CFS           CORNER
Our main objective right now is to get the people with CFS/CFIDS (PWCs), the caretakers, and the
medical personnel to take the effort and time to really help us to gather the histories and common
areas needed to make this site work.  There are those who believe, at last, that finding the real
cause(s) is just around the corner.  It may well be, and we all pray they are right.  However, until that
time comes, including the time needed to develop and deliver the proper treatments, we must live
each day with this "DREADED DISEASE".  Each of you who assist will be supplying the
information that will save us all time, effort, discomfort, and even money in the future.

We hope and believe that we can put together valuable help for all of us by pooling information.  
There are many different stages of this disease and many different ways it affects us.  We believe that
we will be able to categorize this "monster" into helpful information,  We each have a limited amount of
time and energy, but we ask that you use whatever you can to help.

The information used in this site is based upon the 15 years plus that my wife and I have suffered
from CFS, along with tons of past and ongoing research.  Please ask your doctor to review
the site and give us his help.  The website is constantly being updated, changed, and edited
when needed and as often as we can possibly do it from the replies we are getting.  KEEP AN
EYE ON FLASH BULLETINS! As we will put things of major interest and importance there
until we have the time and strength to incorporate them into this site.

This is going to be a major task, and we may be asking for help from volunteers in the future.  If you
are interested in helping, please email us by going to "CONTACT US" and providing the
information for us to get in contact with you.  Otherwise, it is an anonymous communication..

We help define, communicate, and obtain anonymous information from people who
also suffer from CFS to give you the most useful site for CFS/ME.  It is updated
regularly and includes links to some of the other knowledgeable and well-done
websites.

If some of the colors we use on various pages, we have tried to set up
this site to be printer friendly to print to take to your doctor and pages
can be printed in black only (adjustment is required on color printers).

NOTE: Go to the "Website for more information" where you will find a
Yahoo search engine along with notes to help you better refine your
search in order to get the further information you want.  We have
updated our list to be one of the single best sources of infomation
anywhere.
The old cabin above represents the old country store where, in the
winter, everyone came to keep warm around the Franklin stove and
resolve all the problems of the world.  This site is designed for all of us
to sit around and solve the CFS/CFIDS/ME problems.  If no the problems,
ways to make us endure this dreaded illness with a little less pain and
difficulty.

Where as, the picture of the ship is entitled "Arrival".  It indicates our
fondest wish  that a cause(s) and cure(s) will be found soon, and our
ship will finally come home.
Copy write: 2004 - 2005
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Updated: 6/11/05

“Chronic Fatigue Syndrome” is a serious disease that can create damage to the
body, mind, muscles, etc.  At the least, it creates a Chronic Immune Dysfunction.  
We, a husband and wife who have been disabled by CFS for over 15 years, created
this site to share our experiences plus those of many others who have helped us by
responding to our site.  It includes research done on CFS/CFIDS/ME, possible
causes and treatments (pro and con), CFS management, some websites that we
recommend for additional research, and even miscellaneous medical highlights that
we should know. We have tried to make these pages printer friendly to enable you
to print something to discuss with your doctor.  Also, please ask your doctor to
review the website and give us his impute, help, and assistance.

We, the people with CFS/CFIDS/ME, must finally take a stand to help ourselves to
not only feel better, but to also have a QUALITY OF LIFE we can live with!  Too
many people, including doctors, have too many ideas about the cause(s),
treatments, and cure(s); so, we, who have CFS, MUST band together to share our
histories, treatments that have and have not worked, and our own ideas about
DREADED DISEASE.  We would also like to see doctors and other medical
personnel who believe in CFS to stand with us and give us their help and ideas.  We
can take a major step forward if everyone will help us to fully develop this website
with their information.  REMEMBER, THIS IS OUR WEBSITE, AND WE NEED
TO COLLECT ENOUGH HISTORY AND COMMON FACTORS TO FIND
TREATMENTS WHICH MIGHT WORK FOR US FOR A BETTER LIFE UNTIL
THE REAL CAUSE(S) AND CURE(S) ARE FOUND.  Please complete the
"QUESTIONNAIRE".  It is entirely anonymous, so please feel free to really open up.  You
may email us to give us your name and email address if you seek a reply from us.

Please read the rest of this home page before commenting.