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Hi. In Barbara's original posting, she asked for support for her
surgery. Please be so kind to be a bit more gentle when responding to a
person in need of support. I am positive that would be most
appreciated.

I am glad ur brother is doing better.

Sincerely,
Nancy D. Mullen

P&B Fahr wrote:
>
> I have this question to seriously consider:
>
> Why would you want to permanently destroy a part of your brain
> with an operation that has proven --- over time --- to be a
> temporary "fix" in most cases.

> Electrical stimulation of the STN, on the other hand, does not
> destroy brain tissue and can be adjusted to compensate for
> changes in PD symptoms as they occur over time -- if necessary.
> My brother had biSTN DBS in April of 1998 and has needed minimal
> adjustment from his original parameters.  This indicates that his
> previously very rapidly advancing PD (diagnosis to near total
> disability in 5 years) has apparently advanced no further since
> DBS surgery.
>
> Sincerely,
> Paul
>
> ----- Original Message -----
> From: "BARBARA DAVIS" <[log in to unmask]>
> To: <[log in to unmask]>
> Sent: Friday, November 08, 2002 8:03 PM
> Subject: Palladomy
>
> Dose any one live in the Boston area. How has had a Palladotomy.
> I would like to talk to them . I am having the Palladotomy on
> Dec. 4
>
> Barbara A Davis
>
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