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THANK YOU, SO MUCH FOR TAKING THE TIME TO  ANSWER.   I WILL PRINT IT OUT TO 
KEEP IN MY FILE,  TO  TRY.
 
 I ALSO RECIEVED ANOTHER IDEA , FROM HIS NIGHT  CAREGIVER ( ONE HOUR EACH 
NIGHT) TO GET AN EXTERIOR CONDOM  STYLE CATHATER FOR HIM, TO WEAR OVERNIGHT.  
SHE SAID SHE HAS ANOTHER  MALE PARKINSON  PATIENT, WHO USES IT.    SHE PUTS 
THE  CONDOM ON HIM  (WITH MEDICAL TAPE  TO KEEP IT IN PLACE) AT  NIGHT AND 
(HE) OR SHE TAKES IT OFF, WHEN HE WAKES UP,  IN THE  MORNING.  HE WAKES UP  
DRY, IN THE MORNING AND NO WORRY  ABOUT BED SORES FORMING BECAUSE OF  
INCONTENANCE.
 
 
 
 
 
 
 
 
In a message dated 6/20/2013 11:00:32 P.M. Pacific Daylight Time,  
[log in to unmask] writes:

My  husband has the same problem, not being able to make it to the bathroom 
in  time.  To save our carpet he is wearing depends, and we have put the  
walker around the toilet so he has hand grips.

The interesting thing is  that he has been having "Percutaneous tibial 
nerve stimulation" to control the  overactive bladder.  It seems to be working.  
It is a series of 12  treatments.  A needle (similar to an acupuncture 
needle) is inserted in  his ankle and a small electric stimulator is attached to 
the needle and the  charge is left on for 1/2 an hour.  After about 4 
treatments it is  working very well.  He hasn't had to go in the night for 2 
weeks now, and  the usual daytime going isn't happening either.

We'll see how it works  over time.  I don't know if it's supposed to last 
for awhile after the  12th treatment.  It beats botox,which was the other 
suggested  option.

Diane, caregiver to Jay


On Jun 19, 2013, at 12:07  PM, [log in to unmask] wrote:

> DEAR RAY,
> WHAT DO OTHER  PARKINSON MEN AND WOMEN DO ABOUT THE URINE  INCONTENANCE 
> PROBLEM  DURING THE NIGHT HOURS, IN PARTICULAR---TWO DOCTORS  HAVE SAID 
"NO" TO  
> THE EXTERNAL CATATHER AND ANOTHER DOCTOR AND CAREGIVER  HAS SAID  "NO" TO 
> DIAPERS, DUE TO PRESSURE SORES,  AT NIGHT???? 
>  
> I KNOW HE DOES NOT HAVE A BLADDER INFECTION OR KIDNEY   PROBLEM--I KNOW 
> -IT'S PARKINSON AND JUST BEING TOO SLOW TO GET UP TO  GET  TO HIS CHAIR 
SIDE 
> URINAL OR THE BATHROOM, AT NIGHT   WHEN HIS  BRAIN WAKES HIM UP AND TELLS 
HIM HE 
> NEEDS TO  URINATE-----BUT IF THE DOCTORS  ARE SAYING "NO" TO EITHER THE 
>  EXTERNAL CATATHER OR THE DIAPERS---------WHAT ELSE  IS THERE TO DO?   
WHAT DO YOU 
> HEAR FROM THE  OTHER PARKINSON PAITENTS  THAT  HAVE THIS EVIDENTLY 
> FAIRLY--COMMON PROBLEM WITH LATE TERM   PARKINSON?
> 
> THANKS,
> MARGARET
>  

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