Thanks for this, I've been experiencing the discomfort of PD for about a year now and I've been in the care of a respected pelvic floor physical therapist with mixed results (good days and bad days). I'm currently at the point of eliminating treatments that don't work so your video is very useful to me. Sorry to hear that your experience has lasted so long. Please keep posting any information that you find.
Almost 3 years into PN, CPPS pain. I am willing to try anything. I am beyond miserable and losing hope that this is going to be my life from now on. Thank you for this video.
@@mysecretlifeofpain I just finished 8 months of PT, with no measurable benefit. The PT was $110/week! Mutual decision was not to continue as it was wasting their time and my $. Tried a nerve block but the results were not long lasting. This pain is literally destroying my life.
@@DelmarksmanI understand your frustration. I did 6 months with a really knowledgeable PT who at first seemed convinced my PN was caused by thickened connective tissue back at ischial tuberosity and fascial adhesions (despite my pain starting immediately after an invasive surgery). But treating that made no difference and I was discharged :(
@@mysecretlifeofpain I'm not in pain, per se. I have some ear clips but they don't seem to be doing anything. What am I supposed to feel by using them, as it relates to the vagus?
Thanks for the info.
@@cliff_fall you’re welcome! Thank you for liking and supporting my channel.
Thanks for this, I've been experiencing the discomfort of PD for about a year now and I've been in the care of a respected pelvic floor physical therapist with mixed results (good days and bad days). I'm currently at the point of eliminating treatments that don't work so your video is very useful to me. Sorry to hear that your experience has lasted so long. Please keep posting any information that you find.
Me too a year and still no cure. I've had numbing creams and use deep heat! Cocodomal and oddly migraine tabs take the edge off
Almost 3 years into PN, CPPS pain. I am willing to try anything. I am beyond miserable and losing hope that this is going to be my life from now on. Thank you for this video.
It’s horrible I know, mine has been resistant to intervention as well. I hope the TENS brings you some relief
@@mysecretlifeofpain I just finished 8 months of PT, with no measurable benefit. The PT was $110/week! Mutual decision was not to continue as it was wasting their time and my $.
Tried a nerve block but the results were not long lasting.
This pain is literally destroying my life.
@@DelmarksmanI understand your frustration. I did 6 months with a really knowledgeable PT who at first seemed convinced my PN was caused by thickened connective tissue back at ischial tuberosity and fascial adhesions (despite my pain starting immediately after an invasive surgery). But treating that made no difference and I was discharged :(
Great video and pretties eyebrows around. I'm definitely getting a tens machine now for pudendal, pelvic, hypogastric, and vagus nerve stimulation.
@@williamblair1123 thank you! And thanks for leaving a comment. Sorry you’re also in pain. How will you do the vagus stim?
Ear clips?
@@mysecretlifeofpain I'm not in pain, per se. I have some ear clips but they don't seem to be doing anything. What am I supposed to feel by using them, as it relates to the vagus?
Thanks for commenting. I hope you get results with PT!
10 years omg 😢