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These are good guidelines and the suggestions should be reviewed by
someone who is going to take the trouble to set up a new list.  Camilla
started the Caregiver's list, partially b/c (this is MY perspective)
 there was a sentiment on the list that PWP did not necessarily want to
discuss the issues surrounding the end stages of PD - and the
accompanying hardships of their caregivers.

To enforce these guidelines upon an existing list, to me, is the
equivalent of telling people "Shut up, you are boring me.  I want to talk
about what I think is important and your problems and opinions don't
matter."

More and more the tone of this list has become less hospitable and
inviting.  Perhaps it is time to have splinter groups or auxiliary lists.
 Please feel free to start one.

Sara
daughter of Richard, 79/28 yrs with PD


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