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» LymeNet Flash » Questions and Discussion » General Support » " Unrest " documentary on ME/CFS

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Author Topic: " Unrest " documentary on ME/CFS
Bartenderbonnie
Frequent Contributor (1K+ posts)
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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 1/23/2018

http://www.pbs.org/independentlens/videos/unrest/#

Posts: 2294 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
LymeLearned
LymeNet Contributor
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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.

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"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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Keebler
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Excellent film. I saw it last night on NetFlix.
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

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