If someone doesn't have symptoms of any of: fatigue, nausea, dizziness, headache, stomach ache, rashes, itches etc. when they have an O, then they don't have POIS. What other symptoms could they possibly have? A mild sense of dissatisfaction?
I'm not trying to be rude about this and I hope it doesn't seem that way but my interest is in the connection with my symptoms and those of the majority of the people that I'm dealing with, especially people like B_Daniel who are helpful enough to send me their results.
The forum is full of people saying taking X, Y or Z didn't do much for them and some people saying that the same X, Y or Z worked in some capacity. All I can say is what works for me. The same thing that works for me now seems to be working for B_Daniel. That's good.
Having dealt with medical professionals, both generalists and specialists, for 20 years trying to overcome this illness I don't really care what medical professionals think is authoritative information or not. Relatively cheap genetic testing means that genetic mutations and problems are beginning to be identified more easily and the blunt instrument that is much of medical diagnostics will be overshadowed by better doctoring and better cures.
There are millions of people with mysterious illnesses that are not being cured by their doctors. So we have a few possibilities
1) They are all nuts - it's all in their heads
2) They have real physiological problems that their doctors have no idea how to treat.
If 1 is correct then it's
just as likely POIS is all in our heads. So we shut down this website and go back to our psychiatrists admitting we were wrong & they knew best
If 2 is correct then we should adopt some skepticism with our doctors and
insist they adopt some humility with us. I have learnt over many years that unless a doctor has a constructive suggestion for how to deal with POIS, I don't bother to convince them it's real. I spent 10 years a lot of money trying to convince people who were very egotistical that just because they didn't understand POIS that it may still exist.
This year I spoke with a woman with Myaesthenia Gravis who was eventually treated after 8 years of misdiagnosis. She had a similarly dim view of medical infallibility.
We had both ended up paying huge bills for each hour we had spent trying to convince doctors of the validity of an illness they couldn't treat or would not acknowledge.
Never again.