information | commentary | archives on the political issues affecting ME patients, advocates and carers
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ME agenda | information | commentary | archives on the political issues affecting ME patients, advocates and carers | meagenda.wordpress.com Reviews
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information | commentary | archives on the political issues affecting ME patients, advocates and carers
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ME agenda: update on status of this site – ME agenda
https://meagenda.wordpress.com/2013/08/21/me-agenda-update-on-status-of-this-site
Information commentary archives on the political issues affecting ME patients, advocates and carers. ME agenda: update on status of this site. ME agenda: update on status of this site. This site was created in June 2007 for ME patients, carers and advocates and provided information, resources and commentary on the political issues affecting the lives of UK Myalgic encephalomyelitis (ME) patients. In 2009, my primary advocacy focus shifted towards monitoring the development of. DSM-5 and ICD-11 Watch.
Dx Revision Directory – ME agenda
https://meagenda.wordpress.com/dx-revision-directory
Information commentary archives on the political issues affecting ME patients, advocates and carers. Update: New site for monitoring development of DSM-5 and ICD-11 here:. Http:/ dxrevisionwatch.wordpress.com/. The April 2009 report of the APA DSM-V Somatic Distress Disorders Work Group (also known as the “Somatic Symptom Disorders”) can be read on the APA’s site here:. The proposed diagnosis of somatic symptom disorders in DSM-V to replace somatoform disorders in DSM-IV – a preliminary report. Action fo...
Post index – ME agenda
https://meagenda.wordpress.com/post-index
Information commentary archives on the political issues affecting ME patients, advocates and carers. Links to posts in reverse date order back to June 18, 2007 [approximately 980 posts]. For monthly archives see Archives. Widget in right hand column. ME agenda: update on status of this site. Next Meeting of the ICD-9-CM Coordination and Maintenance Committee. New Twitter address and new domain for Dx Revision Watch. Recent posts on Dx Revision Watch: ICD-11 Beta draft updates. Posting of revised draft pr...
Information obtained under FOI Act – ME agenda
https://meagenda.wordpress.com/dx-revision-directory/information-obtained-under-foi-act
Information commentary archives on the political issues affecting ME patients, advocates and carers. Information obtained under FOI Act. Information obtained under FOI Act. FOI Sub page 1. Back to DSM-V Directory. Date request submitted: 18 February 2009. The University of Edinburgh. Email: recordsmanagement@ed.ac.uk. Request for information under Freedom of Information Act. Conceptual Issues in Somatoform and Similar Disorders (CISSD Project). Undertaken between 2003 and 2007. Conceptual Issues in Somat...
Disclaimer – ME agenda
https://meagenda.wordpress.com/disclaimer
Information commentary archives on the political issues affecting ME patients, advocates and carers. Before using this site please read these Disclaimer Notes. DSM; DSM-IV; DSM-IV-TR; DSM-IV-PC; DSM-V; DSM V; DSM-5; DSM 5 are registered trademarks of the American Psychiatric Association. Is not an organisation. This site does not accept advertising, sponsorship, funding or donations and has no commercial links with any organisation, institution, corporation, company or individual. The information on this...
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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 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...
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...
Slightly Alive: My letter to APA on Somatic Symptom Disorder
http://slightlyalive.blogspot.com/2010/04/my-letter-to-apa-on-cssd.html
Subscribe To Slightly Alive. Saturday, May 5, 2012. My letter to APA on Somatic Symptom Disorder. Submission to the Work Group for Somatic Symptom Disorders. 3 The APA has stated elsewhere that many of the changes in DSM-5 are intended to avoid gender biases in existing medical categories. Isn't it strange that the proponents of the new category SSD have often stated 90 percent of victims of CFS (and SSD by extension) are female? I have to say I never thought I would see that book cited as a reputable so...
MErry Christmas | Proper ME News, no PSYCHO babble
https://meworld.wordpress.com/2008/12/25/merry-christmas
Proper ME News, no PSYCHO babble. Email No Psycho Babble. This entry was posted on Thursday, December 25th, 2008 at 9:41 pm and is filed under CBT. You can follow any responses to this entry through the RSS 2.0. Feed You can leave a response. From your own site. Laquo; Previous Post. December 27, 2008 at 8:16 pm. A peaceful Christmas to you, Simon. Let’s hope the coming year will be a better one for all of us and the year in which this illness finally receives proper recognition and research.
DSM-5 timeline | dx revision watch
https://dxrevisionwatch.com/dsm-5/dsm-5-timeline
Monitoring the development of DSM-5 and ICD-11. DSM and ICD links. Coalition for DSM-5 Reform. DSM-5 SSD work group. DSM-5 SSD submissions 2010. DSM-5 SSD submissions 2011. DSM-5 SSD submissions 2012. ICD-11: ME, CFS. American Psychiatric Association (APA). Criticism of DSM-V, DSM-5. DSM-5 in the media. WHO (World Health Organization). Was released in May 2013, at t he APA’s 2013 Annual Meeting in San Francisco, CA. The manual’s publishing dates are May 22, 2013 (USA); May 31, 2013 (UK). Draft proposals,...
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ME agenda | information | commentary | archives on the political issues affecting ME patients, advocates and carers
Information commentary archives on the political issues affecting ME patients, advocates and carers. Information obtained under FOI Act. ME agenda: update on status of this site. August 21, 2013. May 2, 2017. ME agenda: update on status of this site. This site was created in June 2007 for ME patients, carers and advocates and provided information, resources and commentary on the political issues affecting the lives of UK Myalgic encephalomyelitis (ME) patients. In 2010, I created Dx Revision Watch. Suzy ...
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