many many years ago at the beginning of email when the choices of sign in names were few, a computer turned my last name "Spector" into the infamous spectda. Being the amazingly uncreative and lazy person I have been with regards to this, I have used it on many forums. LOL-Just call me dave
Ah; fine vintage indeed :o). It sounds like you’ve come up with a pretty good plan. Does your doctor check you now and then just to make sure you’re still kicking around and living well? Are you watching the press releases or internet chatter regarding protease inhibitors? Telaprevir may be approved as early as next year; has your doctor discussed this or others like it with you?
I am also new to this site. It is a huge kick in the mouth to find out such harsh news. But do remember, that you can live a full and happy life being Hep C positive. The most important thing to do is to remain healthy, and don't binge drink. I wish you all the best of luck.
By the way what country, or city do you live in?
I contracted from a tattoo 22 years ago. I have just finished treatment three months ago, and my viral load is currently negative, so just hoping it stays that way. I am feeling quite okay, and try to remain healthy, but still eat chocolate every day. I don't drink, smoke or do drugs. So hoping to live to see my grandchildren.
Hi there!! Well I don't drink at all, but I smoke weed to much and I hear now it speeds up the liver wear process. but it helps when your on treatment.So I don;t know it sure helps me for now. I get depressed when I dont smoke it. I live in San Diego
I am 33 y/o now, was infected through blood transfusion as a newborn. Diagnosed with "nonA/nonB" in 1977. Never had any symptoms or health problems dut to this though. Almost done with my tx, I optimistic I will achieve SVR this year :)
Best guess is that amazing year of 1970 and doc is on board with this as most probable.
Diagnosed by fluke in 1995 and treated in 2008-2009. Went on to 'SVR', which is what we call a clinical cure around here.
Yup, glad it's gone but I'm one of those who didn't think about it much and was symptom-free. Decided to treat for strange reasons, one being that my older son kept bugging me to take the plunge. There were times during treatment that I wished I hadn't but now I'm so glad I did.
Contracted 2b in 1965 via blood transfusion. Finally decided to do tx and gastro said "You want to add more poison to your body?" Then, he prescribed Nexium for digestive problems. Which gave me IBS that I hadn't experienced for 30 years. Threw them in the toilet. Gastro says I'm basically very healthy. Doesn't matter that I sleep way too much and have a swollen ab every evening. I gave up. I drink and eat any damned thing I want now and wear loose clothing and expect to live until I'm 82.
Oldhepper, How are you sir? read your post, thanks, So you have hep c since 65 and you have no treatment? Your sleepy all the time, and your stomach is swoolen in the evening? You sound like your going to live utill your 92 , how old are you now??
I tried drugs in 1972. One time deal. Got it then, most of the people who were at that party are very sick or dead now. I consider myself lucky in that I quit drinking and doing any drugs back then and have not touched a drop since. So I have had Hep C for 38 years and dx 7 years ago.
i have not attempted treatment. perhaps when the PIs show up in a year or two i will have a go at it. i was in an accident in 1981 that resulted in a fractured liver among other injuries. i was transfused with about 70 units of whole blood and additional units of platelets. since that time i have experienced elevated transaminases. three years ago the docs said that the disease had progressed to cirrhosis. i seem to recall reading that after about 30 years with this disease about 40 percent develop cirrhosis. a more recent article states "Most HCV patients, if untreated, are expected to develop cirrhosis at about 65 years, irrespective of the age at infection. Thus, age itself seems even more important than age at infection for predicting the occurrence of liver cirrhosis." from http://www.medscape.com/viewarticle/554637
In my case, it was discovered during a routine blood test pre-surgery in 1994. However, I also had multiple surgeries prior to 1992 when there was no Hepatitis C test available for donated blood, so who knows how many years, since my first hip surgeries were in 1977. My doctor and I are convinced it was from a blood transfusion since I've never done any drugs except pot in college in 1967... Oh, am I dating myself?
I can actually pinpoint exactly when I got Hep C by my relatively rare genotype which I shared with my sister whom I shared works with a few times in 1972.
Intersting sidenote: Though her liver damage was slightly more significant, she SVR'd easily with just six months of treatment! Me, not so lucky. As are BMI's are strikingly similar, I'm convinced women generally have better chances of clearance. Who said it's a man's world?
Like brainmo, I sometimes think of the talented trailblazers we hung out with and I know many of them didn't make it. I consider both my sister and I so fortunate that we did and I'm real grateful for that.
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