Thursday, December 20, 2012

Emily's death from severe ME prompts Simon Wessely's own charity to give an award to Simon Wessely for decades of ignoring clinical evidence

On Tuesday 6.11.2012, Emily Collingridge was buried. She died from severe MEcfs.

Just hours later Simon Wessely was awarded the Simon Wessely award for vested interest psychiatry for leaving millions of severely ill patients to rot, as Simon Wessely and the other CBT psychiatrist have made sure that there is no proper treatment for this severely disabling neuro immune disease.

Which of the following Simon Wessely charities has awarded Simon Wessely an award?

  • Action for ME 
  • Action for Young people with ME 
  • the MRC 
  • the science media Centre 
  • the RCGP, run by Mrs Simon Wessely a.k.a. Dr Clare Gerada 
  • the BMJ 
  • Sense about Science 
  • the Lancet 
  • Ben Goldenacre 
  • Max Pemberton

See also: The Independent: British psychiatrist Professor Simon Wessely should be stripped of an award, fellow scientists said last night

See also: Another cracker from the CBT school of denial: “The bastards don’t want to get better”…
See also: Harvard Medical School: EEG spectral coherence data distinguish chronic fatigue syndrome patients from healthy controls and depressed patients 
See also: Cerebrospinal fluid profiles can differentiate between Lyme disease, ME/CFS and healthy controls
See also: The main characteristic of ME is an abnormally delayed muscle recovery after doing trivial things, if you don't have that, you don't have ME

See also: The Independent: British psychiatrist Professor Simon Wessely should be stripped of an award, fellow scientists said last night

1 comment:

Hope said...




Hope•in a few seconds −





Here is some ammunition to defeat the enemies of ME. http://www.iacfsme.org/LinkClick.aspx?fileticket=5rQ3LXEp4WE=&tabid=512
Myalgic Encephalomyelitis Case Definitions, by Leonard A. Jason, et al
First-rate article which critically examines the various definitions of ME and shows consensual and essential variables, for researchers as well as clinicians. Reading it carefully, Jason et al have proposed a definition of ME which is integrates that of Ramsay (1991) and Hyde (2007). It excises CFS from ME. Now there is no excuse for ME organisations to fund or publish research or advocate treatments based on CFS patients. Now there is no excuse for our national health institutions to refuse to do research on ME patients.

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