What is Pudendal Neuralgia?
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- Опубликовано: 22 май 2019
- Dr. Allyson Shrikhande provides an in-depth discussion about Pudendal Neuralgia, it's symptoms, potential causes, and potential treatments.
Dr. Allyson Shrikhande, a board certified Physical Medicine and Rehabilitation specialist, is the Vice Chair of the Medical Education Committee for the International Pelvic Pain Society. She is working with other experts in the field of chronic pelvic pain to develop training modules for residents and physicians interested in learning about the diagnosis, treatment and management of chronic pelvic pain. A leading expert on pelvic health and a respected researcher, author and lecturer, Dr. Shrikhande is a recognized authority on male and female pelvic pain diagnosis and treatment.
International Pelvic Pain Society - www.pelvicpain.org/home.aspx
Pelvic Rehabilitation Medicine Practice - www.pelvicrehabilitation.com/
Rose Study - www.pelvicrehabilitation.com/... - The ROSE study won the 2018 Innovation Challenge award for the potential diagnostic test using menstrual effluent (ME).
IRB Guidelines - feinstein.northwell.edu/for-p...
Interstitial Cystitis Association - www.ichelp.org/
Coccyx Pain Resource - www.coccyx.org/index.htm
Endometriosis Foundation of America - www.endofound.org/
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The 2019 Pelvic Health Summit is an online summit created to bring the latest information and top practitioners of pelvic health to you. Our goals for the summit are:
- Educate Men and Women on the importance of Pelvic Health
- Provide multiple perspectives and specialists to weigh in on Pelvic Health
- Provide multiple perspectives and specialists to weigh in on Pelvic Health
- Provide an accepting platform for people to engage, discuss, and support one another
Learn more about the summit, speakers, topics and join our supportive community group at:
Summit - www.pelvichealthsummit.com/
Facebook Group - / pelvichealthsupport
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If you want to learn more here are some resources from our partners:
Pelvic Rehabilitation Medicine - www.pelvicrehabilitation.com/
International Pelvic Pain Society - www.pelvicpain.org/home.aspx
The Women’s Pelvic Health Podcast - www.thewomenspelvichealthpodc...
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How wonderful. I have pudendal neuralgia from damage caused by surgical mesh TOT. Partial mesh removal from major side effects. A huge mess and I know many with the same issues. Sharing!! Thanks again.
Metal Filshie clips used in my tubal ligation migrated. One was on my rectum and it caused my pudendal nerve entrapment. The other went through small bowel. I’m a wreck.
Please come to Los Angeles to help us!!Allyson seems like such an authentic and helpful person. We need your help over here! 💜
Cheers for the Video! Forgive me for chiming in, I would love your opinion. Have you ever tried - Taparton Sturdy Nerves Takeover (erm, check it on google should be there)? It is an awesome one of a kind product for Getting rid of Neuropathy without the hard work. Ive heard some pretty good things about it and my BF after many years got astronomical results with it.
I have endometriosis, interstitial cystitis, and was recently diagnosed with pudendal neuralgia. I’ve been up and down for this year, after 5 years of remission, but today I hit a crippling flare. One where it was somewhat difficult to walk. But I applied cream, did my stretches and I was able to have more movement. It wasn’t where I wanted it, but I have to respect that it’s better than where it was. When she said nerves do heal, they just take time..that did give me hope. I have to accept that I have this condition and life is gonna look different for me..but I have tools now and this pelvic rehabilitation team and physical therapy. All hope is not lost even though it feels that way. Nerves are bitches but they do heal
Please come to u,k as we need your help here. Bless you
I wish I’d understood this was my issue when it started 10 years ago. I finally found a pain management doctor that recognized what was going on, both the cause and the side effect.
Venus De Milo
I’m still getting treated, but I’m having incremental improvement. A knowledgeable pain management doc can really help. I recent had an impar ganglion block and bilateral hypogastric block, and an injection into a knotted pelvic floor muscle, plus ketamine infusion therapy and pelvic floor Phys therapy. It’s taken a few procedures, but the nerves have started calming down.
@@McMomfaceplustwo atleast you have money for treatment. I don't have that either.
Glad that you have found someone to treta you.
@@vaibhavdumaga7229
I’m so sorry, I do understand that situation. I’m perilously clinging to COBRA insurance right now
@@McMomfaceplustwo In my country, pudendal nerve treatments are not covered into any of the insurances.
Please come to Saint Augustine FL as well. There is a Spine Center who you may be able to Team
Up with.
How it can be treated???plz tell
Can u suggest some doctor in San fransisco to heal pudendal neuralgia
I am in the Detroit area. Any recommendations for a doctor? I can travel. Thanks
Thank you so much. I know that this is what I have (Pudendal Neuralgia) a long with (Cystocele Prolapse). My question is, how do I want to exercise with both ? Do I need to speak to my physical therapist about it? Or do I speak to a urogynecologist to help me with the pain?
Where in north Jersey are u in
Damn, wish I was in New York 😢
What if it’s multiple sclerosis related?
I see this sweetie and i cann like see her pain behind her eyes. Dammm sad for people and for myself
Is there any clinics in Manitoba Canada 🇨🇦 where can we reach out to?
THANK 🎁🎁🌈🌈😊😊
My daughter has pudendal neuralgia after using a vibrator. Can you help
I can't do physical therapy for my pudendal neuralgia cause I have severe spine issues.
have had pain since 2011. Been to all the drs, had all the tests. My biggeset issue is a live in a rural area and drs just look at me when I try to explain. Have seen 1 dr who has knowledge but she wants me to go to a dr that is 3 to 5 hours away. Its horrible to deal with on a daily basis
Could you please recommend someone in the Worcester or Boston area of Massachusetts? I have been suffering for almost a year now. Thank you very much.
I can help you.
Dr. Kohli in Wellesley, Ma.
whats the procedure for people from india?
Live in New Mexico, 68 years old male, pelvic pain for 2 years and 3 months suffering! It is causing problems with my marriage. My wife doesn't understand my pain. Have seen regular Doctor, Urologist, even had back surgery, annular tear to take away the pain. Nerve blocks. Have seen pelvic pain therapist, that helped. Who can tell me if I have prudential neuralgia?
Thank you so much, this has given me hope. I have had issues for 6 years now and have given up hope of ever getting better. I am in the UK, are there any clinics that you could please recommend as I'm desperate to get some relief from the constant pain. Thank you so much
Same
Who can you recommend in Los Angeles. My wife has been suffering for two years and finally got a diagnosis of pudendal neuralgia
Lovely Video clip! Excuse me for butting in, I am interested in your thoughts. Have you ever tried - Taparton Sturdy Nerves Takeover (Have a quick look on google cant remember the place now)? It is an awesome exclusive guide for Getting rid of Neuropathy minus the headache. Ive heard some great things about it and my mate at very last got cool success with it.
Has your wife had any surgery using metal clips or mesh?
She may need a guided nerve block into the nerve roots via her buttock.
Is it one side or both sides?
Are you still looking for help? I have some solutions.
Hello, I am in the UK. I think this is what I'm suffering from so can't completely symphasise with your Wife's pain. could I please ask (without being too personal) what treatment did your wife undertake and did it improve her pain and symptoms. I'm desperate to find some relief to the pain I'm suffering and would really appreciate your views on how your wife is feeling now, is she pain free or has it reduced (I hope so)
We need you in Phoenix az
Boy do we ever! Have you found anyone yet to help?
Wow
Is there anyone you can recommend in san diego area who specializes in PN or PNE? I've been suffering for 6 months from a horrible pap smear injury that injured my pudendal nerve. I've seen 2 physical therapists and 4 different doctors and the doctors don't seem to know much about it and they are either saying there are no imaging tests I can get done or they are honest and tell me they don't know what to order. They just keep referring me to different doctors. I'm on several meds for the pain, and it doesn't seem to be helping. I'm suffering a great deal, and any help you can provide would be very much appreciated. Thank you.
Do you have any locations on long island new york?! I believe i have a sense of this. I have abdominal and pelvic discomfort, sexual difficulties, frequent urination and minor incontinence. My symptoms started with a feeling of urine trapped in my urethra which mustve been a nerve sensory issue
There is one in Great Neck! www.pelvicrehabilitation.com/locations/long-island/
Do you have pain in urethra?
I mean not really? In the beginning i had that urine in my urethra feeling. Why what do you feel
Does this physiatrist physician know of a clinic in Canada that can do the injections ?
Thank you for this. My question is, if the pudendal nerve can heal, then why do I hear so many people saying its been debilitating their life for ample years? Is self healing actually common with this, or are the chances slim?
If someone healed, would they even be commenting here? No, they would be going on with their lives. The people commenting online are just the ones with continuing issues.
Also, at what point do u realize it's permanent? I've tried many things w no improvement in 6 months.
I’m miserable I can’t sit or stand or walk. Where can I go In Missouri
I highly recommend physical
Therapy for pelvic pain. A place that does internail and external therapy. My urologist did a cyatoscopy and after that procedure I got the most painfiul spams n my pelvis. I wonder if my pudendal nerve got damage. Therapy is helping me with this issue, but I wish I never had that cystosocpy done since nothing was found in the bladder... my issue was only tight muscles in the pelvis,
have you tried estriol cream? it really can help with bladder and pelvic pain etc and it's a weak estrogen that only acts locally, not systemically so it's safe
Meant for me to see this regarding the cystoscopy. If my urologist suggests one (history of uti's). How were you finally diagnosed & PT started?
@@2b2unit Before the cystoscopy my symptoms were just bad cramps. I never had a UTI and after getting lots of test done the "last option" was the bladder for my doctor. So, I was referred to an Urologist. His first option was to do a cystoscopy. Wrong choice, since my bladder looked fine in the camera. The cystoscopy just caused me a second issue; painful bladder spasm that took me to E.R. I was referred to a PT after that, to help me ease the pain and it has really helped. The recovery has been slow, but it's working :-)
Nvr Mnd I have and it didn’t help at all.
@@venusdemilo3378 He has retired.
OMG U ARE COMING TO NJ!!??
They still can't figure mine out now they want to do cold laser therapy
What kind of Dr. Are you seeing for treatment. Curious for myself. Having issues
@@tiffanylove997 I'm seeing a urogyncolgist
What stretches can a male do to eliminate penis gland pain from this?
I don’t see anything about healing sexual function though. All the videos are about pain management and nothing about living a normal sexual life as before. That feels hopeless to me. Sexual function is necessary to a normal life worth living especially in your 20s.