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CFS CentralCFS Central reports breaking news, research and disputes on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and XMRV.
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CFS Central reports breaking news, research and disputes on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and XMRV.
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CFS Central | cfscentral.com Reviews
https://cfscentral.com
CFS Central reports breaking news, research and disputes on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and XMRV.
CFS Central: IOM Report: Remarkably Positive for ME patients
http://www.cfscentral.com/2015/02/iom-report-remarkably-positive-for-me.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Tuesday, February 10, 2015. IOM Report: Remarkably Positive for ME patients. Is in, and it’s remarkably positive for ME patients. The IOM committee has proposed a new name for ME: Systemic Exertion Intolerance Disease or SEID. OK, it’s a mouthful, and how do you pronounce the acronym? It’s possible that disbelievers will morph the name into:. At sufferers had nothing really wrong with them, except perhaps indolence. At least one of the two following man...
CFS Central: September 2013
http://www.cfscentral.com/2013_09_01_archive.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Tuesday, September 24, 2013. CDC's Two-Day Exercise Test: Not Negotiable. Center for Disease Control's head of CFS research Dr. Beth Unger is slated to do a problematic one-day ME exercise study called the Cardiopulmonary-Exercise Testing. Instead of the two-day test favored by most patients and ME-educated researchers. What’s wrong with Unger's study? Do I really have to answer that question? Dr Chris Snell, an expert in the field of exercise testing f...
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...
CFS Central: A COMMOTION IN THE BLOOD
http://www.cfscentral.com/2010/07/commotion-in-blood.html
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Tuesday, July 20, 2010. The first known cluster outbreak of ME/CFS in the United States occurs in Los Angeles, California. An outbreak takes place in a convent in Fond-du-Lac, Wisconsin. Several outbreaks are reported in Switzerland. An outbreak takes place in Akureyri, Iceland. Goch, Wales; Athens, Greece; Patreksfordur. More outbreaks are recorded in the U.S. (California, New York, Lackland Air Force Base and Dallas-Fort Worth, Texas. Epidemiologists ...
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...
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Pahavit's Universe
http://pahavit.livejournal.com/tag/grass
Coal Mine Ridge Part 2. Coal Mine Ridge Part 2. Heres Part 2 of my recent visit to the Old Spanish Trail at Coal Mine Ridge (Part 1 here. An unusual white form of blue dicks. A live oak is draped in Spanish moss near the crest of the ridge. The Old Spanish Trail goes through a small meadow. A bumble bee visits rose clover. Bracket fungi growing on a fallen log help to break down its tissues and release the nutrients back into the environment for new life to use. The ground-level campus is intended as a p...
Monday Movies: Level Crossing Bell - Pahavit's Universe
http://pahavit.livejournal.com/452503.html
Monday Movies: Level Crossing Bell - Pahavits Universe. Monday Movies: Level Crossing Bell. Monday Movies: Level Crossing Bell. Monday Movies: 20 seconds (more or less) of video from the world around me. This week: Twenty-two seconds of the railway level crossing warning bell (due to a stalled train a block away) at Jack London Square in Oakland during my recent railway excursion ( Part 1. Click - - Monday Movies: Level Crossing Bell. Mind The Abyss, Part 1. Sutro Tower Fan Club. Museum of Lost Wonder.
THE NICEGUIDELINES BLOG: Danish study finds patients with ME/CFS have the lowest health-related quality of life of 21 conditions looked at
http://niceguidelines.blogspot.com/2015/07/danish-study-finds-patients-with-mecfs.html
Doctor Speedy and ME in search of medical honesty. Tuesday, July 7, 2015. Danish study finds patients with ME/CFS have the lowest health-related quality of life of 21 conditions looked at. Published July 6, 2015 @ plosone:. In fact, the ME/CFS HRQoL in this study was the lowest of all the compared conditions. In both the unadjusted analysis and in the adjusted regression analysis. So basically this study confirms that CBT and GET are at best totally useless. Subscribe to: Post Comments (Atom). Revalidati...
The Deep of the Night | Wolfdreams...
https://wolfdreams.wordpress.com/2015/07/08/the-deep-of-the-night
Life, Spirit, and Health: the View from the Mountain. Laquo; #FWF Kellie Elmore. The Deep of the Night. July 8, 2015 by Ash. Awake, yet again, in the deep of the night,. I listen to the breeze sigh through the forest leaves,. Sounding like the gentle caress of waves on the shore. My ever present companion, Kodi,. Lays watchful at the end of the deck,. As I turn to go sit in my porch swing. A loud snort breaks the silence of the Mountain,. Echoing all around us,. And Kodi is instantly alert and by my side.
THE NICEGUIDELINES BLOG: The hell of a disease that is incurable, has inadequate therapies, indifferent government attitudes, social stigma and no strong public voice
http://niceguidelines.blogspot.com/2013/04/the-hell-of-disease-that-is-incurable.html
Doctor Speedy and ME in search of medical honesty. Thursday, April 4, 2013. The hell of a disease that is incurable, has inadequate therapies, indifferent government attitudes, social stigma and no strong public voice. By Llewellyn King, MARCH 30, 2013:. I am a reporter and my beat is hell. But it is neither the eternal hell of the Bible, nor Tartarus, the ancient Greek underworld, where the gods of mythology locked up their enemies. Subscribe to: Post Comments (Atom). Significant impairments in immune r...
Onward Through the Fog: July 2015
http://cfstreatment.blogspot.com/2015_07_01_archive.html
Onward Through the Fog. A practical resource for treating CFS/ME . coping tips, specialists, books, articles, research, and advice on how to recover from this debilitating illness. #NotMyPresident. CFS Treatment Guide, 1st Edition. CFS: A Treatment Guide, 2nd Edition. Marc Iverson's Letter of Resignation from CAA. CDC Spoof of ME/CFS. Friday, July 31, 2015. August Deadlines and Opportunities for Advocacy. Reprinted with the kind permission of Jennie Spotila and Occupy CFS. Here are the details:. Public c...
My Life as I "StandUP2ME" + OI/POTS: October 2011
http://standup2me.blogspot.com/2011_10_01_archive.html
My Life as I "StandUP2ME" OI/POTS. Do not go where the path may lead, go instead where there is no path and leave a trail." Ralph Waldo Emerson. Translate to . with one click. Tuesday, October 18, 2011. 119 Urgent: November CFSAC concerns:. Occupy the CFSAC via EMAILs. Subject: Urgent November CFSAC concerns:. B) Thousands of us have UNITED over the past 2-3 years via watching the CFSAC meetings LIVE online and Sharing the info. Now they are Stating this. NOT ONE WORD ABOUT US WITHOUT US"! If you have ME...
My Life as I "StandUP2ME" + OI/POTS: February 2011
http://standup2me.blogspot.com/2011_02_01_archive.html
My Life as I "StandUP2ME" OI/POTS. Do not go where the path may lead, go instead where there is no path and leave a trail." Ralph Waldo Emerson. Translate to . with one click. Friday, February 4, 2011. 104 PROTEST: McClure in USA- CFS "NIH" SEP. URGENT PARTICIPATION REQUESTED ASAP Please. Please feel free to copy and paste this letter or any part of it to send to anyone you want. Please send this letter below to Kathleen Sebelius, Francis Collins, Dennis Mangan, Dr. Anthony Scarpa ( CSR Director),. 8220;...
THE NICEGUIDELINES BLOG: Another clue that ME/CFS might be an autoimmune disease: Increased Risk of ME/CFS for people with allergies
http://niceguidelines.blogspot.com/2015/07/another-clue-that-mecfs-might-be.html
Doctor Speedy and ME in search of medical honesty. Friday, July 24, 2015. Another clue that ME/CFS might be an autoimmune disease: Increased Risk of ME/CFS for people with allergies. Medicine (Baltimore). 2015 Jul;94(29):e1211. doi: 10.1097/MD.0000000000001211. Increased Risk of Chronic Fatigue Syndrome Following Atopy: A Population-Based Study.Yang TY1, Kuo HT, Chen HJ, Chen CS, Lin WM, Tsai SY, Kuo CN, Kao CH. The overall incidence rate of CFS was higher in the atopy cohort compared with the nonatopy c...
THE NICEGUIDELINES BLOG: Gene expression factors differentiate fibromyalgia, ME/CFS, depression and healthy controls from each other
http://niceguidelines.blogspot.com/2015/07/gene-expression-factors-differentiate.html
Doctor Speedy and ME in search of medical honesty. Saturday, July 25, 2015. Gene expression factors differentiate fibromyalgia, ME/CFS, depression and healthy controls from each other. Arthritis Care Res (Hoboken). 2015 Jun 19. doi: 10.1002/acr.22639. [Epub ahead of print]. Gene expression factor analysis to differentiate pathways linked to fibromyalgia, chronic fatigue syndrome, and depression in a diverse patient sample. Iacob E, Light AR, Donaldson GW, Okifuji A, Hughen RW, White AT, Light KC. Express...
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CFS Central
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Wednesday, May 11, 2016. I’d Like Some Water from Flint, Please. ME research has long deserved real, meaty, physiological research, but will the government ever conduct it? Had Virginia Tech engineering professor and environmental hero Marc Edwards not intervened in both water crises—in the latter case, a Flint resident contacted him. To help—the public may never have known. How many more children would have suffered irreversible brain damage? However, ...
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