| ▲ | kranke155 4 hours ago |
| hopefully we will get somewhere with these studies. The lack of solid research on a disease that affects millions (likely a good percentage undiagnosed) is really tough for patients - and myself really, as I've found i likely suffer from this. Finding out about autonomic dysfunction and small fiber neuropathy as I researched my own fatigue and finding out I likely have this has been very challenging. |
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| ▲ | naturalmovement 3 hours ago | parent | next [-] |
| > as I researched my own fatigue and finding out I likely have this Please don't do this. It's the medical equivalent of copy/pasting shit you don't understand from Stack Overflow. Go see a doctor who has a degree and training. |
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| ▲ | derektank an hour ago | parent | next [-] | | As someone who has gone in to doctors for issues with fatigue, it’s incredibly draining (both emotionally and financially) to be batted around between a PCP and specialists that are unable to provide you with a diagnosis. I don’t blame anyone for just sitting down and trying to learn whatever they can by reading. I agree with your general thrust of course, you’re much more likely to incorrectly diagnose yourself doing this than correctly, and walking around with a false belief is worse than walking around with uncertainty. But simply saying, “go see a doctor,” is rarely helpful. I’ve never heard of someone who tried to diagnose themselves without first presenting the issue to a physician. | |
| ▲ | ksenzee an hour ago | parent | prev | next [-] | | Autonomic neurologists are the relevant specialists. I invite you to look for one in your local area and see how rare they are. The last I checked, the Seattle metro area (and in fact the whole state of Washington) had precisely one board-certified autonomic neurologist. Diagnostic delay is, unsurprisingly, around six years. Combine that with the fact that all the equipment you need to do a basic POTS test is a pulse oximeter and a blood pressure cuff, and yeah, you're going to have people self-diagnosing, for good reason. | |
| ▲ | hombre_fatal 2 hours ago | parent | prev [-] | | If there's no test for it, then what is the doctor going to do for something as nebulous as long covid? |
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| ▲ | zx8080 3 hours ago | parent | prev [-] |
| It's probably more profitable to treat symptoms. |
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| ▲ | jambalaya8 3 hours ago | parent | next [-] | | Hard to treat symptoms with immunological conditions. I mean, there are vitamins and supplements, but noone is gonna generally hand out economy-sized bottles of controlled substances for exhaustion, etc. These sorts of conditions are systemic, and the causes and ways of dealing with the accompanying syndromes are probably always going to be different from individual to individual (well, likely the exact physiological causes anyway). | |
| ▲ | J0nL 2 hours ago | parent | prev | next [-] | | It's true, this is why there are so many government agencies focused on healthcare. The medical field lacks a healthy profit motive. Healthcare CEOs use their fiduciary responsibilities as an excuse and say they'll get sued if they don't exploit situations. There was a SARS vaccine as far as back 2016 which could have changed everything but was ignored. Pharmaceutical execs told them they were, "waiting to see if it comes back yearly" first | |
| ▲ | jmye 3 hours ago | parent | prev [-] | | [dead] |
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