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Support group meetings. I take reams of info from this list to share with my Y.O. group. I also keep the Parkinson office supplied with articles about research, new meds, etc., so they can be published in our news letter. Anything to keep the awareness ball rolling. :) Judith [log in to unmask] At 01:21 am 04/11/97 -0500, Bob & Joy Graham wrote: >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 > >