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welcome about the film trailer “introduction” to synopsis credits “reflections” about me & cfs research and treatment initiatives contributors contributors me specialists translators screenings exercise & me/cfs event at bristol watershed. 2014 reviews & press mill valley discussion contact subscribe to rss feed uncategorized “introduction” video – watch the introduction to the film here. the introduction can be watched on youtube with subtitles... news watch online the film is available to watch on mubi. for most of the world it can be watched ‘on... news trailer video the first trailer for ‘’ released with our announcement of the... welcome this 30 min version was screened at the stanford university me/cfs symposium in 2014 and the talk with prof mark vanness in bristol the original 1 hour film is available to view free of charge on vimeo to go to vimeo click here and enter the promo code voices dvds are not currently available to buy. please remember this film is not suitable for children and young people with me who may be distressed by viewing it. it is intended to educate those who are not familiar with the illness and issues surrounding it. the film is in english with subtitles in swedish, dutch, spanish, french, italian, czech, german, japanese and english. “the reach of this riveting film has been extraordinary, and it has significantly influenced the debate on seriously ill youth with me. this moving documentary has been like a shot heard around the world as it has precipitated an increasing awareness of the severely ill and highlighted the prejudice against patients and the unwitting but pernicious harm done by too many health care professionals.” professor leonard jason, director of the center for community research “” shows the brave and sometimes heartrending stories of five me patients and their carers, along with input from dr nigel speight, prof leonard jason and prof malcolm hooper. it was filmed and edited between 2009 and 2011 by the brother and mother of an me patient in the uk. the film shows the devastating consequences that occur when patients are disbelieved and the illness is misunderstood. severe and lasting relapse occurs when patients are given inappropriate psychological or behavioural management: management that ignores the reality of this physical illness and the severe relapse or exacerbation of symptoms that can be caused by increased physical or mental activity, over exposure to stimuli and by further infections. ( see bristol watershed event videos ) a belief in behavioural and psychological causes, particularly when me becomes very severe and chronic, following mismanagement, is still taught to medical students and healthcare professionals in the uk. as a consequence, situations very similar to those shown in the film are taking place right now, both in the uk and in other countries. ‘’ received its premiere at the prestigious mill valley film festival near san francisco in 2011, where it won the audience award for favourite international doc. the film has been shown in many countries and in different venues – from parliament buildings to cinemas, universities and homes – from the iacfs/me conference in ottawa 20011, to the stanford me /cfs symposium 2014. the original “trailer” can be watched here on youtube or here under the about the film pages on vimeo. watch the “introduction” to the film – the first 4 mins – in english here – or with subtitles in german , swedish , dutch , italian , french , spanish , czech or japanese on youtube. i think the film was powerful and it should be actually part of medical curricula in medical schools in the us… (it) shows how medical arrogance combined with narrow vision knowledge can be so toxic and can bring more suffering to a group of patients that are already suffering at deep levels. dr montoya – professor of medicine, division of infectious diseases and geographic medicine stanford university school of medicine – stanford medical school . watch here . is a poignant documentary, which unveils the reality of people with severe me/cfs and their carers… we hope that this type of initiative helps to promote a revision of preconceptions about me/cfs in health researchers and professionals, and to bring renewed interest for research in this field, particularly in light of mounting biomedical research evidence in me/cfs. dr eliana lacerda – cfs/me observatory at the london school of hygiene & tropical medicine if i could make everyone in the world see just one film, this would be the film i’d choose. it’s my film of the year. it’ll be my film of the decade. as a critic, i spend my life hoping to find films that will speak to me. “” goes beyond that. it is a film that speaks for me. and i want you to hear it. scott jordan harris chicago sun-times the film was born of desperation, made by the mother and brother of a severe me patient. contributors to the film have helped and participated by being interviewed, by allowing us to use to their documentary material and by giving feedback and approval at every stage. news and updates on will be posted on this site and on our facebook page presentation for belfast. 6th june 2016 a parent’s perspective; ‘lost voices’ as the years past. a talk given by natalie boulton at the ‘hope 4 me and fibro’ conference in belfast on june 6th 2016. (dvds available here) you might ask why am i here? – i have a long experience of family members having me. my mother had me until […] posted on june 13, 2016 comments off on presentation for belfast. 6th june 2016 the pace trial discredited recognition of the flaws in the pace trial has become more substantial as a result of david tuller’s investigative reports on virology blog. rebecca goldin, a prof of mathematical sciences, has produced a 7000 word critique and julie rhmeyer has also written an essay – see below. james coyne has blogged at length and george […] posted on june 8, 2016 comments off on the pace trial discredited ‘trial by error’ – by david tuller. ‘’ shows the devastating effects some patients have suffered following exercise programmes. these treatments of graded exercise therapy and cognitive behavioural therapy, used as the primary treatment for cfs and me on the basis that patients have become de-conditioned from resting too much, caught in a cycle of boom and bust as […] posted on october 24, 2015 comments off on ‘trial by error’ – by david tuller. view more posts © 2018 . all rights reserved. josh b - isophia

URL analysis for voicesfromtheshadowsfilm.co.uk

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isophia.co.uk

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