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Hep C Discussion Forum -> New Members Area -> Jumping aboard
Post Info TOPIC: Jumping aboard
Linuxter


Guru

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Posts: 1515
Date:
RE: Jumping aboard
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Hello Indygirl,

Just wondering if you got through treatment ok and how you're doing.

Keep us posted.

 

Linux



__________________

63yy,HCV,2b,F3-A1, Sof/Riba,12wks Tx   SOT: 1/20/16, HCV-RNA 9,816,581, ALT 56, Hb 14.6

4wk: HCV-RNA <15 Detected, ALT 15, AST 17, Hb 13.6 EOT: 4/12/16, ALT 18 , Hb 12.9176a2f85d05d9c965eafe199f2ba9ba5.jpg SVR Achieved 7/8/16

 
wmlj1960


Moderator

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Posts: 1559
Date:
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Hello Mamie, and welcome. That's right - you are not alone in this battle. There are many very helpful, knowledgeable and caring members here who are willing to help. So make yourself at home. We are glad your here. smilesmilesmile



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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

How To Create Your Signature / Forum Abbreviation Definitions

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Cinnamon Girl


Guru

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Posts: 5629
Date:
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Hi Mamie, welcome!

I`m glad  you decided to take the leap and join us here, and congrats on starting your Harvoni treatment 3 weeks ago.

You certainly won`t be alone here, you`re amongst friends and fellow Hep C warriors and you`ll soon be feeling at home here! 

If you`d like to write a few details in your `signature` line that would be very helpful to us when responding, such as the date you started, how long you`ll be on treatment, whether you are tx (treatment) naive or tx experienced, etc.   Our signature lines appear underneath all our posts, you`ll see the kind of things we write. 

Here`s a link which will help you with that, from a very helpful forum member called Mike (wmlj1960).  He has also included a link to the abbreviations we use on the forum as well...

http://hepcfriends.activeboard.com/t58862021/forum-abbreviations-link-and-help-with-creating-your-signatu/

Do feel free to ask any questions!

Very best of luck, keep in touch!   smile

 

 



__________________

Jill 

(71 yo, lives in UK)

Was Gen 3a, 

24wks Peg Ifn/Riba, Sep 2010 - Mch 2011

UND @ Wk.4, UND @ EOT, 

SVR Nov 2011 --> Still UND @ EOT + 4 yrs.

 

 
Tig


Admin

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Posts: 9270
Date:
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Hi Mamie,

Welcome to the forum and a great group of caring people. After three weeks you've gotten treatment well underway and I hope it's going smoothly for you. Let us know. I want to direct you to our thread specifically established for our Harvoni warriors. We call it the Harvoni Train (All aboard!)

There will be several people that will welcome you to the forum. I invite you to join in the discussions and ask any questions you might have. Get ready for a new Hep free life!! Good luck...

http://hepcfriends.activeboard.com/t58762824/all-aboard-for-the-harvoni-treatment-train-enjoy-the-ride-fo/



__________________

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!

Hep C FAQ   Lab Ref. Ranges  HCV Resistance

Signature Line Set Up/Abbreviations   Payment Assistance

 
MzmiffY


Veteran Member

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Posts: 81
Date:
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Hey there Indy,

Delighted you are on your way to becoming virus free.

Feel free to let us know how your journey is going so far!

Be kind to yourself,

x



__________________

42yrs/ f3-f4, gen 1a, 48 wks of Interferon,Ribaviran and Boceprevir. 

VL pre tx-384303, VL @ 4 wks 11095, 8wks- UND.

UND@ EOT, SVR 24!

 
Indygirl


Newbie

Status: Offline
Posts: 1
Date:
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Hello everyone, I've visited this site everyday since starting Harvoni treatment 3wks ago today. It's great to know that I'm not alone in this battle. The info here is great. Tks all.

__________________

I was diagnosised with chronic Hep c in 1997. I started an 8wk Harvoni treatment on May 29th, side effects have been minimal but kinda crazy, anxiety, nausea,  headaches and very tired on & off thru out the day.  1st blood test 6/29/15
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