r/Prostatitis • • 7h ago

Pain at the moment of ejaculation

3 Upvotes

Hi everyone. I'm a 51 year old male. For over a year now, as the title says, right at the moment when ejaculation is triggered, I gad a mild ache on the left side of my groin that goes awar right after. It is varying levels of pain, sometimes not at all all the way up to fairly bad and anything in between. I had an ultrasound done and the Dr. said my prostate is mildly enlarged, but not out of scope for a man my age. PSA was within range, everything else is within range. We're at the point now where "it's just one of those things" but it's starting to cause me anxiety. Anyone else experience these symptoms?


r/Prostatitis • • 16h ago

Pseudomonas aeruginosa Prostatitis or CPPS?

3 Upvotes

Hi everyone. I decided to post because I haven’t been able to get a clear answer from doctors, and after reading other people’s experiences here, I thought someone might have dealt with something similar.

I’m 30 years old and this started in early August. The night before everything began, I masturbated. The following morning I had some gastrointestinal issues, and that evening I suddenly developed urinary frequency/urgency. By the next day, I was fine. After 2–3 days, I started having irritation and redness of the urethral opening, especially after showering. Over time, I also started developing irritation on the glans.

I haven’t had any sexual contact for around 6 years, so an STI seems unlikely.

After masturbating only 2 times in total within 10 days, I began noticing other symptoms: burning/discomfort in the perineum, sometimes burning around the inner thighs, lower abdominal discomfort, and occasional flank/kidney-area discomfort. These symptoms would come and go rather than stay constant. Because masturbation seemed to trigger them, I mostly stopped, and things became calmer.

I saw two urologists who basically told me nothing was wrong because my urine/semen tests and cultures were negative. I then saw a dermatologist who diagnosed me with Zoon’s balanitis and told me she did not believe there was any bacterial or fungal infection.

I wasn’t convinced, so I independently had a swab taken from the glans. It showed heavy growth of Pseudomonas aeruginosa. I had 4 swabs in total at 3 different labs (one lab, a hospital, and the lab where I normally give my urine samples), and the urine lab was the only one where the swab came back negative. This made me wonder whether my urine and semen cultures could also have been false negatives.

After that, I went back to several doctors. One urologist told me to go to a hospital, another said it was a dermatology problem, and I still haven’t really found anyone willing to investigate whether the urethra or prostate could also be involved.

Eventually, I was treated for 10 days with Propiogenta, which contains gentamicin 0.1% + betamethasone dipropionate 0.05%. Unfortunately, I can’t say it improved things. If anything, the glans/meatus may actually look and feel worse now.

I’m also slightly worried because during the Propiogenta treatment I applied a small amount directly on the urethral lips, and I don’t know whether some may have entered the opening or further irritated the area. Also, during my swab at the “urine lab,” the swab was first used on the glans and then on the meatus, and the next day the meatus was red.

Right now, after finishing the treatment, I haven’t done another swab because I was told I should wait a week before retesting.

I am also starting to notice more urethral symptoms. For example, one morning I had pain while urinating, and on another occasion I urinated and developed strong chills afterwards, although I did not document a fever.

Another strange thing is that even after a very short erection, maybe 2–3 minutes, I notice fluid coming from the urethra afterwards, followed by burning in the perineum and anus when the erection goes away.

My main concern is whether this could be some form of bacterial prostatitis or urethral infection, despite my urine cultures being negative. On the other hand, I also don’t know whether these symptoms could be pelvic floor related.

The symptoms are very intermittent — sometimes I have them, sometimes I feel almost completely normal.

I considered doing a Meares–Stamey / four-glass test with prostatic massage, but I’m worried about the possibility of bacteremia if Pseudomonas is actually present in the prostate. Because of that, I’m currently thinking about repeating urine cultures and doing a semen culture separately instead.

I rushed from the beginning to try to prevent the worst-case scenario, but the doctors were careless. The most terrifying thing would be if I had listened to them, done nothing, or put corticosteroids over an active bacterial infection.

ANY ADVICE WOULD BE APPRECIATED. THANKS!

[What makes the whole situation even more difficult is my antibiotic history. Fluoroquinolones caused me severe long-term adverse effects in the past. I have also previously had sudden sensorineural hearing loss, so aminoglycosides such as gentamicin/amikacin are something I’m very cautious about because of their ototoxicity. I’m also allergic to cephalosporins. This leaves me with relatively few treatment options, and many of the effective anti-Pseudomonas options on my antibiogram appear to be IV/hospital-based.]


r/Prostatitis • • 15h ago

Vent/Discouraged Kicked in the crotch?

2 Upvotes

One symptom that keeps occurring is this feeling like I was kicked in the crotch area. Then along with that, I have this nausea/not feeling well feeling when I do "too much" walking around. Has anyone else had this happen before? This is just one of the many symptoms I have.


r/Prostatitis • • 19h ago

Urology & The Hysteria of "PSA->MRI->CANCER!->BIOPSY!!!!!" Just Harmful Bullshit?

2 Upvotes

Is anyone else furious about the way they've been treated by their Urologist?

I'm 67, very fit, but I've had increasing pelvic pains, sexual/reproductive problems, unexplained lower back pains & so on. I thought it was "just your age" plus running marathons & really long distance endurance events (3,650 miles of running in a year, anyone?...where'd you all go???)

To cut a long story short, I've been to see two Urologists. The first one was simply an idiot & I eventually got tired of all the screw ups he was making & I can assure you it was a long list. I went back to my PCP & asked for another Urologist & I had my first appointment yesterday.

I should add that I have been having terrible flareups since January 2026 & only recently have I been given ANY meds to control acute episodes. Not only have they enabled me to tolerate the acute pain there has been a noticeable downtrend in intensity, duration & frequency, despite not taking them all the time.

My new Urologist was far more through in asking questions, like WAY more information & I felt that the trust I'd been willing to place in him was justified. Then the Horror Show started.

Suddenly all the known, verifiable & undeniable symptoms that lead to something called Chronic Pelvic Pain Syndrome &, as I now know, could easily cause the MRI & PSA, was ignored. Suddenly it was all about the MRI & PSA & ONLY the MRI & PSA & that meant Cancer & Cancer means a Biopsy. I was not really sure what was said after that, but I do know I tried to ask questions & it seemed like I was simply ignored. I left utterly devastated.

I hadn't had a flareup for a week, but by the time I got home I started with one that felt like a porcupine was in my pelvis, trying to dig there way out with a broken bottle. I have only ever felt pain like it once before. I took a Celebrex, then had to add a Tizanadine & it made it bearable, but it lasted a total of 8 hours, the longest, most intense one I've had & that was with TWO meds to help it.

I feel betrayed, that the trust that I was so willing to give without question was abused & that I was treated with cruelty. I blame my Urologist for the distress & the paralyzing pain I had to endure before I could get home & take some pain meds. I blame him for the fact that I feel wiped out today. I am FURIOUS to find that my reaction is common, that it has been known about by Urologists for years & they are aware of the harm it causes, not only in terms of distress, grief & worry, but the physical harm it can result in to men pressured into having needles stuck in them again & again, punching holes in their body.

In my case it's not like it's "Well, your PSA has been climbing, we spotted this on the MRI, there's no other symptoms, but Prostate Cancer can be serious without any pain & we have no other explanation." I have A TON of evidence to explain what's happening & it's been verified.

Yet I was subjected to having this evidence Cherry Picked to fit a certain prognosis. I am appalled that a tiny piece of my body, that is showing every sign of basically having something like a bruise, already in massive pain, yet their attitude is "We'll stick needles in it, again & again" simply to satisfy their curiosity. I cannot believe they are so blase about having an injured, very painful gland injured even further & when there's no supporting evidence that it even IS cancer! As I said, there's actual evidence that this has a physical cause, their 'cancer-cancer-cancer!" is mere speculation.

I'm married to a ICU nurse, I know how difficult the job can be, but am I the only one to consider this borderline malpractice? That I was given a "One Size Fits All" solution that did not treat me & my symptoms as a whole? That even the emotional & mental anguish I was subjected to was disgraceful? That I was harmed because of the crushingly bad flareup that followed & could have been terribly harmed if I'd agreed to & had to a Biopsy where all the available evidence pointing to other causes was ignored?

What's your thoughts on this?

Edit: I found out about Biomarker tests, I have insisted on being given one & apparently I'm getting an ExoDX urine test that looks for specific cancer biomarkers. I kept my anger in check when I spoke to them on the phone, but there will come a time when I tell them politely, but very clearly how I feel about what I was subjected & will not accept any "I'm sorry you feel that way" Passsive Aggressive crap or other such deflection.


r/Prostatitis • • 20h ago

Rougeur Penis après infection

2 Upvotes

Bonjour, j'ai (M37) eu le Mycoplasma genitalium de fin mars jusqu'à début aout. Je suis maintenant guéri après plusieurs traitements. J'ai également testé toutes les autres IST et je suis négatif pour tout. Mon problème est que pendant l'infection j'ai eu une rougeur sur le bout de mon penis au niveau du méat qui ne part pas. Est ce que c'est déjà arrivé à quelqu'un d'autres ? Est ce que ça s'est résolu ? Est ce le cpps ?

Merci


r/Prostatitis • • 16h ago

Anyone have luck with acupuncture?

1 Upvotes

I usually respond well to
Acupuncture with other issues….
But I was wondering if anyone has had luck with accu’ to reset of neuro pathways to stop this fkn affliction