that what a friend’s GP did. She died of it 6 months later.
Here’s the deal….
Statistically this is going to happen because there are people who will get various things that do not throw up red flags….I had a lump in my arm once….cyst….lumps in my ear lobes….cyst….the doctor could tell what they were from experience.
BUT there will on occasion be someone that has something that resembles what I had but then ends up dying 6 months later from it.
Now do you want to pay for hundreds more MRI/CT scanners, pathology staff, medical staff that can take biopsies etc….because if you don’t then there is a limit to the amount of people that are sent for testing…..patients have to be prioritized….and someone like me with my 98 percent certain cyst is not deemed a high enough risk to go ahead of other people on a waiting list.
And to compound things further…. if we started scanning/biopsying every single complaint that patients had then the risks associated with testing them might start outweighing the chances of finding something…..so you end up with more ill/dead patients than you had before.