Should there be a primer for employers?

Discussion in 'MEpedia' started by Patient4Life, Mar 3, 2019.

  1. Patient4Life

    Patient4Life Senior Member (Voting Rights)

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    Last edited by a moderator: Mar 5, 2019
    Trish, JaimeS, Sean and 2 others like this.
  2. JaimeS

    JaimeS Senior Member (Voting Rights)

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    Stanford, CA
    I came across a really, really good resource on this recently and it's made me consider precisely that.

    For everyone's edification: https://askjan.org/disabilities/Chronic-Fatigue-Syndrome.cfm

    I'm feeling pretty weird/bad so I apologize in advance if I'm not as responsive as usual lately. I'll pop this into the #MEAction Slack, though.

    It sure is easier to agree to support a project than to take it on. If anyone here wants to take this on, #MEAction can help with staff resources and time -- especially in the spring, with Advocacy Week coming up in April and #MillionsMissing in May, a project leader/collaborator from outside the main staff is absolutely key.

    If anyone feels like they could support this, it would be a great idea. Maybe USA Working Group could help.

    [Edit: #MEAction links to the following resources on its Patients Portal:

    USA
     
    Last edited: Mar 5, 2019
  3. DokaGirl

    DokaGirl Senior Member (Voting Rights)

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    @JaimeS

    Hope you feel less weird /bad soon!
     
    Binkie4 and JaneL like this.
  4. Alvin

    Alvin Senior Member (Voting Rights)

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    I'd love to do it but my ability to organize it is beyond dismal :banghead:
    I don't know if it could somehow be possible, i'm full of information but writing/copy editing i can't do as weird as that sounds.
     
    Patient4Life likes this.

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