I just read about a procedure to dilate the urethra that the Dr can do. I also read that many MS'ers can have Urethra spasms and that it is not uncommon in women with MS.

Has anyone had a dilation of their urethra? If so please tell us about what lead to it and if it helped.

I have many bladder issues including urgency, inability to "hold it" til I get to the commode, problems emptying bladder (I don't have a "steady stream" of urine--it takes me a while to urinate) then I don't even completely empty my bladder. I am on Oxybutanine but only at night.

ANY FEEDBACK IS GREATLY APPRECIATED