Hepatitis Forums
Hepatitis C Main Forums => Post Hepatitis C Treatment => Topic started by: Tess1971 on November 17, 2014, 12:51:26 pm
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Treatment has ended for me and I am "undetectable" after four decades. It is a great feeling. Color is returning to my cheeks after only a few days as I was looking pale and tired all the time last month of treatment. I sleep better already and no longer wake up tired. I really am feeling better than I have in years already. Not sure if it is all physical as the mental relief could definitely be paying some part in it. I am being very positive that this will all continue and just get better. My skin is already doing better and I am hungry more often now. My bloodwork will be checked again in Feb, then yearly after that. i also notice that the mental fatigue I used to get so easily has subsided.
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Hi Tess,
That's great news! Sounds like you slayed the dragon!
Congrats, Mike
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Hello Tess,
This is very good news to end the day.
Only week 5 of 12 for me. Good to hear that you are feeling so much better... very hopeful.
Cheers,
Petra
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I'm finishing up 12 th week of olysio/sovaldi and I feel the same relief you described. I feel more energy, more mental clarity..I just hope that we sustain this - I don't want to go back to how I felt.
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I have my 3 month after treatment blood test results: the virus is UNDETECTED
so I have reached cured status. As a matter of fact all my blood results were in the normal range for the first time in years!
I had to have a D and C for bleeding issues and that scared me but now everything is good and I can enjoy the extra 12 years they say I have gained by getting rid of the virus! All I can say from my point of view is that the treatment was well worth it
Love to you all hope to those who still suffer
Amo curedly haha
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Amocuatli,
You slayed the dragon!!!!!!!! ♪♫♪♫
Click on below link and enjoy:
https://www.youtube.com/watch?v=ioE_O7Lm0I4
Best wishes, Mike
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Amo CUREDLY So nice to hear! You know I was pullin' for you. Really glad for you! Stay Healthy.
Brad
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HaHA LOL! Thanks Mike that was the best surprise!
Brad I am pulling for you. I'll be watching this forum and if you post here I get email notifications, so post here so I know how it is going for you.
Amocuatli
1a
Highest reported viral load 10 million
TX 2014 Olysio/SOVALDI
cured Nov2014 :)
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I started treatment today. I have genotype 2 b. I was previously treated with interferon and ribaviron. It was undetectable for a second but then came back with an even higher than ever viral load. I have not been sick but my liver enzymes are 3xthe norm. I sure hope I am luckier this time with the solvaldi and ribaviron regimen. I was so disappointed after going through the last treatment and feeling so sick and then getting the news that it was not successful.... Wish me luck. I took my 2 ribaviron with the solvaldi this morning. I hope it's ok to take all three pills at the same time.
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Hi Eartheater1,
I think you're suppose to take the RIBV twice a day (1 in the morning and 1 at night). Please check with the pharmacy (they should have a 24 hr hotline). Follow up with your doctor as well to double check.
Also, it should be clearly noted on the prescription bottle or box.
Better safe than sorry!
Best wishes, Mike
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Thanks Mike. I do take the ribaviron twice a day and the solvaldi once daily. I just wasn't sure if it was ok to take the solvaldi and the ribaviron at the same time which is what I did today or if I should wait a couple of hours in between the 2 drugs....it is great seeing so many success stories here...
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Two ribaviron in the morning and two in the evening. One solvaldi daily.
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Hi Eartheater1,
To my understanding, you need to split the RIBV by 10-12 hours, due to the 1/2 life.
Are you taking 400 mg of SOL and 1200 mg of RIBV?
Best wishes, Mike
PS- Make sure you discuss this with your doctor and following the instructions on the RIBV package/script. It can make a difference.
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My solvaldi is 400 mg. the ribaviron is 400 mg in the morning and 400 mg at the end of the day. They go by my weight on the ribaviron. I weight 120 pounds. My ribaviron comes in 200 mg capsules so I take two ribaviron in the morning along with my 400 mg solvaldi. Then at the end of the day I take two more of the ribaviron.
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Hi Eartheater1,
I took 600 mg twice a day. It was easy because the RIBV came in 600 mg doses. They were in boxes that contained 14 pills (1 week) and were separated in the box, 7 marked morning and 7 marked evening.
Best wishes, Mike
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Nice....I'll keep u posted on how things go. What a good feeling it must be for you to be cured. I am a nurse and didn't even know I had this virus until I got a needle stick at work. I had to have blood work to make sure I didn't contract anything from the patient. I was shocked when they called to tell me I had hep c and had to have had it for years. Must have gotten it when I was a teenager because I was a follower and tried something risky back then. I only experimented one time and then realized I was insane and never did it again. So when they say it only takes one time I am living proof. Was never addicted to drugs. Just tried to be cool with a bunch of older kids when I was out and about with my beat friend one night. She I found out also has hep c but I don't know her genotype. I just send her a message on fb telling her about the new treatments available.
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I noticed you have genotype 1a. Is it the same treatment? No injections just ribaviron and solvaldi?
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No. I was on SOL+RIBV+INTF x 12 weeks.
Best wishes, Mike
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Wow...that was hard. I did ribaviron and interferon around 2006. I was in nursing school and working. I had to study while I laid in bed sick as a dog because my boss gave me weekends off and I took the shots on Fridays. Didn't get out of bed until Monday. It was 3 months. The virus was hiding but once I stopped the treatment it came back 10 fold. Was very disappointing. I cried. Oh well maybe this time will be different. The side effects are nothing like last time so far.....
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Hi Eartheater!,
I did 48 weeks of INTF+RIBV in 2001 and it kick my butt. I swore I would never take it again. But the cure rate and short treatment time when Sovaldi was added, made me change my mind.
The 12 weeks I just completed wasn't that bad in comparison.
In any event, hope you have a side effect free treatment and slay this dragon.
Best wishes, Mike
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My Doctor told me that if my genotype was 1a I could have used this brand new drug called harvoni or something like that. It has no side effects what so ever. It's brand new. No injections and no ribaviron needed. It doesn't work on 2b though. I go to Mayo Clinic in Rochester Minnesota. My insurance is covering all but 15 dollars a month for my meds,.,,I am so happy about that or I would not have been able to even try this treatment.....oh and thank you for keeping me company with all of this. I don't talk about it with people I know. Even as a nurse I see even nurses look down upon people with this disease. No one really knows I have this outside of my immediate family.