Pain medications for Pudendal pain
Pain medications for Pudendal pain
Are there any other med. choices for Pudendal pain other than Opiates. I was on Tramadol but my hair really started to thin and I think it was the Tramadol. I am afraid of becoming addicted to Opiates. Are there any other pain meds. effective for nerve pain. Thanks
Symptoms came on so slowly they were hard to explain to anyone much less myself. Discomfort sitting one day and not the next. Foreign object feeling in various private parts. Doctor to doctor. Mis- diagnosed many times. Un-needed surgery, depression pills and finally a diagnosis of PN. EMG testing in NH. Unsuccessful nerve blocks. Will start PT in a few weeks. Finally I don't think I'm crazy!!!
Re: Pain medications for Pudendal pain
No, unfortunately, that's why people move on to surgery.
Some use antidepressants like Cymbalta, or benzos like Valium, or neuropathy meds like Lyrica/Neurontin. If those don't work then they try opiates.
Some use antidepressants like Cymbalta, or benzos like Valium, or neuropathy meds like Lyrica/Neurontin. If those don't work then they try opiates.
PNE as a result of childbirth, 2002. Treatment by the Houston team, with neurosurgery by Dr. Ansell in 2004. My left side ST and SS ligaments were found to be grown together, encasing the pudendal nerve.
I am cured. I hope you will be, too.
There are no medical answers on the forum. Your only hope is to go to a doctor. I was very happy with the Houston team, which has treated the most PNE patients (well over 400), more than any other US provider.
http://www.tipna.org
I am cured. I hope you will be, too.
There are no medical answers on the forum. Your only hope is to go to a doctor. I was very happy with the Houston team, which has treated the most PNE patients (well over 400), more than any other US provider.
http://www.tipna.org
Re: Pain medications for Pudendal pain
There's a thread about possible addiction to tramadol - click here. I am now back on tramadol again, my doctors are all fine with that. For me, it does not make the pain go away but it does usually take it down a notch.
I've not heard of hair loss as a side effect with tramadol. Did you find that your hair loss stopped after you discontinued the tramadol?
I've not heard of hair loss as a side effect with tramadol. Did you find that your hair loss stopped after you discontinued the tramadol?
Re: Pain medications for Pudendal pain
Yes my hair loss stopped after taking Tramadol. I agree with you my pudendal pain did not go away it just took the edge off.
Symptoms came on so slowly they were hard to explain to anyone much less myself. Discomfort sitting one day and not the next. Foreign object feeling in various private parts. Doctor to doctor. Mis- diagnosed many times. Un-needed surgery, depression pills and finally a diagnosis of PN. EMG testing in NH. Unsuccessful nerve blocks. Will start PT in a few weeks. Finally I don't think I'm crazy!!!
Re: Pain medications for Pudendal pain
Hello;
I've been losing my hair like crazy and now I think I know why. Tramadol. I've been on Tramadol for 2 years. It does take the edge off and I've found Percocet, Hydromorphone and Vicodin don't really take the pain down as well. Also I need to take motion sickness pills and laxatives when I take the stronger meds. I can't stop with the Tramadol because I know I couldn't stand the pain, but at least now I know about the hair loss. It's a good thing that I always had a lot of hair to begin with.
Thanks for the info;
Doreen
I've been losing my hair like crazy and now I think I know why. Tramadol. I've been on Tramadol for 2 years. It does take the edge off and I've found Percocet, Hydromorphone and Vicodin don't really take the pain down as well. Also I need to take motion sickness pills and laxatives when I take the stronger meds. I can't stop with the Tramadol because I know I couldn't stand the pain, but at least now I know about the hair loss. It's a good thing that I always had a lot of hair to begin with.
Thanks for the info;
Doreen
Five pudendal nerve infiltrations with good results.
Sixth Injection left me with more burning, more pain, pain in buttocks.
Botox shot didn't notice any difference
Physical Therapy - Aquatic and Myofascial
External and Internal Manual Therapy on the obturator muscle.
3T MRI with Dr. Potter
2nd opinion with Dr. Hibner in Phoenix
Loretta Robertson PT Phoenix
Decompression surgery Nov. 1, 2011
Sixth Injection left me with more burning, more pain, pain in buttocks.
Botox shot didn't notice any difference
Physical Therapy - Aquatic and Myofascial
External and Internal Manual Therapy on the obturator muscle.
3T MRI with Dr. Potter
2nd opinion with Dr. Hibner in Phoenix
Loretta Robertson PT Phoenix
Decompression surgery Nov. 1, 2011
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- Posts: 196
- Joined: Mon Sep 27, 2010 3:42 am
- Location: Vail, Arizona
Re: Pain medications for Pudendal pain
Hope you don't mind me asking but how much Tramadol do you take and how often? I have 50mg and find it does nothing for me, but the one night I took 100mg I felt hungover the entire next day.
Have been dealing with burning pain since Jan 2010.
No sitting since April 2010.
Seen the following dr's: DO, GYN, Dermatologist, Accupuncturist,
URO GYN (his RN is the one who suggested the pain could be PN), Neurologist
Had ECG and MRI both inconclusive, only the SSEP said Pudendal reaction was abnormal and they lost that test result.
Saw Dr. Castellanos April 6, 2011. Next steps, MRI and botox. Having PT while waiting.-Botox denied, appealing to Insurance company now.
No sitting since April 2010.
Seen the following dr's: DO, GYN, Dermatologist, Accupuncturist,
URO GYN (his RN is the one who suggested the pain could be PN), Neurologist
Had ECG and MRI both inconclusive, only the SSEP said Pudendal reaction was abnormal and they lost that test result.
Saw Dr. Castellanos April 6, 2011. Next steps, MRI and botox. Having PT while waiting.-Botox denied, appealing to Insurance company now.

Re: Pain medications for Pudendal pain
I am taking the slow release form of tramadol, on the recommendation of my local pain clinic. They tell me that they have found it more effective for long term pain management than the 'ordinary' sort. My usual dose is 300mg, taken as 150mg tramadol SR morning and evening. But I don't stick rigidly to this, if I am having a bad day I will take it up to 400mg (which is the daily limit) with ordinary tramadol 50mg capsules, if I am having a flare I will take it up to 200mg SR morning and evening, if I am having a good patch then correspondingly I take the dose down to a total of 250mg or even 200mg.
However I do always take something, whether I have pain right then or not, because the pain always does arrive at some point. The pain clinic are most insistent on this, they point out that it is much easier to control pain by having the pain relief already running when the pain arrives, rather than letting the pain get going full blast and then trying to rein it in. Also, a lower total dose is usually needed.
I am lucky in that I tolerate tramadol very well, I don't get constipated or have any other side effects. At the beginning it did make me feel as if I'd had two stiff drinks, and then I'd usually fall asleep. But, as with most side effects, this was short lived and the only thing it does now is take the pain down.
(Edited to correct my grammar)
However I do always take something, whether I have pain right then or not, because the pain always does arrive at some point. The pain clinic are most insistent on this, they point out that it is much easier to control pain by having the pain relief already running when the pain arrives, rather than letting the pain get going full blast and then trying to rein it in. Also, a lower total dose is usually needed.
I am lucky in that I tolerate tramadol very well, I don't get constipated or have any other side effects. At the beginning it did make me feel as if I'd had two stiff drinks, and then I'd usually fall asleep. But, as with most side effects, this was short lived and the only thing it does now is take the pain down.
(Edited to correct my grammar)
Re: Pain medications for Pudendal pain
Hi all;
I was taking Tramadol 50 mg. every 6-7 hours last year. Now, 150mg. in AM 150mg. noon and 100. night. The slow realease did nothing for me. Maybe last year when I was just starting this joy ride it would have been okay, but not anymore. My suggestion would be, take what keeps your pain down to a point you can stand. If you need more as time goes by, you need more. In this PN club we've joined, we all take more stuff as time goes by. I do not have any side effects from Tramadol, except now the hair loss. So glad someone brought that to my attention!!!! I'm sick of doing my hair when I hurt, so maybe a wig, blondish, would be something to think about.
Gotta go.
Have the best day you can;
Doreen
I was taking Tramadol 50 mg. every 6-7 hours last year. Now, 150mg. in AM 150mg. noon and 100. night. The slow realease did nothing for me. Maybe last year when I was just starting this joy ride it would have been okay, but not anymore. My suggestion would be, take what keeps your pain down to a point you can stand. If you need more as time goes by, you need more. In this PN club we've joined, we all take more stuff as time goes by. I do not have any side effects from Tramadol, except now the hair loss. So glad someone brought that to my attention!!!! I'm sick of doing my hair when I hurt, so maybe a wig, blondish, would be something to think about.

Gotta go.
Have the best day you can;
Doreen
Five pudendal nerve infiltrations with good results.
Sixth Injection left me with more burning, more pain, pain in buttocks.
Botox shot didn't notice any difference
Physical Therapy - Aquatic and Myofascial
External and Internal Manual Therapy on the obturator muscle.
3T MRI with Dr. Potter
2nd opinion with Dr. Hibner in Phoenix
Loretta Robertson PT Phoenix
Decompression surgery Nov. 1, 2011
Sixth Injection left me with more burning, more pain, pain in buttocks.
Botox shot didn't notice any difference
Physical Therapy - Aquatic and Myofascial
External and Internal Manual Therapy on the obturator muscle.
3T MRI with Dr. Potter
2nd opinion with Dr. Hibner in Phoenix
Loretta Robertson PT Phoenix
Decompression surgery Nov. 1, 2011