Hi again, King, great to hear you`re getting no side effects so far. It does vary quite a lot from person to person but not everyone experiences sx from Harvoni and you may well find that you don`t either. Drinking enough water is certainly a good thing to do but please don`t feel you have to force it down, but take enough to keep yourself well hydrated.
Keep us posted and best of luck!
hepcinohio said
Feb 15, 2015
Thanks so much Mugsy, Cinnamon Girl, Gator Man, Greg D, Matt Chris, Tig 56 and Firemen Rob. I really appreciate you all taking the time to help me. So I should drink a lot of water? Will have to work at that. Day4 and not 1 side effect. I will continue to post over under treatment. Talk to you all later.
Fireman Rob said
Feb 14, 2015
Welcome King,
You're starting an excellent tx and will likely kill the virus this time! Good luck and keep us posted.
Best,
-Rob
Tig said
Feb 14, 2015
Hi King,
I didn't get the opportunity to say hello, so hello! You've got to be your own best advocate when dealing with people like your Dr., that seem to always be in a hurry. Keep on them if you need or have something to say. They work for you, period. If you feel you need extra time at an appointment, tell them that when you make the appointment. They often forget their bedside manner when they're an hour behind. It's important to get all of your questions answered, especially when you're going through life changing treatment.
I want you to look at yourself in the mirror and tell yourself, "I'm going to slay the Dragon this time"! Attitude is important while you're going through this. Do your best to stay positive and BELIEVE this is the time. The chances for SVR have never been better! I know you've read the posts here and have seen how many have succeeded on this new protocol. You won't be any different, because this is your time. When the flowers start blooming in May and June, you'll be Hep C free, count on it my friend! My Magic 8 Ball says so....
Tig
hepcinohio said
Feb 14, 2015
What a bunch of nice people. Thanks all, day 2. Doctor said I do have cirrhosis but didn't say it was bad. idk Doctor was in a hurry and didn't have time talk. I had to make an appointment to go into his office so he could tell me to take 1 pill a day. He could have done that over the phone. Also said he is positive I will be cured. Okay that sounds good, we'll see though.
Matt Chris said
Feb 13, 2015
Hello King
Welcome to the Harvoni Train, its a short smooth ride with some small bumps on the way, In no time the weeks will pass and SVR will be yours.
matt
Greg D said
Feb 13, 2015
Hi King and welcome back. All the best to you on this treatment. Looks as though you are determined to slay this demon and I wish you all the very best my friend! You must be a little apprehensive starting again after previous medications lol. I think we all admire the people who get back up and battle hard.
Keep in touch.
Gator Man said
Feb 13, 2015
Hi King,
I only made it 6 weeks on Peg/Riba many years back, not enough time to really feel that sick from sx. There have been few complaints from the S/O crowd and even less with Harvoni. Mugsy is absolutely correct that hydration is extremely important and a sensible diet will contribute to overall better health.
I'm not sure how advanced your liver fibrosis may be at this point, but it is amazing how quickly liver enzymes fall back into the normal range after only a few weeks of tx. Many people have commented on improvement in energy and well being after just a short time on Harvoni.
Good luck and glad to have you back!
Cinnamon Girl said
Feb 13, 2015
Hi there, King, welcome back!
I remember you from back in 2013 when you were hoping to start another round of treatment.
Great news that you`ve started Harvoni now, I`m sure you`ll find it a piece of cake compared to the Peg/Riba you were on in 2008, and you stand an excellent chance of success this time around.
Good advice from Mugsy to keep yourself well hydrated as it helps to stave off any side effects, although many people find they don`t have any at all on this tx.
Best of luck and do keep us updated!
hepcinohio said
Feb 13, 2015
Thanks Mugsy glad to have a buddy on here, sure will help
Mugsy said
Feb 11, 2015
I am on the 12 week treatment, too, and I have only 5 more pills to take until I am finished! I would encourage you to drink more water than you normally would to keep yourself hydrated. Relax, this treatment is easy for most people, not at all like your previous treatment. You should do well. Try to keep active, eat healthy foods and take good care of yourself. Can't wait to hear you celebrate UND status in a few weeks. Keep in touch.
Mugsy
PS I know someone else whose first name is also King. Great name!
-- Edited by Mugsy on Thursday 12th of February 2015 12:07:49 AM
hepcinohio said
Feb 11, 2015
I said 4 years ago I did the Interferon, it was more like 8 years ago.
hepcinohio said
Feb 11, 2015
Did the Interferon tx like 4 years back. Made me extremely sick only could take tx for 30 weeks. Unsuccessfull. Been waiting for new tx and now its here. 12 weeks and I start tomorrow. Is this stuff as good as they say?
Hi again, King, great to hear you`re getting no side effects so far. It does vary quite a lot from person to person but not everyone experiences sx from Harvoni and you may well find that you don`t either. Drinking enough water is certainly a good thing to do but please don`t feel you have to force it down, but take enough to keep yourself well hydrated.
Keep us posted and best of luck!
Thanks so much Mugsy, Cinnamon Girl, Gator Man, Greg D, Matt Chris, Tig 56 and Firemen Rob. I really appreciate you all taking the time to help me. So I should drink a lot of water? Will have to work at that. Day4 and not 1 side effect. I will continue to post over under treatment. Talk to you all later.
Welcome King,
You're starting an excellent tx and will likely kill the virus this time! Good luck and keep us posted.
Best,
-Rob
Hi King,
I didn't get the opportunity to say hello, so hello! You've got to be your own best advocate when dealing with people like your Dr., that seem to always be in a hurry. Keep on them if you need or have something to say. They work for you, period. If you feel you need extra time at an appointment, tell them that when you make the appointment. They often forget their bedside manner when they're an hour behind. It's important to get all of your questions answered, especially when you're going through life changing treatment.
I want you to look at yourself in the mirror and tell yourself, "I'm going to slay the Dragon this time"! Attitude is important while you're going through this. Do your best to stay positive and BELIEVE this is the time. The chances for SVR have never been better! I know you've read the posts here and have seen how many have succeeded on this new protocol. You won't be any different, because this is your time. When the flowers start blooming in May and June, you'll be Hep C free, count on it my friend! My Magic 8 Ball says so....
Tig
What a bunch of nice people. Thanks all, day 2. Doctor said I do have cirrhosis but didn't say it was bad. idk Doctor was in a hurry and didn't have time talk. I had to make an appointment to go into his office so he could tell me to take 1 pill a day. He could have done that over the phone. Also said he is positive I will be cured. Okay that sounds good, we'll see though.
Hello King
Welcome to the Harvoni Train, its a short smooth ride with some small bumps on the way, In no time the weeks will pass and SVR will be yours.
matt
Hi King and welcome back. All the best to you on this treatment. Looks as though you are determined to slay this demon and I wish you all the very best my friend! You must be a little apprehensive starting again after previous medications lol. I think we all admire the people who get back up and battle hard.
Keep in touch.
Hi King,
I only made it 6 weeks on Peg/Riba many years back, not enough time to really feel that sick from sx. There have been few complaints from the S/O crowd and even less with Harvoni. Mugsy is absolutely correct that hydration is extremely important and a sensible diet will contribute to overall better health.
I'm not sure how advanced your liver fibrosis may be at this point, but it is amazing how quickly liver enzymes fall back into the normal range after only a few weeks of tx. Many people have commented on improvement in energy and well being after just a short time on Harvoni.
Good luck and glad to have you back!
Hi there, King, welcome back!
I remember you from back in 2013 when you were hoping to start another round of treatment.
Great news that you`ve started Harvoni now, I`m sure you`ll find it a piece of cake compared to the Peg/Riba you were on in 2008, and you stand an excellent chance of success this time around.
Good advice from Mugsy to keep yourself well hydrated as it helps to stave off any side effects, although many people find they don`t have any at all on this tx.
Best of luck and do keep us updated!
Thanks Mugsy glad to have a buddy on here, sure will help
I am on the 12 week treatment, too, and I have only 5 more pills to take until I am finished! I would encourage you to drink more water than you normally would to keep yourself hydrated. Relax, this treatment is easy for most people, not at all like your previous treatment. You should do well. Try to keep active, eat healthy foods and take good care of yourself. Can't wait to hear you celebrate UND status in a few weeks. Keep in touch.
Mugsy
PS I know someone else whose first name is also King. Great name!
-- Edited by Mugsy on Thursday 12th of February 2015 12:07:49 AM
Did the Interferon tx like 4 years back. Made me extremely sick only could take tx for 30 weeks. Unsuccessfull. Been waiting for new tx and now its here. 12 weeks and I start tomorrow. Is this stuff as good as they say?