February 12, 2013
Share your experience with bladder or bowel dysfunction. Get the conversation started.
May 8, 2015
I can't tell when I need to urinate. I put myself on a bathroom schedule. I have not had any accidents, but am wondering if this is a common problem.
August 5, 2015
Yes, and it is very embarking. I have urges but to late, I wear protection all the time now because I never know. I am bedridden and have to wobble to toilet so with urges coming late I try to make it sometimes I do but some I don't. The underwear is plastic and with heat is miserable! But I endure it, because it's better than alt.
Kim Dolce Moderator
May 13, 2015
Skymom, it sure is! I have trouble urinating when I can feel my bladder is full. I used to have urgency, but I take Vesicare for that. It's good that you go on a regular schedule, our doctors say we need to void 4-7 times a day to prevent bladder infections. You're not alone 😀
Kim, MS.net moderator
August 5, 2015
I count each day I go at least 13 times and unfortunate I can not take anything because of allergies and drug interactions. So frustrating and completely exhausting, so much so I have hard time breathing. Round and round we go, where it stops nobody knows.
February 24, 2016
I have bladder urgency and sometimes do not make it to the toilet in time. I work full time and teach classes for adults. This is very embarrassing when I have to make an excuse, practically run from the room and then return in different clothes. I take medication but it does not work very well anymore and I know that most of the drugs can cause "brain fog". Does anyone know of, or has anyone tried anything that works well?
Erin Rush Admin
February 25, 2016
Hi bahunt! I am sorry you are dealing with this issue. Our contributors have written articles on this topic. Many of the suggestions include medication, but some of the non-medical tips might be something to try! https://multiplesclerosis.net/symptoms/urinary-incontinence-frequency-retention-bladder-dysfunction/ This article discusses the issue as well and the comments have some tips you might find helpful -- https://multiplesclerosis.net/living-with-ms/luts-talk-urinary-problems/comment-page-1/#comments. I hope this helps a little. You are not alone in this. Wishing you a good afternoon, Erin (MultipleSclerosis.net Team Member).