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hi sandy,
i agee with you concerning the risks.  i had a very inexperiencd neurologist 
and medtronic rep programming . on my first anversary i was told i had to be 
on 6 volts and as a result my 15 month old kinetra battery was depleted and 
i needed a new one, and btw they though my leads were too deep below the 
midline and i need have a re-do.  i   became very depressed.  it took me a 
year to find sierra farris up in kirkland, wa.  she is my medical ANGEL.
-charlene lustig pd since 1990, dbs 2005

--- Original Message ----- 
From: "Sandra Way" <[log in to unmask]>
To: <[log in to unmask]>
Sent: Friday, December 05, 2008 11:56 PM
Subject: Re: DBS UPdate


>>> It is great to hear how well Brian is going!
>
> However, I have to agree with Craig from Maui that it is a big risk.I  had 
> my DBS 2 years ago and suffered a stroke which left me paralysed  on the 
> left side. I still have not recovered use of my left hand  though I can 
> now walk again. The team told me there was a 1 to 2 %  risk of a bleed but 
> as the surgeon said "It's not much comfort if you  are that 1 or 2%" The 
> electrode placement was also affected by the  bleed so it is not helping 
> my Parkinson's. Before surgery I never  thought of myself as disabled but 
> now I am. Sorry Nigel to give you a  bad story but I don't think when 
> you're told the risks you fully  appreciate them until you've had to live 
> through them. I lost my  independence for a year and that really doesn't 
> help the depression  from the PD or the stroke.
>
> Make sure you choose a good team if you do decide to go ahead. Brian  is a 
> shining example of how good it can be when it succeeds.
>
> Best wishes to all
>
> Sandra Way
> Sydney, Austtralia
>
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