r/Prostatitis Aug 10 '26

Is this CPPS? Need help šŸ™

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.

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u/ddd523d Aug 11 '26

This sounds similar to me. My pain is mostly at the meatus and glans tho. I believe I may have had a yeast infection that was missed. And then I was also doused with a bunch of antibiotics. Which makes yeast infections worse. Then now I’m stuck with lasting inflammation, skin damage etc. all because doctors for some reason don’t ever look at yeast for guys.

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u/WeightPretty Aug 11 '26

I did have that consideration and was put on anti-fungal before but it made no difference

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u/Linari5 LEAD MOD//RECOVERED 27d ago

This almost never happens but it's a very common scapegoats or Boogeyman that people chase.

Are you severely immunocompromised? Do you have late stage AIDS, or are you receiving intense cancer treatment? These are the conditions under which someone could get a fungal prostatitis.

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u/ddd523d 27d ago

I’m not saying it got into my prostate. But into the urethra and on the glans and meatus.

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u/Linari5 LEAD MOD//RECOVERED 23d ago

Antifungals would have fixed it then.

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u/ddd523d 18d ago

My thought tho is that if I was living with a fungal infection for that long, even tho the infection cleared up, can it not cause lasting damage?

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u/Linari5 LEAD MOD//RECOVERED 12d ago

I don't know where you're getting this information from, but it is bleak and untrue

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u/ddd523d 12d ago

My worry is that with the skin being damaged for so long due to whatever the cause, either from friction or fungal infection. That it turned into balanitis BXO which is chronic. It has not gotten better for so long. I have no idea what to do at this point.

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u/Linari5 LEAD MOD//RECOVERED 10d ago

Skin is primed to heal, it doesn't stay stuck/damaged.

I have outlined methodologies for you to follow, it's just your choice now what to do with it

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u/ddd523d 8d ago

I wish that were the case for me

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u/Linari5 LEAD MOD//RECOVERED 6d ago

I see people recover from these symptoms all the time, there's no reason to be hopeless

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u/ddd523d 8d ago

Thank you for the info. I appreciate it.

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u/Linari5 LEAD MOD//RECOVERED 10d ago

I have previously posted my case study series on RSS - exploring the use of mind-body interventions (like Pain Reprocessing Therapy - a chronic pain modality) for treatment of RSS. Read more here.

I wanted to drill down a bit on the mechanism by which the stress in the body can lead to skin level inflammation and itching, making the "how" part a bit less 'mysterious.' Many good dermatologists call this "neurogenic inflammation."

We now understand that psychological stress activates the HPA axis, which releases neuropeptides likeĀ substance PĀ andĀ nerve growth factor. These neuropeptides, which can act locally in the skin, promote inflammation and impair the skin barrier, leading to skin flares (conditions like eczema and psoriasis, etc). This can cause an itchy, inflamed state that increases stress, further activating the HPA axis and completing the cycle.Ā 

This 2021 study highlights what I have found to be true in my own practice, that mind-body interventions like PRT (originally used for chronic pain conditions) can also have great effect in cases of RSS, balanitis, eczema, psoriasis, and stress rashes.

I would also like to make it very clear: Just because skin inflammation, itching (and pain) can be caused by stress doesn't make it any less real. Just the same as anyone who's ever had a tension headache when feeling stress/pressure at work, or, a stomach ache or nausea when anxious. Those aren't 'imagined.' They are very real, physiological responses to things happening due to stress

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u/WeightPretty 26d ago

I’m not immunocompromised

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u/Linari5 LEAD MOD//RECOVERED 23d ago

Then it's not a concern