CFSAC nominations being accepted

Discussion in 'Fibromyalgia Main Forum' started by FM58, Sep 2, 2009.

  1. FM58

    FM58 New Member

    The CFSAC has 5 committee members whose terms expire Jan 4, 2010:

    Dr. James Oleske
    Rebecca Artman
    Dr. Lucinda Bateman
    Kristine Healy
    Dr. Morris Papernick

    Nominations are being accepted until 5 PM September 20, 2009. To view information regarding making a nomination.

    For more information about CFSAC, to to web-site:

    They have not yet posted a meeting date; just stated late October.
  2. skeptik2

    skeptik2 Member

    Why bother? They are worthless.

    Nothing whatsoever positive has happened since their May meeting, and they
    were lambasted back and forth, by me especially.

    They have accomplished nothing in their years of service. One would think
    that they would have insisted on a face-to-face meeting with the head of the DHHS by
    now, but they are just a self-perpetuating loser.

    Someone from the WPI should be appointed; at least they are working
    towards getting results, not words.


  3. kamina

    kamina New Member

    This is why I've missed you so much skep. :)
  4. gapsych

    gapsych New Member

    Are you back on the board?

  5. skeptik2

    skeptik2 Member

    I keep giving up on this board, but you and aunttammie and khaylal
    keep me going!

    I'm so frustrated by the CDC and the CFSAC I can't tell you without
    swearing, so I'll forgo that, ok? LOL...

    BTW, anyone heard from Khalyal?
    Probably spelled that wrong on one of these..ooops!

    K., if you're around, check the heck in, will ya?

  6. simpsons

    simpsons Member

    NEVER GIVE UP - keep the pressure on.

    we need to be clear about what we want and stand united as one all the ME groups need to keep together as one so reeves can.t say its not that everyone feels the same.

    skeptic2 who is our dream team? wpi, plus ? ? ? dr chia pandora ???

    Input on CDC CFS Strategic Research Plan

    Between April 15 and July 30, 2009, CDC received just over 1,000 e-mails in
    response to a request for input to its 5-year CFS strategic plan. Most of
    the e-mails utilized material from the CFIDS Association of America’s Web
    site or supported CFIDS recommendations, reflecting the effectiveness of
    CFIDS advocacy efforts. We greatly appreciate this overwhelming response,
    since it provided an opportunity for members of the CFS community to share
    their concerns.

    Some emails from the general public provided comments specific to the
    strategic research plan and we also received comments on the strategic plan
    from two scientific societies (the International Association for Chronic
    Fatigue Syndrome, and the American Academy of Environmental Medicine),
    scientific investigators, health care providers, and patient advocacy groups
    (CFIDS Association of America, Pandora, Connecticut CFIDS & FM Association,
    National Women´s Health Network, Rocky Mountain CFIDS/FMS Association,
    Phoenix Rising, Wisconsin ME/CFS Association, Share Care & Prayer, CFSActs,
    National CFIDS Foundation, Invest in ME - UK).

    CDC´s CFS research program is currently categorizing comments concerning the
    strategic plan into specific subject areas.

    To see the full CFS Public Health Research Program Draft 5-year Strategic
    click here (links to a
    page last modified on May 29, 2009).

    Page last modified on September 1, 2009

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