Prostatitis After Oral Sex

i think my issue may me partly autoimmune or nerve damage related but i need more tests to figure it out. when i get flare ups i get flushed red burning hands, feet, face and hypersensitive skin over all and heavy fatigue. My sis has similar symptoms minus the pelvic pain and was diagnosed with an autoimmune thyroid condition, just something to consider. I do have very tight muscles everywhere tho, esp legs, hips, chronic back pain n tension (3 bulging disks), neck, scoliosis that prolly causes my hips to be uneven. Lately my anxiety has been insanely bad same with depression and when im going through stress or high emotions it gets worse, but not saying its the cause but i have dealt with it my whole life and even find myself guarding. stretching seems to help tho at least some. wishing everybody luck with this horrible affliction and that we find a light at the end of the tunnel.

whether its infection related or not, I think we'd all benefit by looking at improving issues we can control such as hormone imbalances, gut health, possible mold / fungal issues, toxic exposure (heavy metals, etc), teeth and gum health, all of which affect the immune system. It starts with the diet, I'm cutting out all gluten, dairy, and as much sugar as I can, maybe consuming natural antibacterial/ antivirals and looking into natural medicine. It's worth a try until a definite infection is found. I was having mild symptoms before the sex act so for me personally I'm still open minded as to the causes or causes. Stay hopeful guys

I've been suffering 2 months now with same symptoms, it's so painful really hard to live a normal life. I've changed my diet and get a lil relief but also have pain in my throat area under my jaw when I have a flare up, don't know why but when I'm not in pain my throat dont hurt, you experience this too?

I found out the cause....

CRPS from surgery a year ago.

This is one of the worst diseases known to man and esp when it originates in your private area and ruins your sex life.

There is no cure

I'd give up anything to have tight muscles or even an infection of my prostate.

Take this as a positive guys, at least there is still hope for you , at least its not CRPS.

Signing off this thread. Good luck

well if it is what you have, and youre not experiencing serious neurological symptoms, twitching all over, tremors, crippling fatigue, trouble breathing, chest pains, headaches, severe hearing sensitivity, burning face, pelvic area of course, hands, feet, hypersensitive skin in general, trouble concentrating, planning, finding words, no memory, etc (i could go on) then consider yourself lucky and hope it dont spread. Id focus on fixing your gut health since its a disease of the central nervous system and your gut has most of your neurotransmittors. Clean diet no gluten, no or limited sugar n dairy, supplements and stress control and try to sleep even tho your nervous system is in constant fight or flight

also def limit caffeine esp and alcohol. CRPS can be a genetic predisposition that triggers an autoimmune response of the nervous system after a trauma or surgery or sometimes without one. My sis developed similar symptoms after childbirth and since her thyroid was the only think they could find abnormal, plus they found abnormal immunoglobin readings (crps can affect thyroid and adrenal glands and cause hypothyroidism) they diagnosed her with Hashimotos ( autoimmune condition of thyroid) when really it is likely the nervous system. Its weird cuz ive always had really bad anxiety and a panic disorder, and i could feel when my nervous system was in overload only difference now is it never returns to normal. I feel like a lot if us hsve overactive nervous responses before this sets in but idk. Thats why the multimodel approach is best because you have to address unhealthy thinking patterns, stress, diet, stretching, detox, all to prime your body to be as healthy as possible to calm down and heal itself, as much as it can. Thats all I know to do now until i see a specialist of the disease.

Guys, check your fertility and don’t trust all the tests, they might be unreliable.

My story has bad end...

I received oral sex from one lady (she was not "clean" ) in FEB 2012, after 7 days I began having many problems like burning pain, itching, milky discharge...later on frequency, chronic pelvic pain, pain upon ejaculation... my doctor prescribed me Biseptol (sulfametoxazol/trimetoprim), then my Urologist did cultures and swabbing (4 swabs at the same team, for gono, chlam, tricho, urea/myco...one swab for one bacteria, each next one went deeper into urethra than previous one to not affect the results). enteroccocus faecalis (very minimum volume, detected only after enrichment in cultivation) was the only finding - which I couldn't believe to, but I trusted my Urologist and the lab results at that time.

So Urologist prescribed me Cipro for 5 days only to treat the UTI caused by enteroccocus... It really seemed to be effective, but unfortunately few days after last dosage, all the problems went back...I literally felt like the bacteria was spreading up in my urinary tract and found 'new safe home' in my prostate.. I was given another Cipro for 5 days, it did not help either, Urologist told me it was chronic and there was no cure for it...so I accepted it and tried to live with it though it was nightmare every day:(

After a year anf half (in Oct-2013), I asked my Urologist to completely re-test all STDs (we planned a baby with my girlfriend)... and they found Chlamydia (they did swabbing). I´m sure I must have been infected by Chlamydia in FEB 2012 as I had all typical symptoms at that time)...

So I was given Azithromycin to treat it but my chronic prostatitis was not healed at all (I think it was too late after Chlamydia destroyed my uro-genitaly system - perhaps early diagnostic of Chlamydia and correct and sooner treatment could have healed the prostatitis and avoided turning into chronic disease and after-effects like azoospermia/0 sperm count (which is most sad).

Surprisingly, first test that detected chlamydia was in 2013 and I thought the bacteria was eradicated by Azithromicyn, retest (PCR) was negative, but Lymphocyte transformation test (LTT) again detected Chlamydia in 2017 (no reason for new sti)... I was on Doxy for 3 months in combination with 2 other ATBs, but I still suffer. I can retest it, but I think it is useless...

In any case, unprotected oral started all my problems and bacteria triggered the prostatitis. I also think I could have epididymis in 2012 which resulted in azoospermia.

One oral sex destroyed my life... and my wife was tested negative for chlamydia (vaginal swab), but she has problems with precancerous cells on cervix and cysts on ovaries which is also contributed to chlamydia.

Take care of your partners, chlamydia in prostate can be undetected (forming some biofilms not detected by tests), but you can spread it:(

I have had exactly the same symptoms. It happened to me two or three times after oral sex with my wife, I have had urine cultures, urine tests, sperm cultures without results. Sperm cultures after prostatic massage. I took antibiotics levofloxacin, denvar, and nothing took it from me, finally the sexual abstinence and the knowledge of the Tao table helped me to make my prostate deflate.

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Hi, Have you resolved your prostatitis problem? I also having his problem for past 1 year after receiving oral sex

If there is a biofilm involved in the scenario, I am almost certain about yeast infections. I had similar problems and trying to cure. luckily I have learnt more about yeast infections because my girlfriend diognosed intensine yeast infection.Everyone has in their intensine a level of yeast but when the immune system gets weak, they become too many and hide under those biofilms. Doctors never consider those possibilities. I will get myself checked properly to clear this issue regarding yeast infections perspective. I can share my experience later. look below paper supporting my theory

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077167/#!po=4.16667