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nothing like personal experience murray
thanks for your frankness it helps to guage  and evaluate my symptoms
judy


>From: Murray Charters <[log in to unmask]>
>Reply-To: Parkinson's Information Exchange Network
><[log in to unmask]>
>To: [log in to unmask]
>Subject: DSSE & urination
>Date: Wed, 28 Jun 2000 22:49:24 -0700
>
>On 28 Jun 2000, at 20:33, Judy George wrote:
>
> > janet and all
> > got the dsse from your site
> > i cant open yours marjorie and no children have materialised to assist
> > what a great tool
> > my thanks for your wonderful efforts at your site
> >
> > could i ask
> > how does pd effect urination?
> > what should i be noticing
> > how do muscle cramps manifest themselves
> > often, on the odd occasion, seldom????????
> >
> > the other symptoms i understand well enough i think
> > regards to you all
> > judy
> >
>
>Hi Judy,
>Speaking from personal experience, I have noticed variances in frequency,
>(urge to void more often up to hourly) and the feeling when you get the
>urge
>that ya just might lose it all if you don't go right now.
>
>I can only speculate on a possible cause. Perhaps anxiety & stress, perhaps
>a side effect of a drug, perhaps a minor bladder infection, or perhaps this
>is
>directly related to Parkinson's....  This symptom (with me) goes into
>remission
>by itself after a while and I tend to forget all about it for a year or two
>until I
>again experience the thrill of nearly wetting my pants in public.
>
>I would suggest it is on the sheet because it is something that should be
>noted and discussed with your doctor and is probably very treatable.
>
>I think the things to watch for are abnormalities like frequency, urge,
>leakage,
>volume retained, any burning sensation, any difficulty.
>
>cheers ........ murray
>
>
>
>
>
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