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?
Parkinson’s News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.