the nanoneedle project and work to find something in the blood: [Janet] There are a lot of various threads and tweets about this so I asked Ron to clarify where the research is at and...