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Carole Hercun wrote: > Hi Paul: I am amazed at the paucity of information > available in the average neuro's office, even in the > medical centers like Johns Hopkins and St.Elizabeth's. The > wonderful resource that is this List was only discovered by > me (and I'm sure by others)by accident. So please don't > shut up. Suggestions, anyone? The neuro's office is not a library, meaning that it's no place to get information unless it comes directly from the neuro himself. The neuro's office is for treatment! Public libraries, organizations like the NPF (National Parkinson Foundation), APDA (American Parkinson Disease Association), etc. can give you mounts of information about the disease and various support groups. This list is but a tiny fraction of the PWP population and it is fraught with misinformation as well as correct information, and it is often difficult for an untrained person to differentiate. Thus, do not accept anything stated here unless properly verified or corroborated because the wrong information may be hazardous to your health. Michel Margosis 'Carpe Diem'