Guys, if you can contact My Coyne, please let him see this information if he is to critique PACE and the allied 'evidence based' psychiatric mantra of CFS/ME (which is based on CBT/GET).
If so, he may considering using the following information, to show GET is not safe for ME patients. NB: Also note in the following information, the victims are both
males, yet 'CFS' is promoted as being a 'women's ailment, and in America, placed in 'Women's health'.
So I found out and wanted to share....
That Llewellyn King (Whitehouse Chronical) revealed in a recent online video (6th November, 2015) that a 15 yr old (Child) ME patient died from exercise in a video clip with ME advocate Mary Dimmock.
This is an obvious tragedy, however it is also a warning to other patients, and importantly, to reject the notion that GET is 'safe'.
Llewellyn King:
''There's one lady we both know who's son actually died because he tried to beat it by exercise...killed himself by exercise....He was 15 years old and he thought I will be a man, I will exercise, I will beat this with exercise. A truly terrible situation''.
Source:
MECFSALERT
Chronic Fatigue Syndrome A Disease Looking for Doctors and Researchers WHC 7044 Full Episode.
Video clip below.
Timecode of quote on video:
18.08 - 18.27
Also in the UK a member of Parliament (MP), an adult, also died in 1988 after exercising in the house of commons Gym when he also had ME.
Brynmor John had been diagnosed with the illness, and died suddenly immediately after exiting the House of Commons gym. He had been following an exercise regime based on what is argued to be unfounded and unethical medical advice: that sufferers may exercise their way toward a cure for the illness.
Source:
http://niceguidelines.blogspot.co.uk/2015/01/me-patient-mp-brynmor-john-killed-by.html
I thought this might be useful for any talk on ME CFS done by Mr Coyne, that shows that GET is just a theory, not an evidence based SAFE medical tool for people with ME.
I don't have a twitter account, so if someone can please let him know, and it may or may not interest him. I just though it was worth a mention if it helps saves lives, because we very rarely (if never) have anyone on our side to air their views in public about how serious a diagnosis of ME & CFS can be to the individual diagnosed with it.
Thanks.