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Well said Dennis. It is a great mystery and a huge concern for most PWP-- when will I/they be "hit" by dyskinesias? Now that we have so many other sorts of medications there is no longer the need to rely so heavily on levodopa alone - and this is most encouraging - especially for the newly diagnosed. But how do we tell people (ie. those who do not have access to this List..) about these options? That's what worries me. Joy Graham