Sane advice for the rest of us dealing with the non-motor symptoms of Parkinson's such as urinary incontinence. In my case it is "urge incontinence" which means I have to try and stop from soiling myself when I have actually reached the "destination"! I have tight control until then.
apple.news/Ao59mdT6NTwuQez0...
Anyone else has the same problem? Please share your experiences and we should not be shy about discussing these things.
RKM
I am not shy... I share the same problem as you. I have learned to find a spot outside before there is an issue 
See also this thread from last year:
URINARY URGE.DO YOU EXPERIENCE THIS AS A PWP?
I do find the issue is a lot better since I started B1 thiamine I gm
Urinary urge incontinence is one of the symptoms that I use to gauge whether or not I'm taking the correct amount of B1 at any given time. When I hit my B1 "sweet spot," I have no urge incontinence. If I stop taking B1, take too much, or take too little, the urge incontinence begins to reappear within just a few days.
Hi,May I ask when did you start taking B1,
Thank you
November of 2018.
Thank you, that's very interesting. This means that whatever thiamine high dose is doing, it doesn't stay. It's not a cure. But that's fine, it's already incredible to have a treatment with such an impact (I mean when one looks on the different stories)
This is not relevant, but I read that if, in the UK, everyone peed in the shower, it would save 50 million gallons of water a day.
Not peeing in the shower means I've got to leave the shower to go to the toilet, dripping water the whole way and then back again dripping water and likely slipping on wet tile and slamming my head into the toilet or sink.
Why don’t you like me? 
Incontinence - A major problem
C/L and non motor symptoms
Where are you in the world?
10 Foods High in Glutamate and Why You Should Avoid Them!
