Australia - Adam Bandt MP

Sly Saint

Senior Member (Voting Rights)
Adam Bandt
19 September at 16:53 ·
The effects of myalgic encephalomyelitis, or ME for short, are devastating enough to leave 25 per cent of sufferers housebound or bedbound and an estimated 75 per cent unable to work.

But, there are no government programs supporting ME awareness in Australia, there are no approved pharmaceutical treatments and, sadly, there is no cure.

It's time to take this seriously and increase funding and research for this disease for the hundreds of thousands here and the missing millions around the world.



from Adam Bandt MP on Facebook
" I’ve been reading some very powerful comments here. Thank you to the ME community for helping open my eyes to this debilitating disease and understand better what you’re going through. I hope that together we can raise awareness, get some change in the NDIS experience and boost research funding. Please stay in touch
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"
-PAXP-deijE.gif
 
Adam Bandt
19 September at 16:53 ·
The effects of myalgic encephalomyelitis, or ME for short, are devastating enough to leave 25 per cent of sufferers housebound or bedbound and an estimated 75 per cent unable to work.

But, there are no government programs supporting ME awareness in Australia, there are no approved pharmaceutical treatments and, sadly, there is no cure.

It's time to take this seriously and increase funding and research for this disease for the hundreds of thousands here and the missing millions around the world.



from Adam Bandt MP on Facebook
" I’ve been reading some very powerful comments here. Thank you to the ME community for helping open my eyes to this debilitating disease and understand better what you’re going through. I hope that together we can raise awareness, get some change in the NDIS experience and boost research funding. Please stay in touch
1f642.png
"
-PAXP-deijE.gif

Well done Aussies :thumbup:
 
This makes me very happy. The clip is worth a listen. Adam Bandt is Deputy Leader of the Australian Greens Party, MP for my Australian electorate. I thought he was a good man before he had a view on ME; I was not wrong.

Well done to Christa Callanan (sorry if I have got her name wrong) who approached Adam. Well done to Emerge and everyone else involved. Brilliant.
 
Always a good time to ask when there is an election looming (within 12 months max, more likely a lot less).

By 'formally' do you mean via S4ME or MEAction or a collective approach from Oz patient groups?
 
Always a good time to ask when there is an election looming (within 12 months max, more likely a lot less).

By 'formally' do you mean via S4ME or MEAction or a collective approach from Oz patient groups?
All the groups and individuals as well would be ideal. Yes, I am mindful of a pending election. I do want to keep this free of other political considerations, just on ME.
 
This makes me very happy. The clip is worth a listen. Adam Bandt is Deputy Leader of the Australian Greens Party, MP for my Australian electorate. I thought he was a good man before he had a view on ME; I was not wrong.

Well done to Christa Callanan (sorry if I have got her name wrong) who approached Adam. Well done to Emerge and everyone else involved. Brilliant.

Krista Callinan. She approached Adam at a meeting, and got him to open the screening of Unrest at Bio21. She’s done a great job with cultivating him as an ally!
 
Australian Greens MP, Adam Bandt, formally tabled a petition for Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome (ME/CFS) in Parliament on Dec. 4th.
The Emerge Australia petition asks the National Disability Insurance Agency (NDIA) to collaborate with the ME/CFS community to develop appropriate guidelines for National Disability Insurance Scheme (NDIS) assessors, and for ME/CFS to be added to List B of permanent conditions for NDIS. Close to 1,4000 people signed the petition.

rest here:
https://www.meaction.net/2018/12/05...rliament/?mc_cid=8ba21b5cef&mc_eid=c1fdea04b1
 
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