1. CFS / M.E. Information From CFS-NEWS A project of Roger Burns, the publisher of the Internet newsletter CFS-NEWS. Provides news, information Category Health Conditions and Diseases Chronic Fatigue Syndrome......This is a resource page for chronic fatigue syndrome / myalgic encephalomyelitis/ CFIDS, sponsored by the publisher of CFSNEWS. http://www.cfs-news.org/

Chronic Fatigue Syndrome / Myalgic encephalomyelitis NEWS SOURCES INFO FILES DISCUSSION GROUPS CFS-RELATED WEB PAGES ... Non-CFS links This web page is provided by Roger Burns , the publisher of CFS-NEWS . See also the introductory essays about CFS Latest version: September 19, 2001 NEWS LATEST NEWS CFS-NEWS Newsletter LATEST NEWS about CFS/M.E. CFS-NEWS Electronic Newsletter CO-CURE info exchange: Search Archives ... Brussels CFS medical conference report, Sept. 9-11, 1999 ME-NET (Netherlands) Search Archives CFS Weekly Radio Show Texts ... CFIDS Assoc: News and Advocacy (USA) Youth Action Online (U.K.) CFS NewsWire archive Back to the Top INFORMATION FILES AND DOCUMENTS FAQ Doctors Page QUICK Index CFS FAQ (answers to frequently asked questions) Doctors CFS page CDC Definition article , 1994; Fukuda et al. American Journal of Medicine Symposium on CFS , Sept 1998 Myalgic encephalomyelitis ME-NET Research Papers Royal Colleges Report Psychiatric bias paper , by Jason, et al., 1997 U.K. National Task Force on CFS/ME, 30 Sep 1998 Dealing with Doctors When You Have CFS , by Camilla Cracchiolo, R.N. Where Can I find a good CFS doctor?

2. The No1 Domain Name Information about diagnosis, symptoms, causes, treatments and links. http://www.theno1website.co.uk

theno1website.co.uk Your browser does not support frames. To view our web site click here: http://www.art-is-a-tart.com/web5/cindex.htm For more information contact webmaster@theno1website.co.uk

3. ME/CFS Chronic Fatigue Syndrome. Info For Medical Profession And Sufferers ME/CFS. myalgic encephalomyelitis. Chronic Fatigue Syndrome http://freespace.virgin.net/david.axford/me/me.htm

Search for any word on this web site Enter your words in the box below Use SEARCH to find the word you're looking for. The results will be presented in a list containing the first instance of your word. Click on any of the listed pages to view. Having viewed your word, then use your browsers FIND facility to check for any more occurrences of your word on that page. ME/CFS Myalgic Encephalomyelitis Chronic Fatigue Syndrome What is this diagnosis? Don't forget to mark your calendar too! Countdown to May the 12 th Only year, months, and days left until ME/CFS/CFIDS International Awareness Day Need the latest relevant ME/CFS information? Articles about news and views on the latest information on ME/CFS. Includes the very latest Medical Update, Capita Selecta, Medical Fact sheet, Book Reviews and other relevant medical information. Canada Leads the Way With a Medical Milestone: (Press Release - Feb 2003) A Clinical Definition for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Where can I get help?

4. The Myalgic Encephalomyelitis Association Of Ontario Offers info, tips, and support to those coping with ME/CFS and related illnesses, including youth Category Health Conditions and Diseases Organizations......Whats New. About us. About ME CFS. Parents and Youths. Coping. DisabilityAssistance. Support groups. Other illnesses. Links. Search this site. http://www.meao-cfs.on.ca/

5. Waterloo Wellington M.E. Association The Waterloo Wellington myalgic encephalomyelitis Association (WWMEA) is a registered charitable organization (notfor-profit) http://ca.geocities.com/wwmea

Home  The WWMEA  M.E. - The Illness  M.E. - Self-Help ...  Using This Site MAY 12 IS INTERNATIONAL M.E. AWARENESS DAY SUPPORT YOUR LOCAL M.E. ORGANIZATION Home  The WWMEA  M.E. - The Illness  M.E. - Self-Help ...  Using This Site WWMEA Waterloo Wellington Myalgic Encephalomyelitis Association P.O. Box 20075 Pioneer Park Post Office Kitchener, Ontario, Canada phone: (519) 623-3207 email: wwmea@yahoo.ca 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. M.E. is comprised of numerous symptoms such as impairment in short-term memory, impairment in concentration, sore throat, tender lymph nodes, exhaustion, muscle pain, multijoint pain, headaches (of a new type, pattern, or severity), unrefreshing sleep and post-exertional malaise lasting more than 24 hours.

6. Waterloo Wellington M.E. Association - M.E. - The Illness Copyright © Waterloo Wellington myalgic encephalomyelitis Association. All Rights Reserved. http://ca.geocities.com/wwmea/aboutme.html

Home  The WWMEA  M.E. - The Illness  Children ...  Using This Site WWMEA M.E. - The Illness M.E. can be described as an INVISIBLE CHRONIC ILLNESS There are no visible symptoms to see such as a rash or a cut. Most M.E. sufferers are so ill or in so much pain that they are house-bound.  Thus, they are out-of-sight. M.E. is a chronic, debilitating multi-system disorder comprised of numerous symptoms which include extreme malaise, pain, cognitive dysfunction, and overwhelming fatigue.  At this time there is no cure for this illness.  M.E. has similar symptoms to many disorders, but should not be confused with them. The links at left will guide you through information regarding M.E. The information presented here is not intended to be comprehensive, but rather, to be a starting point for readers to find relevant information about M.E. The links to external web sites are not intended to be a complete listing of all M.E. sites on the internet.  However, you will discover that most of the links that are provided, have many more links to peruse. WHO GETS M.E.?

7. Online Help For Myalgic Encephalomyelitis Information and a number of resources for sufferers from myalgic encephalomyelitis, Post Viral Syndrome Category Regional Europe Chronic Fatigue Syndrome......Online help for myalgic encephalomyelitis, Chronic Fatigue Syndromeand Fibromyalgia. Overton Studios Trust WELCOMES YOU! We http://www.ostrust.freeserve.co.uk/

Overton Studios Trust WELCOMES YOU! We are a UK Registered Christian Charity We provide support and healing for sufferers from: Myalgic Encephalomyelitis (ME) Chronic Fatigue Syndrome (CFS) Post Viral Syndrome (PVS) Chronic Fatigue and Immune Deficiency Syndrome (CFIDS) Fibromyalgia (FM) MISSION Our mission is to help sufferers from these conditions to manage their condition more effectively and finally to bring it under their control. METHODS We produce videos, books, a brochure, newsletters and leaflets. Individual sufferers may consult our resident medical officer in Colwyn Bay, North Wales, UK. He has thoroughly controlled his own ME and is thus in a unique position to help others. We run the OSTrust Club, a unique and ethical club designed to provide world-wide benefit and support for ME / CFS / PVS / FM / CFIDS sufferers, their carers, relatives and friends.

8. Fund For Osteopathic Research Into Myalgic Encephalomyelitis - M.E. / CFS Research into the osteopathic relief of symptoms of M.E. (myalgic encephalomyelitis)/ C.F.S.(Chronic Fatigue Syndrome) http://www.forme-cfs.co.uk/

F.O.R. M.E. .Site created 10th March 1998. Designed by Peevish Web Design Last update 15th June 2001. Visitors to this site since 22 November 1998

9. Action For M.E. - Welcome Information about myalgic encephalomyelitis from national charity campaigning to improve the lives of people with the condition. Includes an appeal for volunteers. http://www.afme.org.uk

Links Help for New Visitors What is M.E.? Action for M.E. Action for M.E. is a national charity campaigning to improve the lives of people with M.E. in the UK. Our aim is to heighten understanding of the impact M.E.* has on the lives of those who have it and to improve the quality of services for people who suffer from this debilitating illness. Action for M.E. is a UK based national membership organisation and registered charity (Reg. No. 1036419). It is supported by its members, donations from individuals, local M.E. groups, businesses and trusts. * or Chronic Fatigue Syndrome as it is sometimes referred to by the medical profession Two new reports on CFS/M.E. DoH directs GPs to Action for M.E. GP Guide Minutes of the All-Party Parlimentary Group on M.E., 10 December 2002 Action for M.E. merges with Westcare UK Action for M.E. response to Medical Research Council Research Strategy Consultation Details of Action for M.E.'s services for members

10. Home Page Mothers Against myalgic encephalomyelitis is an organization dedicated to promoting education and awareness about myalgic encephalomyelitis by utilizing well family and community member volunteers. http://www.mame-net.org/

11. Myalgic Enchephalomyelitis This is a resource page for myalgic encephalomyelitis (ME), sponsored bythe publisher of CFSNEWS. ME syndrome. myalgic encephalomyelitis http://www.cfs-news.org/me.htm

MYALGIC ENCEPHALOMYELITIS Updated: Tuesday, October 5, 1999 Introduction Definitions Lancet, 1956 Acheson, 1959 ... Resources Introduction Recent discussions at the Brussels conference and elsewhere have helped to clarify that myalgic encephalomyelitis (M.E.) and CFS are not the same entity. There has been confusion about this, even in Britain where M.E. was first defined and studied under that name. What exactly is M.E.? According to M.E. experts the key difference between M.E. and chronic fatigue syndrome is that M.E. requires the criterion of easy fatiguability following minimal exertion and a delay in recovery of muscle strength. Definitions M.E. has been described several times in medical literature. It was first defined in an editorial published in the Lancet in 1956 which discussed several epidemic outbreaks of prior years. This first description was rather loose and was not very specific. In later years Ramsay, EG Dowsett and others refined the definition of M.E. in various published papers. After Ramsay died in 1990, Dowsett et al. wrote the latest version of the M.E. definition now known as the "London criteria". These have been used in recent papers by Costa (Brainstem perfusion is impaired in patients with CFS, QJM 1995; 88:767-773) and Scholey (A comparison of the cognitive deficits seen in M.E. to Alzheimer's Disease, Proceedings of the British Psychological Society, 1999, January, 12).

12. Association Of Young People With M.E. - AYME - ME/CFS Charity Support, news and information for children and young people with myalgic encephalomyelitis. http://www.ayme.org.uk/

M.E. Stands for Myalgic Encephalo myelitis Myalgic - means muscle - indicating the pain involved in the muscles. Encephalo means brain - indicating that the brain functioning is involved. myelitis means inflammation of the spinal cord and does not occur in M.E. so 'pathy' Myalgic Encephalopathy is now being used instead which means 'sickness' or 'illness'. Myalgic Encephalopathy (My-al-jik En-kefalo-pathy) or Chronic Fatigue Syndrome is an illness characterised by prolonged, debilitating fatigue and multiple symptoms including headaches, recurrent sore throats, muscle and joint pains, stomach pains, loss of appetite, and cognitive complaints such as difficulty in understanding, concentrating and finding thecorrect word when speaking. In very severe cases, the brain symptoms become severe: vertigo is common, swallowing becomes difficult, shaking fits can occur, and contracture of the limbs and tingling, numbness or even paralysis is not unheard of often down one side of the body The profound fatigue which marks the disorder can come on gradually or suddenly, often after a viral illness. Unlike the short-term disability of an acute infection, M.E or CFS symptoms (by definition - Chronic meaning long-term) persists for at least 3 months in children.

13. Personality Of Patients With Myalgic Encephalomyelitis. The personality of patients with myalgic encephalomyelitis. A controlled followupof cases involved in an epidemic of ‘Benign myalgic encephalomyelitis’. http://freespace.virgin.net/david.axford/articl01.htm

The personality of patients with myalgic encephalomyelitis. A replication of a study by McEvedy and Beard. EM Goudsmit PhD C.Psychol. Chartered Health Psychologist. ME Research Online Volume 1 Number Abstract Introduction Method Results Neuroticism Extraversion Discussion Acknowledgements References Table 1 Table 2 This article was written in 1988. ABSTRACT The aim of this study was to replicate earlier research by McEvedy and Beard, using a group of people with a clear diagnosis of Myalgic Encephalomyelitis (M.E.). Their scores on the EPI were compared to those recorded by a non-symptomatic control group as well as a group of patients suffering from another chronic illness (M.S. group). The results suggest that the slightly raised Neuroticism scores of people with M.S. do not necessarily indicate a hysterical personality or neuroticism. Both the limitations of the EPI as a measure of Neuroticism and Extraversion in people with physical illnesses and the psycho-social sequelae of conditions such as M.E. may have affected the responses on the inventory. These factors should also be considered when interpreting the data obtained by McEvedy and Beard. Consequently, it was impossible to draw any firm conclusions about the role of personality in the aetiology of M.E. INTRODUCTION

14. Tales From Tigercub Towers - These Things Happen! The journal of a Scots writer and photographer struggling with the debilitating condition myalgic encephalomyelitis. http://catsmother.diaryland.com

Tales from . . . . . . . . . . . . . . . . . . Tigercub Towers Just testing Saturday, Mar. 22, 2003 - 3:41 p.m. Just testing, as my journal seems to have disappeared. I'll be back soon, anyway. back forward var site="sm5catsmother" other journals footnotes funny the world cyborgirl discodave kristoli marn buntsign bitter hag Latest Archive Host Email ... Digital Glasgow

15. FibroWhat? - FMS - Fibromyalgia - Fibrositis - Neuromuscular Disorders - Chronic A personal story about FMS, formerly called fibrositis, a chronic pain disorder sharing symptoms of chronic fatigue syndrome (CFS), also known as myalgic encephalomyelitis. http://www.gis.net/~dlowe777

16. The Myalgic Encephalomyelitis Association Of Ontario ABOUT OUR ORGANIZATION. Welcome to the web site of The myalgic encephalomyelitisAssociation of Ontario. Our wish for you as you http://www.meao-cfs.on.ca/about_us/index.shtml

ABOUT OUR ORGANIZATION BROCHURES AND VIDEOS MISSION STATEMENT ABOUT OUR ORGANIZATION Welcome to the web site of The Myalgic Encephalomyelitis Association of Ontario. Our wish for you as you travel through our web site is that you are informed about M.E./CFS and that you feel reassured that you are not alone with your illness. (Throughout the site, we use M.E./CFS as an abbreviation for Myalgic Encephalomyelitis / Chronic Fatigue Syndrome.) We hope you enjoy your visit and gain knowledge and understanding of our illness. However, the information that you will read on our web site is not to be taken as a means of a diagnosis but for an educational purpose only. We do not endorse any treatment, product or service. A diagnosis should only be made by a qualified physician. Understanding the illness, will help you, or those you know are affected, to cope. OUR MAILING ADDRESS The Myalgic Encephalomyelitis Association of Ontario P.O. Box 84522 , 2336 Bloor Street West Toronto, Ontario, Canada

17. National ME/FM Action Network Details about this nonprofit organization dealing with myalgic encephalomyelitis/Chronic Fatigue Syndrome and Fibromyalgia. Includes a downloadable newsletter, information roster, and discusses active projects. http://www3.sympatico.ca/me-fm.action/

18. ME-NET - Chronic Fatigue Syndrome Chronic fatigue syndrome/myalgic encephalomyelitis web site, discussion list, and search engine http://www.me-net.dds.nl

Version: Welcome to ME-NET's Homepage! At this web site, you will find information on "Myalgic Encephalomyelitis" (ME) / "Chronic Fatigue Syndrome" (CFS) / "Chronic Fatigue and Immune Dysfunction Syndrome" (CFIDS). ME-WEB. Links to Official CFS/ME-texts, CFS/ME-resources, and Health Resources on the World Wide Web. ME-NET list. The public archive of the ME-NET list. You can subscribe to this Dutch/English list by sending an E-mail with the text: SUB ME-NET [Your Name] to: listserv@nic.surfnet.nl . The list address is: me-net@nic.surfnet.nl Dutch Page. Go to the ME-NET Dutch Homepage. [Dutch:] Ga naar de Nederlandstalige Pagina. Beginner's Guide. If you don't know anything about CFS/ME or when you are new to the CFS/ME cyberworld, you can learn the essentials here. Contact ME-NET. Address to write to. Phone/Fax numbers and E-mail addresses, colophon, and names of the ME-NET webmasters. Links to Dutch organizations using the ME-NET web site. Log on to ME-NET/ME-InfoNet. How to log on with your computer to ME-NET and the ME-InfoNet BBS in The Netherlands. [Dutch:] Hoe je naar ME-NET en ME-InfoNet in kunt bellen met je computer.

19. ME/CFS List Of Medical Articles Including Medical Updates And Capita Selecta that post partum depression (PPD) and myalgic encephalomyelitis (ME) are fashionable disorders and hysterical http://freespace.virgin.net/david.axford/melist.htm

20. Online Help For Myalgic Encephalomyelitis We provide support and healing for sufferers from myalgic encephalomyelitis. (ME). Chronic Fatigue Syndrome http://www.bigfoot.com/~ostrust

Overton Studios Trust WELCOMES YOU! We are a UK Registered Christian Charity We provide support and healing for sufferers from: Myalgic Encephalomyelitis (ME) Chronic Fatigue Syndrome (CFS) Post Viral Syndrome (PVS) Chronic Fatigue and Immune Deficiency Syndrome (CFIDS) Fibromyalgia (FM) MISSION Our mission is to help sufferers from these conditions to manage their condition more effectively and finally to bring it under their control. METHODS We produce videos, books, a brochure, newsletters and leaflets. Individual sufferers may consult our resident medical officer in Colwyn Bay, North Wales, UK. He has thoroughly controlled his own ME and is thus in a unique position to help others. We run the OSTrust Club, a unique and ethical club designed to provide world-wide benefit and support for ME / CFS / PVS / FM / CFIDS sufferers, their carers, relatives and friends.

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