mecfshints.com
Introduction – Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)
http://www.mecfshints.com/introduction
Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS). Health & Wellbeing. Activities for the Inactive. Children & Teenagers. ME (cfs) Impairment Profiles FAQ. Myalgic Encephalomyelitis (cfs) is a serious and debilitating illness which can affect males and females, children and adults, with devastating consequences for the sufferers, their carers, partners, families and friends. How well sufferers cope with ME (cfs) is dependent on a number of factors, including:. How to maintain mental health an...
wwmea.ca
WWMEA - Summary of Links to Other Web Sites
http://www.wwmea.ca/summary_of_links_to_other_web_sites.html
ME - The Illness. To Other Web Sites. Summary of Links to Other Web Sites. Linking to their respective home pages). Http:/ altmedicine.about.com/. Http:/ canada.gc.ca/. Http:/ chd.region.waterloo.on.ca/. Http:/ communitylinks.cioc.ca/. Http:/ guidance.wrdsb.edu.on.ca/. Http:/ hansardindex.ontla.on.ca/. Http:/ mesh.ncf.ca/. Http:/ www.aacfs.org/. Http:/ www.ablelink.org/. Http:/ www.ahmf.org/. Http:/ www.ahummingbirdsguide.com/. Http:/ www.amalgam.org/. Http:/ www.ayme.org.uk/. Http:/ www.cdc.gov/. Http:/...
kiwikchat.blogspot.com
Sarah's World: Two (more) diagnosis, Lyme and Mast Cell Activation Syndrome.
http://kiwikchat.blogspot.com/2013/12/two-more-diagnosis-lyme-and-mast-cell.html
I write about the best things in life, family, friends and chocolate and how they help me cope with one of life's challenges, M.E. I've changed the blog address from www.sarahsworld.me back to the. Original (badly chosen, but I'm stuck with it) address of www.kiwikchat.blogspot.com . This means that some links to older posts and old links from other sites don't work. :(. Sunday, December 1, 2013. Two (more) diagnosis, Lyme and Mast Cell Activation Syndrome. I want to get better. In hindsight some of the ...
cfscentral.com
CFS Central: HAVE YOU NO SENSE OF DECENCY?
http://www.cfscentral.com/2011/05/next-manhattan-project.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Wednesday, May 11, 2011. HAVE YOU NO SENSE OF DECENCY? Here is my testimony at the Chronic Fatigue Syndrome Advisory Committee meeting on Wednesday at Health and Human Services in Washington, D.C. Below the written testimony is the video clip. My name is Mindy Kitei. I’m a science reporter who’s covered ME/CFS for twenty years. Last June, I began my blog, CFS Central, in honor of my friend Nancy Kaiser. Even when the CDC conducted its XMRV study, it stu...
cfscentral.com
CFS Central: XMRV Conference Recap
http://www.cfscentral.com/2010/09/xmrv-conference.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Monday, September 13, 2010. Despite several positive retroviral findings, by the time the Q and A began at the end of the second day, the upbeat mood many felt due to the recently published FDA/NIH/Harvard murine leukemia virus study. Is it the reagents, the collection, the processing, the methods, the patient cohorts or a combination of the above? Here are some highlights of the conference:. In contrast, Dr. Robert Silverman. Dr Eric Klein,. Of the Uni...
cfsnova.com
CFSupport | Resources | Main
http://www.cfsnova.com/resources.html
The Northern Virginia (NOVA). CFS/ME, FMS, OI. Resources, References, and Links by Subject. Full Directory of Topics. Strategies, Stories, Stress. CAM, Integrative Med. Youth, CFS and School. En Español, Languages. Vitamins, Minerals,. Chats, Pals, Forums. Advocacy, May 12. Poetry, Art, and Film. Advocates for Fibromyalgia Funding, Treatment, Education and Research. Alison Hunter Memorial Foundation. Axford's Abode - ME/CFS. David N. Axford and Ellen M. Goudsmit. CFIDS Association of America. Myalgic Enc...
findacureclub.weebly.com
ALISON HUNTER MEMORIAL FOUNDATION - Find A Cure Club
http://findacureclub.weebly.com/alison-hunter-memorial-foundation.html
Find A Cure Club. Find A Cure Club. Medical Disregard means Increase in Suicides. ALISON HUNTER MEMORIAL FOUNDATION. Stanford School of Medicine. Help is Available in Queensland through Blue Care. Health Impact of M.E. AFTER HOURS MEDICAL ASSISTANCE. Voices from the Shadows. When Medical Practices Fail Us. Pathophysiology of M.E. Heart Problems in M.E. Diastolic Dysfunction and Diastolic Heart Failure. EXERCISE Problems in M.E. We Endure Cancer / Organ Failure and Medical Neglect. Images of Lyme Rashes.
findacureclub.weebly.com
Find A Cure Club - Find A Cure Club
http://findacureclub.weebly.com/index.html
Find A Cure Club. Find A Cure Club. Medical Disregard means Increase in Suicides. ALISON HUNTER MEMORIAL FOUNDATION. Stanford School of Medicine. Help is Available in Queensland through Blue Care. Health Impact of M.E. AFTER HOURS MEDICAL ASSISTANCE. Voices from the Shadows. When Medical Practices Fail Us. Pathophysiology of M.E. Heart Problems in M.E. Diastolic Dysfunction and Diastolic Heart Failure. EXERCISE Problems in M.E. We Endure Cancer / Organ Failure and Medical Neglect. Images of Lyme Rashes.
cfscentral.com
CFS Central: July 2014
http://www.cfscentral.com/2014_07_01_archive.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Monday, July 7, 2014. Is CDC Out to Bury PEM? CDC's head of CFS research Dr. Beth Unger said at last month's Chronic Fatigue Syndrome Advisory Committee meeting. That she couldn't figure out how to measure post-exertional malaise (PEM)- the hallmark of ME- and thus believes problems would ensue if PEM is a mandatory symptom. Studies with patients on the antiviral Valcyte to determine if their exercise tolerance improved on the antiviral. Of measuring PE...
cfscentral.com
CFS Central: January 2014
http://www.cfscentral.com/2014_01_01_archive.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Tuesday, January 28, 2014. Below is my testimony from yesterday's conference at the Institute of Medicine. To watch it, click here. My name is Mindy Kitei, and I’m a journalist. I’ve been reporting on myalgic encephalomyelitis for more than twenty years and started my blog, CFS Central, in honor of my friend Nancy Kaiser, who died of the disease in 2008. Tell that to Nancy Kaiser, who experienced multiple seizures a day. Patients believe that the IOM co...