PLT ~ 215. 170 and above during the last 3 years, the last result was the highest. Thank you for the hint.

2x is for fighting it the second time (the final one hopefully). 1a before INF/RIB, 1a present day. Wanted to exclude the possibility of re-infection (in a way), although I was 99% sure it was a relapse. Maybe 6 months after the therapy was a fail test, maybe test was not sensitive enough those days? I can recognize few risks – dental works, blood test sampling, etc.? Other than that I can’t recall a situation where I was at risk, which does not mean there had not been any.

Low VL is another thing that I am unsure about. Makes me think it was a relapse; then it does not make much sense, because most of people show significant numbers (over million), from what I have seen in other statistics here and there). Maybe it is not important, since low VL is not connected with fewer or milder symptoms, from what I had experienced.

Regards

Just a brief update:

4weeks blood results are not as I expected it to be – lower ALT/AST compared with pre-treatment results. ALT was actually a bit higher. Nothing to worry about, but it would give me some more confidence, to be honest.

8weeks – now this is what I expected to see. I’m aware that only VL counts; however, these results are the best I had in last 5 years (although they had been similar and all in range for that period anyway)

Harvoni high had gone with the end of first month. Brain fog and great amount of tiredness are the only ‘major’ sides I feel and I have to say they are more severe than pre-treatment. With less than 4 weeks until the EOT, nothing to be worried about.

My diet is not as strict as at the beginning of treatment. Increased apetite is an excuse

Warm regards to all fellow patients and FHC team!

Finished my therapy with the end of November. The second half of it was worse than at the beginning, less energy most of all. Nothing unbearable, but I’m glad it is over now it is all about waiting. Yes, sleeping, healthy diet and a lot of water, and exercise will help.

ALT at the EOT was a bit higher than usually, still in range, so no major worries at this point. I will re-test in a week or so anyway.

No VL done at all, that’s the savings for 2016

question: are Fibroscan results and MELD score in line for less fibrotic patients and are they in line in general? Or, is MELD score relevant for general assessment of liver health? They both should be predictive but can MELD say 7 (which should be relatively good), and FS grade 4? I didn’t have a Fibroscan since 2011., so I am trying to fill in the gaps with blood results from the beginning of this year…

SVR 12 for me!

Alt/Ast – 14/14

I could have tell that I was negative even without the testing (yeah, a smart ass ), because I felt improvement in overall health lately. More energy, better mood, a few pounds added etc. Still, very stressed-out waiting for the results…

The plan is to check again by the end of this year, or earlier – in case of any doubt. This is the legacy from my previous treatment with PEG/RIB and it is going to take some time to get rid of this relapse paranoia.

Thanks to all forum members (and dr. F of course) who share their experience and knowledge and keep this site going!

For those who are having or are waiting for a second round of DAA’s – fingers crossed for you guys! You are almost there, just think positively!!