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Thanks, John, for this update on DBS.
In our desperation to rid ourselves of PD's horrible symptoms, many have
turned to DBS (the article said over 25,000 since approval last year by
Medicare).
I wonder if that number included those who had to return to the operating
table for infection, reinsertion of the pacemaker, rejection and subsequent
removal of the "hardware," or battery changes?  I personally know of several
such cases.

This therapy is a godsend for many - but should be carefully considered.
There are risks (high risks!) involved such as mentioned above.  But there
are likewise high risks in having PD! For example:
Falls
Contractures of hands, arms, feet, and/or legs
High rate of divorce & other family problems
Unemployment of patients and uninsurable cases
Mental problems (e.g. depression, psychosis, hallucinations, paranoia, etc)
Greatly reduced quality of life
Suicide or suicidal tendencies increased
And on and on and on . . .

By ALL means, look for a well-qualified neurosurgeon.  The problem that I
see is with Medicare's approval came a free license for any John Q. Public,
MD to "practice" on people's brain.  Be careful when choosing both your
surgeon and your hospital facility.  And remember, IT'S NOT A CURE!  There
isn't one . . . YET!

Be informed!  Read about it from several perspectives:
Medtronic site (from the company's perspective)
http://www.medtronic.com/neuro/parkinsons/activa_qa.html

Re-Wired for Life (from the patients' perspective)
http://www.rewiredforlife.org/

NPF's "Ask the Surgeon:" (from the professional's perspective)
http://www.parkinson.org/site/apps/s/content.asp?c=9dJFJLPwB&b=108269&ct=89596

One Patient/Caregiver perspective:
http://www.parkinson.org/site/apps/s/content.asp?c=9dJFJLPwB&b=108269&ct=132059


Peggy

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