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:
"Elizabeth H. Thiers" <[log in to unmask]>
Reply To:
St. John's University Cerebral Palsy List
Date:
Wed, 23 Jan 2002 08:29:59 -0500
Content-Type:
text/plain
Parts/Attachments:
text/plain (29 lines)
Anthony, you are so right.  It's got to be exhausting work though.  I'm of
the sort, I pay for it, give me my money's worth or I'm bitching.  My friend
is always trying to find care takers for her son, it's an ongoing battle and
they even get to do fun stuff as he needs just minimal assistance with
toileting and feeding, they get to go to fun places, heck, even I would love
to do some of that stuff.  (He mainly needs help because of mental
limitations).

beth the OT


Subject: Re: letter to agency


You have some very good points I have to keep in mind if this treatment
continues, I think that I should definitely go over to the Independent
Living Center to learn more about my rights.  My main problem is I'm
actually paying for this service myself with a trust fund I have, so if I'm
going to take money out of it I expect to get something reasonable back in
return.  But however if I was government funded, I would also expect this
too because the tax payers would be paying the bill, and they better also
receive something reasonable back in return too.  It's like if you hired
somebody to paint your house actually, most painters I know usually charge a
pretty penny, after paying that you expect to have the job done within a
reasonable amount of time.

Thanks,
Anthony

ATOM RSS1 RSS2