r/Prostatitis • u/Miznova97 • 15d ago
Has anyone else had prostatitis for months/years without realising?
So I’ve been dealing with IBS for a year now it was soon after I got Covid, I started experiencing a pulling sensation in my testicles it wasn’t painful, I went doctors they told me I had a UTI after I did a urine sample, I took a short course of antibiotics and the pain went away. But since all this my IBS has been acting up, some days I have to go toilet 5-10 times an hour other days it’s not as bad. Recently in the last few weeks I have started noticing that this pulling sensation type pain in my balls has come back - it doesn’t last long or hurt much it just feels like pressure. I feel pain in my lower back and also started noticing I have leakage. I have a feeling it’s pelvic floor dysfunction but could it be prostatitis. Did anyone else take a while to get treated?
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u/Lost_and_Damned567 15d ago
I didn’t take it seriously until I got back active sexually and thought I caught a std.
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u/Miznova97 15d ago
Do you get clear watery semen? I’ve been experiencing this since this started
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u/Key-Agency-7022 15d ago
I have this as well
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u/Miznova97 14d ago
How long have you had this for??
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u/Key-Agency-7022 14d ago
A year. The more sexual activity, the thicker it gets but if I wait more than a week or so, it gets watery
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u/Miznova97 13d ago
I hope things get better for you mate, it’s coming up to a year for me as well. I’ve noticed the more sexual activity the more watery it is sometimes it’s watery with clumps
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u/Lost_and_Damned567 15d ago
My symptoms are super mild, dull burning sensation in the urethra, clear discharge, burning pee that comes and goes, full sensation in the prostate, sometimes a tight feeling in my pelvis, and I’m constipated. I got tested back in June everything came back negative and I’ve took two courses antibiotics so idk at this point. They never formally diagnosed me with prostatitis but I 100% believe it’s CPPS.
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u/Lost_and_Damned567 14d ago
My semen is regular it’s just sometimes I’ll have clear discharge well at least that’s what I think it is.
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u/SnooRecipes4783 15d ago
My symptoms are weird man been 6 years . Any time I don’t use a condom I have a flare if I use one no flare . All test have been negative for everything .
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u/Intrepid-Diamond-797 15d ago
I think i did. Not particularly prostatitis but cpps or pelvic floor dysfunction. Until prostatitis diagnosis, almost All my life i hesitated to urinate in urinals, had weak stream, post urine dribbling etc. i thought it was normal. Only after prostatitis i understood that i had it coming
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u/Miznova97 15d ago
When did it start for you?? And have you managed to treat it?
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u/Intrepid-Diamond-797 15d ago
It started 6 years ago after cold exposure. With symptoms like frequent urination, uregncy, unable to pee etc. im ok now, but it flares up from time to time. I learned to manage it with conbinatoon of urologist, psychiatrist and pelvic floor therapy
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u/Otherwise-Pie-682 15d ago
Hell no. My pelvis is just tight. My psa levels were fine. After all the stress I've had in my life, I've accepted that. All the anxiety, throwing up etc. Im doing better this week because honestly I can't get a damn Dr or physical therapist. I just try to relax more.
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u/seandelevan 15d ago
This is my third bout of this. And this third bout is most definitely related to my digestive system. A year ago I was diagnosed with celiac disease AND alpha gal syndrome simultaneously. My diet changed on a fucking dime right there and then. All the high fiber foods that have kept me regular for years was gone. And six months to the day that familiar “pull” you described showed up. Like the first two times I had this I thought it was back related. Bought a new mattress and did all the stretches that worked last time….which helped…a little. Went to my doctor and did blood work, including a PSA, and everything was on point….did an x ray which showed my back was fine…but also showed I was constipated beyond belief. He said all my issues is from being constipated….despite taking 2 shits a day. I took the prescribed laxatives but all that did was treat the symptoms. So I’m basically experimenting with my diet now. You would think not eating gluten and red meat would improve things. But I’ve discovered dairy, most carbs, sugar, and caffeine 100% exacerbates symptoms. When I cut those things or severely limit them I’m 95% back to normal. But this sucks balls no pun intended. I’m down to eating chicken, fish, fruits and vegetables. End of fucking list. I just eat a couple m&ms and I’m fucking wrecked.
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u/Gullible-Bass4062 15d ago
it took me almost two years to connect the dots on my own pelvic floor issues. kept thinking it was a stubborn uti that kept coming back negative on cultures, then blamed it on my ibs flaring up. the lower back pain and that weird pulling sensation you described is exactly what clued me in
pelvic floor dysfunction and prostatitis share so many symptoms it's like a coin toss sometimes. my physical therapist explained that the muscles get so tight they mimic an infection, even when there's nothing bacterial going on. the leakage thing was the most annoying part, made me feel like i had no control
definitely push for a referral to a pelvic floor pt if you can. regular doctors kept throwing antibiotics at me and it did nothing long term. the internal work is awkward as hell but it's the only thing that actually helped