August 8th, 2018: Understanding and Remembrance Day for Severe ME
Have you heard of our Severe Myalgic Encephalomyelitis Day of Understanding and Remembrance? Please join Jody Smith in observing this day and honoring the 25% of those with ME/CFS who are most severely ill.
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San Francisco public demonstration: Can you attend? (The week of May 23)

Discussion in 'Action Alerts and Advocacy' started by RivkaRivka, May 17, 2011.

  1. RivkaRivka

    RivkaRivka Senior Member

    ME/CFS/XMRV Patients, Families and Friends -- Invisible No More

    Sick and tired of:
    - your government ignoring you and this illness?
    - being belittled by the media for a very real illness you have suffered with for years?
    - being invisible?

    Be Invisible No More! Join us in telling the government & media that we need more research money dedicated to understanding and treating ME/CFS and XMRV. Join us in a public demonstration to be held outside S.F.'s Health and Human Services building. We'll tell HHS Secretary Kathleen Sebelius to finally help the 1 million sick and disabled Americans with ME/CFS and XMRV.


    WHAT: A demonstration holding a 25 foot banner in front of the San Francisco regional office of the U.S. Department of Health and Human Services. (HHS oversees NIH, CDC, FDA.) This demo will be similar to one held recently on Capitol Hill, Washington D.C., in front of HHS's national headquarters. See video here:

    WHY: Our goal is to tell the HHS that we are expecting more for ME/CFS and XMRV: More respect, more attention, more research money, more clinical trials.

    WHO: People with ME/CFS and XMRV, their family and friends.

    WHEN: The week of May 23, any day we can find 5 people available. Preference for Wednesay, May 24, or Thurs, May 25, 1:30-2:30 pm. Tell us, when might you be available? Do you need help with transportation?

    WHERE: In front of the HHS building at 90 Seventh Street (Federal Building).

    THE ACTION: The large banner reads, "Obama, Sebelius, HHS: Shame on you for abandoning 1 million sick and disabled Americans with ME/CFS and XMRV (Chronic Fatigue Syndrome and a newly discovered retrovirus). Clinical trials now!" Those who wish can say three sentences about your health, years sick, and your needs, and/or read a bit from a previously drafted statement. An edited video of the event will be made public (YouTube) and presented to HHS. Media will be invited. One of us will deliver a letter to HHS officials. We will seek a permit from the S.F. Police before hand, if needed.

    Daughter sick 21 years ME/CFS/XMRV
    Bausubel (at) yahoo (dot) com
    (I am the woman on the right of this video: )

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