Despite all evidence and research to the contrary the British government through its subsidiaries NICE and the Medical Research Council steadfastly refuses to accept any viral or other biological reason for Myalgic Encepholmyelitis.
The whole government funding is geared to defining the disease as a somatization problem. ie. all in the mind. Consequently a whole host of psychiatric doctors have been enrolled at vast government expense who have come up with all sorts of psychiatric models for ME symptoms and have constantly debunked any other possible medical explanation.
No doubt the government is anxious to keep it that way as the costs of funding research and treatment to a retroviral explanation, which is what the XMRV virus is, could be hugely expensive.
There has been one large government funded study on ME in the UK which was carried out by the this government psychiatric research lobby.
The results of this study have never been made public and even more sinister the results of the study are protected by a ban on any publishing of results for 83 YEARS!!
Bans on the results of government enquiries being made public are normally no longer than 30 years. This ban has led to all sorts of speculation that there could be a cover up for a vaccination scandal or some other medical or governmental responsibility for the growth of ME among the population. This sort of speculation is fuelled by the fact that lay members of the study panel have been threatened with the Official Secrets Act if they discose any conclusions of the enquiry.
https://www.meactionuk.org.uk/The-MRC...iles-on-ME.htm
Tests have shown that the XMRV is also found in some types of prostate cancer and there is speculation that it may be spread sexually. More worryingly it was found that 7% of the general population in some controlled studies were carriers of the virus.
Its is a similar type of virus to HIV-1, and part of a family of MULV's(Murine Leukemia Viruses), and while there have been no official drug trials carried out for treatment of this virus, a doctor and her daughter who were among the first to be have been diagnosed with XMRV are at present leading the way in treatment by taking a course of HIV drugs including AZT which appear to be helping.
https://treatingxmrv.blogspot.com/201...1_archive.html
The great fear that this virus can be spread through blood transfusions has forced the Canadian,New Zealand and Australian governments to ban accepting blood from anybody diagnosed with ME. The British blood transfusion service will also enforce a similar ban from November 1st.
Strange isnt it? The British blood transfusion service shortly wont accept blood from ME patients because of a virus that could spread ME, and the British government, who fund the blood transfusion service, at the same time is refusing to acknowledge there could be a viral cause for ME.