← Return to Pudendal Nerve Entrapment/Neuropathy/Damage
DiscussionPudendal Nerve Entrapment/Neuropathy/Damage
Chronic Pain | Last Active: Oct 29 9:41am | Replies (592)Comment receiving replies
Replies to "I am also from Canada and have been experiencing all of the symptoms of Pudendal Nerve..."
I am having a pudendal block done using fluoroscopy and ultra sound on January 4. The sitting pain is stopping me from driving to my grandchildren. I have incidence of urinary and fecal incontinence when the pain goes to the max. At this time I have to do something. Wishing you luck in finding a cure. At this time I am just looking to get to a pain level I can tolerate
Oh I can relate! This is how I got my Pudendal mess! I had emergency laminectomy surgery for Cauda Equina and a year later a fusion. I can’t sit nor lay on my back. It can be excruciating mainly in the rectal area. Maybe it would be worse, but I have partial saddle anesthesia from all my nerve damage.
I go to a pain clinic, (because lucky me I have other chronic pain), and they haven’t even tried to help with this.
I think I’m going to try a TENS unit in this area.