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 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.

ClinicalTrials.gov Linking patients to medical research.

Federal Register; 1995, 1996, 1997 and 1998.

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

MedSpecNet Canadian medical affiliates.

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).

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).

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.



Advocacy Sites


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.

CFS Information Sites


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

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.

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

ME Chat Page

Invisible Disabilities - Chronic Fatigue Syndrome

Pat McClendon's Clinic

Health Information Station

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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