My viral load is 14500 is it true that if you have a low viral load you have a better. Chance of svr on treatment? I took my second shot yesterday and am on day 9 of treatment in a few days ill get bloodwork don't to see how everything is going! I hope things are good I haven't had one single side effect so far I hope that doesn't mean things aren't working I know they can come any time so I'm grateful that its still so far so good
Everything sounds just great re: no side effects. You know what they say about that gift horse... We probably need more info on you, have you had a liver biopsy, your genotype (1,2,3) etc. VL isn't the best indicator of success, but it certainly doesn't hurt to start out so low. Wishing you the best.
What stage of fibrosis are you? The VA site points out viral load does not reflect the amount of liver damage but it does say your chances may be better
The VA site has this:
Q: What does high/low viral load mean?
Viral load is the amount of virus present in the bloodstream. It is expressed as the amount of viral genetic material (RNA) per milliliter of blood. High viral load is often seen in people who have been infected for a long time. People who acquired HCV because of a needle also tend to have high viral load. Viral load is not related to the amount of liver damage, or to how sick someone is. However, people with low HCV-RNA may have a better chance of treatment success.
I'm stage 1 fibrosis geno type 1a I've had a liver biopsy and an eye exam before treatment what my doctor told me from the results was that there was little inflammation I believe I got the virus from sharing a needle because I can't really think of anything else. I'm on 180 Mcg of pegasys And 1000mgs of RIBA tomorrow will be day 10 I hope my whole treatment goes smoothly like the last week has been until then I'm so grateful for the time
It sounds like you're doing great with little/no side effects. Such great news that you have stage 1 fibrosis (F-1). You have made a good decision to treat early before you develop more fibrosis. Way to go!
to keep sx light make sure you drink LOTS of water and try to get some exercise. i did 48 weeks and i worked out 3x/weekly. it really helped me. even when i didn't feel like it i still pushed myself to at least do low impact exercise. good luck. belle
This site complies with the HONcode standard for trustworthy health information.
The Content on this Site is presented in a summary fashion, and is intended to be used for educational and entertainment purposes only. It is not intended to be and should not be interpreted as medical advice or a diagnosis of any health or fitness problem, condition or disease; or a recommendation for a specific test, doctor, care provider, procedure, treatment plan, product, or course of action. Med Help International, Inc. is not a medical or healthcare provider and your use of this Site does not create a doctor / patient relationship. We disclaim all responsibility for the professional qualifications and licensing of, and services provided by, any physician or other health providers posting on or otherwise referred to on this Site and/or any Third Party Site. Never disregard the medical advice of your physician or health professional, or delay in seeking such advice, because of something you read on this Site. We offer this Site AS IS and without any warranties. By using this Site you agree to the following Terms and Conditions. If you think you may have a medical emergency, call your physician or 911 immediately.