usa

  1. J

    Innovative Drugs Save Lives Only if People Can Afford Them, NYT

    https://www.nytimes.com/2019/11/02/opinion/sunday/pelosi-drug-prices-plan.html?action=click&module=Opinion&pgtype=Homepage
  2. Sly Saint

    New ASU (Arizona State University) degree program to provide more nuanced understanding of disability

    full article here https://asunow.asu.edu/20191017-solutions-new-degree-program-provide-more-nuanced-understanding-disability
  3. Sly Saint

    Can Physical Activity Improve the Health of Wheelchair Users? - Bethesda, Maryland (NIH Visitor Information)USA Mar 2020

    March 30, 2020 - 8:30 AM - 5:45 PM March 31, 2020 - 8:30 AM - 1:30 PM Natcher Conference Center, NIH Campus, Bethesda, Maryland (NIH Visitor Information) ME not on list...
  4. Trish

    American Academy of Environmental Medicine Conference on Fatigue, October 10-13 2019, livestream $50/day

    Here's their website: http://aaemconference.com/fall/index.php Details of speakers here: http://aaemconference.com/livestream.php Includes speakers on diverse topics including biomedical, diagnosis, treatment, theories etc about CFS, EDS, MCAS, MCS, GWI mold, toxins... Speakers include...
  5. Adam pwme

    Open Medicine Foundation (OMF) fundraising

    Are you on Reddit? If so, please upvote for OMF to receive a donation of $15,000/1 Bitcoin from an anonymous donor. Upvote the initial comment and keep the chain going. (You must be registered on Reddit to participate.) OMF are really close they just need a few more upvotes. Well worth creating...
  6. Sly Saint

    US - ME/CFS Benefit Concert with Marian Call Saturday, October 5th, 2019 at the Mystic Theatre

    Concert An Evening with Marian Call. Singer-songwriter Marian Call, a native Californian, makes her home in Juneau, Alaska. She has released ten albums since 2007 and her concerts have been well-received on tours in all fifty United States, Canada, Europe, and the UK. full details here...
  7. Andy

    US: Winning and Waiting: A Federal Funding Update for ME/CFS, Sept 2019

    From an email from Solve ME/CFS Initiative What you Need to Know: The Senate Appropriations Committee included our ME/CFS Advocacy Day request for Defense. If approved in the final budget, ME/CFS will be an eligible topic area for the Peer-Reviewed Medical Research Program (PRMRP), which is...
  8. Kalliope

    American Council on Science and Health: Chronic Fatigue Syndrome: Progress Towards Diagnosis And Treatment, Finally?

    Chronic Fatigue Syndrome: Progress Towards Diagnosis And Treatment, Finally? Article is written by Henry I. Miller, physician and Senior Fellow at the Pacific Research Institute. He has also been a Research Fellow at the National Institutes of Health and the founding director of the Office of...
  9. ahimsa

    New website: The Harvard ME/CFS Collaboration

    At the symposium today speaker Ron Tompkins announced a new website, The Harvard ME/CFS Collaboration: http://endmecfs.mgh.harvard.edu/
  10. John Mac

    New Yorker: A Town for People with Chronic Fatigue Syndrome

    Article on the New Yorker Website about Incline Village and Ampligen. https://www.newyorker.com/culture/personal-history/a-town-for-people-with-chronic-fatigue
  11. Sly Saint

    US - Free Webinar: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) & the Pediatric Patient

    Webinar/Online Tuesday, September 10, 2019 at 12:30pm ET - 1:30pm ET Info Speaker(s) Robert Pendergrast, MD, FAAP Professor Department of Pediatrics Medical College of Georgia Augusta, Georgia Credits Offered This event offers 1.0 CE credit to attendees. Accredited by Georgia Nurses...
  12. D

    Open Medicine Foundation (OMF)

    Open Medicine Foundation Canada: https://www.omfcanada.ngo/?utm_source=email&utm_medium=news I donate to the OMF - can now receive a Canadian tax receipt ETA: It would be great to see some OMF funds going to Canadian ME researchers - there are collaborations, but I don't know if funds are...
  13. Sly Saint

    US - The Sleepy Girl Guide to Social Security Disability

    For people in US A lot of information https://howtogeton.wordpress.com/social-security-disability/
  14. Emily Taylor

    USA: Disability Insurance for ME/CFS

    July 2019 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 (employer-sponsored) Policy when disabled from ME/CFS. Register for the webinar here...
  15. rvallee

    Congressman Jack Bergman becomes Champion for ME

    https://www.meaction.net/2019/06/14/congressman-jack-bergman-becomes-champion-for-me/ Always good to thank those fighting for us. They are rare and appreciation always leads to more advocacy.
  16. Kalliope

    Jon Stewart on proper health care to 9/11-responders

    Just noticed a conversation on twitter and thought it might be interesting for the forum as well Jon Stewart has just held a passionate speech on the lack of proper health care for 9/11-first responders before a House Committee in Washington. Here's some of the reactions: And then this...
  17. M

    ME in US medical school curricula

    I didnt see a thread on this but if one exists, could this be merged in? A US medical school, Quinnipiac Medical School, has announced the creation of an endowed chair in family medicine as a result of a donation from a person with ME. As part of his role, the chair intends to bring focus and...
  18. Sasha

    USA Centers for Disease Control (CDC) news (including ME/CFS Stakeholder Engagement and Communication Calls) - next call 4 Dec 2024

    This thread includes posts on general news from the CDC and ME/CFS news including stakeholder calls. Several threads have been merged.
  19. Dr Carrot

    Really interesting project on medical data in the US

    Propublica are an organisation in the US that focus quite heavily on data-driven / accountability-type journalism, and this project they’ve put out is really interesting. Essentially if the data is available they’ve pulled together lots of data on doctors in the US, things like prescribing...
  20. Emily Taylor

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

    Your Advocacy in Action: Our ME/CFS Senate Resolution is Moving! Thanks to your efforts during ME/CFS Advocacy Week, Senators Markey and Collins will be introducing our resolution recognizing International ME/CFS Awareness Day. This is the last chance to urge your Senator to be a part of this...
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