Julie Rehmeyer's 'Through the Shadowlands'
Writer Never Give Up talks about Julie Rehmeyer's new book "Through the Shadowlands: A Science Writer's Odyssey into an Illness Science Doesn't Understand" and shares an interview with Julie ...
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Worldwide premieres of "Unrest"

Discussion in 'General ME/CFS News' started by Sasha, Jan 20, 2017.

  1. Sasha

    Sasha Fine, thank you

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    Thanks, Gary. The question (for us outsiders!) is then how do we find such a nurse or physician and get them to tackle the chair of medicine?

    @Jonathan Edwards, how would patients set about getting showings of Jen's film in hospitals (and medical conferences, and any other relevant places) in the UK? Would this be best done by one of the charities, do you think, perhaps linking up with local patients to push somehow?

    @JenB, do you have thoughts on this?
     
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  2. AndyPR

    AndyPR Senior Member

    From Facebook - https://www.facebook.com/unrestfilm/posts/852095174928217
     
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  3. Old Bones

    Old Bones Senior Member

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    https://www.facebook.com/unrestfilm/

    Exciting news from Jen on the "Unrest" film Facebook page:

    "I am thrilled to announce that Unrest, a feature length documentary about ME and CFS, will be making its European premiere at CPH:OX in Copenhagen, Denmark, March 16-26 in the "Before and After Science" section.

    We are so glad to be bringing this film to Scandinavia, a region that has been home to some of the most exciting scientific advancements in recent memory - uncovering evidence of autoimmunity and metabolic dysfunction in ME patients - while also seeing some of the most unsettling cases of forced institutionalization on the basis of the belief that ME is a psychological illness. We hope that Unrest can help bring to light this contradiction, start a public conversation and through it, increase support for research and for patient rights."
     
  4. Jo Best

    Jo Best Senior Member

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    Regarding increasing support for research and patients rights, currently thirteen countries are represented in the European ME Alliance (EMEA) and formed the European ME Research Group in 2015 - http://www.investinme.org/em-index.shtml
     
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  5. Old Bones

    Old Bones Senior Member

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  6. lnester7

    lnester7 Seven

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    Does it show the whole documentary? I am thinking on going if I can make it so wondering how much family to bring, I hate to show family any CFS documentary unless I see it first.
     
  7. Gingergrrl

    Gingergrrl Senior Member

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    I do not know the answer but please let us know all about it if you do go! I am still hoping the film will eventually come to L.A. so I can see it.
     
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  8. Cheesus

    Cheesus Senior Member

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    Sasha, this is my attempt: http://forums.phoenixrising.me/inde...ing-of-unrest-raise-money-for-research.50077/

    It still needs to all be organised, so we need to wait and see whether or not we can make it happen. If I am not mistaken, this is a screening you could theoretically attend if you're health is up to it as I believe you live somewhere in the region. Even better if we could borrow some of your community initiative to help make it a success.
     
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  9. Old Bones

    Old Bones Senior Member

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    Exciting news for Canadians:

    unrest.JPG

    Unrest2.JPG
     
    Last edited: Mar 21, 2017
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  10. Old Bones

    Old Bones Senior Member

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    MEMum, Never Give Up, Comet and 6 others like this.
  11. Cheshire

    Cheshire Senior Member

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  12. Old Bones

    Old Bones Senior Member

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  13. slysaint

    slysaint Senior Member

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    Sent details to UK TV news people..........still plugging away:D
     
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