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The preliminary test for antibodies doesn't say anything else than that you have antibodies. You can have them if you have hep c or if you had hep c and cleared it yourself. If you test negative, doctors will usually test again in 6 months, just to be sure.
Low liver enzymes are not a marker for having the disease or not. Many people, like myself, have low liver enzymes for years without being diagnosed. I had it for over 25 years and my enzymes were always normal. Until last year.
Many people have low liver enzymes until actually diagnosed with cirrhosis.
Go to another doctor. It is great bullsh1it that he does not want to do further testing.
Usually a RIBA test is performed as well as the antibody test, if thats positive you do have active HCV. Then a HCV RNA PCR is done to check for viral load.
I would get another opinion. Had I been diagnosed properly I could have treated before damage set in. But the norm seems to be damage first then diagnosis.
on my test it says "highly activate" do you know what that means?
Between now and then I've developed the viral load, I've always tested positive for the antibodies, it wasn't until my LFTs came back abnormal that a doc cared.
Now I know there is no such thing as "dormant" HCV.
http://www.filefactory.com/file/a09g77h/n/HCV_Management_October2009_rar
also you need to look for a DR. in your area, maybe some here from your area can guide you with this but, if you start early you can get this sorted with no complications that you don't want to go through, im not really expert but i read, try to learn and help
check out the above file and then you'll know more about it.
http://www.turkjbiochem.com/2007/051-054.pdf
Bottom line...ask for a Quest Heptimax. Straight and simple. If insurance doesn't pay, it costs $440.00 here in Florida.
Hi,
Welcome to JustAnswer!
You have chronic hepatitis C infection.
The liver enzymes are within normal limits which indicates that there is no active inflammation going on in the liver.
The S/C ratio is used for confirmation in low positive cases.
If it is less than 3.8 additional confirmatory test should be done to confirm HCV infection.
Since your S/C is more than that you do not need any additional confirmatory test.
No matter what, get a PCR done. Your doctor should agree to it. Especially if he thinks he is so sure that you have hep C. You will need to know your genotype and viral load. If they come back negative, you will know that you don't have hep C.
Don't I want a PCR test to confirm virus? Someone had told me that Elisa test just means that at one point I had been infected with hep c but that my immune system could have naturally got rid of it, and that many people have the antibody but not the virus, only the PCR test can confirm for sure that i have actual virus, is this true? also my doctor said I was positive Hep C but was not active? I asked to see specialist so I can start treatment if I do have hep C, is this not what I should do?
this is Dr. answer:
There is no need for any confirmatory test as your S/C ratio is quite high.
The next step is to quantitive assay of RNA ( with PCR). This estimates the viral load.
Based on the levl treatment with Peg interferon and ribavirin will have to be started.
Consult a gastroenterologist/hepatologist for further workup.
Get a PCR to determine the viral load and do the genotyping. They usually do it at the same time with the same vial of blood.
Then you will know for sure.
And please don't panic. We have all gone through this here and we will be here to help you.
Probably you have always had that viral load just back then the tests were not nearly as sensitive as they are now so they did not see it in the results.
and Javi again - get the PCR test then you will know for sure one way or the other. If you test positive for the antibodies the healthcare provider really cant refuse you to take it, it's the first of many steps that should be followed.
thanks, Everyone!
I suggest you write down all the questions you have prior to your appointment. Most of us tend to forget stuff by the time we're in their office. Try and read up as much as you can digest, so you are a a bit more prepared and understand what the doc is saying.
I also took notes of what the doc replied on my first visit.
Be sure to request copies of all the lb results; these will help you communicate more effectively here, as well as with other specialists that you might come across.
You can try to discuss treatment options, but it’s still a bit early in the game for that. You might also discuss transmission; I think you had questions about sexual activity in a prior post? This is an opportunity to get authoritative info.
You might also discuss whether this doc prefers biopsy on RNA positive patients; this will be another pertinent question if positive.
Good luck, and let us know how things go—
Bill
then he set me up for Viral load and geno type test, I should get those results back in 5 days.
I think there’s some confusion somewhere; I can’t imagine a medical doctor stating that we cannot be HCV antibody positive, RNA negative. This describes the status of anyone that has successfully treated the virus; not to mention the hundreds of thousands that clear the virus spontaneously in the acute phase.
Regardless, you should have a better idea very shortly where you stand. Good luck with the results; you might be surprised when the results arrive.
Best of luck to you; keep us informed,
Bill
I don't know about that answer, I just want the RNA test to come back clean!
thanks for your help, i will keep you posted.
One will always have antibodies.
These are the most simple facts about HCV. If he doesn't know this, I would not trust him with treatment. If I was you, I would change doctors.
Javi—
Regardless of info your doc provided, you will soon have sufficient info to know where you stand. I’d definitely request copies of the results, given the questionable interpretation given recently. With those results, someone in here can help; it’ll make it easy for other specialists to way in if you have copies too.
Good luck; perhaps you’ll have a diagnosis to work with prior to Thanksgiving holidays.
Bill
jd
Depending on the stage of fibrosis, if I was in your shoes having genotype 1, I would consider waiting for the new drugs to hit the market. You would have a far higher chance of beating the virus than with the current SOC. Also you would be able to treat for 24 weeks instead of 48 weeks.
Another option would be to try get into a trial with the new drugs.
how long after ultrasound should I see results of exam?: i would imaging just a day or two? right? my ultrasound is set for this Monday, I will let you know.
my enzymes are still normal, so this is the only hope I am hanging on to right now that I don't have to much inflamation (inflammation), or damage. im pretty scared right now, I have 4 boys and I want to see them all grow and get married, can't imagine not being here for them:(
Are you getting all your questions answered? Marcia’s a good hand at all this; listen to her words. Also, feel free to get in touch if I can help more,
Bill
Javi
The doctor doing it should be talking to you while he does it. You can talk to him and ask him to explain what he is looking at. Usually they type it into the computer there and then, it is probably just a matter of when they do the print out. I got mine right away, as I was running around the hospital (with my file) for all the different tests on one day and brought the results back to the hepa department. But I'm in Denmark and had treatment at the main teaching hospital. They schedule you for 1 day and take all tests including chest xray, blood, urine.
Hey you are going to be o.k! I have the same geno as you, am 42 years old and found out 17 years ago. I never viewed it as a death sentence. I waited that long for treatment to raise my babies and tried to stay healthy. I kept an eye on it every 6 months for that long. If you are, and have been, kind to your liver don't worry to much, it's not an overnight kind of virus. But you have to check things out like you are to see where you are and if and how much damage you have. Everyone is different.
I didn't know ANYTHING about treatment other than that it didn't always work and made you sick, . I learned it all here after I started (ignorance is bliss in my case).
The ultrasound is easy and even the Biopsy is not bad.
I am in my 34 th week of treatment and I am o.k.
Good luck to you.
Vic
keep me and my family in prayer, I am so blessed that I found this site you guys are all awesome, Bill thanks for talking with me on the phone the other day, you are defenitly a champion on this side, you have a great testimony that you share and even though your cured of disease you still stay around to help us newbies out, your awesome guy! I look forward to the day I also can pay it forward and help others out as well.
so thanks to all who have cleared the virus and your still around to help out it means alot!
why is it everytime i ask for a hepatologist the pcp keeps referring me to a gastro doc?
Hepatologists are normally not listed in searches, but if you do find them, they usually will be listed at larger teaching hospitals and transplant centers. And if your insurance carrier is like mine, you'll only find them listed as GI drs. It's weird, I know. I've made about 200 phone calls in trying to find my own Dr.
You're going to be fine, just focus on one thing at a time. This is the BEST forum so you're doing good staying connected. These people are the finest and have so much to teach us newbies!