Health Organization for Pudendal Education

Has anyone been to Cedars-Sinai Women's Continence and Pelvic Health Center in Los Angeles, CA? On their website, they list "Pudendal Nerve Testing". I'm also interested in researching whether they have doctors who specialize in pelvic pain and adhesiolysis surgery.

http://www.cedars-sinai.edu/Patients/Pr ... th-Center/

Emily B.

I never heard back from my post, so I thought it was worth asking again.

Has anyone been to Cedars-Sinai Women's Continence and Pelvic Health Center in Los Angeles, CA? On their website, they list "Pudendal Nerve Testing". I'm also interested in researching whether they have doctors who specialize in pelvic pain and adhesiolysis surgery.

http://www.cedars-sinai.edu/Patients/Pr ... th-Center/

Emily B.

Hi Em,
I've never been there, nor do I know of anyone who has. I can say that I've had all of that other testing they offer at Mass Generals Pelvic Floor Rehab Services in Boston.
They did not offer or acknowledge PN testing. Probably wouldn't hurt to give them a call to ask for the specifics of what "PN Testing" means. PNMLT? It would be great to have another resource for this condition!
Please let me know how you make out.
Love,
Karyn

Hi Emily,
I see that you have not posted in a very long time and hope you have found medical treatment. Just wanted to mention I know nothing about Cedars Sinai pudendal department, but I have an appointment in 1 week to see Dr Joshua Prager who is in the California Pain Medicine Center at UCLA. If you are still looking for someone in the LA area, give him a call.
Limdsay

Hi, Lindsay. That's so nice of you to think of me. I'm still in so much pain. I'd love to hear how your appointment with Dr. Prager goes.

Thanks,
Emily B.

Emily-

I live in the LA area. My understanding is this group works more with IC / prolapse patients. But Dr Hall is very respected and in my opinion it wouldn't hurt to have a consult with them. I am re-considering the same after seeing your post.

Best-
Merrie

Emily,
I hope I will have some good news to report to you. I also go to a fabulous Dr. in Phoenix. His name is Michael Hibner, he's at St. Joseph's Hospital and he is the most caring, sympathetic dr. who only wants to see you get well. I had 3 pudendal nerve blocks with him and have just, 2 weeks ago, had my second round of Botox shots.
The pudendal ct guided blocks are how they give you a definite diagnosis of pudendal neuralgia. Have you already been diagnosed? I started out with a diagnosis of vulvadynia 4 years ago, then pelvic floor dysfunction 2 years ago, and finally pudendal neuralgia last year. So I felt my next journey was to work with a team of pain management, psychological counseling and physical therapy. Hence, my appointment with Dr. Prager and team. We've rented an apartment at the Palazzo in Westwood and am ready to get started. I'll let you know but if you don't hear from me, write me. I haven't fully learned how to use this website and can get lost easily.
Lindsay

Hi Lindsey,
Ive also been thinking about seeing Dr Prager in LA after hearnig of Lotta Nerve's success stories. I saw that you are about to start working with his group. I hope that all goes well and you get great results. One of my practitioners spoke with him for me and liked him.

I can't go out there right now as my kids are in school and I live on the east coast. I am going to pursue some more options here in my area , but if I have to, am still considering Dr Prager as I have been in pain for a long time, and my goal is mainly to break the centralized pain cycle.

Could you please if you have time keep us posted as to how you do? I could also give you my email address as I am very interested in Dr Prager.
I wish you all the best out there!
Thanks very much.
Kathy

Hi LindseyG
I briefly spotted a post that you sent to Voilet saying you were trying to PM me. I lost track of the post and didn't get to read the entire thing.
I remember that you were starting treatment with Dr Prager and I was very interested in hearing about it.
I so hope that all is going well for you!
I have been in touch with Sharon and she is telling me a bit about pain pumps, as I am working with a pain doc here in the NY area and am awaiting a pain pump trial..The red tape involved in getting it going is taking awhile!
Meanwhile I want to make sure my doc is experienced and hope that I can maybe get him to speak to Dr Prager so that it is done the way he would advise for my pain issue.

Anyway all the best to you and I can email you if you like. Would love to hear about how you are doing with Dr Prager.
Regards,
Kathy D.

Emily B,
I have now been under Dr. Pragers care for three months. He has lowered some of my medications and started me on tegretol. Not sure that has made a difference. I had a pelvic MRI neurogram and that shows my right obturator internus muscle pressing on my pudendal nerve. So finally, a confirmation that my pudendal nerve is causing pain. Dr. Prager does not suggest surgery. He gave me more Botox shots and we will see in 3 weeks if they have helped. If so, we'll continue to do Botox until it stops working. If the Botox is not successful, he suggests a neurostim. So far the Botox is working on the right side where he gave me the Botox shots. However, I am now having pain on the left side. Will give it a few more weeks. He said he will give me Botox on the left before making any decision to do a trial of the neurostim. Are you doing any better?
Lindsay