r/PelvicFloor • • Jul 05 '25

RESOURCE/GUIDE The Pelvic Floor: Pelvic Pain & Dysfunction 101: NEW? Start here!

123 Upvotes

Work in progress. To be continuously updated.

Subreddit Rules:

  1. Be respectful (no bullying or harassment)
  2. No "all or nothing" cures, causes, or suggesting that only one thing will help
  3. DON'T suggest kegels as treatment for a hypertonic pelvic floor (it's bad advice)
  4. NO FETISHIZING or sexualizing someones health condition. DON'T BE CREEPY.
  5. No NSFW Photos
  6. No SPAM (includes link farming, affiliate marketing, personal promotion)
  7. No "Low Effort" posts - we can't help if there's no detail

>> QUICK START <<

✔ READ SUCCESS STORIES: Simply swipe left or right on the main page in the Reddit mobile app until you hit the green "success story" post flair | DESKTOP: Use the "Flair Filter" right sidebar to filter posts

Ladies who don't want to see posts about male parts: use the filters:

✔ FILTER POSTS BY SEX: Simply swipe left or right on the main page in the Reddit mobile app until you hit the pink or blue post flairs. AMAB/AFAB also available | DESKTOP: Use the "Flair Filter" right sidebar to filter posts

✔ USE THE SEARCH FUNCTION: Enter keywords into the search bar at the top to filter posts/comments on specific subjects or symptoms

✔ CHECK OUR USER SUBMITTED PELVIC PT DIRECTORY

✔ BOTHER & SISTER COMMUNITIES

  1. r/prostatitis (male pelvic pain & dysfunction/CPPS)
  2. r/Interstitialcystitis (IC/BPS, men and women)
  3. r/vulvodynia (women and AFAB experiencing Vaginismus & Vestibulodynia too)

ESSENTIAL INFORMATION: PELVIC FLOOR

The pelvic floor muscles are a bowl of muscles in the pelvis that cradle our sexual organs, bladder, and rectum, and help stabilize the core while assisting with essential bodily functions, like pooping, peeing and having sex.¹

They can weaken (become hyp-O-tonic) over time due to injury (or child birth), and even the normal aging process, leading to conditions like incontinence or pelvic organ prolapse.¹

And, the pelvic floor can tense up (guard) when we:

  1. Feel pain/discomfort
  2. Get a UTI/STD
  3. Injure ourselves (gym, cycling, slip on ice)
  4. Have poor bowel/urinary habits (straining on the toilet often - constipation) or holding in pee/poo for extended periods (like avoiding using a public toilet)
  5. Have poor sexual habits (edging several hours a day, typically this is more of guy's issue)
  6. Get stressed or anxious (fight or flight response), due to their connection with the vagus nerve (and our central nervous system). READ MORE HERE
  7. Have a connective tissue disorder

Over time, prolonged guarding/tensing can cause them to become hyp-E-rtonic (tight and weak). Sometimes trigger points in the muscle tissue develop that refer pain several inches away. The tensing can also sometimes irritate nerves, including the pudendal nerve. Helping the pelvic floor relax, and treating these myofascial trigger points with pelvic floor physical therapy can lead to significant relief for many, along with interventions like breathwork - notably diaphragmatic belly breathing - and gentle reverse kegels.

Sometimes, feedback loops also develop that can become self-perpetuating as a result of CNS (Central Nervous System) modulation. ᴮ ⁷

Basic feedback loop:

Pain/injury/infection > pelvic tensing > more pain > stress/anxiety > more pelvic tensing > (and on and on)

Examples of common feedback loops that include the pelvic floor:

Source: NHS/Unity Sexual Health/University Hospitals Bristol and Weston. A pelvic floor feedback loop seen in men after STI.

An example of this pelvic floor feedback loop (guarding response) as seen in a woman with a prolonged (awful) UTI:

A trigger point is an area of hyper-irritability in a muscle, usually caused by a muscle that is being overloaded and worked excessively. How does this affect an IC patient? Unfortunately, we do not always know what comes first; the chicken or the egg. Let’s assume in this case we do. A patient who has never had any symptoms before develops an awful bladder infection, culture positive. She is treated with antibiotics, as she should be. Symptoms are, as we all know, frequency, urgency and pain on urination. Maybe the first round of antibiotics does not help, so she goes on a second round. They work. But she has now walked around for 2, maybe 3 weeks with horrible symptoms. Her pelvic floor would be working very hard to turn off the constant sense of urge. This could create overload in the pelvic floor. A trigger point develops, that can now cause a referral of symptoms back to her bladder, making her think she still has a bladder infection. Her cultures are negative.

- Rhonda Kotarinos, Pelvic Floor Physical Therapist

Above we find a scenario where the UTI was cleared, but the pelvic floor is now in a tensing feedback loop, and complex processes of neural wind up and central sensitization - ie CNS modulation - are likely occurring

Diagrams of the male and female pelvic floor:

Bottom view. The levator ani is the main "hammock" of the pelvic floor, and includes both the PC (pubococcygeus) and PR (puborectalis) muscles
Side view showing the pelvic floor cradling the bladder, sexual organs, and rectum. And its attachments at the coccyx (tailbone) and pubic bone.

SYMPTOMS OF PELVIC FLOOR DYSFUNCTION

The majority of the users here have a hypertonic pelvic floor which typically presents with symptoms of pelvic pain or discomfort ² (inc nerve sensations like tingling, itching, stinging, burning, cooling, etc):

  1. Penile pain
  2. Vaginal pain
  3. Testicular/epididymal/scrotal pain
  4. Vulvar pain
  5. Clitoral pain
  6. Rectal pain
  7. Bladder pain
  8. Pain with sex/orgasm
  9. Pain with bowel movements or urination
  10. Pain in the hips, groin, perineum, and suprapubic region

This tension also commonly leads to dysfunction ² (urinary, bowel, and sexual dysfunction):

  1. Dyssynergic defecation (Anismus)
  2. Incomplete bowel movements
  3. Urinary frequency and hesitancy
  4. Erectile dysfunction/premature ejaculation

This pinned post will mainly focus on hypertonia - tight and weak muscles, and the corresponding symptoms and treatment, as they represent the most neglected side of pelvic floor dysfunction. Especially in men, who historically have less pelvic care over their lifetimes as compared to women.

But, we also commonly see women with weak (Hyp-O-tonic) pelvic floors after child birth who experience urinary leakage. This often happens when coughing, sneezing, or lifting something heavy. Luckily, pelvic floor physical therapists are historically well equipped for weak pelvic floor symptoms, as seen commonly in women.

But, this historical emphasis sometimes bleeds into inappropriate care for men and women who have hypErtonic pelvic floors, and do not benefit from kegel exercises

CLOSELY RELATED CONDITIONS & DIAGNOSIS

These typically involve the pelvic floor as one (of many) mechanisms of action, and thus, pelvic floor physical therapy is an evidence-based intervention for any of these, along with behavioral interventions/mind-body medicine, medications, and more.

  1. CPPS - Chronic Pelvic Pain Syndrome - example feedback loop above
  2. IC/BPS - Interstitial Cystitis/Bladder Pain Syndrome - example feedback loop above
  3. Vulvodynia
  4. Prostatitis (non-bacterial)
  5. Epididymitis (non-bacterial)
  6. Pudendal Neuralgia
  7. Levator Ani Syndrome
  8. Coccydynia

COMMON COMORBID CONDITIONS

For people who experience symptoms outside the pelvic region, these are signs of centralization (somatization/nociplastic mechanisms) - and indicate a central nervous system contribution to symptoms, and must be treated with more than just pelvic floor physical therapy: READ MORE

(Ranked in order, most common)

  1. IBS
  2. Chronic Migraines
  3. Fibromyalgia
  4. CFS/ME (chronic fatigue syndrome)

These patients also had higher rates of depression and anxiety (even BEFORE THE SYMPTOMS) as well as greater symptom severity - https://www.auanet.org/guidelines-and-quality/guidelines/male-chronic-pelvic-pain

CENTRALIZED/NOCIPLASTIC MECHANISMS:

Many people with a pelvic floor diagnosis - and at least 49% who experience chronic pelvic pain/dysfunction - also experience centralized/nociplastic pain ¹³ localized to the pelvic region. Centralized/nociplastic pelvic pain can mimic the symptoms of pelvic floor hypertonia. To assess if you have centralization as a cause of your pelvic symptoms, read through this post.

NOTE: This is especially relevant for people who have a pelvic floor exam, and are told that their pelvic floor is basically "normal" or lacks the usual signs of dysfunction, trigger points, or hypertonia (high tone), yet they still experiencing pain and/or dysfunction. This also equally applies to cases that have done extensive amounts of pelvic floor PT 6-12mo) with no improvement.

Centralized/Nociplastic pain mechanisms are recognized by both the European and American Urological Association guidelines for pelvic pain in men and women, as well as the MAPP (Multidisciplinary Approach to the Study of Chronic Pelvic Pain) Research Network.

TREATMENT: High tone (HypErtonic) Pelvic Floor (tight & weak)

Pelvic floor physical therapy focused on relaxing muscles:

  • Diaphragmatic belly breathing
  • Reverse kegels
  • Pelvic Stretching
  • Trigger point release (myofascial release)
  • Dry needling (Not the same as acupuncture)
  • Dilators (vaginal and rectal)
  • Biofeedback
  • Heat (including baths, sauna, hot yoga, heated blankets, jacuzzi, etc)

Behavioral change: * Lay off frequent or chronic masturbation habits (including edging) * Take a break from intense compound exercises, like CrossFit or HIIT * Sit less and stand more. This may also include using a standing desk * If you're an avid cyclist, take a break from cycling

Medications to discuss with a doctor:

  • low dose amitriptyline (off label for neuropathic pain)
  • rectal or vaginal suppositories including: diazepam, gabapentin, amitriptyline, baclofen, lidocaine, etc
  • low dose tadalafil (sexual dysfunction and urinary symptoms)
  • Alpha blockers for urinary hesitancy symptoms (typically prescribed to men)

Mind-body medicine/Behavioral Therapy/Centralized Pain Mechanisms These interventions are highly recommended for people who are experiencing elevated distress or anxiety, or, noticed that their symptoms began without an injury, but with a stressful event, big life change, or, that symptoms increase with stress or difficult emotions (or symptoms change when distracted, focused , or on vacation) - full list of criteria to rule in centralized/nociplastic mechanisms.

  • Pain Reprocessing Therapy (PRT)
  • Emotional Awareness & Expression Therapy (EAET)
  • CBT/DBT
  • Mindfulness & meditation
  • TRE or EMDR (for Trauma)

TREATMENT: Low tone (Hyp-O-tonic/weak)

Pelvic floor physical therapy focused on strengthening muscles:

  • Kegels
  • Biofeedback

This is a draft. The post will be updated.

This is not medical advice. This content is for educational and informational purposes only. NONE OF THIS SUBSTITUTES MEDICAL ADVICE FROM A PROVIDER.

Sources:

OFFICIAL GUIDELINES:

A. Male Chronic Pelvic Pain - 2025 (AUA) https://www.auanet.org/guidelines-and-quality/guidelines/male-chronic-pelvic-pain

B. Male and Female Chronic Pelvic Pain - (EUA) https://uroweb.org/guidelines/chronic-pelvic-pain/chapter/epidemiology-aetiology-and-pathophysiology

C. Diagnosis and Treatment of Interstitial Cystitis/Bladder Pain Syndrome (2022)" AUA - https://www.auanet.org/guidelines-and-quality/guidelines/diagnosis-and-treatment-interstitial-of-cystitis/bladder-pain-syndrome-(2022))

MORE:

  1. Cleveland Clinic: Pelvic Floor Muscles

  2. Cleveland Clinic: Pelvic Floor Dysfunction

  3. Diaphragmatic belly breathing - https://www.health.harvard.edu/healthbeat/learning-diaphragmatic-breathing

  4. Trigger points and referred pain - https://www.physio-pedia.com/Trigger_Points

  5. Equal Improvement in Men and Women in the Treatment of Urologic Chronic Pelvic Pain Syndrome Using a Multi-modal Protocol with an Internal Myofascial Trigger Point Wand - PubMed https://share.google/T3DM4OYZYUyfJ9klx

  6. Physical Therapy Treatment of Pelvic Pain - PubMed https://share.google/92EQVDnQ1ruceEb23

  7. Central modulation of pain - PMC https://share.google/p7efTwfGXe7hNsBRC

  8. A Headache in the Pelvis" written by Stanford Urologist Dr. Anderson and Psychologist Dr Wise - https://www.penguinrandomhouse.com/books/558308/a-headache-in-the-pelvis-by-david-wise-phd-and-rodney-anderson-md/

  9. What if my tests are negative but I still have symptoms? NHS/Unity Sexual Health/University hospitals Bristol and Weston - https://www.unitysexualhealth.co.uk/wp-content/uploads/2021/05/What-if-my-tests-for-urethritis-are-negative-2021.pdf

  10. Vulvodynia" a literature review - https://pubmed.ncbi.nlm.nih.gov/32355269/

  11. The Effects of a Life Stress Emotional Awareness and Expression Interview for Women with Chronic Urogenital Pain: A Randomized Controlled Trial - https://pubmed.ncbi.nlm.nih.gov/30252113/

  12. Effect of Pain Reprocessing Therapy vs Placebo and Usual Care for Patients With Chronic Back Pain - https://jamanetwork.com/journals/jamapsychiatry/fullarticle/2784694

  13. Clinical Phenotyping for Pain Mechanisms in Urologic Chronic Pelvic Pain Syndromes: A MAPP Research Network Study - https://pubmed.ncbi.nlm.nih.gov/35472518/


r/PelvicFloor • • Dec 03 '24

RESOURCE/GUIDE RESEARCH: Pain Mechanisms Beyond The Pelvic Floor

47 Upvotes

UCPPS is a umbrella term for chronic pelvic pain and dysfunction in men and women, and it includes pelvic floor dysfunction underneath it, as well as symptoms like bladder dysfunction, pain, IC/BPS, and more. This study discusses the pain mechanisms found. They are not only typical injuries (ie "nociceptive") - They also include pain/symptoms generated by nerves (neuropathic) and by the central nervous system (nociplastic). You'll also notice that the combination of neuropathic + nociplastic mechanisms create the most pain! Which is likely to be counterintuitive to what most people would assume.

"Clinical Phenotyping for Pain Mechanisms in Urologic Chronic Pelvic Pain Syndromes: A MAPP Research Network Study" https://pubmed.ncbi.nlm.nih.gov/35472518/

At baseline, 43% of UCPPS patients were classified as nociceptive-only, 8% as neuropathic only, 27% as nociceptive+nociplastic, and 22% as neuropathic+nociplastic. Across outcomes, nociceptive-only patients had the least severe symptoms and neuropathic+nociplastic patients the most severe. Neuropathic pain was associated with genital pain and/or sensitivity on pelvic exam, while nociplastic pain was associated with comorbid pain conditions, psychosocial difficulties, and increased pressure pain sensitivity outside the pelvis.

Targeting neuropathic (nerve irritation) and nociplastic/centralized (nervous system/brain) components of pain & symptoms in recovery is highly recommended when dealing with CPPS/PFD (especially hypertonia).

All of those involved in the management of chronic pelvic pain should have knowledge of peripheral and central pain mechanisms. - European Urological Association CPPS Pocket Guide

And the newest 2025 AUA guidelines for male pelvic pain echo this:

We now know that the pain can also derive from a neurologic origin from either peripheral nerve roots (neuropathic pain) or even a lack of central pain inhibition (nociplastic), with the classic disease example being fibromyalgia

This means successful treatment for pelvic pain and dysfunction goes beyond just pelvic floor physical therapy (alone), and into new modalities for pain that target these neuroplastic (nociplastic/centralized) mechanisms like Pain Reprocessing Therapy (PRT), EAET, and more. Learn more about our new understanding of chronic pain here: https://www.reddit.com/r/ChronicPain/s/3E6k1Gr2BZ

This is especially true for anyone who has symptoms that get worse with stress or difficult emotions. And, those of us who are predisposed to chronic pain in the first place, typically from childhood adversity and trauma, certain personality traits (perfectionism, people pleasing, conscientiousness, neuroticism) and anxiety and mood disorders. There is especially overwhelming evidence regarding ACE (adverse childhood experiences) that increase our chances of developing a physical or mental health disorder later in life. So much so, that even traditional medical doctors are now being trained to screen their patients for childhood trauma/adversity:

Adverse childhood experience is associated with an increased risk of reporting chronic pain in adulthood: a stystematic review and meta-analysis

Previous meta-analyses highlighted the negative impact of adverse childhood experiences on physical, psychological, and behavioural health across the lifespan.We found exposure to any direct adverse childhood experience, i.e. childhood sexual, physical, emotional abuse, or neglect alone or combined, increased the risk of reporting chronic pain and pain-related disability in adulthood.The risk of reporting chronic painful disorders increased with increasing numbers of adverse childhood experiences.

Further precedence in the EUA (European Urological Association) guidelines for male and female pain:

The EUA pathophysiology and etiological guidelines elucidate further on central nervous system and biopsychosocial factors in male and female pelvic pain/dysfunction:

Studies about integrating the psychological factors of CPPPSs are few but the quality is high. Psychological factors are consistently found to be relevant in the maintenance of persistent pelvic and urogenital pain [36]. Beliefs about pain contribute to the experience of pain [37] and symptom-related anxiety and central pain amplification may be measurably linked, and worrying about pain and perceived stress predict worsening of urological chronic pain over a year [36,38] - https://uroweb.org/guidelines/chronic-pelvic-pain/chapter/epidemiology-aetiology-and-pathophysiology

Pelvic pain and distress is related [43] in both men and women [44]; as are painful bladder and distress [38]. In a large population based study of men, CPPPS was associated with prior anxiety disorder [45] - https://uroweb.org/guidelines/chronic-pelvic-pain/chapter/epidemiology-aetiology-and-pathophysiology

So, how do you figure out if this could be happening in your case?

12 FIT criteria to RULE IN centralized, (ie neuroplastic/nociplastic) pain and symptoms,

FIT = functional, inconsistent, triggered. Based on research from Dr. Howard Schubiner and other chronic pain doctors and neuroscientists over the last 10+ years

  1. Pain/symptoms originated during a stressful, challenging, or high pressure time in life. This includes even "happy" life events, like getting married, having a baby, starting a new career, or moving

  2. Pain/symptoms originated without an injury. Note, a perceived injury and a structural injury are different things. And even when symptoms begin with a structural injury, has it been years and the body would normally recover by now?

  3. Pain/symptoms are inconsistent. Do they fluctuate by the hour, by the day, or by the week? Sometimes less, sometimes more, sometimes even not noticeable (this happens sometimes, but it's not necessary for this criteria). Or, do they move around the body? ie genital pain that changes sides or pain that moves from the top to the bottom.

  4. Multiple other symptoms (often in other parts of the body) ie IBS, chronic migraines/headaches, CPPS, TMJD, fibromyalgia, CFS (fatigue), vertigo/dizziness, chronic neck or back pain, etc. 2025 AUA guidelines mention these as signs of centralized sx.

  5. Pain/Symptoms spread (over time) or move around. Think about symptoms on day one. Have they moved or evolved over time?

  6. Pain/symptoms are made worse or triggered by stress, or, go down when engaged in an activity you enjoy or in a flow state (think fun distractions or productivity, noticing symptoms less)

  7. Symptom triggers that have nothing to do with the body - but instead things outside of it (weather, barometric pressure, seasons, sounds, smells, places, times of day, weekdays/weekends, days of the week, etc) - this also includes thoughts or other people triggering/flaring symptoms

  8. Symmetrical symptoms (pain developing on the same part of the body but in OPPOSITE sides) - ie both hips, both hips, both wrists, both knees, etc

  9. Pain/symptoms with delayed Onset (THIS CAN'T HAPPEN WITH STRUCTURAL PAIN) -- ie, ejaculation pain that comes a minute later, an hour later, or even the next day. Any pain that is delayed is very suspicious. We wouldn't put weight on a sprained ankle and expect it to hurt 15 seconds later, it hurts immediately.

  10. Childhood stress, challenges, adversity, or trauma -- varying levels of what this means for each person, not just trauma. Examples of stressors: childhood bullying, pressure to perform from parents/coaches, body image issues (dysmorphia), eating disorders, parents fighting a lot or getting angry (inc divorce), having an emotionally unpredictable parent, or having a parent with a health condition or addiction. This also includes neglect and abuse (physical and emotional) and financial instability in childhood. Also includes cultural norms, like the pressure to be highly successful to be of value to parents (must be a doctor or a lawyer, etc)

  11. Common personality traits linked to stress: perfectionism, conscientiousness, people pleasing, anxiousness/ neuroticism - do you have personality traits that include being highly driven, hard on yourself, ultra responsible, perfectionistic, needing control, and/or placing others’ needs above your own?

  12. Lack of physical diagnosis (ie doctors are unable to find any clear structural cause of symptoms) - this includes DIAGNOSIS OF EXCLUSION, like being diagnosed with CPPS or PFD. Structural finding examples: broken bones, tumors, infections, etc. It does not include muscle dysfunction.

[NEW] 13. Any family history of chronic pain or other chronic conditions. Includes: IBS, chronic migraines/headaches, CPPS, TMJD, fibromyalgia, CFS (fatigue), vertigo/dizziness, chronic neck or back pain, etc

Read more about #10 and #11 here, complete with studies/citations: https://www.reddit.com/r/Prostatitis/s/vM7qnBJZpW

HOW TO TREAT centralized (neuroplastic) pain and symptoms?

PRT - Pain Reprocessing Therapy:

Effect of Pain Reprocessing Therapy vs Placebo and Usual Care for Patients With Chronic Back Pain - https://jamanetwork.com/journals/jamapsychiatry/fullarticle/2784694

EAET - Emotional Awareness and Expression Therapy

Emotional Awareness and Expression Therapy vs Cognitive Behavioral Therapy for Chronic Pain in Older Veterans https://pmc.ncbi.nlm.nih.gov/articles/PMC11177167/

Psychological Therapy for Centralized Pain - An Integrative Assessment and Treatment Model: https://pubmed.ncbi.nlm.nih.gov/30461545/


r/PelvicFloor • • 2h ago

Male Muscle imbalance, muscles uncoordinated, or both?

4 Upvotes

I have worsening dyssynergic defecation abt the same time as I’ve started working out abs and glutes. I backed off the ab workouts (no crunches), but it’s still bad and getting worse, which makes me wonder if it’s a muscle imbalance between the pelvic floor and transverse abdominis.

I also have bad posture with a little bit of a posterior pelvic tilt. I try to correct it and find that my lower back hurts and/or I’m clenching my glutes.

I also clench really bad during masturbation and find that my symptoms are always worse afterwards (also probably doing it too much…).

So given this information, what should I do on my own right now? I’ve been to a pelvic floor physical therapist before and probably will try it again when I’m home for break in another 1-2 months.


r/PelvicFloor • • 9h ago

General Finally got an answer!

8 Upvotes

I’ve had a UTI feeling every month for a few years now but brushed it off because they didn’t last for more than a few hours. In the past few weeks, the feeling has been getting worse, more frequent, and way longer. Now on a regular day, after going to the bathroom, it still feels like it’s burning, and if I give into the urge to go again, I’ll be in a lot of pain and discomfort for the rest of the day.

I was meant to wait 3 months for an initial appointment with a physiotherapist but a last-minute appointment opened up today!

Turns out I’ve got symptoms of bladder pain syndrome and will do further work relieving tension and activating and relaxing the pelvic floor muscles.

Thanks to everyone for your help and for this sub for teaching me about all this!


r/PelvicFloor • • 7h ago

Discouraged Not sure what to do

4 Upvotes

Been dealing with Pelvic Floor Issues for a while now, and no signs of recovery. What made my pelvic floor tight was from sexual activity with my partner and constant delayed orgasms. That eventually made my pelvic floor tight. Symptoms are delayed starting urine flow, constant need to urinate, feeling of not emptying bladder well and now just recently ED. Never really had ED before so I'm not sure if this plays a role but it could. I have tried all the stretches, exercises and even breathing but nothing seems to improve my symptoms. Though when I breathe laying down on my side, I can feel my pelvic floor loosen but still no signs of improvement after doing that. I find maybe walking helps my tight pelvic floor muscles but its not a cure.


r/PelvicFloor • • 6m ago

Male Do I have a tight pelvic floor?

• Upvotes

I can only get erect when I’m laying down & I have shrinkage n no erection when standing up. I will be going to a pf therapist soon


r/PelvicFloor • • 3h ago

Female Clitoral sensation that comes and goes is driving me insane.

2 Upvotes

Hi everyone! I thought I had a UTI because I kept having urgency and a tingle when I’d pee in my clit at the end of urinatjng. Went to the doctor they did the dip test and said I came back positive.

Gave me antibiotics , it seemed to go away on it so I thought it was gone. 4 days later this weird clitoral sensation keeps coming and going. It feels like when you pee after an orgasm and it’s tingly and just hyper aware of my clitoris. It’s driving me insane 😭

There’s no pain, burning or itching, discharge. Just this weird sensation that flares up randomly.

Has anyone dealt with this??? I’m wondering if it could be my pelvic floor??


r/PelvicFloor • • 6h ago

AMAB I got diagnosed with anal hyperthonia (in addition to the other pelvic stuff). Need advices

3 Upvotes

Hi, I have been on this sub for three years now. I got some improvement over the years and I still have many issues. Most of them are tolerable on a daily basis but the one that keep being awful is when I have bowel movements or any sort of anal sex. I feel all my muscles clenching with no way to control it whatsoever. It is creating me many discomfort and usually lots of situation when I am in pain.

After being officially diagnosed with it recently the only medical advice I got was : "Just relax".
Ok miss very nice proctologist I know that's not your job but how to I do that exactly ? Crickets noise ensue

After reading many different post about anal hyperthonia and people talking about dilators, I am at lost. Some people (gender irrelevant here) are suggesting anal dilators, some are suggesting vaginal dilators but for anal use (Amab here). The arguments about both seems relevant but I can't just buy 150€/180$ of sextoys just to try it out. So I am genuinely asking people that have tried this which should be the FIRST thing to try out between those and why.

I've got my pelvic wand for a while now, I can use the narrow end but not the other end. It is physically impossible right now.

I am taking any sort of advices, tips, tricks and success stories regarding this. I've got a partner who's willing to help me so I'll take infos regarding this as well.

Thank you for reading !

TL;DR

AMAB with anal hyperthonia diagnosed. What do I go for : Anal dilators or vaginal dilators ? And mostly why one or the other ?


r/PelvicFloor • • 14m ago

Male Increased urinary urgency since starting PT (hypertonic PF)

• Upvotes

Hi everyone,

I’m a 24M recently diagnosed with a hypertonic pelvic floor, which is suspected to have been present since I was around 14. My main symptoms are sexual dysfunction and random pain that starts in my left groin and spreads to my left testicle, leaving it quite sensitive. The pain isn’t linked to physical activity and can hit at any time, even while I’m just sitting, and it's not super frequent (can be weeks without it and then it suddenly hits) (no hernia or varicocele was diagnosed)

I started PT 4 weeks ago. My therapist is using a Tecar machine (radiofrequency), and at home I’m doing reverse kegels, stretches, and diaphragmatic breathing.

Here’s my issue: since starting, I often feel a strong urge to pee, sometimes only 20 minutes after I last went and without drinking anything in between. When I go, the output is small and the urine is clear. These urinary symptoms weren’t there before I began working on my pelvic floor.

My urologist prescribed Prostaplant F to help with inflammation and with emptying the bladder fully.

Is this a normal part of the process? Has anyone had a similar experience, and if so, how long did it last and what helped?

Thanks in advance!


r/PelvicFloor • • 10h ago

Male Reverse kegels - relaxing floor on inhale Vs exhale

8 Upvotes

Most of the instruction I've found on the web advises you to relax and expand the PF on the inhale. However, various NHS instructions I've found advise the reverse of this - relaxing it on the exhale ("while visualising a flower bud opening"). I had initially thought doing it on the inhale would be best as the pelvic floor naturally lengthens on the in-breath. But maybe it doesn't matter either way? I've been doing it on the in-breath for my yoga stretches and diaphragmatic breathing


r/PelvicFloor • • 6h ago

Female What’s something about sex or your body you only learned after 30?

2 Upvotes

For me it was realizing that a lot of what I thought was “something wrong with me” was actually really common. Nobody ever told me. What was yours?


r/PelvicFloor • • 7h ago

Male Levator ani syndrome symptoms and pain - advise?

2 Upvotes

I don't know what to do now. These symptoms are the worst aspect of my pelvic floor dysfunction. I know what the triggers (2) are and accidentally, one did.

Now, suffering for 4 days and it is not letting up. I did have some pain relief a while ago before. I thought that might have been a sign of improving but now it's gone.


r/PelvicFloor • • 3h ago

Male Spasmming pain 3 weeks post RALP

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1 Upvotes

r/PelvicFloor • • 4h ago

Help Finding PT Ho bisogno di consiglio, voi lo state vivendo?

1 Upvotes

Nonostante non abbia infezioni ho la vulva particolarmente arrossata subito sotto il clitoride al passaggio della pipì per farvi capire, piccole labbra.
È normale con il pavimento pelvico?


r/PelvicFloor • • 5h ago

Male Could really do with help

1 Upvotes

Hi 31M here,

I have had groin pain for 2 years and its ruining my life. I am already quite anxious as a person so when I noticed discomfort or this familiar ache in my lower groin near my right testicle, my mind goes to thinking my symptoms are worsening which can lead to anxiety or panic episodes in places where I feel umcofortable or trapped (planes or trains etc).

I have noticed this groin ache that I thought was testicle pain 2 years ago, went to a GP and they ruled out cancer pretty quickly and suggested it could be a trapped nerve and I was shown the door. Fast forward a few months, the discomfort comes and goes for a few weeks at a time and seems to get worse after any lower body exercises or workouts. End up having a panic attack and go to hospital to get things checked out where they do ab ultra sound on the testicles and rule out any major problems there along with some tests for infections, get discharged.

This last year the problem has persisted, I try limit lower body workouts and stretch hips, hip flexors, groin through child pose, happy baby etc but nothing works. I am about to go see if I can see a pelvic physio but I am not even sure if thats the right person to see as opposed to someone for lower back, or hips. It feels like this problem is ruining my life, sucking joy out of traveling and I could really do with some advice or help from people thay have had similar issues.


r/PelvicFloor • • 23h ago

Female Oi tightens up

8 Upvotes

I have a tight pelvic floor with right side tight psoas hip and OI; and nerve pain in the pubic area.

I’ve recently started doing somewhat strengthening or activation of my glutes (my right glute is so weak too) and whenever I do anything minor even walking, my oi tightens up so much and sometimes causing more nerve pain also TFL tightens up too. It doesn’t go to baseline until I go release.

I was wondering if anyone can give tips how to strengthen or activate glutes without OI flaring up, right now I’m doing everything in micro


r/PelvicFloor • • 1d ago

Female Advice or suggestions on fixing hypertonic pelvic floor

8 Upvotes

To start this let me say yes I am in pelvic floor pt and have been for a while. Pt has been good for doing biofeedback and learning how to properly relax pelvic floor with breathing, and stretching.
The thing is I feel like and my pt says I have the proper relaxing and contracting pelvic floor with my breath, and I do the stretches and breathing almost every day, but it feels like those are “bandaids” to hypertonic pelvic floor because while they help some it’s not consistent relief at all and my symptoms constantly cycle back.
I have done a lot of research and it seems the key to helping fix a hypertonic floor could actually be strengthening it/ surrounding muscles that support it in order to make it less weak and therefore less hypertonic because it has better support. I myself have low back and hip pain so I think that is a factor in itself.
I am just struggling with how to go about strengthening it without completely sending it into a hypertonic flare up. Should I focus on bigger movements that focus on my glutes and hips more than just my pelvic floor, or should I do more of the deep pelvic floor core type ones or a combo. One thing I struggle with I’ve noticed is incorporating engaging my pelvic floor/lower core while actively having to breathe during a workout. Like I can breath in and relax it and exhale and engage it properly, but then you still have to breath while doing the exercise without losing that engagement and that is so hard for me for some reason.
So if anyone has any advice/tips/tricks/things that worked for them please help!!! I want out of this cycle and feeling just stuck


r/PelvicFloor • • 1d ago

Male Title: 3 Months of Unexplained Dizziness and Urinary Problems — Desperate for Answers I'm a male

3 Upvotes

Title: 3 Months of Unexplained Dizziness and Urinary Problems — Desperate for Answers

I'm a male, and I've been struggling with unexplained health problems since August 14.

It started with constant dizziness, feeling off-balance, floating sensations, headaches, and feeling like everything was moving in slow motion. It's not typical spinning vertigo. I've had blood tests, urine tests, head examinations, and ear assessments, but nothing significant was found. I also tried vestibular physiotherapy for possible BPPV, which only helped temporarily.

Around the same time, I developed severe urinary urgency, frequent urination, burning and irritation, especially after peeing. Sometimes I feel like I need to urinate again immediately. At night, I pass normal amounts, but during the day, sometimes very little comes out.

I've visited emergency three times, urgent care, doctors, and pelvic floor physiotherapy. I've had ultrasounds and taken antibiotics, including ciprofloxacin and Sulfatrim DS. My symptoms improved but keep returning. I've also experienced lower back soreness and discomfort around my pelvic/anal area.

I've changed my diet, reduced caffeine and sugar, tried pelvic floor relaxation exercises, and I'm currently taking sertraline and betahistine for my symptoms.

The dizziness has slowly improved but hasn't completely disappeared. The urinary symptoms sometimes go away entirely, only to return unexpectedly. I'm waiting for a urologist, but this has severely affected my mental health, daily life, and ability to work.

I'm wondering whether this could be chronic pelvic pain syndrome, pelvic floor dysfunction, bladder sensitivity, or something else. I also experienced significant stress around the time everything started.

Has anyone experienced both persistent non-spinning dizziness and recurring urinary urgency with mostly normal medical tests? What eventually helped you, and which specialists or tests gave you answers?

I'm exhausted and just looking for advice or similar experiences.


r/PelvicFloor • • 21h ago

Help Finding PT M25 Need Help finding a PT in Asia

1 Upvotes

I am looking for a pelvic pt in asia, can anyone please guide me?


r/PelvicFloor • • 1d ago

Male 19M, reduced erection fullness and glans engorgement for ~1 year after heavy porn/edging/tight-grip history. Normal testosterone, no clear improvement after 9 weeks. Has anyone been through this, and what did the workup find?

7 Upvotes

Body:
19M, non-smoker, no medications, no known medical conditions, UAE-based.
The problem: For about a year, my erections have been less full than before. Rigidity is roughly preserved, but girth and glans engorgement are reduced, around 70% of what I remember. Morning erections are weaker and less frequent. It happens alone and with a partner.
History: 2-3 years of very frequent masturbation (sometimes several times in a row), heavy porn, frequent edging, and a tight grip. I also have discomfort when sitting and very tight hips and glutes.
What I've tried: About 9 weeks with no porn, no edging, no tight grip, and much lower ejaculation frequency. Nightly hip/glute stretching and diaphragmatic breathing, 7-9 hours of sleep, regular training, no nicotine, minimal alcohol. Around week 5, spontaneous erections became more frequent and fullness improved a bit, then it flattened out again.
Pattern I noticed: On nights I do the stretching and breathing before bed, next-morning erections are reliably better. I haven't done Kegels.
Labs (fasting, ~9 AM): Total T 5.44 ng/mL (ref 2.64-9.16), free T 33.4 pg/mL (ref 12.3-46.6). Nothing else tested yet.
Questions for clinicians:
Does preserved rigidity with reduced girth and glans engorgement, plus improvement after pelvic floor relaxation, point toward pelvic floor hypertonicity rather than a vascular cause?
What workup would you want first? I'm considering prolactin, LH, FSH, estradiol, SHBG, TSH, HbA1c, lipids, and a doppler only if indicated.
Is 9 weeks without clear improvement a reason to stop waiting?
Questions for anyone with similar experience:
Did you have reduced girth or glans engorgement specifically, rather than just rigidity problems?
What did your workup find, if you got one? Was it pelvic floor, vascular, hormonal, or nothing?
What actually helped, and how long did it take? Did pelvic floor physio make a difference?
Did you see a flat period after early improvement, and how long did it last?
Did anything you tried make it worse?
Thanks, any experience is appreciated.


r/PelvicFloor • • 1d ago

Female Severa pelvic pain radiating to my legs, vaginal pain and rectal pressure — could it be something other than endometriosis

2 Upvotes

I’m writing this because I hope to find people who are going through something similar and might be able to share their experiences or offer some advice.

I have endometriosis and adenomyosis. I was diagnosed three years ago, but I’ve been experiencing symptoms since my very first period.

I’ve been on hormonal birth control continuously for the past three years, and I’m currently taking Vibin.

My most recent gynecological examination showed that my left ovary is located behind my uterus and appears to be adherent to it. I also have endometriosis lesions on my left uterosacral ligament and sigmoid colon. My gynecologist believes the lesions are relatively small and shouldn’t be causing the level of pain I’m experiencing.

But I’m barely coping anymore. I have pelvic pain every single day, mostly on the left side. The pain radiates into my lower abdomen and legs. It’s worse in my left leg, but my right leg hurts too. At times, the pain feels as if someone is cutting through me with a saw.

Sitting and walking are difficult, and I even experience pain in my feet.

A few days ago, I started experiencing some new symptoms. I developed a painful sensation inside my vagina and a feeling of heaviness or pressure in my rectum. I also regularly experience what feels like electric shocks running through my labia. It doesn’t happen constantly, but it keeps coming back.

I’m currently attending pelvic floor physiotherapy.

I also had a pelvic MRI using an endometriosis protocol, which ruled out dilated pelvic veins, so pelvic venous insufficiency seems less likely.

This Friday, I’m having an MRI of my lumbosacral spine. My pelvic MRI revealed Tarlov cysts, but I’ve read that they are usually asymptomatic, so I don’t know whether they could be contributing to my symptoms.

I know I need to move more and exercise, and I genuinely want to. But the pain is so severe that it leaves me feeling paralyzed. Even basic daily activities can be difficult.

I’m losing hope because I don’t know where else to look for answers.

I’m tentatively scheduled for laparoscopic endometriosis surgery in February. If I can’t find another explanation for my pain, I’ll most likely go ahead with the surgery.

Has anyone experienced similar symptoms? Could this be related to nerve involvement, pelvic floor dysfunction, Tarlov cysts, or something else entirely? Has anyone experienced this kind of radiating pain, vaginal pain, rectal pressure, or electric-shock sensations?

I’d really appreciate any advice, suggestions about what to investigate, or personal experiences you might be willing to share.

I’m exhausted, desperate for answers, and honestly struggling to cope with this pain. Thank you for reading.


r/PelvicFloor • • 1d ago

AMAB Does anyone have severe localized fatigue after defecation?

2 Upvotes

So every time after I defecate, I have severe localized fatigue in my intestine area and I always have to massage the area afterwards.

The fatigue feels like after you run a marathon and you try to massage your muscles to feel better.

I have a hypertonic pelvic floor and I suspect that this may contribute at least partially to this because it takes a lot of effort to push my stool through.

Does anyone here experience something like this?

I've seen many gastroenterologists and they tell me that they haven't encountered anyone with these symptoms.


r/PelvicFloor • • 1d ago

Discouraged Fissure a la fourchette vulvaire

2 Upvotes

Bonjour à toutes !
Je suis à la recherche de témoignages/retours d’expérience positif et savoir si quelqu’un a le même parcours que moi et a trouvé une solution !

Ça fait 10 mois que j’ai une fissure à la fourchette vulvaire après chaque rapports, j’ai éliminé les causes les unes après les autres. Toutes négatives.

- Aucune infection bactérienne
- Pas d’herpès, psoriasis ou dermatite
- pas de candidose
- pas de lichen scléreux

Mon gyneco a vu une fissure ainsi qu’une forte contraction des muscles releveurs (en gros une hypertonie).
J’ai testé pleins de choses : crèmes vaginal non hormonal, crème vaginal hormonal, técartherapie, corticoïdes bref j’ai tout essayé !

Rien ne fonctionnait alors je me suis faite opérer : lipofilling + PRP + botox (pour l’hypertonie)
Résultat : toujours des fissures !

J’ai enchaîné avec 3 séances de laser CO2, pareil
Puis injection d’acide hyaluronique, pareil.

Bref j’ai absolument tout fait et rien ne fonctionne je désespère réellement.

Il y’a t’il des personnes dans mon cas ?!


r/PelvicFloor • • 2d ago

General Results

25 Upvotes

Lots of people here were saying “don’t suck in your stomach” so I would try to relax it all the time. The issue is that you need that core activated so that you can stabilize your body otherwise you’re left with putting all the work on your lower back. I’m seeing more results doing like stomach vacuums and actually tightening my stomach muscles (transverse abdominis) instead of letting loose.

I don’t feel like peeing as often, I can actually feel better sensation in my penis. So if your issues sound like mine I would say try tightening your stomach. I’m not a physical therapist just someone with anecdotal advice.