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power of 3 8 years 3 months ago #8855

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O yes, excellent TV news clip, featuring Hazel and our very own SuperDoc. :+1: :+1: :+1:
NSW Australia. Genotype 1b 30+ years, F0-F1, VL 91,000 Feb 2015 (740,000 in 2010), Tx naive.
Ordered Sof/Dac from Buyers Club 21 Sept, received 14 Oct.
Virus UNDETECTED at 3 weeks AND 12 weeks (EOT) AND SVR4 AND SVR12 AND SVR24. :-)
A thousand thankyous to Dr James and the amazing FixHepC team.

power of 3 8 years 3 months ago #8880

More news from New Zealand however this is not good news its a bloody disgrace!. The Otago Hepatitis Resource Centre has had its funding slashed. This is mine and Hazels home town in which it is estimated there are 5000 living with HCV.

www.odt.co.nz/news/dunedin/370436/hep-c-...-funding-loss-appals
SVR 24

power of 3 8 years 3 months ago #8882

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Great surfing, but bring your wetsuit, here in Otago, Ariel, come see us sometime! It is the Tasmania of NZ....
Genotype 3 30 years, 2x treatment interferon/ribavirin non responder. Cirrhosis 17 years. Fibroscan, decompensating, 40 down to 22 by 29/3/16- now down to 6.5, normal, no cirrhosis. Started Buyers Club Sof/Dac 14 Nov 15. SVR 12 29/0716
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power of 3 8 years 3 months ago #8883

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and I want to say, people say I am 'brave'- I don't see it that way but the reason people do is because of the stigma, which I reject like I do racism and sexism and homophobia and inequality- I know there are people who think like that but they are nothing to do with me or my life. I am very lucky to be not risking my employment or family support or the respect of anyone who has any power over me- that is a freedom I know many haven't got,. So f** 'em, bring it on. We should all be proud of surviving, not ashamed of contracting HCV.
Genotype 3 30 years, 2x treatment interferon/ribavirin non responder. Cirrhosis 17 years. Fibroscan, decompensating, 40 down to 22 by 29/3/16- now down to 6.5, normal, no cirrhosis. Started Buyers Club Sof/Dac 14 Nov 15. SVR 12 29/0716
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power of 3 8 years 3 months ago #8941

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hazelriannon wrote: and I want to say, people say I am 'brave'- I don't see it that way but the reason people do is because of the stigma, which I reject like I do racism and sexism and homophobia and inequality- I know there are people who think like that but they are nothing to do with me or my life. I am very lucky to be not risking my employment or family support or the respect of anyone who has any power over me- that is a freedom I know many haven't got,. So f** 'em, bring it on. We should all be proud of surviving, not ashamed of contracting HCV.


Hear Hear! Oh the people that I learned all about from HCV and their bigotry
You said it so well Hazel
Yes I have a wetsuit and an armoured suit too ;)
Gen 1a
Peg/inf/riba 2012(!) stop @ Wk 43 potassium low +issues (rlps week 4 post tx, VL120,000) scnds eg. adenomas.
pre sof/led VL 240,000 Fibsc F0
Day 25 <30
Day 32 UND
Week 10 UND
EOT UND ALT11AST17GGT19
SVR4 UND ALT10 AST16 GGT13
SVR8 UND ALT <9 AST16 GGT15
SVR12 UND ALT14 AST19 GGT12 Bili 5
EOT +18 ALT13 AST20 GGT9 Bili 5
EOT +21 ALT11AST15
Cured SVR12
Dysplasia Adenomas RemvdAug '16
SVR24 UND ALT11AST16
ColonoscopyClear Nov17
LumpectomyClear ‘18
LithotripsyCytoscopyBiopsy 4/18

power of 3 8 years 3 months ago #8944

Can we expect to see you here Ariel?

Heaps of surf and a room here if you need it :+1: #love
SVR 24
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power of 3 8 years 3 months ago #9239

and so the saga continues......

I find it mad that anyone would think that Gileads asking price of $84000 is fair and that generic medication sourced through Fix Hep C could be a dud.... God give me strength I'm really beginning to lose my patience with these fence sitters.




www.stuff.co.nz/national/health/76120097...lifesaving-medicines
SVR 24
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power of 3 8 years 2 months ago #9248

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Interesting article Tina. Discussed some issues I haven't seen in the media before. Like:

"It was impossible for Gilead to sue any of Freeman's patients because they were protected by patient confidentiality under Australian law." (Some of us aren't exactly confidential on this site)

"Intellectual Property lawyer Sebastien Aymeric said Freeman's buyers club might be guilty of "contributary infringement" of patent law by giving people the means to get around it."

"The secondary drugs were very difficult to make outside of large facilities found in Europe and America" said transplant physician Professor Ed Gane. He's not very well informed is he. :dry:
NSW Australia. Genotype 1b 30+ years, F0-F1, VL 91,000 Feb 2015 (740,000 in 2010), Tx naive.
Ordered Sof/Dac from Buyers Club 21 Sept, received 14 Oct.
Virus UNDETECTED at 3 weeks AND 12 weeks (EOT) AND SVR4 AND SVR12 AND SVR24. :-)
A thousand thankyous to Dr James and the amazing FixHepC team.
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power of 3 8 years 2 months ago #9280

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Yup, I noticed that confidentiality thing too, I have given mine away! but the reality is- there is safety in visibility, and more safety in numbers. How would Gilead look if they went after me, what would be the point? Only would bring massive attention to the fact they need reining in. but the medical profession should be out there beside or behind Dr James in their droves, his head above the parapet should be followed by 100's and where are they? some I know are doing what they can within their systems, but more needed now! what the f** are they afraid of?
Genotype 3 30 years, 2x treatment interferon/ribavirin non responder. Cirrhosis 17 years. Fibroscan, decompensating, 40 down to 22 by 29/3/16- now down to 6.5, normal, no cirrhosis. Started Buyers Club Sof/Dac 14 Nov 15. SVR 12 29/0716
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power of 3 8 years 2 months ago #9290

I have to say I am disappointed with the response from the leading medical professional's - why couldn't they say they applaud James Freeman rather than associate this story suggesting the medication is toxic and untested.
SVR 24
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power of 3 8 years 2 months ago #9506

Allison Beck is an amazing advocate, she was a rock for me when I first found out I was HCV+.

I really hope the Otago Hepatitis C Resource Centre gets funding elsewhere.

www.dunedintv.co.nz/news/government-cuts-funding-hep-c-support
SVR 24
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power of 3 8 years 2 months ago #9514

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Tina-Hill-facebook wrote: Can we expect to see you here Ariel?

Heaps of surf and a room here if you need it :+1: #love


I am so in love with the land of the long white cloud and yes I would LOVE to come over...I have no idea where you are, but I have been all round the Nth Island and done the Marlborough Sounds I stayed out in a Bach on the Queen Charlotte Track it was as close to heaven as I can get without waves lol.....I am so in girls...Hazel and Tina I can get a cheapish fare to Windy Welly later in the year.....
Gen 1a
Peg/inf/riba 2012(!) stop @ Wk 43 potassium low +issues (rlps week 4 post tx, VL120,000) scnds eg. adenomas.
pre sof/led VL 240,000 Fibsc F0
Day 25 <30
Day 32 UND
Week 10 UND
EOT UND ALT11AST17GGT19
SVR4 UND ALT10 AST16 GGT13
SVR8 UND ALT <9 AST16 GGT15
SVR12 UND ALT14 AST19 GGT12 Bili 5
EOT +18 ALT13 AST20 GGT9 Bili 5
EOT +21 ALT11AST15
Cured SVR12
Dysplasia Adenomas RemvdAug '16
SVR24 UND ALT11AST16
ColonoscopyClear Nov17
LumpectomyClear ‘18
LithotripsyCytoscopyBiopsy 4/18
The following user(s) said Thank You: Tina-Hill-facebook

power of 3 8 years 2 months ago #9515

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Tina! How disgraceful of the NZ govt to cut this funding. I know super wealthy people who have fancy holiday homes in NZ...grrrrrrr What is wrong with people!!!!!

Gen 1a
Peg/inf/riba 2012(!) stop @ Wk 43 potassium low +issues (rlps week 4 post tx, VL120,000) scnds eg. adenomas.
pre sof/led VL 240,000 Fibsc F0
Day 25 <30
Day 32 UND
Week 10 UND
EOT UND ALT11AST17GGT19
SVR4 UND ALT10 AST16 GGT13
SVR8 UND ALT <9 AST16 GGT15
SVR12 UND ALT14 AST19 GGT12 Bili 5
EOT +18 ALT13 AST20 GGT9 Bili 5
EOT +21 ALT11AST15
Cured SVR12
Dysplasia Adenomas RemvdAug '16
SVR24 UND ALT11AST16
ColonoscopyClear Nov17
LumpectomyClear ‘18
LithotripsyCytoscopyBiopsy 4/18
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power of 3 8 years 2 months ago #9709

SVR 24
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power of 3 8 years 2 months ago #9740

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RadioNZ are running the story at 0900 local on Monday.

I'll be having a chat and then Prof Ed Gane will be on.

I've had constructive conversations with both the Hepatitis Foundation and Prof Gane this week which, along with the evidence provided by this forum and the brave patients that have spoken out, have helped reduce their perfectly reasonable concerns about the quality, efficacy and supply chain integrity of generics.

With any luck the upshot will be "In a perfect world PHARMAC will fund it, but in the meantime generics are a viable option provided you have confidence in the supply chain."

Moving forward I'm hopeful that will mean less emails like this from NZ:

Hi Dr Freeman,

I emailed you regards to my husband xxxxx, and you phoned me.

I have seen xxxxx's GP and spoken to his specialist. neither
will script the drugs here in xxxxx NZ. What do I do
now? His specialist his happy to monitor him on the drugs
tho. He also said there is a risk of them being fake, where
do I go from here?
YMMV
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