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.
Thank you for the cross link, jeffreyn. I wish that the site had a system for determining prior posts and automatically so , just like Reddit. But oh well, we make do with what we have.
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.
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)
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.
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