Review: 'Through the Shadowlands’ describes Julie Rehmeyer's ME/CFS Odyssey
I should note at the outset that this review is based on an audio version of the galleys and the epilogue from the finished work. Julie Rehmeyer sent me the final version as a PDF, but for some reason my text to voice software (Kurzweil) had issues with it. I understand that it is...
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Register now for ME/CFS Advocacy Day on Capitol Hill!

Discussion in 'Advocacy Projects' started by Emily Taylor, Mar 12, 2018.

  1. Emily Taylor

    Emily Taylor

    Los Angeles, CA
    ME/CFS Advocacy Day on Capitol Hill brings people with ME/CFS, their loved ones, advocates, scientists, clinicians and caregivers from across the country to meet other advocates, share their unique stories with members of congress, and call for action and research funding, together in one voice.

    Check out the May ME/CFS Advocacy Week page for more information.

    To register for ME/CFS Advocacy Day on Tuesday May 15, visit the registration page.

    SMCI will provide:

    • All needed materials for meetings with Congress
    • Advocacy Training
    • Scheduling of meetings with YOUR representative and/or senators
    • A special rest area on Capitol Hill to make the experience as easy as possible, and to spend down time / rest time with other advocates.
    You’ll be responsible for your hotel and travel to the event. SMCI is securing hotel blocks that will be available from May 12-16.

    Advanced Registration is required for Tuesday, May 15th, so that we have time to set up meetings with your congressional representatives.

    To learn more or to register for the event visit our registration page.
    Dolphin and SueJohnPat like this.

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