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Post Info TOPIC: Newbie that need,s advice and encouragement


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RE: Newbie that need,s advice and encouragement
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Thank you everyone for encouraging words :) I have never had a biopsy 3 abd ultra sounds and 1 mri. I am 42 years old and other wise pretty healthy besides the ptsd with panic disorder. I see my new hepatologist sept 9th which I'm sure like the others he will recomend treatment, hopefully my anxiety will be controlled, he is suppose to be one of the best hepatologists in Houston. I feel like I do need meds for anxiety I am fighting this demon alone and it is taking a phydical toll on my body I don't sleep I'm severly fatigued and dizzy and weak its interfereing eith my work and home life.Thank you all again I feel better talking to yall already :)

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Hi Michele, when it comes to HCV genotypes, consider yourself extremly lucky! Genotype 2 is by far easiest to treat. As Malcolm said, success rate is 95-100%!

so relax, don't worry about it. I hope you can get into therapy without interferon.

before taking any antihistamines or other meds, please consult with your hepatologist.

best




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GT 3 dg. 08-2012 / FibroScan: 5 kPa F1 / FibroTest: F0-1 A1 / SoC TX: PegInt 120mcg+Riba 1000mg UND from w8 relapse EOT+4w
01-2016 Sof+Dac+Riba UND from w8, SVR24!




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I totally understand your anxiety with taking meds. I am the same way. I've had celexa sitting in my medicine cabinet for several months because I worry about taking it. It's to help curb migraines and treat my anxiety disorder. I spoke to my nurse yesterday and she said to start taking it now because treatment tends to really make already anxiety filled people a little worse and it takes about a month to start really working.

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Type 1a. Had HCV my entire life via blood transfusion. Did peg & riba in 2000, relapsed. Did triple tx with sovaldi in early 2014 & I am now undetected 



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Hi Michele,

I agree with Tig. With such a low Viral Load and being Geno 2, your chances of a successful treatment are 95-100%. Don't worry, after having HepC for only 10 years you will have little liver damage. Personally, I would not take Zoloft, but make sure your Hepatologist approves it. Some people need antidepressants during treatment, but hopefully yours will be short ( 24 weeks maximum) and successful. Good luck, we're here to support and answer questions.



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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



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Hi, my name is Michele I was dx with hep c in 2002. Genotype 2b viral load 197,000.

I am preparing to start treatment soon but I suffer from panic and anxiety so I need to get that under control first, I have a fear of any kind of medications which seem kinda crazy because there was a time in my life when I really didnt care what I put in my body.

I was diagnosed with severe allergies today and was prescribed nasonex and he wants to do an allergy test next week to find my triggers, will nasonex hurt me liver? Is the allergy test safe to do with hep c? I could really use some encouragement to start the zoloft also so I can start treatment soon smile.

I would like to start treatment within the next few months because a recent ultra sound showed borderline hepatomegely.

any advice would be greatly welcome,



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Tig


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Hi Michele and welcome to the group! First thing you should try and do is relax!! Don't let this freak you out, between all of us here you'll get plenty of good tips and recommendations. I'm not a doctor, but the information I have read on Nasonex doesn't appear to be something you need to worry about. Your doctors and nurses can be trusted to provide you with safe information and its important for you to develop a trust with them. Let them do the allergy testing and get that out of the way first. I have no reason to believe that those tests aren't anything but safe for you to go through. So do your best to not worry about thatsmile I took Zoloft for depression yet he first time I went through treatment in 96 and it worked exactly as it was supposed to and when I was taken off treatment I didn't need it anymore and stopped without a problem. But it worked very well. Some people can make it through treatment without anti depressants, but I'm not one of them. The Peg Interferon is well known for that side effect. I am now taking Wellbutrin XL and have had no symptoms of the deep depression I had the first time. as far as your hepatomegaly, that's very common with Hep C. That just means abnormal enlargement of the liver and that's exactly what "hepatitis" means, liver inflammation. We all have it, don't worry about that. When you can it helps us help you if we have any information you have on your condition. I see you have a 2b genotype and a very low viral load, which is a big plus for you. Have you had a biopsy or fibroscan yet? The younger you are is also a plus, especially with a low VL like yours. It all sounds promising that you'll do well achieving SVR!

i hope that helps you relax a little! You'll have several friendly folks in touch with you shortly! Hang in there you've come to the right place!!



-- Edited by Tig56 on Tuesday 30th of July 2013 03:51:00 AM

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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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