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Rose 54 Hello Everyone. I Would Like To Know If Anyone Have Problems With Incontinency? Since Having Parkinson I'm Having P
Definitely. It's getting worse too. I'm thinking of checking into a device from Axonics. I'll keep you posted.
Important to recognise a difference between insomnia and incontinence me think 🤓
@A MyParkinsonsTeam Member
Me as well thinks you may be missing a couple of o's from your question ?! 😧
@A MyParkinsonsTeam Member
Hi Rose. In response to your question about incontinence. Yes, there are many of us that this has become a problem for. My doctor told me not to try to hold it in if busy. Not to let it build up & to go more often. It does make a difference in my case. I still have the problem, but this does help.😊
Insomnia gets me
Hi Rose, incontinence can indeed be a concern for some people with Parkinson's disease. Parkinson's can affect the autonomic nervous system, which controls bladder function, leading to issues like:
- Urinary urgency: A sudden, strong need to urinate
- Frequency: Needing to urinate more often than usual.
- Nocturia: Show Full Answer
I Feel Cold & Fatigue,More OFF Symptoms,Back Pain
Has Anyone Been Given The Diagnosis Of Multlple System Atrophy Along With Parkinson's Or Instead Of P's After First Thinking It Was That?
I Am Trying To Get The Money Together For Stem Cell Treatment. Has Anyone Tried It? I Don't Want To Waste Money. I'm Looking At Florida.
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