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Author
Topic: " Unrest " documentary on ME/CFS
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177
posted 01-11-2018 10:51 AM
A Harvard PhD student Jennifer Brea, turns filmmaker in this new Acadamy Award nominated documentary titled " Unrest." It is Jennifer's video dairy of her, and others, struggle with ME/CFS myalgic encephalomyelitis/chronic fatigue syndrome . It is available free from PBS till 1/23/2018http://www.pbs.org/independentlens/videos/unrest/#
Posts: 2977 | From Florida | Registered: Nov 2016
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LymeLearned
LymeNet Contributor
Member # 20565
posted 01-14-2018 12:12 PM
Just started watching it. It is just under 1.5 hours, so saving the tab until later today, but we will make it part of our Sunday viewing. I want to see it today in case it I want to refer someone before it goes off the air for free viewing on 1/23. Thank you. When this stuff hits the people with the greatest ability to speak out, it raises awareness, and lifts us all with it. -------------------- "SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT: http://www.youtube.com/TickedOffLiterally
Posts: 183 | From USA | Registered: Jun 2009
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted 01-20-2018 01:12 PM
- Excellent film. I saw it last night on NetFlix. -
Posts: 48021 | From Tree House | Registered: Jul 2007
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