Hepatitis Forums
Hepatitis C Main Forums => On Hepatitis C Treatment => Topic started by: singinasong on October 14, 2017, 02:17:55 am
-
Hi everyone.
I've just hit the two week mark and my experience so far is pretty unremarkable. I have had mild joint pains that are more like phantom pains that only last for a few minutes or so. They are not often.
I am used to having fatigue, but must admit that I actually have more energy than I normally do.
My biggest complaint about HCV is the neurological issues that I have had for the past 11 years. I'm really hoping that treatment helps my symptoms, but I know that this will take time post treatment.
This is my third treatment. I'm genotype 1a. In 2003, I was on the Pegasys Combo with Riba. I only lasted 11 weeks due to having serious thyroid issues. At that time, I was diagnosed with Graves disease and Graves ophthalmology. The next treatment was in 2011/12. I did triple therapy with Victrelis; started at 2.2M VL and ended at 11 weeks 3K VL.
This time, I get to do the full 12 weeks of treatment without a PCR test until I am finished. I will have blood work done every four weeks to monitor my blood cells and liver enzymes. I wish I could see my results at 4 weeks, but I will have to remain patient and wait the full 12 weeks, plus the length it takes to get the PCR results.
Looking forward to journey with you all.
Thanks.
Singin :)
PS. I tried to figure out how to create a signature to list my hx, but I couldn't figure it out ::)
-
singinasong, glad to hear you are getting the energy boost that Harvoni gave me -- it's probably the sofosbuvir that both medicines contain. I assume you will get to see the results of your four-week blood work, and the AST and ALT will be improved and cheer you on.
As to creating a signature, on the middle menu bar (Home Forum Help . . . ), pull down Profile and choose Forum Profile. There's a large box that lets you enter a signature of up to 500 characters.
Best wishes,
Gnatty
-
Hi Gnatty,
Nice to meet you. Thanks for the tutorial; It was right under my nose.
You are right. I will see the AST and ALT drop and that will be enough to keep my patience at bay.
Singin :)
-
I got my 4 week results in for AST/ALT and they are 34/36. Not what I was hoping for, but perhaps these numbers are due to a mildly fatty liver (as per latest ultrasound).
The AST/ALT numbers below during my last tx didn't hit these numbers until 12 weeks in, so I am hopeful. I also take a number of inhaled steroids everyday, so maybe this high normal is my normal.
I do feel better and think better, but I don't look better ;)
Will have to wait and see...
-
Singin, if anyone deserves "third time's the charm," it's you. Amazing that you've stayed at F2 through everything! A big hooray on the AST/ALT numbers -- basing them on your personal hx rather than what's normal for most people makes sense to me.
Gnatty
-
Thanks Gnatty. third time is a charm! :D
Yes, it's pretty amazing that I have stayed at F2 over the past 16 years. The doctor thinks I may have slow progression due to genetics, but that doesn't stop the symptoms. Luckily, I am able to treat it!
Wishing us all success and hope!