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Both my urologists I saw this year recommended I see a Neurologist after my Urodynamic testing. Neurologist has done a number of tests and imaging on me and says he doesn't see anything nerve related to cause my incontinence. My Urologists believe I should get a second neurology opinion and a consultation with a neurosurgeon regarding a disc contacting the S1 nerve. Is getting sent to a neurologist common when Urodynamics doesn't show any incontinence?
 
I went to a urologist who exhausted all his tests so he sent me to a neurologist. Neurologist finally found out I have CIPD (Neuropathy) throughout my whole body. This is one of the factors of my urinary incontinence. Going to a new neurologist, when I can get in, to get confirmation that the 1st diagnosis was correct.Still having to wear diapers and probably always will.This is an autoimmune disease so it can be managed but not completely ever cured.
 
I had a NCS and EMG last week and they say there was nothing abnormal. I have a disc bulging and contacting the S1 nerve. Neurologist doesn’t think it is causing my issues which is incontinence and right toe numbness, both started within weeks of each other.
 
I've done the Urologist routine. No joy. They didn't refer me anywhere. I have a Neurologist for something else, already, and she hasn't suggested anything, but I never asked her if there is a connection to Peripheral Neuropathy. PN isn't related to the S1 nerve, far as i know, but now I'll ask. I had an operation (for cancer) by a NeuroSurgeon, last year. The incontinence increased drastically, no one was willing to talk about it - and i do mean no one, not even the PA and the nurses. That was May. The incontinence has gotten a lot better. I've never seen a connection made in the literature, although maybe when the nerves/spine are damaged in an accident. A bad concussion from a fall sent me to the ER - and one of the symptoms was almost total urinary IC. They discovered the brain cancer. Not sure what conclusions can be drawn from that mess. I do take meds for the PN, and they work.
It seems likely that IC and spinal damage can be related. For example, if you are a paraplegic, or "just" paralyzed from the waist down, what does that mean for IC? Damned if I know. Maybe getting an opinion from a Neurologist, if you can afford it (I can't believe i had to say that. Our medical system is broke), would be worth it.
Anyone here had a Neurologist with an opinion?
 
I have learned that when it comes the the nervous system it is hard to get a diagnosis and the doctors just shrug and say "deal with it". I have problems related to a motorcycle accident, but none of them should give me bowel problems, yet here I am still wearing a soiled diaper 20 years later. As long as its not getting worse I guess I pretty much have to deal with it and the insurance companies wont pay for any more tests.
 
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