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List of news articles on ME and CFS
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=== Funding === '''Chronic fatigue syndrome recognized at last'''<ref>{{citation |last = Solomon | first = Rivka | date = 9 November 2015 | title = Chronic fatigue syndrome recognized at last|url= http://www.sfchronicle.com/opinion/openforum/article/Chronic-fatigue-syndrome-recognized-at-last-6620617.php|newspaper= San Francisco Chronicle|location= |access-date= }}</ref> ''San Francisco Chronicle'' By: [[Rivka Solomon]]. (09 Nov 2015) "After 30 years of neglect, the federal government promised late last month to bolster research on myalgic encephalomyelitis/chronic fatigue syndrome — the equivalent of promising to help multiple sclerosis or Parkinson’s, two other important neurological diseases with no known cause or cure." '''Rethinking chronic fatigue syndrome'''<ref>{{citation |last = Rowley|first = Sylvia | date = 6 August 2016 | title = Rethinking chronic fatigue syndrome|url= https://www.thesaturdaypaper.com.au/2016/08/06/rethinking-chronic-fatigue-syndrome/14704056003560|newspaper= The Saturday Paper|location= Melbourne|access-date= }}</ref> ''The Saturday Paper'' By: Sylvia Rowley. (06 Aug 2016) "Despite world-class research into chronic fatigue syndrome being undertaken nationally, government funding and support for sufferers is grossly lacking." (Note: This article was also in the Aug. 6, 2016 hard copy edition with the title "What about ME?"; online non-subscriber readers are allowed one free article per week.) '''ME is often dismissed – but sufferers like Emily Collingridge are dying'''<ref>{{citation |last = Harris | first = Scott Jordan | date = 30 March 2012 | title = ME is often dismissed – but sufferers like Emily Collingridge are dying | url = https://www.theguardian.com/commentisfree/2012/mar/30/me-emily-collingridge-chronic-fatigue-syndrome|newspaper= The Guardian|location= London|access-date= }}</ref> ''The Guardian: Opinion'' By: Scott Jordan Harris. (30 Mar 2012) ''"How many young people have to die before 'chronic fatigue syndrome' merits properly funded biomedical research?"'' '''The Tragic Neglect of Chronic Fatigue Syndrome'''<ref>{{citation |last = Khazan | first = Olga | date = 8 October 2015 | title = The Tragic Neglect of Chronic Fatigue Syndrome|url= http://www.theatlantic.com/health/archive/2015/10/chronic-fatigue-patients-push-for-an-elusive-cure/409534/|newspaper= The Atlantic|location= Washington, D.C.|access-date= }}</ref> ''The Atlantic'' By: Olga Khazan. (08 Oct 2015) "It leaves people bed-bound and drives some to suicide, but there's little research money devoted to the disease. Now, change is coming, thanks to the patients themselves." '''Stigmatized Chronic Fatigue Syndrome sufferers seek recognition'''<ref>{{citation | author=<!--Staff writer(s); no by-line.--> | title = Stigmatized Chronic Fatigue Syndrome sufferers seek recognition | url = http://www.ctvnews.ca/health/stigmatized-chronic-fatigue-syndrome-sufferers-seek-recognition-1.3067130|newspaper= CTV News|location= Toronto | date = 10 September 2016|access-date= }}</ref> ''CTV News''. (10 Sep 2016) "As many as 400,000 Canadians suffer from Chronic Fatigue Syndrome, or Myalgic Encephalomyelitis. But according to a federal review, their condition is all in their minds. Canada's largest scientific funding agency recently decided that ME/CFS is not deserving of research funding because it is not a legitimate disease, and more likely made up by patients."
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