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Not sure whether you got this so I am resending it.  Responses to this by
hitting reply to sender will also likely have been lost
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----- Original Message -----
From: [log in to unmask]>Charles T. Meyer,MD
To: [log in to unmask]>Parkinson's Information Exchange Network
Sent: Wednesday, April 05, 2000 11:43 AM
Subject: Re: Re: My Dad was just diagnosed

Dan, 
 
Where is your father and where are you?  We have a reasonably active PD support group here in Madison.
 
Your question about Mirapex and l-dopa is a good one.   Most (many) neurologists feel that the longer one can hold off the use of l-dopa the better.  Mirapex is an agonist of dopamine.  It acts as dopamine (to which l-dopa is converted to in the brain.)  But it is supposedly less likely to cause dyskinesias 0-- which are random movements which are difficult to control (except by surgery).  If the Mirapex is helping a lot he should stay on it but if he has any significant problem with the drug he should consider adding l-dopa.  It sounds as though he is getting some reasonably good advice. 
 
Charlie
 
 
From: [log in to unmask]>Daniel Wachula
To: [log in to unmask]>[log in to unmask]
Sent: Tuesday, April 04, 2000 10:58 PM
Subject: My Dad was just diagnosed

My father was diagnosed about a week ago.  He is taking a drug called Mirapex.  I guess that this drug is about 2 years old.  He lives in Illinois and he needs to be active all the time - he worksout every other day.  My question is - does anybody have any information about this drug? and what about the drug called levodpa?  I have heard that l-dopa wears off after a few years which is why he is taking Mirapex?  Any comments will be great. 
 
Thanks for the newsletters on Web sites for PD.  My Dad does not have a computer so I need to gather as much information on this as I can. 
 
Thanks!
Dan in Wisconsin