The Call for Opposition: Challenging the P2P and IOM Processes
In our second article on how to react to the publication of the draft P2P report, Gabby Klein provides her view of why she and a large group of advocates and patients are continuing their protest of the government’s ongoing control and manipulation of our disease via their processes...
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UK: Jen Brea wants eyecatching stats re UK ME prevalence, diagnosis, research, treatment

Discussion in 'Advocacy Projects' started by Sasha, Aug 14, 2014.

  1. Sasha

    Sasha Fine, thank you

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    UK
    Looks like Jen with her Canary in a Coalmine documentary (can't wait!) is going to be mentioning the UK.

    She just posted on FB:

    https://www.facebook.com/canaryfilm/posts/438195219651550

    I've got no reason to think that she reads Phoenix Rising or will see this thread so please post your responses on FB or presumably it's OK to use her main website contacts page:

    http://www.canaryinacoalminefilm.com/#!contact/c24vq
     
  2. Countrygirl

    Countrygirl Senior Member

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    When reading the above, I ask what diagnosis,research and treatment????

    We are mis-diagnosed, mis-treated and no funding has been given for medical research over the decades in the UK.
     
  3. Leopardtail

    Leopardtail Senior Member

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    well, given yes, but mostly to Psychiatry
     

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