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I have been taking 1mg permax per day since diagnosis a year ago last May. I have had no problems since I finished titrating. The reason my MDS suggested permax is it doesn't seem to have the sudden sleep attack problems some of the others do. It has worked very well for me. I began having symptoms in late 1997 or early 1998, finally went to a neuro in May 2000, who diagnosed ET. Changed to an MDS is May 2001 who diagnosed PD. No apparent progression since that time (touch wood). PJ -----Original Message----- From: Parkinson's Information Exchange Network [mailto:[log in to unmask]]On Behalf Of Carol Gray Sent: Thursday, October 10, 2002 8:15 AM To: [log in to unmask] Subject: Re: Drug prices I would like to hear more from those of you who are taking permax, I am taking 3 mg. per day and I asked my neuro if I could change to another similar medication and he said no! carol gray ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn