What do you do for your Incontinence? - My MSAA Community

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What do you do for your Incontinence?

rjoneslaw profile image
14 Replies

I’m lucky mine always happen when I’m at home.

I wear depends with a pad . I do that because if something happens I can remove the pad if needed and use another one

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rjoneslaw profile image
rjoneslaw
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14 Replies
greaterexp profile image
greaterexp

There are when it would be nice to just change a vowel... like “e” to an “a.”

jimeka profile image
jimeka

Depends give you the security you need 🚽

carolek572 profile image
carolek572CommunityAmbassador

I try to not drink after 8pm, and during the day, I stay close to the bathroom. However, that is not always convenient, so Depends will be it for me ~ sooner rather than later. Are they good to be worn at night as well?

CynthiaS profile image
CynthiaS in reply to carolek572

Yes! Great 24/7

carolek572 profile image
carolek572CommunityAmbassador in reply to CynthiaS

Good to know! Thank you for this info :-D

I self cath, and other times I sprint

carolek572 profile image
carolek572CommunityAmbassador in reply to MS_Indestructible

My sprinting days are long gone, my friend! :-D

MS_Indestructible profile image
MS_Indestructible in reply to carolek572

my sprinting is my moving as fast as I can without hurting myself. Too many, it is a snails pace, to me, it is too fast, but I do it with reason, LOL

carolek572 profile image
carolek572CommunityAmbassador in reply to MS_Indestructible

I agree, it's all in the eye of the 'pea'holder! :-D

MS_Indestructible profile image
MS_Indestructible in reply to carolek572

more like a 'fire hose' sometimes, LOL

carolek572 profile image
carolek572CommunityAmbassador in reply to MS_Indestructible

:-D

RoseySawyer profile image
RoseySawyer

I guess to me it all "Depends" 😂 how far I go and how long I will be gone. And I use pee pads everyday. Thin pads around the house and thicker ones if I'm on the go. I use depends on the days my body decides to go Wacko. 😊❤🌷

sashaming1 profile image
sashaming1

Lots of advice and recommended treatments on MS websites because it may be a problem getting nerve signals to-and-from the brain and bowel. I've self-cathed recently - I guess I can cross another one off my "Bucket List." A urologist can help figure out what the issue is and figure out what to do about it. I've done "Bladder" Therapy (including sticking an electrode up my anus and getting my "Pelvic floor" muscles to respond like they should - another one to cross off my "Bucket List"), Kegel exercises, "Pelvic floor" exercises.

Jackjosh profile image
Jackjosh

I wear depends only when I leave the house my bowels are bad idk if that's incontinence but it sucks

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