Hi everyone,
I’m wondering if there any folks out there who have had redo unilateral pudendal nerve decompression surgery, ideally with Dr. Hibner and had a better outcome. I unfortunately am starting to think that my pudendal nerve have become “entrapt” either between ligaments and/or fibrotic scar tissue over the last 2 years. My symptoms were pretty severe prior to surgery and failed conservative treatment including multiple rounds of pelvic floor therapy and pelvic floor stretching. Would appreciate any insight any of you have on your experiences with Dr. Michael Hibner.
Success with redo decompression surgery
Re: Success with redo decompression surgery
Redo was a failure for me. And re-entrapped again with scar tissue
Devastated and no dr will help
Devastated and no dr will help
Re: Success with redo decompression surgery
Have you considered surgery with a physician that does it laproscopic? It's a much easier recovery time and I chose laproscopic because of some claims I read in the literature about reduced scar tissue and better visualization of the fibrotic tissue with the laprascope. When I consulted with Dr Hibner, his approach was much more invasive and also included botox at the time of surgery. He just seemed really convinced botox fixes everything every time I met with him and it really made it worse for me. Just my thoughts and I wish you well in your decision making.
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aussie_surfer
- Posts: 29
- Joined: Sat Jan 25, 2025 7:08 am
Re: Success with redo decompression surgery
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Last edited by aussie_surfer on Sat Apr 25, 2026 8:55 am, edited 1 time in total.
Re: Success with redo decompression surgery
I would love to see answers to this question as I am in the same situation, considering a redo surgery and Hibner appears to be the only surgeon I've found who definitely does redo decompression surgery. But man...it is a big gamble to spend that much money and go through the brutal recovery from transgluteal surgery again.Natedogg91 wrote: ↑Wed Jul 23, 2025 2:05 am Hi everyone,
I’m wondering if there any folks out there who have had redo unilateral pudendal nerve decompression surgery, ideally with Dr. Hibner and had a better outcome. I unfortunately am starting to think that my pudendal nerve have become “entrapt” either between ligaments and/or fibrotic scar tissue over the last 2 years. My symptoms were pretty severe prior to surgery and failed conservative treatment including multiple rounds of pelvic floor therapy and pelvic floor stretching. Would appreciate any insight any of you have on your experiences with Dr. Michael Hibner.
May 2002 - developed disabling PN.
Aug 2002 - started 4 rounds of CT scan guided nerve blocks
Feb 2003 - had bilateral decompression surgery. The surgeon found a very obvious abnormal issue on the left side that was wrapped around my nerve and squeezing it flat. Slow improvement over the next 6 years.
6 years after surgery Egoscue Method helped me completely get rid of lingering symptoms.
No issues with PN for 14 years.
Nov 2023 - accident triggered disabling PN again
Aug 2002 - started 4 rounds of CT scan guided nerve blocks
Feb 2003 - had bilateral decompression surgery. The surgeon found a very obvious abnormal issue on the left side that was wrapped around my nerve and squeezing it flat. Slow improvement over the next 6 years.
6 years after surgery Egoscue Method helped me completely get rid of lingering symptoms.
No issues with PN for 14 years.
Nov 2023 - accident triggered disabling PN again
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Natedogg91
- Posts: 24
- Joined: Tue Oct 03, 2023 10:10 pm
Re: Success with redo decompression surgery
My options are pretty limited at this point. I unfortunately had a regression of symptoms and have pudendal neuropathy (rectal dysfunction, erectile dysfunction, rectal/perineal/scrotal burning). Symptoms had improved significantly after my initial pudendal nerve decompression. As life went on and I started getting back to a more normal life including more sitting, the nerve didn’t like that and my symptoms started coming back. My wife and I want to try for kids soon and your standard ED treatments aren’t working as this is largely a neurogenic problem. I have an upcoming consult soon with Dr. Hibner and I’m willing to do whatever it takes to improve my symptoms. I have exhausted conservative therapies (yet again) without significant improvement in my symptoms.
Re: Success with redo decompression surgery
If you're open to sharing, I would love to hear the outcome of your consult with Hibner. I'm in such a similar situation, have thoroughly exhausted all conservative therapies and am considering "betting the farm" on surgery with Hibner as I'm pretty much out of other options at this point. Mind if I send you a DM to stay in touch?Natedogg91 wrote: ↑Thu Jul 31, 2025 9:21 am My options are pretty limited at this point. I unfortunately had a regression of symptoms and have pudendal neuropathy (rectal dysfunction, erectile dysfunction, rectal/perineal/scrotal burning). Symptoms had improved significantly after my initial pudendal nerve decompression. As life went on and I started getting back to a more normal life including more sitting, the nerve didn’t like that and my symptoms started coming back. My wife and I want to try for kids soon and your standard ED treatments aren’t working as this is largely a neurogenic problem. I have an upcoming consult soon with Dr. Hibner and I’m willing to do whatever it takes to improve my symptoms. I have exhausted conservative therapies (yet again) without significant improvement in my symptoms.
May 2002 - developed disabling PN.
Aug 2002 - started 4 rounds of CT scan guided nerve blocks
Feb 2003 - had bilateral decompression surgery. The surgeon found a very obvious abnormal issue on the left side that was wrapped around my nerve and squeezing it flat. Slow improvement over the next 6 years.
6 years after surgery Egoscue Method helped me completely get rid of lingering symptoms.
No issues with PN for 14 years.
Nov 2023 - accident triggered disabling PN again
Aug 2002 - started 4 rounds of CT scan guided nerve blocks
Feb 2003 - had bilateral decompression surgery. The surgeon found a very obvious abnormal issue on the left side that was wrapped around my nerve and squeezing it flat. Slow improvement over the next 6 years.
6 years after surgery Egoscue Method helped me completely get rid of lingering symptoms.
No issues with PN for 14 years.
Nov 2023 - accident triggered disabling PN again
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Natedogg91
- Posts: 24
- Joined: Tue Oct 03, 2023 10:10 pm
Re: Success with redo decompression surgery
Sure you can, I’ll be honest I don’t check this website as often as I used to after dealing with this for 3+ years. But we’ll see what he says! I’m starting with a virtual consult and likely flying down to Arizona soon after if he offers some options.
Re: Success with redo decompression surgery
Hibner is big on Botox it was a complete waste for me
I think it’s another money making gimmick for him
I think it’s another money making gimmick for him