Sunday, 18 May 2014

project description (shared with other group members)

the project aims to explore how chronicle fatigue syndrome has affected Ren Gill's life as a music career pursuer. The documentary was based on an interview with Ren and 



my group work:

Me VS M.E. Project Description

            Me VS M.E is a documentary account of a young mans life after being diagnosed with Myalgic Encephalomyelitis in 2011. It explores and encapsulates the journey of 24 year old Ren Gill, from diagnosis to imminent recovery and his use of social media to connect with other M.E. patients. It engages with some of his most inner thoughts and feelings about the condition and about himself.
                        M.E.s unrecognised significance in young people today demonstrates how little people understand the seriousness of the illness. Commonly connected to older adults, the effects of M.E. in teenagers and young adults is not frequently discussed on many media or social platforms. The absence of medicinal support methods and lack of funding for a more advanced, professional research program of M.E. has triggered diagnosed sufferers to share their own forms of remedies and therapies online through their personal blogs and video diaries.

            The aim of this documentary is to provide a nonfictional account of the reality of living with M.E. as a young person on a daily basis and thus to give an insight into the life of a sufferer. The documentary shows what it is like from a humanistic approach, focusing on Rens personal story to provide a moving and uplifting account of life with M.E, with an emphasis on the subjects state of mind and psychological outlook. This nonfiction film critically engages with the documentary genre by using psychological realism to explore the interior life of the main protagonist of Me VS M.E.           

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