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Sorry for a rather crude set of questions.........but...... I'm having a lot of difficulty getting the muscles to relax so I can go to the toilet......l'm pretty much numb down there.......any experience of this out there..........??

Hi all, After a recent (just before Christmas) 6 days in hospital with uro-sepsis I have now found myself having to self catheterize due to urine retention! Following on from that I am now also finding it more and more difficult to naturally empty my bowels as I'm constantly feeling constipated! Do...

Hi I’m a newbie here currently stuck in hospital with not being able to pee or poop properly how is everyone

Bladder and Bowel appointment today, don't want to do this today.

When someone asks me about MS, if they know anything, it's usually that it affects a person's ability to walk. If only it was that simple....We (MSers) have a little of almost every disease to deal with. Think about it - the brain controls everything the body does. MS causes brain damage and causes ...

Hello my fellow MSers I have RRMS and one of the permanent issues I have are bladder and bowel control. I've returned to work after a relapse (triggered by work-related stress) and have asked if I could have the ability to reserve a desk near the bathroom (we book desks) as part of my OH workplace...

I had the day from hell on Saturday. I've been really poorly with a chest infection for about three weeks. Due to being on Fingolimod my immune system is very weak. It wouldn't seem to shift even with antibiotics. Then last Monday I developed numbness in my lower back accompanied by some severe nerv...

Hello all, I'm wondering if other people get confusing messages from bladder and bowel, i.e. 'need to go... don't need to go' once you get to the toilet. Very frustrating from the effort it takes me to get up/down & jeans off/on again. My husband says it's all in my mind, but I'm pretty sure it'...

Hello 👋 new here, please be nice. I've been living with MS a while, and have declining bladder and bowel function which is causing fun issues. I've been offered SNS as a longer term solution to botox. I'm wondering what experience others have had? Issues? Unexpected consequences? Benefits? Thx