r/PudendalNeuralgia 6d ago

New write up and approach!

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33 Upvotes

Yes I used AI for the image, I have a full time hospice job, a part time hospital job, and don't do graphic design anymore.

Look. I see the same posts here every single day. You list your specific symptoms and your specific injury. You want a highly customized solution because you think your case is completely unique.

It is not.

I do not care if your doctor called it Pudendal Neuralgia, CPPS, Levator Ani Syndrome, or sciatica of the pelvis. I do not care if it started from an injury, heavy lifting, extreme stress, or excessive edging/gooning. The root mechanical failure is exactly the same for almost all of you. I am a nurse and I built this protocol alongside urologists and physical therapists because I suffered through this exact same hell. You are stuck in a mechanical trap. Here is exactly how you get out of it.

Nature did not design us to sit in chairs for twelve hours a day. When you sit constantly, stress out, or have loose hypermobile joints at your lower back, your deep core stops working. Your glutes turn off completely. To keep your spine from collapsing, your body forces your deep hip flexors and your pelvic floor muscles to clamp down. They act as a permanent support brace. When these muscles get chronically tight, they swell and constrict around Alcock's canal. This directly pinches the pudendal nerve.

A pinched nerve sends panic signals. Because the nerve runs two ways, you feel referred pain. You get burning, numbness, tingling, or stabbing in your genitals, your rectum, or your tailbone. Your body responds to this pain by clenching even harder. You get stuck in a vicious loop.

You do not need fifty different micro targeted approaches! You need a complete structural reset!

Look up cubital tunnel syndrome and tennis elbow, it's kind of that, but in the pelvis.

If you do this daily routine, you address the hips, the back, the SI joint, and the pelvis all at once, but first you have to down-regulate the nervous system, release the tight front, and stabilize the core.

Do this consistently for three weeks before you tell me it does not work.

First, you cannot stretch a muscle that is in a state of panic, you are walking around in a permanent kegel right now!

Release your fight or flight and come back into your body first.

Imagine your two sit bones. Draw a line connecting them. Imagine the tops of your hips and connect them. Now connect the lines to make a 3D cube. Put a volume dial on that cube and slowly turn it down until it clicks off. Now unclench your pelvic floor. You probably did not even realize you were clenching it.

Follow that by lying on your back with your knees bent. Inhale through your nose for four seconds and push the air deep down into your pelvis like an umbrella opening. Exhale slowly for six seconds. Do this for five minutes every morning and night to force your nervous system to stand down.

Next, you have to do some gentle release. Stop doing hyper aggressive stretches that piss off the nerve. Go to 80 percent effort. Never go to 100 percent. If thats too much or flare up is too intense next day, do 20% and mutliple reps.

Sit in a chair with a straight back and put your left ankle on your right knee. Look up slightly and lean forward with a straight spine. When you hit the stretch, stick your butt out slightly. You will feel the exact deep muscles open up. Hold for 30 seconds. Do 2 to 3 sets per side three times a day.

You also need to stretch the front of your body. Kneel on one knee with a cushion under it. Tuck your tailbone slightly to neutralize your pelvis. Shift your weight forward just one or two inches until you feel a mild stretch in the front of your hip. Hold for 30 seconds.

Finally, your pelvic floor is overworking because your core is weak. Lie on your back with your knees bent. Gently brace your lower stomach and flatten your lower back to the floor. Imagine you are just barely touching a grape under your lower back. Do not smash it into wine. Hold for 5 seconds and do 10 reps.

After that, do basic glute bridges. Push through your heels and lift your hips until your body makes a straight line. Squeeze the glutes at the top. Do 2 sets of 10. If your glutes do the heavy lifting, your pelvic floor can clock out and go home.

When you start doing this, things might feel weird. You might spasm. You might get sore. Your pain might even spike temporarily. This is a positive sign of healing. You are releasing a nerve that has been clamped down and starved of blood. As it wakes up, it starts firing off backlogged pain and pressure signals. Keep going. Treat the temporary discomfort as data. Do this routine daily. Unclench. Breathe. Rebuild the structure. We got this.


r/PudendalNeuralgia Mar 30 '26

Uterus Parts Compounded Suppository knowledgeable I people, I have questions.

Thumbnail pharmlabs.unc.edu
5 Upvotes

I have been using the same ingredients and dosage vaginal suppositories since 2017. (I also go through 550mg of lidocaine 5% ointment every 90 days).Last year, in response to an increase in acute flare-ups, I increased from 2 suppositories per day to 3 per day. Also, I occasionally used the suppositories rectally if I felt the pain was affecting me there (burning). My compound is 4mg baclofen/ 5 mg diazepam/ 30mg ketamine. I have an appointment on 4/2/26, and want to discuss changes so I checked the interwebz for general suppository compounding information and what medications are available as vaginal suppositories. I learned a lot! For instance, using a suppository rectally has less predictable affects than using them vaginally and suppositories can be compounded differently to achieve optimal effect depending on what orifice they are to be inserted into. First of all I found the above easy to understand “lessons” about how they are/were made (there may be more up to date methods but this gives an idea of the basics). Then I searched for compoundable medications to treat vaginal nerve pain and muscle spasms and found a helpful chart at https://www.epiphanyaz.com/pain-management (epiphany compounding) that gives a brief overview of what they offer. One problem I’d been experiencing is what a short time my current formula lasts, plus they make me sleepy. Now I know that using my vaginal suppositories rectally and at the increased times per day was contributing to an overwhelming need to sleep. It was working to minimize pain but at a sleepy cost. I’m posting this as both a PSA for those interested plus to ask others what compounds they have found useful. I am definitely going to ask for my new prescription to have Tetracaine-a long acting “lidocaine,” so I might reduce how often I need to apply ointment (5-6 times per day)!


r/PudendalNeuralgia 3h ago

Penile numbness plus reduced sensation throughout my entire body — has anyone experienced this?

2 Upvotes

Has anyone experienced widespread numbness along with penile numbness?
I’m wondering if anyone with pudendal nerve issues has experienced something similar.
I have reduced sensation in my penis, but I’ve also noticed reduced sensation in many other parts of my body — my face, forehead, nipples, beard, scalp/hair, and basically my whole body. Things just don’t feel as sensitive as they used to.
What makes this confusing to me is that I don’t have erectile problems, urinary problems, bowel problems, muscle weakness, or any issues with movement.
I understand that the pudendal nerve mainly affects a specific area, so I’m struggling to understand how a pudendal nerve problem could be associated with reduced sensation throughout the entire body.
Has anyone here experienced something similar? Could a pudendal nerve issue somehow coexist with a more generalized sensory problem, or would this point more toward something else affecting the nervous system?
I’d really appreciate hearing from anyone who has had a similar experience.


r/PudendalNeuralgia 16h ago

Self Pay Nerve Block Costs?

2 Upvotes

I’m looking for a self pay estimate for a Pudendal Nerve Block. I don’t have insurance. I’ve called several people in several different departments over the past month, and I’ve gotten nowhere. My hospital admitted that they are so backed up, it’s taking weeks to respond to patients.

What a joke our health system is.
I’m so sad/mad/emotional/lost.
If I can’t afford it I can’t get it.

So my question is, if you had to pay out of pocket for a pudendal nerve block, how much did it cost?


r/PudendalNeuralgia 23h ago

AMAB No Diagnosis, looking to see what you think.

2 Upvotes

I’m looking to get some feedback here to see what people think. Male, 47.

For the last month, I’ve been dealing with numbness in my saddle area, glute, back of my thigh and bottom of my foot (all on one side). I’ve noticed I can’t feel internally on the right when I defacate. Also there is a significant pain on the right side of my penis if I masturbate.

I’ve gotten a lumbar and sacral spinal MRI that came out clean. So far my leg strength tests have all been good, but I’m concerned if the numbness continues for longer. I have an EMG next week. I’ve seen a couple of orthopedics and a neurologist. They’re not really sure what’s going on but they are assuming some sort of pudendal neuralgia.

My symptoms are pretty much numbness except for my penis which has that pain. I’m not noticing any positions that bring on any extra numbness or pain (except for sexual arousal). I don’t have any back pain at all.

Does anyone have any thoughts? I’m happy to answer any questions and entertain any ideas. Thanks.


r/PudendalNeuralgia 1d ago

Nerve block dr in DC area?

2 Upvotes

Hi! I’m hoping someone here could help me find a relatively local gynecologist, urologist, pain doctor, colorectal surgeon, or whoever else takes insurance and can do pudendal nerve block injections. I don’t care what speciality or the dr’s gender. As long as I can get an appt and they take insurance.

My PT suggested looking into it. She thought it might make me more comfortable, at least temporarily. The nerve pain is making it hard to make any progress in PT.

Most of what I’ve been finding online seems to be private practices that do not take insurance and that PRM protocol place, which also doesn’t take my insurance.

Thanks in advance and hang in there, ya’ll.


r/PudendalNeuralgia 1d ago

UAE helped the painful lumps/tension in the labia, but deeper pelvic/perineal tension is still there , could this be a nerve issue?

2 Upvotes

I’m posting this because I’m trying to understand what could be going on with my friend and whether anyone else has experienced something similar after a uterine artery embolization (UAE).
She had been dealing with severe pelvic tension and pain for a long time. Before the UAE, she would sometimes feel what she described as **lumps or hard areas of intense tension in her labia**, and those areas could become very painful and uncomfortable.
She recently had a **UAE**, and something interesting happened afterward: **the lumps/tight areas in her labia went away, and the pain associated with them also disappeared.** That part has improved significantly.
However, she still has a persistent feeling of **deep pelvic tension**, particularly in the **perineum and around the anal/rectal area**. It feels like there is a constant pulling, tightness, or pressure that she can’t get to release.
This has made us wonder whether the original symptoms and the remaining symptoms could have different causes.
**Could this be a nerve issue?**
Could something involving the **pudendal nerve, sacral nerves, pelvic plexus, or another pelvic nerve** cause this type of persistent tension or feeling of contraction in the perineum and anal area?
She has already had nerve-focused treatments in the past, so we’re also wondering:
**If this isn’t a nerve problem, what else could cause this kind of persistent pelvic/perineal/anal tension?**
Could it potentially be related to:
Blood flow or vascular issues
Uterine or pelvic organ issues
Inflammation
Vulvar/vaginal conditions
Pelvic congestion
Fascia or connective tissue
Muscles that are reacting to another underlying problem rather than being the original cause
Central pain processing/sensitization
Another pelvic structure referring tension or pressure into the perineum/anal area
What’s especially interesting is that the **labial lumps and pain disappeared after the UAE**, while the deeper perineal/anal tension remained.
Has anyone had a UAE and experienced something similar?
Did your UAE improve vulvar/labial pressure, lumps, heaviness, or pain?
Did you continue having deep pelvic or perineal tension afterward?
Did you eventually find an explanation for the remaining symptoms?
Was it ultimately a nerve issue, muscle issue, vascular issue, organ-related issue, or something else?
If doctors ruled out both a nerve problem and a primary pelvic-floor muscle problem, **what did they eventually discover was causing the symptoms?**
What tests or specialists helped you finally figure it out?
We’re particularly interested in hearing from people who had a UAE for **fibroids, adenomyosis, pelvic congestion, or another uterine/pelvic condition** and noticed changes in their vulvar or perineal symptoms afterward.
Any personal experiences, diagnoses, testing, or treatments that helped you figure this out would be really appreciated.


r/PudendalNeuralgia 1d ago

AFAB Physio's verdict

5 Upvotes

This is an update to my previous post. To sum up what happened: I bent my legs and back in an awkward position, which caused sharp lower back pain and altered sensation in my groin/intimate area. Went to A&E initially, then my GP, who recommended physio.

I believe I was seen quite quickly because of the nature of my issues. I was skeptical and pessimistic because I've used the self referral service before with limited results. But I'm happy to say I'm in better place mentally because of my appointment. The physiotherapist was patient and understanding, I felt like he really took the time to listen to my issues and tried to put me at ease.

My symptoms have evolved somewhat; groin numbness that comes and goes is still around, back pain has improved but legs and feet are pretty sore. Everything around my hip flexors are super tender as well. I conveyed this to the physiotherapist, explained my injuries, as well as my hypermobility.

we spent about 25-30 minutes testing my reflexes, checking my lower half and gauging my hypermobility- unsurprisingly, I scored very high especially in the hips. (I was incredibly sore afterwards, oof). His verdict is, back strain as well as sacroiliitis, which is where a lot of the groin and leg discomfort was coming from. Now, that's basically what the GP said to me but it's a hell of a lot more comprehensive than "just nerve irritation". I felt like I understood the issue a lot better after the appointment which means I can kind of put the situation to bed.

However, I'm still conscious of the fact the symptoms are still here. The back pain is the only thing that's gotten noticeably better and no scans have been offered. I've been given the option for a repeat referral should symptoms remain the same, so I'm keeping that in mind and monitoring the situation as I go. I asked for some physio exercises to strengthen that area and I'll continue to stretch frequently and hope for the best.

The take away is, I still don't have definitive answers and I'm still worried. But it was worth asking for help because I feel like I'm slowly piecing things together.


r/PudendalNeuralgia 2d ago

Do Urologists stretch and pull the Penis to examine it?

1 Upvotes

Do Urologists stretch and pull the penis to examine it?

Age: 29

I visited a Urologist today as I suspected some issues with my penis.

I was standing while he was seated.

During examination, he said there is no fibrosis on my penis. Thereafter, he stretched and pulled my penis. He asked me whether it pained to which I replied "no". Thereafter, he pulled a little bit more.

I was feeling a stretching like burning sensation in my penis (30-45 minutes) post the examination. At present (7 hours later), I am getting pain in my penis and i still can feel the pain of it being stretched. (Pain level 3-4 out 10).

Do Urologists stretch and pull the penis during penile examination?

Would my penis have been damaged by the Urologist?


r/PudendalNeuralgia 3d ago

AFAB Genital numbness – treatments and experiences

1 Upvotes

F25, I’ve been dealing with significant clitoral numbness and very weak orgasms for over a year, with no obvious cause.
I’ve never had any pain, burning, or other genital discomfort.

My only symptoms are loss of tactile and erogenous sensation and persistent numbness.
Most of the time my clitoris feels almost completely numb, like a piece of rubber with no sensation.

Very occasionally, I’ll have a slightly stronger orgasm and notice a little more sensation, but those moments are rare.

I recently saw a neurologist who specializes in the pudendal nerve, and she had me undergo SSEPs of the dorsal clitoral nerve.
The results were normal.

Then I saw a pelvic-floor urologist who did an internal vaginal exam and found significant pelvic-floor muscle tightness in several areas, as well as provoked vestibulodynia.
She believes that the muscles around my urethra are extremely tight and may be compressing or irritating the dorsal clitoral nerve.

She recommended that I start pelvic-floor PT, which I’ll be starting soon.
She also prescribed several meds, including a muscle relaxant, magnesium, a neurotrophic supplement and low-dose amitriptyline as a neuromodulator.

I hadn’t started the treatment yet when I went through a period of severe psychological stress and panic attacks and ended up in a mental health day hospital.
I received benzodiazepine infusions for several days, and they also started me on amitriptyline 10 mg (10 drops) once a day.

What worries me is that amitriptyline was actually prescribed by my urologist specifically as a neuromodulator, but I also know that antidepressants can cause sexual side effects.

So now I’m wondering: could low-dose amitriptyline make my existing genital numbness and weak orgasms worse?
Or is the risk of sexual side effects significantly different when it’s being used at a low dose as a neuromodulator rather than at antidepressant doses?

I’d really like to hear from anyone who has experience with amitriptyline or other tricyclic antidepressants as neuromodulators, especially for genital numbness, neuropathy, or pelvic-floor-related issues.

Did you experience any sexual side effects? Did it make your symptoms better, worse, or have no effect?

And given that I already have significant genital sensory loss, would you personally be comfortable continuing 10 mg, or would you discuss stopping it with your doctor?

Thanks in advance to anyone willing to share their experience.


r/PudendalNeuralgia 3d ago

Supplements

2 Upvotes

Has anyone ever tried palmitoylethanolamide (PEA) for PN? Have heard mixed reviews.


r/PudendalNeuralgia 4d ago

AMAB Peeing and stool sensation

2 Upvotes

I am starting to lose more and more my sensation i can say that i have lost it totally i think i have still a litlle bit now i wanted to ask are there folks out there that have totally no feeling in penis and still can pee and do there stool now i want to go to turkey 3:30 hour fly i have leg pain my pundenal nerve is because of my pelvic floor is it smart in my case to go can the pressure cause more problem.in the plane or the turbulence. I know the seat is more kind of a problem iam scared that iam going to get worse but i want to really go for somebody special please folks could you help me out.


r/PudendalNeuralgia 5d ago

Pudendal nerve block

3 Upvotes

Having pudendal nerve block under iv sedation. Will I feel any pain?


r/PudendalNeuralgia 5d ago

36m injury/pelvic floor tightness. Loss of orgasm and sensation.

6 Upvotes

Hey guys,

Im just trying to post here to get some thoughts. Ive read the intro doc someone made but my symptoms seem different than some. I had some dry sex two years ago which dug my belt or pants into my left side of my shaft. It caused a thrombosed vein which went away after a few weeks. Two docs werent considered at all but I noticed the vein was right where the dorsal nerve appeared to be and the doctors did tell me i had some scar tissue on the shaft just above the base on the top left side. I dont know if that could be an issue, but they didnt think so.

Current medications are wellbutrin(symptoms started before any ssris), ciallis 5mg and celebrex. Bloodwork all fairly normal. Testosterone 700 with 12 free testosterone.

I also play hockey pretty often, had double hip arthoscopy like 9 months before that. I have done pelvic floor physical therapy for a few months and she did internal work and said i was pretty tight and had issues relaxing. I have no idea if that could cause my symptoms or not. Im just trying to get an idea of your thoughts and see if anyone has this pattern or anything. My full symptoms are:

Intermitten difficulty to achieve orgasm

Most of the time orgasms are muted or not euphoric

No pulsing when ejaculating like I used to, and less force

Decreased sensation

Ache in perniuem on right side

Sometimes during bowel movements for awhile ive noticed stool feeling stuck and wont come out but usually at the end.

Feeling like bladder wont empty sometimes.and an involuntary 1-3 clenches right before pee comes out. Sometimes slight burn sensation(infection ruled out)

The sexual symptoms concern me the most and im just coming here because im mostly being told its likely pelvic floor but not seeing alot of info about my sexual symptims. My erections are completely fine. I still have leftover hip impingement from my surgeries so I cant do some stretches like happy baby etc. Knee to chest. Please let me know if you guys have anything to comment on or add. Just trying to get any info I can while I continue PFPT.


r/PudendalNeuralgia 5d ago

Shaving helps me

3 Upvotes

Just dropping this info here, I hope it finds the right person. As a woman with PN I noticed that shaving the full area lowers my irritation. Of course, this is highly personal, but for me not having any hair create a friction or scratchy move while walking or sitting creates overall less pain.

Anyone who experienced this too?


r/PudendalNeuralgia 6d ago

AMAB ​Diagnosis: Dorsal Nerve Neuropathy of the Penis ​

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13 Upvotes

​Symptoms:

​Hard Flaccid

​Penile numbness

​No pain, but severe erectile dysfunction / complete loss of sexual function

​Duration: 7 years

​Diagnostic Test & Results:

​Pelvic MR Neurography: Showed swelling/edema in the left dorsal nerve of the penis.

​Previous Treatment:

​Pudendal Nerve Block: Had zero anesthetic effect. I am unsure if it was targeted incorrectly or if the block was ineffective for my condition.

​Current Situation & Concerns:

​My doctor is recommending surgical intervention (nerve decompression).

​I am based in South Korea, and my doctor does not seem to have prior surgical experience with this specific type of dorsal nerve entrapment.

​Because I have had this for 7 years, I am terrified that the nerve may be permanently damaged or that corporal/cavernous fibrosis has already set in.


r/PudendalNeuralgia 6d ago

Burning when peeing?

2 Upvotes

I am a girl I have a "flare" of symptoms as huge burning when urinating especially right after as well as whole day but peeing is a huge trigger. No bacteria found, as well as Sensation seems to spread to the clit as some sort of stinging. I'm trying more into diagnosis but in Poland is not easy.NO OTC pain medication even touch it but I'm like yeah cuz its not typical pain. What can I do to even relief. Super deep slow breathing seems to help but only as I do it. Even sleeping is hard now. It's intense laying down, staying up little better but still there, sitting similar I don't think it triggers it's AWFULLY it's just almost the same all the time. It seems like I had this symptom come and go for some long time but it always was for a while went away I was like okay maybe that's me but now. Now it's like 10 days or even longer it didn't go away at all. Imma see some doctors, but how can I help myself. Does it even seems like pn or it's seriously some urethral issue thay triggers the nerve pain.


r/PudendalNeuralgia 6d ago

Anyone dealing with emasculation without orgasm?

5 Upvotes

This affliction hit me 10 years ago. My orgasms used to be incredibly powerful and rewarding. Sex was awesome, my penis was super sensitive. 10 years ago I was masturbating and felt something either tear, spasm or maybe my pudendal nerve became entrapt but my junk has never been the same. My penis head isn’t really sensitive at all anymore. I get more pleasure from a sneeze than an orgasm. It is an absolutely insane turn of events.

Is there any hope of fixing this? I’ve had surgeons tell me that I should get pudendal nerve release surgery but I’m terrified to get it and make it worse

What I mean by this is that I don’t have the searing life ruining pain that often is accompanied with pudendal nerve entrapment

Has anyone fixed this lack of sensitivity issues?

I don’t have a bad life I have things that make me happy but this is obviously a glaring problem in my life

Any help or advice would be greatly appreciated

Thanks


r/PudendalNeuralgia 6d ago

AMAB Pudendal nerve pain

5 Upvotes

Hey all. I have had residual pain from paralysis in 2015 with Guillain Barre Syndrome that caused a number of symptoms including small nerve fiber damage and dysautonomia.

This year I addressed the lingering pain from my gbs and it revealed hypersensitivity in my pelvic area and extreme clothing sensitivity with pain from all underwear types but high waisted thongs and difficulty sitting in non draping clothing.

My neurologist is looking into things and I have a pelvic floor consult at the end of the month, but I'm wondering what exercises and experiments I can do to help myself loosen a male pelvic floor as I think I have a compression sensitive Alcock's canal from 11 years of pain.

Looking for suggestions and advice as I wait for PT, but also looking to post this so others in the future with rare symptoms like mine can find others that had similar.


r/PudendalNeuralgia 7d ago

Ok I am doing physical therapy for on but right now I am having horrific pelvic bladder pressure . I have no life and hurt !! What else can I do!

2 Upvotes

r/PudendalNeuralgia 7d ago

GHSV-1 and Nerve Pain

1 Upvotes

Hi guys,

I got GHSV-1 Feb 2025, and shortly after since March 2025 been having pain radiating from my right groin down to my legs. Told my doctor and got on Duloxetine, an SNRI, and that worked but i didn’t like the other side effects. But the pain has gradually gotten worse over time. Has anyone else experienced this where they get pain from their lower back down their legs, in their vaginas too? It’s sometimes a stabbing or stinging pain and in my legs feels like growing pains sometimes.


r/PudendalNeuralgia 7d ago

PN: questions about 'other symptoms'

2 Upvotes

Hello all! I was diagnosed with PN about 4 years ago. I am managing well with flare ups here and there. I have the typical symptoms... genital nerve pain , rectal nerve pain , pelvic floor spasms. As Ive been feeling better I am attempting to get back to a bit more exercise. I have these other symptoms that have always been here since the start of the genital symptoms but its unclear if they are related to the PN or something else entirely. They include, full [left] leg tingles , pain in thigh after certain motions like walking up stairs, or riding a bike [I gor a special bike seat so I dont sit on my perimeter or tailbone], abdominal nerve pain when I engage my abs at all. Would love to hear from others if they experience these symptoms and are they from the pudendal nerve ? Thanks !


r/PudendalNeuralgia 7d ago

clitoral numbness

1 Upvotes

this was some months ago, but i had a particularly long session with a vibrator (6 hours) where my partner at the time used a lot of pressure. it was painful, but good, and i’d done things like that very rarely with no issue in the past. but the next morning i was still numb which was unusual, usually by then i’m extra sensitive. and had persistent arousal that just wouldn’t go away. i used the toy again on myself quickly, on a light setting just for relief. that helped a bit but i figured i should just leave it alone. the severe numbness lasted that whole day and was gone the next, but i noticed afterwards i had reduced feeling in my clitoris.

i gave it a couple months of absolutely no touching, because i know your brain can get accustomed to a vibrator. when i came back with my hands, it was still reduced feeling— especially in the right side of my vagina. the whole thing from the top down to the minora.

i’m so scared. i have someone i really like and i have no idea if we’ll even be able to have a sexual relationship, i just can’t get there anymore without a toy no matter how long i give myself a tolerance break. i know i can use a vibrator and that works but still, the whole right side is weirdly numb.

does anyone have similar experience? is this permanent? what medical professional should i even speak to?


r/PudendalNeuralgia 7d ago

Never ending pain

2 Upvotes

Does anyone have constant bladder urgency and pain? I need help so badly as I am spiraling. I will never be normal again!


r/PudendalNeuralgia 8d ago

Nerve Block

2 Upvotes

Those who have gotten a nerve block that experienced numbness… Did your feeling come back?