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Scott Ludlam
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== Senate hearings == At the [https://en.wikipedia.org/wiki/Australian_Senate_committees Australian Senate Community Affairs Legislation Committee] hearings, Senator Ludlam's direction asked questions about the little funds and poor medical health support for Australia's myalgic encephalomyelitis patients and GPs trying to treat them. He mentioned the good job [[Emerge Australia]] does on little funds. A 9 minute video of theone of the hearings was uploaded on February 10th, 2016 (FB time stamp 5:51PM) .<ref>[https://www.facebook.com/SenatorLudlam/videos/10153980238139470/ The Senate Community Affairs Legislation Committee - Senator Scott Ludlam FB Page - Video Feb. 10, 2016 5:51PM]</ref> In 2015 Ludlam told the hearing “I am struggling to think of a cohort of people in our community that large for whom there is so little”. [https://meaustralia.net/2016/03/03/aust-senator-questions-government-on-lack-of-action-on-me/ 'Australian senator questions government on lack of action on ME]'. In 2016 Ludlam asked the NHMRC “outside NHMRC grants, is there any Commonwealth support for people with this condition that you are aware of?" [https://meaustralia.net/2016/03/03/australian-health-dept-answers-questions-on-me/ Australian Health Department answers questions on ME]. Later in 2016, he asked the NHRMC "about two-thirds of the funding appears to be going to into research that, however worthy, actually has nothing at all to do with ME/CFS.Can you correct either the record or point out how this research is directly relevant to the questions that I asked?” [https://meaustralia.net/2016/03/03/australian-health-department-pins-its-hopes-on-nih-research/ Australian Health Department pins its hopes on overseas research instead of funding our own]. Read Sasha Nimmo's article for more http://www.meaction.net/2016/02/12/australian-health-department-pins-its-hopes-on-nih-research/
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