God bless you Stacy. You are a true encouragement. i watched your day 22 and wish to hear how you are. I know there are many here that care . Thank you n know you r loved.
You're not alone. I'm also on a support group on Facebook, Harvoni Family and Friends. I'm ending day 5, going into day 6 myself with stage 4 liver disease cirrhosis. I also know about the ups and downs of tired vs alert then tired again, also irritability and mood swings. It's a roller coaster ride. But all worth it to become UD - Undetected. Keep at it and slay that dragon!!!!
Sharon Horney Congratulations on starting Harvoni! It is quite a rollercoaster ride but you're right, it's totally worth it! Some of my side effects have started to get better. That gives me hope. The sugar cravings are worse though! Lol! That probably isn't good for a diabetic! Do your doctors have high hopes that this treatment can reverse your liver damage? I really hope so! Here's to slaying the dragon together!!! Please keep me updated on how you're doing and thanks for commenting. It really is nice to know you're not alone!
I just received word today that my 8 week course of Harvoni has indeed cured my hepatitis c. God bless this drug. I personally had no real side effects to speak of either.
Hi Stacey..Im Jerry and I'm very glad to hear you qualified for Harvoni . I started treatment a month ago and had a blood test after day 10 and went from a viral load of 8 million to just 19. Tomorrow I go for the 30 days blood test and hope to be cleared but still have to do a full 6 months of Harvoni. Only because I went thru 5 previous treatments on Intron, Interferon and Rebetron ..that and I have advanced Cirrhosis.. Wish you the best and if anyone has any questions feel free to ask..jerry
Hi Jerry! That's so amazing to hear about your blood work! 8 million to 19!!!! I'm so happy for you. Good luck with your next blood draw. It sounds like the medicine is working and I'm sure when you get the results from tomorrow's test you'll be undetected! I'm guessing this round of medication must be a piece of cake compared to the other 5! I'm kind of embarrassed complaining about my side effects. That's a lot of heavy meds! You must be a very strong man to have gotten through all of that. Please keep me updated on how you're doing and what the blood test says about your viral load. Or lack there of. Thanks for commenting and have a great night!
j maedl Hi Jerry.It's TarandonDesigns. I'm trying to respond to your question directly but having some issues doing that. So I popped over here. You asked if my missing appts. was because I was sick from the hepC or was I sick from the Harvoni. It was from the Harvoni. There were nights that I could not sleep at all because of the joint pain, the awful itching and burning, the headaches and the sweating. These are all hepC symtons that were incredibly magnified by the Harvoni. After being up all night I was not able to drive myself to my appts. The Drs. is an hr. from my house. I would sleep most of the day because of the horrible nights. While driving home from my University of Washington appt. I feel asleep while driving on the highway during the 3hr. ride home. I drifted into the next lane. It was very scary...
Wow..hope your doing better now..pretty scary falling asleep at the wheel 😲 I agree witb ya too about being undetectable... I have been there twice and not for long..all the interferon i injected in my body was for .nothing...The Harvoni worked wonders as I just got a call from my new gastro " UNDETECTABLE " and only after a ,month of Harvoni.***** They told me that being undetectable is a 0-15 viral load and I have heard that before as the virus leaves a tell tale scare if you will...I am trying to find out what 5years of inteferon will do to one as far as lifelong side effects? All my joints extremely hurt..I have been on oxycontin and they allowed me to work but now even walking is a challenge.. I now take lortab but Im getting ones that dont have the acetaminophen in them called Zohydro. Who should take Tylenol? NOBODY SHOULD...Instant liver damage...Now if i can just get my sugar under 200..I take 80 units daily and Im not responding very well..one thing at a time i guess...Jerry
j maedl Good news! Only 2 mos. to go! 5 yrs. of Interferon? I've never heard of anyone being on it for that long. Hopefully this is it for you. It's very hard to get prescription pain meds in WA. right now. They are treating everyone here like a drug addict. I personally know 2 people that have very real pain issues and have to get their medication on their own - if you know what I mean. I take about 12 or more advil a day plus gabapention. I had a nurse yell at me for taking too many advil because she said they would cause kidney damage. When I asked her what the **** I was suppose to take for pain since they won't give me anything for it she told me to take tylenol. I laughed in her face. Perhaps the sugar levels will be easier for you to manage once the hepC is finally under control.
I'm in line waiting to be approved for harvoni . I have been told its comparable to chemo therapy is this true ? I'm in tears now so scared. watching these vids trying to find hope .
Just me again. I forgot to say that I consider myself in remission and won't consider myself really "cured" until the virus is still undetectable 3 mos. after stopping treatment. This is what I have been led to believe at this point. This worries me a little as the drug is so new. It hasn't even been out for a year yet so I wonder how there can be enough data to support that statement. I have also been told that once off the med it will take about 2 weeks to completely get out of my system.
Stacy, congratulations on starting your journey. I applaud your efforts to reach out and support other people by sharing your story. I started Harvoni on xmas eve. I searched for help, information and support at that time but there really wasn't any. Thank goodness for all that are infected that things are different now. I will be taking my last pill on mon. 3/16. I am counting the hrs. I posted some of my story on Paulas HepC video blog. If you get the chance please read it. I don't want to scare you but please be aware that the adverse side effects if you are going to experience them probably won't start until you are on the medication for about 2 weeks. I think it takes that long for the Harvoni to really get into your system.I wish that I had been prepared or had more information. The really good news is that it is a fast acting medication and when you are at week 4 you will get the good news that the virus is "undetectable". This is what gave me the mental and emotional power to go on. I had no idea what to expect. My Drs. were very ill informed and not caring enough to share the little they did know.I had to be very proactive in my own treatment. There were times that I was too sick to go for my blood tests or my appointments. I wish I had been more prepared but now I know enough to write a book.I kept a very detailed diary.I was not not brave enough to share my story online. Please keep us posted and contact me if you have any questions or just need to share.
Hello Tarandon Designs..thanks for posting..I read that you were too sick to get blood work or keep Dr. appointments..In your opinion was that a result of the side effects from Harvoni or something else? I have been on Harvoni about a month now and I had a pretty good headache for 3 days..thats all. I do have alot of experience with former treatments over the last 20 years tho too. . thanks..jerry
Hi Paula! I have to admit something to you... You're the reason I started this diary! I was desperately searching for information about Harvoni and it led me to your video blog. As I listened to your story and heard what you had been through, I knew it would be helpful for me to start one too. You inspired me and gave me the courage to tell my story! Thank you! I've commented on your videos just under my other account. I hope you don't mind but I talked about you in my 2nd video. I didn't say your name but I talked about your lab work being undetected and how much hope that had given me! Even though we've never met. I'm so happy that you're almost done! I'm doing a happy dance for you and will continue to check in on your page and say hi! Thank goodness you were there because my doctor seems to be clueless when it comes to the side effects. I'm guessing its because the medicine is new. Please stay in touch and please put up more videos! You never know who you're going to help. Thanks again Paula!
j maedl Hi Jerry! I know you were commenting on Paula's comment but I just started to experience headaches too! I'm not sure if they're the Harvoni or just allergies! Lol! It seems like anytime I sneeze now I want to blame it on the medicine. Hope you're having a great weekend and enjoying some of this sunshine!
Harvoni Video Diary I'm not Jerry but I wanted to respond to this. The headaches are a Harvoni side effect. Harvoni seems to effect the sinus's. Many people complain of allergy like symptoms - runny nose, sneezing,headaches.I think the med is very dehydrating which can cause headaches. I have found that drinking lots of water will help with any dehydration headaches. I once had a headache so bad that it lasted for 2 days. I thought I was having a stroke. I went to the er and they started IV fluids which helped alot.
TarandonDesigns Hi Paula! I tried to respond to your post but I think it got lost between the other posts. Lol! I wanted to let you know that you're the reason I started this video diary! I've commented on your videos under my other account! I actually mentioned you in my 2nd video! I didn't say your name but mentioned that you just found out you were undetected and how hopeful and happy that made me even though I didn't know you! I wanted to thank you for being such an inspiration to me and for helping me to find the courage to make this video diary! Please post more videos and keep me up to date on how you're doing! Miracles happen everyday and you're living proof!
Im sorry to hear your suffering. You know Genetics is the most important thing with diseases. I have a friend who was positive and I used needles with her everyday because I assumed I had it and all my friends that used with her (at least 15 positive hep c) friends so I just thought I had it so I told everyone I had it and my friends that didn't I would tell them and eventually they'd use with patient 0 or 2 and catch it. I finally got tested(takes 6 months to come up) didn't have it. I told doc that's impossible. I got tested again 18 months after and kept using with hep positive people, I didn't have it. They then said I am either immune to the virus or my body has fought it off. P.S. I got tested after getting clean 3 and half years after first exposure(exposed hundreds maybe a thousand times or used dirty needles 4-6 times a day for 5 and a half years) and Im hep c clean. No good diet. Nothing special.
Day 12 the first 4 days I had this incredible energy and a lot of aches and pains gone. Later on I notice constipation, fatigue, mild headache, nausea. The fatigue is different from the hepC fatigue. This feels like you have low blood pressure or anemic walking around carrying weights. I take my dosage in the morning. I wish I had started at night instead.
I'm on day 5. I was having really bad joint pain before, but now it's become almost unbearable. Everything else seems fine. I have a bit more fatigue,some sleep issues and headache bit yeah joint pain is bad. Any suggestions?
bILL stegura Hi Bill! Congratulations on your sobriety! That's a blessing in itself! I'm originally from Maryland but live in Illinois now. I actually lived in PA for a bit in York and Red Lion. Are you anywhere near there? Congratulations on starting Harvoni! I know you're one a few days in but how are you feeling? The last few days have been sort of rough for me but this too shall pass! One thing I've learned from others suggestions is to drink a lot of water. It really helps! I look forward to keeping in touch and going through this journey together! It makes it easier to know that you're not alone. I'll be looking for your next video so please keep posting them! You never know who you're going to help. Talk to you soon! -Stacy
I live in allentown, but yourk is in my region. Im a member of Na thats how I got and stay clean. Iny problems I've had so far was some headache but nothing too bad. Hooe you feel better.
bILL stegura I know right where that is! I come back to town a few times a year because I still have family there. I got sober in CA but definitely qualify for NA and AA. Lol! I'm super glad to hear your side effects have been mild. I just started getting headaches too. It's all going to be worth it though to hear... Undetected! I can't wait!
If you don't mind, what insurance do you have, because I have upmc for you medicaid, and I got denied in 2017 for some reason, and now I'm going through the process again for the second time around, and I called my insurance, and they said that they cover the medication, but does that mean that they will approve me now just because they said that the medication is covered, or do they still have to approve it? Anybody who has any idea about this please?
+Lynsey p It could be a few different things. Normally it is one of three things. 1. Doesn't have a metavir score of F3-4 2. The type of test used to give the score. Some places like Blue Cross will only accept Fibrocan or a liver biobsy. MRI's, Fibrotest, and many other tests would not be accepted. 3. They want him to take something else, that is less expensive, that does the same thing. Normally Viekira Pak.
I am I the process for trying to get approved for this treatment. Is there anything that you or anyone can help me with or anything I need to know. I have Fl blue, if that says anything. I just turned 28 and I nee help getting help.
+Angie Lopeman Florida Blue through Prime Therapeutics? They cover Harvoni, but you need to make sure you have either a liver biopsy or Fibroscan showing F3-4 metavir score. If you have that it's really easy, if not you still can get approved, but your doctor's office will have to be clever about it.
No problem, I spend a few days a week doing solely Harvoni approvals and before that I worked at an insurance company reviewing claims, so I know just about everything there is to know about that process.
+Angie Lopeman Hi Angie, Harvoni is not the only option to cure Hepatitis C. Nano-medication is another option you have. The advantages of nano-medication include, 1. Absolutely no side effects (i.e. fatigue, headache, anxiety, nausea, etc.); 2. Cured well within 12 weeks (SVR60 is still no problem.); 3. Regardless of genotypes; 4. Cirrhosis is treated at the same time (cirrhosis can be cured by nano-medication.); 5. Feel energetic and alive in the very first week of the treatment; 6; Entire treatment cost: only $10,000 (excluding shipping cost). Check out the link, www.glordavi.com
The Harvoni support group supports Harvoni, not the patients. They tell people they're ungrateful, when they say they're having a hard time with the drug.
Thank you for being brave enough to share your story! Your information is definitely helpful to others who are considering this course of treatment.
I had mild side effects the first 2 days, but none since, so far. On day 16 of 84
God bless you Stacy. You are a true encouragement. i watched your day 22 and wish to hear how you are. I know there are many here that care . Thank you n know you r loved.
You're not alone. I'm also on a support group on Facebook, Harvoni Family and Friends. I'm ending day 5, going into day 6 myself with stage 4 liver disease cirrhosis. I also know about the ups and downs of tired vs alert then tired again, also irritability and mood swings. It's a roller coaster ride. But all worth it to become UD - Undetected. Keep at it and slay that dragon!!!!
Yes also to the vivid dreams and sugar cravings, not good for a diabetic!
Sharon Horney Congratulations on starting Harvoni! It is quite a rollercoaster ride but you're right, it's totally worth it! Some of my side effects have started to get better. That gives me hope. The sugar cravings are worse though! Lol! That probably isn't good for a diabetic! Do your doctors have high hopes that this treatment can reverse your liver damage? I really hope so! Here's to slaying the dragon together!!! Please keep me updated on how you're doing and thanks for commenting. It really is nice to know you're not alone!
I just received word today that my 8 week course of Harvoni has indeed cured my hepatitis c. God bless this drug. I personally had no real side effects to speak of either.
i am on my 3rd day of Harvoni, Thank you for these videos, the tablet is mashing me.
Medicare Will give Harvoni. I have hepc & cirrhosis. But waited so long for a non interferon drug. Just started 8 days ago.
Hi Stacey..Im Jerry and I'm very glad to hear you qualified for Harvoni . I started treatment a month ago and had a blood test after day 10 and went from a viral load of 8 million to just 19. Tomorrow I go for the 30 days blood test and hope to be cleared but still have to do a full 6 months of Harvoni. Only because I went thru 5 previous treatments on Intron, Interferon and Rebetron ..that and I have advanced Cirrhosis.. Wish you the best and if anyone has any questions feel free to ask..jerry
Hi Jerry! That's so amazing to hear about your blood work! 8 million to 19!!!! I'm so happy for you. Good luck with your next blood draw. It sounds like the medicine is working and I'm sure when you get the results from tomorrow's test you'll be undetected! I'm guessing this round of medication must be a piece of cake compared to the other 5! I'm kind of embarrassed complaining about my side effects. That's a lot of heavy meds! You must be a very strong man to have gotten through all of that. Please keep me updated on how you're doing and what the blood test says about your viral load. Or lack there of. Thanks for commenting and have a great night!
j maedl Hi Jerry.It's TarandonDesigns. I'm trying to respond to your question directly but having some issues doing that. So I popped over here. You asked if my missing appts. was because I was sick from the hepC or was I sick from the Harvoni. It was from the Harvoni. There were nights that I could not sleep at all because of the joint pain, the awful itching and burning, the headaches and the sweating. These are all hepC symtons that were incredibly magnified by the Harvoni. After being up all night I was not able to drive myself to my appts. The Drs. is an hr. from my house. I would sleep most of the day because of the horrible nights. While driving home from my University of Washington appt. I feel asleep while driving on the highway during the 3hr. ride home. I drifted into the next lane. It was very scary...
Hi all..just got the call from gastro., " UNDETECTABLE " 😀
Wow..hope your doing better now..pretty scary falling asleep at the wheel 😲 I agree witb ya too about being undetectable... I have been there twice and not for long..all the interferon i injected in my body was for .nothing...The Harvoni worked wonders as I just got a call from my new gastro " UNDETECTABLE " and only after a ,month of Harvoni.***** They told me that being undetectable is a 0-15 viral load and I have heard that before as the virus leaves a tell tale scare if you will...I am trying to find out what 5years of inteferon will do to one as far as lifelong side effects? All my joints extremely hurt..I have been on oxycontin and they allowed me to work but now even walking is a challenge.. I now take lortab but Im getting ones that dont have the acetaminophen in them called Zohydro. Who should take Tylenol? NOBODY SHOULD...Instant liver damage...Now if i can just get my sugar under 200..I take 80 units daily and Im not responding very well..one thing at a time i guess...Jerry
j maedl Good news! Only 2 mos. to go! 5 yrs. of Interferon? I've never heard of anyone being on it for that long. Hopefully this is it for you.
It's very hard to get prescription pain meds in WA. right now. They are treating everyone here like a drug addict. I personally know 2 people that have very real pain issues and have to get their medication on their own - if you know what I mean. I take about 12 or more advil a day plus gabapention. I had a nurse yell at me for taking too many advil because she said they would cause kidney damage. When I asked her what the **** I was suppose to take for pain since they won't give me anything for it she told me to take tylenol. I laughed in her face. Perhaps the sugar levels will be easier for you to manage once the hepC is finally under control.
I'm in line waiting to be approved for harvoni . I have been told its comparable to chemo therapy is this true ? I'm in tears now so scared. watching these vids trying to find hope .
Just me again. I forgot to say that I consider myself in remission and won't consider myself really "cured" until the virus is still undetectable 3 mos. after stopping treatment. This is what I have been led to believe at this point. This worries me a little as the drug is so new. It hasn't even been out for a year yet so I wonder how there can be enough data to support that statement. I have also been told that once off the med it will take about 2 weeks to completely get out of my system.
Stacy, congratulations on starting your journey. I applaud your efforts to reach out and support other people by sharing your story. I started Harvoni on xmas eve. I searched for help, information and support at that time but there really wasn't any. Thank goodness for all that are infected that things are different now. I will be taking my last pill on mon. 3/16. I am counting the hrs. I posted some of my story on Paulas HepC video blog. If you get the chance please read it. I don't want to scare you but please be aware that the adverse side effects if you are going to experience them probably won't start until you are on the medication for about 2 weeks. I think it takes that long for the Harvoni to really get into your system.I wish that I had been prepared or had more information. The really good news is that it is a fast acting medication and when you are at week 4 you will get the good news that the virus is "undetectable". This is what gave me the mental and emotional power to go on. I had no idea what to expect. My Drs. were very ill informed and not caring enough to share the little they did know.I had to be very proactive in my own treatment. There were times that I was too sick to go for my blood tests or my appointments. I wish I had been more prepared but now I know enough to write a book.I kept a very detailed diary.I was not not brave enough to share my story online. Please keep us posted and contact me if you have any questions or just need to share.
Hello Tarandon Designs..thanks for posting..I read that you were too sick to get blood work or keep Dr. appointments..In your opinion was that a result of the side effects from Harvoni or something else? I have been on Harvoni about a month now and I had a pretty good headache for 3 days..thats all. I do have alot of experience with former treatments over the last 20 years tho too. . thanks..jerry
Hi Paula!
I have to admit something to you... You're the reason I started this diary! I was desperately searching for information about Harvoni and it led me to your video blog. As I listened to your story and heard what you had been through, I knew it would be helpful for me to start one too. You inspired me and gave me the courage to tell my story! Thank you! I've commented on your videos just under my other account. I hope you don't mind but I talked about you in my 2nd video. I didn't say your name but I talked about your lab work being undetected and how much hope that had given me! Even though we've never met. I'm so happy that you're almost done! I'm doing a happy dance for you and will continue to check in on your page and say hi! Thank goodness you were there because my doctor seems to be clueless when it comes to the side effects. I'm guessing its because the medicine is new. Please stay in touch and please put up more videos! You never know who you're going to help. Thanks again Paula!
j maedl Hi Jerry!
I know you were commenting on Paula's comment but I just started to experience headaches too! I'm not sure if they're the Harvoni or just allergies! Lol! It seems like anytime I sneeze now I want to blame it on the medicine. Hope you're having a great weekend and enjoying some of this sunshine!
Harvoni Video Diary I'm not Jerry but I wanted to respond to this. The headaches are a Harvoni side effect. Harvoni seems to effect the sinus's. Many people complain of allergy like symptoms - runny nose, sneezing,headaches.I think the med is very dehydrating which can cause headaches. I have found that drinking lots of water will help with any dehydration headaches. I once had a headache so bad that it lasted for 2 days. I thought I was having a stroke. I went to the er and they started IV fluids which helped alot.
TarandonDesigns Hi Paula! I tried to respond to your post but I think it got lost between the other posts. Lol! I wanted to let you know that you're the reason I started this video diary! I've commented on your videos under my other account! I actually mentioned you in my 2nd video! I didn't say your name but mentioned that you just found out you were undetected and how hopeful and happy that made me even though I didn't know you! I wanted to thank you for being such an inspiration to me and for helping me to find the courage to make this video diary! Please post more videos and keep me up to date on how you're doing! Miracles happen everyday and you're living proof!
I was in the Harvoni support group, on facebook. They kicked me out, when I started asking questions they didn't like.
Im sorry to hear your suffering. You know Genetics is the most important thing with diseases. I have a friend who was positive and I used needles with her everyday because I assumed I had it and all my friends that used with her (at least 15 positive hep c) friends so I just thought I had it so I told everyone I had it and my friends that didn't I would tell them and eventually they'd use with patient 0 or 2 and catch it. I finally got tested(takes 6 months to come up) didn't have it. I told doc that's impossible. I got tested again 18 months after and kept using with hep positive people, I didn't have it. They then said I am either immune to the virus or my body has fought it off. P.S. I got tested after getting clean 3 and half years after first exposure(exposed hundreds maybe a thousand times or used dirty needles 4-6 times a day for 5 and a half years) and Im hep c clean. No good diet. Nothing special.
i see no post on here for year ..are you all ok?Amen
Day 12 the first 4 days I had this incredible energy and a lot of aches and pains gone. Later on I notice constipation, fatigue, mild headache, nausea. The fatigue is different from the hepC fatigue. This feels like you have low blood pressure or anemic walking around carrying weights. I take my dosage in the morning. I wish I had started at night instead.
Wonderfull human being
If you have time look up Challenger Eagle here on UA-cam. He is the spokes bird for the American Eagle Association..pretty cool **
thankyou.
I'm on day 5. I was having really bad joint pain before, but now it's become almost unbearable. Everything else seems fine. I have a bit more fatigue,some sleep issues and headache bit yeah joint pain is bad. Any suggestions?
Stacy I`m in pa where are you? I got clean in 2002.
bILL stegura Hi Bill! Congratulations on your sobriety! That's a blessing in itself! I'm originally from Maryland but live in Illinois now. I actually lived in PA for a bit in York and Red Lion. Are you anywhere near there?
Congratulations on starting Harvoni! I know you're one a few days in but how are you feeling? The last few days have been sort of rough for me but this too shall pass! One thing I've learned from others suggestions is to drink a lot of water. It really helps! I look forward to keeping in touch and going through this journey together! It makes it easier to know that you're not alone. I'll be looking for your next video so please keep posting them! You never know who you're going to help. Talk to you soon! -Stacy
I live in allentown, but yourk is in my region. Im a member of Na thats how I got and stay clean. Iny problems I've had so far was some headache but nothing too bad. Hooe you feel better.
bILL stegura I know right where that is! I come back to town a few times a year because I still have family there. I got sober in CA but definitely qualify for NA and AA. Lol! I'm super glad to hear your side effects have been mild. I just started getting headaches too. It's all going to be worth it though to hear... Undetected! I can't wait!
If you don't mind, what insurance do you have, because I have upmc for you medicaid, and I got denied in 2017 for some reason, and now I'm going through the process again for the second time around, and I called my insurance, and they said that they cover the medication, but does that mean that they will approve me now just because they said that the medication is covered, or do they still have to approve it? Anybody who has any idea about this please?
Hi, can someone tell me if they have had visual changes as I have (pretty severe) and when will it go away?
What genotype do you have if you don't mind me asking, I have genotype 1 and tomorrow will be day 3 of Harvoni for me.
my dad has medicare which wont cover it, how can i help him!?
+Lynsey p It could be a few different things. Normally it is one of three things.
1. Doesn't have a metavir score of F3-4
2. The type of test used to give the score. Some places like Blue Cross will only accept Fibrocan or a liver biobsy. MRI's, Fibrotest, and many other tests would not be accepted.
3. They want him to take something else, that is less expensive, that does the same thing. Normally Viekira Pak.
I am I the process for trying to get approved for this treatment. Is there anything that you or anyone can help me with or anything I need to know. I have Fl blue, if that says anything. I just turned 28 and I nee help getting help.
+Angie Lopeman Florida Blue through Prime Therapeutics? They cover Harvoni, but you need to make sure you have either a liver biopsy or Fibroscan showing F3-4 metavir score. If you have that it's really easy, if not you still can get approved, but your doctor's office will have to be clever about it.
Thank you. I am going through the marketplace because that's all I can afford but I will look into it. Thank you again.
No problem, I spend a few days a week doing solely Harvoni approvals and before that I worked at an insurance company reviewing claims, so I know just about everything there is to know about that process.
+Angie Lopeman Hi Angie, Harvoni is not the only option to cure Hepatitis C. Nano-medication is another option you have. The advantages of nano-medication include, 1. Absolutely no side effects (i.e. fatigue, headache, anxiety, nausea, etc.); 2. Cured well within 12 weeks (SVR60 is still no problem.); 3. Regardless of genotypes; 4. Cirrhosis is treated at the same time (cirrhosis can be cured by nano-medication.); 5. Feel energetic and alive in the very first week of the treatment; 6; Entire treatment cost: only $10,000 (excluding shipping cost). Check out the link, www.glordavi.com
Hi Stacy. Wondering how you are doing?
The Harvoni support group supports Harvoni, not the patients. They tell people they're ungrateful, when they say they're having a hard time with the drug.
Hey Tracey I want to ask u do u get any bad smell in ur mouth while ur taking it?
Great
look up Dr Joel Wallach...trust me
Can reach anyone who wants to get affordable price
irritating-is that u attack people? do u know what r u doing, after reception,pls?
want some cheese to go with your whine .. NEXT video .. waaaaaaaaa.........