Guest guest Posted May 1, 2004 Report Share Posted May 1, 2004 Hi everyone, I am a new member But I am not new to the pain. I have had vulvar pain for almost 5 years now. It started right after my hysterectomy. I am 34 years old. I have been to every kind of Dr. you can think of I have been poked and proded to the hilt. I went to a vulvar specialist this past week and she was my last hope. After spending almost 3 hours in the office and only seeing her for about 15 minutes of that time. She looked and since she didn't se anything unusual, she too doesnt seem to think anything is wrong. She didnt take me seriously. I give up! I told my family Dr. no more doctors but him! No more needles! I have Pudendal Nueralgia. My clioral nerves are damaged to the point where it hurts all the time and it keeps me up nights and totally destroys my days. He was the first of about 15 doctors who took the time to do research on the subject. I found out most of the information myself. I even talked to specialist in 2 different states. I was wondering if anyone in the group had anything close to this or knows anyone who does. I am currently on Vicoden and Topomax. My family doc is sending me to one last pain clinic, on the condition that they don't want to put needles in my vagina . To perhaps try a low, low dose pain patch of some sort. I am so tired of taking pills all the time. I have 2 kids and I don't like the way the pills make me feel. I appreciate any suggestions or information that anyone has to offer Thanks so much Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2004 Report Share Posted May 1, 2004 Hi kid, listen, I don't fully understand what is causing your pain, but I was on elavil which is for nerve pain for years and it worked. Just an idea. Ask your doctor, hope I havent' adivsed and said something I shouldn't. I am new and see there is an issue about giving medical adivce. I am only telling you what worked for me. I don't know where you live, but try and go to a big university hospital if you can, you will find that all these other doctors don't know a thing. This is rare. Call the Universtiy Hospital in the state you live. Hope this has helped. Had enough!!! > Hi everyone, I am a new member But I am not new to the pain. I have > had vulvar pain for almost 5 years now. It started right after my > hysterectomy. I am 34 years old. I have been to every kind of Dr. > you can think of I have been poked and proded to the hilt. I went > to a vulvar specialist this past week and she was my last hope. > After spending almost 3 hours in the office and only seeing her for > about 15 minutes of that time. She looked and since she didn't se > anything unusual, she too doesnt seem to think anything is wrong. > She didnt take me seriously. I give up! I told my family Dr. no more > doctors but him! No more needles! I have Pudendal Nueralgia. My > clioral nerves are damaged to the point where it hurts all the time > and it keeps me up nights and totally destroys my days. He was the > first of about 15 doctors who took the time to do research on the > subject. I found out most of the information myself. I even talked > to specialist in 2 different states. I was wondering if anyone in > the group had anything close to this or knows anyone who does. I am > currently on Vicoden and Topomax. My family doc is sending me to one > last pain clinic, on the condition that they don't want to put > needles in my vagina . To perhaps try a low, low dose pain patch of > some sort. I am so tired of taking pills all the time. I have 2 kids > and I don't like the way the pills make me feel. I appreciate any > suggestions or information that anyone has to offer > Thanks so much > > > > > > *****END OF MESSAGE/REMOVE WHEN REPLYING***** > --------------------------------------------Yahoo members can go to: > http://groups.yahoo.com/group/VulvarDisorders > to search our archive or view our files. > > *** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2004 Report Share Posted May 1, 2004 In a message dated 5/1/04 11:16:59 AM, VulvarDisorders writes: << It started right after my hysterectomy. >> Hi , Do you still have your ovaries? An hormone imbalance could be making the pain worse. Was your hysterectomy vaginal? Several women have attributed their vv/vvs with nerve damage done during vaginal hysterectomies. I'm assuming that's when your pudental nerve was injured. << My clioral nerves are damaged to the point where it hurts all the time and it keeps me up nights and totally destroys my days.>> Have you tried Neurontin? It's similar to Topomax. I know you mentioned that you were tired of taking pills and Neurontin does require diligence, since one has to take it 2-4 times a day. Kristy is having some luck with nerve blocks, have you tried that? I think hers are injected through the vulvar area which you said you want to avoid, but other women have mentioned theirs are injected through the lower back. I would not suggest surgery to sever the nerve to the clitoris. A woman on another list did that and ended up in even worse pain, the wrong nerve was severed. Pain patches usually do not come close to touching nerve pain. If Vicodin isn't doing much, you probably won't have much luck with a low dose pain patch. What dose are you taking of the Topomax and how long have you been taking it? I'm going to assume the dose has to be escalated like Neurontin does until you find a level that works for you. Have you tried combining it with Elavil? Some times a combination of nerve signal disrupting drugs works best. And Ora took a drug that had Atropine in it that solved her clitoris pain. I can never remember the name of it. It might be Urised. There are several women on the Vulvodynia lists with clitoral pain, you may want to post to that list and see if anyone has any other ideas. I know Jac has had some clitoral pain reduction in the past few months but I don't remember exactly what treatment she has been following. Good luck with the pain clinic. Debbie Tiger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2004 Report Share Posted May 2, 2004 Michele, Can u be evaluated at a Women's Therapy clinic for physical therapy in the pelvic area? Please consider that, it may well help reduce the pain you experience. Many women use antiseizure meds to control nerve pain - is that what Topamax is? So do you think that nerves were damaged during the hysterectomy procedure? Dusty Had enough!!! Hi everyone, I am a new member But I am not new to the pain. I have had vulvar pain for almost 5 years now. It started right after my hysterectomy. I am 34 years old. I have been to every kind of Dr. you can think of I have been poked and proded to the hilt. I went to a vulvar specialist this past week and she was my last hope. After spending almost 3 hours in the office and only seeing her for about 15 minutes of that time. She looked and since she didn't se anything unusual, she too doesnt seem to think anything is wrong. She didnt take me seriously. I give up! I told my family Dr. no more doctors but him! No more needles! I have Pudendal Nueralgia. My clioral nerves are damaged to the point where it hurts all the time and it keeps me up nights and totally destroys my days. He was the first of about 15 doctors who took the time to do research on the subject. I found out most of the information myself. I even talked to specialist in 2 different states. I was wondering if anyone in the group had anything close to this or knows anyone who does. I am currently on Vicoden and Topomax. My family doc is sending me to one last pain clinic, on the condition that they don't want to put needles in my vagina . To perhaps try a low, low dose pain patch of some sort. I am so tired of taking pills all the time. I have 2 kids and I don't like the way the pills make me feel. I appreciate any suggestions or information that anyone has to offer Thanks so much *****END OF MESSAGE/REMOVE WHEN REPLYING***** --------------------------------------------Yahoo members can go to: http://groups.yahoo.com/group/VulvarDisorders to search our archive or view our files. *** Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2004 Report Share Posted May 6, 2004 Hi, Was that doctor from the U of M? I cant remember her name, right off. It took months to see her, and she did nothing for me. I ended up having nerve blocks in my low back, I am totally pain free, and on no drugs at all. I don't think that I had PNE but, I do feel I had PN. The nerve wasn't entrapped, but sure was irritated, for some reason. Sue~ Quote Link to comment Share on other sites More sharing options...
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