Blotchy red rash/irritated skin on penile head (lasted for over 3 moths now)?

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Part of the skin on the head of my penis has become slightly red and is causing some pain/irritation.

It first appeared the day after I used a condom so I think I must have had a reaction to the latex or some other substance in the condom.

The tip of the penis became super sensitive and noticeably hurt whenever it touched my underwear.

The skin was and still is noticeably red close to and directly around the meatus. This redness gets worse and bigger after I've come out the shower or masturbated.

An hour or so after ejaculation, I get a slight burn/irritation at the very end of the urethra when I urinate and this can last for a few days before subsiding. This has put me off from masturbating as much now.

This has lasted for about 3 months now with no signs of improvement.

I saw a doctor and was prescribed timodine/hydrocortisone cream and this didn't have much effect and am slightly worried it may just make things worse so have stopped using it for now.

It almost seems as if the redness comes from within the skin rather than on the surface.

I don't think its balanitis as I haven't had that for over 12 years when I was a kid and that was with the usual smegma discharge etc, whereas this is just redness. 

I've attached images to show how it looks straight after showering, which is when the redness is at its worst and the contrast between the normal skin colour and the redness can be clearly seen.

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  • Posted

    I also tend to think that it's virus related nerve irritation. I'm not familiar with HPV symptoms so I lean to Herpes family viruses since they usually cause nerve irritation, CMV, EBV, VZV, HSV.

    Have you guys tried any antiviral meds?

    • Posted

      This may sound strange but since I’ve had this issue I’ve been talking lecsipro for two months and now have tingling in my feet and hands,any one else?
    • Posted

      Hey mate is lecsipro an anti depressant? I have take a lot of Valium myself and do wonder sometimes the effect it had had on me. I also have noticeable tingling in my hands, not all the time but definitely seems unusual.
    • Posted

      I'm unfamiliar with that drug. I've taken metranizodol (sp) and had a similar response and was told to come off it immediately to avoid any complications. Have a look at the packaging insert and ensure it's not a side-effect that requires ceasing taking the drug.

    • Posted

       I just hope it’s from the drug and not this penis thing 
  • Posted

    Hi everyone, I have the exact same redness as the pictures of Jason, only difference is I have two what I call nods/lips on my meatus on both the left and right sides. I have had this for two and a half years now and have been to my GP, two Urologist’s and a Infectious decease doctor. My problem started with unprotected sex and oral sex with a girl, 3 days after first encounter I went to go to toilet and pipe was a little blocked before urine came out, didn’t think much of it as there was no pain or anything. 3 days later while having sex with same girl when ejaculating I had this pain which was that bad I pretty much pushed her off me. From that point on I had what I can only describe as a little creature crawling up and down and scratching at my Ureathra and I had these little nods/ lips starting to protrude from my meatus. So after seeing my GP and having all the tests which were all negative and trying all the creams and different antibiotics he sent me to a Urologist, he put me on Cyprofluxcin for 8 weeks, after the first week that little creature itching at my Ureathra was gone (thank f*ck) but the pinching pain and nods/ lips still stayed, he dicided to go in and have a look with the old camera up the front and backside to which everything was fine, no prostititus and prostate fine, his final answer was there’s a problem which I can’t detect (fair dinkum Einstein) so there’s nothing more I can do if the pain is still there in a couple of months I will send you to a pain specialist lol, at this point it had been 4 months from initial first sexual encounter. Went and seen another urologist this time this urologist was older (50-60) first urologist was in his 30’s and did not really thinks outside the box, this one however does. We tried everything all the bacterial antibiotics and so on, he then sent me to infectious decease doctor who again did all the tests blood, urine, swabs you name it Iv had it and talked to a sexual decease doctor and came up with this- I had some type of infection which is gone but I have been left with damage to which I disagreed with, this is now 15 months. I went back to Urologist and we discussed what had been done and I said the only antibiotic I haven’t tried is flamclovir/famvir and I want to try it, now this is where it gets really interesting, he put me on 2/ 250mg tabs a day just to see, ok after a week of taking this medication all of the pinching pain had gone, the only time I got this pain was after urinating and ejaculation which only lasted 5-10 minutes at the most but the redness and nods/lips were still there. Ok now I am on 2/500mg tabs a day of famclovir and the pain has all gone but again the nods/lips are still there as is the redness. At this stage now it has been 2 and a half years and I am waiting to go and see a different infectious decease doctor as this is the only medication (since first taking cypro) that has had any type of reaction. In a way it is very pleasing as now I have something to work with, I’m definitely thinking now after this new finding that it is only two things for me, one is that it’s obviously some type of herpes or a superbug bacteria that is resisting all of the existing antibiotics that are out there, I’m also going to ask for another microplasma genitalium  test which my previous test was negative but as I have just learned as of last week that here in Australia they have just come up with a brand new way to test microplasma genitalium which can exactly identify the type of bacteria you have and then doctors can give you the right antibiotic to rid the bacteria, with this new test it will definitely rule out Bacteria which will leave me with working in the herpes side of things. Just some advice on going to doctors and specialists is that I personally found if you can try and find an older and more experienced  doctor, they seem to think outside the box more where as I found the younger ones just do there A+B=C and if there’s no answer we’ll that’s it( not saying all young doctors are the same) just my personal opinion. Another thing is try everything it’s a headache and takes time but you have to rule out things one by one and again try everything as in my case I had been told not to worry about famclovir because I’m negative for herpes 1 and 2 but as I found out this is the only drug that is doing something which as I said before now gives us something to work off. I’m sorry for the long story but I feel telling you men everything it might help. I will post more once I have been to new infectious disease doctor. Cheers and good luck to you all, I know this has ruined my life for two and a half years now so let’s hope we can come up with a cure if not a cure at least something that can give us our normal everyday life back.
    • Posted

      Your findings are very interesting. 

      ?You mention that you're negative for HSV1/HSV2 but have you been tested for CMV or EBV? Or maybe you recall fatigue and fever like symptoms after your exposure?

      ?Also have you done prostate fluid culture for bacteria?

    • Posted

      Hey mate yes this new finding is very interesting it has even stumped my GP and my Urologist. I have been tested for CMV and EBV in the beginning and also when first urologist went in and did the camera work he massaged the prostate and then tested the secreation, all come back negative. Initially he seemed to think it was prostititus but ruled this out with also testing my sperm for any  culture of bacteria and also there was no sign of enlarged prostate either. I myself have always said that it is some type of bacteria not herpes and I still think this but the finding from taking the famiclovir has me stumped now as this has only just happened, I only started with the famiclovir at the beginning of November so until I go and see the new infectious disease doctor which I can’t wait for I will just have to be patient AGAIN. I will be asking for all the tests again plus the new microplasma genitalium test as well as those old tests were done at the beginning back in July 2015 when I first got this. I am waiting to see a really well known and a very experienced infectious disease specialist which is a sexual decease specialist and also is a specialist in overseas deceases, spoke to the nurse that makes the appointments this morning and she said I can’t get an appointment until beginning of April but after she received my referral and all my information she is going to try and speak to doctor and see if she can get me in earlier as it even has her curious lol, so waiting for them to ring me back. Once I have been to this specialist  I will post. Stay strong 
    • Posted

      Yes I have also read about Adeno virus relation to urethritis, this was very interesting for me as of my condition with my meatus but like you said not to sure if it would last for this long. But again it is one thing I will be asking about as I agree it has to be ruled out. I am booked in to see infectious disease specialist at the end of March, can’t wait.
    • Posted

      hey again,

      ?forgot my password so had to create another account.

      ?anyway just found some interesting stuff - first time ever I saw some doctor to confirm that virus may cause urethritis. my real life experience is that everyone denies any possibility of virus being responsible. https://www.medhelp.org/posts/STDs/Urethritis-Diagnosis-3-weeks-after-receiving-oral-sex--antibiotics/show/449267[/b]

      ?you might try contacting him about your interesting case.

      ?by the way I tried Valtrex for a week - haven't noticed any relief so I stopped to avoid possible side effects.

    • Posted

      Hey mate yes we all do that lol, my Urologist did say at one stage that it could be a viral infection which he said if it is there is really nothing to take for it, i know there’s nothing wrong inside as my Urologist checked for any think unusual and found nothing, all ok inside. His situation was interesting as well with having oral sex and then having the itchyness which is what my first real symtom was but I never had the runs or any flu toe symptoms, I will try and contact him for sure. For me I definitely know I contracted something but what I do not know, and it’s why for me as I said I really think some type of bacteria infection, I’m just gonna wait until I see infectious decease Doc now as this new information with the famiclovir should give them something to work with, whether it’s just something in the antibiotic that is for some reason reacting and killing the pain or it is a type of herpes well we will find out, but my Urologist did say that he couldn’t explain why but also said it doesn’t mean I have herpes either as I have tested negative for both 1&2. Yes I have tried all creams and even natural oils but they only inflame the meatus even more so Iv given up on using anything topical. Good luck and stay strong 

    • Posted

      Hi San,

      You mentioned in your post that the  Cyprofluxcin took your irritation away. Just curious did the tip of your penis irritated you when rubbing against your boxers? or was it something different? and did the cyprofluxcin clear the irritation? 

    • Posted

      Hey Sego, sorry to hear about your problem. The Cyprofluxin got rid of the crazy pain in my Ureathra (that’s the little creature scratching at my Ureathra I mentioned in my first thread), but no it didn’t fix the iratation of my meatus or gland(head). First thing you need to do is stop wearing boxers when at work, exercising or doing anything like that, where undies, keep him packed in there nice and snug so it doesn’t flip flop around, this is what I found helped me, didn’t remove iratation but it helped. Now I’m waiting to see infectious disease specialist at the moment because  if you read my last thread you’ll see that I have just found out in the last 5 months that flamclovir removed that iratation, stinging, pinching pain to the meatus/gland up to 95% of the time now. It does come back at stages but no where near what I had, it’s the first time since taking the cyprofluxin that any antibiotic has worked and it’s the first time in 2 and a half years that my penis has felt how it used to feel, like it’s not there lol. I would try Flamclovir and see what it does for you as I haven’t heard of this helping anyone else with our type of problem and the feedback would be truly helpful to us all.  I take 2 x 500mg tabs a day of flamclovir, oh and also remember just because you get a reaction to this drug doesn’t mean you have herpes, I test negative to both HSV 1&2. Good luck with your problem and please let me know if it has worked for you because as I said any feedback will help everyone with this crazy and messed up thing we all have. Stay strong 

    • Posted

      Hey mate,

      ​have you already visited that famous disease doc? any news about your situation?

    • Posted

      Hey mate

      Sorry for the late reply been flat out. Yes did go and see specialist last Friday, as this is the first visit to him he has sent me for all the normal tests all over again but is doing some extras. We chatted about the whole story from start to finish and some, as you only have a limited time with first visit he obviously has made no diagnosis at this stage pending results. He wants to work through things one by one and go from there (obvious being new to this doctor) he did mention at one stage that with my story and condition that it was a chance that it was a bacteria infection and that it has damaged the nerve endings in gland. I did ask why the famiclovir got rid of the pain when I test negative to Herpes and he really had no answer for this other then we will talk more on that next time, he has put me on APO-Valaciclovir 500mg once a day until I go back at the beginning of May, I personally think this is a waste of time as I don’t have Herpes and have no real pain anymore other then a little stinging pain after ejaculation which goes within a minute anyway, I will take it for a couple of weeks and see but I will stop if nothing happens and I’ll just wait for all results and see what he comes up with next. My condition as of today is 95% better then 2-3 months ago and I really only have the two little nods on my meatus and a bit of redness at times so I am leaning towards nerve damage now as it seems to slowly and I mean slowly getting better month by month, also started taking probiotics and working out and swimming again, also been meditating which to be honest is working wonders with everything even the anxiety as well (didn’t really think this would do anything) but has, really mate just trying to live a normal life again. Will let you know results and an update once iv been back to see him. How’s your situation going? Stay strong 👍

    • Posted

      Thanks for your update.

      It’s great to keep us all in the loop. I think most on the forum are struggling to work out what has happened and what to do.

      With us all in the same boat and trying a variety of treatments we will eventually find the thing that makes the difference.

      Hang in there - it’s only a matter of time for us all!

    • Posted

      I'm quite ok. The pain hasn't gone but its milder. Still haven't found the cause which sometimes drives me nuts smile At one point I have convinced my self that its lyme disease, but ruled it out. There is huge community in US for lyme disease and if you believe everything they write in forums, lyme can be the cause of any mysterious illness even if your blood test is negative.

      ?Anyway my latest obsession is tuberculosis which usually affects lungs but also can be found in other organs. I guess I'm going to do a blood test to rule this one out also.

    • Posted

      Ok that’s good to hear, yes it’s the worst thing when you can’t work out what the cause is so we can fix it (Very frustrating). For the first 18 months I was checking out all the forums and trying to figure out what it was but then realised that this was not a good thing for my mental health but hey when something like this affects our lives like this does it’s just a natural thing that you would do, especially when the medical community can’t work it out as well. I decided to take a break for a while but of course it got the better of me and I started to check them out again (obviously again due to doctors not being able to fix it), but it ended up getting me down again, that’s when I found this forum and decided to just stick to this one and no others, one of the best things I did for my mental state. Anyway stay strong and best of luck to you and everyone else on here and will keep the updates coming when more is known. 👍

    • Posted

      Hey yes I hope everyone keeps updating their findings, stories on here as I know it can help us all, best of luck with your situation and stay strong 👍

    • Posted

      Oh just want to add it’s now going on three years for me and when I first started reading these forums certain men would say that they had what we all describe, some symptoms different and some different reasons how it started that “it eventually goes away after a few years, live healthy build your immune system up and also stop looking at it and get your head right and in time all will be fine”. At the time I didn’t believe obviously, at this stage it was only a month in so I was all over the place, what I’m thinking now is that I’m at that stage and again with my story I’m heading towards nerve damage from a bacteria infection, Im thinking maybe this is what it is NERVE DAMAGE at the end of the day for everyone whether it caused from unprotected sex, oral sex, masturbating to much, creams, soaps, penis pumps, skin infection, I could go on but with all the reading and research I have done and the doctors responses i have listened too it seemingly points to damage to our gland one way or the other. I think mentally we don’t want to except that this is damage and that maybe just maybe it will never go away and we all keep asking that question “WHY and HOW we can fix it” instead of accepting that its there and moving on. Once you accept and you start to live healthy again in mind body and soul, only then will it start to heal and clear, not saying this is easy to accept and is for everyone but for me I was the one who had unprotected sex with a girl I didn’t know and am the one to blame, I have now accepted  it and have moved on and with that and other positive things I can see improvement. Again please if this does happen to you obviously you have to go through all the motions which I must admit takes a long time but after a certain amount of time I think you have to just ACCEPT it and move on what ever the look is or the pain. Sorry for the long stories but I think much information for us all on this forum will be beneficial whether you believe or not, stay strong everyone and will update my specialist results once I get them. 👍

    • Posted

      Did you ever take the advanced mycroplasma test you spoke of?
    • Posted

      Yes it was done last week waiting for results on all plus that one, will update once iv been back to specialist at the beginning of May 
    • Posted

      hey San,

      it's been a while. Any news? Have you gotten better?

      I still haven't found the cause, very frustrating ... ruled out tuberculosis. now leaning back to some HVP strain which would be logical explanation even without visible warts.

    • Posted

      Hey aubag25

      It has been a while, ok my update at this stage is I have been back to Infectious Desease specialist and as for all test results they all came back negative even advanced microplasma genitalium was negative, iv now had all tests multiple times over and have had everything that can be tested come back negative and to date it has been 3 and a half years since initial contact, the final conclusion for my problem is, it was a bacteria infection that I got from unprotected sex, this is why the Cyprofluxin killed that creature like feeling I mentioned in first post, but bacteria is a bad bugger and it has left me with damage to my gland/head and to be honest I think internally as well thus why the severe pain remained. At the final consult with IDS there was also a Sexual health Specialist who said she had seen this before in 3 other males who had received bacterial infections from unprotected sex and were left with severe damage to the head of the penis and that it does heel but can take a long time, there advice was to eat healthy, excercise cut stress down all the normal things they say lol. At this stage I’m at 95% heeled at the 3 and a half year mark, in the last 9 months I had already started to change my diet and eat healthy, started to exercise and also got into yoga and meditation which has done wonders, also at the beginning I did a body detox got on the probiotics really did a good flush and started new, best thing I ever did. I still do get the occasional bit of pain in the tip( meatus) but it is only after I wee lasts about a minute and also when I ejaculate lasts about an hour or so, But this does not happen all the time. Iv found now for me knowing I’m clean and moving on from this and giving the body a good detox/cleanse, eating the right foods exercising basically just getting the body back to good health it has done wonders. I still drink alcohol coffee and have a bit of bad stuff here and there but I keep it to a minimum as I said you still have to enjoy life. I definitely would say that if you have had this problem now for more then 12 months and you have had all the tests possible and you still have pain then I think you could put it down to damage whether it’s nerve damage and skin damage the gland is a sensitive thing that once hurt, damaged it can take a long time to heel if ever, hey we use it to release our waste so if the pipe is damaged your gonna know about it lol. Iv read a couple of others on here who have sort of done the same thing in getting there bodies right and have improved their conditions so again I think this is the main issue for everyone once all other possibilities are tested and ticked off the list, I did mention nerve damage in my last couple of posts as a possibility and have read on other forums that this is the main reason for everlasting pain and conditions in the Ureathra, as for me I am now 100% sure that it’s  bacterial damage that is slowly repairing itself and will one day get back to normal, I hope this helps you and others out there, good luck and stay strong everyone. 

    • Posted

      Hey San13220,

      I think you are right . This needs time to heal. As the urine keeps on irritating it. O noticed when I drink less water and pee less often the irritation levels have minized. I would like to get into the healthy eating pattern too. I can certainly say it has to do with diet since as soon as I eat JUNK FOOD my stomach reacts and the bacteria I had was a nasty one which only got cured from clintamicin ABX.

    • Posted

       Good for you, glad things are going in a positive direction...

       I'm about 7 months into a BAD bacterial infection (most likely lyme, myco or some other bacteria)....and I feel like things are going in a positive direction, feels like the backside of the infection after the climax.......lot's of symptoms subsided or minimized..THANK GOD....but still more time needed....if you have lyme (borrelia burgdorferi), they specifically like nerves, lymph system and collagen.....that fact explained so much about  my symptom picture..

      Anyone with this sort of infection, these bugs are TOUGH to beat and do cause damage while the infection is going on, some cases worse than others...but the body can rebound and heal in incredible ways, so don't think what you're going through is going to be permanent.

      You need to throw EVERYTHING you can at this, good eating, research all the supplements to fight bacterial infections/parasites....put anything stressful off for now and rest....do a few rounds of Abx, that's very important. Try Bactrim DS (this is a go to for skin infections, try to get the longest course possible) try doxycycline, minocycline, amoxicillin etc. etc. there are many but bactrim is pretty standard for anything skin related...

      Bactrim DS really did the trick for me, brought me from a plateau of 75%(couldn't get past it) to like 95%, brought the bacterial load down and gave my body the fighting chance I think.. recently, I've been experimenting with ivermectin horse paste and albendazole, these are very common, world renown de-wormers, people use them for scabies and other mite like parasites also....they're very safe, ivermectin has been well researched... even without this bacterial infection issue, de-worming is a smart thing to do and should be a habit to do atleast once a year.... as mentioned above, I know the majority of my symptoms are bacterial related but I tried to cover all the bases, cause who really knows....could even throw some protocols for fungal infections in there also....bottom line, gotta reduce the load, make your body an inhospitable host, rebuild the immune system and DETOX... #1 easy thing for detox is standardized milk thistle capsules (1200mg) take every night before you go to bed. Drink fresh lemon water through out the day. If you have lyme, red root powder or extract helps with lymph drainage... since I started posted on here this spring, I've put about 6 months of research into all things infection related...STD's, Lyme/Morgellons and parasites..... pretty much the only positive I can about this experience is that it's changed my life in terms of knowledge, awareness and preparedness.... 

      By the way, you mentioned you've tested negative for most of the common bacteria....well, the only reason why I think my case is lyme is because I expressed as Morgellons at the infective peak (98% of people showing Morgellons are positive for lyme bacteria, borrelia burgdorferi, still unknow if it's the cause tho) without those clues, I still would probably be treating this a fungal infection.... but again, nothing says this isn't a combo bacteria/fungal so I hit it with everything and it seems to be working @ 7 months into this...

      PS... to get tested for lyme disease if VERY tough, they don't stay in the blood, they hide in tissue so getting a sample can be tough. One thing I learned from my research is that lyme disease and testing for it is surrounded by HUGE controversy in the medical community and people are suffering because of it, it's a deep rabit hole.. you need to choose your words carefully if mentioning it to a standard doctor.....best to see someone who is better researched in it...

      Also, I've read 5 herbal books from a world renoun herbalist Stephen Buhner, the guy is basically the God of herbs and there was a quote that struck me, basically the fact is there are millions of bacterial strains that still have not been discovered, we've only figured out and studied a handfull so far in the past 100 years....so who knows what's out there.... as you guys are all finding out, unfortunately, getting a mysterious infection is not a simple quick trip to the doctor for that one magic pill... it takes time to figure things out and that's why so many are coming back with negative test results, they only test for like maybe max 20 strains of the most common stuff out there...... sad

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