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Dale Severance said in part: > 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. I think a website listing the support groups in the US is an excellent idea. What good is your list if it isn't made available to pwp or those who work with and care for pwp? I can think of no reason why a support group would not want this exposure unless the group leader indicated a need for privacy when sending you the data. Does the database list the place/date/leader of each group? Jeanette Fuhr