POISCENTER
POIS Life Style => The Down Side => Topic started by: haidcat on October 24, 2012, 09:21:00 AM
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Who here urinates frequently during POIS? I am talking about more than 7 times per day, or where you pee out the water you just drank 15 mins ago?
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i just urinate as ever during pois
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increased thirst, increased urination and peeing 15 minutes after drinking are common pois symptoms to me.
I know it is not a common symptom, but I know others have it too.
Risking credibility: in my worst days, I am talking about 7 liters a day. Try an antihistamine before ejaculation.
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Do antihistamines reduce your symptoms? I thought they didn't? Which one do you take?
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It could be an UTI. Let your urine get checked.
The other thing is I drink a lot when in POIS. That's because I dried out, my mouth, nose, skin. And I get thirsty. So if you drink a lot you have to pee...
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I pee somedays about 20 times a day...Don't know if it has something to do with POIS
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yeah they do reduce about 20-30%. Brand didn't really matter, tried a few: ceterizine is quite good. Its non-description.
Huge difference; I had consistent results for over a year or so. Now pursuing desenz.
I had my urine checked but no infection. I am not surprised about 20 times (in pois that is).
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Who here urinates frequently during POIS? I am talking about more than 7 times per day, or where you pee out the water you just drank 15 mins ago?
Yea, frequent urination is very common for me in the days following ejaculation. I notice that I carry more water weight when my POIS is more active because of inflammation. For me personally, exercise is key in helping to remedy that symptom. Yet, I do not take any antihistamines because Ive been on Depakote ER for years because my inflammatory symptoms present themselves similarly to many as other neurological, psychological, and infectious diseases hence being misdiagnosed in many times over. Regardless, I found the drug did help with inflammation, mood and migraine like symptoms in spite of it being used under false pretenses. Although I would not recommend you delve into a broadband anti-seizure/psychotropic like Depakote because of the possible side-effects and dependence. Try those antihistamines combined w/ good exercise and see whats effective for you.
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If they don't find a virus or bacteria in the urine, it doesn't mean that there is no infection.
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I do have that
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yes, more frequent for me.
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Yes
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Yes, and it's almost always clear (not yellow).
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Yes, and it's almost always clear (not yellow).
Same thing happens here.Though i have been diagnosed with urinary problems and POIS has no relation with it.
I also cannot empty very well.I have some residuals in the urinary tract after pee that leaves the urethra later as urine leaks.
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Overactive bladder here. I rarely take Ditropan (Oxybutinin) because its a Catch-22: these type of drugs (all very similar) cause dry mouth...which make you urinate more frequently!
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I experience this for at least 3 days following release, I think it’s more like 7 days. Frequent urination. Someone on reddit mentioned this a few weeks back & I didn’t believe something like this would be connected to POIS. However I have noticed I do not experience it when I begin to abstain past 3-7 days.
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For me its not just increase in Volume but also a very nervous bladder while in POIS.
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I also have something like "nervous bladder". And i urinate frequently when i am in a POIS attack.
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I have this, this is a symptom that came much later, i did not have it in the begining.
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I have this, this is a symptom that came much later, i did not have it in the begining.
I anecdotally feel this has been true for me as well, but who knows.
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I also have this problem. The cause is evidently the burning pain that I had since as long as I can remember. Even so I had no really issues with this until my late twentieths. I could urinate as usual and had no real problems with retention, so it was more like an inconvenience. Since my late twentieths it became more difficult to urinate while standing as the flow is often weak and intermittent. Retention is not a real problem at least as I can hold it as long as I want, however it is often difficult to start the flow and it is more than just due to the pain as it was ways more excruciating several years ago. I guess some permanent damage was caused to the nerves, so I can no longer control this function adequately. While I can hold the urge indefinitely it is still rather problematic to do so, as my POIS symptoms would usually escalate rather quickly then and sometimes some really bad chest inflammation can occur due to this. Thus I try to go to the loo as often as I can even if only to leak a few drops. Waking up in the middle of the night due to the urge also became an everyday issue. It is interesting though that even then the amount I produce is often very small, sometimes only a few drops. I don’t like this as if I don’t get up I often can’t sleep back as it bothers me so much, however if I get up and take a leak I get too aware and then I can’t sleep either. Similarly to other members if I don’t sleep more than an average man would my POIS symptoms are much worse and my whole day is messed up doubly so.
I had many urine tests throughout the years, but doctors had never found anything wrong, so they were kind enough to deny any kind of pharmacological help as well.
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I also face the same problem
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I also face this issue. Went to doctors, took some medication. But nothing helped.
Then I realized that if I leave out my morning cup of coffee, I don't have to go as often. Still, perhaps more often than some people but not a huge problem. Also I have to avoid drinking coke and stuff like that aswell. But when I'm out of pois, when I avoid these then it's alright. Hope this piece of information is helpful
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I can confirm both the urination and that coffee makes it worse.
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Yes, and it's almost always clear (not yellow).
yes i can say that i m facing the same issues like for 5 year. and in tests: no infection, no swollen prostate, no problem with uro dynamic.
drug like Tamsulosin or Tolterodine didn't help