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solve mecfs initiative

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  1. Andy
    Thread

    A letter from the NIH ME/CFS Collaborative Research Center consortium Community Advisory Committee to Francis Collins, Apr 2021

    "Dear Dr. Collins, We are a Community Advisory Committee established with the support of the NIH to advise the ME/CFS Collaborative Research...
    Thread by: Andy, Apr 19, 2021, 2 replies, in forum: Epidemics (including Covid-19)
  2. Andy
    Thread

    Video: ME/CFS Alert, Episode 124: Interview with Oved Amitay, CEO of the Solve ME/CFS Initiative

    In this episode Oved Amitay, who is the new CEO of the Solve ME/CFS Initiative and a pharmacologist by training, talks about the organization's...
    Thread by: Andy, Mar 22, 2021, 1 replies, in forum: General ME/CFS News
  3. Andy
    Thread

    USA: News from Solve ME

    The Solve Newsletter thread has been merged with this thread. Spring 2018 Contents: Page 2 - SMCI This Quarter: A Summary of Our Work Page 5 -...
    Thread by: Andy, May 18, 2018, 17 replies, in forum: News from Organisations
  4. Andy
    Thread

    News from The Long COVID Alliance (set up by SOLVE)

    Solve M.E. Spearheads “Long COVID Alliance” to Accelerate Post-Infectious Research From a Solve email. Today, Solve M.E. warmly welcomes 50 new...
    Thread by: Andy, Feb 25, 2021, 23 replies, in forum: News from Organisations
  5. ahimsa
    Thread

    Solve M.E. Presents: Legislative Cafe Chat on Thursday, Jan. 21

    I found the following announcement at the bottom of this page -...
    Thread by: ahimsa, Jan 16, 2021, 2 replies, in forum: General Advocacy Discussions
  6. Andy
    Thread

    Solve ME/CFS: The 5th Annual ME/CFS Advocacy Week April 18-24, 2021

    From an email from Solve. >>>>> The 5th Annual ME/CFS Advocacy Week will take place from Sunday, April 18, 2021 to Saturday, April 24, 2021. To...
    Thread by: Andy, Oct 28, 2020, 8 replies, in forum: Advocacy Projects and Campaigns
  7. ahimsa
    Thread

    Solve ME/CFS: $547,000 Awarded from Defense Department for ME/CFS Research

    Solve ME/CFS tweeted this today:https://twitter.com/PlzSolveCFS/status/1319407326621827078[MEDIA] I wanted a bit more info so I searched their...
    Thread by: ahimsa, Oct 23, 2020, 7 replies, in forum: General ME/CFS News
  8. ahimsa
    Thread

    USA: Rep. Jamie Raskin introduces legislation to address potential rise in ME/CFS from COVID-19 pandemic

    Raskin Introduces Legislation to Address America’s Hidden Health Crisis CDC labels chronic fatigue syndrome “America’s hidden health crisis” as...
    Thread by: ahimsa, Jun 4, 2020, 14 replies, in forum: General ME/CFS News
  9. Emily Taylor
    Thread

    ME/CFS Advocacy Day is TODAY!

    [IMG] Today is ME/CFS Advocacy Day! Not participating in meetings? If you have a few minutes throughout the day, you can still support and...
    Thread by: Emily Taylor, Apr 21, 2020, 1 replies, in forum: Advocacy Action Alerts
  10. Andy
    Thread

    Solve M.E. partners with University of California to issue an ME/CFS-specific funding announcement

    Solve M.E. is partnering with the University of California, Los Angeles (UCLA) Iris Cantor Women’s Health Center to issue an ME/CFS-specific...
    Thread by: Andy, Mar 31, 2020, 1 replies, in forum: BioMedical ME/CFS News
  11. 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, 0 replies, in forum: Advocacy Projects and Campaigns
  12. Emily Taylor
    Thread

    You + M.E. (International ME/CFS Registry) Website Live!

    [IMG] Registries are foundational in understanding, treating, and curing diseases. This approach is desperately needed in ME/CFS. That’s why...
    Thread by: Emily Taylor, Dec 24, 2019, 25 replies, in forum: General ME/CFS News
  13. Sly Saint
    Thread

    US News : Western Wisconsin Residents struggle with chronic illness Nov 2019

    [MEDIA] (not posted direct link to article as unsure of copyright/distribution permissions)
    Thread by: Sly Saint, Nov 21, 2019, 3 replies, in forum: General ME/CFS News
  14. Andy
    Thread

    Solve ME/CFS Initiative: Ramsay Grant program 2019 awards

    2019 is our biggest year yet! We have over 30 researchers working across seven projects. The group represents 12 academic centers and...
    Thread by: Andy, Oct 31, 2019, 21 replies, in forum: BioMedical ME/CFS News
  15. Andy
    Thread

    Solve ME/CFS Initiative: The Advances in ME/CFS Research Webinar Series

    From an email from them. Our “Advances in ME/CFS Research and Clinical Care” Webinar Series features presentations by researchers who contributed...
    Thread by: Andy, Oct 23, 2019, 7 replies, in forum: General ME/CFS News
  16. Andy
    Thread

    Empowerment in the Doctor’s Office: Overcoming White Coat Syndrome - Solve M.E. EmPOWER ME Conf 2019

    From the video description As part of 2019 ME/CFS Advocacy Week, Solve M.E. hosted the first EmPOWER M.E. Roundtable on April 2, 2019. Part 1,...
    Thread by: Andy, Jun 25, 2019, 2 replies, in forum: Advocacy Projects and Campaigns
  17. Emily Taylor
    Thread

    July Solve ME Webinar: Disability Insurance for ME/CFS

    Disability Insurance Attorney Andrew Kantor from Kantor & Kantor, LLP joins us to explain the ins and outs of filing for disability under an ERISA...
    Thread by: Emily Taylor, Jun 17, 2019, 8 replies, in forum: General ME/CFS News
  18. Andy
    Thread

    Video: Science for ME Q&A with Dr Sadie Whittaker from Solve ME/CFS Initiative, May 2019

    [MEDIA] The Science for ME forum are delighted to talk to Dr Sadie Whittaker from Solve ME/CFS Initiative about Solve's work, in particular their...
    Thread by: Andy, May 9, 2019, 14 replies, in forum: Researcher Interactions
  19. Emily Taylor
    Thread

    Advocacy Action: Urge Your Senator to Support ME/CFS Resolution

    [IMG] Your Advocacy in Action: Our ME/CFS Senate Resolution is Moving! Thanks to your efforts during ME/CFS Advocacy Week, Senators Markey and...
    Thread by: Emily Taylor, May 8, 2019, 1 replies, in forum: Advocacy Action Alerts
  20. Andy
    Thread

    Solve ME/CFS Initiative: Register now for the EmPOWER M.E. Roundtable Livestream!

    Solve ME/CFS Initiative (SMCI) is hosting our first ever EmPOWER M.E. Roundtable on April 2, 2019 moderated by Board Certified Patient Advocate,...
    Thread by: Andy, Feb 27, 2019, 13 replies, in forum: Advocacy Action Alerts
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