Print

Print


I take the regular C/L now, although I've tried all of them at one time or 
another.  I get nauseous, too, but I don't see any alternative.  Thanks for the 
tip about ginger ale--I've tried that before, but maybe I'll try it again.  I'm 
sorry you have had trouble with your DBS-what makes the stimulators stop 
working?  I thought the battery rook care of that.  You are not alone--we have a 
small support group in Bloomington, IN, and there is one other person besides 
myself who has had DBS, and he is not doing well at all.  I hope the 
reprogramming helps you.  It just goes to show how very individualized this 
disease is.  I wish my meds would help ME lose weight!! 




________________________________
From: Rayilyn Brown <[log in to unmask]>
To: [log in to unmask]
Sent: Thu, October 14, 2010 9:52:07 PM
Subject: Re: New member

Hi  Marti

I  had 2 DBS in 2003 (one was redo of one side) at age 67. I've had the 
stimulators replaced twice now.  I never took PD  meds much as they didn't seem 
to help, but when I "crashed" when  my stimulators died in August 
carbidopa/levadopa enabled me to move a little.  My new neuro gave me CR 
carbi/leva but I 'm waiting to try it again after I stabilize after some 
reprogramming.  Do you take the regular  C/L or do you have the controlled 
release kind?  it gives me slight nausea but  helps me lose weight.  my neuro 
said to drink ginger ale.

Although I can barely speak, at least I can move and don't tremor.  I'm a big  
DBS booster but I guess some PWPs have not had good results.

--------------------------------------------------
From: "Marti Coleman" <[log in to unmask]>
Sent: Wednesday, October 13, 2010 4:35 PM
To: <[log in to unmask]>
Subject: New member

> Hi all!!  I was a member of this group several years ago but let my membership
> lapse because I didn't have time to read all the input.  Now I'm semi-retired
> and think maybe I can keep up with it.
> 
> 
> I am a 61 year old female, and this is my 24th year with Parkinson's.  Two and 
>a
> half years ago, I had the deep brain stimulation operation on both sides of my
> brain.  I still take carbidopa/levadopa 10 /100 and Amantadine, but I quit
> everything else cold turkey because the meds were making me feel sick all the
> time.  I've tried just about everything in the arsenal of meds during my 24
> years with PD, but for now this combination seems to be adequate.  I would
> encourage anyone who is interested to look into DBS seriously, as it has
> definitely proven helpful to me.
> 
> 
> I would welcome any questions about the operation, or anything else for that
> matter.
> 
> Thanks for listening.
> 
> Marti Coleman
> Bloomington, Indiana
> 
> ----------------------------------------------------------------------
> To sign-off Parkinsn send a message to: mailto:[log in to unmask]
> In the body of the message put: signoff parkinsn 

----------------------------------------------------------------------
To sign-off Parkinsn send a message to: mailto:[log in to unmask]
In the body of the message put: signoff parkinsn


----------------------------------------------------------------------
To sign-off Parkinsn send a message to: mailto:[log in to unmask]
In the body of the message put: signoff parkinsn