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Post Info TOPIC: New Member from Texas
Txmike


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RE: New Member from Texas
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Thanks to all for the warm welcome!

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Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Thanks matt!



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Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Matt Chris


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Welcome to the forum Mike

You have found a good place to hang out at and become part of the family.

Happy for your progress and hope the best for you.

Matt

 



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"And in the end, the love you take is equal to the love you make"

61 year old Geno type A1, F4 Cirrhotic, started 24 weeks on Harvoni 12-17-14 ,EOT-5 week = UND, 8-31-15 =UND , SVR-24 Baby YES! 
Dillo


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Hi Mike

Good to see a fellow Texan. I'm finishing up Triple Treatment myself in about 5 weeks but with Incivek instead of Victrelis

Good luck with your treatment and let us know whats happening. Lots of good info and people here.

 



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GT 1a Started triple tx with Incivek, Pegasys, and Riba 2-6-2013. UND at 4,6,12,23,& 24 wks EOT 7-26-2013. Probably had Hep C for 20-30 years. Don't really know when I got it.

Txmike


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I hear ya about that rollercoaster ride! I know he's glad to be almost done with this mess! thanks!



__________________

Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Posts: 10
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I hear ya! Thank You!



__________________

Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Status: Offline
Posts: 10
Date:
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Thanks



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Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Zlikster


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Hi Mike, glad to hear you are UND :) this forum has a lot of experienced people who went even thru multiple tries with interferon based therapies. Also a lot of support and tips for clinical trials going around in USA (mostly). So you will have proper way of online support here



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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!
Kellie


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Hi Mike welcome! - I'm glad you found us. I'm not on the Victralis, but I'm on the Incivik, riba and interferon. I'm on week 9. I've received so much kind sincere & compassionate help here. I wouldn't be able to do this w/o them. Use the search button at the top of the page for questions - or just ask. biggrin Kel



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HCV 1A 1980. Dual tx 2003 -UND at wk 11-discontinued due to severe depression

Started Triple 4/16/13 for 24 weeks

UND wk 4,6,8,12,17 & 24

E.O.T. 9/29/13

EOT + 12 weeks=SVR, and EOT +26 weeks=Cured!
JoAnneh


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Hey Mike,
Glad you found the forum!
It helped me thru 48 weeks.
I am post treatment 8 weeks
And starting to have a life again.
Great info on forum.
Yes, better than doc office:)
Keep up the good fight

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JoAnne

Genotype 1a, Triple therapy w/Invicek started May 19, 2012

DET 4 wk. UND 2,6,12,24 48 treatment. Achieved SVR 2013!
Txmike


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Man that's great, I get wait for that day to come! Glad you made it. I think I can make it if the meds don't jack me up anymore than where I'm at now, Thanks!



__________________

Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Posts: 10
Date:
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Thank you nurschic!



__________________

Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Posts: 10
Date:
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At week 8 VL was 25ul/ml and at week 10 was und. I was so happy about that and after that visit I got really sick again but feeling better now, Thanks mallani.



__________________

Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Txmike


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Posts: 10
Date:
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Thank You JoAnneh!



-- Edited by Txmike on Wednesday 19th of June 2013 02:30:53 AM

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Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
Bloomster


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Posts: 235
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Hi Mike and welcome - my husband is another who is also just finishing up on 48 weeks with Victrelis with 5 days to go.  He's had a bit of a rollercoaster ride at times, but has managed to get through it all.  This forum is a great support.  All the best.  Caroline



-- Edited by Bloomster on Wednesday 19th of June 2013 01:21:07 AM

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My husband had genotype 1a, 46yo, started triple therapy (peg/rib/vic) 23rd July 2012, VL prior to treatment 14 million, UNDET 12, 24 weeks, EOT 24th June 2013, EOT +1.5 weeks UNDET, EOT +12 weeks & EOT +27 weeks UNDET; SVR January 2014
mallani


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Hi and welcome, Mike.

As an F4 you can expect low platelets particularly with the Victrelis triple. I did 48 weeks and ended up with a platelet count of 38,000 but they soon come up again after EOT. How was your 8 week VL? The fatigue and Sx are worth it and we've all had them. The Forum was a great support for me, and helped get me to the finish line. The Rant'n Rave section was very useful at times. Best of luck. 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
nurschic


Senior Member

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Posts: 143
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Welcome Mike!!! The forum is full of great people and great advice and tips.....have a question, just ask! It has been a real life saver for me!!



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Dx:2007; Genotype 1; VL 1.4mil, start triple therapy (peg/rib/inc) 6/2/13 (Failed), Harvoni 12 weeks EOT undetected, 6 month EOT UNDETECTED!
Biggyb


Guru

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Welcome Mike, lot's of info here. I just did my last 48th shot of peg. I was on same treatment you are on. Hang in there, if i can do it anyone can.



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58 yo..Relapsed in 99 and again in 2004. Started triple therapy with Victrelis July 22,2012.  genotype 1a. week 8,12,16,24 VL Undetectable..E.O.T -- 6-22-2013,,,EOT + 24., UND. 

SVR !!!

 

~Bob~
Txmike


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Hello from Texas. My name is Mike and been on the TX for 11 weeks now. I have had some good day's and very bad day's. My Sx are feeling very weak,dizzy,headaches, body aches,congested, confused,etc. I had low platetes and Dr put me on Promacta which is slowly bringing the count up and starting to feel a little better but not much. I really like the forum and it's like you get more help here than I do at the Dr office, Thank You!



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Geno type 1a, Chronic Hep C, F4 cirrosis,  Interferon, Ribavarin, Victrellis.

Started TX April 19th, 2013
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