I am scheduled to start interferon/ribavirin (Pegasys) treatment for
hepatitis C today. In January (3 months ago) I tested positive for
Hep-C antibodies at a blood donor clinic and promptly followed up with
PCR testing at a local Liver and Hepatitis Clinic. Obviously, the PCR
test confirmed I have Hep-C.
My labs included the following information:
Hemoglobin: 14.4 g/dL
Hematocrit: 43 %
Platelet Count: 209 THOU/uL
HCV RNA Genotype Result: 3
Albumen 4 g/dL
Bilirubin (Total) 0.5 mg/dL
AST: 30 U/L
ALT: 48 U/L
Hepatitis C Quantity Result: 57,667 IU/mL
As the practitioner who discussed my lab results with me said, as far
as the Hep-C lottery goes, I'm looking pretty good. All the blood
values--including liver enzyme and bilirubin levels--are within normal
limits; my viral load is very low; and I have genotype 3.
I want to thank all of you who post here in alt.support.hepatitis-c for
the information that I've found here as I have prepared for treatment.
I will post more later and look forward to your correspondence.
-- BG in Seattle
Steve - 28 Mar 2006 17:50 GMT
You are lookin' good.
Good luck and don't the tx get to you. You're chances are to good not
to go through the full treatment.
Steve
mags - 28 Mar 2006 18:22 GMT
Welcome Burke. Interesting how many lurkers are out there. Glad to
see you join in. Yup I would say this is dam good looking - and the
big bonus is only 6 months of treatment. Who ever thought you guys
wanted to be known as good looking labs lol.
Mags
okay other lurkers start typing
Paul - 28 Mar 2006 19:51 GMT
On 28 Mar 2006 08:23:27 -0800, "Burke Gilman"
<burkegilman@moxmail.net>, in message ID
<1143563007.397265.6720@i40g2000cwc.googlegroups.com>, in the
newsgroup alt.support.hepatitis-c wrote:
>I am scheduled to start interferon/ribavirin (Pegasys) treatment for
>hepatitis C today. In January (3 months ago) I tested positive for
[quoted text clipped - 27 lines]
>
>-- BG in Seattle
Well I don't understand *all* of the numbers but the ones I do
understand look OK - especially the genotype. It's great fortune only
having to do it for 24 weeks rather than 48. I had a favourable
genotype as well (2b) and by the time thew tx starting getting really
messy, I only had a few weeks left to do.
Russ - 29 Mar 2006 06:04 GMT
Good luck on the tx Burke and welcome to the group. I hope you do ok on the
treatment.

Signature
Russ
Visit Alaska @ http://www.tannersacre.com
> I am scheduled to start interferon/ribavirin (Pegasys) treatment for
> hepatitis C today. In January (3 months ago) I tested positive for
[quoted text clipped - 27 lines]
>
> -- BG in Seattle
flifla - 29 Mar 2006 06:34 GMT
Wow! Blood looks good, lucky you! I am new here too so I feel weird
"welcoming" you...lol,,,
anyways this is a fabulous place. In fact, the only place for hepC.
ghibelno - 29 Mar 2006 08:40 GMT
Burke Gilman ha scritto:
> I am scheduled to start interferon/ribavirin (Pegasys) treatment for
> hepatitis C today. In January (3 months ago) I tested positive for
[quoted text clipped - 27 lines]
>
> -- BG in Seattle
Hi BG,
I do agree with you. Yes, your labs look _good_, your LFTs are low
and so is your viral load. You have a genotype 3 and this usually mean a
shorter treatment (24 weeks). So, as you can see, everything looks fine
and you should stay as positive as you seem to be now.
Treatment isn't going to be like taking a pill for a cold, there are
some side effects that affect everyone differently.
Usually almost everyone has a bad first injection night, then it goes
better and, after some weeks, some start having a bad time because of
different side effects like severe anemia, thyroid issues, weight loss
et cetera.
Anyway it is not like that for everybody. A lot of people don't develop
this severe side effects and just go through the whole of it managing
their saturday's fevers and headaches.
For almost everyone, it is quite a bad time, but definitely DOABLE.
Some pieces of advice:
. keep drinking a lot of water;
. keep eating good and genuine food;
. stay positive and have something to do other than thinking "I have HCV
and I'm on treatment", but have friends to talk about what you're going
on when you feel the need of it;
. ask your doctor opinion about a safe ("liver-friendly") vitamin
supplement (folic acid worked for me) to prevent or help preventing
development of severe anemia;
. have frequent blood test to keep an eye on your values (I haqd the
first after two weeks of treatment to monitor anemia synptoms and one
after 4 weeks to check the viral load) and keep a copy of them;
. ask anything you want and you think might help to your doctor;
And as far as support, information and sharing are concerned this is a
GREAT place, though not always perfect.
Good luck,
jeeb.
elmoemerson@webtv.net - 29 Mar 2006 14:04 GMT
Good luck, BG!! Slay the dragon!!!!!
elmo
http://community.webtv.net/elmoemerson/DocElmosHepFile
http://community.webtv.net/elmoemerson/TheFamilyAlbum
dortski - 29 Mar 2006 22:14 GMT
> I am scheduled to start interferon/ribavirin (Pegasys) treatment for
> hepatitis C today. In January (3 months ago) I tested positive for
[quoted text clipped - 27 lines]
>
> -- BG in Seattle
Hello Burke!
I just wanted to let you know 24 weeks is very doable. I breezed through
most of it. The last month....got me, I had to take time off work. I have 1
shot to go. It's good to hear you learned a lot from this group and that you
decided to join in the group. You did your homework, and you sound like you
are well prepared for this journey!
All the best to ya!
dort