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Unrest now on Netflix

Discussion in 'General ME/CFS news' started by Joh, Jan 15, 2018.

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  1. Joh

    Joh Senior Member (Voting Rights)

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    I asked people with Netflix to check and Unrest is not available in Germany. It's strange that it's on Netflix for our smaller neighbors the Netherlands and Belgium (even with German subtitles) but not in Germany. It would have been a great opportunity to ask more people to watch Unrest and to reach a mainstream audience. I wonder if Netflix deciding to not show it in Germany says something about the non-existing interest in the topic here. No media report or blog post so far and only 2 screenings. I translated the trailer and was so excited and nobody in the German forum was interested or commented. No one commented after it was available as stream with subtitles. Hard to understand.
     
  2. Andy

    Andy Committee Member

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    Perhaps Unrest not being on German Netflix is due to some kind of broadcasting rights issue? Hopefully, whatever the reason, if Netflix see high enough viewing figures elsewhere they'll extend it to Germany.
     
  3. Joh

    Joh Senior Member (Voting Rights)

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    Sounds like more countries might be added - just saw the Unrest email from today, Unrest will be on Netflix in 190 countries and in 20 languages! :woot:
     
  4. Alvin

    Alvin Senior Member (Voting Rights)

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    Thats not enough, we need to expand that by 6 to 196 :woot:
    j/k thats extremely impressive
     
  5. Rick Sanchez

    Rick Sanchez Senior Member (Voting Rights)

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    Unrest being released on Netflix in Denmark has made the news on one of the most popular and most well respected news sites in Denmark. Appears smack in the middle of the front page.

    https://politiken.dk/forbrugogliv/s...rfilm-sviner-dansk-tilgang-til-mystisk-sygdom

    Title: Documentary scolds danish approach to mysterious illness

    The documentary 'Unrest' exposes the treatment of the illness chronic fatigue syndrome / ME by Danish doctors. The movie has just been released on Netflix.

    (My somewhat liberal translation, hard to translate the word ''sviner'')

    The article also discusses how Denmark appears as the villain of the movie with excerpts from a earlier interview with a danish ME/CFS patient.
     
    Last edited: Jan 15, 2018
  6. Alvin

    Alvin Senior Member (Voting Rights)

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    Something i have wondered does Jen get any royalties from being on Netflix?
    If so is it based on the number of views?
     
    Nellie likes this.
  7. TiredSam

    TiredSam Committee Member

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    That's annoying, I told a colleague yesterday to watch it on Netflix. Hopefully it'll turn up soon.
     
  8. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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    Last edited: Jan 16, 2018
  9. Valentijn

    Valentijn Guest

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    I'd be careful about using a fake VPN to get international Netflix access. They started cracking down on that a few months ago, to the point that we couldn't even use their own national IPv6 servers anymore because it registered with them as tunneling :confused:
     
  10. Joh

    Joh Senior Member (Voting Rights)

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    ahimsa, Philipp, Skycloud and 6 others like this.
  11. TiredSam

    TiredSam Committee Member

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    Brilliant, I can tell everyone to watch it :)
     
    ahimsa, MErmaid, Joh and 2 others like this.
  12. Valentijn

    Valentijn Guest

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    I finally watched Unrest with my fiance tonight, and it was really really good. I'm saying this as a lifelong hater of documentaries :p I could have lived without the mold-avoidance adventures, but so much of it resonated with our experiences and there were some profound moments that would impact anyone watching it.

    I think they also did an excellent job of taking on the psychosomatic paradigm, and how horribly serious the disease is. Even the anti-"CFS" advocacy nuts couldn't claim it wasn't taken seriously if they'd actually watched the movie. Unrest features a lot of severe and very severe patients, as well as the deadly consequences ME/CFS can have.

    Additionally, I am now a movie star, appearing at around 1 hour 27 minutes on a giant poster during a Millions Missing protest :cool: Just think of the lucky bastard that has me hanging up on their wall!
     
    ahimsa, Revel, MESteveW and 17 others like this.
  13. dannybex

    dannybex Senior Member (Voting Rights)

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    I agree with all your points @Valentijn. My only, tiny -- and selfish quibble -- is that they didn't feature any patients dealing with this by themselves. But overall, an excellent film, and the cra-cra opponents of the film and Jen Brea's efforts should be ashamed of themselves.

    Now I'll have to watch it again so I can slow it down at the 1 hour 27 minute mark. :)
     
    Binkie4, ahimsa, MESteveW and 10 others like this.
  14. Valentijn

    Valentijn Guest

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    My blurry moment of fame:
    unrest_small.jpg
     
    ahimsa, Revel, MESteveW and 14 others like this.
  15. Andy

    Andy Committee Member

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    I can take it down it if it's too creepy... ;)
     
  16. Valentijn

    Valentijn Guest

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    Nah, it's okay ... I've got a poster of you on my ceiling:
    [​IMG]
     
  17. Alvin

    Alvin Senior Member (Voting Rights)

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    Cool, i wondered if you looked at all like your avatar.
    Can i ask why you used your screen name while protesting?
     
    Joh likes this.
  18. Allele

    Allele Senior Member (Voting Rights)

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    Is it on Netflix France?
     
    TiredSam and Joh like this.
  19. Valentijn

    Valentijn Guest

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    Not really ... I make a habit of never wearing orange :p

    To keep somewhat anonymous.
     
    Joh and Alvin like this.
  20. Alvin

    Alvin Senior Member (Voting Rights)

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    So we do have something in common :woot:

    Did you need a name at all to protest?
     
    Last edited: Jan 20, 2018

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