Picture kindly supplied by HR.
From Horace Reid:
From: Wessely, Simon
Sent: 12 December 2012
To: MAR, Countess
Subject: RE: My letter of 5 December 2012
Dear Lady Mar
May I ask, genuinely respectfully, am I writing to you, or am I writing to all the internet?
==============
He and his journalistic catspaws spent the summer of 2011 and the autumn of 2012 stigmatising the ME community in the broadsheets. He purported that he was exposing the "militants". But in fact he and Dr Esther Crawley and others were attempting to silence us all.
All that was public. It was very public.
He abused his power as a prominent member of the medical establishment, to get a platform for his personal perspective on ME, and so far lazy journalism has let him get away with that. The ME patient community was never afforded any proportionate right of reply in the media - until now.
But once the Countess of Mar, Dr. Weir, and Professor Hooper secured a hearing in the mainstream press for the patients, suddenly the "courageous" winner of the Maddox prize gets stage fright.
At the first sign of a fair fight he wants to duck into anonymity.
Pathetic.
From Horace Reid:
From: Wessely, Simon
Sent: 12 December 2012
To: MAR, Countess
Subject: RE: My letter of 5 December 2012
Dear Lady Mar
May I ask, genuinely respectfully, am I writing to you, or am I writing to all the internet?
==============
He and his journalistic catspaws spent the summer of 2011 and the autumn of 2012 stigmatising the ME community in the broadsheets. He purported that he was exposing the "militants". But in fact he and Dr Esther Crawley and others were attempting to silence us all.
All that was public. It was very public.
He abused his power as a prominent member of the medical establishment, to get a platform for his personal perspective on ME, and so far lazy journalism has let him get away with that. The ME patient community was never afforded any proportionate right of reply in the media - until now.
But once the Countess of Mar, Dr. Weir, and Professor Hooper secured a hearing in the mainstream press for the patients, suddenly the "courageous" winner of the Maddox prize gets stage fright.
At the first sign of a fair fight he wants to duck into anonymity.
Pathetic.
4 comments:
Most with ME, CFS and Fibromyalgi diagnoses has multiply chronic infections, also known as chronic Lyme disease or Lyme Borreliose Complex (Google Dr Joe Burrascano and see him on utube)
If you go to have your blood better tested you will find the reason, I did and thousands with ME/CFS has too..
We are missdiagnosed most of us and unfortunately many has for years and then is treatment very hard and for some can it be to late, so we can't recover this bad life threatening disease.
Let everyone know, the sooner the better - don't rely on a negative test in your healthcare system, I did for way to long..
Most with ME, CFS and Fibromyalgi diagnoses has multiply chronic infections, also known as chronic Lyme disease or Lyme Borreliose Complex (Google Dr Joe Burrascano and see him on utube)
If you go to have your blood better tested you will find the reason, I did and thousands with ME/CFS has too..
We are missdiagnosed most of us and unfortunately many has for years and then is treatment very hard and for some can it be to late, so we can't recover this bad life threatening disease.
Let everyone know, the sooner the better - don't rely on a negative test in your healthcare system, I did for way to long..
Most with ME, CFS and Fibromyalgi diagnoses has multiply chronic infections, also known as chronic Lyme disease or Lyme Borreliose Complex (Google Dr Joe Burrascano and see him on utube)
If you go to have your blood better tested you will find the reason, I did and thousands with ME/CFS has too..
We are missdiagnosed most of us and unfortunately many has for years and then is treatment very hard and for some can it be to late, so we can't recover this bad life threatening disease.
Let everyone know, the sooner the better - don't rely on a negative test in your healthcare system, I did for way to long..
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