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:
"Cleveland, Kyle E." <[log in to unmask]>
Reply To:
St. John's University Cerebral Palsy List
Date:
Mon, 25 Feb 2002 13:04:06 -0500
Content-Type:
text/plain
Parts/Attachments:
text/plain (24 lines)
Right!  Most folks don't have a category for it, so it must not be "real".
Same with fatigue.

I hate to "dis" my wife, Laura (especially here), but she never had pain
issues with her leukemia, so there's precious little patience and
understanding on that front.  No wonder people find themselves with no
alternative but "ending it."  You have a medical community that's too scared
to treat it and an at-large society that condemns the meds that relieve it.
Jenn knows what she's talking about, and her asshole doctors need to listen.

The Hippocratic Oath has become the Hypocritical Oath.

-Kyle

-----Original Message-----
From: Barber, Kenneth L. [mailto:[log in to unmask]]
Sent: Monday, February 25, 2002 12:56 PM
To: [log in to unmask]
Subject: Re: My Mom, my physiatrist in Ottawa


NO ONE UNDERSTANDS HOW MUCH DEALING WITH CONTINUOUS PAIN WILL TAKE out of a
person unless they have it to deal with themselves.

ATOM RSS1 RSS2