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Hep C Discussion Forum -> On Treatment -> Just a few ???
Post Info TOPIC: Just a few ???
JimmyK


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RE: Just a few ???
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Greetings,

That is correct regarding Antibodies. In fact I intend to die having them but NOT the Dragon. It is like comparing a puppy to a MONSTER.

Welcome and please add some info so we can assist. That is one thing each of us here are more than happy to do.

Regards

 

JimmyK

 



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Harvoni TX 2 12 weeks. UND weeks 4, 12 and now EOT + 4 Weeks. SVR-12 09/29/16. All Glory, Honor and Thanks be to God.

"I go to war with the brothers I trust."
mallani


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Having HepC antibodies doesn't mean you have chronic HepC. It merely means you have been exposed to the virus at some time, and your immune system has produced antibodies.

You now need a Viral Load test, and if that is positive, they will also do a Genotype test. Cheers.



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Geno 1b, IL28B CT,  x3 prior relapser,  ex-cirrhotic, 75 yo, did 48 weeks with Victrelis/Peg./Riba.  VL 1.28m at start, UNDET. at 8 ,12 ,16 ,24 ,30  and 48 weeks.  EOT 15 Feb 2013 , UNDET. at EOT + 28 weeks. SVR!  Still Undet. at EOT +5 years

Malcolm
wendyo


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Hi Chuck and welcome. I have a feeling the stomach is nerves/anxiety. For me, staying off the internet (google, self diagnosis, etc) as far as health items is often best as I can manufacture my own misery. Treatment is not as bad as it once was and I suggest start having conversations with your doc about treatment options and deal with this dragon and knock him down sooner rather than later.

Explore this message board, it is a wealth of knowledge and support. 

All best,

wendy

 



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Wendy 53 y/o, DX 1994, geno 1A F1

1999 TX 1 - Inter -non responder 2001 TX 2 - Peg + Riba - viral load tripled and taken off

T3:  Harvoni 12 weeks Sept. 19, 2015 ALT 41 AST 30 VL 541800 UND at EOT and SVR 24 ALT 18 AST 26 platelets 223

 
Ari-anna


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Hi Chukelle, welcome to the forum.

I can relate to your deciding Dr Google wasn't a good option! Sometimes Googling does my head in, however it did lead me to this forum so not all bad )

All the best on your journey,

Aroha
Ari

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Genotype 1a diagnosed 2005, Cirrhosis.

Pyglated Interferon/Ribavirin 2006, non-responder 

Viekira Pak/Ribavirin 24 weeks, virus undetected EOT 12 weeks SVR Feb 2016

New Zealand 64 yo
wmlj1960


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 Hi Chuck and welcome to the group. I'm sorry you were told you have this but it is not anywhere near as big of a problem to resolve as it has been in the recent past. The new DAA medications we have now are curing people every day with almost 100% effectiveness. And this is a slowly progressing illness so you have time to get set-up with a treatment plan without worrying about being in a big hurry. Try to relax a bit and know that this can be dealt with and you can continue to live a long happy life free of Hep C.
 Have a look around the site and if you have any questions just ask. If you need help with setting up your signature that Tig56 mentioned then information on that can be found by clicking the link below. There is also a link there to definitions for all the abbreviations you will be seeing in the member post and signatures.
 There will be other members along too so make yourself at home and join us all in our common journey to a Hep C free future.

Forum Abbreviations Link and Help with Creating your Signature



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60 yo, geno 1a, Dx 1994 HCV-HIV co-inf, Dx 2013 decompensated cirrhosis
Tx #1 - 24wks Sov+Riba /SOT 7-24-2014/UND@EOT/DETECTED@EOT+16 wks
Tx #2 - 24wks Harvoni /SOT 7-25-2015/UND@EOT,+12,+24,+52 = SVR

Mike

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Tig


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Hi Chuck,

Welcome to the group! Sorry you had to get that sort of news at any time, but it's far better today than it was just 2 years ago. The new oral medications, for 8, 12, or 24 weeks are much easier to tolerate. I wonder if your stomach problems may not be from stress and some anxiety? It's very common to be a bit freaked out to discover you're carrying around a virus like this and then trying to comprehend treatment. It's hitting you all at once and thats difficult for anyone. Take a deep breath and relax, it's not that hard to go through and will be done and over with in no time. Waiting to start is the hardest for many. 

You'll hear from others soon and you'll get a lot of good advice. We're here to share some experiences and see you through this part of the journey. Feel free to ask any questions, use our search function above and you'll find the topics discussed here on the forum. If you can provide some information like genotype, viral load, fibrosis stage, anything you know, will help us provide knowledgeable opinions. We can help you get that set up in your signature line if needed. I'm glad you're here.



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Tig

67yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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chuckelle


Newbie

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I start my treatment next hopefully (Lord willing everything goes as planned) and have not had any symptoms.  Found out April 2015 after donating blood at a local blood drive that I had the antibodies which of course started me on the road I am on now.  My main question is I have started feeling like my stomach is literally tied in a knot.  Right in the middle, not towards either side at all.  I googled a few things and quickly decided that was not a good option.  Called the doctor and waiting for a call back now.  Just wondering if this has anything to do with Hep C.  Any and all info would be appreciated.



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