Several weeks ago I started experiencing slow and weak urine stream for first time since diagnosis almost 6 years ago. This, coupled with rise in PSA, triggered my oncologist to order both MRI and PSMA scan. Would appear things are progressing and got referrals to radiation oncologist and urologist. Met first with urologist who strongly recommends scheduling a TUAP procedure. After taking a deep dive into procedure I have a few questions for my beloved peers:
1) the procedure itself is already causing me sleepless nights. From those who’ve gone down this path I would love to know your opinion on side effects and results.
2) Aside from Flomax , which did nothing for me, has anyone had any success enhancing the flow within doing TURP?
3) Any thoughts on which, radiation or TUAP, should I do first?
As always, thanks a million for your consideration of this request. Till then, best wishes on your continued journey.
Dave
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3putt
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3 Putt - I created a post just earlier this week with lots of good info in it. I can seem to find link now but should be easy to navigate to.
One lingering question though - why does all the damn fluid in out bodies seem to want to come out when sleeping - it seems more so than when awake right?
I’m in the uk and went from peeing a couple of times in a night to half a dozen, and increased daytime frequency. Tamulosin helped a little, but the urologist did a flow rate test, and found it very poor.
After a cystoscopy, he offered me bladder neck incision, to widen it where it meets the urethra. Not fun having a catheter for a day or two but it worked and has restored my QOL.
If you are suffering now, my advice would be to get it done now.
I had a TURP procedure about 9 months ago, and it was the best thing that happened to me. I was getting up 5 or 6 times a night just to dribble half a cup of urine. After the TURP, which cost me 2 days in hospital, the catheter was removed and I went home. Passed a fair amount of blood for about a month, but not too uncomfortable. Now I only get up about twice a night, which is I think normal for my age (72) and I have a stream like a fire hose. My urologist said that he had removed about 50% of my prostate. I am very glad I opted for the procedure.
I had a TURP 4 days ago on my prostate that was radiation treated a year ago. When I finish urinating I am getting several drops of red blood. You mentioned blood for a month. Is this something you were told was normal during recovery? Yes, I pee like a fire hose now.
My partner had a TURP operation about a year ago. About no side effects. By far better flow of urine. No need for Flomax anymore. No nocturia anymore. But quite a degree of incontinence still remains. All in all he is content with the result of the operation..
I went from say 5 night times down to 3 , 2 on good nights with 3 to 4 hrs good sleep in between flow rate much improved How ? certain herbs and supps, oh and patience giving them a chance, to work. I don't need no cut burn poison so far , but not , but just sayin.
Thanks for asking, Prostatesure sold by Activeherb, Bittermelon,Vitex, Pao Pereira, Andrographis, Zeolite ( detox/ drug carrier agent ), Melatonin ( sleep ). Also started taking DCA ( sodium dichloroacetate ) along with my ongoing Fenben as a treatment protocol. dcaguide.org/dca-for-cancer... . I don't know what single one is helping . As I write last night only 2 night trips 11pm and another at 5am wake up. Just type in anyone along side prostate cancer for info. Vitex ( natural ) reads as an anti androgen - lowers testosterone. Kinda makes ya wonder what may be in the realm of possibilities . Most of all my guidance to gaining knowledge comes through prayer and asking the allmighty to lead the way. Oh I also do cycles of Ivermectin, and plan on taking Laetrile again . Happy trails on doing the research on all said.
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