Hello everyone,
My story isn’t a heroic story where patients developed chronic pain after a difficult childbirth or elite athleticism. I’m a 42-year-old man who developed chronic pain following the use of a prostate massager—a single misstep that profoundly disrupted my life. It’s not easy to share, but I believe honesty is important in communities like this.
I experienced immediate electric/shooting pain in the rectum and perineum after using the device.
Lacking awareness of PN at the time, I pursued unrelated diagnoses and treatments for several months.
Eventually, after extensive research, I began to suspect pudendal nerve involvement.
I worked with three different pelvic physiotherapists. Unfortunately, none produced meaningful results.
Since then, progress has plateaued.
My current status:
Pain levels: Usually range between 1–3 on a typical day.
Pain location: shifts, but still within distribution area of pudendal nerve.
Unable to sit more than 15 minutes due to pain
Flare frequency: Despite trying to avoid known triggers, I still experience at least one flare-up per week.
I am 12 months into this horrible journey and starting to realize that even though what triggered my pain was physical action, my pain in reality is TMS:
1) Pain almost disappears when I am engaged in activity or talking to friends;
2) I have no pain when I wake up and stay in bed. Even if I stay in bed for an hour;
3) Pain is emotionally driven. When I am upset or scarred I feel burning sensation;
4) The more I read about pudendal neuralgia the more symptoms I developed:
a) initially I was able to sit, but then I learned that PN patients cannot sit and my sitting tolerance diminished to 15 minutes;
b) My pain was only in rectal area/right buttock. But then I read that it can migrate... Well and of course it migrated to my testicles;
What points to the fact that the pain has a physical component to it:
1) I feel burning after bowel movement. I am not sure if brain can control this sensitivity;
2) I feel pull/discomfort in my testicle and buttock when I urinate or have an erection
3) Sitting causes pain
4) Squats or leaning down causes discomfort/pulling sensations
5) I feel numbness in my buttock on the affected side if I sit on it for a certain period of time
6) I feel discomfort if I lay in bed on affected side
I was hoping to get some expert opinion from the community on what I am dealing with and how to overcome this nightmare. I hope that the community can help me and guide me in the right direction in my healing journey.
Thank you everyone for listening to this embarrassing story!
My story isn’t a heroic story where patients developed chronic pain after a difficult childbirth or elite athleticism. I’m a 42-year-old man who developed chronic pain following the use of a prostate massager—a single misstep that profoundly disrupted my life. It’s not easy to share, but I believe honesty is important in communities like this.
I experienced immediate electric/shooting pain in the rectum and perineum after using the device.
Lacking awareness of PN at the time, I pursued unrelated diagnoses and treatments for several months.
Eventually, after extensive research, I began to suspect pudendal nerve involvement.
I worked with three different pelvic physiotherapists. Unfortunately, none produced meaningful results.
Since then, progress has plateaued.
My current status:
Pain levels: Usually range between 1–3 on a typical day.
Pain location: shifts, but still within distribution area of pudendal nerve.
Unable to sit more than 15 minutes due to pain
Flare frequency: Despite trying to avoid known triggers, I still experience at least one flare-up per week.
I am 12 months into this horrible journey and starting to realize that even though what triggered my pain was physical action, my pain in reality is TMS:
1) Pain almost disappears when I am engaged in activity or talking to friends;
2) I have no pain when I wake up and stay in bed. Even if I stay in bed for an hour;
3) Pain is emotionally driven. When I am upset or scarred I feel burning sensation;
4) The more I read about pudendal neuralgia the more symptoms I developed:
a) initially I was able to sit, but then I learned that PN patients cannot sit and my sitting tolerance diminished to 15 minutes;
b) My pain was only in rectal area/right buttock. But then I read that it can migrate... Well and of course it migrated to my testicles;
What points to the fact that the pain has a physical component to it:
1) I feel burning after bowel movement. I am not sure if brain can control this sensitivity;
2) I feel pull/discomfort in my testicle and buttock when I urinate or have an erection
3) Sitting causes pain
4) Squats or leaning down causes discomfort/pulling sensations
5) I feel numbness in my buttock on the affected side if I sit on it for a certain period of time
6) I feel discomfort if I lay in bed on affected side
I was hoping to get some expert opinion from the community on what I am dealing with and how to overcome this nightmare. I hope that the community can help me and guide me in the right direction in my healing journey.
Thank you everyone for listening to this embarrassing story!