Just to say if anyone doesn’t normally do social media there are many positive comments in response to George Monbiot’s posts. but also as ever the usual mix of people who are advocating various “approaches” to ME including Lightning Process GET and so on. And the cynics and nasty people as...
Is there a link for the paper @John Mac
Based on the extract It’s positive that most of these 11 teachers were able to recognise the impact of ME on their pupils.
Concluding that Clinical services should consider collaborating with teachers is hardly cutting edge thinking.
But in reality any conclusions we’d be attempting to draw are speculative and I’m sceptical that there’s any benefit from discussion of other people’s symptoms based on articles.
https://www.webmd.com/schizophrenia/side-effects-aripiprazole#3-7
insomnia is a very common side effect
We would only be speculating on whether that is the case for Whitney.
It’s useful to know that a symptom is not a one off so it’s a step up from an individual account. Obviously large scale surveys such as Action for ME/ME Association in the U.K. with thousands of participants have more use as evidence of issues being widespread.
I know some people have these tremors regularly. I have only had them a handful of times. I had a realisation that I was visiting friends in Provence my neuropathic pain was aggravated by heat so I took pregabalin for a couple of weeks which I don’t normally take. I checked the side effects...
Yes I was asked about this at a family do by someone 80 a couple of years ago. And I said a more colloquial version of this. When I mentioned it’s like having the flu a lot it really hit home
I think the inventors Lightning, Reverse, Mikel, Gupta, and the other multi level scam “therapies” best you to it as some of those they hook into their marketing scams are supposedly people who had ME
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