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The HTML address reads "dr-klinghardt-a-future-without-me" which—though less preferable to a future free of M.E.—might actually be a step forward.

If only everyone in our community did!

The microbiome is not just in the 'gut' but elsewhere including on/in the skin.

https://www.medicalnewstoday.com/articles/327486.php#3 "A group of researchers has brought the idea of food as a medicine one step closer. They have identified certain common foodstuffs that alter our microbiome."

Yep this is what I thought. Also the project seems to have a very broad scope, almost verging on the social sciences.

I'm surprised the GWAS is mentioned given it is not funded yet. I wonder if the project is contingent on ME-biomed being funded. Possibly not.

https://www.ed.ac.uk/inflammation-research/postgraduate-training/phd-programme/research-projects The M.E. project is one of several advertised on this page. Mentions the GWAS study....

I have seen similar articles in the past, perhaps from the same website. Bizzarely, they often come from people who otherwise have a good knowledge of M.E. I don't know what such articles aim to achieve.

what a mess.

The whole process needs to be standardized too - you can't just bring together data from different tests.

I'm a cynical bugger online, so let me do something productive and positive, and link you to downloadable PDF copies of the posters: https://www.roche.com/sustainability/philanthropy/science_education/pathways/pathways-ordering.htm

I didn't know ME Advocacy had a European Office....

This has reminded me of this radio show that was posted here a couple of weeks ago about Doug Lindsay who came down with a sort of M.E like illness, after his mum and aunt had suffered for decades, and pretty much self diagnosed and got someone to do surgery on his adrenal glands...

Really, huh - what are the chances of getting Lyme and mono at roughly the same time?

This sort of wave of publicity is the type of thing the CMRC project could do with if funded.

I do get a slight bluriness on bad days. This is perhaps the only vision symptom that is an actual eye (or rather eye muscle) issue.

For reference, here is a past post in which I describe my experience of some of these symptoms and a related issue with my brain seeminly not able to process my vision properly...

PS Thanks for posting the entopic phenomena video. I have this and didn't know it had a name! Like swirls of ink of slightly different hue moving around when my eyes are closed.

I looked into the connection about 18 months ago when my visual disturbances started. You'll find some forum threads I started if you do a search on here. Another area that desperately needs looking into in more detail. The only work I saw on ME and vision was from Leicester and it didn't...