.Here is me thinking that the U K approach to M E care pathway was to forget that people with m e actually have an illness and fob us of so often that we stop seeing them .i have very little faith in the medical industry when it comes to serving patient needs first.
IT really would be cheaper for doctors to tell patients we do not know of any way to really help you but will try to reduce their symptom burden through proven treatments ie pain meds anti nausea etc.
seems like the usual papermill copy paste garbage we have seen so many times before . They are still recreating the same false evidence base simply to give themselves more useless busywork. Easy job if you leave out any ability to think critically.
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I think that patients who have no previous experience with this test will have raised heart beats simply because it is a new procedure to them and do not fully understand everything that will happen . results would be skewed by this.
they are making a rather large assumption that those patients being fobbed of with bs explanations are not going to do any research of their own .resulting in a huge loss of confidence in their gps and the entire medical industry . personally i prefer that a gp has the common sense and decency...
It is absolutely stunning that so many doctors have to experience disease symptoms before they find empathy for some patient groups .This shows that way to few medical professionals actually feel any duty to understand what patients go through .
I have never owned a mobile phone never mind an expensive smartphone. I always thought that tech at the time was way to intrusive and was exploited by employers .
So not pointing out how broken the entire system of academic publishing is . Has been since the fifties when various people saw how lucrative such publishing houses could become .
they really like to tag on anxiety and depression to everything don't they . those two words seem to be very dismissive of two very serious comorbidities .
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