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Since February 22, we have had 146 new members join us. Many of them, and many others who have not joined us (yet), are requesting information on pallidotomy. I have replied to them, mostly suggesting they read the archives of the list. Since there is a wide variety of opinions on the subject of pallidotomy (our one and only flame war!) and since my only qualification re Parkinson's is that I have it, I would appreciate it if two or three members of the list would volunteer to send these people the information which has been posted to the list. I think it would be most helpful if these people got as wide a sample of opinions as possible so they, along with their doctors, can make a more educated decision about the surgery. Another thing most of them are requesting is a copy of David Devor's message. So....any volunteers?? Please let me know if you are able and willing to take this on. Barb