r/Prostatitis Oct 19 '22

Starter Guide/Resource NEW? START HERE! Prostatitis 101/Checklist + Sub Rules

419 Upvotes

» QUICK START! «

  1. SUCCESS STORIES in this subreddit
  2. TOP TIPS AND INFO (All Posts)
  3. NEW 2025 AUA TREATMENT OUTLINE
  4. See below 'Subreddit Rules' for the full 101 prostatitis guide and newbie checklist

The information provided in this subreddit is not medical advice, including the information here. It is for educational and informational purposes only

SUBREDDIT RULES

  1. No harassment, abuse, or disrespect is tolerated here, especially to the volunteer mod team
  2. No promotion of pseudoscience, conspiracies, and/or fringe doctors
  3. No graphic photos allowed (NSFW)
  4. No self-promotion/selling of products (SPAM)
  5. One post per person, per day. Leave room for others
  6. No fear mongering

VIOLATIONS: Depends on the severity of the violation, but generally:

  1. First infraction is a warning
  2. Second is a temporary ban (~3 days)
  3. Last is a permanent ban

POSTING REQUIREMENTS

  1. To prevent abuse and spam we have an Automod in place. Accounts with very low comment karma and/or less than 36 hours old cannot post.

  2. Also, please tag any pessimistic/hopeless posts with the "vent/discouraged" flair, and any positive progress updates with "positive progress."

NEWBIE ORIENTATION: CPPS vs Prostatitis

The vast majority of prostatitis cases are non-bacterial, i.e. NIH Type III non-bacterial prostatitis. Expert consensus (of the research) estimates this number to be around ~95% of all cases. True chronic bacterial prostatitis (CPB) is rare. Read more about the prevalence of CBP here, complete with journal citations.

CBP also prevents with unique and specific symptoms. Here is how to identify bacterial prostatitis based on symptoms.

Q: If I don't have an infection, then why do antibiotics make me feel better? FIND OUT WHY

The rest of us have (or have had) NIH Type III non-bacterial prostatitis, now referred to as CPPS or UCPPS - (Urologic) Chronic Pelvic Pain Syndrome. Type III non-bacterial prostatitis can present either with or without actual inflammation of the prostate, but overt prostate inflammation is very uncommon. Most men with CPPS (non-bacterial prostatitis) have small, firm, 'normal' prostates upon examination. This means that the common 'prostatitis' diagnosis is very often a total 'misnomer,' as most cases have no prostate inflammation whatsoever.

While CPPS is officially a syndrome (The 'S' in CPPS), or a collection/pattern of symptoms with no single cause officially agreed upon by the larger medical community, there are leading theories with significant bodies of high quality evidence behind them.

The top theory backed up by research: CPPS is a psycho-neuromuscular chronic pain + dysfunction condition. It often affects the muscles of the pelvic floor, the peripheral nerves that innervate the pelvic region, and the central nervous system (which includes the brain) - among others. This means that treatment requires a multi-modal, integrated treatment approach, and that there is no single pathway or 'pill' to recovery.

I must emphasize that the central nervous system (ie centralized/nociplastic mechanisms) of CPPS affect at least 49% of all cases according to the MAPP study (Multidisciplinary Approach to Pelvic Pain). Do not neglect these. We recommend reading the centralization section below 👇

RECOMMENDED: 1. Centralized Pain Criteria and Citations

  1. Psycho neuromuscular CPPS - with journal citations and techniques to apply.

Things that are known to trigger CPPS (chronic pelvic pain and dysfunction)

These commonly happen via central (nervous system) or peripheral (pelvic floor or nociceptive/neuropathic) mechanisms

  1. Pelvic injuries (falls, hernia, accidents)
  2. Perceived injuries
  3. Infections (UTI/STD)
  4. Stressful experiences and trauma, including sexual abuse/assault
  5. Regretful/anxious sexual encounters
  6. Poor bowel/urinary habits (straining on the toilet often - constipation) or holding in pee/poo for extended periods (like avoiding using a public toilet)
  7. Poor sexual habits (edging/gooning excessively)
  8. Cycling or intense gym habits

SYMPTOM VARIABILITY:

CPPS also presents differently from person to person, and you may exhibit only a few symptoms from the total 'pool' of possibilities. For example, you may only have a 'golfball sensation' and some minor urinary urgency. Another person may have tip of penis pain, testicular pain, and trouble having bowel movements. A third may have ALL of those, and also have sexual dysfunction (ED/PE) and pain with ejaculation. But they are all considered to be CPPS. Here is the full list of symptoms of non-bacterial prostatitis (ie CPPS) - https://emedicine.medscape.com/article/456165-clinical?form=fpf

The chief symptom reported by patients with abacterial prostatitis/CPPS is pain. Genitourinary symptoms include perineal, penile tip, testicular, rectal, lower abdominal, or back pain.

Patients can also have irritative or obstructive urologic symptoms such as frequency, urgency, dysuria, decreased force of the urinary stream, nocturia, and incontinence. Other symptoms are a clear urethral discharge, ejaculatory pain, hematospermia, and sexual dysfunction.

Note: If your symptoms extend BEYOND the pelvis, this is a classic indication of centralized mechanisms (ie nociplastic mechanisms) - What some doctors have in the past called "central sensitization." According to the American Urological Association, these include symptoms like headaches and migraines, IBS, fatigue, fibromyalgia, and more.

So how do we treat it?

The most evidence based approach to treatment is called "UPOINT," a treatment/phenotyping system for Prostatitis/CPPS that was developed by the American Urological Association. UPOINT Stands for:

Urinary, Psychosocial, Organ Specific, Infection, Neurologic/Systemic, Tenderness (ie, Muscles)

it's been shown to be very effective (around 75%) in treating CPPS, as it takes each patient and groups them into phenotypes based on symptoms, then treats them in a customized, integrated, and multi-modal manner. Every case is treated uniquely by symptoms, and this leads to much better patient outcomes. UPOINT is what a good urologist uses to treat patients with CP/CPPS. If your urologist isn't aware of UPOINT, find a new one. You're probably not in good hands. Citation: https://pubmed.ncbi.nlm.nih.gov/34552790/

EXCELLENT MEDICAL/SCIENTIFIC VIDEO RESOURCE - 2015 AUA (American Urological Association) Meeting: https://www.youtube.com/watch?v=4dP_jtZvz9w

✓✓✓ NEW SUFFERER TREATMENT CHECKLIST

ENGAGE WITH A PHYSICIAN:

  • Do see a urologist to rule out any serious structural issues
  • Do get a LUTS and/or bladder ultrasound (check residual urine/voiding issues) along with a DRE for prostate size assessment
  • Do get a urinary culture and/or EPS localization culture, if infection is suspected (based on symptoms) - AUA guidelines DO NOT recommended semen cultures - full text, page 21
  • Do get any physician-specified blood tests
  • NOTE: Cystoscopy is typically reserved for suspicion of IC/BPS - but not typically recommend for CPPS
  • Do not use antibiotics without meeting specific diagnostic criteria. Only ~5% of all prostatitis cases are bacterial (even less if your case is > 90 days)

! ! WARNINGS ON INDISCRIMINATE USE OF FLOROQUINOLONE ANTIBIOTICS (Like Cipro or Levo) ! ! Click to Read FDA & EMA Warnings

Thinking about MicrogenDX testing? Please think again, the 2025 AUA Guidelines specifically advise against it's use: READ OUR MOD MEMO

ENGAGE WITH A PELVIC FLOOR PT - Muscles and Nerves

  • See a pelvic floor physical therapist, one who has experience TREATING MEN and can do INTERNAL AND EXTERNAL trigger point release. Studies suggest that 47% - 90% of CPPS cases have pelvic floor myalgia (pain, tenderness, trigger points), and multiple studies show 70-83% of people improve significantly with pelvic floor physical therapy
  • Practice diaphragmatic belly breathing daily
  • Practice pelvic stretching daily (and combine with the breathing)
  • NOTE: 2025 AUA Guidelines suggest that ESWT, acupuncture, dry needling, and TENS help some cases

CENTRALIZATION/BIOPSYCHOSOCIAL:

  • At least 49% of cases have centralized/neuroplastic mechanisms according to the MAPP research network study
  • EXTERNAL: Manage and reduce stress and anxiety in your external environment (work, relationships, finances, etc.)
  • INTERNAL: Address the fear towards your own symptoms. And, avoid obsessive preoccupation & problem solving with symptoms, redirecting your attention to things that are meaningful and enjoyable (distractions and hobbies)
  • Belief/perception of safety or danger (including assumptions about assumed injuries or assumed infections) is also shown in studies on chronic pain to affect our physical pain experience
  • Take time for yourself and do things to relax and engage in self care. Find SAFETY in your body again: mindfulness/meditation, yoga, baths, etc
  • See a chronic pain therapist, coach or psychologist who practices PRT, EAET, and/or CBT: Examples: Pain Psychology Center (LA), the app "Curable" for chronic pain/symptoms (Note on CBT - this is typically found less helpful for pain in controlled experiments, compared to newer PRT and EAET)
  • Recommended readings: Alan Gordon (LCSW) - 'The Way Out' or Dr. Howard Schubiner 'Unlearn Your Pain'

Urological (Pharmacological) Treatments to Discuss With A Doctor:

  • Discuss alpha blockers (Alfuzosin etc) for urinary/flow/frequency with physician, if you have urinary symptoms. Be aware of possible side effects in some users: PE, Retrograde ejaculation, etc
  • Alternate to above, if they don't work for you or you have side effects, discuss Cialis with your physician. Cialis (Generic: Tadalafil) also helps with ED and can be used at low doses of 2.5mg/day.
  • Discuss low dose amitriptyline (off label usage) with your doctor, which can help approx. 2/3 people to relieve the neuropathic pain associated with this condition
  • Discuss rectal suppositories for pain management, often containing meds like: diazepam (Valium), available via a compounding pharmacy - this is a controlled substance; always discuss with your doctor - not meant to be used daily.
  • You may try NSAIDs for pain during flair ups, but caution for daily, ongoing use. MOST find this class of meds unhelpful.
  • Oral Steroids are NOT RECOMMENDED, per 2025 AUA Guidelines

HERBS/SUPPLEMENTS:

  • Phytotherapy (Quercetin & Rye Pollen, ie Graminex) - highest level of evidence for CP/CPPS
  • Magnesium (glycinate or complex) - less evidence
  • Palmitoylethanolamide (PEA) - less evidence

BEHAVIORAL CHANGES (Lifestyle):

  • Avoid edging or aggressive masturbation; limit masturbation to 2-3/week, and be gentle. No "Death grips"
  • Less sedentary lifestyle - walk for 1 hour daily or every other day (I would recommend you build up to this, start with 15 minutes daily, easier to start a habit with a gentle, but regular introduction)
  • Get your blood pressure, body weight, and blood sugar under control (if applicable)
  • Gym goers and body builders: lay off the heavy weights, squats, and excessive core workouts temporarily. Ask a physical therapist to 'OK' your gym and exercise routine. This is a possible physical trigger
  • Cyclists and bikers: Lay off cycling until your physical therapist OKs it - this is a known physical trigger
  • STAND MORE! Get either A) a knee chair, or B) an adjustable standing desk. You'll still need the regular chair, because you can't sit on a knee chair or stand all day, basically, although conceivably you could do both A and B, and skip the regular chair
  • Try a donut pillow if experiencing pain while sitting

BEHAVIORAL CHANGES (Diet) Note: Dietary triggers affect a MINORITY of cases

  • Try reducing/eliminating alcohol (especially in the evening, if you have nocturia)
  • Try reducing/eliminating caffeine
  • Try eliminating spicy/high acid foods
  • Try eliminating gluten and/or dairy
  • Try the IC Diet (basically this is all of the above, and more)
  • If eliminating or reducing doesn't help, then it probably doesn't apply to your case, enjoy your food and drinks!

NEW 2025 AUA TREATMENT OUTLINE

Others suggestions? Beyond this abbreviated list, work with a specialist. This includes urologists who have specific training in CPPS (through continuing education), pelvic floor PTs, and chronic pain specialists, including PRT practitioners.

Welcome to r/Prostatitis, follow the rules, be respectful, and we'll be happy to have you in your recovery journey.

The content of this subreddit is not considered medical advice, including the information here. Even if a flared user (verified urologist or PT) makes a comment, this is not prescriptive advice, nor is it medical advice.

This guide was co-written by your moderators u/Linari5 and u/Ashmedai


r/Prostatitis Apr 07 '21

Starter Guide/Resource Confusion over ANTIBIOTICS

117 Upvotes

Tony's Advice for Beginners

Top Rated Thread of all time in this Reddit: The experience of an MD with CP/CPPS

Antibiotics

Every day numerous questions are posted here about the effects of antibiotics. How can my case be nonbacterial if antibiotics help me (for a while anyway)?

The simple fact is that antibiotics are ANTI-INFLAMMATORIES and also have other immunomodulatory effects. In fact they are used for these effects in many conditions (acne and other skin conditions, ulcerative colitis, Crohn's Disease, and more).

Sadly, even many doctors don't know this (it was only acknowledged this century and medical school curricula have mostly not been updated yet). But the research is all there. (Note that due to our genetic differences, some people react more to the anti-inflammatory effects and some people less, or not at all. This is known as pharmacogenetics).

Acute bacterial prostatitis does happen, and it's pretty obvious: very sudden abrupt onset, fever, chills, nausea, vomiting, and malaise (feels like having the flu). Nothing like what 99.9% of readers here have. It's often a medical emergency that requires a trip to the ER.

But you may still think your case is bacterial, perhaps a chronic and not acute case. Professor Weidner says:

"In studies of 656 men with pelvic pain suggestive of chronic prostatitis, we seldom found chronic bacterial prostatitis. It is truly a rare disease."Dr. Weidner (Professor of Medicine, Department of Urology, University of Giessen, Giessen, Germany)

Chronic bacterial prostatitis also has a distinct picture. It presents as intermittent UTIs where the bug is always the same (often E coli). Here's an example:

I have chronic bacterial prostatitis that responds well to antibiotics. ... The doctor will express some prostate fluid and run a culture to determine the bug and prescribe an appropriate antibiotic. My bug has consistently been shown to be E-coli.

That being said, my symptoms usually start with increased frequency of urination, burning and pain on urination, and pus discharge. But no pain other than that and it usually goes away after a few days on the antibiotics. I continue the antibiotics for 30 days which is well after the symptoms have disappeared. I can usually expect a relapse in 6 to 12 months. ... This has been going on for more than 30 years. .... My worst experience a number of years ago was when I thought I would tough it out and see what happened. The pain got excruciating, testicles inflamed, bloody discharge, high fever. But this responded well to antibiotics and I haven't tried to tough it out again after that experience. I know when it starts and go on antibiotics right away.

I know that guys who have chronic pelvic pain syndrome may scoff at what I say and I know that they are in the majority. I really don't know what they are going through but then, they don't know my experience either.

So here are the key points to look for in chronic infection:

  1. Relapsing UTI picture (dysuria [painful urination], discharge)
  2. Consistently identifiable bug (the bug does not change)
  3. Generally no pain unless accompanied by fever and discharge. So for most of the time, men with chronic bacterial prostatitis do not have any pain.

All the rest have, sigh, UCPPS (CPPS).


r/Prostatitis 22h ago

Any advice? 2 months with urethritis today and not coping very well.

3 Upvotes

I understand this is a prostatitis sub, but given how the two are linked I figured I'd post here.

Any advice healing post urethritis inflammation?

I never tested positive to any bacteria, this all stemmed from an unprotected sexual encounter on may 16th, noticed first symptoms (discharge, pain, acute inflammation) on may 21st, the day my life changed for what feels like will be forever at this point.

Whilst the discharging and urinary frequency has stopped, my glans has distinct white patches/splotches and feint brown dots that seems like swolen glans that do not itch, the meatus is inflamed (dark glans colour/redness that fluctuates, fish/botox lip opening) but not bright red or as bad as it was first pre treatment (1g azith, 14 days 100mg doxy)

Even light/quick masturbation on the very few times I have tried, results in the redness temporarily flaring for an hour or two, and i feel tightness/pinching in the urethral tube right on climax with lingering pain for an hour or so after followed by worsened pelvic feelings and general discomfort/awareness, i could not imagine what actual sex would do to it and how i would even explain this to a partner without scaring them off, not that I'm in a rush to engage in sexual activity after this nightmare anyway but the point is, im still not okay and my function is far from normal..

If anyone in a similar position who eventually recovered can share their story, wisdom or any advice whatsoever and maybe give me some hope, it would be greatly appreciated.

Next Monday, I have an appointment with a sexual health clinic that saw me 3 weeks ago that told me "give it two weeks you'll be back to nornal, if not, call us" and am hoping i can form a good plan moving forward, it will also be 3 weeks since my last antibiotic test so im in a good testing window now and plan to test for everything they possibly can just to rule out residual infection, the person I had that fateful encounter with is also testing and is now supporting me through this which i greatly appreciate, she gets results tomorrow from her urine and swab tests, we're both pretty nervous however she is completely asymptomatic.


r/Prostatitis 19h ago

Urine sample after prostate massage: initial stream or midstream?

2 Upvotes

My doctor asked me to give a urine sample for bacterial infection after a prostate massage. Should I collect the initial urine (first part of the stream) or a midstream urine sample after the massage?

If you've had this test done or know the standard procedure, I'd appreciate your advice.


r/Prostatitis 1d ago

Prostatitis ureaplasma/mycoplasma

4 Upvotes

I have a complicated case of chronic prostatitis that started after sexual contact with a woman who had a sexually transmitted infection (STI). I had multiple standard cultures performed, but no bacteria were detected, even though I initially had urethral discharge and severe pain during urination. Later, my symptoms progressed to urinary frequency and pain in my lower abdomen and perineum.

I have received several courses of antibiotics: first 15 days of doxycycline (Vibramycin), then 20 days of levofloxacin, followed by another 15 days of doxycycline, 14 days of azithromycin (Zithromax), 14 days of cefixime for suspected gonorrhea, and I also received an injection of ceftriaxone.

More recently, Escherichia coli (E. coli) was detected on a urethral swab. I then saw an infectious disease specialist, who prescribed 6 weeks of trimethoprim-sulfamethoxazole (Bactrim) and 4 weeks of doxycycline.

What would you recommend I do? I still think a persistent Ureaplasma or Mycoplasma infection may be responsible and that it has caused chronic prostatitis. Has anyone experienced something similar or have any advice?

I also have balanitis. I'm not sure whether it is related to all of this.


r/Prostatitis 2d ago

Vent/Discouraged Torsion and orchiopexy as CPPS trigger?

0 Upvotes

Disclaimer (AI drafted): I've been inputting my various symptoms and experiences to Gemini and I asked it to summarize my experience to date in a digestible format for this Reddit post.

TL;DR: Had sudden, unbearable 9–10/10 left testicular pain 6 weeks ago. Emergency surgery (orchiopexy) performed; surgeon saw no active 360° twist but stitched testicle to scrotal wall anyway. Ultrasounds confirm testicle is healthy and fully healed, but I’m left with 1–2/10 pain aggravated by walking and tight clothing. Also had pre-existing shaft symptoms. Looking for thoughts/experiences regarding nerve irritation, CPPS, or pelvic floor involvement.

Pre-Event Symptoms (2 Months Prior)

  • 37M, located in Europe.
  • For ~2 months leading up to the main event, experienced an intermittent itchy or needle-like pain inside the penis shaft, particularly noticeable during erections.
  • Avoided seeing a doctor at the time.
  • A few days before the acute event, applied over-the-counter thrush/candida cream to the tip of the penis.

Acute Event & Surgery (6 Weeks Ago / Mid-June)

  • Sudden, severe ache in left testicle while walking to the store. Escalated to unbearable 9–10/10 pain within 20 minutes (hardly able to speak/walk).
  • Went to ER. ER doc suspected testicular torsion; administered strong painkillers and attempted manual detorsion.
  • Emergency Orchiopexy: Under general anesthesia within 2 hours of pain onset.
  • Surgical Findings: Surgeon reported no visible evidence of active torsion upon opening, but performed left testicular fixation (stitched testicle to scrotal wall) as a preventative measure.

Post-Op Course & Medical Workup

  • Hospital Stay: Discomfort & brief severe pain spike overnight; discharged after 2 nights following a clean ultrasound.
  • Infection Suspicion: Developing pain days later led doctor to suspect infection.
    • Urine culture: Negative
    • Semen culture: Negative
    • CT Scan: Negative (ruled out kidney stones)
  • Antibiotics Taken:
    • Course 1: Amoxicillin (finished late June) -> temporary mild improvement.
    • Course 2: Doxycycline (1 week in early July) -> minimal change.
    • Course 3: Amoxicillin again (7 days) -> minimal change.
  • Prostate Check: Doctor examined prostate recently, noted nothing major.

Current Status & Triggers

  • Ultrasound Results: Multiple follow-up ultrasounds show the left testicle is healthy, structurally intact, and well-perfused.
  • Current Pain Level: Settled at a low-grade, persistent 1–2/10 ache/tenderness (down from a 4–5/10 flare-up early July).
  • Specific Triggers:
    • Walking: Repetitive movement triggers a cumulative dull ache.
    • Clothing: Any pressure from tight underwear seams or pants against the scrotum creates tenderness.
    • Ejaculation: appears to trigger pain in following hours but not sure if this is imaginary.

Questions for the Community:

  1. Has anyone experienced persistent mechanical/nerve pain after testicular fixation (orchiopexy) even with clean ultrasounds?
  2. Could the pre-existing shaft itching/needle sensation combined with the traumatic pain event point toward pelvic floor muscle guarding or nerve entrapment (CPPS / Genitofemoral / Ilioinguinal nerves)?
  3. If you had similar symptoms post-surgery, did pelvic floor physical therapy or nerve-modulating treatments help?

r/Prostatitis 2d ago

Positive Progress Symptoms improving after doing baby post exercise

8 Upvotes

I just started baby Pose exercise a day ago and I see my symptoms approving like less urgency after peeing and less frequency.

I also have little pain and burning in ureatha and left side penis pincing pain which have decreased alot.

Idk if anyone wants to give it a try.
I do it in the morning for two minutes and afternoon and before bed.

I almost feel normal and i hope this progress continues


r/Prostatitis 2d ago

Ejaculation quality is the only variable.

4 Upvotes

Not anxiety, posture, etc. The only thing that seems to decide whether I have CPPS or not is how good the ejaculation was.

If I have a really strong, satisfying orgasm: CPPS completely disappears and stays gone.

If the orgasm is weak or unsatisfying: CPPS, agiation, hard flaccid, etc. all come back immediately and stay there 24/7 until I have a good one again.

Of course, once it comes back I start trying to force a good orgasm, which obviously makes it worse and usually leads to another lackluster one lmao

Anyone else?


r/Prostatitis 2d ago

Is Blood in Semen Common ?

2 Upvotes

I'm 29 years old male , healthy no medications no other issue , no urinary issue or blood in urine

about a month maybe even a month and a half i noticed blood in semen , at 2 weeks mark it went away and then came back and still present .

if i dont ejaculate for a lot of days the blood gets heavier and more concentrated .

I did 2 semen culture checks and STD check .

STD came back as negative and Semen Cultures came with a rare bacteria called "Strep. dysgal./canis" .

This bacteria is from dogs and cats and I have a dog but no clue how it was transferred .

Ether way I started Antibiotics based on the resistance test they did in the semen culture but after 7 days nothing changed .

Urologist said that this strep bacteria is not the issue and antibiotics should have solved the issue even in less than 7 days ,

He gave me other type of antibiotics and said that he suspects Protstatitis as a main cause .

Further investigation will be done later if it persists but wanted to ask you guys if that’s reasonable and common for Prostatitis ?


r/Prostatitis 2d ago

Vent/Discouraged PRP injections (P Shot)

1 Upvotes

Wanted to talk to anyone that has had PRP injections into the glans, meatus and shaft for glans and meatus damage, inflammation and pain.


r/Prostatitis 2d ago

Doxycycline side effects?

1 Upvotes

Ive been prescribed 100mg of doxycycline twice a day for 2 weeks for what the dr says could be difficult to detect bacteria in the prostate since all labs come back negative. Did a ureaplasma test im still waiting results on but he said to take it anyways. Ive been reading some stories about people getting psychological (even psychosis) side effects from doxycycline. Whats been your experience at treating prostatitis/ non bacterial prostatitis with this antibiotic ? Should i wait for my appointment and ask the doctor for an alternative? Im a very anxious person when it comes to taking medication that pose these type of side effects


r/Prostatitis 2d ago

Vent/Discouraged Help new flare. Help

1 Upvotes

Usually whenever I drink a lot of water . It causes burning urine mainly inside of glans . It burns and stinging . So today it happened . After it went away . If I get aurosed or erect muscle in penis pain .what's happening .iam panicked


r/Prostatitis 3d ago

Dull orgasms only symptom

3 Upvotes

Some background, Late 30s M, Caucasian. I have been having dull orgasms where it's not painful but I feel a warming sensation when ejaculating, but no other symptoms. Not sure when this started but I feel like it was a boiling frog. I'm noticing it now. I've not been diagnosed but think I have PE as well, and have had a history of edging/stopping while having sex to last longer. I've also been very horny lately.

I've been doing the reverse keagles and other stretches, recently discovered massaging my perenium at the point of orgasm helps a lot to make it feel more normal.
Is this cpps or something else?

My urologist put me on antibiotics but it didn't help and I have a follow up next week where I believe next step is cialys and a prostate exam. Does anyone else only have this symptom out there? It's not painful ejaculation, but pleasure is very muted, the rest of sex pre orgasm still feels good. I think maybe I lost sensation in my pereneum for a while and am starting to get it back (maybe?), but I'm trying to figure out if anyone else out there is similar.


r/Prostatitis 3d ago

Vent/Discouraged PRP Injections in Glans and Meatus

1 Upvotes

Has anyone had PRP injections in their glans, meatus and shaft to heal damaged glans and meatus?


r/Prostatitis 3d ago

21M need help with diagnosing

2 Upvotes

hello! not sure if this is the right subreddit because I don't know what this could be.

on July 9, i developed pain at the base of penis, slightly to the left, after masturbation. it hurt only when touched (during palpation). after about 3 days, the pain became much less noticeable, so I masturbated again on July 12 and 13.. after that i noticed another symptom that freaked me out: both times semen was too liquid, watery (there was some white cum clumps though) after those sessions the pain came back, so i haven't masturbate since.

on July 17, i saw a urologist, he examined my penis, testicles, prostate, nothing abnormal was found. I didn't even have the pain during the examination. later that day, after i had an erection and touched the area, the pain returned.

i also had a urinalysis: no signs of UT infection. an urologist recommended me to do a semen analyses to rule out an infection, which currently I am afraid to do, because I assume that pain will come back after an erection/masturbation.

(TL;DR) my symptoms are:

  • pain at the base of penis, when pressing the area, which worsen after masturbation/erection
  • extra effort to squeezy out the last drips of urine (is it urine dribbling?)
  • watery semen, which worries me the most

any advice needed, any similar cases? does this sound more like a muscular/soft tissue injury, or could it be something like prostatitis or seminal vesicle inflammation? the thing that scares me the most is watery semen.. should i do a semen analyses anyway?


r/Prostatitis 4d ago

Positive Progress Another medical paper showing Zyrtec helps with CPPS

18 Upvotes

I posted a different paper showing linkage between CPPS and mast cell / tryptase. I also said that since taking Zyrtec twice a day my CPPS is gone. It’s still gone. I only hope that this helps someone else.

https://pmc.ncbi.nlm.nih.gov/articles/PMC10592376/


r/Prostatitis 4d ago

Vent/Discouraged My story... Numbness, losing hope

3 Upvotes

Hello everyone.

For me it all started 4 years ago after severe stress.

I got symptoms out of nowhere pain and irritation in pelvic floor and penis I also got hardflaccid. When it started it was 10/10 for about a month and a half. Anxiety and stress over symptoms made it that severe. After about a month and a half after I stoped caring about it it all went away. I was completly symptom free for a month. Then it came back but it was only 1/10 this time and wasnt constant.

First 2 years my symptoms were very minimal. Most of the time in first 2 years I was symptom free.

Now about a year and a half ago symptoms slowly got worse and I again suspect because of my fear and anxiety over them. I read tons of horror stories and worried about everything that was happening to me.

Every symptom every change frightened me and I spiraled in very dark toughts. All this made it worse.

Now about 9-10 months ago I started experiancing numbness in penis after a very normal sex. Nothing rough, no injury, absolutly nothing abnormal.

My penis just went numb after sex and I only noticed in the shower after. The water felt weird. Like my penis is covered with condom. Also temperature sensation is very very minimal.

Didnt think much of it as I tought its just maybe a flare up and will go away. Well it didnt. My sensation since then is minimal in my penis. In the shaft and in the glans. But I do still have normal sensation in inner foreskin area tight under glans where I was circumsised. I feel temperature and touch well there.

This is now starting to scare me. Im not sure what im dealing with as I never had an actual injury.

I had spine MRI and its clean.

I had Pelvis MRI and its clean

Blood work also clean

No diabetes

No vitamin deficency.

Prostate ultrasound - normal size normal results

Test for bacterias - negative multiple times so no infections ever

Ive been to pelvic floor PT last week and here is what she said.

She did internal work and it went like this.

General pelvic floor tension is not bad.

She said most muscles are 3/10 tension in resting tone and she said that is normal for males.

She did find very tight coccygeous muscle.

Prostate area was very painful. When she pressed around prostate a sharp pain was felt at my penis glans.

Sitbone area also painful.

Im pretty much lost at this point. Why did numbness aprear like this and I never had it before.

Hope someone can help me out.

Can I still recover sensation ?

I still feel temperature but very little.

I feel light touch but its muted.

I feel a bit of pressure but also muted.

Other symptoms:

Pain in perineum and pelvic floor ranging from 1-4. Trouble sitting.

The scar area under glans from circumsision is normal tho.

I can get erect and have sex. Orgasm actually still feel good. Usually I feel it in penis glans and shaft.

thanks for anyone who read this and I hope for all of you to recover from this. God bless you all


r/Prostatitis 4d ago

27M hematospermia but no clue

2 Upvotes

I've had symptoms of hematospermia for about 5 days and have no other symptoms (fever, pain). I went to the doctor and he did urine and blood tests. There's a very small amount of blood in my urine. There's no inflammation in my blood or urine and PSA is okay. How many days will it take to clear up and what will the doctor's next step be? Each new ejaculation produces bright red semen btw.


r/Prostatitis 4d ago

Vent/Discouraged Prostatitis inflammation and a great London doctor to help . Please advise .

1 Upvotes

I’ve tried anti biotics , diet , PT nothing helps . Need some
Hope

Has anyone see a urologist in London that just didn’t tick boxes ?


r/Prostatitis 5d ago

Could MCAS cause prostatitis?

1 Upvotes

Im 46band have had symptoms for almost 3 years. Just diagnosed with MCAS. Im on dupixent, hydroxyzine and quercetin specifically for that and will be adding a few more soon. Probably Ketotifen.

Wondering if the inflammation from these hyper active mast cells is causing prostate inflammation? Its causing asthma and EOE and my symptoms started at the same time of a huge flair that led me to the er multiple times right after covid.

Ever since, my psa numbers have been a roller coaster up and down. Lowest was 3.2.. highest was 5.9. Im currently 4.8 but just started all these medications 2 weeks ago. Im also starting pelvic floor therapy and an intense exercise routine to strengthen my legs after leg surgery a few years ago that wasn't properly addressed.

If I do get better, I won't know if its the medication, exercise, or the pelvic floor stretches. Oh and I also might start taking lexapro for anxiety. Im basically doing everything possible to finally get better.

Im wondering though. Has anyone with confirmed MCAS noticed any difference after starting specific MCAS medications?


r/Prostatitis 5d ago

Vent/Discouraged Having lower abdomen tightness and veins buldged out

0 Upvotes

Hi I'm having a lower abdomen discomfort and some of the veins become prominent I had also taken some antibiotics but nothing happened

It's quite irritating for me

Link to the image: https://kommodo.ai/i/xwJ58MbPg5OSKeCyOUiR


r/Prostatitis 5d ago

Seeking advice for my Dad

1 Upvotes

Hi all! My Dad (61) was diagnosed with prostatitis about 12 weeks ago. He was on a long course of Cipro, but no changes besides his mental health (the gut brain connection is real and insane). We also have no idea if it was even bacterial or not in the first place. He is in so much pain he is having near panic attacks and the shakes constantly. The urgency is also a real problem. He is not himself at all. He has to lay down—he can’t really sit, even with cushions. Walking does help and he paces a lot. He’s a bucket of anxiety over this? completely spaced out. His hands shake, a symptom he’s had on and off for a year or so, but it’s become much more severe and constant. Not sure if it’s related or not. Either way, this is all really scaring me. He has always been an independent and stoic man, very reluctant to ask for help. When he asked for help, I knew it was bad. He has a procedure coming up to take a biopsy and clean out some “excessive tissue” they saw on the testing he’s already had. He’s been trying stretches, ditching caffeine, etc. He can only take OTC medication or non-addictive because he is 20+ years sober. What else can I do to help him? Thank you!


r/Prostatitis 5d ago

32M, diagnosed at the ER yesterday with prostatitis. Questions!

1 Upvotes

Since last week, maybe Wednesday, I noticed my urine stream/output wasn't as strong as it usually is. Like in the morning I’ll have two water bottles and then have to urinate like crazy for an hour or so since I chugged water lol. But I noticed it wasn’t coming out as strong still. Also noticed a little groin pain on The left, and my pelvis area would sometimes feel pressure. But I never had a fever or burning or anything like that, just difficulty urinating sometimes. But then sometimes it comes out fine and fast. Right now I don’t have a PCP, but I found one and set it up for July 31st, the earliest they could see me. Also set up a urologist Appointment for August 11th.

Anyway, I went to my local urgent care and they did a urinalysis and it was all good except for a trace amount of blood and the clinician there wasn’t too concerned about it but sent it out for a urine culture And put me on cephalexin. I called back Wednesday and got the results and they were all negative, no infection, and they even did some STD tests to be sure and they were negative (I’ve only had one sexual partner, my girlfriend, that we have a child together). So I suffer from bad anxiety and stress, and definitely am a hypochondriac. So I went to the ER yesterday, and told them my problem and that I went to urgent care. They ran tests, urine and blood and did a CT scan. My urine and blood tests were okay and fine and didn’t show infection or white blood cells, but the CT scan showed my prostate was enlarged/mildly inflamed, and so the NP told me she was gonna put me on antibiotics to deal with it. I was kinda just flabbergasted and was trying to ask questions, but I never saw that NP again after she left the room to go see if my blood work was done. A regular nurse came in and he discharged me and gave me a first dose of ciprofloxacin. I then looked up that antibiotic and see that it can cause all these issues like tendon ruptures and tendinitis and nervous system problems. I take 1mg of clonazepam in the morning, and I was told it would be fine to still take it with it. I was so annoying since I kept calling the ER back about my bloodwork and the antibiotic and they said that’s what I was deemed to be put on by the NP for my inflamed prostate. I picked up the medicine today and took my second pill, and am going to take the second for the day around 10pm tonight.

But basically I’m wondering if it’s even bacterial? They said they werent totally sure I believe when I asked and called, but my symptoms pointed to that. But then I keep thinking it might be CPPS, since I have a lot of anxiety and stress and maybe made my pelvis floor weak from it. So I’m just sitting here constantly googling stuff since I can’t be seen by a urologist until next month and can’t get in earlier to my new PCP. And calling the hospital saying this antibiotic scares me to take, they say it’s the best one for prostatitis and that once they discharge you they can’t really change anything. And not to get TMI, but I noticed when I was going to ejaculate last night I reached climax but only like a drop came out. When earlier in the day it came out fine. So I tried again this morning and I barely ejaculated again, so that has me all nervous now why that started happening, I’ve never had that.


r/Prostatitis 5d ago

26m with urethral burning prescribed cialis

2 Upvotes

So ive been dealing with daily urethral burning that increases after ejaculation, sometimes peeing and after bowel movements for a year. Ive seen many urologists who have told me a range of things. The last one said it could be prostatitis/cpps and prescribed daily 5mg cialis + a 2 week round of doxycycline antibiotics. So far semen culture, std, urine culture, uti tests have all comeback negative. Im still waiting on a ureaplasma test i did yesterday. Question is, has cialis worked for any of you with similar symptoms? Its frustrating because this started one day last july and has stayed with me for a year now without a cure. I also have pain in the left side of my testicle although not thr testicle itself, more like the veins beside it/on top of it. Im also scared to do thr antibiotics bc ive seen they cause insane sunburns even with little sum exposure (i work in the sun)


r/Prostatitis 6d ago

Positive Progress How long does it take for cialis to work and help you relax your tight pf muscle?

4 Upvotes

It seems to work pretty quickly for me which makes sense as it's just supppsed to relax your pelvic floor muscle.

Does it take it a few days of taking cialis for you guys?

Thanks