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Hello new guy here 4 years 6 months ago #26598

  • DrJames
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Hi Nick,

I'd be happy to help with the prescription.
YMMV
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Hello new guy here 4 years 6 months ago #26599

okay wednesday i am going to schedule an appointment with you on the application on my phone.
Contracted 2011
Gen 3
VL 13000
Treatment Start Date: SOON
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Last edit: by Nick-Campfield-facebook.

Hello new guy here 4 years 6 months ago #26600

Ditto to what Greedfighter said here splitdog!!!
GT1a; Got it some time in the 70's; Diagnosed @1976
Tx naive
METAVIR: A2-F2
SOT May 18, 2016: CMP: AST 162 ALT 241 VL 13000000
3 weeks after SOT: AST 27 ALT 31 VL 138
Reached EOT Aug. 10, 2016 / Received svr4 results Sept. 20, 2016: AST 22 ALT 24
Hep C RNA "NOT DETECTED"
AS OF 3/20/2017 ,Hep C RNA PCR "NOT DETECTED" THAT'S SVR24!
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Hello new guy here 4 years 6 months ago #26601

Hey Nick, I’m really glad you’re going forward ... you absolutely will not regret it.
Looking forward to you progressing to being free of this ... you’re being a responsible father and husband is touching ... stay strong man!
GT1a; Got it some time in the 70's; Diagnosed @1976
Tx naive
METAVIR: A2-F2
SOT May 18, 2016: CMP: AST 162 ALT 241 VL 13000000
3 weeks after SOT: AST 27 ALT 31 VL 138
Reached EOT Aug. 10, 2016 / Received svr4 results Sept. 20, 2016: AST 22 ALT 24
Hep C RNA "NOT DETECTED"
AS OF 3/20/2017 ,Hep C RNA PCR "NOT DETECTED" THAT'S SVR24!
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Hello new guy here 4 years 6 months ago #26604

thank you so much
Contracted 2011
Gen 3
VL 13000
Treatment Start Date: SOON
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Hello new guy here 4 years 6 months ago #26612

so i got my fibroscan done. to keep it short indont qualify for treatment intill i have a f2 or f3..
Contracted 2011
Gen 3
VL 13000
Treatment Start Date: SOON
Attachments:
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Hello new guy here 4 years 6 months ago #26613

Yeah, here in the USA it can prove next to impossible to get approved unless your dying and/or in need of a liver transplant. My insurance denied me treatment 2-3 times for the same reason you say you don’t qualify.
DO NOT wait for permission to save your life and continue being the husband and father you want for your family. Go through with what Dr. James advises. You’ll get started long before you meet those dire “qualifications” they require.

Best regards,
Matt
GT1a; Got it some time in the 70's; Diagnosed @1976
Tx naive
METAVIR: A2-F2
SOT May 18, 2016: CMP: AST 162 ALT 241 VL 13000000
3 weeks after SOT: AST 27 ALT 31 VL 138
Reached EOT Aug. 10, 2016 / Received svr4 results Sept. 20, 2016: AST 22 ALT 24
Hep C RNA "NOT DETECTED"
AS OF 3/20/2017 ,Hep C RNA PCR "NOT DETECTED" THAT'S SVR24!
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Hello new guy here 4 years 6 months ago #26621

My insurance "Blue Cross/Blue Shield" (same as Nick) denied me because I was not on the "transplant waiting list" :huh: :-1:

WTF - I guess the person judging eligibility is related to Satan?

I've said it before, but it bears repeating. When you go through this site, you not only get a cure, but you regain your dignity and humanity. Or you can wait until Satan's spawn thinks you are sick enough to receive treatment.
Gt 1a, F0, VL 6.5 million, AST 59, ALT 62
Started Twinvir 1/15/16
6 wk. labs VL UND, AST 27, ALT 20
EOT labs VL UND, AST 23, ALT 19
SVR 16, VL UND, AST 28, ALT 17
SVR 24 , VL UND, 10/8/16
SVR 125, VL UND, 9/22/18
SVR 230, VL UND, 10/3/20
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Hello new guy here 4 years 6 months ago #26623

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"WTF - I guess the person judging eligibility is related to Satan?". Sure seems like it :lol:
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Last edit: by Mar.

Hello new guy here 4 years 6 months ago #26626

Nick-Campfield-facebook wrote: so i got my fibroscan done. to keep it short indont qualify for treatment intill i have a f2 or f3..


Hello all,

me thinks that if they are going to approve funding DAA's when you are F2 or F3 anyway, why not approve it at first point of call. Maybe save some liver damage on the way through.

I know I have heard this type of thing before ...., but it still amazes me to hear it again. I'd be just as worried about becoming a gibbering wreck using your system over there. Does my head in just to hear about it.

Don't know what the costs are to get generics to the States, but I guess it is still a significant amount if you are short a quid. Using generic DAA's here too before they were fully subsidised cost a bit, but no more then copping an expensive servicing bill for the car.

I like my car, but I like my liver too.

Yours

Jeff
GT3a 1990 Failed Inter 1998, comb in 2000. HCC 2012
Started 24/52 Sof/Dac 27th October 2015.
1. Bloods 2 October 2015: AST - 165 (20-40), ALT - 265 (5-40), GGT 189 (5-50)
2, Bloods 20 November 2015: ALT etc normal; VL 19
3. Bloods 8 January 2016: AST - 40, ALT - 59, GGT 48 VL RNA UND
4. EOT 12 April 2016 - blood tests: all is well, CT scan: okay
5. AFP 11 June 2016: 4 ref< 11
6. VL July 2016: DET
7. Oct16 start treat - June17 UND
8. Jun 18, lfts okay, platelets a bit low.
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Last edit: by sabrecat.

Hello new guy here 4 years 6 months ago #26656

Nick said "to keep it short I don't qualify for treatment until i have a f2 or f3"

But Nick, you can get your medication here for under $1500, which is less than the cost through your insurance company. Contact Dr. James, we're all hoping you see this opportunity to save your life. I'm waiting to hear you tell us you're cured :cheer: :+1:
Gt 1a, F0, VL 6.5 million, AST 59, ALT 62
Started Twinvir 1/15/16
6 wk. labs VL UND, AST 27, ALT 20
EOT labs VL UND, AST 23, ALT 19
SVR 16, VL UND, AST 28, ALT 17
SVR 24 , VL UND, 10/8/16
SVR 125, VL UND, 9/22/18
SVR 230, VL UND, 10/3/20
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Last edit: by Greedfighter.

Hello new guy here 4 years 6 months ago #26658

Hi Greedfighter,

This is not so much relevant to this thread, but when I go on this forum I usually have a glance down the bottom to see how many Guests are there. Today at 12.09pm (Australian Eastern Standard time) there are 110. I wonder where they are living as well, and what time they are staying up to looking for information about how they can kiss HepC good bye.

I didn't blink when I first used generics late 2015 as there was an article about Dr Freeman in the Sydney Morning Herald. The SMH paper is a bit like the NY Times would be to Americans? Due diligence wise this was a good as it gets.

Treatment failed first time and second time worked (so far so good).

Must be hard in some countries where big pharma has 'the powers that be' declare that you have to wait until you are f2 or f3. We used to be warehoused in Australia too. For f.ck sake! Look at the first line of my signature to see where f2/f3 got me!

Due diligence wise, any Guests not so sure what's going on here may care to click on someone's profile and follow it back over the years. Mine goes back to November 2015.

Yours


Jeff
GT3a 1990 Failed Inter 1998, comb in 2000. HCC 2012
Started 24/52 Sof/Dac 27th October 2015.
1. Bloods 2 October 2015: AST - 165 (20-40), ALT - 265 (5-40), GGT 189 (5-50)
2, Bloods 20 November 2015: ALT etc normal; VL 19
3. Bloods 8 January 2016: AST - 40, ALT - 59, GGT 48 VL RNA UND
4. EOT 12 April 2016 - blood tests: all is well, CT scan: okay
5. AFP 11 June 2016: 4 ref< 11
6. VL July 2016: DET
7. Oct16 start treat - June17 UND
8. Jun 18, lfts okay, platelets a bit low.
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Hello new guy here 4 years 5 months ago #26719

Well, we never heard what happened here, hopefully Nick got his meds
Gt 1a, F0, VL 6.5 million, AST 59, ALT 62
Started Twinvir 1/15/16
6 wk. labs VL UND, AST 27, ALT 20
EOT labs VL UND, AST 23, ALT 19
SVR 16, VL UND, AST 28, ALT 17
SVR 24 , VL UND, 10/8/16
SVR 125, VL UND, 9/22/18
SVR 230, VL UND, 10/3/20
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Hello new guy here 4 years 5 months ago #26721

Hey Nick, I hope by now you've received your meds and are on your way to a cure. When I contracted HepC, over 50 yrs ago, there was no cure and not even one on the horizon. Fast forward to the dawn of Hiv and the anti-viral drugs and the development HepC drugs. The cost in the US is still 60-80,000 USD for the drugs anybody can get through Dr. Freeman and this program for $1500.00. I have to give my own personal physician for pissing me off one day, claiming that I would never beat these little "buggers" with my attitude of saying it was just too expensive. That led me to go online and find the "light at the end of the tunnel." Once I became aware of the program, I was taking my first pill less than one month later. I did not even bother to go through my insurance, of which is very good, because of the time and hassle. Besides you can deduct the expense as medical on your taxes, if you're in the US. Since you have your phone with you most of the time, set your alarm for a time of day that is good for you, mine is 5pm, and you should never miss your pill. Good sleep, pale urine, good food, and NO ALCOHOL. I had a viral count after nine pills and it went from 16 million to 2300. These do work. I will get another blood draw in two weeks and there is a good chance it may be zero. Lets hope. Good luck again Nick
mrcleanrt
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Hello new guy here 4 years 4 months ago #26840

Great post here mrcleanrt,

You were inspired by your anger at the system, just like I was when I was told I was denied treatment "because I was not on the transplant waiting list" :angry: :-1:

Anyone else who has Hep C needs to realize the best course of action is contacting Fix Hep C. They will help you get cured right away

You made it here, now get your cure, this is not a scam
Gt 1a, F0, VL 6.5 million, AST 59, ALT 62
Started Twinvir 1/15/16
6 wk. labs VL UND, AST 27, ALT 20
EOT labs VL UND, AST 23, ALT 19
SVR 16, VL UND, AST 28, ALT 17
SVR 24 , VL UND, 10/8/16
SVR 125, VL UND, 9/22/18
SVR 230, VL UND, 10/3/20
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Last edit: by Greedfighter.
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