Rusty J: Is this what the secret UK documents are about?
Maybe biological warfare experimentation that went wrong? Found this on the internet......
"Large-scale mouse mutagenesis experiments were first begun at two government-based "atomic energy" laboratories: the Oak Ridge National Laboratory in Oak Ridge, Tennessee, in the U.S. and the MRC Radiobiological Research Unit first at Edinburgh, Scotland, and then at Harwell, England, in the U.K. Both of these experimental programs were begun initially after World War II as a means for quantifying the effects of various forms of radiation on mice and, by extrapolation, humans, to better understand the consequences of detonating nuclear weapons. The U.S. effort was directed by W. L. Russell and the British effort was directed by T. C. Carter (Green and Roderick, 1966).
*XMRV comes from mice and both the UK and USA embraced 'CFS' with a passion to hide ME.
*The secret UK files on ME are owned by the MRC (Medical Research Council) who refuse biomedical funding into ME, but do spent a fortune on psychiatry and CFS.
*ME is not a psychiatric disease, yet is dismissed and ridiculed in public by a famous epidemiologist psychiatrist employed by the UK military and with direct links to the MRC.
* 4,000+ articles on biomedical research on ME/CFS exist. No excuse to think ME/CFS is a psychiatric illness whatsoever.
We'll never know why this was done to us and the bigger picture doesn't matter as we aren't privy to the classified information and never will be. It is interesting though. If we had treatment we'd not care, we'd just take our meds and have a life, like people with HIV can do. They don't have to postulate if an SV40 polio vaccine caused their state of AIDS, but probably would if left to rot at home and blamed for the condition as we are.
A key failing in the political cover up of ME/CFS was that the people paid to deny it, had far too much of a field day in the deception campaign. By default, they never appeared genuine by using awful words to describe people with obvious serious non psychiatric symptoms. No professional scientist or doctor would call their patients (mentally ill or not) those derogatory words. So this raised suspicion in the public eye that something was up. (Only psychiatrists and pro psychiatric theorists were funded). Of note, in medicine, just ME/CFS patients meet this level of hatred from medics, a level so discriminatory that if used in any other condition would have lead to the researcher or doctor's dismissal from the professional bodies they belonged to. Yet to ME/CFS patients detriment, these people were soon termed 'experts' in ME/CFS and given titles and even medals/awards by the state for their 'service' towards CFS. Even worse, the medical profession always refused to attend conferences to hear of latest research, such was the level of negativity towards fellow scientists studying these maligned and ignored patients. Even now the Royal college of Physicians in the UK invite not biomedical researchers, but psychiatrsits to talk in conferences on ME/CFS. All the talk in the press of 'better' attitudes of ME/CFS in the medical profession is a total falsehood. Who is science advisor to the UK media again? Ohh yes...... Medics now believe not in ME/CFS as a neuro immune disease, but a 'genuine' mental health problem that needs CBT to change 'attitudes' and 'beliefs' about viruses keeping people ill. Everything is hopeless.
But...
The language used to describe ME/CFS patients in the psychiatric profession is not far removed from the Nazi's opinion of the jews, gypsies and the disabled. Yes the psych profession don't call for ME/CFS patients to be killed, but they
do kill the severe patients via medical neglect, which is quiet genocide. They do say that ME/CFS patients should not receive social welfare payments and are the 'undeserving sick' of society. They do place themselves as government advisors for social welfare in the UK, to guarantee that ME/CFS patiens will often be denied money to care for themselves, money they are entitled to and that non ME/CFS patients get. The public are not aware of this, they trust doctors and don't consider they could do sick and twisted things like throwing children into swimming pools to see if they are lying. (That's what Nazi's did to people they hated, for fun, before doing more uspeakable things).
It's sadistic to put people onto exercise bikes as a 'therapy' who's muscles are in terrible pain and who's central nervous system is abnormal and immune system is highly activated.
It's sadistic to tell people they must self brainwash themselves via CBT, in order to ignore a relapse and a flare of symptoms that come from this exercise.
It's sadistic to tell people once they have relapsed (usually within a few hours to days), this is fake and deny pain medications or access to a doctor if suffering from cardiac pain etc.
It's sadistic to refuse diagnostic tests that can save patients lives, such as brain scans, checks for cancers, and investigative cardiac tests.
This sadism, became 'evidence based treatment' at the institute of psychiatry for ME/CFS in the UK, who then sold (literally) these beliefs and 'treatment packages' to governments around the world, much to well known psych's delight. We became slaves to a twisted ideology. CFS was such a bad word, patients wouldn't even tell their best friend they had it, and rarely would tell doctors how ill they felt, from fear of being labelled an attention seeker.
None of this manufactured social and medical stigma ever made the news in the UK, because the psych's controlled the press as 'science advisors' and still do. Instead the UK media was full of recovery stories, talking about a disease with no cure. Again the public sucked it down and believed it all. Once the ME/CFS charities were infected too, the game was up. All was left for ME/CFS patients to do, was take their own lives. Suicide is the biggest killer in ME/CFS. Isn't this important? Not towards a society that is brain washed to view us with distain and sometimes, disgust. (social welfare cheating fakes they call us).
Next time the powers that be need to cover up a condition as disabling as end stage AIDS and COPD, it would be sensible not to have a few psychiatrists who own sole access to the media, funding, and to steer guidelines. That was their undoing, and a huge 'howler' in terms of people thinking, hang on a second; what exactly is going on here?!
A conspiracy has to be effective not lazy. They got lazy and ran out of ideas to blame people for causing ME/CFS:
1) Rich wealthy people - tried that didn't work.
2) Women - tried that didn't work
3) Depressed people - tried that didn't work
4) Exercise phobic people -tried that didn't work
5) People who were ill with a common virus, who are now obsessed they are still ill - tried that didn't work
6) People who are lazy as kids and never exercise causing them to have CFS as adults - tried that didn't work.
7) People who have been sexually abused as children - tried that didn't work *
*Is this not the lowest of the low and deeply offensive to people who have been sexually abused?
There was literally no excuses left to blame people with ME/CFS, so they had to dilute what CFS more and more until 'Reeves Disease' was born and even 'fatigue and one symptom' proposed to become the new hybrid CFS. Ironically, the CFS 'experts' disapered their own imaginary illness meaning the cover story evaporated and the people with original CFS were saying we dont' even have your CFS so we must have something else. What's that ME (Myalgic Encephalomyelitis thing again?).... hmm that sounds more appropriate. So people dumped CFS and went with ME or 'Neuro Immune Disease'. Sensibly advocacy groups latched onto this and also the WPI who knew that using the words ME or CFS in their title was pointless. Neuro Immune disease was accurate, honest and correct, it also (by defaullt) included people with original (non Reeves disease) CFS and ME.
Patients were happy, and the people sent to discredit you and I were left thinking and realising they just lost the grip onto the bubble of CFS patients were trapped in. Somone poked it with a pin and it burst, leaving the reality of XMRV to be found by scientists now researching 'Neuro Immune Disease' and not CFS, an umbrella term that contained too many types of patient to ever know that scientists were researching the same people. Which is why the CDC chose it. It lasted for nearly 25 years, but the game is up now. The idea the WPI is leading world research on XMRV should be laughable, but the jokes on the employees of the CFS section of the CDC for not absconding from the 'plan' and putting their hands up and admitting they were wrong about people contained within the label 'CFS'. Possibly, some were threatend, or felt scared and didn't want to have an 'accident' or get stiched up by the UK GMC (General Medical Council) like other serious ME/CFS reseachers did?
How sad that humans can treat other humans in a sub-human manner, purely by greed and selfishness caused by being offered total power and becoming dictators in the world of psych theory CFS. When they're old and bed riddden themselves, maybe the people who committed these crimes will consider just what they have done, that they cost the lives of tens of thousands of people (if not more). What a horrible legacy to be involved in.
