1 year with CPPS
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doverwhite
1 year with CPPS
i hate this shit more than you can amagine..... although some days are worse then others.. I find that ajaulating causes the most pain but not derectly after ..but when I wake up the next day o m g its a nighmare,sore balls nausating stomach fatuge urgencey the whole nine.my girl friend has been living with me since it started and before it started. I have no erectile prolbems in fact I get harder then I ever did now.. plus I can last longer than before also... but it all sucks for me because my orgasms are, well not there when I cum it feels like a .5 second orgasm and its very mild.. the the pain in the morning after is a nighmare. I can feel a mild burn in my rectum.. been seeing a uro for a year seemed that antioatics work in the beging but symptoms always returned.. I statrted quirtuin plus but see no results so far....do ibs an chronic prostatitis / chronic pelvic pain syndrome come together? or is the ibs a result of the antibotics...
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webslave
- Maintenance

- Posts: 11432
- Joined: Wed Oct 30, 2002 3:18 pm
- Location: Please give your location so we can help better
Your description is very typical. Orgasms don't feel as good when you have pelvic myoneuropathy. The dysfunctional pelvic floor musculature and disturbed nerves can severely inhibit the complex neuromuscular phenomenon that is orgasm/ejaculation.
Good News! The great ProstaQ is BACK at last! You must try it.
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