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Right on!


>From: rayilynlee <[log in to unmask]>
>Reply-To: Parkinson's Information Exchange Network
><[log in to unmask]>
>To: [log in to unmask]
>Subject: Invisibility
>Date: Wed, 1 Feb 2006 12:10:40 -0700
>
>We are not only invisible to our government, but to our fellow citizens.
>
>Although millions are afflicted by incurable diseases and conditions,
>millions are not, and for most people it has to happen to them to pay
>attention.  They quite naturally don't think it will happen to them and are
>busy living their lives.  Things would be different if EVERYONE got PD or
>Huntington's disease.
>
>Ask yourself, how interested were you before PD?  When I was young I
>volunteered in a spinal cord injury ward, but didn't last long because it
>was so depressing and hopeless.
>
>Advocacy is left mainly to patients and/or their CGs.  It is very difficult
>to fight a disease and politicians and their supporters who oppose
>research.  When people were protesting IVF, blood transfusions, organ
>transplants, etc. the government was not opposing it, as I recall.
>
>I have pretty much accepted the fact that there will be no progress in my
>lifetime.  Being a teacher and student of history has taught me that life
>is terribly unfair.  My  philosophy (my minor) is simple:  we should do all
>we can to change that injustice.
>
>Before the lights go out,
>
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>Ray

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