Insane - how is it covered by the Official Secrets Act?
Go here:
http://www.nationalarchives.org.uk
Search: Myalgic Encephalomyelitis
Choose 7th down the list
''Medical Research Council: Registered Files, Scientific Matters (S Series) F...''
Please see screen grabs showing the result attached. It should be noted
someone did get to apply to see the file, but they were told it's a censored version. (Unsurprisingly). The word used was ''Redacted''. What use is a censored version?
If you click on FULL DETAILS, once you find the file it says it's blocked for 73 years and this starts in 1989. In 1990/1 De Frietas found XMRV and the CDC
said they couldn't afford the plane ticket to come verify her findings.
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The word ME was denied, and CFS was created in the USA in it's place and sold to the UK and then the world as a 'life-style choice'.
Check this little beauty:
'''During the life (1998-2002) of the Chief Medical Officers Working Group on ME/CFS, members were ordered not to discuss the deliberations and were even threatened with the Official Secrets Act. If the psychiatric lobby which dominated that Working Group was so confident that they were right, why the need to force the suppression of opposing views by resorting to threats of prosecution under the Official Secrets Act in a Working Group that had nothing to do with State security but was supposed to be acting simply in the best interests of sick people?'
Source:
http://www.meactionuk.org.uk/Corporate_Collusion_2.htm
Sticking with the MRC (Medical Research Council) who hold the secret file on ME, I have a PDF somewhere of a court case in the UK that tried to find out why all funding only ever goes to psychiatry, but is always turned down.
http://www.meresearch.org.uk/information/publications/casetoanswer.html
The MRC (Medical Research Council) won the case with the judge saying the anonymity of the MRC members, was overiding that of the public to know what the research applications where, that were turned down. (It's a well known fact that the MRC block bio-medical funding into research applications in ME CFS - yet they cannot explain why). Psychiatry gets funded for 'Nurse lead therapy' over a telephone, but not research into muscle fatigue and lactic acid in MR scanners. Interesting....
I want to keep on track here about HIV and XMRV. I am just sure XMRV must be the cause of post infective/viral ME. Why did the British get a military Psychiatrist (Simon Wessely), and place him, in charge of a disease he says doesn't not exist? Here's a good quote from Wessely:
''I will argue that ME is simply a belief, the belief that one has an illness called ME.'' (ME is of course a neurological disease classified by the World Health Organisation, since 1969. ICD-10 G93.3
Are people in denial of Autism, put in charge of health programmes who deny Autism exists? I think not. Why did the Department of Health get an HIV/AIDS specialist on a panel of 'experts' who obsesses over CBT/GE/Pacing and 'Life style management'? It just doesn't add up. He should be talking about immunology, yet not one word.
Regarding XMRV transmission, in the UK one cannot donate blood in the UK with ME CFS if you 'active symptoms'.
http://www.meassociation.org.uk/content/view/444/70/
Again an incredible turn of events when ME CFS is labelled officially as, and I quote: 'Chronic Long Term Tiredness.' The Department of Health says 'Evidence Based Medicine' only exists for CBT/GE/. So why can we not donate blood?
HIV patients get 'Crimson Crescents' in their throat, I believe due to HHV-6? infection that leads on to cancer (Kaposi's Sarcoma).
ME patients also get 'Crimson Crescents' . I was diagnosed with this myself, or should I say - observed as to having this.
Yet I don't have HIV. But maybe I have XMRV.