1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
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A Little Poisoning Along the Road to ME/CFS
Looking at my symptoms, many of which are far less these days and some are gone, it would be easy to figure that I'd just been dealing with some heavy-duty menopausal issues.
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World Premier: A New Play about Chronic Fatigue Syndrome (ME/CFS)

Discussion in 'Action Alerts and Advocacy' started by RivkaRivka, Jul 11, 2011.

  1. RivkaRivka

    RivkaRivka Senior Member

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    Hey everyone, please spread the word: Our new play about the lives of people living with ME/CFS (Chronic Fatigue Syndrome) has its world premier this week. Thanks to the patients -- Laurel, Ben, Janine, Joey (and me) -- for allowing us to tell their stories publicly. And thanks to the director, Ivy Nelson, and the Missouri actors she has assembled for this world premier of I REPRESENT: INVISIBLE NO MORE. See link below for more info. Consider doing the play in your community as a fundraiser for your local ME/CFS support group, or for the Whittemore Peterson Institute. To request the script, email me.

    https://www.facebook.com/event.php?eid=121323907958246#!/event.php?eid=121323907958246

    Best,
    Rivka
    Rivka (at) ThatTakesOvaries (dot) org
     
  2. Nielk

    Nielk

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    Queens, NY
    Thank you Rivka for all you do for us!
    I just posted the event on my fb wall.
    If everyone could do the same, we could reach a lot of people.

    Thanks to all who participated in this for us,
    Nielk
     
  3. RivkaRivka

    RivkaRivka Senior Member

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    wonderful, nielk! thank you! -- rivka
     

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