This forum is for questions about medical issues and research aspects of
Hepatitis C such as, questions about being newly diagnosed, questions about current treatments, information and participation in discussions about research studies and clinical trials related to Hepatitis. If you would like to communicate with other people who have been touched by Hepatitis, please visit our new
Hepatitis Social/Living with Hepatitis forum
Some HCV patients will have iron storage problems; until you’re doctor performs an iron study, you might benefit from a no-iron multi like Centrum Silver.
Bill
i have read that pineapple,beetroot mmm cant really think of the rest....brain fog,is good for the liver,but dont go eating to much of the good foods cos to much of 1 thing wouldnt be a good idea,moderation is the key.
Milk thistle is very good,but people here say dont take it on the tx but take it if you are not on the tx,its a herb you bye in pill form.
So what do you all think? 20 years to get to this point, don't drink alcohol, exercise, try to eat right, and wait? The alternative of taking treatment now, with all the side effects, is frightening.
Yeah, there are some warnings our about shellfish; good catch. I seldom eat shellfish due to cost, so it wasn’t on my list of biggies at the time.
Genotype 2 is fortunately quite responsive to treatment; it only requires a 24 week treatment duration with a roughly 90% response. All the trial drugs are currently being used as adjuncts to the interferon/riba combo therapy, and most probably will for some time to come. If your doctor was somehow suggesting otherwise, I’d like to hear his thoughts.
When I was diagnosed, I had stage 3-4 fibrosis with genotype 1 HCV. It took me several years, but I managed to get through it, and am now SVR, or sustained viral response. It can be done, although it might not be pleasant at times. I probably contracted this stuff in 1973-’74, and wasn’t diagnosed until 2004.
Understand that many, if not most of the people that post in internet discussion groups are having significant problems managing their treatment and disease. Those that aren’t affected severely continue on with their lives, and are therefore under represented in these groups. Not all of us get slammed by treatment; although almost all of seem to get hit with fatigue, etc. I have yet to speak with someone that slid through this stuff completely unscathed.
Welcome to the group, by the way—
Bill
It would be great to hear from people that have had less negative results from treatment but this is a good place for people to download some 'bad time' frustrations.
Thanks for your comments. You as well Rocker
Good luck to you with whatever course of action you decide to take—
Bill