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List of news articles on ME and CFS
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=== Advocacy and awareness === '''Cool customer Tom hopes to race into record books'''<ref>{{citation |last = King|first = Susan | date = 16 September 2016 | title = Cool customer Tom hopes to race into record books|url= https://twitter.com/staplessarah1/status/777868529039204352|newspaper= Sussex Express|location= |access-date= }}</ref> ''Sussex Express'' By: Susan King. (Sep 16, 2016) A superfit Crowborough teenager is running from Lands End to John O'Groats to say thank you to an inspirational teacher. '''Carol Head Receives Prestigious Honor from Oprah Magazine, Is Named 2017 Health Hero'''<ref>{{citation |last = P|first = C | date = Jan 2017 | title = Carol Head Receives Prestigious Honor from Oprah Magazine, Is Named 2017 Health Hero|url= http://www.solvecfs.org/wp-content/uploads/2016/12/Oprah-Magazine-Flier.pdf | newspaper= O, The Oprah Magazine|location= New York|access-date= }}</ref> ''O, The Oprah Magazine'' By: C. P. (Jan 2017) Print Only [LINK Reprint available via Solve ME/CFS] "Chronic fatigue syndrome (CFS) is the Rodney Dangerfi eld of diseases: It gets next to no respect. “We’re all fatigued” is the response Carol Head sometimes hears when she tells people she’s fundraising on behalf of CFS. “They don’t realize it’s a debilitating condition affecting up to two and a half million Americans,” she says." ====Millions Missing==== '''Chronic Fatigue Patients Fight for Research, Funding, and Recognition'''<ref>{{citation |last = Ducharme | first = Jamie | date = 27 September 2016 | title = Chronic Fatigue Patients Fight for Research, Funding, and Recognition | url = http://www.bostonmagazine.com/health/blog/2016/09/27/millions-missing-boston/|newspaper= Boston Magazine|location= |access-date= }}</ref> ''Boston Magazine'' By: Jamie Ducharme. (Sep 27, 2016) "On Tuesday, in 25 cities around the world, myalgic encephalomyelitis (ME) patients and allies will raise the voices they feel they’ve been denied for decades. Under the name Millions Missing, the ME community is protesting the neglect it says it’s felt from the government and the medical field—a neglect spokespeople say has left millions of people undiagnosed, untreated, and unnoticed." '''Life-draining disease needs research'''<ref>{{citation |last = Vastag|first = Bonnie | date = 23 September 2016 | title = Life-draining disease needs research|url= http://www.greenbaypressgazette.com/story/life/2016/09/23/life-draining-disease-needs-research/90843430/|newspaper= Green Bay Press-Gazette|location= |access-date= }}</ref> ''Green Bay Press-Gazette '' By: Bonnie Vastag. (Sep 23, 2016) "Myalgic encephalomyelitis (ME) — It’s the difficult to spell, hard to pronounce illness that afflicts our son, Brian Vastag, and millions of sufferers in the U.S. and around the world. On Sept. 27, the second Millions Missing protest is scheduled for Washington, D.C., and worldwide. I have mailed a pair of shoes to D.C. representing Brian — missing from the job he loves, missing from socializing with his friends, missing health care professionals who understand his disease. They’ll be displayed with thousands of other pairs as advocates work for adequate research dollars to help solve this scourge." '''Rows of empty shoes outside the Radcliffe Camera, Oxford will represent Chronic Fatigue Syndrome sufferers at Millions Missing'''<ref>{{citation |last = Hughes | first = Pete | date = 27 September 2016 | title = Rows of empty shoes outside the Radcliffe Camera, Oxford will represent Chronic Fatigue Syndrome sufferers at Millions Missing | url = http://www.oxfordtimes.co.uk/news/yourtown/oxford/14765529.Rows_of_empty_shoes_will_represent__hidden__sufferers_of_debilitating_condition/|newspaper= The Oxford Times|location= |access-date= }}</ref><ref>{{citation |last = Hughes | first = Pete | date = 27 September 2016 | title = Rows of empty shoes outside the Radcliffe Camera, Oxford will represent Chronic Fatigue Syndrome sufferers at Millions Missing | url = http://www.oxfordmail.co.uk/news/14765529.display/|newspaper= Oxford Mail|location= |access-date= }}</ref> ''The Oxford Times'' and ''Oxford Mail'' By: Pete Hughes. (Sep 27, 2016) "MORE than a hundred pairs of shoes will be lined up outside the Radcliffe Camera in Oxford tomorrow to represent sufferers unable to attend a demonstration to raise awareness for one of the most debilitating and least understood conditions of our time." '''Commentary: A day of action for a hidden epidemic'''<ref>{{citation |last = Solomon | first = Rivka | date = 26 September 2016 | title = Commentary: A day of action for a hidden epidemic|url= http://www.courierpostonline.com/story/opinion/columnists/2016/09/26/commentary-day-action-hidden-epidemic/91123178/|newspaper= Courier-Post|location= Cherry Hill, NJ|access-date= }}</ref> ''Courier-Post'' By: [[Rivka Solomon]]. (Sep 26, 2016) "A hidden epidemic has swept the globe — and your neighborhood is not immune. In its wake are millions of lives ruined. Its silent victims are all ages and backgrounds, in every state across America: Up to 99,000 in Illinois, 152,000 in New York and 211,000 in Texas. There is no prevention, no treatment and no cure for this barely acknowledged disease that gets barely any government funding." '''Dozens Rally To Bring Attention To Incurable Disease'''<ref>{{citation |last = Fielding|first = Lisa | date = 27 September 2016 | title = Dozens Rally To Bring Attention To Incurable Disease|url= http://chicago.cbslocal.com/2016/09/27/dozens-rally-to-bring-attention-to-incurable-disease/|newspaper= CBS Chicago|location= |access-date= }}</ref> ''CBS Chicago'' By: Lisa Fielding. (September 27, 2016) "It’s called Myalgic Encephalomyelitis or Chronic Fatigue Syndrome and it affects 17 million people worldwide. “This particular illness is more functionally debilitating than chronic congestive heart disease and cancer. The quality of life is significantly less. There’s over a million people in this country with this illness, 25% are homebound or bedbound,” said Leonard Jason, DePaul University, who’s been studying the disease for 25 years." '''Silent shoe protest at lack of funding for ME'''<ref>{{citation | author = <!--Staff writer(s); no by-line.--> | title = Silent shoe protest at lack of funding for ME|url= http://www.itv.com/news/westcountry/2016-09-27/silent-shoe-protest-at-lack-of-funding-for-me/|newspaper= ITV News|location= London | date = 27 September 2016|access-date= }}</ref> ''ITV News''. (Sep 27, 2016) "More than a hundred pairs of shoes have been laid out on College Green in Bristol in a silent protest at the lack of funding for research into ME, also known as Chronic Fatigue Syndrome. The empty shoes represent people who couldn't be at the protest because of the condition." '''Shoes for a syndrome'''<ref>{{Cite news | last = Michael|first = Pascal | date = | title = Shoes for a syndrome|url= http://sandtonchronicle.co.za/165664/shoes-for-a-syndrome|newspaper= Sandton Chronicle | date = 2016|access-date= }}</ref> ''Sandton Chronicle'' By: Pascale Michael. (2016) "On 27 September, residents are encouraged to put out a pair of shoes to remember the sufferers of myalgic encephalomyelitis (ME), also known as chronic fatigue syndrome (CFS)." '''100 pairs of shoes used to make poignant protest on ME research in Bristol city centre'''<ref>{{Cite news |last = Clensy|first = David | date = September 27, 2016 | title = 100 pairs of shoes used to make poignant protest on ME research in Bristol city centre|url= http://www.bristolpost.co.uk/100-pairs-of-shoes-make-silent-protest-on-me-research-in-bristol-city-centre/story-29755005-detail/story.html|newspaper= Bristol Post|access-date= }}</ref> ''Bristol Post'' By: David Clensy. (Sep 27, 2016) "A hundred pairs of shoes were laid out on College Green in a poignant silent protest against the lack of funding for research into the causes of ME, also known as Chronic Fatigue Syndrome (CFS). Each pair of shoes represented a sufferer of ME who was unable to attend the rally in Bristol city centre, but was too exhausted as a result of their condition to attend in person." '''Demonstrators at Stormont urge more research into chronic disease ME'''<ref>{{citation |last = Simpson | first = Claire | date = September 28, 2016 | title = Demonstrators at Stormont urge more research into chronic disease ME|url= http://www.irishnews.com/news/northernirelandnews/2016/09/28/news/demonstrators-at-stormont-urge-more-research-into-chronic-disease-m-e--712221/|newspaper= The Irish News|location= Belfast|access-date= }}</ref> ''The Irish News'' By: Claire Simpson. (September 28, 2016) "A major demonstration urging more research into M.E. was held at Stormont on Tuesday as part of a global day of action. Protests took part in 25 cities across the world, including Belfast, Melbourne, London and New York." '''Protesters Demand Increased Funding or ME/CFS Research'''<ref>{{citation | last1 = Schlossman | first1 = Fallon | last2 = Dugyala | first2 = Rishika | date = 28 September 2016 | title = Protesters Demand Increased Funding or ME/CFS Research|url= http://www.usnews.com/news/articles/2016-09-28/protesters-demand-increased-funding-or-me-cfs-research|newspaper= U.S. News & World Report|location= Washington, D.C.|access-date= }}</ref> ''U.S. News & World Report'' By: Fallon Schlossman and Rishika Dugyala. (Sep 28, 2016) "Protesters placed dozens of pairs shoes in front of the Department of Health and Human Services Tuesday, symbolizing people so affected by Myalgic Encephalomyelitis, or Chronic Fatigue Syndrome, that they're unable to fully live their lives." '''MillionsMissing: A Hidden Epidemic and a Day of Action'''<ref>{{citation |last = Solomon | first = Rivka | date = 28 September 2016 | title = MillionsMissing: A Hidden Epidemic and a Day of Action | url = http://www.huffingtonpost.com/rivka-solomon/millionsmissing-a-hidden-_b_12183114.html?|newspaper= The Huffington Post|location= New York|access-date= }}</ref> ''The Huffington Post'' By: [[Rivka Solomon]]. (Sep 28, 2016) "A hidden epidemic has swept the globe — and your neighborhood is not immune. In its wake are millions of lives ruined. Its silent victims are all ages, from all backgrounds and in every state across America: Up to 99,000 in Illinois, 152,000 in New York and 211,000 in Texas. There is no prevention, no treatment and no cure for this barely acknowledged disease that gets barely any government funding." '''More than a million Americans are suffering from a debilitating disease that makes simple tasks impossible — and they're sick and tired of being ignored'''<ref>{{citation |last = Letzter | first = Rafi | date = 29 September 2016 | title = More than a million Americans are suffering from a debilitating disease that makes simple tasks impossible — and they're fed up with being ignored | url = http://www.businessinsider.com/me-cfs-protest-government-2016-9|newspaper= Business Insider|location= New York|access-date= }}</ref> ''Business Insider'' By: Rafi Letzter. (Sep 29, 2016) "Imagine living with a disease that renders you disabled and exhausted, unable to meet the physical demands of daily living. Now imagine that much of the medical establishment refused to believe your disease was "real" in the sense of a physical illness, and failed to fund research into its true causes and treatment." '''Millions Are Missing: Will The World Finally Notice?'''<ref>{{citation |last = Hanson | first = Maureen | date = 30 September 2016 | title = Millions Are Missing: Will The World Finally Notice?|url= http://www.huffingtonpost.com/maureen-hanson/millions-are-missing-will-the-world-finally-notice_b_12184042.html?|newspaper= The Huffington Post|location= New York|access-date= }}</ref> ''The Huffington Post'' By: Maureen Hanson. (Sep 30, 2016) "This week, demonstrations occurred in 25 global cities world-wide to focus attention on a neglected, devastating disease — Myalgic Encephalomyelitis (ME), an illness that also goes by the misleading name Chronic Fatigue Syndrome (CFS). At this event, the most powerful demonstrators were those who could not attend — the bedridden and housebound patients." '''Brock's Banter: Beyond “Sick and Tired”'''<ref>{{citation |last = Weir | first = Brock | date = 2 November 2016 | title = Brock's Banter: Beyond “Sick and Tired”|url= http://www.newspapers-online.com/auroran/?p=15705|newspaper= The Auroran|location= |access-date= }}</ref> ''The Auroran'' By: Brock Weir. (Nov 2, 2016) "The predicament in question was finding the wherewithal to get through a peaceful demonstration in Toronto to help facilitate a solution. But, when you’re mad as hell and you’re not going to take things lying down, how are you going to make a difference if the thing you feel like most in the world is lying down?" ==== Unrest film ==== '''‘[[Unrest]]’ documents lives of ME patients'''<ref>{{citation |last = Moody|first = Frances | date = 17 January 2017 | title = 'Unrest' documents lives of ME patients|url= http://www.parkrecord.com/entertainment/sundance-slamdance/unrest-documents-lives-of-me-patients/|newspaper= Park Record|location= Park City, UT |access-date= }}</ref> ''Park Record'' By: Frances Moody. (Jan 17, 2017) "Trying to ignore bouts of excruciating muscle pain, Jennifer Brea forced herself to walk home after a doctor diagnosed her with myalgic encephalomyelitis, commonly called chronic fatigue syndrome." '''Sundance 2017: ‘Unrest’ Is An Emotional Look At Human Strength'''<ref>{{citation |last = Booth|first = Kaitlyn | date = 23 January 2017 | title = 'Unrest' Is An Emotional Look At Human Strength|url= https://www.bleedingcool.com/2017/01/23/sundance-2017-unrest-emotional-watch/#comment-anchor|newspaper= Bleeding Cool|location= Rantoul, IL |access-date= }}</ref> ''Bleeding Cool'' By: Kaitlyn Booth. (Jan 23, 2017) "Unrest takes a very frank look at the often misunderstood illness known as ‘chronic fatigue syndrome’ that is both informative and hard to watch." ''''Unrest': Film Review | Sundance 2017'''<ref>{{citation |last = DeFore | first = John | date = 23 January 2017 | title = 'Unrest': Film Review Sundance 2017|url= http://www.hollywoodreporter.com/review/unrest-review-967867|newspaper= The Hollywood Reporter|location= Los Angeles, CA|access-date= }}</ref> '''The Hollywood Reporter'' By: John DeFore. (Jan 23, 2017) "Late in Jennifer Brea's Unrest, a doctor informs us that Multiple Sclerosis, the devastating nervous system disorder, was viewed by doctors as a "hysterical" illness — one essentially invented in the sufferer's own mind — right up until the CAT scan was introduced, allowing previously dismissive doctors to see what was going on inside their patients' bodies. Unrest finds a similar difficulty facing people with Chronic Fatigue Syndrome, a debilitating but controversial disorder that is barely understood and in some quarters denied entirely. Using her own experience with the syndrome as a springboard, Brea offers an affecting film that, when made available on video, will be embraced by the millions suffering CFS worldwide." '''Sundance Film Review: ‘Unrest’'''<ref>{{citation |last = Harvey|first = Dennis | date = 23 January 2017 | title = Sundance Film Review: ‘Unrest’|url= http://variety.com/2017/film/markets-festivals/unrest-sundance-film-festival-1201966610/|newspaper= Variety|location= Los Angeles, CA|access-date= }}</ref> ''Variety'' By: Dennis Harvey. (Jan 23, 2017) "A largely mysterious condition that reportedly afflicts as many as 17 million people worldwide, Chronic Fatigue Syndrome still flummoxes most physicians, and remains frequently dismissed as a psychosomatic “illness” — including by some nations. Still, it’s hard to buy the “all in your head” diagnosis when seeing the long-term, sometimes entirely bedridden victims of CFS in “Unrest.” Director Jennifer Brea is one of them herself, and this first-feature documentary chronicles her own struggles while taking in the perspectives of other patients and experts around the globe. Though the “Patient, film thyself” concept is starting to risk overexposure — Sundance alone premieres two such features this year, the other being ALS-themed “It’s Not Dark Yet” — “Unrest” is a high-grade example of the form that’s consistently involving, with content diverse enough to avoid the tunnel-visioned pitfalls of diarist cinema." '''Jennifer Brea Filmed Her Sundance Premiere Without Leaving Bed — And it Saved Her Life'''<ref>{{citation |last = Buder | first = Emily | date = 23 January 2017 | title = Jennifer Brea Filmed Her Sundance Premiere Without Leaving Bed — And it Saved Her Life|url= http://nofilmschool.com/2017/01/unrest-jennifer-brea-interview-sundance-2017|newspaper= No Film School|location= Brooklyn, NY|access-date= }}</ref> ''No Film School'' By: Emily Buder. (Jan 23, 2017) "One day, Jennifer Brea woke up to find that her life had been stolen from her. The newly engaged Harvard PhD student couldn't write her own name. She couldn't get out of bed; when she tried, she would collapse on the ground in pain and utter exhaustion. She could barely talk. She couldn't even draw a circle." '''How Great Human Beings Find Their Purpose'''<ref>{{citation |last = Kasanoff|first = Bruce | date = 22 January 2017 | title = How Great Human Beings Find Their Purpose|url= https://www.linkedin.com/pulse/how-great-human-beings-find-purpose-bruce-kasanoff|newspaper= LinkedIn - What Inspires Me|location= Mountain View, CA|access-date= }}</ref> ''LinkedIn - What Inspires Me'' By: Bruce Kasanoff. (Jan 22, 2017) "It's probably a mistake to think you were "born to be" an entrepreneur, cure cancer, or become an actor. Your purpose is not just a function of your inherent talents, but rather the product of how those talents interact with what life throws in your path." '''Entrepreneur Needed To Cure Anti-Initiative Disease'''<ref>{{citation |last = Kasanoff|first = Bruce | date = 26 January 2017 | title = Entrepreneur Needed To Cure Anti-Initiative Disease|url= http://www.forbes.com/sites/brucekasanoff/2017/01/26/entrepreneur-needed-to-cure-anti-initiative-disease/#4f1a7bb52d88|newspaper= Forbes - Leadership|location= Jersey City, NJ |access-date= }}</ref> ''Forbes - Leadersip'' By: Bruce Kasanoff. (Jan 26, 2017) "Perhaps 20 million people worldwide have had their lives curtailed by what I'm calling the Anti-Initiative disease. (In a moment, I'll tell you its more traditional names.) This disease is horrific in that it literally punishes its victims when they display initiative. For example, if a patient who can't get out of bed for weeks then has a good day and decides to go sit in her backyard, she may then be dramatically worse for months." '''‘Unrest’ Review: A Personal Look at Chronic Fatigue Syndrome, With Powerful Results — Sundance 2017'''<ref>{{citation |last = Kohn | first = Eric | date = 27 January 2017 | title = 'Unrest' Review: A Personal Look at Chronic Fatigue Syndrome, With Powerful Results — Sundance 2017|url= http://www.indiewire.com/2017/01/unrest-review-jennifer-brea-sundance-2017-documentary-1201774204/|newspaper= Indie Wire|location= USA |access-date= }}</ref> ''Indie Wire'' By: Erik Kohn. (Jan 27, 2017) "Chronic Fatigue Syndrome — otherwise known as Myalgic Encephalomyelitis — receives little exposure in the media and often goes misdiagnosed, even as it afflicts tens of thousands of people worldwide. Jennifer Brea’s stirring documentary “Unrest” goes a long way toward explaining the nature of the disease and the devastating impact it can have on family life, deriving much of its power from her own encounter with it." '''Sundance review: ‘Unrest’'''<ref>{{citation |last = Means | first = Sean P. | date = 26 January 2017 | title = Sundance review: ‘Unrest’|url= http://www.sltrib.com/home/4867522-155/sundance-review-unrest|newspaper= The Salt Lake Tribune|location= |access-date= }}</ref> ''The Salt Lake Tribune'' By: Sean P. Means. (Jan 26, 2017) "Filmmaker Jennifer Brea gets deeply personal in her documentary "Unrest," as she chronicles her debilitating illness and meets other sufferers around the world — all without leaving her bed." '''10 Kick-Ass Women Filmmakers to Know from Sundance 2017'''<ref>{{citation |last = Farmer | first = Shelly | date = Jan 25, 2017 | title = 10 Kick-Ass Women Filmmakers to Know from Sundance 2017|url= http://www.papermag.com/10-women-filmmakers-watch-sundance-2017-2201353209.html|newspaper= Paper|location= NY City|access-date= }}</ref> ''Paper'' By: Shelly Farmer. (Jan 25, 2017) "Princeton alum Jennifer Brea was pursuing a PhD in political science at Harvard when she was suddenly struck with a mysterious, debilitating illness. Left bedridden and only able to shoot two days a month, Brea – a Sundance Institute Fellow – turned the camera on herself in Unrest, chronicling her struggles with the little-understood myalgic encephalomyelitis (better known as Chronic Fatigue Syndrome) and her connection with four other families grappling with similar health issues." '''Sundance: Medical Mystery Doc 'Unrest' Nabbed by PBS (Exclusive)'''<ref>{{citation |last = Siegel|first = Tatiana | date = 31 January 2017 | title = Sundance: Medical Mystery Doc 'Unrest' Nabbed by PBS (Exclusive)|url= http://www.hollywoodreporter.com/news/sundance-medical-mystery-doc-unrest-nabbed-by-pbs-968176|newspaper= The Hollywood Reporter|location= Los Angeles, CA|access-date= }}</ref> ''The Hollywood Reporter'' By: Tatiana Siegel. (Jan 31, 2017) "The medical mystery doc Unrest has been solved by PBS. The network has acquired U.S. broadcast rights for its Emmy Award-winning series Independent Lens." '''Sind Vorurteile gegen kranke Menschen geschlechtsspezifisch?'''<ref>{{citation |last = Schickendanz|first = Melanie | date = 2 January 2017 | title = Sind Vorurteile gegen kranke Menschen geschlechtsspezifisch?|url= http://www.huffingtonpost.de/melanie-schickedanz/sind-vorurteile-gegen-kra_b_14544026.html|newspaper= The Huffington Post - Germany|location= Munich|access-date= }}</ref> German Language ''The Huffington Post - Germany'' By: Melanie Schickendanz. (Jan 2, 2017) "Im Oktober 2013 startete Jennifer Brea eine Kampagne über Kickstarter, bei der es darum ging, Geld für eine Dokumentation namens Unrest (damals Canary in a Coal Mine) über die Krankheit ME (Myalgische Enzephalomyelitis, auch bekannt als chronisches Erschöpfungssyndrom bzw. CFS) zu sammeln. Nach drei Tagen waren schon 50.000 US-Dollar zusammengekommen. Am Ende hatten über 2.500 Unterstützer eine Summe von 212.692 US-Dollar gespendet." '''If you have to shoot your own illness to show that you are not crazy?'''<ref>{{citation |last = Thorup|first = Mette-Line | date = 16 March 2017 | title = If you have to shoot your own illness to show that you are not crazy?|url= https://translate.google.com/translate?sl=auto&tl=en&js=y&prev=_t&hl=en&ie=UTF-8&u=https%3A%2F%2Fwww.information.dk%2Findland%2F2017%2F03%2Fnoedt-filme-egen-sygdom-vise-tosset&edit-text=&act=url|newspaper= Information |location= Denmark|access-date= }}</ref> ''Information'' By: Meete-Kine Thorup (Mar 16, 2017) Google Translated "A woman moans tormented in a gritty dark. She is lying on a wooden floor and trying to rise by supporting arms against the ground, but fail back. She pushes instead toward the bed under the great effort and with a camera turned against itself in one hand." '''New film about chronically tired: their cells are sick - doctors and friends say they just need to get their act together'''<ref>{{citation |last = Rasmussen | first = Lars Igum | date = 17 March 2017 | title = New film about chronically tired: their cells are sick - doctors and friends say they just need to get their act together |url= https://translate.google.com/translate?sl=auto&tl=en&js=y&prev=_t&hl=en&ie=UTF-8&u=http%3A%2F%2Fpolitiken.dk%2Fforbrugogliv%2Fsundhedogmotion%2Fart5874906%2FDeres-celler-i-kroppen-er-syge-%25E2%2580%2593-l%25C3%25A6ger-og-venner-siger-de-bare-skal-tage-sig-sammen&edit-text=&act=url|newspaper= Politiken |location= Denmark|access-date= }}</ref> ''Politiken'' By: Lars Igum Rasmussen (Mar 17, 2017) Google Translated "The American graduate student at Harvard University Jennifer Brea could everything."
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