- for research into Myalgiac Encephalopathy / Chronic Fatigue Syndrome. Here is the best collection of research and medical information about CFS/ME/CFIDS available on the internet. This collection is always being updated.
-This is the place to begin your web search for information concerning Chronic Fatigue Immune Dysfuntion Syndrome, Myalgic Encephalomyelitis, Chronic Fatigue Syndrome..or whatever you'd like to call it. There are information links here to sites around the globe.. from research archives to personal web pages where the voices of those who suffer are presented for the entire world to hear. This site belongs to my deal friend Mary Schweitzer, Ph.D.. who is herself another survivor of what we call the Da** Disease (DD).
The CFIDS Report provides a credible, cutting edge news and commentary on CFIDS. This site stands out by showing editorial discretion in their choice of content, giving those with CFIDS a trustworthy site they can confidently refer skeptical family and friends.
-CINDA (Chronic Immunological and Neurological Diseases Association) Inc.; for Public Relations; marketing, development and information, regarding "invisible" diseases such as CFIDS, FMS, GWS, MCS and more.
- Professionally Selected & Edited Information on ME/CFS. On this site you'll find more than 4000 files on CFS/FM and overlapping syndromes. The files are organized in 90 main sections.
Welcome to Our FM/CFS World, Inc and Our FM-CFIDS WORLD Organization .Our FM/CFS World Inc. is a non-profit organization maintained by sufferers of Fibromyalgia and Chronic Fatigue Immune Deficiency Syndrome. Our Mission is to improve the quality of life for fellow sufferers, while increasing public, governmental and medical awareness of these diseases.
-I have created this web page to provide an extensive resource of information on FM, CFS and other related conditions. I am constantly researching and adding additional information on these related conditions as well as adding additional links.
- Womens Web Construction Company has provided this site as a place where the voices of those stricken with the Da** Disease are brought together and are presented for the world to look in on. This is the personal side of this chronic illness of many names. Come, look around.. share in our joys as well as our sorrows.. and come away enriched by the experience.
- CFIDSer's(Cfids Emergency Relief Services) Inc. is a non-profit organization that aids people with ME/CFS/CFIDS during times of financial crisis.
Marilyn J. Kerr RN
- At this web site, you will find information on "Myalgic Encephalomyelitis" (ME) / "Chronic Fatigue Syndrome" (CFS) / "Chronic Fatigue and Immune Dysfunction Syndrome" (CFIDS).
Search the ME-NET and CO-CURE databases:
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"The National ME/FM Action Network is a registered, charitable, non-profit organization dealing with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and Fibromyalgia (ME/FM)--offering support, advocacy, education and research into the many, varied, anomalies connected with these illnesses. We work hand in hand with the General Public, Educators, Government Agencies, and the ME/FM Community to achieve these goals that are so important to sufferers under duress everywhere. Enjoy your visit, and please contact us if we can be of any further help!"
Offering support, news and research information.
-from About.com .
- The name "Co-Cure" stands for "Cooperate and Communicate for a Cure for CFS & FMS."
-A very informative site.
A guide for parents of chronically ill children who are mistakenly told their children are just lazy.
Information from Australia for people with Myalgic Encephalopathy: Fibromyalgia, Chronic Fatigue Syndrome, Myalgic Encephalomyelitis etc., and Chronic Pain.
-A happy place to visit.
![[LOGO]](wecan.gif)
In May of 1996, Mary Schweitzer had a vision of an
online activist organization made up of People With CFIDS, (PWC's). With
the backing and support of many other PWC's on internet
mailing lists and newsgroups, WECAN came into existence on June 1, 1996.
WECAN has grown to over 220 members working on committees to help with
insurance, government, public relations, research
compilation and media issues regarding CFIDS. Although, the media and the
U.S. Centers for Disease Control use the term CFS, or
Chronic Fatigue Syndrome when referring to our disease, we voted for the
names more prevalent within the CFIDS/M.E./FMS community
itself. CFIDS, or Chronic Fatigue and Immune Dysfunction Syndrome, is the
acronym chosen by the U.S. Congress when referring to the
disease; M.E., or Myalgic Encephalomyelitis, is the name by which this
disease has been known in the U.K. and Canada for many years;
FMS is Fibromyalgia Syndrome, an illness very similar to CFIDS.
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The primary mission of the Center for Complex Infectious Diseases is to determine the nature, origin, disease associations, modes of transmission, methods of diagnosis and responses to therapy of complex infectious diseases, and to disseminate such information. CCID is currently specializing in the detection and characterization of viruses which have undergone a "stealth" adaptation to avoid elimination by the immune system.
Remedyfind is a non-commercial, non-sponsored, patient owned site that allows individuals and healthcare professionals to rate the effectiveness of the treatments they have used for specific illnesses.
-NACPAC is a self-help organization dedicated to providing support to people in chronic pain, and to giving them assistance in living their lives to the fullest.
-An Internet Health Resource Database and Index
- ChronicIllnet is the first multimedia information source on the Internet dedicated to chronic illnesses including AIDS, cancer, Persian Gulf War Syndrome, autoimmune diseases, Chronic Fatigue Syndrome, heart disease and neurological diseases.
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e-mail lists index that includes some subscription information.
-A mailing list support group for Canadians with Fibromyalgia and/or Myalgic Encephalomyelitis.
-The About.com Index of internet mailing lists relating to Fibromyalgia and CFS/CFIDS/ME.
*My Print Materials Reference List*
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this page last modified
November, 2002 