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...
livingwithchronicfatiguesyndrome.wordpress.com
My ME Treatments- A January 2014 Update | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2014/01/29/my-me-treatments-a-january-2014-update
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; One Thousand Paper Cranes. My ME Treatments- An August 2014 update. My ME Treatments- A January 2014 Update. January 29, 2014 by cfssufferer. A lengthy period of time has again passed between my blog entries. This article will hopefully inform readers of the different treatments I have trialled over the past few months. The Neuroimmune Disease Alliance funded a trial of Moringa Oleifera on ME/CFS patients, to be run by the Op...
livingwithchronicfatiguesyndrome.wordpress.com
Sulforaphane, Nicotine Gum, Curcumin and VNS | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2015/02/01/sulforaphane-nicotine-gum-curcumin-and-vns
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; My health- A 2015 Update. Ten years of M.E. Sulforaphane, Nicotine Gum, Curcumin and VNS. February 1, 2015 by cfssufferer. Sulforaphane is a compound found in high doses within cruciferous vegetables, most notably broccoli sprouts. Sulforaphane may benefit ME patients due to:. Protecting against oxidative stress. A study published in late 2014. I started taking broccoli extract capsules on the 7. Studies have shown that nicot...
livingwithchronicfatiguesyndrome.wordpress.com
Oxymatrine | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2009/11/03/oxymatrine
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; My Abnormal Blood Tests. November 3, 2009 by cfssufferer. The White Tiger brand contains 200mg of oxymatrine per tablet. My dosing structure is flexible based on any reaction to the oxymatrine however at the moment stands at:. 100mg each day for 2 weeks. The tablet is to be taken with water before or with meals. 100mg 2x a day for 2 weeks. 200mg at am and 100mg at pm for 2 weeks. I must stress that it is imperative to slowly ...
livingwithchronicfatiguesyndrome.wordpress.com
An ME Update- August 2013 | Living With Chronic Fatigue Syndrome
https://livingwithchronicfatiguesyndrome.wordpress.com/2013/08/05/an-me-update-august-2013
Living With Chronic Fatigue Syndrome. Just another WordPress.com weblog. Laquo; Nimodipine- The Results. One Thousand Paper Cranes. An ME Update- August 2013. August 5, 2013 by cfssufferer. It has been a lengthy period since my last blog. This entry will attempt to outline my ME related journey from the past 6 months. In a previous blog entry here. There exists a plethora of ME treatments that I have lined up and ready to trial. The one prohibiting factor for testing these treatments involves the wei...
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...
niceguidelines.blogspot.com
THE NICEGUIDELINES BLOG: Evidence that a disease is psychosomatic doesn't exist
http://niceguidelines.blogspot.com/2015/06/evidence-that-disease-is-psychosomatic.html
Doctor Speedy and ME in search of medical honesty. Saturday, June 13, 2015. Evidence that a disease is psychosomatic doesn't exist. Doctors or others who say that a disease is psychosomatic do not have any evidence for that; why not because it doesn't exist. The mere fact that routine testing is normal is not evidence that something is psychosomatic. But many doctors do not understand or realise this. In Parkinson or ALS for example, routine testing is also normal. Venus Williams, the successful American...
