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Links to Other
CFS Sites


Pages by Government agencies
CFS Organisations
Advocacy Sites
CFS Information Sites
CFS Sites on the Web
Need a CFS Specialist?After tons of emails asking for CFS specialists all over the world...I'm starting to compile a list of site that will offer many choices for CFS Specialists everywhere

Pages by Government Agencies and Central Authorities

American Association for Chronic Fatigue Syndrome

ATSDR Agency for Toxic Substances and Disease Registry, Public Health Assessments. ATSDR, is an agency of the U.S. Public Health Service. It was established by Congress in 1980 under the Comprehensive Environmental Response, Compensation, and Liability Act, also known as the Superfund law. This law set up a fund to identify and clean up our country's hazardous waste sites. The Environmental Protection Agency, EPA, and the individual states regulate the investigation and clean up of the sites.

American College of Physicians (ACP).

AHA Central Office. This site is an integral extension of the AHA's Central Office on ICD-9-CM.

AHAData.com provides comprehensive healthcare data online.

American Medical Association.

American Psychiatric Association.

American Psychological Association.

Chronic Fatigue Syndrome Information Page has been put together by the National Institute of Allergies and Infectios Diseases. It is a good overview of the illnesses and current theories about its cause.

A CFS page has been set up by the Centre for Disease Control (CDC), with sufficent information on who gets CFS, popular treatments, ideas on its cause and more.

Canadian Institute for Health Information.

Canadian Medical Association Online (CMA).

CDC CFS Home Page.

CDC Home Page Center for Disease Control and the CDC WONDER, which provides a single point of access to a variety of CDC reports, guidelines, and even numeric public health data.

Central Office on ICD-9-CM The International Classification of Diseases, Ninth Revision, Clinical Modification, ICD-9-CM, is a classification system that groups related disease entities and procedures for the reporting of statistical information. The clinical modification of the ICD-9 was developed by the National Center for Health Statistics for use in the United States.

CFSCC (DHHS CFS Coordinating Committee) Web site.

ClinicalTrials.gov Linking patients to medical research.

CRISP Database. CRISP (Computer Retrieval of Information on Scientific Projects) is a searchable database of federally funded biomedical research projects conducted at universities, hospitals, and other research institutions.

Dept. of Labor (U.S.) line to the ERISA Act Employee Retirement Income Security Act (ERISA), (29 USC §1001 et seq., 29 CFR 2509 et seq.). ERISA is the keystone of U.S. federal legislation concerning employer-provided health and welfare plans (pensions, health and disability insurance, etc.), and is administered jointly by the U.S. Dept. of Labor and the U.S. Internal Revenue Service.

FedStats More than 70 agencies in the United States Federal Government produce statistics of interest to the public. The Federal Interagency Council on Statistical Policy maintains this site to provide easy access to the full range of statistics and information produced by these agencies for public use.

Federal Register; 1995, 1996, 1997 and 1998.

Food and Drug Administration, with pages on Nonprescription Medicines: What's Right for You?

Health Canada Online.

Health Canada Laboratory Centre for Disease Control

MedSpecNet Canadian medical affiliates.

MigDB - The Mitochondria Interest Group.

National Center for Health Statistics (NCHS) (USA) and the International Classification of Diseases, 9th Revision, Clinical Modification (ICD-9-CM)

NIAID (USA). National Institute of Allergy and Infectious Diseases Home Page, has produced several fact sheets and brochures on CFS.

NIDCD National Institute on Deafness and Other Communication Disorders Webpage (part of NIH, USA).

NIH National Institutes of Health (USA)

NIH Special Interests Groups - Epidemiology & Clinical Trials Interest Group (USA).

NIH Clinical Research Studies: Search and Browse Page (USA). Search the collection of research studies being conducted at the NIH Clinical Center by: entering the diagnosis, sign, symptom, or other key words or phrases; or browse by institute of primary investigator or primary disease category.

Overview of NIAID Chronic Fatigue Research Program

Projekt ICD 10.

RCPSC Royal College of Physicians and Surgeons of Canada.

Social Security Online (USA) has a factsheet on Providing Medical Evidence to the Social Security Administration for Individuals with Chronic Fatigue Syndrome; a Guide for Health Professionals.

The CFIDS Association of America

U.S. National Library of Medicine (NLM).

World Health Organization

CFS Organizations

The Worldwide Electronic CFIDS/ME Action Network (WECAN).

The American Association for Chronic Fatigue Syndrome (AACFS) is a non-profit organization of research scientists, physicians, licensed medical healthcare professionals, and other individuals and institutions interested in promoting the stimulation, coordination, and exchange of ideas for CFS research and patient care as well as periodic reviews of current clinical, research and treatment ideas on CFS for the benefit of CFS patients and others.

AYME is the Associtation for Youth with Myalgic Encephalomyelitis, based in England.

The CFIDS Association of America is the nation's leading charitable organization dedicated to conquering chronic fatigue and immune dysfunction syndrome (CFIDS).

The National CFIDS Foundation, Inc. in America was founded in February 1997 by two 14 year activists of the CFIDS movement. The goals of the Foundation are to help fund medical research to expedite a treatment and eventual cure, to provide information, education, and support to those people who have CFIDS and related illnesses including FMS, GWS, and MCS.

Two Australian links: The Northern Rivers ME/CFS Society web page, with details of supports groups in northern NSW and southern Queensland; and the ME Society of NSW has a web page, with info on becoming a member and services available.

MPWC Is Medical Professionals With CFS. This group was formed in 1993 by Gail Dahlen and Meghan Shannon to give MPWC's an opportunity to coordinate their efforts, support each other, and make a difference for all PWC's.

RESCIND ("Repeal Existing Stereotypes about Chronic, Immunological and Neurological Diseases"), Inc. is a non- profit 501(c) 3 corporation. RESCIND's primary goal is to change the name "CFS" to something more accurate and less pejorative.

The Chronic Syndrome Support Association, Inc. is a 501(c)3 non-profit corporation. It was founded in order to educate the general population and health-care professionals who lack current knowledge of the research being done, and potential research that needs to be done,Ê on these serious, yet invisible, conditions [CFS and others].Ê It is our goal to promote awareness of these conditions, and in the process we hope to contribute to the growing body of knowledge about them.

Mediconsult Another great resources for CFS Sufferers.



Advocacy Sites


Listening to CFIDS: Works by PWCs and others who care has, among other things, a postcard utility where you can spread CFS awarness by sending postcards to others on the net.

The Memoriam Site for PWCs is a list of CFS sufferers of all ages. Add yourself or a sick friend and help remind everyone of the pervasiveness of this disease - both sexes, all ages.

WECAN has got a special May 12, 1998 CFS Awareness Day site going, with details of the Washington Rally and people's efforts from around the world.

B.R.A.M.E., Blue Ribbon Awareness for ME.

CFS Information Sites


Jaime has compiled and categorised many CFIDS-related sites at the Chronic Fatigue Syndrome Info Source .

The CAMEO Survey needs PWCs to fill out its questionnaire so accurate information on the symptomology of CFS can be gathered.

Moira Smith's Canberra Fibromyalgia and Chronic Fatigue Syndrome Page contains information on how to find Aus/NZ support groups, how to join various mailing lists and newsgroups, and a huge collection of links to useful websites all over the world where people can find information on the symptoms and management of FM, CFS and all the rest. It also contains four fairly long book extracts on how to manage your FM or CFS; the text of an excellent booklet from the ACT ME-CFS Society on Coping with CFS; factual articles about what CFS and FM are; six personal stories; a page of links to articles by people like Cheney and Lapp, including stuff about managing the illnesses and their symptoms; plus a page of links to articles on chronic pain management.

Gossamer's CFS page has an Open Letter to non CFS Sufferers, where the problems and thoughts of people with CFS are explained.

Jenn Munn's extensive CFIDS Site contains information on research, recent media mentions of CFS, and her own experiences.

Mary Schweitzer has written an article explaining why the CFS community hates the 'F Word' - Fatigue - so much. Read about it here.

From the M.E. & F.M. Manual are Charts showing the differences between ME and depression, the difference between ME and FM, effects and recovery rates, and the percentage of people able to return to work full- or part-time.

Abstracts presented at the Sydney 1998 CFS Conference show strong support for the case of CFS as a physical illness, and some interesting information on possible causes.

Robyn's CFS Index is one of the premier CFS web pages, having won both an A-List and Featured Page award from Geocities. Her NMH page is one of the biggest Neurally Mediated Hypotension information sites available on the web.

Ted Shaw's CFS Pages include a database of 1100 papers on CFS with abstracts categorised into 58 topics.

"Somebody help M.E." is an easily read, comprehensive book about living with CFS/ME. Written for young people with CFS and their families, information about it can be found at the AYME (Associtation for Youth with Myalgic Encaphalomyelitis) web page.

CFS Sites on the Web
Chronic Fatigue Syndrome FAQ

Chronic Fatigue Links on the Internet

Chronic Fatigue Syndrome

CFS Home Page

ME/CFS Links

CFS/ME Information - New Site by Roger Burns

CFS/CFIDS/ME/... Reference Guide© v1.2

CFS Hot List

The Nightengale Research Foundation - The reseach Foundation founded by Dr. Hyde. This organization is also in Ottawa, Ontario, Canada but Dr. Hyde travels all over the world and has given many many TV and radio shows on CFS/ME

ME Chat Page

Welcome to Alex Chapman's Link Page

ME/CFS Society

The Cheney Clinic Information Services

MJC Online

Chroniclllnet Home

Invisible Disabilities - Chronic Fatigue Syndrome

Dr. Roger G. Mazlen, MD

Pat McClendon's Clinic

The Mining Company

PWC's Address Book

Health Information Station

Need a CFS Specialist? Then the CoCure Organization is one source that may help. It has doctors by country, state/province and town/city.

Co-Cure Good CFS Doctors

If you know of any links that offer information on CFS Specialists anywhere, please email me and I'll add a link. Thanks!!

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