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ME/CFS AUSTRALIA (SA) INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 322,
Modbury North,
South Australia 5092

Office:
Suite 506,
North Terrace House,
19 North Terrace,
Hackney, SA, 5069


Phone:
1300 128 339

Office Hours:
Wednesdays, 11am-3pm

ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

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ME/CFS Australia (SA) Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

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"City of Ghosts," "Unrest" Take Sheffield Doc/Fest Awards

Friday 16 June 2017

 

From Realscreen:

 

Sheffield Doc/Fest
 

“City of Ghosts,” “Unrest” take Sheffield Doc/Fest Awards

By Meagan Kashty
June 13, 2017
™ Realscreen is a trademark of Brunico Communications Ltd. Site copyright © 1997-2017
Realscreen title, tagline and logo are trademarks of, and the events are produced by Brunico Marketing Inc

SHEFFIELD - City of Ghosts and Unrest; took home top prizes at the annual Sheffield Doc/Fest Awards.

The six-day UK festival, which wraps tomorrow (June 14), handed out awards at a Tuesday evening (June 13) ceremony in Crucible Theatre, hosted by local radio presenter Paulette Edwards.

...

Jennifer Brea (pictured, right) picked up two awards, including the inaugural Illuminate Award, which explores the screen chemistry between vibrant storytelling and innovative filmmaking inspired by science. Brea was given the Illuminate Award for Unrest and the alternative reality award for Unrest VR.

The doc follows Brea as she tries to make sense of a debilitating, leaden tiredness that took hold of her, leaving many questions unanswered by medical experts. Brea turns to the internet and finds not only that her condition has a name—myalgic encephalomyelitis (ME)—but along with it a supportive community of sufferers.

 

Full article…

 

 

 


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