I haven't been on here for over a month, but I saw your post and wanted to reply. I was diagnosed with CPPS earlier this summer (before that, non-bacterial prostatitis), and very nearly had an empirical surgery (e.g. 'hydrodissection') for pudendal nerve entrapment (because my doctor had no idea what else it could be). I went to multiple doctors, urologists, urgent care clinics, sports doctors, physical therapists, chiropractors . . . nothing really much worked, or if it did, it only worked for a short while before failing.
I'd stumped about every medical professional I saw. Around late October of this year, I very seriously considered that TMS might be at play, and started to treat it as such.
It's pretty much gone now, about two and a half months later. I may get stressed out and experience some vague burning for a half hour, but it dies down and disappears once I quit thinking about it. It continues to recede. It's only about 1/4 as bad as it was a month ago, and a month ago, it was only 1/4 as bad as it was when I first looked into TMS in October. When I do think about it, it creeps up (I can feel it a little now, haha! It's sneaky, but if I ignore it, it'll drift away).
Before, I'd only sit on a cushion and was afraid of making things worse or of causing more nerve damage. At first, because I'd conditioned myself to have more pain while I did certain triggering activities, I would feel more pain without the cushion. But enough time driving around without the cushion broke that association.
I've now ridden my bike 20 miles without any increase in pain, which, if you know what pudendal nerve entrapment is, is a fairly unthinkable activity to do. I never sit on cushions anymore, and have given away all three seat cushions I had. I'm basically back to normal. And I still can't believe that that's all happened. Just a few months ago, I was convinced I'd have a life full of chronic pain.
If I had to offer any coping advice, it would be to believe it's psychological. If your doctors have cleared you, then the key is to lose the fear of the pain. Like I said, I went from being afraid to sit at my desk for more than an hour (with a cushion) to riding by bicycle 20 miles with no change in pain. I let go of the fear and quit letting the pain take center stage in my brain.
Another bit of advice is to have patience. For a good while, I still felt the pain, but I got my life back. I felt the pain but quit thinking about the pain, and eventually, with time, it subsided. Everyone's experience is different though, and you need to be patient with yourself.
Another success by losing fear and moving on
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carbonevo
- Intermediate Member

- Posts: 99
- Joined: Tue Feb 23, 2016 1:43 pm
Another success by losing fear and moving on
Few months back this guy was crying for help on the pudendal and TMS site, @Ezer convinced him to check at the psychological aspects of this disorder, few months after here's his reply to Chriss who happens to be a member on this forum:
Onset Age: 23 , Current Age: 24 Symptoms: Pain in butt/ prostate area, buttocks when sitting for long, pain during sex - especially erections were very painful... pain moved slowly to the left side after reading about the PNE bullcrap. Helped By: Relaxation, massage (temporary relief), the real difference made for me understanding that this is induced by the Brain/Central nervous system as tension, therefore addressing the tension psychologically, not physically. During flare ups I use a strong dose of tramadol - 100mg extended release, works magic for me. If your symptoms improve when distracted or during vacations and stress worsens your symptoms I urge you to:
* Read John Sarno's books
* Read Ezer's story on this site.
* Explore the TMSwiki site and read every single success story there. (even the non CPPS)
* Pay a special attention to Alan Gordon's posts.
* Read Clair Weeks book Hope and help for your nerves (apply the concepts to CPPS).
Current status: more or less cured if stressful events and emotional conflicts did not flare up my symptoms. This does not affect my life in any aspect anymore, because I dont allow it to.
* Read John Sarno's books
* Read Ezer's story on this site.
* Explore the TMSwiki site and read every single success story there. (even the non CPPS)
* Pay a special attention to Alan Gordon's posts.
* Read Clair Weeks book Hope and help for your nerves (apply the concepts to CPPS).
Current status: more or less cured if stressful events and emotional conflicts did not flare up my symptoms. This does not affect my life in any aspect anymore, because I dont allow it to.
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dailysuffering
- Beginner

- Posts: 56
- Joined: Mon Mar 28, 2016 8:30 pm
- Location: Canton, Illinois
Re: Another success by losing fear and moving on
truly amazing
Age:22 | Onset Age:21 | Symptoms: weak stream, pelvic pain, muscle spasms, ejaculation pain, start stopping urine flow, sometimes bladder pain, and pain while urinating, frequent urination, feeling like i have to urinate constantly when i don't actually have to. | Helped By: Quercetin, and stretches, diaphragm breathing helps with urine flow. | Worsened By: Stress!! acidic foods and drinks, | Other comments: prostate is not enlarged, only had minor issues back when i was 17 at 21 that all changed for the worse been in a flare ever since.
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MajorSky1
- Old Hand

- Posts: 378
- Joined: Mon May 25, 2015 3:13 pm
- Location: Grand Rapids, Michigan
Re: Another success by losing fear and moving on
Awesome!
Age: 49| Onset Age: 47| Symptoms: Pain locations: Intermittent left and right front pelvic floor lateral to urethra; occasionally left side tailbone pain (rarer); left spermatic chord pain (become rare); Post BM-Pain helped by distraction during Bowel Movement.| Current meds: None. Helped by: deep breathing, mediation, hiking, distractions, exercise. Approximately 98% improved, varying depending on stress levels.
