I have Gt 1a, diagnosed 30 years ago, 6.5 million VL, F0, liver function AST 59, ALT 62 (done 8/15) . My journal will not be as comprehensive as others since I am just going to get blood work from my GP after 6-8 weeks to see how I am doing.

I was denied twice by insurance, and again on appeal. I realized no one will give me treatment, but I get tired at the end of the day more than other people do, so I know I am being affected by this virus. I didn't want to wait until I am approved by insurance and have real problems.

I got an RX from GP2U.COM for 12 weeks sof/led (book the longest session available, 20 or 30 min.to discuss with Dr.). I was able to arrange for 12 weeks of meds (Twinvir) to be shipped to me in USA by a third party.

I started meds on 1/15. All I can tell you is I feel great. It's not a placebo effect. It is unreal how my daily fatigue has been lifted after just 2 days. I know this is working; no side effects at all. I just pray that 6 months after treatment I am VL undetected

Good luck! We are starting at the same time. I just started sof/dac on 1/16. I slept ok which is rare and feel fine today. Now to see how work goes tomorrow night.
Congrats! Glad you are feeling better already

Welcome and a big Congrats to you Greedfighter for being pro-active in taking your health and wellbeing into your own hands. I'm G3a, started Sof/Dac 13/01, 16 weeks Tx.
Good Luck and post how little or more you want as we all appreciate everyone's experience and sharing of info.

Good luck GF from another GT1a
I wish you every success for the best possible outcome.

Welcome aboard! All the best with your Tx

Hi GF,
Glad you got your meds instead of waiting & waiting & waiting....for your insurance people to allow you the goodies (if ever)
Now's your time, happy for you.
Good luck

Hi GF good luck to you and a successful outcome

I have G1a as well and my experience has been just like yours. After just a couple of days i started to feel way better. Enjoy feeling normal again. It is a blessing.

That is so great to hear. Looking forward to the undetected post.

Congrats for taking the reins and deciding enough was enough, GF. Another 1a here, in a few similar position to you fibrosis & stats-wise. I too thought why wait until we have become more symptomatic and our livers more compromised in order to access tx at some future date?

Good on you for being proactive and kicking off the fight now. And hard as it is to believe, it does work, as you've noticed already. All the best

Thanks everyone for your encouragement and good luck wishes! I really appreciate it! Thanks also to everyone who can relate and has posted their story here too! My story is by no means unique on this site....we're all here because either an insurance company, or national health system won't help us! Feel free to post whatever you would like here!

I posted initially that I had my daily fatigue greatly reduced; just thought I'd share 2 new side effects I had on day 3. I find that I think much more quickly and clearly (I guess this is the infamous "brain fog"). I never really thought I had any.....but now I realize this crummy disease really paralyzes you in many ways. Because of the brain fog being lifted, I have side effect 4: I'm more upbeat and have a more positive outlook.

I'm still having no physical side effects from the treatment.