Prostatitis with zero pain, just horrible 24/7 urge to urinate/frequency

Posted , 85 users are following.

Hello All,

I am a healthy 25 year old male with no history of urinary issues.

I am at my wit's end. Last Sunday, I started having terrible urinary frequency. I will literally go to the bathroom, urinate, flush the toilet, and then have to use the restroom again RIGHT AWAY. In other words, I have constant urinary urges 24/7... It has been this way for one week.

I don't have any pain or discomfort in my pelvic area, and there is no burning sensation during urinating. However, I feel as if the urine is at the tip of my penis - that is where the urge sensation is most prevalent. If I hold it for a long time and it accumulates, there is quite a lot of urine. However, most of the time (especially in the middle of the night) hardly anything comes out even though it feels so urgent.

I can't sleep since it feels like I have to urinate constantly... last night I was going every 5 minutes, and most of the time only a few drops came out. I am having anxiety now because of this.

I went to the urologist last Tuesday (2 days in). Urinanalysis showed no UTI and bladder ultrasound was okay. However, during the rectal exam, he said my prostate was "off" and did a test of the urine that came out after the exam. At that point, I was told that I had a prostate infection and that the enlarged/inflamed prostate was causing the frequency. In other words, there was bacteria.

I was given 500 mg of Levaquin to take once a day for 30 days. However, it has not helped after 6 doses. I'm trying Motrin (ibuprofen) to no avail. I was told it takes a while for the antibiotic to reach the prostate. I have no fever, and no chills.

I am terrified that I have the chronic pelvic pain (CPP) form of prostatitis. However, I don't know if I do, since (1) there WERE bacteria present upon running the urine after the rectal exam and (2) I have ZERO PAIN. The only symptom is the 24/7 need to urinate. Any ideas on this? I hope I have the acute prostitiis form since this is cured with more antibiotics, but if I have the lifelong CPP form I don't know what to do... I feel like I will have to quit my job since I can't sleep with the need to urinate.

Please help!

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  • Posted

    I'm feeling the same as you, this has been going on for almost 2 weeks and it's driving me crazy. I went 3 days after the sensation started to the ER and they did an urine test and didn't find a bacteria or anything, they told me to just drink a lot of water. The feeing didn't go away so I went to a clinic and the doctor thought it was an UTI so he gave me "Sulfamethoxazole"  but it didn't work, I took it for like 4 days and the feeling was the same, so I did an urine culture and he didn't find any bacteria so he gave me "Doxycycline" I took it for 7 days and nothing changed,I still have the same feeling of having pee in the tip of my penis and it is so annoying, I pee and 30 seconds letter the urge comes back. I have already waste so much money. I have an appointment with an urologist in 3 days. does any one know any medicine to cure this.

  • Posted

    Hi guys, I felt I should share my story with you as it may help someone. I am a mother of a 16 years old boy who suffered from the same thing you are describing here. This is why I was following this discussion.

    For him it all started 2 years ago, one night after defecation, he felt a terrible pain in the perineum area, he managed to fall asleep but when he woke up next morning there was no pain, or burning, just a horrible 24/7 day urge to urinate, nothing else. We went to a couple of urologists, they performed all types of lab tests, have tried different antibiotic therapies, Ditropan to relax the bladder and urinary tract and several similar new drugs, nothing helped, he was then send to a psychologist but nothing was really effective....no one (even me) could not understand what is happening and how awful this is for him as there was nothing wrong in the results, I am a pharmacist and I was aware that some  small number of bacteria that was found sometimes (over those 3 months) could not give these type of sensation. But after about 3 months it calmed a little bit,  for him it became bearable, it was better during the day, worse during evenings and he had problems to fall asleep, but anyway much better than before.

    And then in February 2018, we moved to the UK a year before, and one Sunday (that was particularly relaxed family day) out of the blue, it all started again, and it was worse than ever, again no pain no burning nothing but a constant feeling that he needs to urinate. And the agony started, he spent the first 7 days in bed, refusing to communicate, we were seeing urologist, again the same drugs, antibiotics, ditropan and similar, with absolutely no effects, then they suggested the cystoscopy (awful thing for a teenager, but he agreed)..and again everything came clear, we were referred to the neurologist, MRI of the brain, spine, sampling spinal liquid,  everything came clear, and the whole time psychological support....on the other side we have tried acupuncture, Bowen therapy, restriction diet for interstitial cystitis, gluten free, dairy free diet, bioresonance, chiropractice, everything and no effects at all. He was not able to go to school and after 6 months of agony and not even one meaningful result or opinion, he started to lose his hope.And then in June we moved to Dublin, as I got a job here. I was still trying to find how to help him and I googled a physiotherapy clinic here in Dublin that is specialized in both male and female pelvic pain. After the initial consultation for the first time after 7 months I had a feeling that someone really knows what we are talking about, you could clearly see that they do have patients like that all the time. We were told that although those urinary symptoms are not specific, and they can be caused by various things, the fact that doctors could not identify anything pathological supports the notion that pelvic floor muscles are causing the problem. So we were told at the beginning that this is a long process and it can last for months, that in men you can reach and treat those muscles only internally (through the rectum) but before they start with the internal treatment, other muscles need to be treated too (abdominal gluteal and inner thigh muscles)  because if they are contracted and spastic they will not allow the pelvic floor muscles to relax (they are pooling the pelvic floor muscles as according to the newest theory there are no individual muscles they are all connected with something called fascia)... Anyway, he started his therapy, they have showed some stretches that he was doing 2 times a day and some breeding exercises, and he was seeing a therapist once a week for treating abdominal gluteal and inner thigh muscles, after 4 weeks they concluded that these external muscles are in better condition and that they can start with the internal treatment, again once a week, he was advised to continue with his stretches and breeding at home, he could include yoga if he wanted (and he was doing that) but to avoid anything that would put more pressure on those muscles (abdominal, gluteal and inner thigh) including running.  But after almost 6 weeks he could still not see any improvement, he was more elastic the abdominal, gluteal and inner thigh muscles were not so painful as at the beginning, but the urinary symptoms were still the same. However, the therapist was supportive, telling him that he needs to be patient as it does not work like that, it is not a gradual improvement, those inner, pelvic floor muscles will release the tension at one point and then the improvement will come almost instantly. But when that will happen is an individual thing. And we both trusted them. And it really happened like that, after about 7 weeks of therapy in total, and after 3rd internal treatment it just improved drastically, just like that, something happened inside and the relief came, the feeling is not gone totally, well he still feels it mostly after defecation, but since than it is going better and it has been 11 weeks now since the beginning. There is still a lot of work and it will last for couple of months we were told, but he is a different child now, he goes to school, he does not mention this at all, stretching became his routine, he goes to PT once a week but other than that he is just a normal happy teenager like he was 2 years ago. Well, this is just our story and even if the problem is with the pelvic floor it is probably individual, but I strongly suggest to consider this type of treatment. If this is a case, and I think that as a pharmacist I have the right to say this, there is no pill that will help, the only way to help yourself is with PT and most importantly with exercises and breading techniques at home.  I can also suggest a book that I was recommended at the clinic: Ending Male Pelvic Pain, A Man's Manual by Issa Herrera, it is a very good book. 

    And at the end my son was obsessed why this happened to him, as I was honestly, and I think no one could answer this, but I realize now that it is more important for him to understand that his body does react like this and that he needs to have an active approach and change his life style to prevent this to happen again, to exercise, do yoga (which is mostly stretching), to learn how to relax and I believe this is the way to live a normal life....and it is all part of healthy living anyway...

    At the end ...I wish you all the best...and I hope you will all  find the solution that will work... 

    • Posted

      hi, how are you doing...i think i have same problem...your message gives me hope..i have appointment with phiyotherpist after 2 month..i hope for best..

  • Posted

    Thanks for taking the time. 

    Would u mind telling who was your PT

  • Posted

    So to update on my current situation, I've been pretty much feeling normal for the past couple of days. Very little sensation, no real urgency issues to speak of unless bladder is full or fairly full, and I'm definitely not having much in the way of frequency, I maybe pee about 4-6 times a day. The way my bladder feels when it's full is a bit different than what I'm used to, but I'm thinking this is apart of the anxiety portion of this, or perhaps just a new normal, or pelvic issue or dysfunction that thankfully has drastically improved over the past week or two. I was on Cipro 500mg for 5 days, and even before then, my symptoms had lessened a bit. I'm hoping mine is an extremely temporary case and it clears up, but I do have weird inconsistent aches and pains in my groin area, some pain in the lower back, and around the thighs, and that weird rash (thrush or jock itch) resurfaced for a few days but I'm trying my best to battle it back. 

    I still get a slight sensation in the tip of my penis that makes me feel like I have to pee, like right now... but it's not nearly as horrible as it was from the start, and there's sort of a fluid sensation in the tubing, but it dissipates, and when I kegel, I feel nothing in there (usually), so I think it's just a matter of retraining my brain. I don't know if I stated this in earlier replies, but I've experienced this sensation before, and it made me a depressed mess when I first had it which was right after I had a testicle removed due to cancer. It eventually went away, but the first few days, or weeks, or however long I experienced it were tough. I thought my genitals were falling apart. It did recede or go away almost to the point of no issues, but I've had post-urination dribble since... which is apparently common, and referred to as the "shilling spot" when it leaks out. Just requires some extra shaking. I have a feeling it's linked to the scar left from surgery on my abdomen since everything down there works harmoniously.

    I've found that the sensation is the most apparent when I'm laying on my back, so I'm assuming this is some sort of impacted nerve or minor spinal injury maybe. If I sit up more, the sensation usually leaves. I don't have constant pain however, but I do feel some lower back pain from time to time as mentioned, and maybe on the front of the pelvis above the penis, but nothing constant, or super severe. I chalk it up to my posture mostly. I'm hoping I can eventually shake this sensation altogether, but if I had to give a percentage rate comparing normalcy to how I feel now, it's probably about 85-95%. Keep in mind, my only active treatment was the 5 days of Cipro, but given that there's no consistent pain in the pelvis, or blood in the urine or semen, I feel like this probably isn't the bacterial form of prostatitis if any form at all, so I doubt Cipro did much to help really. I have been walking a bit more at night, and I went to the gym yesterday... not going to train legs and glutes for a while to see how this works out, but I'm  hoping to feel normal in a few weeks. Keep praying for me, and I'll say some for you guys as well but hopefully this disappears completely. 

  • Posted

    Hi all,

    Just another update here. I'm still about 90% back to normal. It varies day to day. some days a little better and some worse. I feel like I'm almost there. I wrote a post earlier mentioning that It seemed to be going away fully however since my uro highly recommended PT for the pelvic floor I've decided to go to a specialist for that even though I'm feeling better. I figure if anything it will be preventative in the future. I never really did much PT work but I figure I might as well.  

  • Posted

    First off - to the poster who said something like "It is impossible to commicate to a doctor that I am feeling an itching / urge to go, but it is in the top of my penis... NOT in my bladder". This has never felt like simply an urge to go bathroom. I've seen it described on forums and google as "urine stuck in the tip of my penis" because the sensation is in the urethra, and not with a matching feeling in my bladder.

    I am 40 year old male, and I have had this on and off since I was young, but now with very increased frequency. When I was younger ( 16-30 or so ) I would have an episode maybe once or twice a year. I would usually notied it when trying to fall asleep, but I also remember it happening in the middle of the day. It was annoying, but I found early on that sitting on the toilet and just drinking glass after glass after glass of water would relieve my symptoms. It would usually take an hour or two, and I would just sit there and read a book.

    In my late 20s I spoke to my GP about it - he didn't run any tests, but suggested it was happening because the muscles were spasming, or fired "out of order" during an orgasm, or maybe something else - I don't remember it's been a while. But that reinforced my idea that drinking lots of water would either flush out, or retrain/relax my bladder muscles so would work properly again and quit sending "you are about to pee" signals to my brain.

    At 30, I started having erection/ejaculation problems, which lead to a round of doctor visits. This was most likely as a result of increasing my antidepressant, Effexor ( venlafaxine ). I had never had sexual issues on lower doses. I started having semen discharge sometimes when I had a bowel movement. I suspected this was due to not ejaculating as much ( went from masturbating daily, to maybe once a week ). I saw a urologist about this change, but he brushed me off, saying I was too young to have prostrate issues. It didn't occur to me to mention the peeing issue, for some reason. Just bringing it up, because I've wondered if there is a connection between my Effexor, and increased occurrence of this peeing urge problem.

    Over the last 10 years, the peeing itch has gotten more common, and less treatable - and lasts MUCH longer. I had this happen one time, and no amount of water relieved the symptoms. It lasted an entire weekend, most of which I spent on the toilet. At this point I started looking for ANY type of relief. Pyridium tablets, cranberry, etc did not help. Urine tests all came back negative. I received medicine for overactive bladder Tolterodine. The first time I took this, it worked like a miracle. I was so happy! However the second time I tried using ( months later ) it did not relieve the symptoms.

    I saw a urologist 5 years ago, and we found that I had several symptoms of prostatitis. I had weak urine stream. The doctor said I had "urgency", even though I tried to explain it isn't urgency like I have to rush to the bathroom. I guess technically it is "frequency", but its not that I have to empty my bladder 10 times day - it is that it feels constantly need to pee to relieve the itching. It feels more like I have already started peeing or something. It's in my penis, not in my bladder. He gave me the usual "don't drink caffeine, no spicy foods, lose weight" and put me on Filofax. I did not change my habits, and quickly found that the Flomax was very uncomfortable when I ejaculated. So I stopped using it.

    I was fine for several months, and after that my episodes were relatively short - so I didn't bother seeing a doctor about it. I felt that I was not really being listened to, and just rubber stamped with a BPH diagnosis, even though my prostate has never appeared swollen or enlarged.

    So I'm going to try the flomax again I guess. The frustrating part is the flomax could be doing nothing, and my episodes are so far apart it is hard to tell if something specific is working. I have been having this for a week now though, so I gotta do something.

    I suspect that I've always had some underlying physical condition, which is why I was affected early on in life. And now that I'm getting older the relentless growth of the prostrate ( BPH ) is making it worse.

    If you want to search more on this issue, try "pee stuck in tip of penis". lots of other people with these symptoms.

    • Posted

      As we age, our prostate increases in size, so you are right around the brackets where the prostate does have the most growth. It does eventually stop growing, but if all things kinda come back clear, I have to assume you might be experiencing some form of pelvic floor dysfunction. However, getting your prostate fluid checked out might be beneficial to rule out some sort of long-term infection. Don't forget, however, that chronic non-bacterial prostatitis is commonly misdiagnosed, and is usually pelvic floor dysfunction. PT seems to help others, so you might want to look into a PT who specializes in pelvic floor. Prostatitis does not improve on its own though, unless it's non-bacterial, and BPH doesn't decreases or go away either. Any other form of urinary issues aside from bladder/kidney stones typically are not chronic, or if they are, do not decrease in symptoms, or improve on their own. 

    • Posted

      "chronic non-bacterial prostatitis is commonly misdiagnosed, and is usually pelvic floor dysfunction"

      That is interesting - where do you get that information from? Most of the time when I run across pelvic floor information or sites, they seem to be shilling for themselves, an "Alternative" treatment or a book like "headache in the pelvis." I've also noticed almost all of these speak about Pelvic pain, which I have never experienced. 

      I do kegels, but honestly, I tend to forget once I haven't had an episode for a while. I'm definitely open to an alternative solution - I'm just a bit skeptical.

      "However, getting your prostate fluid checked out might be beneficial to rule out some sort of long-term infection."

      I think I am going to do this with a new doctor. I disliked my last one - he charged me for wasted tests ( eg: charged for a urine analysis when I was unable to pee, did an ultrasound to check for voiding, even though I told him I had not urinated beforehand - and wanted my Wife to come into our meetings for some reason? ). I hate having to be my own advocate.

      What relief have you found for your own symptoms?

      Do you know of people who have cured this problem with PT? I'm definitely open to

    • Posted

      edit: Sorry - I see that you have provided recent updates - I'll reread those smile

    • Posted

      While I'm also in the boat of "homeopathic is trash" there is some basis to pelvic floor disorder. When the prostate is no swollen, or inflamed, it's not exactly a resulting issue from the prostate. You're looking at overly tense muscle structures in the pelvis, and while I never had any issues in pelvic pain, there are tons of lads in this thread who have gone to PT to alleviate their issues with great success. For me, it's hard to speculate, or persuade as I'm not a personal reference for it, but my urologist has confirmed to me that non-bac prostatitis is normally misdiagnosed, and the only time he's seen the prostate inflamed without any trace of bacteria is because the patient had several cases of bacterial prostatitis before due to an abscess in the prostate after a cyst... or tumor was removed? 

      Relief for me came naturally. I was literally sitting around trying to find out why a 15 year old node on the side of my penis hurt suddenly, when I got a massive urge to urinate and couldn't get off the toilet for an hour. Weak stream, fluid feeling in urethra, pressure on bladder. I thought it was a UTI. It stayed pretty constant like that for about a week, on ceasing during sleep, and when I first woke up. After that, it came right back. I took Cipro for 5 days at 500mg for it even though symptoms had improved already, and it got a bit better even still, but at this point, I'm almost 100% back to normal, without issues. Occasionally symptoms do return, but only for a short period usually, and I don't ever have a weak stream when the urge to urinate presents itself. I have been drinking a lot of water though. I've also been taking saw palmetto too, as someone suggested it would help. My only real complaint is a bad case of jock itch I have still that got worse after the antibiotics. Trying to kick that has been a true pain in the ass, literally. 

      As stated though, check out this entire thread. Many found relief through pelvic floor stretches and relaxation, but the one thing they tell you is to quit the kegels, and rest the pelvis. Change your typical desk chair, get more movement, lay off heavy lower body workouts, etc. Obviously it's hard to say what everyone has here... literally every damn issue in the lower half of the body presents itself as urgency to urinate. Even if you accidentally get hot sauce on your balls, you'll notice you have an urgency to urinate as your muscles and nerves tense up in the crotch, testicles, and pelvis and this results in that sensation to "cleanse". 

    • Posted

      Thanks - I'll dig through the thread again. I come here every few months when I have an episode, and keep meaning to post something, but never do. It's nice to talk about this stuff. Appreciate your quick responses.

      Ill look into the PT angle. Even if that isn't "the cause" it would still be good for my body. And if it IS, then it would be awesome know.

      I have a female friend who has something very similar - constant irritation / urge to pee, and she spent thousands of dollars and has tried everything from anti-biotics to pelvic floor work to using bio-feedback with electrodes on her pelvic floor. She has basically given up and "learned to live with it". It makes me sad that medical science has progressed so far, but so many things still are a guessing game.

    • Posted

      Did she come across a diagnosis? She could have IC which affects women far more than men. Similar symptoms, only it normally has bladder pain too, but not always. 
    • Posted

      I don't know - she never mentioned a specific diagnosis, just that they never found a way to address it, so she just learned to live with it. I've looked up IC a bit ( it's inevitable to read about when looking up my own problems... that fear that its permanent and un treatable ). She doesn't experience pain per se, but does experience the constant "itch" at her urethra and frequent trips to the bathroom. She has a complicated medical history - transplant recipient, multiple surgeries - and she's on all kinds of odd meds - like daily anti-biotics and stuff. I think when things get that complicated, it becomes even hard to narrow down a possible cause.

      I've encouraged her to start seeing a doctor again, since I know medicine has progressed in the 10 years since she sought treatment. I feel bad - when we first started hanging out, and realized we had similar symptoms - I basically locked her in the bathroom until she had drunk gallons of water. That worked for me, and I was convinced it would work for her too smile This was back when "drink water till it goes away" still worked for me. I was so bummed that it didn't help her.

      I'll ask her about her diagnosis next time I get the chance.

       

  • Posted

    yes. many of the above symptoms i have... every night every hour im up to p**s like 5 drops. but it feels like i really have to go. way worse if i eat lots (i guess less room down there if large intenstine full). the pain comes and goes- this started 2 years ago when i moved to nyc. it started with some pain here and there. then progressed to dribble after peeing. now finally the increased frquency is destroying my quality of life. i have way less energy and am getting sick easily because of the chronic sleep loss, which means even less energy. trying to make it in music in nyc is incredibly stressful- so maybe that contributed, is contributing- but I'm not giving up my dream because of this B*******. no way.

    so far i have tried abstaining from masturbation (a week), which seems to help. so i'm gonna try to keep going. i switched to vegan for a week also seemed to help but i'm thinking it may just have been that i was eating less so there was less in the intestines prrssing up against prostate and bladder, bc i ate a lot more of the same stuff and it's as bad as always.

    it all just seems to be getting worse at a terrifying rate, no matter what i try. i'm seeing urplogist tuesday...but am skeptical. there are so many possible causes and treatments...tons on this thread. gonna try some and see what works.

    • Posted

      Urologist is a must. Two years without ceasing or decreasing symptoms is definitely worth seeking answers from a medical professional. Don't stop till you get some. Give us a shout here after your appointment, so we can see what your doc thinks. 

    • Posted

      so. doc checked me out- said my prostate is "bogged down," "spongy", i said, "swollen?" he said no "spongy, like, infected." i gave urine sample. gonna call for lab results but i know bacteria easily evade this method of detection. he prescribed antibiotics. i want to wait to see if bacteria problem before taking. but might just do it. my quality of life is horrifically down because of this. the chronic sleep loss jjst keeps piling up, shortening my temper by the day, watching my willpower go down, and chronic splitting headaches are now common. i had so, so much joy. and now, i'm telling myself, don't worry, you'll die some day. i have to believe this can be fixed.

    • Posted

      The headaches, and mood, depression... all due to the stress and lack of sleep. Get the antibiotics asap, and start on them. You'll need to source a decent probiotic as well to take along with it, so your gut doesn't plug up. Getting a confirmation on a diagnosis is a good thing though. Getting steps towards any diagnosis and subsequent treatment is. I'm just hoping your doc is smart enough to determine a plan of attack for this in particular. He should've taken a sample of seminal fluid from the prostate as well so they can test/culture that. If not, call his office BEFORE taking antibiotics and have them collect a sample from you. Otherwise they can't treat the bacteria if they don't know what kind... then you end up being stuck on antibiotics for months, taking crap shots in the dark. If they don't test the prostate fluid, they won't understand what bacteria is currently in it, causing problems. Urine cultures rarely produce prostate infection bacteria. 

      I still can't believe you lasted 2 years like this. I would've gone insane, personally. 

    • Posted

      24. and 2 years it started and got gradually worse. it didn't start ruining my life till a couple months ago-

      and no. he didn't take prostatic fluid and frankly i don't think he's up to this challenge. i guess just call around asking before appt if the doc will do that? then go from there... i dont want to blast my gut with antibiotics with no certainty of bacteria let alone the strain

    • Posted

      If he's unwilling or unable, new doc. Urine cultures aren't going to give you a solid answer to your prostate bacterial infection if that's what is going on. At 24, you're kinda young to have prostate issues, but guys sometimes have a genetic pre-disposition to it. Get a second opinion. Keep us posted, buddy. We'll try to help as best we can. 

    • Posted

      hey again. so, there was bacteria in the urine sample, turns out. not sure what this means. doc has me on levofloxacine, 2 weeks. we'll see what happens...

    • Posted

      You might do better on Cipro, but see how you feel in the 2 weeks. 
    • Posted

      Hey Ryan-

      So here is update. Levofloxacin (levaquin) worked ALMOST PERFECTLY. frequency was ANAHILATED. i could finally.sleep.

      BUT. once 2 weeks up- As SOON as stopped the levoflox- it came back, FULLY, maybe even worse. My original.doc says wont do any more levoflox, is a pussy, afraid of side effects (i had NONE)- i have researched and seen 28 days is usual course on levo for prostatitis, so WTF. this guy is incompetent moron.

      he says wait 2 weeks see if it clears up. then if not switch to BACTRIM (less side effects).

      IMPORTANT... apparently i had a urinary tract infection, showed up in urine sample, bacteria. which is why he said levoflox. they say very odd for man to get that. Today had ultrasound of kidneys bladder and prostate.

      I saw a new doc. Seems better. had me drop off a semen sample.for prostate fluid at lab today. doesnt want to do levofloxacin before getting more info even tho i told him it worked. he also said UTI, bizzare. and odd that levaquin worked.

      i plan to take the ulttasound results from the s****y guy to this new seemingly smarter more capable one.

      THIS guy did rectal exam and said "YOUR PROSTATE IS FINE- idk what the other guy was talking about. you can't FEEL an infected prostate."

      SO-

      clearly...it is bacterial. if levoflox worked like a CHARM, it thusly must be.

      if this guy right- prostate ok (im young, makes sense), then??

      a bacterial infection in bladder?

      in urethra?

      a central nervous deregulation, causing incorrect overactive bladder signals? (levoflox.i read has some kind of effect on the nervous system)

      i aim to study levaquin and WHAT it does and TO what...and piece together the puzzle.

      BUT. my thought- levaquin worked. why not BLAST the motherfu**er for a full 28 day course....???

      additional.info-

      • glutten makes frequency worse. makes gut feel bloated and seems to put preasure on bladder (on levoflox it was fine. everything felt pretty much normal

        eating more in general makes frequency WAY worse.

      • masturbation seems to make it worse and cause what seems to be a "urethral" pain, sharp pain.

      Awaiting ultrasound results, and the semen culture result. HOPEFULLY this new guy knows WTF to do.

      THANKS FOR YOUR HELP...!!

      Best,

      • Nick
    • Posted

      As long as bacteria is present, I don't think this is a nervous system issue. Antibiotics normally work against the bacteria's ability to thrive, so that your immune system can kill it on its own, so the levo was just meant to give your immune system a boost.

      Your old doc is right though, you gotta be careful on floxacins, they can cause permanent damage if taken for too long, or your body is sensitive to them. They ruined my thyroid for sure. I'm glad the new doc seems proactive, but have you thought about possibly getting scoped for interstitial cystitis? Is it just urgency for you or do you have pain anywhere else?

    • Posted

      hey man-

      um- there is some mild intermittent pain in the urethral area...like a sting sometimes, not bad nor often.

      and- so youre saying a cystoscopy? the first doc said we should do that...

      it actually does seem like it might be getting a bit better, immune system may be working.

      thanks...

      -Nick

    • Posted

      Yup cystoscopy would be the best way to rule out IC. IC normally only affects women... why? I don't know. Could be something to do with chronic UTIs but basically the bladder wall is constantly inflamed and causes discomfort, pain, frequency urges, and chronic UTIs. Men can be diagnosed with it, but I feel your pain. I have some sort of Sciatic nerve pain in my back right above my buttocks on the right side. It causes spasms and pain all along the pelvic sling, but more notably under my inguinial scar which feels like a mild bladder spasm. It's getting a little better, but my first symptom was a dull ache in the penis head, which dulled and went away, and moved to urine frequency and pressure, and then onto the back pain. I was on bed rest for a month with mono 2-3 months ago, so I'm assuming I screwed something up in my pelvis while laying on a crappy bed for so long. It's slowly going away, and not nearly as severe as it was. In your case, since bacteria was found, that's the obvious line of treatment for you. It might have progressed into cystitis by now which is a bladder infection and those can be tough to treat.

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