Hello
Fellow sufferers, I am happy to find you. (as sadistic as it sounds)
I am from another community that has been sharing information on POIS (or what we have called Sexual Exhaustion) for 5 years and has 1600 members. The evidence of existence our groups as separate for so long time proves the point that we are not easy to find online. There are many, many others like us. I know that for a fact!
We haven’t got a cure (yet). But hopefully we can draw doctors’ attention to research us and the data we have gathered. We need to show that this condition is extremely serious – I would trade my disorder for some milder form of cancer anytime! I see the potential of Dr. Waldinger’s last paper as a tool to create awareness, even though I totally disagree with his findings. It generated news on regular media and helped me to find you!
Let’s get acquainted and start sharing information and hopefully start group efforts, because our pursuits as individuals have proven to be unfruitful.
Let’s get well!
Research of sexual exhaustion/dysfunction and other biochemical/deficiency diseases:
http://recover.forumup.org/