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

Discussion in 'ME/CFS research news' started by MyalgicE, Mar 27, 2019.

  1. MyalgicE

    MyalgicE Senior Member (Voting Rights)

    Messages:
    146
    Location:
    Australia
    Health Minister Greg Hunt announces $3 million for biomedical research funding for chronic fatigue syndrome!
     

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    svetoslav80, Tilney, JaneL and 27 others like this.
  2. Alvin

    Alvin Senior Member (Voting Rights)

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    Who is the money going to?
     
    rvallee likes this.
  3. hixxy

    hixxy Senior Member (Voting Rights)

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    Please let it not get sucked into the black hole that is NCNED or even worse to BPS researchers.
     
    EzzieD, Cheshire, Andy and 3 others like this.
  4. Patient4Life

    Patient4Life Senior Member (Voting Rights)

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    ugh...it would be a shame if they got the money. Their biomarker research is ridiculous. In the US, no researchers are heralding their "discovery".
     
    Andy likes this.
  5. dreampop

    dreampop Senior Member (Voting Rights)

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    They actually have done a lot of neuro imaging stuff (Barnden) and are at least looking at a variety of angles. They are also ready to talk to the newspapers about how bad the illness/that it's real etc.. So they have definitely done some good.
     
    Londinium, pteropus, Hutan and 2 others like this.
  6. MyalgicE

    MyalgicE Senior Member (Voting Rights)

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    146
    Location:
    Australia
  7. MyalgicE

    MyalgicE Senior Member (Voting Rights)

    Messages:
    146
    Location:
    Australia
    @hixxy
    There is a danger of that and we can see UNSW gearing up, releasing a review recently calling for more biopsychosocial studies into ‘mecfs’ (although they don’t use the Canadian Consensus Criteria).
     
    Last edited: Mar 27, 2019
    Milo likes this.
  8. Sean

    Sean Moderator Staff Member

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    7,159
    Location:
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    I smell an election.
     
    Lidia, MEMarge, pteropus and 6 others like this.
  9. BruceInOz

    BruceInOz Senior Member (Voting Rights)

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    414
    Location:
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    First the Greens, now Liberals. Must be Labor's turn now.
     
    alex3619, pteropus, Wonko and 5 others like this.
  10. Simone

    Simone Senior Member (Voting Rights)

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    Location:
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    This is the second recommendation from the NHMRC ME/CFS Advisory Committee which has been implemented, which is really encouraging, given that the committee’s final report hasn’t been released yet. The first was for a health economics study: https://www.grants.gov.au/?event=public.GO.show&GOUUID=8E688A94-D501-6184-7128C473FE3CD789

    This has truly been a community effort. In addition to the committee’s work, many advocates have written letters to MPs and had meetings with politicians (with several meeting with Hunt). The combined efforts have paid off!
     
    Hutan, alex3619, Ron and 17 others like this.
  11. oldtimer

    oldtimer Senior Member (Voting Rights)

    Messages:
    645
    Location:
    Melbourne Australia
    Thanks Simone and everyone for their efforts!
     
    MEMarge, pteropus, Wonko and 6 others like this.
  12. InitialConditions

    InitialConditions Senior Member (Voting Rights)

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    I still don't know where the money is going...!
     
  13. Andy

    Andy Committee Member

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    It's not been allocated yet. As I understand it, it is a $3 million pot of cash that researchers will be able to put proposals forwards, asking for funding from that pot.
     
  14. Cinders66

    Cinders66 Senior Member (Voting Rights)

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    1,205
    This is very good news.

    In pounds It’s equivalent to £1.6 m of state funds for research. Australia has a population of just under 1/3 of UK (23m), so it’s quite a large sum. In proportion UK should be investing £4m and the USA £20m odd (I think)

    We need several countries having a significant research effort to make proper progress. They’re doing what our MRC refuse, putting up money to stimulate research interest which imo is obviously the right thing to do.

    Edited for Australian dollars not US.
    Edited to note the 1% prevalence rate quoted in article
     
    Last edited: Mar 27, 2019
  15. Simone

    Simone Senior Member (Voting Rights)

    Messages:
    445
    Location:
    Australia
    Yep, that’s exactly right.

    A worst case scenario would be for someone like Andrew Lloyd to get a grant from this, but at the very least we know he won’t get all of it, because it will be multiple grants. And, hopefully, the emphasis in the ME/CFS Advisory Committee’s report itself (that NHMRC funding should prioritise biomedical research and use CCC to select patients) will make it more difficult for psychosocial researchers to be successful in getting a grant from this.
     
    Last edited: Mar 27, 2019
    andypants, Lidia, Sean and 8 others like this.
  16. Sunshine3

    Sunshine3 Senior Member (Voting Rights)

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    @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 :)
     
    pteropus, andypants, Sean and 3 others like this.
  17. Sunshine3

    Sunshine3 Senior Member (Voting Rights)

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    I hope Neil McGregor gets some of this stash.
     
    chelby, andypants, Lidia and 6 others like this.
  18. Sean

    Sean Moderator Staff Member

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    Location:
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  19. MyalgicE

    MyalgicE Senior Member (Voting Rights)

    Messages:
    146
    Location:
    Australia
  20. BruceInOz

    BruceInOz Senior Member (Voting Rights)

    Messages:
    414
    Location:
    Tasmania
    I presume/hope that a commitment is being sought from the Labor party to match or better this. I am guessing minister Hunt's announcement won't be set in stone before the May election so may be overturned in the somewhat likely event that they lose. Getting Labor on board now seems vital.
     
    rvallee, Sean and andypants like this.

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