Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
Misssy2
I swear I pee every 20 minutes...its super annoying.. I had an MRI...and may or may not have MS...but has this been a symptom for anyone?
I don't have diabeties..as far as I know...and I have been tested...its getting worse..I know it can be a signal of menopause as well..I'm 51...and this is REALLY disrupting my life...I don't think menopause..does that...so much
I don't have diabeties..as far as I know...and I have been tested...its getting worse..I know it can be a signal of menopause as well..I'm 51...and this is REALLY disrupting my life...I don't think menopause..does that...so much
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I just do not feel well and I really think that it's because I cried yesterday on my way to work about my Aunt who is in the hospital. I don't think that we will have her much longer. She is very frail. Now she needs help eating. So, this is the third time in a year that I felt this way after crying. I think crying releases toxins into my body. I also worked up a sweat at the gym...

What my urologist found was that the bladder never emptied completely on its own and that was the reason for the frequent desire to go. Self Catheterization is a great help for this. I can't imagine life without it although I'd like to count on it less through doing kegels and exercise.
You don't have any UTI symptoms, do you? This can be difficult to diagnose if you don't experience any pain with UTI's as it my case.
Hope you get some relief! (the spinal lesions are the contributing factor in bladder problems so far as I know.)
lorr...your right...I'm lazy at kegel...but I don't have a UTI....I mentioned this to my Dr...but we really didn't identify anything...
I thought maybe MS...even thou I don't have a diagnosis yet...because when I was studying the parts of the brain...there is a part that is responsible for "incontinence"....and that part (I don't remember what it was, I think pons)....was showing a lot of hyperdensity on my scan.
So regardless if I have MS or not...I will still ask the Neurologist about it.
I just wanted to know from you all if it was common with MS...and it seems for some it is...but it could be that some (including me) just have urinary problems period..
Its just really troublesome to be needing a bathroom frequently. Minor symptom of anything but an annoying one!
So I do have that practice now..getting old is trying...:)
But remember I too don't know if I have MS. Still waiting to hear results of the test..grrrrrrr...I hate not knowing.
Missy2 I took a pill that helped with slowing down frequency. I can't remember what it was called but I stopped it because I started feeling like I wasn't completely emptying my bladder & it was hard to get a flow going. I decided to take my therapist's suggestions-- kegals, I always try to go before I leave the house, I scope out bathroom locales immediately upon entering an unknown place & poise pads.
Now i,m ok at home but when i go out i fit a penile sheath and a leg bag wrap around upper leg if i wear shorts or lower leg if in trousers it allows you to get about worry free not after constantly looking for toilets oh i i have to wear one at bedtime NO MORE ACCIDENTS IN BED.
It might not even be MS....It could be just incontinence...as much as I would like to blame it on something..
ya know what?
we are who we are...
Take me or leave me...I worry more about others thoughts about it. Stupid..but true.
I have been on two different meds, which I am not entirely convinced work/have worked, but I read everywhere that the drugs don't seem to be fool proof for anyoe but help enough to make it worth it.
I now always TRY to empty my bladder every two hours, even during the night (I have something by the bed because I wouldn't make it otherwise). Where I live, something like Poise is super expensive, so I combine a cheap pad with a panty liner. That way, if I leak slightly, I just change the liner.
Gentle hugs, Linda