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  1. Sunshine3
    Post

    Australia’s Health Minister Greg Hunt announces $3m for medical research

    From Emerge, a reply on their Facebook page: our understanding is that this research money has gone into the upcoming budget. This budget is...
    Post by: Sunshine3, Mar 29, 2019 in forum: ME/CFS research news
  2. Sunshine3
    Post

    Australia’s Health Minister Greg Hunt announces $3m for medical research

    So does this mean that the 3 million isn't fully guaranteed at present.... That this could change depending on election outcome... Sigh.....
    Post by: Sunshine3, Mar 28, 2019 in forum: ME/CFS research news
  3. Sunshine3
    Post

    David Tuller crowdfund: Trial By Error: Reporting on ME/CFS and Related Controversies

    I've never met you David but you are a true hero and I feel so grateful to have you with us. You are our superman!!
    Post by: Sunshine3, Mar 28, 2019 in forum: Fundraising
  4. Sunshine3
    Post

    Australia’s Health Minister Greg Hunt announces $3m for medical research

    I hope Neil McGregor gets some of this stash.
    Post by: Sunshine3, Mar 27, 2019 in forum: ME/CFS research news
  5. Sunshine3
    Post

    Australia’s Health Minister Greg Hunt announces $3m for medical research

    @Simone thank you for keeping us informed and clarifying information, much appreciated. Hope we see Emerge video clips soon, not that I'm eager or...
    Post by: Sunshine3, Mar 27, 2019 in forum: ME/CFS research news
  6. Sunshine3
    Post

    Australian Greens party announce ME and CFS policy

    Any idea when this money will be released so that research can get going
    Post by: Sunshine3, Mar 25, 2019 in forum: General ME/CFS news
  7. Sunshine3
    Post

    Frontiers review - Chronotropic incompetence an overlooked determinant of symptoms and activity limitation in ME/CFS (prov. 2019) Davenport et al

    Makes so much sense to me, I always feel that my heart can't sustain any simple activity..like I'm in some kind of heart failure. I'm delighted to...
    Post by: Sunshine3, Mar 25, 2019 in forum: ME/CFS research
  8. Sunshine3
    Post

    NIH Request For Information: Soliciting Input on How Best to Advance ME/CFS research

    Is the NIH's current position in relation to funding of trials for ME/CFS going to change anytime soon? There is no mechanism in place for us at...
    Post by: Sunshine3, Mar 20, 2019 in forum: General ME/CFS news
  9. Sunshine3
    Post

    ME/CFS International Research Symposium, March 2019, Australia

    The Norwegians have also noted something in the blood. Mark Davis is surely looking for it. I only saw one video clip from Ron Davis but I thought...
    Post by: Sunshine3, Mar 18, 2019 in forum: ME/CFS research news
  10. Sunshine3
    Post

    ME/CFS International Research Symposium, March 2019, Australia

    Having no luck with that but thanks @andypants
    Post by: Sunshine3, Mar 17, 2019 in forum: ME/CFS research news
  11. Sunshine3
    Post

    ME/CFS International Research Symposium, March 2019, Australia

    @Simone any idea when videos from Emerge Conference will be made available? Thank you.
    Post by: Sunshine3, Mar 17, 2019 in forum: ME/CFS research news
  12. Sunshine3
    Post

    Pharmaceutical interventions in CFS: A literature-based commentary, Richman, Morris, Broderick, Craddock, Klimas, Fletcher, March 11, 2019

    @Alvin I thought they were trying to reboot homeostasis and effectively get us back to normal... Did they mention that in Australian presentation?
    Post by: Sunshine3, Mar 16, 2019 in forum: General ME/CFS news
  13. Sunshine3
    Post

    ME debate in Danish Parliament March 12 (2019)

    Jeez I'm emotional... Great news!!
    Post by: Sunshine3, Mar 14, 2019 in forum: Advocacy Action Alerts
  14. Sunshine3
    Post

    ME/CFS International Research Symposium, March 2019, Australia

    Wow that transcript from Greg Hunt is super news!!
    Post by: Sunshine3, Mar 14, 2019 in forum: ME/CFS research news
  15. Sunshine3
    Post

    Assessment of Post-Exertional Malaise (PEM) in Patients with Myalgic Encephalomyelitis (ME) and Chronic Fatigue Syndrome (CFS). Holtzman et al. (2019)

    I'm delighted to see this study.. A true reflection of this awful illness.
    Post by: Sunshine3, Mar 6, 2019 in forum: ME/CFS research
  16. Sunshine3
    Post

    ME/CFS Discovery Research Network (MDRN) - Australian research collaborative

    Can't wait to hear some news from Emerge Conference.. Anyone know who will be providing such news...
    Post by: Sunshine3, Mar 5, 2019 in forum: ME/CFS research news
  17. Sunshine3
    Post

    Article: The role of mitochondria in ME/CFS: a perspective, 2019, Tomas and Elson

    So do I big time
    Post by: Sunshine3, Feb 28, 2019 in forum: ME/CFS research news
  18. Sunshine3
    Post

    Article: The role of mitochondria in ME/CFS: a perspective, 2019, Tomas and Elson

    It's easy to make a diagnosis of M. E if doctors knew anything about it.. But they don't. I totally agree with you @Mithriel... I've often thought...
    Post by: Sunshine3, Feb 28, 2019 in forum: ME/CFS research news
  19. Sunshine3
    Post

    Letter from the 25% ME group to NICE re: CBT and GET, Feb 2019

    Nobody knows what the figures for M.E are! How could we know when many doctors can't diagnose it or diagnose depression or fibromyalgia instead....
    Post by: Sunshine3, Feb 24, 2019 in forum: 2020 UK NICE ME/CFS Guideline
  20. Sunshine3
    Post

    SMCI RAMSAY 2018: “Characterization of Janus kinase (JAK) activation profiles in ME/CFS subgroups”, Lombardi

    The holy grail, clinical trials!
    Post by: Sunshine3, Feb 19, 2019 in forum: ME/CFS research
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