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Incontinence, something no one wants to talk about
Urinary/Bowel incontinence have been identified as a non movement PD symptoms. 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. Short of never straying far from a bathroom, how do you handle incontinence issues?
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