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I had many thyroid tests done before i was diagnosed, they never revealed much, though since then i have learned to get the results myself instead of assuming the doctor will interpret them correctly (which i didn't do back then). Perhaps i should try to get them redone?

We need to be ready for this next time, when interviewed spokespeople should probably say the "leading" researchers continue to cling to their debunked and poorly conducted studies that claim therapies that make patients worse are good for them and in the UK "experts" commit people against their...

If they teach this in philosophy classes then i would be very impressed :D It might not be a bad idea, i can see someone starting a new course called Modern and technological philosophical perspectives on thought (or similar) :thumbup:

Cool, but did you know that over 95% of all Wikipedia articles link back to philosophy? :geek: https://en.wikipedia.org/wiki/Wikipedia:Getting_to_Philosophy

I certainly do, confirmed by multiple MRIs, though it seems to be the typically ME type reports, eerily similar to one of the ones posted in JenB's twitter threads a while back :(

If my mind gets any sharper i'll be considered comatose This obviously doesn't apply to our type of brain damage

She is going for broke

Of course

Its a reply to your post So i'm rude but disparaging sign language and claiming Whitney's signs are cult like behaviour is not? She made a request, there is no obligation or force involved. If you like it then feel free to add your voice of support, if you don't then no action is necessary...

Indeed, i have become recently interested in the concept of cultural policing, which is something we all do to varying degrees, we have cultural norms we 'protect' without realizing, staying in them ourselves and calling it out in others to get them back into cultural norms. Culture does change...

It seems the popular position is that anything outside the "norm" is to be avoided because it will backfire but inside the norm can also backfire but thats not a forefront concern despite being the same issue. Of course i expect few to agree with this analysis, but thems the breaks

Just wow :emoji_face_palm: I don't even know where to start :emoji_rolling_eyes:

Would we say the same thing if he used a few words of sign language instead?

Thats completely different, you see baldness and stem cells for hair loss are unrelated and our research only covers whichever one is not in vogue and then we will claim its both in a different conversation and assume everyone has forgotten this one (which we can then claim is subterfuge) [/MS]

Did we not have a hair loss cure thread already? If not and i am experiencing déjà vu then perhaps more CBT is in order...

I don't recall him saying that (then again my memory is shot), his talk was basically a warning to be aware that taking multiple medications can cause dangerous interactions and side effects and that long term use of drugs and especially multiple drugs can also harm patients, which really...

It was a good talk, though only peripherally related to ME/CFS I felt it will be more relevant when we have more treatments available, though its one that more GPs should be attending in regards to their non ME/CFS patients.

Did anyone else get an e-mail entitled Evaluation - ME/CFS Conference - Montreal 2018 The link included appears non personalized https://fr.surveymonkey.com/r/MECFS2018

Indeed, i could also never build up any muscle. Without realizing it i was still pacing where possible... I wish i had known what i had and could have done things differently, i might not be so bad today :emoji_face_palm: