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Author Topic: New to forum  (Read 4223 times)

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Offline Vee

  • Newbie
  • Posts: 2
New to forum
« on: February 22, 2015, 02:55:28 pm »
Hello,
I am new to forum and thankful to have the option of reaching out to people who truly understand.  I was diagnosed back in 1995 and tried Interferon/Ribaviron with no results.  Just horrible side effects.  I am currently on week 12 of Harvoni and have side effects but not as horrible as previous treatment...Terrible headaches and fatigue.
Tomorrow I find out results of viral load as of now.
I wish everyone good luck and remain positive if you can.

Offline Mike

  • Global Moderator
  • Member
  • Posts: 993
Re: New to forum
« Reply #1 on: February 22, 2015, 06:05:35 pm »
Hi Vee,

Good luck tomorrow and I hope it will be joyous, happy and great news (it should be). :)

Here's to slaying the dragon!

Best wishes, Mike
Genotype 1a
Treated 2001 with PEG and RIBV
Treated in 2014 SOL+PEG+RIBV
Cured July 2014

Offline Vee

  • Newbie
  • Posts: 2
Re: New to forum
« Reply #2 on: February 23, 2015, 10:23:31 am »
Thanks so much for your kind words.  Much needed.

Offline BubbaT

  • Member
  • Posts: 267
Re: New to forum
« Reply #3 on: March 12, 2015, 11:33:41 pm »
Hi vee, what took you so long?

We were waiting on Ya, to tell you your gonna make it, in fact you have already made it!   I'm on week 2, and going for the gusto!   After fighting this thing for 20 years, I'm ready to win!   Welcome to board!

Is water helping your headaches?  And can you take aspirin?
Age 57 male
Infected late 70's
Diagnosed 95
1a, 2 prev biopsy 95, 2004
Ct 2007, 2015
Treatment Naive
F4 A3. Fibrosure/ CT 2-5-15. Ammonia 222
VL 2.2 mil.
Started Harvoni  3-3-15. 12weeks, finished 5-26-15
4 week VL undetected
12 week EOT undetected

 


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