Does anybody here suffer from urinary incontinence? I don't very much but feel like it's starting down that road.
Urinary problems: Does anybody here suffer... - My MSAA Community
Urinary problems
Urinary incontinence was one of my first symptoms. I get bladder botox every 6 months and self-cath. As terrible as this may sound, versus the alternative, it works we wonderfully. My nerves in that region are on a permanent vacation.
I lost a lot of weight this last year and now if I sit on a hard surface I know when I stand up I will need the toilet. And yes if I donβt go right away accidents will happen, and especially if I have had a coffee. Here in the U.K. we have Always Depends. I had a hysterectomy so I donβt have the womb to support the bladder, anyway the Depends saves any embarrassment, let us know how you go, blessings Jimeka π¦
yes, I self-cath 3-4 times a day. and have accidents if I don't make a beeline to a restroom when being called upon. You get used to it and it is not as big a problem as it may sound.
Occasional accidents. I go frequently and when I gotta go, I gotta go.
I also some problems, but they aren't that bad. I've taken to wearing depends. They aren't that bad.
That was one of my probs. Ikeeptrying I take oxybutynin for it now. They called it bladder spasms. Although there are mornings when I'm running to the bathroom!ππ
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Jπ π¦
I'm sorry you struggle with this. It's very inconvenient, at the very least. Have you informed your doctor?
Thank you all for being so forthcoming. I'm not quite so afraid now.
Yes I do & that started in early in this battle with occasional problems now I wear pads 24/7 as I don't know when or where it will happen. Some times when I stand up it'll just start running. My pcp put me on Oxybutynin 5mgs 3x day it helps BUT I still use the pads
It's part of the aging process but when we have MS β¦ we adapt!!!
i don't know anyone with ms who doesn't have urinary issues!