1st ME/CFS Canadian Collaborative Conference

Discussion in 'General ME/CFS news' started by Hoopoe, Feb 12, 2018.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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  2. Sly Saint

    Sly Saint Senior Member (Voting Rights)

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  3. JaimeS

    JaimeS Senior Member (Voting Rights)

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    Yessica, Helen, MEMarge and 19 others like this.
  4. Londinium

    Londinium Senior Member (Voting Rights)

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    From the minimal twitter scan I've done so far, there's a lot to like about this conference.
     
    MEMarge, dangermouse, Hutan and 3 others like this.
  5. Milo

    Milo Senior Member (Voting Rights)

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    Today was dedicated in priming physicians new to the field in understanding the illness. It was basically ME101. Tomorrow there will be a deep dive into the research. Most of the research presentations will be reserved to physicians and researchers. There will be a separate agenda for patients- and this will be webcast.
     
  6. Trish

    Trish Moderator Staff Member

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    It sounds like a really good conference. I hope it contributes to improving the situation for patients in Canada.
     
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  7. Pechius

    Pechius Senior Member (Voting Rights)

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    Does anybody know if recordings will be available?
     
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  8. JaimeS

    JaimeS Senior Member (Voting Rights)

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  9. andypants

    andypants Senior Member (Voting Rights)

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    My arm is getting worn out from hitting refresh on Twitter, so much promising info:) Can't wait for the summaries and hopefully more actual publications soon. Packed audiences in the doctor/researcher section is maybe the best thing about the entire conference.
     
    Yessica, Dechi, MEMarge and 9 others like this.
  10. JaimeS

    JaimeS Senior Member (Voting Rights)

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    Yesterday I was getting up and moving around a lot... this time I am totally captivated. I still WANT coffee and to stretch my legs but rn I'm consumed by the flow cytometry diagrams!
     
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  11. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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    This conference is good (for being the first). Thanks for tweeting.
     
    Yessica, MEMarge, dangermouse and 6 others like this.
  12. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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  13. JaimeS

    JaimeS Senior Member (Voting Rights)

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    Nacul now, but Cort and I had to flee around about the same time... we ran out of energy. He was leaving as I was coming back inside...
     
  14. Snowdrop

    Snowdrop Senior Member (Voting Rights)

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    Looks like there are lots of interesting findings being shared.
     
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  15. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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    ukxmrv, Yessica, JaimeS and 13 others like this.
  16. dangermouse

    dangermouse Senior Member (Voting Rights)

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    Wow, so much going on here..in a very good and positive way! :thumbup:
     
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  17. Snowdrop

    Snowdrop Senior Member (Voting Rights)

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    I look forward to having these various findings explained in more detail.
     
    JaimeS, MEMarge, Aroa and 6 others like this.
  18. Milo

    Milo Senior Member (Voting Rights)

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    The conference has wrapped up, there is this tweet from the institute that takes care of ME at the Canadian institutes for health research. Please like and retweet. This person may well be an agent of change for all of us.

    https://twitter.com/user/status/992833405254488065
     
  19. Snowdrop

    Snowdrop Senior Member (Voting Rights)

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    Done.

    I'm curious though. I had thought there were a few suspect people (central sensitisation theorists) who were to present their ideas. Haven't heard anything but reports of real science so far. Which is very good. I am relieved.
     
  20. Sunshine3

    Sunshine3 Senior Member (Voting Rights)

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    Ron Davis said at some point, I saw on a tweet earlier, we don't want to just treat this disease, we want to cure it. That statement used to fill me with hope in the past, not so much now.......it just seems a bit unrealistic.
     

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