C-PALSY Archives

Cerebral Palsy List

C-PALSY@LISTSERV.ICORS.ORG

Options: Use Forum View

Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Betty Alfred <[log in to unmask]>
Reply To:
St. John's University Cerebral Palsy List
Date:
Mon, 5 Jun 2000 18:20:28 EDT
Content-Type:
text/plain
Parts/Attachments:
text/plain (14 lines)
I didn't really mean it like that.  I meant that parents of children who have
disabilities might be more inclined to answer parents of children with
disability questions (if that makes any sense).  I could be wrong in what I
said though.

In a message dated 06/05/2000 12:20:33 PM Eastern Daylight Time,
[log in to unmask] writes:

>       I would hope that a "sub-division" does not exist between adults
>  and parents. We are a community centered around a neuromuscular impairment.
>  I often wish my mother had had access to a similar list. I don't think she
>  ever talked to another parent with a CP child.
>

ATOM RSS1 RSS2