Embarrassing
Ever since I've been diagnosed with my multiple sclerosis I have been having some trouble holding my urine. I try not to drink many liquids and even take oxybutynin but nothing seems to work. I am just looking for any advice on how to control this over active bladder.
The only reason I have been wearing a catheter ever since I was diagnosed
Don’t restrict fluids it will make it worse, one infection and two the bladder shrinks and it holds less urine,so having more bathroom visits, it’s hard, i was diagnosed in May but have had bad symptoms since Christmas including bladder- not being able to control it , needing to go right now 😬 I work in care and seen bladder issues lots, im no expert but I have tried to keep my fluids up and regular bathroom visits , has improved control so far 🤞