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3 years post surgery - still require a pad

User
Posted 18 May 2026 at 13:09

I’m now just over 3 years post surgery. Main thing PSA remains at <0.01.However despite doing squeezes 4x a day I still require a pad only one a day level 2. Some days I am basically dry other days it quite damp. I do occasionally get a sense of a leak - if sneezing or laughing and I do try to squeeze when I know there’s a chance of a leak. Other times I’m surprised why the pad is wet. I’m wondering is this normal and it’s now what I can expect going forward as I’m one of the unlucky ones or should I see if anything else be done? Immediately post op I could not hold water as they say and went through 9/10 pads a day until about 4 weeks when something clicked and I started to get a semblance of control such that after around 7/8 months I was down to the 1 pad a day I’m now on. Most of the guys in the support group I’m in were dry after a few months. Thanks

User
Posted 27 May 2026 at 17:26
I still have urinary incontinence more than 6 years after surgery, so I must be part of the "10%" It's not as bad as it used to be, although two years ago I had surgery to the neck of the bladder (due to blood in my urine, caused by radiation scarring, apparently), which made my incontinence a lot worse for a while. This is sadly only one of several "consequences of treatment" that I have learned to live with.

I meant to write something to cheer people up, but I don't think I have succeeded!

User
Posted 22 May 2026 at 02:19

Andy62 - may look at the physio route as an option. 

Adrian -I don't feel that I'm bad enough for anything as drastic as surgery as 1 pad a day is not life changing and it doesn’t really impact me now as its come part of my life and routine. I was just wondering if this is something that is normal. 

Debbie - sorry to hear about Steve’s issues. Along with all the hassle of surgery and worry about the diagnosis it’s not something you want. 

User
Posted 27 May 2026 at 09:15

Originally Posted by: Online Community Member
I was lucky to have had no incontinence issues and  near full erectile function post RARP (which I’m convinced was down to years of physical training and good pelvic floor muscles), so was surprised about 6 months ago (2.5 yrs post surgery) to experience arousal climacturia for the first time. I now get it regularly when aroused.

Hi, Eddie.

I'm also three years RARP. I have very few incontinence issues, only an occasional, very slight and surprise dribble, when I'm over exerting myself. As for climacturia, initially I got it every time I orgasmed but now its very intermittent. It helps to empty my bladder before having a bit of 'how's your father'. The wife avoids men like the plague when I come home from the pub with a belly full of beer and I'm feeling a bit fruity. 😀 

Edited by member 27 May 2026 at 09:18  | Reason: Additional text

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User
Posted 18 May 2026 at 14:13

Hi MGOR

My experience is not very encouraging. Following prostatectomy 15 years ago I am still using a small pad a day. I suffer from arousal climacturia: leakage of urine when sexually excited and at orgasm. Not exactly conducive to any intimate connection. However we have had to rethink our intimate life and have managed to re-establish our sex life within the new normal, with unexpected benefits.  If you are interested in reading about our experience please have a look at the following link:

https://community.prostatecanceruk.org/posts/t28948-Re-establishing-Sex-Life

 'Physics is like sex: sure, it may give some practical results, but that’s not why we do it.'                    Richard Feynman (1918-1988) Nobel Prize laureate

 

 

User
Posted 18 May 2026 at 20:13

Pratap - thanks for that. I am similar to you in so much that I also leak when excited. Just needs a different approach. It’s not something which bugs me as the main thing is fingers crossed I remain cancer free. I’m just curious if I’m one of the unlucky ones. 

User
Posted 18 May 2026 at 21:26
MGOR, if it's any consolation I shared your experience. The considerable leakage after catheter removal settled down but I continued to need a pad a day - albeit some days fairly dry but unpredictable in advance - and occasionally, usually after some activity keeping pressure on the bladder, a second pad.

10 years later, including salvage radiotherapy, I still need pads.

One of the things I have learnt from this forum is that we are all different. Some men are lucky (from my point of view) by returning to complete continence, some leak at a manageable level (like us), and a few have significant ongoing problems. My solution is to take life positively, because I never need more than two pads I know that having a spare in my pocket will see me through the day. Crises only occur if I can't access a discreet place to change.

User
Posted 18 May 2026 at 22:59

MGOR - one pad a day, PSA <0.01 it is unlucky but not too  difficult to have a reasonable life. How is your erectile function. I have permanent ED but we are still enjoying sex. So everything is possible.

 'Physics is like sex: sure, it may give some practical results, but that’s not why we do it.'                    Richard Feynman (1918-1988) Nobel Prize laureate

 

 

User
Posted 19 May 2026 at 01:48

Hi guys, slightly off piste, I recently got a very sore looking penis ,it is under the penis quite close to the scrotum. It sometimes stings ,a bit like when you trap a few pubic hairs in the foreskin.  I was going to fill in a triage form at the docs, we can't ring for appointments any more, anyway good old Google came to the rescue.  I have a suprapubic catheter but still dibble around 2.5 mls a day into a pad. Being conscious of urine smelling at night I rinse my penis at the sink night before going to bed. Sometimes I use water sometimes I use soap, I think the soreness is caused by not rinsing off the soap. Anyone else with a similar experience.

Thanks Chris 

User
Posted 19 May 2026 at 12:09

I count my blessings that I was diagnosed early and treatable. Using 1 pad a day is a minor inconvenience and is now part of life. I was 50% nerve sparing and initially there was no life even with silenafil. After some 18 months /2 years post surgery I was surprised and my wife even more so when there was all of a sudden life (not quite as we know it!) so much so that neither of us could remember what to do! Anyway it’s not consistent but every little helps. 

User
Posted 19 May 2026 at 12:52

After 3 years of pelvic floor exercises, your pelvic floor isn't going to get better, at least not by doing the same exercises. There is a possibility you aren't doing them correctly, in which case a session with a pelvic health physiotherapist could help. They could also identify if there's some other issue which needs investigating. It would be worth asking for a pelvic health physiotherapy referral.

You might also try easing off on the pelvic floor exercises to see if that helps. I have come across several people who were over-doing it, and making it worse. 

User
Posted 20 May 2026 at 07:06

Originally Posted by: Online Community Member

Hi guys, slightly off piste, I recently got a very sore looking penis ,it is under the penis quite close to the scrotum. It sometimes stings ,a bit like when you trap a few pubic hairs in the foreskin.  I was going to fill in a triage form at the docs, we can't ring for appointments any more, anyway good old Google came to the rescue.  I have a suprapubic catheter but still dibble around 2.5 mls a day into a pad. Being conscious of urine smelling at night I rinse my penis at the sink night before going to bed. Sometimes I use water sometimes I use soap, I think the soreness is caused by not rinsing off the soap. Anyone else with a similar experience.

Thanks Chris 

May be over washing drying it out, try a moisturiser. Or  possibly a fungal infection?

Edited by member 20 May 2026 at 07:16  | Reason: Not specified

User
Posted 20 May 2026 at 08:39

Any part of the genital area, particularly the penis, when constantly damp causes irritation. I experience this on the foreskin. I find that the most effective method to reduce irritation is to wash and dry the area and then apply some barrier cream - such as what parents use on babies to help with nappy rash.

 'Physics is like sex: sure, it may give some practical results, but that’s not why we do it.'                    Richard Feynman (1918-1988) Nobel Prize laureate

 

 

User
Posted 20 May 2026 at 08:40

Chris, for the same purpose I use a skin friendly flushable toilet wipe. My plumber hates them so I rip it up before flushing. 

Peter

 

User
Posted 21 May 2026 at 01:37

Originally Posted by: Online Community Member
May be over washing drying it out, try a moisturiser. Or  possibly a fungal infection?

Interesting. I wonder if this is why mine looks like a dehydrated button mushroom. 🤔 

Hi, MGOR.

I'm sorry to hear that you've still got incontinence issues, mate. Apparently only 10% of those who've had RARP have incontinence 18 months after surgery. May be, as you said, you're just one of the unlucky ones.

I dont know if you've read what our site says

https://prostatecanceruk.org/prostate-information-and-support/living-with-prostate-cancer/urinary-problems

I suppose, after three years, it's a case of are you happy enough to continue as you are or would you consider surgical intervention?

Best of luck, pal.👍

Edited by member 21 May 2026 at 01:39  | Reason: Add link

User
Posted 21 May 2026 at 22:41
Hi MGOR

We feel your frustration with this issue. Steve had his RARP in January 2024 and is one of the unlucky ones who has never regained continence. They like to leave it 12-18 months or so to make sure it’s not going to happen, then he had tests to see what was going on (cystoscopy etc.) before he was told he would remain like this unless he had further surgery. We had guessed this was the case 6 months ago so started researching. Surgeon recommended an AUS but we are going down a different route, a newer surgery called ATOMS, it isn’t right for every situation and damned difficult to get on the NHS, it has only been done in Reading so far but they are going to introduce it in Edinburgh and Newcastle. Steve is having the op privately in July and there’s a 75% chance he will be totally dry afterwards. Will update on here afterwards.

Debbie

User
Posted 22 May 2026 at 02:19

Andy62 - may look at the physio route as an option. 

Adrian -I don't feel that I'm bad enough for anything as drastic as surgery as 1 pad a day is not life changing and it doesn’t really impact me now as its come part of my life and routine. I was just wondering if this is something that is normal. 

Debbie - sorry to hear about Steve’s issues. Along with all the hassle of surgery and worry about the diagnosis it’s not something you want. 

User
Posted 27 May 2026 at 08:56

Hi MGOR

Like you I’m just over 3 years post RARP and nearly 2 years post RT. My PSA post RT has remained undetectable which is the main thing. I was lucky to have had no incontinence issues and  near full erectile function post RARP (which I’m convinced was down to years of physical training and good pelvic floor muscles), so was surprised about 6 months ago (2.5 yrs post surgery) to experience arousal climacturia for the first time. I now get it regularly when aroused. However, I’m thankful overall and see it as a small inconvenience which I have to live with. At the moment I’m not using pad as only get it at home lol! If it was to progress then would start padding up! Enjoy the beautiful weather folks!

User
Posted 27 May 2026 at 09:15

Originally Posted by: Online Community Member
I was lucky to have had no incontinence issues and  near full erectile function post RARP (which I’m convinced was down to years of physical training and good pelvic floor muscles), so was surprised about 6 months ago (2.5 yrs post surgery) to experience arousal climacturia for the first time. I now get it regularly when aroused.

Hi, Eddie.

I'm also three years RARP. I have very few incontinence issues, only an occasional, very slight and surprise dribble, when I'm over exerting myself. As for climacturia, initially I got it every time I orgasmed but now its very intermittent. It helps to empty my bladder before having a bit of 'how's your father'. The wife avoids men like the plague when I come home from the pub with a belly full of beer and I'm feeling a bit fruity. 😀 

Edited by member 27 May 2026 at 09:18  | Reason: Additional text

User
Posted 27 May 2026 at 09:27

Adrian, this is a cracker reply 🤣🤣🤣! Cheers 🍻 

User
Posted 27 May 2026 at 17:26
I still have urinary incontinence more than 6 years after surgery, so I must be part of the "10%" It's not as bad as it used to be, although two years ago I had surgery to the neck of the bladder (due to blood in my urine, caused by radiation scarring, apparently), which made my incontinence a lot worse for a while. This is sadly only one of several "consequences of treatment" that I have learned to live with.

I meant to write something to cheer people up, but I don't think I have succeeded!

 
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