I have finally finished reading and making comments on the NICE guidelines for CFS/ME. I've sent a copy to NICE and also a couple of copies to other interested parties I know.
The awful thing about it is that it wasn't nice at all. Most of the document is deeply insulting to sufferers of true ME. When 61% of the Guideline Development Group is firmly sitting on the pysychiatric side of the table before the discussion even starts, we ME sufferers know we have problems.
I am always a believer in the adage 'The Truth will out'. In this case it may take a very long time, but oh yes it will, believe you me, it will.
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