As posted by others- the international paediatric primer has " treatment" options for many symptoms - I printed off a copy for both GP and paediatrician. Far more comprehensive and empathetic. perhaps MEA could reference to it if they comment on this paper?
I have not had the heart today to look at this, but will work up to it
From Trish's comments,
Re largest trial
how were children diagnosed and referred?
do we have a definition of what "recovery" is?
do we know that we are actually studying ME ?
were outcomes subjective/ objective?
From other...
there was a conference last year - food the forgotten medicine by the College of Medicine which I tried to persuade a relative ( geriatric consultant) to attend without success
https://www.collegeofmedicine.org.uk/wp-content/uploads/2016/03/College-of-Medicine-revised-1-low-res.pdf
I can't find...
Unfortunately public screenings ( such as at med schools) require a license to screen - c £200
The DVD is also priced at higher end of market ( probably due to distribution costs?) - not everyone has itunes / netflix.
The Youtube generation expect everything to be " for free"....
From the guardian.
I have reservations about appropriate care for those with severe ME being able to be provided.
https://www.theguardian.com/society/2018/mar/27/disabled-people-independent-living-care-homes
I' m crap at Twitter. There are a number of tweets re BMJ exposure of dodgy paper on stents ( switching end points) . I follow aseem malhotra who has picked up on this. It might be useful to link to the thread to highlight this and the dodgy stats underpinning this illness paradigm for those...
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