Hepatitis C Support Group
Hepatitis C is a blood-borne viral disease which can cause liver inflammation, fibrosis, cirrhosis and liver cancer. The hepatitis C virus (HCV) is spread by blood-to-blood contact with an infected person's blood. Many people with HCV infection have no symptoms and are unaware of the need to seek treatment. Hepatitis C infects an estimated 150-200 million people worldwide.

I had to have a liver biopsy and an ultrasound, but I am not sure if they are still doing biopsies. I have had this a long time, over 25 years.
Once they figure out your genotype, then they decide on what treatment will work for you.
You are very fortunate to start when they now have drugs that really work!!! Consider yourself blessed in this respect.
I am one year post treatment and I am cured!!
Good luck and don't be scared, they are really nice and used to it.
I also kept my status to just my Hubby and then to my adult kids. I have been dealing with this Hep C since they only had the name:
Non A/Non B Chronic Hepatitis with no real treatment available.
Your liver should be in decent shape yet. If you aren't having side effects from your liver - that is fantastic news!!
I did the "HIV test" myself (through the mail), but in the long run, I had to tell them my name and stuff as how could I get the test sent to me? I was blessed NOT to have HIV also.
You will be fine...I know how it changes your life from "the sun is shining and everything is good and suddenly the floor falls out from under you. Stay with this support group and any other groups you are comfortable with. It helps so much.
I am not sure if I could have made it without getting support and not being judged. It helps a great deal..
God Bless.
They'll need to determine your geno type & order tests to assess level of liver damage.
It's all a slow process. It's a slow moving disease so don't worry, don't be impatient.
Be kind to your liver. No alcohol. Alcohol detecting in your blood could postpone treatment.
Look up liver friendly diets to get ideas on what changes you can make.
Get all the rest you can.
Don't be afraid. Just do what you need to do and fight it. Stay here with folks going through the same thing as yourself, it makes it easier.
Good luck and hang in there.
Prayers!
Bill
I really only agreed to be tested, b/c they were giving out gift bags to people who agreed to do it, which was movie tickets, McDonald's free coupons, etc. Mine was done by mail , anonymously. When I called for result i was floored. Had not thought it would be positive. The lab gave me the name & number of the American Liver Foundation , who I called and got much helpful info and also calmed me slightly. I know my first question was about how I sometimes cut my fingers , while preparing dinner for my stepson......(my mind was racing, thinking of all the possible ways I may have infected him & others) They assured me, even if my blood got in the food before cooking, the virus would not live in the human digestive tract. I went back to where I got the test kit and talked them in to giving me 2 more, for my hubby and son. Son was negative, husband was positive.
Ten years , is nothing as far as liver damage with this virus. If you are not drinking and other bad habits. You should not drink alcohol and certainly nobody with or without HepC, should ever take tylenol and drink , together.
tylenol is often still prescribed to me, btw, It is ok when taken as directed but talk to the doctor. I apologize for how long my message is but I want to hug you and tell you , you will be ok. It is good you are going t finally face your fears and get rid of it. You are blessed that you are doing it now, with the miracle drugs they have now.
It depends on your genotype (which version of the virus you have) and possibly, your ethnicity, as it does affect tx. If there is a best time to have this disease, it is now. :) I agree with whoever said to just think about who you share this with, beyond your doctor. There is a stigma and a lack of knowledge about it......though it is better than in the past. Just like the early days of HIV/AIDS awareness when children were kept from going to school because community did not know the facts. And , you do not owe anyone any personal info you do not feel comfortable sharing. Except your doctor and whichever close people you feel you can trust. I mean, I have had random nurses in non related visits to hospitals etc ask me "how did you get that ?" and sometimes I lied, sometimes I shrug and don't answer. I am now , at this moment clear of it. I just finished my treatment recently (Sovaldi and Ribavirin) And it is true , when you've had it a long time , you don't realize how many aches and pains , etc, might be from it.
I am starting to feel younger ....kind of strange , to be chronologically older , but mentally feeling younger. I better shut up now. Stay strong! There is nothing to fear, but fear itself. If you don't understand something the doctor tells you, ask. and , you can always ask us.