I live in Southern California and have gone through two
combination therapy trials to rid myself of type 1 hepc.
(still positive) I read the messages this morning
and was shocked to read your claim that pegalatyed interferon
does not work with type 1. I have not heard this
before and need to see solid proof of your claim. Not
a day goes by that i curse sherring-plough for the devastating
effects of the combination therapy prescribed by my gastro
dr at Kaiser. I am absolutely convinced that my
right eye was permanently damaged as a result of the drug,
and i saw both optometrists and optomologists at Kaiser
and complained loudly that my eyes were effected by the
drug. They didnt beleive interferon could effect
my eyes, but sherring supplied literature to me which
i gave to the eye dr's.
If you know of any lawyers getting involved for a class
action suit, please let me know immediately. I'm also
convinced that this program may have done other unknown
damage to me that is undetectable at this time.
My dr thinks i may have had the virus for close to 20
What are you doing about your eye situation? My
right eye feels like i have sand in it constantly and
I use drops all day long to keep them wet. During the
therapy, i had massive veins bulging in my eyes and constant
severe irritation. I never had problems prior to
my experience with peg-intron. I'm convinced it
is pure poison and i was a lab rat. Please provide
a link to the lawyers ...tia.
Thanks & best regards
Look on message board, oct. 2002 and there is a link.
Thank You for sharing your stories with others with hep
c. I do not know what to do about what interferon
did to my right eye. I have gone to some
eye doctors but I get nowhere. I just live with
it, nothing else I can do.