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solve mecfs initiative

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  1. ahimsa
    Thread

    USA: Register now for ME/CFS Advocacy Week and DC Lobby Day 2020

    The Solve M.E. group is organizing another ME/CFS Advocacy Week this year for April 19 – 26, 2020. ME/CFS Advocacy week returns from April 19 –...
    Thread by: ahimsa, Jan 17, 2020 at 8:10 PM, 0 replies, in forum: Advocacy Projects and Campaigns
  2. Andy
    Thread

    Video: Carol Head: "ME As A Worldwide Civil Rights Issue"

    The 13th Invest in ME Research International ME Conference, one of the premiere scientific conferences for myalgic encephalomyelitis (ME) /...
    Thread by: Andy, Dec 29, 2018, 4 replies, in forum: General Advocacy Discussions
  3. Sly Saint
    Thread

    Dr. Jose Montoya On Believing ME/CFS Patients

    " [IMG] SolveCFS Published on Dec 12, 2018 At a recent SMCI gathering in Redwood City, Dr. Jose Montoya, a clinician who has fought for people...
    Thread by: Sly Saint, Dec 13, 2018, 4 replies, in forum: General ME/CFS News
  4. Andy
    Thread

    Solve ME/CFS Initiative: Chronicle Newsletter, Fall 2018

    Contents: SMCI This Quarter: A Summary of Our Work in Research, Advocacy and Beyond Updates from Ramsay Researchers Class of 2016 SMCI’s Research...
    Thread by: Andy, Dec 9, 2018, 0 replies, in forum: General ME/CFS News
  5. Andy
    Thread

    Solve ME/CFS Initiative: "Congress to HHS: What's replacing CFSAC?" [easy form to fill in to contact your reps]

    Congress to HHS: What's replacing CFSAC? ME/CFS must be represented! On September 6, the Secretary of Health and Human Services disbanded the...
    Thread by: Andy, Dec 4, 2018, 8 replies, in forum: Advocacy Action Alerts
  6. Andy
    Thread

    NIH Launches New Working Group Dedicated to ME/CFS

    The NIH (National Institutes of Health) recently formed The ME/CFS Working Group of the NINDS (National Institute of Neurological Disorders and...
    Thread by: Andy, Sep 14, 2018, 4 replies, in forum: General ME/CFS News
  7. Andy
    Thread

    Member questions for Dr. Sadie Whittaker, new Chief Scientific Officer of Solve ME/CFS Initiative

    Hi all. I have the chance for an interview with Dr. Sadie Whittaker at some point, so I wondered if you had any questions that you'd like asked?...
    Thread by: Andy, Jul 4, 2018, 28 replies, in forum: General ME/CFS News
  8. Andy
    Thread

    Solve ME/CFS Initiative: Research Highlights from 2018 So Far: Notable Study Developments

    The first half of 2018 has yielded over 100 publications specifically addressing various aspects of ME/CFS. Reports encompass familiar domains...
    Thread by: Andy, Jun 24, 2018, 0 replies, in forum: General ME/CFS News
  9. Andy
    Thread

    Solve ME/CFS Initiative: Chronicle newsletter Spring 2018

    Contents: Page 2 - SMCI This Quarter: A Summary of Our Work Page 5 - SMCI Welcomes Two New Members to Its Board of Directors Page 6 - What’s in a...
    Thread by: Andy, May 18, 2018, 2 replies, in forum: General ME/CFS News
  10. Andy
    Thread

    Solve ME/CFS Initiative: Discovery Forum 2017: Presentation of Dr. Elizabeth Unger

    Solve ME/CFS Initiative’s 2nd Annual Discovery Forum, held on October 14th in Washington DC, brings together leaders from across industry,...
    Thread by: Andy, May 6, 2018, 7 replies, in forum: General ME/CFS News
  11. Andy
    Thread

    Video: Fighting for M.E. with Carol Head | April 2018

    In this episode of “Fighting for M.E. with Carol Head,” Carol talks about ongoing work in SMCI’s research program and our efforts to storm Capitol...
    Thread by: Andy, Apr 21, 2018, 4 replies, in forum: General ME/CFS News
  12. Andy
    Thread

    Solve ME/CFS Initiative: Discovery Forum 2017: Presentation of Dr. Rick Williams

    This recording is the full presentation of Dr. Rick Williams, Principal Investigator for Medical & Public Health Research at RTI International...
    Thread by: Andy, Apr 13, 2018, 1 replies, in forum: General ME/CFS News
  13. Andy
    Thread

    SMCI: National ME/CFS Patient Registry Meet the Community Guide – Brian Vastag

    The Solve ME/CFS Initiative (SMCI) National ME/CFS Patient Registry, developed in partnership with the Genetic Alliance and Platform for Engaging...
    Thread by: Andy, Apr 4, 2018, 2 replies, in forum: General ME/CFS News
  14. Andy
    Thread

    Solve ME/CFS Initiative: Discovery Forum 2017: Presentation of Dr. Maureen Hanson

    [MEDIA]
    Thread by: Andy, Apr 1, 2018, 10 replies, in forum: General ME/CFS News
  15. Andy
    Thread

    Solve ME/CFS: "Tell Congress To Give ME/CFS Research a Fighting Chance!"

    Tell Congress To Give ME/CFS Research a Fighting Chance! Did you know that Congress oversees a $11.9 billion medical research budget independent...
    Thread by: Andy, Feb 17, 2018, 9 replies, in forum: Advocacy Action Alerts
  16. ahimsa
    Thread

    Solve ME/CFS Initiative (SMCI) has updated their website

    For those who aren't on the email list, the Solve ME/CFS Initiative group has updated their website. Here's the announcement from their mailing...
    Thread by: ahimsa, Feb 9, 2018, 0 replies, in forum: General ME/CFS News
  17. Andy
    Thread

    Advances in ME/CFS: "Scientist Advocate Spotlight: Zaher Nahle, Ph.D., M.P.A."

    Blog from the Jackson Lab, an interview with Zaher Nahle of Solve ME/CFS Initiative. For our next spotlight series, I took advantage of a recent...
    Thread by: Andy, Feb 7, 2018, 0 replies, in forum: General ME/CFS News
  18. Andy
    Thread

    Solve ME/CFs Initiative: Research 1st Newsletter, January 2018

    [IMG] Go direct to the newsletter, http://go.solvecfs.org/webmail/192652/56034262/84e1d7841020482702d2f139eb54c656adcc7b303ed3a93305e4ab13b6313018...
    Thread by: Andy, Jan 25, 2018, 2 replies, in forum: General ME/CFS News
  19. Andy
    Thread

    Solve Me/CFS Initiative: Discovery Forum 2017: An Interview with Dr. Nancy Klimas

    Solve ME/CFS Initiative’s 2nd Annual Discovery Forum, held on October 14th [2017] in Washington DC, brings together leaders from across industry,...
    Thread by: Andy, Jan 23, 2018, 12 replies, in forum: General ME/CFS News
  20. Andy
    Thread

    Solve ME/CFS Initiative's ME/ CFS Patient Registry: You + M.E.

    Preview of the project. The Solve ME/CFS Initiative (SMCI) is in the final stages of constructing a new state-of-the-art patient registry...
    Thread by: Andy, Jan 12, 2018, 10 replies, in forum: General ME/CFS News
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