Hi Vatisloff, and thanks for having taken the time to register, and for contributing to the forum. I hope more and more of the "silent lurkers" will join and share their experience, their questions, their frustration, their success, or anything related to their life with POIS. IT is so important ofr us all to be in contact with others who have to live with the same ailment. We can, finally, talk with others who truly understand our situation. And it is also a place to vent, from time to time, and be understood about why we need to vent!
Even if medicine is not as good as you would like in Canada, It would not be better anywhere in the world right now, because POIS is not known, its causes are not known, its pathopysiology is not known, and because of that, no physician or specialist have anything to offer as a treatment. There is a handful of specialist who know about POIS, and they are still in the "observation mode", except, maybe, dr Waldinger, who is currently searching for an antigen in the prostate fluid, in line with his view of POIS as an auto-immune disorder.
We hope soon another team will start another POIS research, with the money of our grant, through NORD.
I hope you will find some safe and effective alternatives for your POIS symptoms in what is presented on the forum by other members.