Hello folks. I am new, obviously. I am 62, female, married and have 4
grown children. Got hep c in a transfusion in 1976. Thank God it
moves slowly, else I would not be here posting.
I have had one round of treatment - schering -Plough brand of drugs for
24 weeks and was clear for 4 months then relapsed. I have now just
about got financing lined up for a 48 week round with Roche. My doc
says this drug is less hard on the body and has a better success rate.
Any others had it? What results?
Sharon
Solo - 16 Mar 2005 13:10 GMT
It is basically the same drug, but have heard it has less side effects,
don't really know that it is more affective though. I did the Shering brand
3 years ago for the big 48 weeks and am still clear of the virus. I think it
to be weird that you responded and relapsed while still taking tx.
Good luck.
> Hello folks. I am new, obviously. I am 62, female, married and have 4
> grown children. Got hep c in a transfusion in 1976. Thank God it
[quoted text clipped - 6 lines]
>
> Sharon
Russ - 16 Mar 2005 15:12 GMT
I think she meant she relapsed after finishing. Though I can't prove it from
lack of testing, I could "feel" the relapse about 3 1/2 months after
finishing treatment. It was very obvious to me it was back.
Welcome and the best of luck on your round two of treatment.
As for sides? I did the 48 weeks of Pegaysys/Riba. The first couple of
months weren't too bad, but I came down with interferon induced thyroiditis
around month 4 and that was very troublesome for me. I hope you don't have
that problem!
Good luck!!

Signature
Russ
Visit Alaska @ http://www.tannersacre.com
> It is basically the same drug, but have heard it has less side effects,
> don't really know that it is more affective though. I did the Shering brand
[quoted text clipped - 13 lines]
> >
> > Sharon
elmoemerson@webtv.net - 16 Mar 2005 15:20 GMT
newbie
Group: alt.support.hepatitis-c Date: Wed, Mar 16, 2005, 3:12am (CST-2)
From: csharonxoxo@msn.com (sharon)
Hello folks. I am new, obviously. I am 62, female, married and have 4
grown children. Got hep c in a transfusion in 1976. Thank God it moves
slowly, else I would not be here posting. I have had one round of
treatment - schering -Plough brand of drugs for 24 weeks and was clear
for 4 months then relapsed. I have now just about got financing lined up
for a 48 week round with Roche. My doc says this drug is less hard on
the body and has a better success rate. Any others had it? What results?
Sharon
///////////
Hi Sharon, and welcome to the group. Yes, I've used Pegasys/Copegus as
well as Schering's Peg and Schering's 3Xweek interferon, both with
ribavirin. Neither of Schering's products got me the desired SVR
(sustained viral response), although the virus went undetectable after
16 weeks of their PEG, only to relapse after the 11 month course of tx
ended. My third attempt involved daily Infergen in the beginning, two
weeks overlap of the daily shots of Infergen with weekly Pegasys, then
just Pegasys til I finsished 11 months total. I took 1400mg/day of
ribavirin for the first 6 months, then reduced to 1200mg for the last 5
months. I was also taking Amantadine. The virus went undetectable in
the 9th week and has not resurfaced. My lack of viral load was verified
6 months post tx.
The info I've seen about Pegasys indicates it's only slightly more
effective than Scherring's. I attribute my success in getting an SVR to
daily Infergen, especially when it was combined with Pegasys over a
couple of week period as well as a heavy dose of ribavirin.
Looking back on the 4 different tx regimens I've experienced and their
side effects, daily Infergen was the toughest followed by the
rollercoaster ride of 3Xweek shots of Schering's non-peglyated
interferon. Of the two peglyated interferons, Roche's was easier, for
me. Of course, after doing daily Infergen, a ball bat would have seemed
easier. LOL.
You gave us just enough info about your situation that if brings up more
questions. What is your genotype? At which week in your tx did the
virus go undetectable? Why only 24 weeks of tx? What shape is your
liver in?
Best of luck to you this time. Slay the dragon!!!!
Elmo
http://community.webtv.net/elmoemerson/DocElmosHepFile
http://community.webtv.net/elmoemerson/TheFamilyAlbum
sharon - 19 Mar 2005 12:15 GMT
I guess I did not say much. Now I have been recuperating from a puter
crash. AAARRRGGGHHH
I think it's all up and working now.
I am genotype 2a, stage 1 fibrosis, and I think the virus fell to a low
at about 3 months and stayed that way. THen, at the end of tx, it was
undetectable. Then at 4 months later, it was back with 14,000. The dr
I was seeing at the time thought that because of my age, 24 wks was
enough torture. I was 60 then and it was rough, still have scars from
the rash, but I would rather suffer this now than liver cancer later.
I feel I'm never too old to try. My mind is stuck at 40 anyway, so
that's how old I am. lol
I understand that the treatment at least rested my liver a bit and I am
not too damaged anyway. I should get drugs to start within the next
week, I hope.
I am happy to have found a cheerful group and can't imagine why I
suddenly began to get the posts when I joined weeks ago!! Guess I had
no need then and do now??
Sharon Thanks for all the welcomes.
JV - 19 Mar 2005 18:28 GMT
Hi Sharon its a real nice group in here.
I did 44 weeks of peg-intron/riba cleared all virus by 5 shot. 1a geno
type. I was stage 3 fibrosis.
Its amazing how some of the folks in here had to do 3 tx attacks of
different interferon and cocktails. and won. Its a very educational
place in here lots of pros.
You have come to the right dragon slaying org. hehe
Welcome Juanita
pajaritaflora - 19 Mar 2005 18:42 GMT
> I guess I did not say much. Now I have been recuperating from a puter
> crash. AAARRRGGGHHH
[quoted text clipped - 9 lines]
> I understand that the treatment at least rested my liver a bit and I am
> not too damaged anyway.
Hey Sharon, I take on that belief myself also. I,m committed to doing
it for the liver rest , and possibility of less cancer risk.
Good luck with this round. Glad your machine is up and running and you
are here.
Mary Ann
I should get drugs to start within the next
> week, I hope.
> I am happy to have found a cheerful group and can't imagine why I
> suddenly began to get the posts when I joined weeks ago!! Guess I had
> no need then and do now??
> Sharon Thanks for all the welcomes.
Mark Emerson - 16 Mar 2005 16:52 GMT
Hello Sharon-
Welcome to the group. I am currently on Schering's meds and so far so good.
I cleared at week 12 and I have done 35/48 weeks so far.
There are many here to help with your questions. Some are currently on tx,
some have went through tx several times to finally win, some have relapsed
like yourself and are waiting to make the next move, and still others that
are on transplant lists or even worse. So there's a vast pool of knowledge
and wisdom here to draw from. Also a few jokes to lighten up things from
time to time :-)
Life is good
Mark
> Hello folks. I am new, obviously. I am 62, female, married and have 4
> grown children. Got hep c in a transfusion in 1976. Thank God it
[quoted text clipped - 6 lines]
>
> Sharon
pajaritaflora - 16 Mar 2005 17:46 GMT
> Hello folks. I am new, obviously. I am 62, female, married and have 4
> grown children. Got hep c in a transfusion in 1976. Thank God it
[quoted text clipped - 6 lines]
>
> Sharon
Hi Sharon,
Welcome to the group. I'm doing the Pegasys, sorry I don't know info
about the Schering- Plough treatment. But I do wnat to welcome you and
am sure you will get helpful information here.
Mary Ann
Kozure Ookami - 16 Mar 2005 23:52 GMT
>Hello folks. I am new, obviously. I am 62, female, married and have 4
>grown children. Got hep c in a transfusion in 1976. Thank God it
[quoted text clipped - 6 lines]
>
>Sharon
I did the roche and am awaiting my results to see if it was
successful. I found the sides to be mostly mild. Good luck with
round 2. How is your liver? Not too bad? I've heard these two
interferons are pretty much comparable with results and sides.