“Cooking The Books” and Margaret Williams 2016 Letter Re PACE Trial

cookthebooks

 

“Cooking The Books” and Margaret Williams 9/2016 letter “PROOF POSITIVE ? (REVISITED)” on the PACE Trial

 

Basically, Margaret Williams points out more details in how the PACE Team “Cooked The Books” and with their own money to boot!!!!

 

How stupid can one be- they are stupid crooks that’s why!

 

I noticed, everyone spends years on debating “scientific” data. If everyone would look at how the “books are being cooked”, we would solve these matters sooner!

 

In other words- STOP WASTING TIME WHILE PATIENTS SUFFER!

 

Stop being “politically correct” and worrying if your insulting some “supposed” “top” guy at a “supposed” research institution.

 

THEY WORK FOR US, WE DON’T WORK FOR THEM, THEY SHOULD BE QUESTIONED FROM THE GET-GO!

 

Here are a few examples in the letter that is in the link below:

 

 

“Facts to be considered:

 

1. Peter White has used his own money, as well charitable money and public money, in order to lobby support for his belief that ME/CFS is a psycho-behavioural disorder that can be overcome through “cognitive restructuring” and graded aerobic exercise

 

2. he has egregiously used large sums of public money (£250,000) to prevent the disclosure of data that would falsify his belief

 

3. for nearly 30 years, he has ignored evidence that disproves his belief, including evidence from his own trials

 

4. he has failed to correct errors of fact after being alerted to them

 

5. he has consistently failed to disclose significant financial, institutional and ideological conflicts of interest

 

6. he has been in breach of his NHS contractual obligations in that he has persistently ignored mandatory directives and has wilfully encouraged other clinicians to do the same

 

7. as a consequence of his actions:

 

-money which should have been used for biomedical research into the aetiology of ME/CFS has been diverted to fund studies into therapies which were already known to be ineffective and even harmful

 

– patients have been stigmatised as sociopaths and malingerers who refuse to accept they have a behavioural disorder,

– patients have been denied financial support from private insurers for whom Peter White and his colleagues work,

(for example, he was Chief Medical Officer for the giant re-insurer Swiss Re and was also CMO to Scottish Provident),

-and from the Department for Work and Pensions (where he was lead advisor on “CFS/ME”

-and was a prominent member of the group who re-wrote the chapter on “CFS/ME” in the DWP’s Disability Handbook used by Examining Medical Practitioners,

-by DWP decision-makers and by members of the Appeals Services Tribunals);

-he also works for the US Centres for Disease Control, and for defendants in legal actions (BMC Health Services Research 2003:3:25)

– patients with ME/CFS have been wrongfully sectioned and detained under the Mental Health Act

– clinicians who oppose his views about ME/CFS have been sanctioned by the General Medical Council and prevented from working.”

 

 

 

 

Unfortunately we have gangsters in our field, and there are more, all you have to do is look around and pay attention!

 

Crooks, gangsters, medical researchers included, etc.. always leave a paper trail and most of it is online now.

 

 

Before you donate your money to research, do your own research to see where the money is going!

 

 

Hopefully more people start paying attention to these details!

 

 

 

Thankyou Margaret Williams for another awesome piece of investigation!

http://www.margaretwilliams.me/2016…Margaret Williams 2016 Letter

 

 

R. (2003). Cook The Books. Retrieved September 22, 2016, from http://www.investopedia.com/terms/c/cookthebooks.asp 

 

“The Other Side Of The Stretcher” (c) 2016

This blog is not for medical advice.
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About The Other Side Of The Stretcher

Nurse turned patient, but not by choice. I was became a Registered Nurse in 1985 when I was 21 years old. That career was cut short the end of 1994 when I was unable to work anymore because of the illness M.E. or Myalgic Encephalomyelitis. I have 3 adult children including twins, A daughter and 2 sons. View all posts by The Other Side Of The Stretcher

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