IMPORTANT NOTES FOR FIRST-TIME READERS
Select title in catalogue entry index to display summary details of article,
select title in summary to display full text of article
![[ Previous ]](../buttons/newblibrcatprevious.gif)
![[ Catalogue Index ]](../buttons/newblibrcatindex.gif)
![[ Next ]](../buttons/newblibrcatnext.gif)
- Title: Let's
Sleep With Our Nightmares and Follow Our Dreams
Also reproduced in Issue
No.8 - November 1997 of LINK-PIN.
Author(s): Sunny Roller, M.A.
Original Publication: Keynote speech given at the Atlanta
Post-Polio Conference, "Been There, Done That, Movin' On" in Atlanta Georgia,
September 12-14, 1997
Abstract/Extract:The title of our presentation today is "Let's
Sleep With Our Nightmares and Follow Our Dreams." Living with polio for 40,
50, or 60 plus years has filled each of our lives with a generous supply of
both nightmares and dreams. I believe that from time to time it is important
for us to reflect on our very private nightmares and dreams, if we are to
live an abundant and healthful life in the years ahead. As we take time consider
this dual challenge today, thinking about following our dreams or being led
by our hopes is one thing. We've been doing that successfully for years, but
sleeping with an array of nightmares - now that is quite another thing! How
could I suggest such a thing? Well, let's stop and contemplate. Maybe I shouldn't
ask, but have you ever slept with a nightmare? Well, I'll tell you a secret,
I've slept with a few horrible nightmares during the course of my adult life
and I highly recommend it. It can be liberating, rejuvenating and VERY good
for your mental health!
![[ Index ]](../buttons/rwindex.gif)
- Title: Polio
Survivors Abroad: Canadian Roulette, Rue Britannia
Author(s):
Dr. Richard Louis Bruno
Abstract/Extract: Over the past few years much heat has been
generated by suggested solutions to the difficult problem of reforming the
American health care system. A solution promoted by the Clintons', but despised
by their free-market Republican opponents, is a single-payer health care system
very much like the ones in Canada and Great Britain. Such systems, where treatment
is paid for by the government, provide medical care to all citizens regardless
of their ability to pay. Or do they?
![[ Index ]](../buttons/rwindex.gif)
- Title: POST-POLIO
SEQUELAE AND THE PARADIGMS OF THE 50's:
Newtie, Ozzie and Harriet versus Paradigms of Caring and a Future for Rehabilitation
in America
Author(s): Richard L. Bruno,
Ph.D.
Original Publication: Presentation: The 45th annual John
Stanley Coulter Memorial Lecture presented to the American Congress of Rehabilitation
Medicine, Alexandria, Virginia, June 24, 1995
Archive: Archives of Physical Medicine and Rehabilitation, 76 (12): 1093-1096.
Abstract/Extract: We find ourselves at an extremely interesting
and extremely extreme point in our nation's history. The pendulum of what
American's believe government should do has swung all the way from FDR's New
Deal, gaining momentum as it flew past LBJ's Great Society to hit Bill Clinton
squarely between the eyes. In listening to the political rhetoric since last
year's Republican coup, I believe that not only have the times changed but
also that time itself has changed. I have the feeling it is not June 24, 1995.
It feels to me as if the clock has been turned back exactly forty years. So,
put on your poodle skirts, slick back your D.A. and let's return to those
thrilling days of yesteryear so we can view the childhood and adolescence
of rehabilitation through the eyes of those who have grown up with it: the
survivors of America's polio epidemics. Let's see what lessons have been learned,
now that both the polio poster children and rehabilitation have reached mid-life,
and ask this most important question: Given the current ideological timewarp,
will polio survivors - will rehabilitation itself - have any future at all,
let alone enjoy their golden years?
![[ Index ]](../buttons/rwindex.gif)
- Title: POST-POLIO
SYNDROME: WHERE DO WE GO FROM HERE?
Author(s):
Mary T. Westbrook, PhD
Original Publication: Paper presented at the final plenary
session of the Australian International Post-Polio Conference, Sydney, November,
1996
Abstract/Extract: One overwhelming impression I have from
the conference is that we polios are opening up with each other in ways that
did not happen in the early days of our support groups. We are acknowledging
that dealing with PPS is difficult. We still too frequently downplay our problems
and criticise ourselves for not coping more effectively. As one participant
said, we need to learn to ask for help and to say 'No' to demands that overtax
us. One of the main messages of this conference has been that we need to be
caring of ourselves and that we can gain much through mutual friendship and
support.
![[ Index ]](../buttons/rwindex.gif)
![[ Previous ]](../buttons/newblibrcatprevious.gif)
![[ Catalogue Index ]](../buttons/newblibrcatindex.gif)
![[ Next ]](../buttons/newblibrcatnext.gif)
It is the intention of the Lincolnshire Post-Polio Network to make
all the information we collect available regardless of our views as to it's
content. The inclusion of a document in this library should not therefore be
in any way interpreted as an endorsement.
People who had polio and are experiencing new symptoms need to be assessed
by medical professionals who are experienced in Post-Polio to determine what
is wrong and to give correct advice. We can only make these documents available
to you. YOU must then take what you believe to be relevant
to the medical professional you are seeing. We are collecting and collating
everything we can to enable medical professionals to make informed decisions.
Other medical conditions must be looked for first, Post-Polio Syndrome is by
diagnosis of exclusion.
Whether you are a Polio Survivor, a friend or relation of a Polio Survivor,
or a Medical Professional, we would advise you use this catalogue only to assist
in determining your reading priorities. Every article in this library
is likely to contain information of interest to both Polio Survivors
and Medical Professionals.
![[ Index ]](../buttons/rwindex.gif)
![[ Reception ]](../buttons/newbrecpt.gif)
![[ Library ]](../buttons/newblibr.gif)
![[ Networking ]](../buttons/newbnetw.gif)
![[ Directory ]](../buttons/newbdir.gif)
![[ What's New? ]](../buttons/newbwn.gif)
The Lincolnshire Post-Polio
Network
Registered Charity No. 1064177
An Information Service for Polio Survivors and Medical Professionals
The Lincolnshire Post-Polio Network takes great care in the
transcription of all information that appears at this site. However, we do not
accept liability for any damage resulting directly or otherwise from any errors
introduced in the transcription. Neither do we accept liability for any damage
resulting directly or otherwise from the information available at this site.
The opinions expressed in the documents available at this site are those of
the individual authors and do not necessarily constitute endorsement or approval
by the Lincolnshire Post-Polio Network.
© Copyright The Lincolnshire Post-Polio Network 1997 1998
1999 2000 2001 2002
Document preparation: Chris Salter, Original
Think-tank, Cornwall, United Kingdom.
Primary Document Reference: <URL:http://www.ott.zynet.co.uk/polio/lincolnshire/library/cc_3.html>
Secondary Document Reference: <URL:http://www.zynet.co.uk/ott/polio/lincolnshire/library/cc_3.html>
Last modification: 7th January 2002
Last information content change: 29th February 2000