I can't believe it, but yea, I've been Hep C free for 2 years.... after all those years and years of treatments! I still am being followed for fibrosis though, as that has not completely gone away. My LFT's have been normal for the 2 yrs as well. Now, just doing the social distancing like everyone else. Stay well!
I'll be 7 years SVR this May! Good to see some of you on here. I beat liver cancer with a transplant 5 years ago. I wonder where some of the others have gone.
Hit me up if you want to chat.
Love you All XO
No Hep C but now liver cancer. I promised my son that I would live to be 70 but not feeling so hopeful at the moment.
Six for me and soon six after the transplant.
Almost 5 years post successful Harvoni. Never had any side effects, and not after effects. Fibroscan does show very slight worsening of fibrosis though, and is probably due to my age (80's).
Contracted HCV in 1998 and was very ill in acute stage. Then after it became chronic just a low energy level. Interferon/Ribaviron 2008-2010 made me terribly ill, needed 22 pints of transfusion and failed anyway. After that was left with astronomical iron from the transfusions which then required IV chelation for several months, and several years til normal level. Finally in 2014 started Harvoni, cleared 3 wks later and continued on it for 24 wks. Absolutely NO side effects from Harvoni. SVR since then and feeling excellent (age 83) but disappointed that Fibroscan is going UP regardless and considered moderate fibrosis (doc says it is not from the HCV, diet or any unhealthy behavior but from age).
18 years for me. After Interferon/Rabi treatmeant althouch hep c clear my life was destroyed due to great dec line in my health ie foggy mind fatigue bone/ joint pain flu like symptoms low immunity etc. I was unable to work my career ended etc . Should be grateful I know but so tired of not being heard by GP etc
I just got the news, TODAY 8/13/18 , that I am officially SVR!
Been awhile since I came on this site.
I recognise some of your names from when i was being treated (successfully, yay) with incivek interferon and ribavirin in 2013.
The post tx side effects took a long time to go away.
I am feeling pretty good now.
The weird side effects have gone. Eg the moving patches of weird itching.
I am feeling pretty darn good except for the tiredness though I am working full-time in a sometimes stressful job.
Ideally I should work 4 days a week.
I watch my diet and do lots of hiking and work out at a gym.
It's taken 5 years to get to this.
I was diagnosed with HCV in 2008, and cured by Sovaldi/Olysio in 2016. However, my fibrosis was F4 when I was cured, and cirrhosis was diagnosed.
My latest ecoDoppler (ultrasound) shows the beginning of fatty liver disease, which my hepatologist says will double my chances of getting HCC, already double the norm because of HCV.
I have no idea how to stop the fatty liver disease except to stop eating altogether, since I already diet.
I think that age (74 now) is catching up with me, and maybe the HCV will get me in the end despite having eliminated the virus.
If there's any moral to this story, it's that everyone should be tested and those with HCV treated immediately, before serious liver injury has occurred. I may have waited longer than I should have.
I was diagnosed in 2005 with cirrhosis. SVRed with with peg/riba and took Heptech's fibrosis cocktail on and off. Fibroscan from last year says all is well.
I was diagnosed 10 years ago this month with cirrhosis.
Still kicking :-)
Celebrated my 4 years post transplant on the 2nd and still performing here in Arizona. All is well...
So hard to tell as the baseline for what it felt to be 'normal' vanished years ago. Survived Hep C but on to the next bit that aging brings
I'm three years clear of Hep C. I do an MRI every 3 months for cancer check. I am at stage 4 cirrhosis.
My concern is the memory loss. I am experiencing this and I'm reading that could have caused by the combination of interferon and ribavirin.
Hi don't worry. Doing well after treatment but having unrelated health issues.
Been outta touch and hope everyone in the Hep community is doing well. Happy to see u r thriving.
Just over 8 years post failed Combo tx, I'm 1 week in with Harvoni. I was left with panic attacks that started during tx and never left. I started a new drug for that, Effexor about a week before I began the Harvoni. Both drugs cause blurry vision so that is my only complaint. My computer has drop shadows on the letters and my night vision was already pretty bad. I'm hanging tough with both, actually feel pretty good other than the blindness :/
2.5 years cured still have cirrhosis now for 9.5 years but otherwise good