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The current theme of the list appars to revolve around concepts of information sharing and privacy to the group. As many of you know I have bilt a database of pD support groups in the US. The number of listings various from 1850 to 1950. I agreed with my self to make this information available to anyone with a reasonable PD need. I was planing to place the database on a web site for easy access to all. What are your thoughts on this matter. Dale Severance [log in to unmask]