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Billie, et al....

Like other list-family members, I've been trying oh-so-hard not to
drop "Me toos" all over the List in response to various posts,
however, I feel absolutely COMPELLED to respond to Billie's
message.

Billie.... I've had PD for 24 years, have had a unilateral
pallidotomy, and by now while I'm no neurological genius, I'm
pretty darn PD-savvy.

I KNOW you're skating VERY, VERY close to the edge with that scary
collection of drugs!!!  In fact, I don't recall EVER hearing of
any Parkie taking so many contra-indicated drugs at one time and
still being alive!

M'dear..... If you haven't been evaluated by a movement disorder
specialist, I STRONGLY urge you to do so, ASAP!!!  THAT'S the Md.
who should be coordinating your meds intake.

Please pay heed to the advice of our fellow List-members 'cause
you won't find a more PD-savvy bunch of individuals anywhere....

We CARE 'bout you!

Barb Mallut
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-----Original Message-----
From: Murray Charters <[log in to unmask]>
To: [log in to unmask] <[log in to unmask]>
Date: Friday, March 19, 1999 7:22 PM
Subject: Re: Progress report


Hi Charlie and Katherine and Billie,

Billie, I am not a Dr. , nor do I have any medical training or
background.   I'm a mechanic who happens to have Parkinson's.

Thus I feel no restraint in stepping on the toes of those who may
not share my opinions.   Your list of medications scare the Hell
outa me.

I have seen nothing but the most negative results when the list of
drugs taken is this large.  There are overwhelming odds against no
interreactions.

My opinion is that you need to work very carefully with your
neurologist to find the least amount of drug(s) that will give you
a
positive result.

Remember.... there are no "magic bullets" and your list of
medications sounds too close to Russian Roulette.

Look after yourself ... Please.

All the best ............... Murray
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