Pudendal Nerve Entrapment/Neuropathy/Damage
Hello from a new member. Am wondering if anyone suffers from the monster Pudendal Nerve Entrapment/Neuropathy/Damage? I do. And I'm very alone in it. It is a very uncommon condition, and because of its personal nature, one that many people may not be comfortable opening up about. There seems to be a more vocal/visible presence of patients in the US, AUS and France. I hope, I need, I want - for it be made more aware of here in Canada. If there is any one who suffers from it, or who thinks they might, please feel free to open up about it. Please join me in advocating for ourselves in this horrible condition.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
can you tell me what medicine was that?
Topamax. It's nasty and I stopped it after 2 weeks. But it was long enough for me to realize my butt felt better after 14 years of sitting on a donut. I was taking it for migraine and daily persistent headache. My former pelvic PT said she just read about it helping pudendal nerves. That was awhile after I was treating with her. But, it makes sense.......it's for seizures and that pudendal nerve is in a spasm. What have you got to lose?
Mikayla
I'm thinking of going to Dr. Tollestrup for this. Did you go to him? How was your outcome?
Pudendal Nerve pain:
After 2 solid years of horrific pain, visiting 7 local doctors, I made a appt at Mayo Clinic, Jacksonville, Fl MAYO CLINIC. I flew each trip. He gave me my life back. Horrific striking pain except when in a hot tub of water or elevating my feet. Was pretty much a home body. Sat on a doughnut cushion.
After exhaustive research, I found MAYO CLINIC’s Dr Paul Pettit, Urogyn. Year 2012. Under sedation, he used skillfully Used Botox injection. First one, helped a little. He told me that… Came back when he told me ( about 2-3 months?). After second injection , one day… it magically left me! To date, no pudendal nerve pain. I am forever grateful to MAYO and Dr Paul Pettit.
I had this monster for 14-1/2 years so I know you are more than ecstatic. What finally helped me was anti-seizure medicine that I was taking for another issue.
hey
I suffer from pudendal neuralgia, loss of penile sensation. I would very much like to have conversation with you
can you contact me? ***
Okay, Christopher, I will email you later today.
Hi @tullson, I'm happy to see that you've already connected with @mikaylar. You'll notice that we removed your email address. Connect is a public forum. We recommend sharing personal contact information using the secure private message function.
I might also add that by sharing here in the forum, you are connecting with several people where all can benefit from group support.
Good idea, John. It is probably best to stay on this site. What is the secure personal contact information?