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

Home The WWMEA M.E. - The Illness M.E. - Self-Help ... to Other Web Sites MAY 12 IS INTERNATIONAL M.E. AWARENESS DAY SUPPORT YOUR LOCAL M.E. ORGANIZATION WWMEA Waterloo Wellington Myalgic Encephalomyelitis Association Free Public Lecture Tuesday September 21, 2010 7 p.m. Special Presentation Do you know your legal rights as a Fibromyalgia or Chronic Fatigue Syndrome Patient? Tuesday, September 21, 2010 7:00 p.m. click here for details. Waterloo Wellington Myalgic Encephalomyelitis Association P.O. Box 20075 Pioneer Park Post Office Kitchener, Ontario, Canada email: How to Live Toxin Free 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.

82. 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

83. 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

@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"; home about us contact us donate ... partnerships Search health centers Aging and Memory Allergies and Asthma Alternative Medicine ... Home Chronic Fatigue Syndrome Email Print Chronic Fatigue Syndrome Like This Article? Click to rate Average: Select rating Poor Okay Good Great Awesome No votes yet Article Medically Reviewed By: Suzanne Vernon, PhD Scientific Director, The CFIDS Association of America, Charlotte, NC What is it? Diagnosis Treatment Prevention ... Organizations and Support What is it? Overview What Is It? 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.

84. 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

Fibromyalgia. No longer a completely unexplainable pain, but observed and coherent mechanisms. Chronic Fatigue Syndrome. No longer 'Yuppie Flu' but a condition that 14 disciplines of USA CDC researchers can measure. The research on both illnesses aided by the latest medical technologies. Years of research have proven them. Take a new look... There are now respected clinical diagnosis and treatment guidelines. Please make a donation. Support our drive for progress. We need you. Thank you! Information Connections Research English Français Spotlight's Top News: A New, Collaborative, Campaign! New Web Site! and! Our Latest Free Video about FM/CFS/ME. Click here for Part 1! Part 1 also available on YouTube Our Latest Free Video about FM/CFS/ME. Click here for Part 2! Part 2 also available on YouTube From the author of Seabiscuit "...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..." Laura Hillenbrand - August 9th 2006 after 20 years of CFIDS Site updated by MyMason.ca

85. 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

showMenus(1,'Horizontal') A Non-Profit Organization To make a financial donation to P.A.N.D.O.R.A., click the button below. 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 It is estimated that 20 MILLION AMERICANS are stricken by Neuroendocrineimmune Disorders. Worldwide the estimates can be staggering. Recently a demographics expert suggested that between 23-28 million individuals are now suffering with Chronic Fatigue Syndrome or ME worldwide. Despite of these high numbers, our single voices have no impact. We are yet to estimate the total financial, social and demographics impact of all the illnesses that we embrace in our mission. But we are working on it. 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;

86. 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/

87. 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/

Home Search Home About Us ... Contact Us Home Home About CFIDS/ME About Fibromyalgia Diagnosis ... Contact Us XMRV one year later… Inconsistencies in study results confuse researchers and patients. Read our commentary… A video of Dr. Anthony Komaroff's recent lecture, The Latest Research on CFS, is available for viewing. 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

88. 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/

Home Research Information Support us ... Donate Make a one-off donation or set up a standing order Shop at Amazon Shop via our Amazon link and we will receive a donation. Support us Ideas for fundraising to help support ME research Just four quid Everyclick Raise money for ME Research UK by searching the web Shopping Raise money for ME Research UK by shopping on the web Leaflet Download our leaflet (pdf 111 KB) Poster Download our poster (pdf 1 MB) Breakthrough Download back issues of our magazine Making a breakthrough Welcome to ME Research UK, a national charity funding biomedical research into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (also known as ME CFS 10th anniversary celebration ME Research UK celebrated its tenth anniversary this year, and we celebrated the event with lunch together at Murrayshall House Hotel. Pain in ME/CFS Biochemical abnormalities in children A newly published study from the University of Dundee looking at biochemical abnormalities in children with ME CFS See also media coverage Christmas cards 2010 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. Call for ME/CFS Centre of Excellence Our article in The Herald newspaper calls for an ME/CFS Centre of Excellence in Scotland Research database update The latest update of our database is now available, containing over 3,000 research publications on

89. 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

90. 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/

91. 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/

92. 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/

Bookmark Contact us Home About Us ... Donations 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 Support Organisations by State ME/CFS Australia directs enquiries from members of the community about frontline support for people with ME/CFS to independently run state organisations. News Retrovirus XMRV and ME/CFS Scientists have identified the retrovirus XMRV in the blood of 68 of 101 people with ME/CFS. For the latest updates regarding XMRV, please click here. XMRV and ME/CFS Click here for more news News article: New study links HIV-type disease to chronic fatigue syndrome Read more Journal Article: An update on the management of glandular fever and its sequelae caused by Epstein–Barr virus (HHV-4) Results of a recent study.

93. 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/

94. 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

95. CFIDS Articles written by medical and research professionals. http://www.cfids.org/archives/research-review-issues.asp

96. The CFS Report News and commentary for the CFS Community. Covers recent research articles and press releases. http://www.cfidsreport.com

97. CFS Research Foundation UK charity that funds investigation towards diagnosis and treatments. Provides list of ongoing projects and published articles. http://www.cfsrf.com/

98. 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/

ME International ME symptoms CFS symptoms ME/CFS symptoms Pediatric Definition WELCOME to ME International Myalgic Encephalomyelitis - ME 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.

99. 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/

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.

100. 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

What is the Perrin Technique™ ? 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 Follow our link to the website of The Fund for Osteopathic Research in M.E you can view the film The Perrin Technique™ 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.

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 5     81-100 of 103    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20