LymeNet Flash: " Unrest " documentary on ME/CFS

This is topic " Unrest " documentary on ME/CFS in forum General Support at LymeNet Flash.

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Posted by Bartenderbonnie (Member # 49177) on :

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/#

Posted by LymeLearned (Member # 20565) on :

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.

Posted by Keebler (Member # 12673) on :

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Excellent film. I saw it last night on NetFlix.
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