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!

My insurance “Blue Cross/Blue Shield” (same as Nick) denied me because I was not on the “transplant waiting list”

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.

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

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

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