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Urinary and bowel incontinence
Urinary and bowel incontinence have been identified as a non motor symptoms of PD. http://parkinsons.stanford.edu/incontinence.html
I have experienced both and it is not pleasant. One thing I have learned is to never pass up an opportunity to use a bathroom, even if I don’t feel I need to use it. If you have experienced either of these symptoms, short of never straying far from a bathroom, how do you handle incontinence issues?
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