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Carol, glad you find my participation useful.

Rick

-----Original Message-----
From: Parkinson's Information Exchange Network
[mailto:[log in to unmask]] On Behalf Of Carol Irish
Sent: Monday, February 25, 2013 9:17 AM
To: [log in to unmask]
Subject: Re: Musical people with Parkinson's

thanks to both of you for your posts.  You make me have hope.
 
 
In a message dated 02/25/13 2:19:58 A.M. Eastern Standard Time,
[log in to unmask] writes:

Rick

I used to play piano when I was a young adult.   Can't play at all now.   
Had 
DBS almost 10 years ago when I'd  had PD 7 years.   Like Lisa, the big 
benefit was no more  tremors.  I don't take PD meds at all and wish I could.

The thing  with PD is you get worse no matter what you do.  There are
degrees of  disability and I am  learning about them. It is harder and
harder to use  
computer, poor balance leads to falls, etc., but no more  tremors!!   I 
think
my motorized cycling helps.  I would  bee a real basket  case without DBS. 
Don't know how  much my  speech difficulty is due to PD or DBS.


-----Original Message-----
From: onelove
Sent: Sunday, February 24, 2013 9:55 AM
To:  [log in to unmask]
Subject: Re: Musical people with  Parkinson's

Hello I am Lisa main problem a budding singer I have  Parkinson's
since1993,  I am also an, Artist I do mosaic art  with stained glass. Had
DBS surgery in July and August ,i can't  say enough about how happy I am
with the results, I don't want to  sound like I am complaining but there
are still things that  are not  perfect ((but they weren't perfect
before the surgery)my  balance  is off...I feel like I am about to tip over
most of The time,butttti have no more tremors or flailing limbs reduction of
medication by about 60percent iihave have a hard time typing .  So i  will I
Will send this out now.  I would love to chat w/you. I  remember your name
from a few years..u mightnm remember me asnLisa in  paradise st John virgin
islands.....talk Moore . What ave u found about  DBS

By

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