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Chronic Fatigue Syndrome: more books (104)

Chronic Fatigue Syndrome: An Integrative Approach to Evaluation and Treatment by Mark A. Demitrack, 1999-05-01
Kicking: Chronic Fatigue Syndrome and Fibromyalgia - A Step-by-Step Plan to Restore Your Health and Vitality by Debra Dimas, 2010-06-14
The Night-Side: Chronic Fatigue Syndrome & The Illness Experience by Floyd Skloot, 1996-09
Treating & Beating Fibromyalgia and Chronic Fatigue Syndrome: a step-by-step program proven to help you get well again! by Rodger H. Murphree, 2006-10-31
How to Reverse Immune Dysfunction: A Nutrition Manual for HIV, Chronic Fatigue Syndrome, Candidiasis And Other Immune Related Conditions by Mark Konlee, 1996-07
50 Things You Should Know About the Chronic Fatigue Syndrome Epidemic by Neenyah Ostrom, 1993-02-15
Understanding Chronic Fatigue Syndrome: Better Ways of Managing Your Lifestyle by Dr. Alastair Jackson, 2001-04-01
Chronic Fatigue Syndrome: A Biological Approach
Chronic Fatigue Syndrome (The Facts) by Frankie Campling, Michael Sharpe, 2008-09-15
Chronic Fatigue Syndrome: A Comprehensive Guide to Effective Treatment ("the Natural Way" Series) by Gill Jacobs, 1998-04
Chronic Fatigue Syndrome: Advances in Epidemiologic, Clinical, and Basic Science Research by Roberto Patarca Montero, Roberto Patarca-Montero, 2000-05-17
Chronic Fatigue Syndrome and the Body's Immune Defense System (Haworth Research Series on Malaise, Fatigue, and Debilitation) by Roberto Patarca Montero, 2002-10-08
Clinical Management of Chronic Fatigue Syndrome: Clinical Conference, American Association of Chronic Fatigue Syndrome by Nancy Klimas, 1996-04-16
Chronic Fatigue Syndrome, Genes, and Infection: The Eta-1/Op Paradigm by Roberto Patarca-Montero, 2003-10-15

lists with details

Waterloo Wellington Myalgic Encephalomyelitis Association
Canadian registered charity offering coping and self-help strategies, and help with finding a physician.
http://www.wwmea.ca/

Extractions: The Waterloo Wellington Myalgic Encephalomyelitis Association (WWMEA) is a registered charitable organization (not-for-profit) that provides support group meetings and information for those affected by M.E. (Myalgic Encephalomyelitis). M.E. is a painful, chronic, debilitating illness that affects many bodily systems. The WWMEA operates in Southwestern Ontario within Wellington County and the Region of Waterloo serving cities such as Cambridge, Guelph, Kitchener and Waterloo (KW). This area is also referred to as the Golden Triangle of Ontario as well as Canada's Technology Triangle. The WWMEA relies on membership fees and donations to cover operating expenses. Charitable Tax Receipts will be issued for donations from within Canada. Funds are also raised through the Zehrs Save-A-Tape Program of Zehrs Supermarkets.
CFIDS
Symptoms. Although its name trivializes the illness as little more than mere tiredness, chronic fatigue syndrome (CFS), also known as chronic fatigue and immune dysfunction
http://www.cfids.org/about-cfids/symptoms.asp
Chronic Fatigue Syndrome | HealthyWomen
What is it?DiagnosisTreatmentPreventionFacts to KnowQuestions to AskKey Q AOrganizations and SupportWhat is it?OverviewWhat Is It?Chronic fatigue syndrome is an illness
http://www.healthywomen.org/condition/chronic-fatigue-syndrome

Extractions: @import "/sites/all/modules/contrib/print/css/printlinks.css"; @import "/modules/comment/comment.css"; @import "/sites/all/modules/contrib/fivestar/widgets/hw/hw.css"; @import "/sites/all/themes/healthywomen/css/reset.css"; @import "/sites/all/themes/healthywomen/css/default.css"; @import "/sites/all/themes/healthywomen/css/healthywomen.css"; Search Like This Article? Click to rate Chronic fatigue syndrome is an illness characterized by prolonged, debilitating fatigue severe enough to affect one or more aspects of a person's life. It is also characterized by multiple nonspecific symptoms such as headaches, recurrent sore throats, muscle and joint pains, memory and concentration difficulties.
FM-CFS Canada, Splash Page, Welcome To A World Of Information
National registered-charity that provides guides for doctors and pharmacists, nursing, assessment and treatment of patients, and guidelines for support groups.
http://fm-cfs.ca

Extractions: "...this disease cleans you out, it takes everything from you that was normal...sometimes I don`t get downstairs at all... when you (overdo and) go backwards, you really really go backwards fast and disastrously, and it can be many many years before you get better...we can`t hold marches on Washington..."
PANDORA, Fibromyalgia, FMS, Chronic Fatigue, CFS, CFIDS
American patient advocacy group for CFS and other neuroendocrineimmune disorders. Provides scientific articles, support and educational resources, newsletters.
http://www.pandoranet.info

Extractions: WWW www.pandoranet.info WELCOME TO THE WEB SITE OF P.A.N.D.O.R.A.! IT IS OFFICIAL! We did because of you! P.A.N.D.O.R.A. wins a $20K grant from Chase Community Giving. Our final ranking was with votes. Click here! to go to the winning page. ONE VOICE, ONE COMMUNITY, ONE OUR MISSION IS... We are in our neuroendocrineimmune community. We are lending our voice to create awareness of the plight of individuals suffering with neuroendocrineimmune disorders. Our mission is to address and alleviate many of the issues that affect the quality of life of persons who are diagnosed with chronic fatigue syndrome (CFS) , (also known as chronic fatigue immune deficiency syndrome (CFIDS) in the U.S., and abroad also known as M.E. or ME;
ME Association Of Ontario
Canadian charity that offers info, tips, and support to those coping with CFS and related illnesses, including youth and parents.
http://www.meao-cfs.on.ca/
Massachusetts CFIDS/ME & FM Association - Home
Articles on diagnosis, coping, advocacy, treatment, and disability. Assists patients with referrals to health care providers and gives guidance on disability issues.
http://www.masscfids.org/

Extractions: Go to the video... Advocacy Alert! Advocacy Alert – CDC needs to hear from CFS/CFIDS/ME professionals and activists Dr. Fred Friedberg, the president of the International Association for CFS/ME ( IACFS/ME ), urges for letters to be written to the Centers for Disease Control ( CDC) by CFS/CFIDS/ME professionals and patient-oriented activists regarding the selection of a new Chief of the Chronic Viral Diseases Branch. The CDC had posted an opening for this position, which closed on September 17, and is now in the process of reviewing applications. This is a very important development, particularly in how it may affect the direction of CFS /CFIDS/ME research, and an opportune time to make our voices heard on this and other critical issues. Letters should be addressed to Dr. Stephan Monroe with copies sent to Dr. Thomas Frieden. Please review and use Dr. Friedberg’s announcement as a guideline for your letters which appears on the home page for the
ME Research UK — Home
National charity that funds scientific investigation into causes and treatment. Offers educational literature, reports of conferences and workshops, and a bi-annual magazine.
http://www.meresearch.org.uk/

Extractions: Welcome to ME Research UK, a national charity funding biomedical research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (also known as ME CFS ME Research UK celebrated its tenth anniversary this year, and we celebrated the event with lunch together at Murrayshall House Hotel. A newly published study from the University of Dundee looking at biochemical abnormalities in children with ME CFS See also media coverage Our new collection of Christmas cards for 2010 is available to order now. Have a look through the designs and print off a form to place your order. Our article in The Herald newspaper calls for an ME/CFS Centre of Excellence in Scotland The latest update of our database is now available, containing over 3,000 research publications on
The Connecticut CFIDS & FM Association Home
Provides email and telephone support, online library of medical articles, and quarterly newsletter.
http://www.ct-cfids-fm.org
Home - The Hummingbirds' Foundation For M.E.
Provides an overview of known medical facts, diagnosis and basic treatment, comprehensive symptom list, research and advocacy information, and a monthly newsletter
http://www.hfme.org/
Sussex & Kent ME/CFS Society | Main
UK registered charity offering support through newsletters, meetings, and telephone contacts to patients in East Sussex, West Sussex, and Kent.
http://www.measussex.org.uk/
ME/CFS Australia
Nationwide non-profit with resources on diagnosis, possible causes, symptoms, treatment and management. Also helps patients to find a local support group.
http://www.mecfs.org.au/

Extractions: Diagnostic Criteria Resources About ME/CFS Latest News Donate Now Resources Critical resources for people with ME/CFS include the diagnostic guidelines for medical practitioners and fact sheets to support people managing ME/CFS; available in ten languages. ME/CFS Fact Sheets Documents for Medical Practitioners Information in Other Languages Research Research into ME/CFS is occuring across the globe. Follow the links below for research resources. Alison Hunter Memorial Foundation Australian Research Institutions International Research Institutions Latest Research Articles
Association Of Young People With ME - AYME - ME/CFS Charity
Includes phone helpline, assistance with study problems, and guide to request a disabled students allowance. A UK-based charity.
http://www.ayme.org.uk/
National ME/FM Action Network > Home
Includes a quarterly newsletter, online library of articles, list of support groups, and discusses active projects. A Canadian registered charity.
http://www.mefmaction.net
CFIDS
Articles written by medical and research professionals.
http://www.cfids.org/archives/research-review-issues.asp
The CFS Report
News and commentary for the CFS Community. Covers recent research articles and press releases.
http://www.cfidsreport.com
CFS Research Foundation
UK charity that funds investigation towards diagnosis and treatments. Provides list of ongoing projects and published articles.
http://www.cfsrf.com/
Myalgic Encephalomyelitis G93.3 Post-viral Fatigue Syndrome : "Benign Myalgic En
Contains Canadian clinical working case definition, diagnostic and treatment protocols, and pediatric criteria for ME.
http://myalgic-encephalomyelitis.com/

Extractions: Chronic Fatigue Syndrome - CFS This site was created in response to the continued marginalization of people suffering from Benign Myalgic Encephalomyelitis, also incorrectly referred to as Chronic Fatigue Syndrome , Chronic Fatigue Immune Dysfunction Syndrome, Myalgic Encephalopathy and many others. For those looking for Fibromyalgia try this link Fibro Down Under ME is not CFS this is the current CDC position . The paragraph below is from the 'Overview of CFS', a part of the CME course offered on the CDC web site(http://www.cdc.gov/cfs/cme/wb1032/chapter1/overview.html). "Various terms are incorrectly used interchangeably with CFS. CFS has an internationally accepted case definition that is used in research and clinical settings. The name chronic fatigue and immune dysfunction syndrome (CFIDS) was introduced soon after CFS was defined; there is no case definition for CFIDS, and the name implies an understanding about the pathophysiology of CFS that is not fully supported in the medical literature. The name myalgic encephalomyelitis (ME) was coined in the 1950s to clarify well-documented outbreaks of disease; however, ME is accompanied by neurologic and muscular signs and has a case definition distinct from that of CFS.
The National M.E. Centre - Caring For People With CFS / ME
Provides help, care and support to patients and their families in the United Kingdom.
http://www.nmec.org.uk/

Extractions: Home The ME Centre What is M.E? Contact Us ... Useful Links Esther Rantzen has long been a campaigner and advocate for the "underdog". From her early days in radio to her rise in the world of television, she has never been afraid to question authority. She has always shown great empathy when tackling sensitive issues such as organ donation, stillbirth, drug abuse and more recently, her very important and public campaign on child abuse. This led to the setting up of ChildLine which has been instrumental in helping thousands of children and has been used as a model for similar organizations in other countries. From a personal perspective, Esther's daughter Emily, became very ill and was bed bound for many months after being diagnosed with ME/CFS. Esther learnt firsthand the devastating effect this illness has not just on the patient, but on the whole family. As with every other project she has been involved in, Esther set about learning as much as she could about this illness. It became apparent to her that there was very little information and even less support for this group of people and once again, she found herself at the forefront of a campaign. Esther currently is very involved in the ME world as the President of the Association of Youth with ME and, we were honored that she agreed to become Vice President of the National ME Centre.
The Perrin Clinic :: Leading The World In Osteopathic Treatment Of CFS/ME :: 016
Dedicated to helping patients using osteopathic diagnosis and treatment. Includes details about the technique and a list of practitioners.
http://theperrinclinic.com

Extractions: We at the Perrin Clinic believe that Chronic Fatigue Syndrome/Myalgic Encephalitis and Post Viral Fatigue Syndrome is a physical disorder that leads to a build up of toxins within the brain and the spine. The Perrin Technique� has been developed to diagnose CFS/ME by identifying definite physical signs and to treat the disorder by improving drainage of these poisons from the central nervous system. The Perrin Technique� Book Dr Perrin's book: 'The Perrin Technique' published by Hammersmith Press, is now available in bookshops or you can order here on this website Research Raymond Perrin's research at the University of Salford in conjunction with the University of Manchester has provided strong evidence that an important component of CFS/ME involves a disturbance of lymphatic drainage of the brain and muscles. The novel osteopathic treatment developed by Raymond Perrin has been statistically validated in both clinical trials, emphasising the need to focus future research on the biomechanical aspects of this disorder. Raymond has expanded our knowledge of CFS/ME , which led to a doctorate awarded by the University of Salford.

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