Heres the podcast here http://mpegmedia.abc.net.au/rn/podcast/2015/10/ras_20151022_1306.mp3

Almost exactly the same situation as in the UK – although NICE have recently approved the treatments for some patients, not all. Unfortunately, while the headlines look good, the reality is, they have 3 months to implement it and there are severe waiting lists and as the current Gvt are conveniently devolving health authorities to their own devices, there are many hospitals that just don’t have the funds to provide the treatments. In other words, just because they are ‘approved’ – it doesn’t mean patients will get access to them and it will be a post-code lottery.

Excellent interview with Mr Freeman senior, maybe someone in England could listen and learn.

Just listened to the podcast Thx Archer and Sir Paul. Score Dr John Freeman 10 -Helen Tyrrell nil.What hypocritical rubbish she came out with.The” wait-wait we will provide” has been going forever.In my own case I spoke to my GP a year ago about accessing tx from India.My fibroscan reading was 5.”Wait” he said.I was actually going to Sri Lanka where sof was available at the time,and could have easily accessed it.2 mths ago I saw my GP again.”Wait” he said.By this time my fibroscan reading was 14,By lucky chance i had discovered the Greg Jeffreys blogsite,and insisted he write out some scripts..Within 3 wks I had the sof from India and the Dac from Mesochem.I am now 3wks into tx and have never felt better,What would the result have been if I had continued to wait?.Helen Tyrrell should be grateful that I have saved the PBS a heap of money as have all the others who have done the same.Why could she not have just come out and said “If you can afford $2000 then I endorse your effort” .In fact, an unlikely, but sensible solution would be for the PBS to subsidise people who cant’t afford the $2000 odd dollars while the Govt arm wrestles with Big Pharma over the price.
A concern is. that if the Govt makes a deal with Big Pharma ,it will only be a partial solution and it will include a caveat that all efforts must be made to close down groups such as the Fx buyers club.
If you haven’t already,get your meds now,even it means using your credit card.Its a tiny price compared with your life.
Don’t trust the Govt bureaucracy and the likes of HelenTyrell.

Oh man, Helen Tyrell lives in a richly embellished fantasy world.

Wish Mackenzie had asked her if Hepatitis Australia receives any sponsorship from Gilead or other Big Pharma.

Just catching up a bit late on some of the forum threads; this was a great interview by Dr Freeman, a breath of fresh air compared to the seemingly wilful mass self-delusion perpetuated by those in the Hep C ‘industry’ like Helen Tyrell. When I started yelling at the computer is when I realised this is why I’ve stopped watching the news on TV inch:

She really refused to address the fact that its simply not affordable to treat everyone…or even a fraction of everyone. The same illogical mantra being peddlled to keep those afflicted thinking there is some publicly-funded hope..do they think there would be rioting in the streets if we were told the truth? I wonder. She is indeed living in a fantasy world if she thinks Gilead will drop their pricing so catastrophically…not with a $5 bil profit over the last quarter lol

Hepatitis Australia definitely do receive money from Pharma.

In the Hepatitis Australia Annual Report 2013/14

https://static1.squarespace.com/static/50ff0804e4b007d5a9abe0a5/t/55c03fbbe4b05b83500ef619/1438662587534/Final+annual+Report_2013-2014sml.pdf

If you scroll down to page 42 to the “2 Revenue and other income” you will see in 2014

Government Grants: 884,687
Sponsorship 203,046

And on page 48 it looks like Helen got paid $153,248 in the 2014 year.

And page 53 rather seals the case where the sponsors are listed as being:

• Abbvie
• BMS
• Gilead
• Janssen
• MSD
• Roche

It is so so obvious without knowledge of their financials, that something smelt with old Helen’s stand. This information confirms it.
The Dog.