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jen brea

  1. Sly Saint
    Thread

    Media Impact Award 2019 Invisible Disabilities Association goes to Jen Brea

    [MEDIA] "Jennifer Brea is impacting the world for people living with the invisible disability, M.E. with her award winning film, "Unrest!"...
    Thread by: Sly Saint, Jan 18, 2020, 2 replies, in forum: General ME/CFS News
  2. Dr Carrot
    Thread

    Jen Brea: My ME is in remission

    This is a hard post to write because there are no words that can do this justice. I can hardly believe it myself. My ME is in remission. For the...
    Thread by: Dr Carrot, May 20, 2019, 305 replies, in forum: General ME/CFS News
  3. Sly Saint
    Thread

    Canada: 19th Annual Illuminations Jan 2019 - guest speaker Jen Brea

    "Date January 24, 2019 Time 11:30am - 2:00pm Location Fairmont Waterfront, 900 Canada Pl, Vancouver BC Illuminations is our much-anticipated...
    Thread by: Sly Saint, Nov 9, 2018, 0 replies, in forum: General ME/CFS News
  4. Andy
    Thread

    #MEAction: Next steps: a letter to our community [from Jen Brea]

    Hi everyone, I just wanted to take a moment to comment on some of the confusion and concern of these last few weeks and offer some steps forward...
    Thread by: Andy, Jun 28, 2018, 3 replies, in forum: General ME/CFS News
  5. Andy
    Thread

    Jackson Labs blog: Patient Advocate Interview: Jennifer Brea

    We are very excited to present our next “People in ME/CFS Research” spotlight this week, which is my interview with patient and advocate Jennifer...
    Thread by: Andy, May 8, 2018, 1 replies, in forum: General ME/CFS News
  6. Sly Saint
    Thread

    Australian radio program: Jen Brea & Panel Discussion

    Uncommon Sense with Amy Mullins "Tuesday 13th March: US film director Jennifer Brea will talk to Amy about her Oscar-shortlisted documentary...
    Thread by: Sly Saint, Mar 10, 2018, 18 replies, in forum: General ME/CFS News
  7. Sly Saint
    Thread

    Jen Brea - Lavin agency speaker

    " THE LAVIN AGENCY is the world’s largest intellectual talent agency, representing leading thinkers for speaking engagements, personal...
    Thread by: Sly Saint, Mar 8, 2018, 3 replies, in forum: General ME/CFS News
  8. Sly Saint
    Thread

    ProHealth is Proud to Announce its 2017 ME/CFS Patient Advocate of the Year: Jennifer Brea

    " In 2017, Jen Brea did the impossible. She catapulted ME/CFS onto the public stage, and into the international spotlight, all in one fell swoop...
    Thread by: Sly Saint, Mar 8, 2018, 9 replies, in forum: General ME/CFS News
  9. Alvin
    Thread

    Jen Brea comments on Esther Crawley's behaviour

    I've made a practice of not publicly calling out Esther Crawley in part because the issues we face are so much bigger than any one researcher. 26...
    Thread by: Alvin, Dec 31, 2017, 47 replies, in forum: General ME/CFS News
  10. Sly Saint
    Thread

    Unrest - Screenings 2018

    Galway Premiere of the award winning medical documentary film 'Unrest' (97 mins) about Myalgic Encephalomyelitis (M.E). " The screening of...
    Thread by: Sly Saint, Nov 23, 2017, 19 replies, in forum: General ME/CFS News
  11. Sly Saint
    Thread

    Unrest - reviews and general articles

    When Fatigue Disables - Newcastle Herald Australia Chronic fatigue syndrome documentary UNREST to screen in Newcastle 10 Nov...
    Thread by: Sly Saint, Nov 12, 2017, 156 replies, in forum: General ME/CFS News
  12. Skycloud
    Thread

    ME - The Movie. Ouch Disability Podcast BBCRadio

    An interview with Jen Brea on the Ouch Disability Podcast On BBC iPlayer Radio http://www.bbc.co.uk/programmes/p05mgjjz 19 minutes long eta -...
    Thread by: Skycloud, Nov 9, 2017, 7 replies, in forum: General ME/CFS News
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