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Hi Everybody.
I recently joined the PIENO list (a couple of weeks ago). I'm 53, was just
diagnosed, and have had symptoms for about 3 years. I am taking a big load
of "supplements" at this point, but no "Parkinson's med."

A friend referred me to a movement disorders specialist--Shawn Bolton,
DO--in Farmington Hills, MI. I live in Ann Arbor, so it's a bit of a drive.
But after my Mom's treatment at the Movement Disorders clinic at University
of Michigan (here), I'm wanting to look elsewhere.

I've emailed Dr. Bolton. Here's an excerpt of her response to me...

<<<...some info about me!   I finished my neurology training in 1996, and
completed my movement disorder fellowship in 1998.  About 80% of my current
practice is Parkinson's.  I am also conducting several clinical drug
trials...one of which, if I agree about the Parkinson's...you would be an
excellent candidate for.  It involves a new dopamine agonist, Sumanirole,
not yet approved by the FDA.  The study has 3 groups of patients...one group
will take the Sumanirole, one will receive Requip (already on the market)
and one group (the smallest, about 20-25%) will receive placebo.  The study
is designed for the earliest patients, even perhaps people who do not yet
require treatment.  There is a lot of info in the works about the newer
dopamine agonists, (Mirapex, Requip, and this Sumanirole) the debate is
whether or not they will provide neuroprotection, or help slow the progress
of Parkinson's.  So, being such a young woman, it would be terribly
important to explore all aspects of potential treatment, especially the
cutting edge studies that are available to you! >>>>

Dr. Bolton certainly sounds "qualified" to me and my friend really likes
her. I particularly am impressed by her willingness to communicate with
patients via email. So I expect to go see her--unless any of you knows of
her and has a problem with her.

But what about participating in the study??? In some ways I'm concerned
about starting any meds before I really need to. Also, I'm terribly
sensitive to about 1/2 the meds that are out there. And I'd be signing up to
get either something as yet untested on humans, or Requip (what experience
does any of you have?)--or of course a placebo.

I sure would appreciate the thoughts that any of you might be willing to
share with me.

Thanks!

Sally

Sally Lattuca
Turn of Phrase
carefully crafted communications
When the words sing. . .the ideas dance!

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