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There was no reaction at all to the questionnaire being posted, after sooo much work. And only one person has even filled it out. This is the key to getting help -- to getting researchers' attention. I had planned on bringing some of the forms to some research physician friends, but I can't do that if there is nothing to show.If you are currently testing a treatment, and are worried you won't get a chance to write about it, that isn't the case. We will have another opportunity in a few months. And if you urgently want to add something, we will include it in whatever is put together to present.The website again is: pois.olympe-network.comCheers.
Did you test cortisol too ?
Hi,I'm new to this forum. I'm female and experiencing similar symptoms. What baffles me is the fact that these symptoms usually get called post-traumatic stress disorder, flashback or dissociation when you have them as a woman. So I'm wondering- do men and women exprience the same thing? Is it due to trauma or a physical problem, or what? I don't know if anyone has brought up this aspect before, and I don't feel quite comfortable to adress this, but it's just too strange. Aloha
I finally told my younger son about POIS (and that I have it). His immediate reaction was that it is "psychosomatic". My early upbringing was with religious teachers who taught that sex is "dirty", so he has a point.I insisted that POIS is not psychosomatic, but I was weak in defending that. To me, it really is just my best educated guess after 30 suffering years plus the wonderful journey with you all here.ANY IDEAS TO EXPLAIN WHY POIS IS NOT PSYCHOSOMATIC?Thanks!