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    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 'just another' budget from the ruling coalition. Budgets get passed and then are inherited by the next government. In our view it is absolutely safe...
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    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.. @BruceInOz @Simone
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    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!!
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    Australia’s Health Minister Greg Hunt announces $3m for medical research

    I hope Neil McGregor gets some of this stash.
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    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 anything :)
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    Australian Greens party announce ME and CFS policy

    Any idea when this money will be released so that research can get going
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    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 this study published. Also, HR has nothing to do with pem for me. I can get severe pem from having a visitor.
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    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 present. The use of stricter diagnostic criteria, the presence of PEM is an absolute must. @Michiel Tack are you compiling a document or is there...
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    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 he seemed optimistic, more alive and upbeat than usual. He presented very well. He is on no holiday, he is on a mission. I think Phair equally wants...
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    ME/CFS International Research Symposium, March 2019, Australia

    Having no luck with that but thanks @andypants
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    ME/CFS International Research Symposium, March 2019, Australia

    @Simone any idea when videos from Emerge Conference will be made available? Thank you.
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    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?
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    ME debate in Danish Parliament March 12 (2019)

    Jeez I'm emotional... Great news!!
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    ME/CFS International Research Symposium, March 2019, Australia

    Wow that transcript from Greg Hunt is super news!!
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    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...
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    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 there are other illnesses with no biomarkers such as migraine and they can be diagnosed. Id diagnose M.E in 10 minutes because I know what the...
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    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. In fact some doctors think fibro and M.E are the same disease. I personally don't think M.E is that common. Chronic fatigue is conflated with M.E..so...
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