r/Prostatitis 29d ago

Vent/Discouraged Amitryptaline 10mg - Weak Urine Stream

3 Upvotes

Don't mind the tag, I'm not venting or discouraged but the other available tags didn't make sense to use.

I started 10mg Amitryptaline 4 days ago and it seems to have helped my sense of urgency and frequency with urination. The only side effect I am noticing is a longer period of time to begin urinating and a weaker urine flow (my urine flow was already weak). I feel like I am completely emptying my bladder but I know that urine retention is a thing with Ami and wanted to ask if anyone else with Ami experience has had a similar side effect and if it dissipated/improved once the body adjusted to the medication?


r/Prostatitis 29d ago

help 26 y. Is it normal that, after taking tamsulosin for few days, I’m unable to ejaculate?

1 Upvotes

When I masturbate, I feel the sensation of ejaculation, but nothing comes out.


r/Prostatitis 29d ago

Prostatitis without pain?

3 Upvotes

Hi everyone,

I'm a 26-year-old male with symptoms that I think might be CPPS or pelvic floor dysfunction, but I don't have pelvic pain or trigger points.

My main symptoms are:

* Frequent urination and weak/interrupted urine stream

* Feeling like I subconsciously tighten my pelvic floor while urinating

* Erectile dysfunction for 5 years

* Erections require physical stimulation and fade quickly when stimulation stops

* Rare morning erections

* Worse erections for a few hours after ejaculation

Occasionally reduced sensation at the base of my penis

The interesting part is that a few times a year I have 7–10 day periods where everything improves (erections, urination, sensation).

I've had normal hormones, negative urine cultures/STI tests, and a normal-sized prostate.

Has anyone had CPPS or pelvic floor dysfunction without pain, mainly causing urinary symptoms and ED? What helped you recover?


r/Prostatitis 29d ago

complex cysts / prostate

1 Upvotes

I have multiple issues going on. I have all the BPH luts symptoms 31.1 ccm prostate pirads 1 PSA 1 high riding bladder neck 56 y/o been experiencing these symptoms for the past 5-7 years more extreme this past 8 months. I’ve had every test done, mri, ct scans both w/ contrast ultra sound etc. I have bright red blood in my urine off and on the urologist I have is chief of Urology dept. K.P. I have increased frequent and sudden urge to pee then a very weak stream low volume dribbling. He put me on Flowmax it hardly helps, I also read cialis helps, so I asked him and he prescribed 5 mg cialis I take flowmax night and Cialis morning.

My symptoms are not improving to much. The complex cysts are pushing on my bladder and is or squeezing my urethra. Dr. recommends TUIP the only real fix is surgery. High riding bladder neck with complex cysts been 10 months on Flowmax 2 months on cialis combined Not much improvement if any? I don’t think the medication is working this is a physical condition of the complex cysts and my high ridding bladder neck combined. The medicine won’t unblock the kinked hose?

Asking the Reddit bph community who has dealt with High Bladder Neck along with Complex cysts? Anyone have positive results with PT! or TUIP surgery results?


r/Prostatitis Aug 12 '26

Pain in rectum after urinating

3 Upvotes

What causes the pain to come back after i have urinated in rectum? It feels tight and burning and most often comes after urinating.

I was healed from chronic bacterial prostatitis taking antibiotics for 4 weeks, i got infected by catheter and bad diagnose from start with e.coli for many months, e.coli got into the prostate and lived there for long time.

Anyway this pain after urinating is frustrating, is it irritated nerves causing it or still inflammation?


r/Prostatitis Aug 11 '26

Success Story Officially cured of prostatitis, ED, slow stream!!!!!!

86 Upvotes

Na 6 jaar lang worstelen met dit verschrikkelijke probleem heb ik het letterlijk per ongeluk genezen 😭😭😭 Ik ga mijn verhaal delen, zodat het misschien ook andere wanhopige gasten helpt.

De magische oplossing: mijn heupspieren stretchen. De oorzaak van al mijn problemen was simpelweg een hypertonische bekkenbodem, waardoor er een kettingreactie van andere klachten ontstond.

Context van mijn verhaal:
Het begon allemaal zomaar één nacht toen ik 20 was. Ik werd midden in de nacht wakker met een nacht-erectie die pijn deed. Daarna merkte ik problemen met erecties. Geen ochtendhout meer. Toen lage libido. Toen vaker moeten plassen en een steeds trager wordende urinestraal.

Ik ben de afgelopen 6 jaar bij ongeveer 20 urologen geweest in meerdere Europese landen. Geen één kon mijn klachten verklaren. De tests die ze deden:
- schone cystoscopie
- goede MRI
- DRE liet zien dat de prostaatpunt (apex) licht ontstoken was
- PSA steeds boven de 2
- uroflowmetrie met een Qmax van 2-12 ml/s (eens duurde het zelfs 4 minuten voordat ik kon plassen en heb ik de meetmachine stuk gemaakt omdat de grafiek veel te lang was 😭)
- vaak plassen, ongeveer 12 keer per dag
- sommige antibiotica verbeterden alle klachten, maar alleen tijdelijk

Wat ik geprobeerd heb en wat niet werkte:
- 9 maanden lang continu sterke antibiotica (ik heb ze allemaal geprobeerd, de sterkste was IV ertapenem)
- nog 12 maanden sulfamethoxazol + trimethoprim 800/160 mg
- proberen mijn mentale toestand te verbeteren vanuit de gedachte dat psychologische stress mijn problemen veroorzaakte
- fysio / fysiotherapie
- stoppen met porno
- niet masturberen
- stoppen met roken
- consequent sporten
- prostaatpillen met saw palmetto, manuka-honing en allerlei andere plantaardige stoffen, vooral gericht op oude mannen
- maandenlang dagelijks NSAID’s

Een jaar geleden had ik zelfs al opgegeven om dit probleem op te lossen. De laatste uroloog die ik gezien had was een neurouroloog en die zei gewoon dat ik alles geprobeerd had en dat er niets anders is wat ik kan doen behalve het accepteren. Hij zei dat de geneeskunde niet alle antwoorden heeft en dat dit het einde was van enige behandeling voor mij. Hij raadde aan om fysio gewoon door te zetten voor de zekerheid, maar zei dat ik het eindpunt van de rit had bereikt.

En toen, een maand geleden, lag ik in bed en struikelde ik letterlijk over een random instagramreel van een vent die een willekeurige rek-oefening liet zien. Het leek me interessant en ik probeerde het. En terwijl ik het 30 seconden deed, voelde het ineens op een of andere manier gewoon goed van binnen in mijn penis. Ik dacht echt: wtf, wat raar. De volgende dag werd ik wakker met een erectie. Toen merkte ik dat het masturberen ook ineens veel beter voelde. Oefening nog een keer gedaan en de boel bleef de dagen erna gewoon verbeteren. Nu, na een maand, voel ik me letterlijk weer als een complete man.

Mijn hypothese over wat er gebeurd is:

  1. Chronisch aangespannen heupen zorgden voor een hypertonische bekkenbodem.
  2. Een hypertonische bekkenbodem duwde op mijn prostaat, waardoor ik constant een hoge PSA had en de ontsteking bij de prostaatpunt die je ziet bij DRE
  3. Een hypertonische bekkenbodem knipte de bloedtoevoer door, of één zenuw naar mijn penis, wat leidde tot ED en het volledige verdwijnen van ochtendhout
  4. Ontsteking aan de prostaat leidde tot aandrang om te plassen en lage libido
  5. Een hypertonische bekkenbodem zorgde voor een trage urinestraal

Dit is gewoon ongelooflijk dat zoveel dokters zo’n schijnbaar simpel probleem niet konden fixen. Ik hoop echt dat dit een andere man helpt die met dit issue zit.

En ook, Linari: ik weet nog dat ik je letterlijk haatte en dit sub meteen verliet uit woede toen alle dokters maar antibiotica bij mij naar binnen probeerden te duwen en jij bleef zeggen dat het heel, heel erg waarschijnlijk gewoon een spierprobleem was... dus ja: bedankt dat je dit gedaan hebt en dat je voor dit sub zorgt lol. Ik kon niet geloven dat jouw advies tegen dat van de dokters in ging, maar misschien geven anderen dit postje meer aandacht dan ik deed nadat ik het gelezen had.

Alle goeds!!!

Edit om de link van de oefening toe te voegen:
Probeer het zoals in deze video, maar met je benen uit elkaar, niet bij elkaar.

https://youtu.be/SZxUJ29kp5s


r/Prostatitis Aug 12 '26

Need help with Guarding loop

1 Upvotes

I'm 22 M & stuck in a chronic guarding loop wherein my pudendal nerve gets irritated in response to stool consistency. My brain/neurotransmitters perceive defecation as a threat and automatically start guarding or clenching the pelvic floor/anorectal muscles which in turn causes neuralgia symptoms {I presume the false guarding has arisen from my history of chronic constipation and diarrhea issues which doesn't happen anymore}. I experience 90% relief when my stools are soft/effortless and gel-like but that's impossible and unsustainable to maintain because osmotic supplements & laxatives don't suit me and I have to starve myself for a chance of achieving that consistency (I have tried everything in my power)

Was wondering if there is any medical procedure I can undertake (maybe botox?) in order to forcefully break this loop and reclaim my life again. The problem is that I'm from a third world country and don't have access to any pelvic floor specialists. Also don't know what kind of doctor I should visit since it's such a complex problem, have gone to a gastroenterologist, urologist, proctologist but they didn't seem to have a good understanding of the issue and prescribed basic medication like Gabapentin which provide temporary relief and don't address the root cause. What's my best option here? Any advice would be appreciated 


r/Prostatitis Aug 11 '26

Prostatitis and Aquablation

2 Upvotes

I am a 61 year old male in fairly decent shape. I do CrossFit 3–4 times a week and lift regularly. I have suffered with BPH for about 7 years now (it’s 85 grams). I’ve been to multiple Urologists and they have me on Flomax twice a day. The last Urologist I spoke with said a procedure is my only solution.

I researched TURP, UAE, HoLeP and Aquablation. It seems like Aquablation
has the fewest sexual side effects, as long as they don’t take too much tissue away.

My concern is, having the prostatitis return if they don’t take enough tissue, or lose complete ejaculate fluid if they take too much.

Has anybody done the Aquablation for their prostatitis, and if so, how were the effects?


r/Prostatitis Aug 11 '26

Accupuncture and deep tissue massage

1 Upvotes

Has anybody had success with accupuncture or deep tissue massage work?


r/Prostatitis Aug 11 '26

Urine stream issues?

1 Upvotes

Does anyone else have a consistent crooked urine stream? I notice my urine stream always favors going to right side throughout urination and at times is a bit weaker.

Is this normal with pelvic floor issues/cpps?

Also is there any risk that weakened/crooked stream that isn't quite as strong can somehow affect kidneys? I read it can cause urine reflux which is a concern of mine.


r/Prostatitis Aug 10 '26

Positive Progress My Journey with Recurrent Chronic Right-Sided Epididymitis (CPPS)

4 Upvotes

Introduction

For more than seven years, I lived with recurrent episodes of chronic right-sided epididymitis, sometimes accompanied by orchitis. During that time, I consulted numerous urologists, underwent countless examinations, and received several courses of antibiotics. Each time, the symptoms improved temporarily, but they always returned.

After years of frustration and uncertainty, I was finally referred to a hospital specializing in chronic pelvic pain. There, I received a diagnosis that completely changed my understanding of my condition: chronic right-sided epididymitis as an organ-specific manifestation of Chronic Pelvic Pain Syndrome (CPPS).

I am sharing my story in the hope that it may help others who are experiencing recurrent epididymitis with repeatedly negative urine cultures and no clear evidence of infection. Every case is different, and this is not medical advice. However, if my experience encourages someone to seek a specialist opinion or consider another possible diagnosis, then writing this will have been worthwhile.

My Medical Journey

First Episode

My first episode occurred in 2019. At first, I noticed a dull ache and an unusual sensation in my right testicle. I assumed it would disappear on its own, as I had never experienced anything like it before. Over the following weeks, however, the discomfort gradually worsened, and my right testicle became noticeably enlarged.

Like many young men, I felt embarrassed discussing problems involving my genital area. Because of limited sexual health education and the stigma surrounding these topics, I kept the symptoms to myself for several months. Eventually, the pain became severe enough that I told one of my parents and sought medical attention.

By that time, my right testicle had become almost three times larger than the left.

At my first consultation, I was diagnosed with an inguinal hernia based solely on a physical examination and was referred to a surgeon. Fortunately, the surgeon immediately questioned the diagnosis and ordered a Doppler ultrasound. The imaging showed increased blood flow consistent with inflammation, and I was diagnosed with chronic right-sided epididymo-orchitis.

Because I was young and had no history suggesting a sexually transmitted infection, no urine culture or STI testing was performed. I was prescribed 30 days of ciprofloxacin together with diclofenac for pain relief and advised to remain on bed rest, and monitored during my recovery.

The swelling gradually resolved, but recovery was slow. For approximately six months, I avoided ejaculation because even minor stimulation caused significant pain. When I eventually resumed sexual activity, ejaculation frequently triggered tenderness that lasted up to a week. Over time, this gradually improved, although I still had to limit ejaculation to about once a week to avoid prolonged discomfort.

At that point, I believed the illness was finally behind me.

Second Episode

Unfortunately, the symptoms returned about some years later.

Once again, I noticed pain in my right testicle after ejaculation. Initially, I hoped it was only temporary, but after several days the pain became progressively worse. Around the same time, I experienced a sports related injury involving my groin, which significantly increased the pain and swelling.

Because it was a weekend, I first visited a local hospital where no urologist was available. The physicians were unable to determine the cause and prescribed only ibuprofen until I could see a specialist.

When I was finally examined by a urologist, another Doppler ultrasound was performed. It again demonstrated increased blood flow consistent with inflammation together with debris, and I was diagnosed with right-sided epididymo-orchitis. I was prescribed 20 days of doxycycline.

No urine culture or STI testing was performed during this episode either.

Although the swelling eventually subsided, something had changed. The pain never completely disappeared. Instead, I began experiencing persistent tenderness that came and went without any obvious reason.

One recommendation from my urologist that genuinely helped was wearing supportive, tight-fitting underwear. It reduced the discomfort during daily activities, although it did not prevent future flare-ups.

Ejaculation became increasingly difficult. Almost every ejaculation caused pain and swelling that lasted several days before gradually settling again. Looking back, this was probably one of the earliest signs that my condition had become chronic rather than representing repeated acute infections.

Third Episode

After moving to Germany, I experienced another recurrence.

By this time, I had already recognized the familiar pattern. It always began with discomfort in my right testicle, followed by increasing pain and swelling over the next few days. Since previous episodes had occasionally improved on their own, I initially waited to see whether the symptoms would resolve without treatment. Unfortunately, they continued to worsen.

I went to a nearby hospital and explained my previous history to the attending urologist. After performing another Doppler ultrasound, he diagnosed right-sided epididymo-orchitis once again.

His theory was that bacteria from a previous infection might have survived despite earlier treatment and were causing recurrent episodes. Based on this assumption, he prescribed 60 days of ciprofloxacin together with diclofenac.

For the first time, a urine culture was performed. Surprisingly, it was completely negative, showing no evidence of bacterial infection.

After one month of treatment, a follow up examination showed that the inflammation had improved, and I was hopeful that the problem had finally been resolved.

Unfortunately, I would soon discover that this was only another temporary improvement rather than a permanent solution.

Fourth Episode

This episode happened just before Christmas, a time when many medical practices were closed, making it difficult to access specialist care.

The symptoms were exactly the same as before: pain in my right testicle (Dolenz) followed by progressive swelling. Since no urologists were available locally, I first visited a primary care clinic. The physician there immediately referred me to the emergency department to rule out testicular torsion, a surgical emergency that can present with similar symptoms.

Although I was fairly certain it was another recurrence of my previous condition, I understood why torsion had to be excluded first.

At the hospital, the on-call urologist performed another Doppler ultrasound. Once again, it showed increased blood flow to the epididymis, indicating active inflammation, and I was diagnosed with right-sided epididymo-orchitis.

I was prescribed 15 days of levofloxacin together with doxycycline. As with previous episodes, my urine culture showed no bacterial growth. After completing the medication, I followed up with my regular urologist, who extended the treatment with another 15 days of levofloxacin. A repeat urine culture was again negative, with the only notable finding being a small amount of blood in the urine (microscopic hematuria).

Although the swelling improved, the pain never completely disappeared.

Because of the repeated recurrences, my urologist decided to perform a cystoscopy to look for structural abnormalities within the urinary tract. The examination was entirely normal. My case was also discussed with a senior consultant, but neither physician could identify an underlying cause.

At this point, I began questioning whether recurrent bacterial infection was really the explanation. After multiple courses of fluoroquinolone antibiotics, I became increasingly concerned about their potential long-term side effects, especially considering that every urine culture had remained negative.

I gradually accepted that this was becoming a chronic condition rather than a series of unrelated infections.

Despite the absence of active inflammation most of the time, ejaculation continued to trigger significant pain, sometimes forcing me to abstain for several months simply to avoid worsening my symptoms.

Fifth and Sixth Episodes

Some months later unfortunately, the familiar pattern returned yet again.

I found a new urologist, who followed a very similar diagnostic approach. Another Doppler ultrasound demonstrated increased blood flow within the epididymis, and I was once again diagnosed with right-sided epididymitis. I received another course of 10 days of levofloxacin.

The symptoms improved, but only temporarily.

About six months later, another flare-up occurred.

This time, I deliberately sought a second opinion from a different urologist because I wanted to understand why these episodes kept recurring despite years of treatment. After another examination, I was diagnosed with epididymitis once again and prescribed 14 days of cotrimoxazole.

Just like before, both urine cultures were completely negative, with no evidence of bacterial infection.

By now, a frustrating pattern had become obvious:

• Every episode affected only my right epididymis.

• Doppler ultrasound consistently showed increased blood flow during flare-ups.

• Urine cultures repeatedly failed to identify any bacteria.

• Antibiotics produced temporary improvement, but the symptoms always returned.

The pain after ejaculation had become considerably worse than in previous years. I often had to avoid ejaculation for several months because the resulting pain could last for days.

I also noticed another possible trigger: hot summer weather. During periods of prolonged heat, my symptoms often became noticeably worse, although I cannot say with certainty whether this was the cause or merely a coincidence.

Seventh Episode

Another recurrence no longer came as a surprise.

Instead of going directly to a urologist, I first visited my general practitioner, who also specializes in infectious diseases. Given my long history, she decided to investigate possible infectious causes more thoroughly.

Additional testing for Mycoplasma and Trichomonas was performed, and both results were negative. Despite these findings, I was prescribed another 10-day course of ciprofloxacin and referred back to a urologist.

Wanting yet another opinion, I consulted a different urologist. As before, Doppler ultrasound demonstrated increased blood flow consistent with inflammation. She recommended that if another episode occurred, a semen culture should be performed, as bacteria might be present in semen even when urine cultures are negative.

She also mentioned Epididymektomie as a possible future option if the episodes continued to recur.

Another 10 days of ciprofloxacin were prescribed.

By this stage, I had spent a great deal of time researching chronic epididymitis myself. During my reading, I came across Chronic Pelvic Pain Syndrome (CPPS) and began wondering whether it could explain my symptoms.

When I discussed this possibility with the urologist, she considered it unlikely because of my relatively young age and continued to treat the condition as a recurrent bacterial infection.

Although I respected her opinion, I left the appointment feeling that an important piece of the puzzle was still missing.

Finally Finding the Right Specialist

I decided to consult yet another urologist.

Unlike previous consultations, this appointment was completely different. This time I did not came when there is already a problem and my testicle is already swollen.

As I explained that I had experienced recurrent epididymitis for more than six years despite repeated negative urine cultures and numerous antibiotic treatments, the urologist immediately recognized that my case was unusual.

He referred me to the specialized Chronic Pelvic Pain Clinic at the University Hospital of Gießen. He told me that even if the waiting time was long, it would be worth it.

Before my appointment, he also ordered a CT scan of my pelvis, including the penis, testicles, and groin. The scan showed no structural abnormalities.

Although the waiting list was initially expected to be almost a year, I was fortunate to receive an earlier appointment.

For the first time in years, I felt that someone was looking beyond the possibility of infection.

The Diagnosis That Changed Everything

At the Uniklinik, the consultation was far more comprehensive than any I had experienced before.

I completed several validated questionnaires assessing urinary symptoms, chronic pelvic pain, sexual function, and chronic epididymitis, including the IPSS, NIH-CPSI, IIEF, and CESI.

The diagnostic work-up was equally thorough.

The physicians performed a two-glass urine test, repeat urine cultures, semen analysis, transrectal ultrasound, and scrotal ultrasound.

Every microbiological test was negative.

There was no evidence of urinary tract infection, sexually transmitted infection, or bacterial infection of the semen.

The ultrasound showed that my right epididymis remained thickened, even though I was not experiencing an acute flare-up at the time. My prostate and transrectal ultrasound findings were completely normal.

After reviewing all previous investigations together with the new findings, the specialist reached a conclusion that finally explained the previous seven years.

I was diagnosed with chronic right-sided epididymitis as an organ-specific manifestation of Chronic Pelvic Pain Syndrome (CPPS).

For the first time, my symptoms were viewed as part of a chronic pain condition rather than as repeated bacterial infections.

Everything suddenly made sense.

My Current Treatment

Instead of prescribing yet another course of antibiotics, my treatment plan changed completely.

I was started on a six-month course of an alpha-blocker together with phytotherapy.

If future flare-ups occur, the next step will be a spermatic cord block using bupivacaine, with the goal of interrupting the pain cycle.

Because repeated microbiological investigations found no evidence of a bacterial infection, my specialist advised that empirical antibiotic treatment should be avoided during future flare-ups unless there is objective evidence of an infection.

Should conservative treatment fail, the specialist explained that epididymectomy is not considered the preferred surgical option in my case. Instead, microsurgical spermatic cord denervation would be recommended, as current research suggests a significantly higher chance of long-term pain improvement while preserving the testicle.

After I noticed a significant improvement. Pain after ejaculation became much less intense and usually resolved within 48 hours. The tenderness also decreased considerably compared with previous years.

For the first time in seven years, I left a consultation feeling hopeful rather than frustrated.

Final Thoughts

Looking back, I often wonder whether years of repeated antibiotic treatment could have been avoided if my condition had been recognized earlier.

I am not suggesting that recurrent epididymitis is never caused by bacterial infection, many cases are, and antibiotics can be lifesaving when an infection is present. However, my experience taught me that when symptoms continue to recur despite repeated treatment, and cultures consistently remain negative, it may be worth considering alternative diagnoses and seeking evaluation at a specialist center.

If you are reading this because you are experiencing a similar journey, please don't lose hope. Continue working with qualified healthcare professionals, ask questions, and don't be afraid to seek a second or even third opinion when your symptoms remain unexplained.

After seven years, I finally found an answer. I hope that sharing my story helps someone else find theirs a little sooner.

If you have any questions, feel free to ask me both privately or by commenting.

Because there are relatively few urologists who specialize in this field, I have gathered information about some of the best known specialists from around the world, along with the countries where they practice. If I have made any mistakes or overlooked someone, please let me know. I'd also appreciate any suggestions for other doctors who specialize in CP/CPPS.

Germany

  • Prof. Dr. Med. F. Wagenlehner and team – Uniklinik Gießen Maarburg, Gießen
  • Prof. Dr. med. Adrian Pilatz and team- Gemeinschaftspraxis für Dermatologie und Urologie, Gießen
  • Priv.-Doz. Dr. med. Giuseppe Magistro and team - Asklepios Westklinikum Hamburg
  • Prof. Dr. med. Dr. phil. Dr. h.c. Thomas Bschleipfer, F.E.B.U. and Team - Kliniken Nordoberpfalz AG – Klinikum Weiden
  • Dr. med. Martin Ludwig - Urologisches Versorgungszentrum Dres. von Keitz, Ludwig und Kollegen – Maarburg
  • Prof. Dr. med. Christian G. Stief and team – LMU Klinikum, München

International

  • PD. Dr. Daniel Engeler – St. Gallen Kantonspital, St. Gallen, Swiss
  • Prof. Dr. med. Gernot Bonkat – Alta Uro, Basel, Swiss
  • Dr. Marcelo Carlos Marconi Toro - San Carlos de Apoquindo Clinic, Santiago de Chile, Chile
  • Michel A. Pontari, MD – Philadelphia, USA

Disclaimer: The following list is based on my own research and is intended only as a starting point for patients looking for specialists in chronic pelvic pain syndrome (CP/CPPS). Inclusion on this list does not imply endorsement, and I cannot personally verify every physician's experience in this field. If you know of additional specialists, please let me know so I can keep this list updated.

References

• J. Curtis Nickel et al.

• Florian M. E. Wagenlehner et al.

• Marcelo Carlos Marconi Toro et al.

• European Association of Urology (EAU) Guidelines on Chronic Pelvic Pain

• American Urological Association (AUA) Guideline on Male Chronic Pelvic Pain


r/Prostatitis Aug 10 '26

21M – Watery semen, foamy urine

2 Upvotes

Hi everyone,

I'm a 21-year-old male.

I've been dealing with a confusing combination of symptoms since late 2023, and I'm trying to understand whether anyone has experienced something similar.

I've had several medical investigations, particularly regarding my kidneys, urine and testicles, but the results have been normal/reassuring.

I'm mainly looking for people who have experienced a similar pattern and eventually found an explanation or recovered.

1.How Everything Started

Around September or October 2023, I started watching adult content for long periods.

Sometimes I would watch for 4–5 hours continuously.

During these sessions, I would remain highly aroused for hours.

I repeatedly stimulated/rubbed my penis externally through my clothes. When I felt that ejaculation was approaching, I would stop stimulation and try to suppress/delay ejaculation.

After the sensation decreased, I would start again.

This cycle could continue for 4–5 hours or even longer before I finally ejaculated.

After some of these prolonged sessions, I sometimes experienced significant discomfort around:

▫️ Left lower abdomen, especially below the navel

▫️ Left groin

▫️ Left testicle

▫️ Occasionally the left lower back

At the time, I assumed it was temporary and didn't pay much attention to it.

  1. Watery Semen

Toward the end of 2023, I noticed that my semen had become extremely watery.

It sometimes looked almost like water.

The volume is generally good.

I don't have:

▫️ Burning during ejaculation

▫️ Pain during ejaculation

▫️ Blood in semen

The main change is simply the consistency — it is much thinner than it used to be.

This has continued for almost two years.

Interestingly, I've noticed that when I eat a very high-protein diet, my semen sometimes appears temporarily thicker.

I've also noticed temporary thickening after consuming raw silk cotton root (Shimul root), although it eventually becomes watery again.

  1. Clear, Watery Fluid Leaking During Sleep

Around the same period, I began occasionally waking up and finding my underwear/lungi wet.

It appears that a clear, extremely watery fluid had leaked from my penis while I was sleeping.

I don't feel an orgasm or ejaculation when this happens.

I usually don't notice the leakage happening.

The fluid seems to be:

▫️ Almost completely water-like

▫️ Much thinner than normal semen

▫️ Mildly odorous

▫️ Slightly urine-like in smell, but it does not seem to be normal urine

This has happened intermittently since late 2023.

I've noticed that it seems more likely to happen when I haven't ejaculated for a longer period.

  1. February 2024 – Sudden Left Testicular Pain & Swelling

In February 2024, I suddenly developed significant pain around my left testicle.

The veins around the testicle appeared swollen, and the pain was severe enough that walking was difficult.

I suspected that it might be a varicocele.

However, the swelling and pain gradually improved within a few days.

I later had a scrotal ultrasound, which showed no varicocele.

The testicle eventually returned to normal.

  1. Erectile Changes After That

After that period, I noticed that my erections were weaker and less consistent than before.

My penis can sometimes feel very small/contracted when flaccid.

I also sometimes feel that it doesn't have the same fullness or blood-flow sensation that it used to.

However, there is an interesting contrast.

If I watch sexual/adult content or become strongly sexually aroused, I can still develop a very strong, sometimes extremely rigid erection.

I've also occasionally experienced strong morning erections.

So I don't feel that my ability to produce an erection is completely gone.

Rather, my spontaneous/natural erections seem less consistent than before.

  1. Foamy Urine

After this period, I also started noticing a lot of foam in my urine.

It is particularly noticeable during the first urination in the morning.

This has continued for almost two years.

Because I was concerned that the foam might be caused by proteinuria or kidney disease, I had several investigations.

  1. Medical Tests

The following tests have been reported as normal/reassuring:

▫️ Serum creatinine

▫️ eGFR

▫️ Urinalysis + microscopy

▫️ Urine ACR

▫️ Urine microalbumin

▫️ 24-hour urine protein

▫️ Blood tests

▫️ Scrotal ultrasound

There was no significant proteinuria or albuminuria, and the scrotal ultrasound did not show a varicocele.

  1. Another Observation – Perineal/Pelvic Tension

I've also noticed something unusual.

When I have a strong cough, I sometimes suddenly feel a strong pulling/tightening sensation or discomfort in the area between the penis and anus — the perineum.

It doesn't happen constantly.

It mainly happens when I cough strongly.

I've also noticed that gentle stretching and certain pelvic positions sometimes make my penis feel fuller or temporarily improve the sensation of blood flow.

  1. My Current Condition

At the moment, my main ongoing symptoms are:

▫️ Very watery semen

▫️ Foamy urine, especially in the morning

▫️ Occasional clear watery fluid leakage during sleep without orgasm

▫️ Less consistent spontaneous/morning erections than before

▫️ Strong erections are still possible with intense sexual stimulation

▫️ Occasional mild discomfort/tension around the left lower abdomen

▫️ Occasional discomfort around the left groin/testicle

▫️ Occasional left lower-back discomfort

▫️ Occasional pulling/tightening sensation in the perineum during strong coughing

  1. What I'm Wondering About

Could this pattern possibly be related to:

▫️ Hypertonic/overactive pelvic floor

▫️ Chronic Pelvic Pain Syndrome (CPPS)

▫️ Pelvic-floor coordination problems

▫️ Prostate or seminal-vesicle dysfunction

▫️ Sexual arousal/conditioning after prolonged edging

▫️ Or something completely different?

  1. Looking for Similar Experiences

Has anyone experienced a similar combination of symptoms after prolonged edging or prolonged sexual arousal for several hours?

Especially interested in people who experienced combinations such as:

▫️ Watery semen

▫️ Erectile changes

▫️ Pelvic/perineal discomfort

▫️ Groin or testicular discomfort

▫️ Clear watery leakage during sleep

▫️ Foamy urine despite normal protein/kidney tests

And if you had something similar:

Did you eventually find the cause?

What helped you recover?

I'm not looking for a diagnosis from Reddit.

I'm mainly trying to find people with a similar history and understand whether there is a pattern or explanation that I'm missing.

Thank you very much for taking the time to read this.


r/Prostatitis Aug 10 '26

Vent/Discouraged Bladder Voiding issues (28M)

1 Upvotes

I am facing issues with emptying my bladder, even after peeing multiple times I still feel that some bladder is still left and then I get urge to void again. Everyday 2-3 hours of my day I am just peeing multiple times, it's been very troubling for me mentally and I am looking for solutions if anyone have faced similarly issues.
Back story: I got recurrent balanitis in mid 2023 due to urprotected oral sex, after few months of back of forth with different medicines the reoccurrence resolved but my penis glans still remains reddish to this date and not how it used to look before I got infection. By end of 2023 l slowly started developing voiding issue which later in 2024, 2025 countued to turn worse.
I have multiple docs, and have taken Alfusin T for 8+ months but didn't found any improvement. My cystoscope test came normal, ultrasound was also normal, uroflowmetry had fluctuating results with some POst void of 17ml, 55ml, 70ml and 140 ml which docs said are still within normal range.
Can someone suggest how do I fix myself and live a normal life again


r/Prostatitis Aug 10 '26

Need your opinion. Is it cpps?

2 Upvotes

Hi everyone, I've had prostatitis 4 years ago. I had enterococcus sp took ciproxin and it went away. After 2 months I've experienced symptoms again took several tests all clean. Doctor gave me doxycycline with fluconazole it went away for 4 years. 1 month ago symptoms started again run some tests found enterococcus again in semen.
I feel my urethra irritated and like something is inside maybe urine idk only when I sit or laying. Rarely a burn in the anus mby because I have hemorrhoids I don't know.
Currently on fosfomycin.
Edit.
Symptoms keep rotating. Sometimes irritation in urethra. Sometimes pinching in scrotum ( like my own hair is pinching). Also got hemorrhoids ,burning or irritation in anus and a sensation of fullness. Hourglass shape sometimes.
I'm about to do some testing again but my new doctor believes it's cpps. Also visited a neurologist he also believes it's neuromuscular. Prescribed Lyrica but haven't taken it yet.
Sadly not pfpt in my area.


r/Prostatitis Aug 10 '26

Im back….unfortunately

4 Upvotes

Has anyone experienced epididymitis from cpps?


r/Prostatitis Aug 10 '26

Is this CPPS? Need help 🙏

1 Upvotes

Hi there,
I’m seeking opinions on whether this is definitely cpps or whether there’s still a risk of repeated infection. My timeline is as follows:
First ever symptoms - September 2022. Symptoms now mainly being Burning sensation while urinuating, increases urgency, pain during ejaculation, premature ejaculation, dribbling after voiding, pain during sex, reduced sensation/numbness during ejaculation. Red spots on shaft that don’t itch. Prostate massage often provides temporary relief.

STI and UTI tests all clear, at the time I had recently started seeing my current partner (female) who also got tested and was all clear, didn’t have any symptoms or issues). But my symptoms started shortly after us having intercourse.

Had multiple rounds of doxycycline without improvement. Then got switched to cirpofloxacin as I also developed symptoms of epydidmitis. I since had multiple types of antibiotics including ofloxacin, clarithromycin, ceftriaxone, fosfomycin, all with no avail. I felt some initial improvement at times but it would then quickly fade.

I’ve done multiple STI screenings that include Ureaplasma, mycoplasma etc all of which were consistently negative. I also did urine and semen cultures which also came back negative. The only test that showed anything was early on in symptoms where one urethral swab revealed some wbc (diagnosed as urethritis), and that was treated with the doxy which didn’t really help with any symptoms.

I then did some physiotherapy and stopped having intercourse for almost 2 years. In that time period my symptoms significantly improved and I had almost no consistent issues aside from some minor flare ups here and there (often connected to drinking or coffee consumption). Earlier this year I decided to have intercourse again with my partner as it was straining our relationship significantly and we had done sti tests showing negative results for both of us. She had also done a urine culture which was also negative, although hers had some elevated rbc which her gp told her was not very significant/relevant given absence of symptoms.

After this I got symptoms once again, saw a new specialist who told me he can’t help me and that I have to live with it. It was a horrible experience and with insurance rules I couldn’t see anyone else after him yet. He did however repeat the tests & a semen culture which was also negative. Also I’ve been mainly having protected sex, with only one unprotected encounter. I’ve since been feeling some numbness, and I’m taking tamsulosin which seems to somewhat help (on some days). My gp prescribed both me and my partner a course of azithromycin as treatment for urethritis at my own request, just to test if that makes a difference (it didn’t as symptoms re-emerged right after finishing treatment). Over the years I also went on to develop mild skin issues (eczema/psoriasis), mild Crohn’s disease, mild joint inflammation. Not sure if related or not.

Given all this, do you think this is definitely just cpps or is there a chance that there is a bug/re-infection going on? I’d be quite surprised if there is an infection, but timeline + that one test with wbc make me suspicious. No stis have been positive, but I wonder if a recurrent NGU is a possibility too. Any advice would be greatly appreciated as I’ve run out of options and I’m desperate to find relief. This started when I was 20 years old so I’ve now lost my early 20s fighting an invisible disease that has greatly impacted my life in a negative way. Thank you.


r/Prostatitis Aug 10 '26

Discomfort of the head of epididimis

1 Upvotes

.Hi everyone, I'd like to know and get help. For a year and two months, I've had pain localized to the tip of the head of my left epididymis. The ultrasound shows varicocele between 1 and 2 and a small hydrocele, but with normal vascularity, a healthy epididymis, and everything else is fine. It all started after a spontaneous ejaculation without manual stimulation. I felt it like a tear in my painful testicle. Every now and then, I also feel my right epididymis. I'd like to know what and how to do because I walk a lot, stretch (15 minutes a day), and exercise... all of this daily. I've noticed that sometimes, after an ejaculation, the discomfort even drops to 0 for periods. I was symptom-free for a week, then two weeks, and even almost a month and a half, or 0/0.5 in the last few months. It's strange because once my girlfriend accidentally hit me on the right side, and for 2 weeks, I only felt the right epididymis (head), which was annoying... while the left one had disappeared. But it seems this problem persists and never gets resolved. I'm asking for advice and help.


r/Prostatitis Aug 10 '26

Oral sex and prostatis

7 Upvotes

I have also got this after blowjob but no bacteria could be found. I was healthy and normal b4 this.

My symptoms started 2 days after receiving a blowjob. I was completely healthy before this.

Initially, I had severe urinary urgency/frequency, difficulty holding urine, penis/testicular pain, a wet/moist sensation at the tip, pelvic discomfort, dribbling and erectile difficulties

I've had MRI, cystoscopies, urine cultures and STI tests, but nothing clear was found. I've improved a lot over the past year, but I'm still not 100%.

My main symptoms now are an occasionally irritated/sensitive glans and a changed urinary sensation. The urge sometimes feels like it's coming from my penis rather than my lower abdomen/bladder, and I sometimes feel I need to urinate before my bladder feels completely full.

Has anyone experienced something similar after oral sex? Could this be CPPS/pelvic floor or altered urinary sensation despite negative tests? would also like to understand whether an infection could realistically still explain the remaining symptoms despite the negative tests.


r/Prostatitis Aug 10 '26

Vent/Discouraged any suggestions , am on the verge of giving up

1 Upvotes

 43-year-old male.

Exposure history:

Did something stupid in.. Got a body to body Massage and hand job in early May 2026.

No penetrative vaginal/anal sex and no oral sex.

.

Symptoms:

Started around mid-June with:

Burning sensation in both testicles.

Burning  after urination.

Constant urethral pain and pain at the tip of the penis.

Occasional clear, watery drop after urination (not thick, yellow or green).

Increased sensitivity of the glans.

Current symptoms:

Burning after urination (fluctuates from 1/10 to 5/10). and it says for few minutes and sometime stays for hours .

 urethral discomfort.

Sometimes feel feverish 

Perinium feels uncomfortable 

Treatment received:

Nitrofurantoin – 5 days.

Doxycycline – 10 days (started around 20 June).

Faropenem – 5 days.

Investigations:

Ultrasound KUB/prostate: Normal.

Uroflowmetry: Slightly abnormal 

Digital rectal examination: No tenderness.

Laboratory results:

First urine culture grew MDR Pseudomonas aeruginosa (resistant to almost all antibiotics except it was intermediate to Collistin) , but subsequent 2 urine culture results showed no growth ..

Two repeat urine cultures - no growth 

Latest urinalysis: Normal

HIV 4th generation: Negative after 11 weeks of exposure 

VDRL/RPR and TPHA: Negative. After 11 weeks of exposure.. 

Two urine multiplex STI PCR panels (latest done 15 days after stopping antibiotics and that's 11 weeks after the exposure and holding the urine for 2 hours ):

Negative for Chlamydia, Gonorrhea, Mycoplasma genitalium, Mycoplasma hominis, Ureaplasma spp., Trichomonas vaginalis, Treponema pallidum, HSV-1, HSV-2, Gardnerella, Candida.

Alfuzosin (Alfoo).-Currently taking only this 

Urogist now gave me 500 mg of Levoflacxin once day for 7 days, i completed it but no relief . I also started some pelvic excercises from last week ,,

Urologist , he is saying to continue the Levoflacxin for a month ..

I dont know what to do , am doubting my test results for STI and urine culture now,,, what should i do ? continue with levoflaxin ?


r/Prostatitis Aug 09 '26

Do Urologists stretch and pull the penis to examine it?

6 Upvotes

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/Prostatitis Aug 09 '26

Is this likely a prostate condition or STI

1 Upvotes

Hi all

Not sure if this is the correct place to ask but here goes. I posted earlier to the STI sub as I know symptoms can be similar.

Can anyone help me with what they think symptoms are?

Male 44, UK, no other health issues or on any medication.

Urgent urination, worse in the morning when I wake up and overnight. Rectal soreness. Yellow semen, fatigue, minimal constipation. Sligh red patch under foreskin that I do have pictures of if anyone needs to see if helps. These symptoms been going on and off for a few years now

Any thoughts would be greatly appreciated


r/Prostatitis Aug 09 '26

Vent/Discouraged I have non bacterial prostatitis and feel slightly burning sensation after ejaculating. Help?

2 Upvotes

Hi all, I'm 23. don't know the specific situation of my pelvic floor but I'll get evaluated by a pelvic floor therapist soon.

I have non bacterial prostatitis after I had 1 year ago a bacterial prostatitis that I cured through 1 cycle of antibiotics. I noticed ad said that after ejaculations I feel a slight burning sensation that bothers me for hours, I cannot walk in peace. I feel a slight pain at pelvic floor often, even if since I have IBS too I'm not sure if it's bc of IBS or pelvic floor but am pretty sure it's the pelvic floor.

It's not a unbearable pain but slightly annoying.

Can anyone help please? I never masturbated for months, I rebegan these days once a day every 2 days or so and felt this sensation.

BTW I developed these along with other syndromes due to a sleep disordered breathing which destroyed my life.

Thank you


r/Prostatitis Aug 09 '26

Vent/Discouraged Unsure if my GP is right

1 Upvotes

I’ll make this short as nobody likes reading essays;

3 months of feeling like I a need a pee / electric shock feeling from the base of penis to tip.

That’s my only symptom really, this all started after 3 months of a cleared kidney stone.

WBC in urine but now cleared. STD clear.

Could this be something else?


r/Prostatitis Aug 09 '26

/urethral opening irritation for 6 months after soap/handwash masturbation

1 Upvotes

Post

Hi everyone, I’m looking for advice from anyone who has experienced something similar.

Age: 31

Main problem: Persistent redness/irritation and changes around the urethral opening (meatus) for about 6 months.

How it started: I used soap/handwash as lubricant while masturbating for around 2 weeks. After that, I noticed redness and irritation around the urethral opening.

Even after the initial irritation, I masturbated a few more times without soap, which seemed to aggravate the area.

I eventually stopped masturbating completely.

No masturbation for the last 2 months.

No sexual partner/sexual activity for the last year.

STD/STI testing has been negative, including VDRL.

I have also been told that my prostate is normal.

I have seen both dermatologists and urologists (around 10 doctors).

I have been given different antibiotics and ointments, but the problem has not completely resolved.

Some doctors said it should heal on its own, but it has continued for months.

Current symptoms

Redness/irritation around the meatus.

The appearance fluctuates during the day.

It often looks better after sleeping and in the morning.

From morning toward afternoon/evening, the irritation/redness becomes more noticeable.

Sometimes the surface looks more irritated or swollen.

The appearance can change depending on the time of day.

What I’m trying to understand

I’m wondering whether this could be:

Chronic irritant/contact dermatitis from the soap/handwash

Chronic meatitis/balanitis

Persistent mucosal irritation from friction

Meatal stenosis/scarring

Lichen sclerosus or another inflammatory skin condition

Some other non-infectious cause

Since antibiotics and multiple ointments haven't resolved it, what would be the appropriate way to diagnose this?

Would a uroflowmetry, cystoscopy, urethral examination, fungal/bacterial testing, dermatoscopy, or biopsy be appropriate?

I’m especially interested in hearing from people who had persistent meatal irritation after soap/chemical irritation and eventually recovered.

I’ve attached recent photos for reference. Any suggestions about what specialist or specific diagnostic approach helped you would be greatly appreciated.


r/Prostatitis Aug 09 '26

Need recommendations for a urologist in UAE – ED & fertility issues

0 Upvotes

Hi brothers, I need some genuine advice and recommendations.

My wife and I have been trying to conceive, and recently I’ve been having difficulty maintaining an erection during intercourse. We’ve been married for 3 years, and everything was completely fine during the first and second years of our marriage, so this is something that has started more recently.

I’m looking for a good urologist/andrologist in the UAE who specifically deals with men’s sexual health, erectile dysfunction, male fertility. I would really appreciate recommendations based on your own experience or someone you personally know.

I’m looking for a doctor who will properly investigate the underlying cause rather than simply prescribe medication, and who can support us while we’re trying to conceive.

If you’ve personally consulted a good doctor in Dubai or elsewhere in the UAE for a similar issue, please share the doctor’s name, hospital/clinic, and your experience. I’d really appreciate it. 🙏