niceguidelines.blogspot.com
THE NICEGUIDELINES BLOG: My response to the medically unexplained nonsense from Professor Moss Morris
http://niceguidelines.blogspot.com/2015/07/my-response-to-medically-unexplained.html
Doctor Speedy and ME in search of medical honesty. Friday, July 10, 2015. My response to the medically unexplained nonsense from Professor Moss Morris. Dear Professor Moss Morris,. As professor Hooper wrote a few years ago when does ignoring evidence become serious professional misconduct? It's clear that the Pinocchio Psychiatrists have crossed that line a long time ago. Please do keep in mind that evidence that something is psychosomatic or all in the mind, because that's basically what you say whe...
niceguidelines.blogspot.com
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...
niceguidelines.blogspot.com
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...
niceguidelines.blogspot.com
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...
niceguidelines.blogspot.com
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...
raisingawarenessforcfs.wordpress.com
Raising Awareness for ME/CFS | Research, treatment options and my personal chronicles with ME/CFS | Page 2
https://raisingawarenessforcfs.wordpress.com/page/2
Raising Awareness for ME/CFS. Research, treatment options and my personal chronicles with ME/CFS. Newer posts →. Update on Andrew McGorrian. June 26, 2012. Last May I posted about a little boy named Andrew McGorrian. In Northern Ireland with severe ME/CFS whose family and friends were trying to raise money for treatment in the United States with Dr. Jamie Deckoff-Jones. To read Dr. Jamie’s blogpost click here. May 12 International Awareness Day 20th Anniversary. May 10, 2012. On Saturday May 12. May 12 w...
standup2me.blogspot.com
My Life as I "StandUP2ME" + OI/POTS: December 2010
http://standup2me.blogspot.com/2010_12_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, December 24, 2010. 100 Please SPREAD this video NOW! THx♥ OUR WikiLeaks. Please make your Holiday present to the World, just a few emails about this video and to the NIH Thx♥. Ladies and Germs, I think that Dr. Judy and Annette Whittemore did was HEROIC! We have a link on our site at www.rescindinc.org. Harvey Alter's comme...
livingwithchronicfatiguesyndrome.wordpress.com
June | 2015 | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2015/06
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Archive for June, 2015. Ten years of M.E. On June 23, 2015 13 Comments. Today marks an anniversary for me with this illness. A decade ago to the day, my first symptoms emerged, although they were relatively mild at the time. This is my journey…. I have spent the last ten years of my life living with Myalgic Encephalomyelitis. Specialised testing ascertained that the blood wasn’t flowing freely around my brain and my immune system wa...
agentforchange.blogspot.com
One Agent for Change: April 2011
http://agentforchange.blogspot.com/2011_04_01_archive.html
One Agent for Change. Well-Come to Agent for Change, a blog created by Marly Silverman, to serve as a catalyst for change that is much needed on the issues affecting millions of individuals stricken with neuroendocrineimmune disorders worldwide. Through this blog I want to share ideas, exchange, communicate and find solutions for everyday living. The goal is to pursue quality of life that will make a difference in the lives of individuals with neuroendocrineimmune disorders (NEIDs). May he never experien...
