La-u-rie, I must inform you that we do not tolerate anyone using inappropriate language to any of our members, even in a private message. It is totally unacceptable behaviour. It is also against forum rules to open more than 1 membership account with this forum.
I`m ending your membership with us. ~ Jill
Cinnamon Girl said
Feb 26, 2013
Hi there Laurie, welcome. It`s good to hear that things are improving for you, although I would be cautious in recommending the advice given by someone like Lloyd Wright, who no doubt makes a lot of money from selling his publications to people with Hep C.
Best of luck with getting on the trial! Jill
J2theB said
Feb 26, 2013
Glad your liver is improving. Ya think it may have just been cutting out the drinking? What ever it was its good!
la-u-rie said
Feb 26, 2013
Hi just joined went in and had a fibro scan about 2 yrs ago it was 27.5kpa so chirrosis after alt ast all through the roof i have had hepc probably 33 yrs blood transfusion,started using lloyd wrights stuff which i honestly believe turned my chirrosis around,which is nearlly unheard of,but its true,went back for another scan 8mths later no alcholol during all of this. Fibroscan came back at 17.6 still into chrrosis another year later 8.5 which is fibrosis 2 or boardering on 3 .The liver speciallist did this twice so all good news just thought i would write this for people with compensated chirrosis it is possible to turn it around.I would love to here from luv2ride ,who is on the sapphire trial i have been screened and waiting for results,so il say hello to every one and its nice to be on here.regards laurie (brisbane austarlia)
Groo said
Feb 25, 2013
Was diagnosed Hep-C 2-b positive in 2005. Did the pegasis for 43 weeks as I was a slow responder, beat is and will be going on 8 years clear as soon as I get the next blood test. Just wanted to try and boost the morale of others who are newly diagnosed and let them know its not the end of the world, and as long as they are willing to fight they will win. Hey all.
La-u-rie, I must inform you that we do not tolerate anyone using inappropriate language to any of our members, even in a private message. It is totally unacceptable behaviour. It is also against forum rules to open more than 1 membership account with this forum.
I`m ending your membership with us. ~ Jill
Hi there Laurie, welcome. It`s good to hear that things are improving for you, although I would be cautious in recommending the advice given by someone like Lloyd Wright, who no doubt makes a lot of money from selling his publications to people with Hep C.
Best of luck with getting on the trial!
Jill
Glad your liver is improving. Ya think it may have just been cutting out the drinking? What ever it was its good!
another year later 8.5 which is fibrosis 2 or boardering on 3 .The liver speciallist did this twice so all good news just thought i would write this for people with compensated chirrosis it is possible to turn it around.I would love to here from luv2ride ,who is on the sapphire trial i have been screened and waiting for results,so il say hello to every one and its nice to be on here.regards laurie (brisbane austarlia)
Was diagnosed Hep-C 2-b positive in 2005. Did the pegasis for 43 weeks as I was a slow responder, beat is and will be going on 8 years clear as soon as I get the next blood test. Just wanted to try and boost the morale of others who are newly diagnosed and let them know its not the end of the world, and as long as they are willing to fight they will win. Hey all.