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I cannot wait for you to prove that doc wrong Topcat. I can't believe he/she said that. 20 years ago, my doc said, so long as you stay sober, you will die from something else, not this. A year ago, his exact words to me were, I will get you cured before I retire. So far, so good. We are on our way.



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Wendy 53 y/o, DX 1994, geno 1A F1

1999 TX 1 - Inter -non responder 2001 TX 2 - Peg + Riba - viral load tripled and taken off

T3:  Harvoni 12 weeks Sept. 19, 2015 ALT 41 AST 30 VL 541800 UND at EOT and SVR 24 ALT 18 AST 26 platelets 223

 



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Those ALT / AST results look really good and your upcoming VL test will likely be very encouraging also. If you're feeling good right now then your next 68 days should be a breeze and then you can start your countdown to SVR 12 and proving that "doc" wrong. Keep doing what you're doing. You got this! smile



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60 yo, geno 1a, Dx 1994 HCV-HIV co-inf, Dx 2013 decompensated cirrhosis
Tx #1 - 24wks Sov+Riba /SOT 7-24-2014/UND@EOT/DETECTED@EOT+16 wks
Tx #2 - 24wks Harvoni /SOT 7-25-2015/UND@EOT,+12,+24,+52 = SVR

Mike

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Tig


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Hey Terry,

Those are excellent numbers and can be pleased with the direction things are going! If your previous numbers were in the 60's, this is an excellent improvement. It shows the treatment is working as planned. Some medications, like Ribavirin cause some anemia, and we look at the hemoglobin and red blood cell count. Harvoni doesn't tend to affect those, so the ALT/AST are the ones we interested in. The next test we're anxious to see results for will be the viral load. They will probably draw that the next time you go in. 

I'm glad you're feeling good. Let's hope you'll avoid any side effects at all. Keep drinking that water, that will help keep things at bay. Keep it up! Let us know how things progress smile



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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I had my first blood test since starting Harvoni Monday. After 16 pills mu alt is 18, ast is 22. I have to go back and look at some older blood test but I believe I was in the 60 range on both before. 

What other numbers should I be looking at? Thanks all. I feel very good so far. 



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Hello Topcat

Welcome from me as well, you have found a good place & a excellent treatment protocol 'Harvoni' You have started on the road to recovery, stay 100% compliant and keep your diet a healthy one and all will go well.

matt



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"And in the end, the love you take is equal to the love you make"

61 year old Geno type A1, F4 Cirrhotic, started 24 weeks on Harvoni 12-17-14 ,EOT-5 week = UND, 8-31-15 =UND , SVR-24 Baby YES! 



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Thanks to all. I had total hip replacement June 18 and i can't believe how great it went. And now to be getting rid of the virus! 

I will never forget what the first specialist said over 20 years ago when I first was detected. 

"If you live long enough, this will be what takes you down."

Not exactly the words a 36 yr old father of 2 wanted to hear. Well, hopefully I get to prove that doc wrong with the help of insurance & Gilead. 



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Welcome. You will find a wealth of knowledge here and lots of support. It has helped me immensely and hope you find the same. 



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Wendy 53 y/o, DX 1994, geno 1A F1

1999 TX 1 - Inter -non responder 2001 TX 2 - Peg + Riba - viral load tripled and taken off

T3:  Harvoni 12 weeks Sept. 19, 2015 ALT 41 AST 30 VL 541800 UND at EOT and SVR 24 ALT 18 AST 26 platelets 223

 



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Hi there, Topcat, welcome from me too!

Congrats on starting your Harvoni treatment, and I`m glad to see you`ve already found our Harvoni Treatment Train thread. 

Most people feel anxious and apprehensive before starting their treatment, we all understand what it`s like, and it must be a relief to you to have begun your journey, and not to be experiencing any side effects.  As Mike said, make sure you drink enough water every day to keep yourself well hydrated, and you should find your 12 weeks to be very doable.

Feel free to join in any of the discussions and ask questions, and note that we have a `Search` button at the top of the page if you`re looking for something specific.  We have many experienced and helpful people here, you`ve landed in a good place!

Keep us updated, we`ll be following your progress..  smile

 

 



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Jill 

(71 yo, lives in UK)

Was Gen 3a, 

24wks Peg Ifn/Riba, Sep 2010 - Mch 2011

UND @ Wk.4, UND @ EOT, 

SVR Nov 2011 --> Still UND @ EOT + 4 yrs.

 

 



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Hi Terry.

 That's good news you got approved and are on your way to beating Hep C. Harvoni is generally easy on side effects but there are some things you can do to help. Staying adequately hydrated is proving to be very helpful in keeping Sx's to a minimum. Get adequate rest. Take care of your liver by staying away from junk food, excessive salt or sugar, alcohol, etc. There are some herbs and supplements that should be avoided in order for Harvoni to be 100% effective. More information on that can be found in the link I will include below.

If you have any questions about anything related to Hep C, fire away. We have a great group of knowledgeable members who are always willing to help. If you have a question about what all the abbreviations mean, such as in member signatures, information on that and on creating your own signature can be found HERE.

  Make yourself at home and join the ride along with the rest of us into SVR land. We are glad you are here. smile

Harvoni Full Prescribing Information .pdf



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60 yo, geno 1a, Dx 1994 HCV-HIV co-inf, Dx 2013 decompensated cirrhosis
Tx #1 - 24wks Sov+Riba /SOT 7-24-2014/UND@EOT/DETECTED@EOT+16 wks
Tx #2 - 24wks Harvoni /SOT 7-25-2015/UND@EOT,+12,+24,+52 = SVR

Mike

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Hi Topcat. Welcome to the forum.Glad you got your treatment drugs. It seems people are getting aproved for R/X easier  now than 15 months ago. Your deniel turned around pretty fast! Congratulations , get on the treatment train,your on for a smooth ride.  RC



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 M-64) 3 Treatments)( SOF-RIBA 2014)(SOF-RIBA-PEG 2016)(HCC 2016) (LIVER TRANSPLANT 8-2017)(VOSEVI-RIBA 2017)   SVR-12. 3-13-18   



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hi all. Just started harvoni Saturday. 57y/0 m.. 2 mil load. I was diagnosed 20+ years ago. Type 1. 12 weeks of treatment. 

when the Meds came in the mail Friday I was scared and hopeful that this virus could be taken down. So far after 3 days no side effects. 

Blue cross initially denied paying for the meds. I went back to see my specialist got a new biopsy, and he resubmitted the results. No cirr but some scarring.  Thank God they approved the meds!



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