Just reading the title increased my hypertension 

By extension of this nonsense, it would also make Parkinson's disease a functional whatever, since everyone knows dopamine is the happy hormone, therefore it must mean they are depressed. Deal with the depression, increase dopamine, and you fix the mood disorder.
I think another problem is that it is easy to think that whatever test was used in a published paper is a validated one. After all, it's been peer reviewed! The number of times I've explained that certain tests for anxiety or depression doesn't work for pwIllness due to symptom overlap I'm left with blank stares and/or that the authors must have thought of that. A few months (or maybe two years? can't quite remember) a psychologist wrote an opinion piece on how many scales used in clinical practice should not be used like that because they were tools developed for research and had not been validated for a clinical setting. She argued that unfortunately we use them because we lack something else (and the knowledge that they are not validated).I don’t understand how people don’t kick these charlatans out of the profession. My guess is that the broader medical establishment feels these conditions don’t warrant legitimate research and should be de-medicalized. Thus, there is absolutely no scrutiny or oversight.
Opinion piece said:Imagine that your GP on your own initiative had made a test at home on the kitchen counter and used it to check if you were ill. Or that your doctor left it to the health secretary to interpret the test result. What would it have done with confidence in the test result, in the doctor, yes, in the health care system?
For most people, the answer is self-explanatory. Transferred to mental health practice, the answer is not as obvious. A large number of psychological tests and surveys are performed daily in the health service. There are key tools in the work to investigate and diagnose patients with mental disorders.
...
But today psychological tests are used such as:
Opinion piece said:
- is not sufficiently quality assured,
- does not follow international standards and guidelines for testing
- and which are imported from outside, but are not authorized for and translated into Norwegian conditions.
The messages from medicine on cardiac symptoms are completely contradictory.Referring to the scoring questionnaire in post #11, some of the "sensations" they ask about are things that we are told we must always take seriously e.g. chest pain and choking/throat closing. When and why does it become a stick to beat the patients over the head with?
Yes! There was another opinion piece a while back In Norway on this, that how can we expect patients to know if it is a heart attack or something else when the medical profession need tools to do so? Are we putting too much responsibility on patients?The messages from medicine on cardiac symptoms are completely contradictory.
It is worse than even that. What they are really trying to say is that patients must do their own diagnosis. We are supposed to know if it is the 'right' kind of chest pain before we go to a clinic.
If we get it wrong either way, we are stuffed, and get the blame for it.
Wish I could get a job like that.
The messages from medicine on cardiac symptoms are completely contradictory.
It is worse than even that. What they are really trying to say is that patients must do their own diagnosis. We are supposed to know if it is the 'right' kind of chest pain before we go to a clinic.
If we get it wrong either way, we are stuffed, and get the blame for it.
Wish I could get a job like that.
I had my OI under control, more or less, but the last few months I have nearly fallen many times and actually fell twice, once leaving a large bruise on my forehead. Yes, I fall forward, common in OI. I want to add I don't know for sure it was OI, but I am sometimes more vigilant than I used to be. I also completely forget a lot, which is when I am most likely to nearly fall.They found that people who have POTS symptoms, including potentially falling over if they don't sit down when feeling faint, think about their body sensations more than people who don't regularly have such symptoms.
This is actually a teaching moment about the flaws in medicine. A single mediocre study of no merit whatsoever, and you have physicians declaring from this single mediocre study how it proves the condition is psychogenic. That's all it takes for them, good enough to make life and death decisions about millions. Since it obviously can't be falsified and it's so easy to pretend this is valid by not caring about outcomes ("my patients seem to get better" is all it takes), it can sustain itself indefinitely as long as no one checks anything, which is already the default.This drivel is, sadly, gaining immense traction. It’s so gut wrenching to see how gleefully pseudoscience is embraced by medical professionals. The simplicity is too seductive I suppose. Anyway, when patients inevitably fail to improve via CBT, we can just attribute it to a lack of motivation and keep on failing upwards.
This drivel is, sadly, gaining immense traction. It’s so gut wrenching to see how gleefully pseudoscience is embraced by medical professionals. The simplicity is too seductive I suppose. Anyway, when patients inevitably fail to improve via CBT, we can just attribute it to a lack of motivation and keep on failing upwards.
When I first got sick, I contacted the NYU Dysautonomia Clinic (where the authors see patients). And they sent back a referral form clearly stating that they ***DO NOT SEE POTS PATIENTS***
Fantastic twitter thread by E Krebs, thanks AndyTwitter thread exploring the issues with this paper
I think your fear for the outcome of the wet tissue is causing this unreasonable thought process of yours, I'm sure a short course of AI-delivered CBT will be sufficient to correct that for you....These people should not be trusted with a wet tissue.