It has been 4 weeks now. I had my first blood draw Tuesday. And will find out results next week. I have had a few side effects but nothing i couldn't handle. Knock on wood. Mostly have just gone about my daily routine. I am thinking I will start exercising again. As my joint pain has subsided. I so...
Tuesday, November 27, 2012Sexual transmission of HCV among monogamous heterosexual couples: The HCV partners study. The efficiency of hepatitis C virus (HCV) transmission by sexual activity remains controversial. We conducted a cross-sectional study of HCV-positive persons and their part...
Well, it had to happen! After 37 weeks of not being even 5 minutes late for a dose, I forgot my 3pm Victrelis. I have 2 alarms for the 7am and 11pm, but have got a bit casual about the 3pm. I discovered the error at 6pm and had sheer panic and disbelief! After gulping them down, I had to work out how to get back on...
Well seen doctor and as of 2:00 p.m. I have started the Vict. 12 per day. Hemo was at 100 and he hopes with eprex can keep me at least around 85, still low but still only treatment mood left. only doing 3 rib per day and shot. Doctor figures the Vict will hammer my hemo, but what I have been reading the hemo i...
#18 6 To Go. I have been in a study, where I have been negative since week 1.Heres a salute to all that are doing this treatment for extended amounts of time.I have been a angry untouchable person. I find the only relief is to hide myself away. It also provides grand relief for my family !! LOL
im in week 9 of incivik and pegasus.Everytime i see nurse she never has much good to say and has a hard time remembering who i am and ,asks everytime if im still drinking.I have told her repeatedly that i dont anymore its been three years since my last one. this treatment is really getting to me,with the bu...
Hello everyone, This is my first post, but I've been reading for a while and getting lots of useful information. I've read quite a few high fat options here, but I was hoping someone might have suggestions for low carb meals without cheese that are 20 g of fat. My husband just started treatment last Thur...
Happy Thanksgiving to all. I'm thankful that aside from this pesky HCV thing I have my health. I'm grateful that it's a treatable disease and that I have wonderful friends on this forum to help me through it. I'm happy that today I get to relax and cook a good meal with my wife Jen who I love. I'll even get to...
Since the 1990's, volumes have been written about the differences between Genotype 1a and Genotype 1b. Researchers have gone to extraordinary lengths to try to highlight any differences. This is a summary of what was thought, and how it is today with the new Trial drugs. The geographical distribut...
I haven't posted in awhile, treatment made me pretty sick & was quite a rollercoaster ride! I was on triple therapy with victrelis & the doc stopped my treatment yesterday. I have an artificial eye and it keeps bleeding--like bloody tears when I blink, my lab results are just getting worse...
I was just wondering how members and the medical community will look back on the current SOC's. Will we look back on them as the lifesavers they appear to be or will we look back on them as some form of barbaric medieval torture that was rushed into production to satisfy the stockholders of Big Pharma...
Well it's been 27 weeks since tx, I have been checking in from time to time but had nothing to update. My labs on 11/12/12 were wbc 7.2 rbc4.77 hgb 15.7 plt 205 sgot 11 sgpt 34 total bilirubin 0.5 Viral load UND!! Was also Und at week 6 and 16 post tx. Still not feeling as well as I had hoped but getting the...
My husband took his last Riba pill tonight. It is over!!! I hope he starts feeling better it has been a tough road. This forum has been a source of strength. Thanks.
Hey guys, just checking in after going through a bad week or so with hubby. He's coping the best he can at the moment, but is suffering with fatigue, sickness, loads of hair loss and the general yuckiness that goes with treatment. I feel upset seeing him like this. He told me today that he can see a mas...
Nail salons should be regulated to help prevent the spread of infections: report Link to article...http://hcvadvocate.blogspot.ca/2012/11/nail-salons-should-be-regulated-to-help.html
I reported a side effect to my Drs office today . what a mistake Instead of just making a note and asking how I was doing, they said go to the ER, they wont see me until 10 days after my4 week blood which I done earlier today before I called my Drs office. So off to the ER, who is having the busiest day theyve...
I recently had both a HCV fibrosure and ASH fibrosure done. The ASH test came back with a Fibrosis score of .46(borderline F1/F2) and a Steatosis score of 0.66-moderate Steatosis. The HCV test resulted in a 0.46(F1/F2) Fibrosis score and a Necroinflammat Activity score of 0.21(A0/A1). When I went...
Well my blood count is all messed up. I am going to the hospital on Friday to get some blood. I was told it will take about 10 hours. Hope they hane a tv in the room. If i need a second pint I will have to stay over night. They say I will feel like a million dollars when I am done. Ken
So Today is my LAST SHOT! Lindsay and I are having our friend over; Joanie who is a love :) and she was present for my first shot so we thought it only right to complete the circle Linds and I are working on cleaning up lol, when Joanie gets here we are going to le...
I have found a good way to remember the difference between the two Q tests: Quantatative:" the quantity" the amount of virus being replicated in your liver Qualitative: "the qualifier" the test done to see if you have the C virus I.D. (is this correct Malcolm? please feel free...
I was on incivek w/interferon and riba for 48 weeks 12 weeks with incivek. Since week 3 and1/2 less than 43 udetected all the way till last blood test maybe 8 weeks ago. Took blood test last week after 2 weeks of finishing therapy results less than 43 but detected. Doctor said lets wait for another blo...
I am on my 19th week of TX (triple with vic). Since approximately week 5 I have really bad taste in my mount but from what I read here on this forum it is common. Some days it was worst and some it was better. However, in the last 3 weeks I am walking with a taste that feels like someone dumped a nuclear waste int...
I took my 12-week post-treatment blood test last Friday (Oct 26). I was tempted to tell the doctor not to give me the results on the basis that, emotionally, no news would be better than bad news. I was afraid to even hope for success, lest I be so very disappointed yet again. What I dislike most about H...
As a veteran of the Incivek 20-grams-of-fat wars, I know all too well the misery of gagging down that quantity of vile substances not once but THREE times a day for twelve weeks. But those of you who are mid-battle are in luck! 'Tis the season for eggnog! -- my all time favorite secret fat weapon. A sin...
Been on triple therapy since October 19th, ribavarin, peg interferon and incivo. Am due to collect next months medication this week. Discovered tonight I should have been taking 600 mg of ribavarin. have only been taking 200mg. Thought I had been given too much ribavarin, realised tonight that the...
I recently started a new job in the biotech field and durring me prospecting for new clients I came across Monogram Biosciences. They recently developed an assay (test) for resistance to boceprevir and telapravir. Have any of you had this? I didnt...I had my IL28B tested but not this test...I don...
I have ben treated for Hep C 5 times in 8 years with failure.My last treatment of Pegatron ended in Jan 2007.Since then my life has taken a drastic fall.I have lost all energy,ringing in one ear constantly,stomach pain,depression,fibromyalgia,can't take the cold, major brain fog and much,much mor...
Hello everyone! I feel groggy and tired all the time due to the hep..and im about to start tx....after treatment is all said and done, does the tiredness and fatigue from the hep go completely away?? thanks! none of my doctors have been able to give me an answer so far lol
Hi everyone! I'll be starting tx in a few weeks. I know most things about the disease but don't know much about the tx. Im 25 and have geno 1a..my vl is 50,000 and so far my biopsy said there is no liver damage. I was diagnosed at 17 with hep. Being young and stupid and influence of an older sibling I used pill...
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Lindsay and I are having our friend over; Joanie who is a love :) and she was present for my first shot so we thought it only right to complete the circle 
Linds and I are working on cleaning up lol, when Joanie gets here we are going to le...