MyHep LVIR

I have stated to use this drug a bit less than a month ago (5 more days and it is going to be one full month). My doctor told me that I only need 8 weeks of treatment with it and it should be enough to help me. I am trying to do everything my doctor told me to do, exactly as he said. I am taking in the morning after I am eating my breakfast, I have been warned that it is going to be more effective if it is taken with meal, whether it is true or it is not – I am not sure but I try to do whatever I am told. So far I am 4 weeks in the treatment ( as I have said ) and I am having absolutely no side effects from it. I mean, nothing at all. it seems to me that I won’t have any. Or at least I hope so. But I don’t feel anything it is feeling like I am taking a vitamin or something. I am going to start my second bottle in one more week. Gotta say that I am very happy that my insurance has covered this medication for me and I don’t pay anything at all. I’ve looked for it online and I’ve found out that it is the same thing as a drug called Harvoni (at least Harvoni and this one both have the same active ingredients) but I’ve found out that Harvoni is more expensive. I guess this is why my insurance covered MyHep LVIR instead of it but whatever. What really matters is that I am feeling fine while using it and I hope that I am going to be cured after I would end the course. But I feel that it will. I really feel like I have been given a second chance in my life and to be honest I really cannot wait until I could finally say that I have done it and that I have beaten up the Hepatitis C. I’ve read online some reviews and I’ve seen that there are a lot of people writing that the combination of the active ingredients it has (ledipasvir / sofosbuvir) really helped them. I’ve seen much more people saying that it did helped them than those saying that it did not helped so it seems that most people do find it helpful. I hope that I am among “most of the people” here.

I am still not 100% sure when and where I have got the Hep C even though I am having one idea. I’ve always been thinking (but once again, can’t be sure) that I must have gotten the Hep C back in the 90’s when I have had a heroin shot for a fun experience that nowadays I regret so much. it has been such a bad and guilt feeling when I have found out approximately 7-8 years ago that I am having Hep C. as soon as I have found out about it I have been involved in a trial by using interferon injections that has turned out to be a complete disaster and the treatment has been completely discontinued for me because besides the fact that it did not work for me – the side effects I’ve been getting were horrible. It has destroyed my thyroid and since that day I have issues with it (big issues), I have lost my hair and I have got very sick. Anyway, yesterday I have started my treatment with this drug. of course it is too early to say anything about it but so far (after the yesterday dosage and the today dosage) seem to be fine. I have tried to do a bit of reading and learning about it and that’s how I have found out about a lot of experiences that people have with ledipasvir / sofosbuvir, about the side effects that it has and so on and so forth. That is why I would really like to thank those who have made this drug real, those people who have written the reviews (and here I am trying to help too) as well as those people who have helped me to get this drug MyHep LVIR for free. I can say that so far I have no side effects from it. either it is too early for them to appear or not – we have to wait and see. Also, either it would be helpful or not. I have to wait and see.. I really hope that it is going to be helpful because if this combination of ledipasvir / sofosbuvir is not going to help me then I would lose my hopes that there would be something that it is going to be helpful. I am going to return back after a while after I end my treatment and leave a review about it letting you know how did it worked.