Severe ME Day of Understanding and Remembrance: Aug. 8, 2017
Determined to paper the Internet with articles about ME, Jody Smith brings some additional focus to Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance on Aug. 8, 2017 ...
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UK: Do survey on need for individual advocates for patients to get health & social care, benefits

Discussion in 'Action Alerts and Advocacy' started by Sasha, Apr 28, 2015.

  1. Sasha

    Sasha Fine, thank you

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    I just did this worthwhile survey on this important topic and it took me 15 minutes, even though I had quite a bit to say on the open-ended questions. The questions were thoughtful and relevant - I thought the survey was generally well-designed and asking the right things.

    I'm aware that not all are fans of AfME but I don't see a downside to taking part in a good project that will help make the case for funding for advocates.

    I wanted to copy and paste the intro that's on SurveyMonkey but now that I've done the questionnaire, I can't get that page back. It would be good if someone could grab it and copy it here - it mentioned a June deadline, among other info.

    https://www.facebook.com/permalink.php?story_fbid=873449132712746&id=171411469583186

     
    Bob, Matthew Jones, SOC and 2 others like this.
  2. mango

    mango Senior Member

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    Sasha likes this.

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