ScottTriGuy
Stop the harm. Start the research and treatment.
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Just want to echo that therapists are in positions of authority.
CBT in not harmless.
CBT in not harmless.
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Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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When you read those GET materials they use this type of authority to assert that up is down, that the scientific consensus is that there is no physical problem other than being deconditioned.
This is a strong abuse of authority
I think in the case of ME/CFS patients, who have a lot of frailty of mind and emotional hypersensitivity, a medical professional with a strong personality or adherence to a particular methodology can come over as an authority figure, even though to a healthy person the same doctor would seem quite normal and even quite empathetic.
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So I think the emotional hypersensitivity may create the image of an authority figure in the ME/CFS patient's mind, when in fact there may be none there.
Nevertheless, even if this is just a perceived aura of authority, rather than a real one, it does have a very real effect on ME/CFS patients.
Sorry, but I have to say something to this. CBT is not just offering a different explanation for your symptoms. CBT goes much further. CBT tries to change your maladaptive thinking, which usually leads to maladaptive behaviour. Or in other words, the therapist teaches you how to recondition your thoughts and tries to fix your cognitive distortions. CBT was and still is heavily influenced by the theories of conditioning.
A doctor telling a cancer patient that treatment X will lead to Y and Z is in a position of authority and is asserting power.
That is not the normal meaning of the words authority or power. Authority would be where a doctor has the power to enforce their treatment.
It depends what type of CBT. The Chalder protocol is potentially harmful in that it aims to increase activity. For most other disorders, CBT is focused on resolving specific issues that en has e.g. depression. It is therapeutic. It can help or it has no effect.Just want to echo that therapists are in positions of authority.
CBT in not harmless.
That is not the way Simon Wessely sees ME/CFS etiology. Wessely posits that all the mental and physical symptoms of ME/CFS are caused by the patient having a belief that they are ill. His view is that if you can change or oust this belief that you are ill, and replace it with the belief that you are well, then ME/CFS will disappear.
So for the Wessely school, CBT is used in order to expel these illness believes that he thinks maintain the ME/CFS state. The fact that this sounds rather like the hocus pocus you find in religious exorcism has not stopped Wessely's theory from being published in scientific journals.
Fault as in blame? Agreed, its not their fault for the most part. Fault as in responsibility? They have the responsibility to do better.Not really the doctor's fault
This is a specialized use of the term. Authority can have many shades of meaning.Authority would be where a doctor has the power to enforce their treatment.
So not because she's a woman, then?Oh, here's another, tweeted 19 hours ago: "Cyberbully has returned to diminish me (on Phoenix rising). Frustrated by psychiatrists, I'm the Prof. Wessely manqué. Bash bash."
Nope. When I did that (cancelled my upcoming therapist appointments at a fatigue center), they responded by removing their diagnosis of ME/CFS and replacing it with a diagnosis of obesity.Are you allowed to agree CBT is a complete waste of everybodys time?
Nope. When I did that (cancelled my upcoming therapist appointments at a fatigue center), they responded by removing their diagnosis of ME/CFS and replacing it with a diagnosis of obesity.
Maybe for you. But I've never automatically viewed any doctor as a threatening source of authority, before or after becoming ill. I still get on well with my GP, but I actually see her as being disempowered by the medical system. She does the best she can in that framework, but can't force specialists to see an ME/CFS patient, or write certain prescriptions without the involvement of those specialists.I think it is the mental state of ME/CFS patients that makes medical professionals come over as authority figures.