 |
 |
In a message dated 97-08-29 03:31:30 EDT, you write: << <<errrrr... I guess I'm saying I don't trust his medical opinion when it comes to PD and me?> >> That is true and I might add I know even less than your neuro; I hadn't even learned what he has forgotten. We (my Barbara and I) have utmost confidence in our neuro who is a PD and movement disorder specialist; she knows about the vagaries of the new drugs coming onto the market, and WE discuss the merits of the treatment being prescribed. Moreover, she is the most caring MD we have been connected with. I would highly recommend you seek an expert opinion. Our individual anecdotal experiences are interesting but should not be the guide for medicalnor pharmaceutical practices. This coming Wed. we are to be re-evaluated for possible switch to Mirapex, although our neuro mentioned that dyskinesia may still be a problem. Good luck. Warmly Michel M.