Good to see some media coverage on this: The medical breakthroughs to watch out for in 2025
Just to note that this study is covered in an article on the landing page of the Financial Times today: Anti-viral protein found to be important...
I found this very interesting - thanks for laying it out so clearly. Do you have thoughts on what an initial/small study could look like to test...
NBC News has just run a story on this: Long Covid study reveals major insights on a potential cause (nbcnews.com)
The Times has an article on this study today, which includes mention of ME. Long Covid changes your muscles, scientists find (thetimes.co.uk)...
Thanks everyone for all the replies and perspectives - useful as always in putting the study's conclusions into context.
On a related note to the studies mentioned above, I wonder if anyone has a view on the clinical trial conducted for laser light therapy in...
Do you know if a recording of this will be made available? Thanks!
Welcome to the forum Audrey and best of luck with your project.
In case useful as background context for those attending, here's the list of all active NIH research projects in ME/CFS that are NOT run out of...
Thanks Hutan for these v helpful pointers.
Hello all, this study came onto my radar after reading the following media article on the search for a biomarker and treatments for Long Covid,...
Title: Cutaneous α-Synuclein Signatures in Patients With Multiple System Atrophy and Parkinson Disease Authors: Christopher Gibbons, Ningshan...
That is certainly my experience.
This is excellent, thank you Joan for writing it.
Post copied from the DecodeME thread: I agree the 85% response rate is fantastic - unheard of really. Decode ME is such a brilliant study. On a...
I agree the 85% response rate is fantastic - unheard of really. Decode ME is such a brilliant study. Posts about the MS study discussed below...
Thank you to everyone who has posted - especially the longer posts which really get to the heart of the challenge and which I suspect reflect...
Dear all, I'm keen to sound out opinion on what the ideal ME/CFS research institute would look like. Much of the forum discussion is (rightly)...
Thanks for sharing. I find this area of research hard to follow in the details as a non-expert but my intuitive sense/lived experience of ME/CFS...
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