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

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...

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

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..........??

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

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...

So like many I have the pesky bladder and bowels issue. Going on a cruise and starting to buy my supplies . Going for one week and I am going to pack 4 packs of disposable underwear..... figure I'd feel safer over packing then under 😉 #MSUnfiltered

I had to to pee Real Bad and there was a line so I went in the sink. I was shamed and I think I creeped out my new friend. I'm depressed about my pending MS diagnosis and I'm stressed in not going to be able to do the things that spark joy. The bladder and bowel stuff are totes lame! 🤬

A friend's clearly struggling with symptoms which range from tingling, numbness, heat patches to pain, cognitive impairment and fatigue, spasticity to trigeminal Neuralgia bladder and bowel issues recently too. Athough she has had an MRI, which a muscosceletal doctor has said looks normal, she is s...

Hi all! I am new to group and newly diagnosed. Haven't been told what type of MS, but after researching myself, looks like PPMS. Not on any prescribed medication yet. My main symptoms are numb feet, pins and needles and general weakness in legs as well as attacks of fatigue, partial loss of control ...