Prostate :: Strong Connection Between Coeliac And Prostatitis


Nov 3, 2015

I have been officially diagnosed with celiac disease and I have been gluten free for about 3 years now. However, I have been having on again off again inflammation of my prostate for the past few months. Some have suggested that there is a strong connection between celiac and prostatitis. I try pretty hard to avoid gluten, but could cross contamination cause flare ups? This last flare up has lasted a few days with no signs of letting up.

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Prostate :: Chronic Prostatitis For 18 Years - My Experience

I am 36. I have chronic prostatitis for 18 years, that's half my life. My experience in the disease and treatment follows:

The pain is intense and crippling. I have to be in bed all the time. Intense spasms. Symptoms move from urethra to prostate, back,ass, testicles so when you feel you finished with a symptom there starts another. I also may have difficulty urinating and some time ejaculating. This condition has remained idle for a total of 6 years out of 18 and whenever I feel it is gone I have a really good flare up the very next day. Idle means I am not in pain but I get to wet my pants after urinating.. That is the closest I can have to normal life. My sex life is not good because I get erectile dysfunction when chronic prostatitis is active. When it moves to being idle there is a tendency for restoration of erectile capacity however it is clear to me that I do not respond to visual stimuli any more . Reason for ED is venous leakage. Location of pain is as such that I frequently check both my urinary system and intestines.

Findings: High bladder neck, non typical inflammation of colon, prostate has no infection

Medical checks so far: Urethroscopy, Colonoscopy. prostate, testicular, bladder, kidney ultrasounds. urine and prostate fluid cultures.

All cultures have come back negative. Bladder ultrasound shows some urine remaining after fully urinating.

Experience with medication: I have used antibiotics, a-blockers, mesalazine for my intestines and cortisone (buddy cole). For ED I have used Viagra and Cialis.

When I have flare ups NO medication works to control the pain. Or it may work for some weeks and then all of a sudden stop working. Medication for ED seems to be effective provided my symptoms are either gone or are not too intense. Symptoms come and go and it seems I cannot really control them.

Psychological impact: I am desperate and seriously considering suicide when I have flare ups

Social impact: No friends left. I do not have the energy to move out of bed

Fertility: Thankfully no problems whatsoever. However I am extremely worried whether my offspring will have the same problems as I do.

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I can only remember once in my whole life experiencing a rock hard erection whilst standing, maybe 3 years ago. Maybe I was particularly aroused, I don't know, but never since then. It felt great at that time and I would love to get that way again.

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