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Thank you for inviting me to join the Forums.
My name is Chattypie and I am in London, UK.
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Hi John,
If you have not had the Hep C that long then chances are your fibrosis is relatively low.
With GT1b 12 weeks is long enough and with insurance coverage, they should give you Vosevii if you fail the first round so you have a good plan B. An extra 4 weeks insurance is nice for peace of mind if it’s going to worry you.
Here is a copy of my eBook on weight loss. The key for most people is getting enough protein rather than low fat or low carb. Anyway I’ve taken people from 300 pounds to 160 so it can certainly be done.
Attachments:
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Hi Balance,
I think you’ve made the right choice.
There is no doubt that PEG Interferon and Ribavirin was hard going, but most of that was the PEG.
Most people tolerate the Ribavirin pretty well with 25% getting nothing much, 50% getting a few sides like the irritability, and only a few getting significant issues.
We can always reduce the dose or stop it if needs be…
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Hello vedruss,
At 8 weeks there is not long to go now…
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15 March 2018 at 2:38 pm in reply to: Cimivir-l purchased in India/ Other medical judgments of Hep. C #27598Hi Gert,
Great news. I’m very happy for you!
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Hello kullboys,
Sorry to hear you’ve got a dose of the insomnia side effect. It’s about a 1 in 5 problem.
You know those cooking shows where they go “Here’s one I prepared earlier”?
Well… here’s one I prepared earlier!
https://fixhepc.com/blog/item/82-how-do-i-fix-my-insomnia.html
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Hi John,
Only a biopsy can give 100% certainty of what’s going on – everything else is a surrogate way of looking at it where the results correlate but that correlation is not 100%.
Being on the large size means ultrasound can be a challenge and fibroscan is a form of ultrasound.
As a big guy there is no surprise you have some fatty liver disease.
At the end of the day. You have a working liver that will be progressively damaged by ongoing Hep C infection, so the obvious thing to do is treat the Hep C.
With an F4 fibroscan result you could well leverage that into funded treatment under insurance/Medicare/Medicaid (if you have any of these). If you can’t get access that way generics work and with GT1b being the easiest to treat 12-16 weeks (the extra 4 is insurance and because of the ? over fibrosis) of Harvoni or similar should do the trick.
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Hello Tigerfan,
That’s great news!
Congratulations…
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Thanks for the update Redhead,
Looking forward to hearing about your SVR! Fingers crossed, knock on wood, not walking under any ladders…
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Hello Smp123,
Magnesium is just a salt so should not cause any problems.
5htp is a byproduct of L-tryptophan metabolism so should also not cause any problems.
So, yes you can continue to take them, but to be safe maybe a couple of hours before or after the Sof/Dac so they have basically no physical contact/mixing in your gut.
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Hello Balance,
Ribavirin needs to be started at the beginning to deliver full benefits.
If you are GT3 with high fibrosis (fibroscan >10 kPa) then you definitely need either Ribavirin or 24 weeks Sof/Dac without ribavirin.
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I’m looking forward to hearing about the results of your first test!
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Hello Balance,
Welcome!
Yes, there is a fair bit of jargon but you’re right that it does not take long to get a handle on it…
It is all explained in the Glossary (which is a tab up the top of the forum)
https://fixhepc.com/forum/glossary.html
How long are your planning to treat for with the Sof/Dac?
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Hi Sunflower,
Taking the pills +/- 4 hours is fine. The important bit is the daily bit so don’t worry about the daylight savings change – it makes no difference at all.
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Maybe ‘retreaters’ like me have gone the way of the Dodo? If so, well and good.
Hi Jeff,
Nothing has really changed in terms of success rates although going a little longer in GT3 definitely helps.
The peak of originator DAA use was around 2015Q2 – 2016Q1 when there were around 160,000 patients being treated each quarter. In 2017Q4 that number was 80,000 so over the last 2 years, the number of people treating with originator medication has fallen to 1/2 what it was. The situation for generics appears similar and we only help about 1/2 as many people as would have been the case a year ago.
So the major reason is there are less people treating so fewer people relapsing.
Another reason you don’t see much here is that most of the hard cases (cirrhotic past treatment failure) have either been successfully treated or died. This leaves a relatively easier population to treat where the SVR rates are over 95%.
The other significant change is that 3 years ago I was one of the only doctors prescribing generics. Over time other doctors have seen the results themselves and started prescribing and of course, have had relapses. The conversations have tended to be in the background involving me the patient, their doctor and sometimes others. Mostly we’ve settled on adding Sofosbuvir to Viekira or Zepatier or adding Asunaprevir or Simeprevir to Harvoni or Sovaldi/Daklinza to produce the Vosevii you have when Vosevii does not exist. Anyone who has worked with HIV understands that 3 drugs (targets) are much better than 2, however, the guidelines (both AASLD and EASL) and the various government/insurance funding requirements, and to a degree ethical and medicolegal considerations, dictate this is better done on the QT with informed consent from those that need to know.
Almost all the patients who relapsed the first time have been successfully retreated the second time. There are a couple of exceptions – one who failed 12 weeks Sof/Dac and then 24 weeks Harvoni who cleared on 24 weeks Viekira/Sof/Riba. Another GT3 who is still on maintenance Sof/Dac while we wait for something better (they were bucket list unwell prior to treatment and travelling well on HIV style maintenance).
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