Constant need to urinate with radiation therapy for prostate cancer
I am currently undergoing radiation treatment for prostate cancer. I am on treatment 14 of 28. The first week or so was ok but now I am having serious issues. I have gone from the need at night to urinate every 45 minutes or so to every 10-15 minutes. I have gone 3 nights with zero sleep. As soon as I get back in bed and I have to go again. I stop drinking anything at dinner other than what I need to take meds. Sometimes it's an inability to completely empty my bladder but other times I completely empty and still have to go 10 minutes later. My Dr. doubled my Flomax and recommended a product called AZO but neither have been much help. They tell you to take with a full glass of water which seems counterproductive. I have also developed bowel problems and hemorrhoids which is giving me issues as well. I still have a long way to go, and I have to find some way to get some sleep. Has anyone else had these issues and found anything that provides relief. I seriously wish I had gone with surgery but was convinced this was the easier path. I am at my wit's end. Thank you!
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
Just bleeding.
I have had bleeding but believe it due to hemorrhoids I developed from the treatments. Some of the meds I am taken cause constipation. I am scared it is going to cause anemia which I have dealt with in the past
Thanks for getting back to me. At the moment I am exploring all available options near where I live.
I have not had any bleeding to date but still early in my treatment (18/40 sessions). I think the psyllium has really helped firm up my bowel movements and maybe the retinol is doing something as well. It probably helps too that IMRT is a lower dose therapy. Don't know if you are around a facility that offers it, but hyperbaric oxygen therapy is supposed to be helpful for bowel problems. Hopefully I won't need it as the nearest clinic is 4 1/2 hours away.
My urination is still not good but I just added another 5 mg Cialis to my daily routine, one in the morning and one in the evening so we'll see how that shakes out.
Just wondering about your bowel problems-does this include bleeding or is it restricted to very loose bowel movements. I had 5 high power radiation treatments last July/August and started having blood during bowel movements 5 months after. Tried sulcafate enema and supporitories but neither worked. Now waiting to see a gastrointestinal specialist. I'm wondering if the psyllium you took in the morning would be helpful.
wear a catheter or catherize yourself to get it all out / or much easier wear a diaper.sweet dreams.
Same problem with TURP
dave1957, I am going on 10 weeks post radiation therapy (28 treatments). Still have some of those same issues myself. It seems to keep improving, but much slower than I would like. My Doc tells me to be patient. But, sometimes my patience runs thin. I have to remind myself that it is better than the alternative.
Thank you! The side effects with surgery weren't appealing either and I wasn't impressed with the surgeon that I was referred to.
Sorry you are going thru all this but believe me when I tell you that surgery is no picnic either - just different side effects that are equally frustrating and exhausting.
Prostate cancer sucks and so do all of the treatments. But you will live to laugh about it down the road with others who’ve travelled the same path. Hang in there baby!