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new to board
(Preview)
Hello everyone. From my bio. Im 63, gt 1a, F2, VL 5m, F2. Last checkup 7/13 and all numbers were normal. First diag. 1996. Had this since 1970. Been reading this board for a couple of years. I waited a lotta years for a better treatment to come along. I thought Incivek was it-had followed its progress for...
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jimbob
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13
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1053
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newbie
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Hey All Names Gig post Liver Trasplt 3 yr peg and rib 6 yr ago non responder. Got Liver Cancer moved me up on Transplant List got Tranplt was home in 3 days was like being born again. Went from feeling so bad for so long told the Dr. as soon as I woke up after surgery I feel better couldn't believe the differenc...
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Gig
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2
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669
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Trying to understand why symptoms after so long undetectable
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Hi all, this is my first post. I was diagnosed in early 1993. I was young and resigned myself to the fate of an early death. I lived recklessly with drinking and drugs but after about 5 years passed, I realized I was healthy and had no symptoms. I got proactive and saw a doctor, the doc said I was undetecta...
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Dave
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2
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887
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News from Spain
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Yesterday I had an appointment with my hepatologist. He check my viral load ( in 8 months up to 1.300.000,from 800.000 , do you know if this is significant? ) . Another lab test, normal. We commented, about future treatments with sofosbuvir ,when approved in Europe, and the possibility of waiting ....
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rebeca
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3
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976
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Side Effects after Peg
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Hi I am into my 7th wk of triple therapy with peg/rib/vict. I have noticed my side effects are not as bad every other wk after I get my injection on the left side of the abdomen, than on the right. I find the side effects are pretty bad when I have the shot on my right side. Could it be, because the liver is on th...
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kristi6
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12
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1585
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I have a question about medication
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Hi guys,I havent been in awhile the last time I was here I got some really good advice and encouragement from some senior members :). I have a couple things to discuss and hopefully ya,ll can help again. I recently visited with my ENT because I have been haveing some sinus and throat issues, i have a horri...
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michele
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2
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1026
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Hi Everyone, new member
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Hi All, Just an intro from my biography....contracted HCV in Feb 91 (from anti-D, I'm Rhesus Negative), told in UK in 95 (it was non-A/non-B then.) Moved to Ireland in 97, treated by Prof. Hegarty at St.Vincent's hospital Dublin. Was one of the first people in Europe to use Ribavirin/Pegylated Inte...
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Irish Lass
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5
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1107
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Post Treatment
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Hi everyone I'm Eliza & I'm new here. I've come to this forum to look for some answers and hopefully find that I'm not alone. I finished Hep C combination treatment in March this year so it's been about 8 months. I had a horrid time with side effects whilst on treatment some of which have had a lastin...
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Eliza
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12
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1747
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Hi Folks
(Preview)
Just a posting from my "biography", introducing myself. HCV over 35 years, liver cancer survivor, triple therapy patient (Interferon, ribavirin, victrelis) one week to go to end of treatment, 48 weeks - genotype 1a. Viral load from 5 million+ to non-detectable by week 8, been that way...
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DeRanger
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19
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2128
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Week 9 of Treatment and Looking for Encouragement Please
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Hi - this is my first time posting so I'm hoping I'm including everything you need to give me some advice. I started treatment with Pegatron on Sept. 6 for what I had hoped was 24 weeks. I have genotype 3 and my liver is a stage 2. I was told I have a 70-80% chance of a cure. My starting viral load was low at...
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PL
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19
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3057
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Victrelllis for 44 weeks instead of 12?
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My doctor just told me that the protocol for Victrellis has recently changed. I'm in week 9 of the Vic and was told I would only take it for 12 weeks. Now that's been changed and I have to take it for the remainder of my 48 weeks! Anyone else been told this? My Hgb is at 10 now and the Vic has been much more dif...
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Ginny
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2
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925
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To wait for new medication
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My wife Julia has been diagnosed with Hep C. She is Chinese and apparently when she had an hysterectomy in China 27 years ago a blood transfusion was infected. Tests have shown no liver damage. We have talked to 3 doctors, one advised starting treatment right away, another said we could wait until t...
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gerewolf
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22
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1711
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just starting triple drug treatment with boceprevir
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hello all, just starting treatment with boceprevir. Have tried ribavirin and interferon before , but due to side effects and not good response quit and tried to wait til all oral treatment came out. Now have progressed to stage 4 cirrhosis and am hoping can get svr with this triple treatment. Know it...
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newmex
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14
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1295
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hi mallani
(closed)
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Hi mallani
This is about your post on the other thread that I started. You have said that I have tried several IP addresses. I do not get you.
And you say that I am here to have fun.
I do not understand why did you get such an impression.
I am not here to have fun. There is nothing funny about this disease....
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newtohep
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2
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802
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Anyone here got HCV from sex?
(closed)
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I have had sex with a sex worker 2 months back. I used protection. When, I removed the condom, I felt something sticky on my fingers - it was the vaginal fluid. Without washing my hand, I used water to clean my penis with the same hand. After this, I took some water on the same hand and repeatedly gargled and...
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newtohep
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14
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1372
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Good News
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All three of my children are clear of the virus. This is such a relief, now I can focus on my own care & getting better. I am Very thankful right now.
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LTChaos
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3
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816
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Newly Diagnosed & terrified
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I am feeling very overwhelmed, sad, ashamed, devastated. I am 44 years old, mother to 3 elementary aged children. I started feeling stomach pain recently, and thought I was having gallstones. During the ultrasound, they said there was a small hemangioma on my liver, and my liver enzymes were sli...
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LTChaos
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17
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1599
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paperwork results my high numbers help
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I have my paper work her it tells me what number I have that are high right now Iron 159 reference 35-150 so just a little high This number are label as hep panel I have 3 high numbers in this category Total protein 8.5 reference 6.4-8.2 Alt 232 reference 30-65 this is the one the doc is most concerned a...
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jtthatsme55
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7
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1173
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Just started treatment and looking to learn from the pros
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I am genotype 1, VL of 7,700,000 on combo treatment. I took my first shot two days ago, and other than a headache I feel fine. Is this the honeymoon period??
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Calgarygal
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4
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1029
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well its offical
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I got the results of my blood test today im genotype 1 with a viral load just under a million with stage 2 liver damage im going to start treatment in either Dec or January
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jtthatsme55
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9
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1155
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new here looking for support
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I have just recently been told I have hep a and hep c im 21 and I contracted them threw IV drug use I am now clean and just looking for support with people who live with hep c and have gone threw treatment. Tomorrow I go to my first appointment with my hepatalogist what should i expect on my first visit
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jtthatsme55
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19
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1837
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frightend
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hello i was in a 2 year relationship w/ someone that was diagnosed w/ hep c and i went to get tested and it came back clear i was not infected. we have been split up for 2 weeks now and i feel lost i love him very very much and he has the same feelings for me too ( we went to junior high school together) and he was in...
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dragonfly79
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12
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939
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I need some support
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Today I feel really depressed, last week I decided not to treat with dual therapy, because there are a % 50 of healing in genothype 1a. As you now, in Spain,at the moment I can´t take another way. Yesterday I started to beat myself about it. Now I´m thinking here the new therapies will not arrive a...
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rebeca
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11
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1447
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Hello, the forum!
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Hello! I was diagnosed in 2002. 1b. Liver in relatively good shape, hope to start new drug treatment next summer... I'm looking for support and community. Thanks... Lida Rose -- Edited by Lida Rose on Friday 25th of October 2013 02:29:05 AM
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Lida Rose
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11
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990
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decided to wait for sofosbuvir
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I finally got to see the specialist again. I was ready to start treatment in August but for some reason they were dragging their feet with it. I'm kind of glad they did because I want to see if sofosbuvir is going to make it's way to the public in a few months. The doctor said there is no reason why I can't wait...
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AngieV123
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2
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745
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Nervous about biopsy
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I am haveing a biopsy done next week and I am very nervous, my genotype is 2b and they are comeing out with a new treatment after the first of the year to treat my specific genotype that dosent affect anxiety or depression because I suffer from both.......my liver tests are always normal and my viral load...
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michele
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6
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998
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Starting treatment
(Preview)
Greetings I recently made the decision to start treatment. I got the results of my biopsy, Hep C genotype 1...Stage II Cirrosis. Happy to find a support network and I'm sure i'll be using you guys advice alot. I'm scared to death from all the horror stories I've heard about treatment but I'm 38 years old...
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bigedawg23
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3
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716
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I have to decide to treat or not
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Hello everyone, As you know I live in Spain so, at the moment I can only access the dual therapy. Next december, I have an appointment with the hepatologist, and I have to decide. My status: 50 yo. Genotype 1a.VL 800.000. Fibroscan, in June 2013, (7.4.) F2 (in beginning of F2 ). IL28B CC genotype. I hav...
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rebeca
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7
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1149
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I feel guilty
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Hello all, I want to share a very strong feeling and very bad for me. I´m 50 years old. When I was 23, I tried intravenous heroine,3 or 4 time, I left this world without any problem. I studied and I got a good job. Now I have a couple and a good life. In 1993,20 years ago, my doctor detected the virus. I have nev...
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rebeca
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13
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1514
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Hiya's
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Nine weeks into triple tx incivek. I was on a trial about ten years ago, back when you had to mix the inter. I was about 190lbs and could bench 300lbs typical 1970's biker. You know the look that gave hep c its bad name hahaha. Only side effect I had was the first shot. I didn't respond well so tx was stopped....
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Scruffy
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9
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1826
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