Saturday, 4 February 2012

Voices from the Shadows

http://voicesfromtheshadowsfilm.co.uk/

Please buy this DVD! It has been made to educate people about the reality of severe ME. It is not a Christian film, and I would not advise showing it to children or to those newly diagnosed with the illness, but I would certainly recommend it. For those who believe ME to be simply “chronic fatigue”, the contents will come as something of a shock.

About the film -
http://voicesfromtheshadowsfilm.co.uk/about-the-film/

Who made the film?

The film has been made by Natalie Boulton and Josh Biggs – the mother and brother of a severe ME sufferer. Josh is a young professional freelance editor and cameraman. Natalie was an artist/teacher and is a full time carer for her daughter who has been ill for over 20 years. This is the first time we have worked together on a film and we are both first time director/producers. The making of the film has been entirely financed by our family and we are grateful to unpaid help we have received. The music was written, recoreded and kindly donated to the film by Emmy nominated composer David Poore . Full credits are here

People have asked us if we made the film for a particular charity, as we did with the book ‘Lost Voices from a Hidden Illness’, but we did not. It is an independent project which we felt compelled to make as a family, to try to help make a difference to the lives of so many wonderful young, and not so young, severe ME sufferers. We need you to help by using the film to inform others about this situation. Please buy copies of the film to give to others, particularly to those professionals who could help change the lives of so many people living in fear and isolation. We are not in any way making a profit from this project, we just need others to help too please.

Why did you make the film?

‘Voices from the Shadows’ was born of utter desperation. Having struggled for nearly 20 years to care for my daughter, I found that we were caught in a trap.

Like most patients and their families I believed the medical profession had this disease in their sights and was working at a cure. With an awful shock, after attending Invest in ME and MERUK conferences, I realised that was not the case. NOTHING – absolutely NO biomedical research was being funded by the Medical Research Council in the UK and international biomedical research was just being totally ignored. The illness, which had been taken seriously, identified and studied for decades, had just disappeared off the radar. Instead the name had been changed and research funds were being allocated to psychiatric/behavioural management, using up millions of pounds that could have been used to more fully identify the organic causes and develop more effective treatments.

The illness that trapped my daughter and her friends had been ‘disappeared’!

This was being supported by government policy and the media had been doing an excellent job of trivializing the illness and denigrating patients. Nowhere in the public domain was there any sign of the terrible severity of the illness I saw driving many intelligent, creative, positive and courageous young people, into lives of devastating dependency, isolation, pain and steadily deteriorating health. Not only that, but the abuse suffered by some patients who were being harmed by professionals was going totally unrecorded and unnoticed. Patients were, and are, dying invisibly…..

Between 2007-9 I worked on a book for the charity Invest in ME – ‘Lost Voices from a Hidden Illness’ – which started to give patients a ‘voice’. This opportunity was particularly appreciated by young people who had been severely ill for 15-20 years or more; since childhood. I was helped by my son Josh who taught me the computer techniques I needed to carry out the project.

We realized that one of the problems is that severely ill patients with ME become completely isolated and invisible to the world at large. Few people see them, they are too ill to take part in most research projects and so very few people are aware of the severity and nature of the illness. When ‘Lost Voices’ was finished we realized that more needed be done. Josh offered to help with making what was intended to be a short film using his professional expertise and his close involvement with the subject. We started filming, not really knowing what direction the film would take, but our work on ‘Lost Voices’ did not prepare us for the shocking revelations that came to light when we spoke to patients, carers and doctors – of the abuse of children and patients. The project grew and evolved in a direction we hadn’t foreseen. As with ‘Lost Voices’ we worked very closely with the families in the film, many of whom we had known for years, to make sure they were accurately represented and in a collaborative effort we were given access to personal documentation which had not previously been publicly available.

To buy the DVD please go to http://voicesfromtheshadowsfilm.co.uk/shop-dvds/


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