I just read an article on 'ProstateCancer. net' that drinking more water can reduce incontinence problems.
"Because of his urinary incontinence, R--- avoided drinking water. This can irritate the lining of the bladder walls and actually worsen urinary leakage in all humans, whether or not they have had prostate cancer."
I have always read that anyone plagued with urinary incontinence should reframe from drinking any liquids a couple of hours before bedtime.
Comments please?
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E2-Guy
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Hi, Before my diagnosis I was really struggling with incontinence. If I was active, I had to urinate almost every 20 minutes, and once I felt the urge I couldn’t stop the urine from flowing. So, I started drinking less water. Then, I started occasionally urinating painful blood clots. Turns out the clots encompassed bladder stones. When the urologist was scoping my prostate he found a large bladder stone that he attributed in part to my reduced water intake, and also to my inability to completely empty my bladder when I did urinate. I upped the water again and feel better as a result, but I now have to rely on Depends whenever I leave the house. That took a while to adjust to, but it is now just the way thing are…
Yep just the way things are. Seems like every bump in the road causes me to bottom out. I had a MGB that would scrape the muffler each time I hit a speed bump. With my health I can't anticipate the next bump in the road, just that I will need to make some adjustments. Good luck!
I've tried drinking more water; however, 'no joy'! The leaking just increases. I guess I'm kinda like the three hundred plus cacti on my balcony...I do better with less water!
There is a book by Anita Gaglani , a physical therapist in Florida, who works with men with Urinary incontinence and in her book she stresses drinking more water. It helped me get continent until that got destroyed by the radiation therapy. Never could regain continence so had an AUS ( Artificial Urethral Sphincter) placed.
The AUS has been really good. It gave me back the quality of life that I lost. It was more painful than my Prostatectomy, but worth it. The idea of drinking more water has to do with the the concentrated urine is an irritant to the bladder and so it will expel the urine. Also in Anita’s book, she has various exercises used to strengthen the pelvic floor so that you can gain control. I tried for 10 months to regain control. I live in Texas but did video conference calls and texts with her.
Burnett1948. I had the AUS. The surgery was easy. It was the best decision I have made. Previously the exercises didn’t work, neither did the stint. Recommend AUS.
ronromHU. That is what I experienced. But so far after 3 months settling down this latest the AUS 800 is working well. It was a 2.5 hour operation. No deep cutting and I was out of hospital after two nights feeling good. It’s the best procedure I’ve had. I had a good surgeon.
I am sure you already know to keep doing Kagel exercises “a lot” might help you build up more control over time.
Regarding water - i find that drinking a lot of water all day helps me. Still have to go frequently since what goes in must come out, but with better control. Cut off water at about 6 pm so sleeping is a little better.
One more thing, monitor what you drink to see if it matters. I found that iced tea caused me more problems so i stopped drinking it. My UO said tea should not cause issues but if i thought it did then to quit drinking it. Lol
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