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I encourage people to try this. 7 years 2 months ago #307

I've just started tx under Dr Freeman. I'm 6 days into the medicine for genotype 3. I have no side effects at all.

I'm 49 and a year and a half ago I had had some bad blood results at my local GP, who sent me to a specialist who, who sent me for a liver scan and then told me I was ok liver wise and explained the new drugs and that I could either wait for gov to put them on the PBS or maybe try and get them in India. To be honest I just wrote it off and didn't think about it.

Then recently Dad showed me an article on the man from Franklin Tas who is importing from India and told me to try it out. I was still reluctant to even begin asking about it. I had had Interferon tx at Royal Hobart Hospital in 2006, which was a nightmare to deal with. It was a horror show on all levels, from administration exhaustion, total lack of support available (which I really needed) and the shocking symptoms of the Interferon.

My Dad nagged me until I googled and found the man from Franklin and emailed him, he explained how he went about it and I put it aside again as the secondary drug wasn't available in India yet. Then again Dad was asking me to do something and said he wanted me to do it now as he was worried the gov or drug company would shut down the importing. To me that made sense so we googled and got Dr Freeman, emailed him and he emailed right back and them telephones me within a day or two and explained it all.

The drugs via Dr Freeman being in powder form from China put me off again, so I left it a few more weeks. Then I just thought fuck it, just do it and made an appointment.

My fears, administration, no secondary drug, lack of support and powder were addressed. There is stuff all admin, no paper work to get the powdered drug through customs. The Chinese company has all the various secondary drugs to go with the Sofosbuvir for the various genotypes, mine was Daclatasvir. With Dr Freemans office, there are shrinks that will see me even by skype and bulk bill if I get distressed and the drug is tested at Hobart Uni to see if it is proper.

So all I did was:
1. Go and get my blood tests, (only as Hobart hospital didn't have my genotype or record anymore).
2. Revisit Dr Freeman for the prescription and receive an emailed invoice from the company in China that same day.
3. Take my payment & invoice to my bank to be wired to the China Drug Company.
4. Get the drugs in my mailbox a few weeks later, all tested and packed into capsules.

So if you have had a bad experience in the past, please don't let it stop you now.

Here is a pic of my drugs Dr Freeman emailed me as they arrived from China, just before they went to the Hobart Uni.


Diagnosed in the early 90's, geno 3, had Interferon 2006, currently on Sofosbuvir & Daclatasvir

NO VIRUS @ 4 WEEKS of Sofosbuvir & C Daclatasvir

Still free - SVR4 and at 8 weeks too

Still free at 7 months, CURED!!
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I encourage people to try this. 7 years 2 months ago #309

Hey WIshIwasAwombat,

Thanks for your message. Where to find Dr Freeman? I just need the tested and encapsulated Daclatasvir.

Thanks
Iftikhar
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I encourage people to try this. 7 years 2 months ago #311

Hello Ahmad,

Dr Freeman is on this forum or his email is This email address is being protected from spambots. You need JavaScript enabled to view it.

gp2u do appointments by skype if you aren't in Tasmania.

Wish you all the best.
Diagnosed in the early 90's, geno 3, had Interferon 2006, currently on Sofosbuvir & Daclatasvir

NO VIRUS @ 4 WEEKS of Sofosbuvir & C Daclatasvir

Still free - SVR4 and at 8 weeks too

Still free at 7 months, CURED!!

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Hep C CLEAR....... I encourage people to try this. 7 years 1 month ago #1847

Just got my results in mail



It's GONE GONE GONE!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
Diagnosed in the early 90's, geno 3, had Interferon 2006, currently on Sofosbuvir & Daclatasvir

NO VIRUS @ 4 WEEKS of Sofosbuvir & C Daclatasvir

Still free - SVR4 and at 8 weeks too

Still free at 7 months, CURED!!
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Hep C CLEAR....... I encourage people to try this. 7 years 1 month ago #1848

  • crazy8
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Congrats!
GT 3, F3, Contracted 1993 Tx Naive
V/L 1,267,000 AST 67 ALT 65 6/10/15
commence Sof/Dac (Mesochem) 6/11/15
AST ALT normal 24/11 *
*V/L UNDETECTED 24/11*
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I encourage people to try this. 7 years 1 month ago #1849

  • Alsdad
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Congrats. This forum lacks a 'thumbs up' smiley.
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I encourage people to try this. 7 years 1 month ago #1852

  • poodle
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Well done Wombat
Geno1a 35years fibrosis 2 or 3 different results from different hospitals ??
24weeks mesochem sof/led as unsure of fibrosis status.
currently UND. No bad side effects
Have svr12 ... waiting for svr 24
I now have SVR 36 weeks.
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I encourage people to try this. 7 years 1 month ago #1854

Bloody Brilliant !
Two time relapser.

SVR 4 achieved 12/16 at last
SVR 12 achieved 22/02/2017 The Bastard has been defeated :):):)

GT 3 - about 28 yrs with HCV
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I encourage people to try this. 7 years 1 month ago #1856

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Top stuff mate
Long live the Wombat :cheer:
52 y.o. G3a for about 30 years
Previous tx 2004 interferon/ ribavarin
2004: ALT 624 AST 263

Pre tx test 23/10/15: ALT 153 AST 128 VL 11 849 493
6/11/15: Sof/ dac started
26/11/15: ALT 41 AST 41
7/12/15: ALT 36 AST 30 Virus undetected

2004 biopsy F3
Fibroscan appt Jan 11 2016.
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I encourage people to try this. 7 years 1 month ago #1860

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Excellent news Wombat!

Party party party?

I agree Alsdad, we need a thumbs up/smiley button. There's going to be a lot more celebrating yet.
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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I encourage people to try this. 7 years 1 month ago #1867




Thank you for the well wishes guys, I can see a few other threads with same news from people...


:woohoo:


here's a few pics of the last day of interferon hell a decade ago... For me the fall came after interferon, I quickly put t on 40 odd kilos and went totally gray.. :(

I got mail at 9am this morning and have just slept ALL day :) First thing I did was write an email to James Freeman to tell him & thank him. Then rang and mailed family & friends, then slept.. lol... Two nights ago I had a fear dream Dr Freeman was telling it it hadn't worked, then read the log explanations of my results letter this morning first and thought they were my results 2 log what ever, lol...

25 years of half life ended.. so fucking amazing.

I reckon if there isn't one all ready, to make a CURED section and move our strings to it as we all clear. :woohoo: :silly: :blink: :whistle:
Diagnosed in the early 90's, geno 3, had Interferon 2006, currently on Sofosbuvir & Daclatasvir

NO VIRUS @ 4 WEEKS of Sofosbuvir & C Daclatasvir

Still free - SVR4 and at 8 weeks too

Still free at 7 months, CURED!!
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I encourage people to try this. 7 years 1 month ago #1879

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I'm so happy for you, Wombat!
Congrats! :lol:
Virus not detected from 14.10.2015
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I encourage people to try this. 7 years 1 month ago #1888

Well done Wombat :cheer:
GT1a Dec14 F2/8.7 VL 900000-2.5M
Jan16 Hepcivir-L MonkMed/Redemption
Baseline: VL 913575 Alt 76 Platelets low
Wk2 VL1157 Alt 23
DET Wk 8 VL 32 Alt19 'In the slow lane'
June16 Fibro 5.7 F0/1 LIF 1.5
Wk 11 VL<12 Alt 13 Det/Unq
Extending tx 12 wks Mylan Sofo/Dac MonkMed
Wk 14 VL <12 Det/Unq
Wk 16 VL UNDETECTED
Wk 22 + 4 Wks Sunprevir FixHepC
Wk 24 UNDETECTED Alt 13
Wk 12 post tx SVR12 Wk 26 SVR24
Thank-you Tim, Dr Debasis @ MonkMed & Dr Freeman @ Fix HepC
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I encourage people to try this. 7 years 1 month ago #1894

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Thanks for sharing your story,
I too have geno 3 & was on tx 10 years ago with that soul & body destroying toxic cocktail. :angry:

It's interesting what you said that many of your health problems started after you finished that tx 10 years ago as same happened to me, including my hair went grey where before they were naturally brown. :unsure:
Before the old tx I was healthy & fit 40 years old, after I felt like 80 years old woman!

It is great to hear you are now clear , yes indeed 25 years of life only half lived… :(
I can totally relate to all you're describing,
Geno 3, Fibro 8.7 pKA, tx experinced in 2005 - Peg/Riba, relapsed.
Started tx 1/12/2015 with Indian Sofo & Chinese Dac.
5 weeks result all normal, ALT 18 - down from ALT 73 at the start of tx.
5 weeks HCV PCR RNA - UND. - down from 2 ML
9 weeks HCV PCR RNA - UND.
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I encourage people to try this. 7 years 1 month ago #1908

  • Joan
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Thats Great News!! Congratulations!!!
GT2B Diagnosed 1989
Started Tx 6.Nov.2015
F3 Fibroscan 17: April.2015
Alt PreTx: 186 Ast PreTx: 157 VL PreTx: 733,000 27.10.2015
Alt Week 4: 14 Ast Week 4: 28 VL Week 4: UND 7.12.2015
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