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Medical Forum / Diseases and Disorders / Hepatitis / March 2007

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anemia and Hep c

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golfgirl - 24 Feb 2007 03:14 GMT
I just finished my last needle last week.  I have genotype 2B and have
developed anemia late into my treatment.  I have been put on Eprex and
I take it 3 times a week.  I was non detectable after 4 weeks of
treatment and my liver enzymes have been normal to the end of my
treatment.  Through your experiences here are my questions

#1  How long should I expect to have anemia problems after treatment.
I have never had the problem before.  Is this something that will just
adjust itself or should I continue to take the medication?????

#2 For all of you who have finished treatment, what are the chances of
this coming back based on my genotype and my age, (43 Year old Male)
and I am in excellent physical condition.
greyhackles - 24 Feb 2007 03:34 GMT
>I just finished my last needle last week.  I have genotype 2B and have
>developed anemia late into my treatment.  I have been put on Eprex and
[quoted text clipped - 9 lines]
>this coming back based on my genotype and my age, (43 Year old Male)
>and I am in excellent physical condition.

I was deeply anemic by the middle of the second month on therapy. Eventually I
was put on the max recommended weekly dosage of Epogen for the last 35 of my
48 weeks on therapy (g1b). My last Epogen shot was one week after my last
handful of Ribavirin, which was one week after my last shot of Peg-IFN. So,
figure within two or three weeks you won't need the Eprex any more. The
recovery is that profound. You'll feel like a million bucks in short order.

The odds of relapse for a g2 super-responder who was fully compliant through
the 24 week plan are virtually wired in your favor. It almost doesn't happen.

Cheers

/greyhackles
greyhackles - 24 Feb 2007 03:43 GMT
>>I just finished my last needle last week.  I have genotype 2B and have
>>developed anemia late into my treatment.  I have been put on Eprex and
[quoted text clipped - 23 lines]
>
>/greyhackles

btw: As a 48 year old male, should we be interested, alarmed, or aloof about
your pen name? ;-)

/greyhackles (not that there's anything wrong with...um....never mind)
golfgirl - 24 Feb 2007 03:47 GMT
> >>I just finished my last needle last week.  I have genotype 2B and have
> >>developed anemia late into my treatment.  I have been put on Eprex and
[quoted text clipped - 28 lines]
>
> /greyhackles (not that there's anything wrong with...um....never mind)- Hide quoted text -

> - Show quoted text -

LOL!!!  You have a good eye!!!  Do Not be alarmed, a girl friend of
mine has posted these questions for me!!!!  And it is her choice of
name.  She is much more savy on the computer than me!!!!!
Jeff - 26 Feb 2007 02:55 GMT
I'm glad you cleared that up, I was beginning to wonder myself. Also glad
you asked those questions as I have yet to begin tx and every piece of
information helps at this point.

tx
Jeff

>> On Fri, 23 Feb 2007 22:34:47 -0500, greyhackles
>> <greyhack...@NOSPAMyahoo.com>
[quoted text clipped - 47 lines]
> mine has posted these questions for me!!!!  And it is her choice of
> name.  She is much more savy on the computer than me!!!!!
golfgirl - 27 Feb 2007 02:11 GMT
> I'm glad you cleared that up, I was beginning to wonder myself. Also glad
> you asked those questions as I have yet to begin tx and every piece of
[quoted text clipped - 56 lines]
>
> - Show quoted text -

The information we share is all we really have.  The doctors can't
tell us that much because this is all relatively new and forever
changing!!!  All we have is each other

golfgirl
elmoemerson@webtv.net - 01 Mar 2007 14:16 GMT
Re: anemia and Hep c  

Group: alt.support.hepatitis-c Date: Mon, Feb 26, 2007, 6:11pm (CST-2)
From: yellowmustang2000@rogers.com (golfgirl)
On Feb 25, 9:55 pm, "Jeff" <j...@comcast.net> wrote:
I'm glad you cleared that up, I was beginning to wonder myself. Also
glad you asked those questions as I have yet to begin tx and every piece
of information helps at this point.
tx
Jeff
"golfgirl" <yellowmustang2...@rogers.com> wrote in message
news:1172288859.498747.206210@8g2000cwh.googlegroups.com...
On Feb 23, 10:43 pm, greyhackles <greyhack...@NOSPAMyahoo.com> wrote:
On Fri, 23 Feb 2007 22:34:47 -0500, greyhackles
<greyhack...@NOSPAMyahoo.com>
wrote:
I just finished my last needle last week. I have genotype 2B and have
developed anemia late into my treatment. I have been put on Eprex and I
take it 3 times a week. I was non detectable after 4 weeks of treatment
and my liver enzymes have been normal to the end of my treatment.
Through your experiences here are my questions
#1 How long should I expect to have anemia problems after treatment. I
have never had the problem before. Is this something that will just
adjust itself or should I continue to take the medication?????
#2 For all of you who have finished treatment, what are the chances of
this coming back based on my genotype and my age, (43 Year old Male) and
I am in excellent physical condition.
I was deeply anemic by the middle of the second month on therapy.
Eventually I
was put on the max recommended weekly dosage of Epogen for the last 35
of my
48 weeks on therapy (g1b). My last Epogen shot was one week after my
last
handful of Ribavirin, which was one week after my last shot of Peg-IFN.
So,
figure within two or three weeks you won't need the Eprex any more. The
recovery is that profound. You'll feel like a million bucks in short
order.
The odds of relapse for a g2 super-responder who was fully compliant
through
the 24 week plan are virtually wired in your favor. It almost doesn't
happen.
Cheers
/greyhackles
btw: As a 48 year old male, should we be interested, alarmed, or aloof
about
your pen name? ;-)
/greyhackles (not that there's anything wrong with...um....never mind)-
Hide quoted text -
- Show quoted text -
LOL!!! You have a good eye!!! Do Not be alarmed, a girl friend of mine
has posted these questions for me!!!! And it is her choice of name. She
is much more savy on the computer than me!!!!!- Hide quoted text -
golfgirl
/////////
FOUR!!!!!

Mind if we play through?
elmo

http://community.webtv.net/elmoemerson/DocElmosHepFile

http://community.webtv.net/elmoemerson/TheFamilyAlbum
Puckertoe - 24 Feb 2007 15:21 GMT
I was thinking the same thing about the name.

I'm also a 2x genotype as well. My first 6 month tx faied due to a screw up
on my part. My second tx has come back undetectable during the fist month
off tx.

As a 2x yourself you have a better chance than 1x genotypes.

The odds are in your favor. Good luck and keep us posted.

-Puckertoe

> On Fri, 23 Feb 2007 22:34:47 -0500, greyhackles
> <greyhackles@NOSPAMyahoo.com>
[quoted text clipped - 39 lines]
>
> /greyhackles (not that there's anything wrong with...um....never mind)
golfgirl - 27 Feb 2007 02:10 GMT
> I was thinking the same thing about the name.
>
[quoted text clipped - 53 lines]
>
> - Show quoted text -

Hi there
You said you had to do treatment again????  How did you screw up if
you don't mind me asking????

golfgirl
 
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