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New Theories / Re: Post Orgasmic Illness Syndrome (POIS)
« on: 25/08/2010 19:30:33 »
The cyste and POIS came six years ago. I don't know if there is a connection. A few weeks ago I had a scan in the prostate. There was nothing to see. This research was done by a replacer because my urologist was called for an emergency case. One appointment before I mentioned the cyste to my urologist. I said that maybe the cyste oppress the prostate. He said that it's possible and that we have to wait the scan. But his replacer didn't mention it. And I was forgotten it because I was happy that it wasn't cancer in the prostate.
But the only unusual thing about the cyste/prostate is that I couldn't have a full O since I discovered the cyste. That was the reason to go to urologist. He said that it was just a UTI.
But in stress the cyste grows. It's more internal.
About a few weeks I already have an appointment with my familydoctor to discuss the resultst of the last blood test (low Vitamin D) and my experiment with Thyrax. So if the cortisol test is not out of range, I will ask him to send me to the endo.
P.S. I saw on B_Jims list that you use Relora. Isn't that strange because Relora brings cortisol down. And you have already a low cortisol level because of Addison.
Maybe the cyste is blocking the actual ejaculation process in the prostate thus not able to have an orgasm unlike before having the cyste .. i had low vitamin d3 blood results as well .. got it up to 80 with 10000iu of VIt D3 liquid emulsion.
Body wouldnt absorb vit d3 capsules/gels etc
Low vit D comes with the pois territory, from the symptoms I stayed in 99.99% of the time all year no sun so less vit d3 and also less thyroid hormones which Im on armour for hypothyroidism as well.
hehe that was a few years ago in regards to the relora, i first posted on this thread on page 4 dispite my low newbie post count