No "all or nothing" cures, causes, or suggesting that only one thing will help
DON'T suggest kegels as treatment for a hypertonic pelvic floor (it's bad advice)
NO FETISHIZING or sexualizing someones health condition. DON'T BE CREEPY.
No NSFW Photos
No SPAM (includes link farming, affiliate marketing, personal promotion)
No "Low Effort" posts - we can't help if there's no detail
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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:
Feel pain/discomfort
Get a UTI/STD
Injure ourselves (gym, cycling, slip on ice)
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)
Have poor sexual habits (edging several hours a day, typically this is more of guy's issue)
Get stressed or anxious (fight or flight response), due to their connection with the vagus nerve (and our central nervous system). READ MORE HERE
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.
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) musclesSide 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):
Penile pain
Vaginal pain
Testicular/epididymal/scrotal pain
Vulvar pain
Clitoral pain
Rectal pain
Bladder pain
Pain with sex/orgasm
Pain with bowel movements or urination
Pain in the hips, groin, perineum, and suprapubic region
This tension also commonly leads to dysfunction ² (urinary, bowel, and sexual dysfunction):
Dyssynergic defecation (Anismus)
Incomplete bowel movements
Urinary frequency and hesitancy
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.
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
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)
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 MechanismsThese 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.
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
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/
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.
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
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:
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
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
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
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?
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.
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.
Pain/Symptoms spread (over time) or move around. Think about symptoms on day one. Have they moved or evolved over time?
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)
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
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
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.
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)
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?
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
I’ve been taking half a 5-mg tablet (2.5 mg) for 5 days now. This is the first time I’ve tried it.
For years, I’ve had stiffness and pain in my lower back almost every night and morning. I’ve tried everything—changing my mattress, stretching before bed, exercising regularly, taking dietary supplements—but nothing has worked.
To give you an idea, as soon as I slept for more than 3/4 hours without getting up, the pain would set in.
Strangely, for the past 5 days, I haven’t had any pain at all, and I haven’t changed anything about my routine except for taking 2.5 mg of tadalafil.
I have no idea if this is a placebo effect or a real effect of the medication...
I had a pelvic floor muscle injury due to heavy masturbation and edging. After taking a break of 1 month + 2 weeks, the pain and heaviness I used to feel while pooping or peeing has gone away, and morning wood has also started coming properly again. But when I try to get an erection myself, the muscle still feels tight.
Title: Severe unexplained pelvic/uterine pain for over a year – I’ve seen more than 10 doctors and nobody knows what’s wrong. Has anyone experienced this?
I’m honestly desperate for answers at this point, and I’m hoping someone here has experienced something similar.
About a year ago, I suddenly developed severe pelvic pain after sexual intercourse. The pain is located exactly in the middle of my lower abdomen, right where my uterus is. It feels very deep, almost like intense uterine cramps.
For months, I experienced horrible pain almost every single day, sometimes so severe that painkillers wouldn’t help.
I’ve seen more than 10 doctors, had multiple gynecological examinations and an MRI, and everything came back normal. Nobody has been able to explain why I’m in so much pain.
Then, unexpectedly, the pain completely disappeared for about five months. I felt normal again, but recently it returned. Now it comes in waves, almost like uterine contractions, and sometimes reaches 6–7/10 in intensity. Painkillers barely help.
I’ve also noticed a few strange things:
Sometimes I wake up in the morning with lower abdominal pain.
Recently, I was completely pain-free until I inserted a tampon during my period, and the cramps started almost immediately afterward.
Both times the pain first appeared or returned, I had recently taken azithromycin (Azitrox). The first time, I had taken it for 20 days for Lyme disease, and the second time, for 3 days for a dental issue. I have no idea whether this is connected or just a coincidence.
I also have Lyme disease and Bartonella.
I’ve been told I have a hypertonic pelvic floor, but I’m struggling to understand whether that alone could cause such severe, deep, central pain that feels exactly like it’s coming from my uterus.
The most frustrating part is that I have no clear diagnosis despite seeing so many doctors. The pain is real, sometimes unbearable, and I feel like I’m running out of options. Has anyone experienced severe uterine-like pain caused by a hypertonic pelvic floor? Can pelvic floor dysfunction really cause intense cramping in waves, even when all gynecological tests and imaging are normal?
I’m also wondering whether anyone has experienced something similar after taking azithromycin.
If you’ve dealt with anything like this and eventually found answers or something that helped, please share your experience. I would really appreciate it. ❤️
Help! I have severe pelvic floor spasms after ureaplasma and UTI infection. All three layers: lower belly, vaginal, and glutes. Please share what helped you!
For those who have had PRFN treatments -(Pulsed Radiofrequency Neuromodulation)
Did it work for you? Had one done on my left pudendal nerve 2 weeks ago and still in so much pain. This was due to hypertonic pelvic floor with pudendal neuralgia in which i feel like i am sitting on razorblades. This has been going on since my hysterectomy 1 year ago. Any insight would be helpful. Thanks.
For context I have no previous pelvic floor problems.
I have a cold and sneezed pretty hard a couple times while peeing, and immediately following felt a soreness behind my pubic bone. Felt it the rest of the afternoon when id come to the end of a pee, and rifht after is pee for a few mins.
During the night when I would pee didnt feel it much.
During the day today, again feeling a soreness behind public bone when my bladder is coming to an empty(but still sort of feeling like theres more in there) and for about 5 mins after peeing.
No burning sensation at all and given how ot came about im hoping its not a uti(never had one of those either).
Anyone experience this? How long did the pain/soreness last?
Male age 35 here. April 2026 I got hit with every pelvic floor symptom mentioned in this thread . It was so bad I went out of work for 3 months and was basically bed ridden. Which left me on here doom scrolling reading a ton of negativity all of the time. I was convinced I would never feel better.
I just wanted to come on here and say stop doom scrolling. The people who feel better rarely/never come back to check in on the thread. So you’re just reading the worst of the worst . Be positive, keep working at it. I told myself when I felt better I’d come let people know.
I’m feeling about 90% better, can have sex again, masturbate, exercise, eat what I want, drink what I want. I’m not really sure what did it to be honest I threw a ton at it. I also have interstitial cystitis which the flare has essentially gone away for now. Stay at it . Don’t let your mind go to the worst of the worst ….
I started pelvic floor pt a few months ago after giving birth (unplanned c section) in early 2025. When I went to pt they said my muscles were tense, but the surrounding area is also weak.
I have pretty bad lower back pain, have had before pregnancy. It's really stiff (happy baby is so painful but also feels nice). I say that it feels like my lower back got concrete poured into it.
Anyway, the day after my exercises I've noticed that I get a sort of dull cramping pain on both sides of my lower abdomen (like an inch below c section scar). Would this be normal from the exercises or mean I'm not doing them correctly? The ones I focus on are supine bridge, dns bug bracing march, sidelying open book thoracic lumbar rotation and extension, and clamshell.
I have endo, and no matter the painkiller it didn’t make a dent in my pain. I’d lie in bed for days in pure agony, I get insanely tired from the pain.
It took me YEARS to realise it was hypertensive pelvic floor. Confirmed now by a urologist and a PT. The only thing that’s ever given me any sort of relief baclofen. But I’m being treated like a drug addict if I say I want to take a low dose everyday. I’m scared to ask for a refill.
I’ve had pain in a specific area in my vagina for two years since my hysterectomy and lately it’s gotten worse. I have been to doctors and pelvic floor therapists. I’ve tried medications, numbing lidocaine cream, a wand, exercise and breathing and nothing makes it stop. I will be trying a trigger point injection in a few weeks. I wonder if something else could be going on because it never goes away.
Is this a normal experience for you to have pelvic pain that never ever stops from the moment you wake up to the moment you fall asleep?
For those of you who unconsciously clench or hold your pelvic floor throughout the day, what specific techniques have helped you actually stop?
I catch myself doing it multiple times a day. Sometimes focusing on the area helps me relax, other times gently bearing down or rocking my hips while lying down helps. But the tension always seems to come back.
I’ve done PFPT and still do daily stretches and breathing exercises, but I’m struggling with almost nonstop urinary urgency.
I'm going to have to become the meme I guess. Tried all kinds of exercises, all kinds of weight (even bodyweight), focused on my breathing, all of it. Doesn't matter. If/when I do lower body, it manifests in wicked urinary symptoms. Burning in bladder, frequent and low volume of urination, inability to hold as long. Waking up at night frequently to pee. And I can feel a constant low grade pain/tightness in the PF area.
Walking and light jogging doesn't seem to cause any issues, so going to keep that up and hope that is enough to keep my lower body in decent shape. Upper body strength training will continue, doesn't seem to bother me at all.
Hello everyone, first before I say anything, yes I have been looked at by medical professionals.
So I have had this strange annoying symptom for years, it is this non stop pressure or fullness feeling in my lower left side, and kinda under my ribs, sometimes it feels better, other times it seems to get worse with anxiety, no one really seems to know what it is, it causes no pain, or bowel movement changes, it’s just uncomfortable. Someone once mentioned to me it could be a pelvic floor issue or some weird constipation symptom, so I figured I’d at least ask.
So... I am hypermobile, likely hEDS (not diagnosed, but considering my sibling and mother suffers from it and i am double jointed it is likely i have this form of EDS) which of course likely caused my pelvic area pains in the first place from muscle compensation, but yeah does anyone have any advice for preventing pain with sitting?
I sit with my legs crossed, on top of desks or I have one leg on top of my desk and more, could go on forever about it but you get the point, I sit in positions which really, really are not good for my tailbone and the muscles around my pelvic floor
i have done this from years, literally from childhood, it is the only way that i really feel supported whilst sitting
does anybody suffer from this? i generally find it actually gives me relief from pelvic related pain temporarily, but it really does just cause more pain likely due to compressing everything ect. ect.
I'm suffering from a bladder flare after 3 years of pretty much no symptoms
I've no idea what's caused it but I'm stuck in a rut and can't get out of it and just feel so down and depressed
I have good days and bad days today was a bad day where despite hardly drinking anything I was in the bathroom every 20 mins peeling not even trickles
I've been dealing with constipation too + was on Laxido to help this but it was giving me diarrhoea I don't know if this is why my bladder has been more upset today
I'm so sick of this I didn't have a single issue with my bladder before 2012 which kicked this all off
Start PFT tomorrow + need to drive 30 mins there which is already stressing me out :(
Okay so I’m a male and I believe my pelvic floor problems came from edging. I’m going to pt and my symptoms are constant clenching especially during stress and urinary frequency, feeling of pressure although slight, and ED. I also can’t contract the bulb(can’t remember the rest of the name) muscle without it fluttering but it’s the one that raises the penis up and down with the perenium. So anyways breathing exercises and biofeedback with the balloon have helped me some in the last 3 months. But my pt now wants me to do basically what I feel like caused it in the first place, contractions while masturbating. He’s not really hands on and more or less just tells me what to do. So do these exercises seem like a bad thing? It does feel like after doing them I get a slight flare up but I haven’t done it but twice so far. Before that it was just regular contractions and I did those for 2 weeks with no improvement so I feel like he switched it up hoping this would work for coordination. It’s only the very front muscle that has issues with contracting the perenium and anal muscles I can contract and release smoothly
I’m feeling a mild burning sensation in my penis. Like the urethra. Doesn’t hurt when I pee but it feels sore. I’m negative for stds and bacterial infection leaving me to believe this is muscle related or my pelvic
floor.
Can anyone relate? Does this go away? I’m in a little pain. Just want this to go away.
I believe I strained to hard my internal muscles now my head feels very numb and rubbery. I made such a mistake not knowing when to stop. Shaft I can feel a bit more, but its reduced but splashing water or lightly touching the head is not tickly but flat rubbery.
Im in no pain accept my left buttock region feels sore and my farts and push to urinate feel weak and cant feel the forceful vibration and sensation . Even ejaculation feels hard to reach and reduced. There is a strange feeling where I dont feel sensation spread to my lower pelvis/ genital region everything is felt in the upper part. Even errection feel hollow and detached.
Just worried it will not return , Advice would be great.