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M.E. In BC [British Columbia]: How the healthcare system for M.E. impacts clinicians and patients

Discussion in 'ME/CFS research news' started by Milo, Apr 2, 2021.

  1. Milo

    Milo Senior Member (Voting Rights)

    Messages:
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    M.E. In BC [British Columbia]: How the healthcare system for M.E. impacts clinicians and patients

    This is a preliminary study assessing the unmet needs of patients living with ME; 25 patients were either interviewed or participated in a focus group. Over 170 health care professionals/ administrators filled out an online survey.

    https://twitter.com/user/status/1377727469827031043


    You can find the link to the short and long versions of the reports at the link above, and while you are there, please give it a like and a retweet if you are so inclined
     
    Andy, Michelle, Helene and 16 others like this.
  2. Milo

    Milo Senior Member (Voting Rights)

    Messages:
    2,107
    There are several graphics for viewing in the long-version report.



    8C9BC29E-E7F0-4BA7-93D2-335B8C174FE1.jpeg
     
    Andy, ME/CFS Skeptic, Helene and 4 others like this.

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