Guest guest Posted May 24, 2002 Report Share Posted May 24, 2002 I agree with not taking things to the extreme...we do need to enjoy our lives. But I am careful not to eat things that are particularly hard on the liver and I try aromatherapy, meditation, deep breathing, etc. before I start popping pills for things like headaches, aches, etc. I have considerable liver damage although I don't have cirhossis and I'd just as soon as not push my liver to further damage...I do enjoy life and there are so many things I still want to do...like having Willem marry me in name only so I can immigrate to Holland <g> Tatezi <who wants so badly to live in Holland where humyns are treated with respect and dignity> > I just said " the hell with it " and eat what I dam well want. > ..... " forget it all....quality of life over quantity " . -- " It is in the shelter of each other that the people live. " ~Irish proverb~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2002 Report Share Posted December 22, 2002 Hey, I'm jealous <g> Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2002 Report Share Posted December 22, 2002 Hey, I'm jealous <g> Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2002 Report Share Posted December 22, 2002 Hey, I'm waiting for the cat fight. LOL. Carol Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2002 Report Share Posted December 22, 2002 Hey, I'm waiting for the cat fight. LOL. Carol Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2002 Report Share Posted December 23, 2002 LOL...no cat fights here.... Willem, you wouldn't dare, would you????? <g> I've been collecting feathers for my cape.... Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2002 Report Share Posted December 23, 2002 Hi.Ok like to meet you 2,instead of a electronic person I become a person of flesh and blood but don.t take that literally.Tat is jealous and Carol thinks there.s going to be a cat-fight but when I look into the mirror I don.t see a Knight riding a white stallion but a Hepper in drag,it takes all kinds to make a world,but Tat wearing a costume made from chicken feathers does.nt look very attractive either.Instead of marrying her in a barn I would like to get her over here and Caroll too to get the treatment they deserve.I believe you hve friends in Holland,give them my phonenumber,020-6680020.Nog een prettige dag verder,Willem. Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2002 Report Share Posted December 23, 2002 Hi.Ok like to meet you 2,instead of a electronic person I become a person of flesh and blood but don.t take that literally.Tat is jealous and Carol thinks there.s going to be a cat-fight but when I look into the mirror I don.t see a Knight riding a white stallion but a Hepper in drag,it takes all kinds to make a world,but Tat wearing a costume made from chicken feathers does.nt look very attractive either.Instead of marrying her in a barn I would like to get her over here and Caroll too to get the treatment they deserve.I believe you hve friends in Holland,give them my phonenumber,020-6680020.Nog een prettige dag verder,Willem. Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2002 Report Share Posted December 23, 2002 Willem, When you look in the mirror behind that hepper in drag is a sensitive, caring and very special person. I don't have to see you in flesh to know that. And besides, my cape will not be chicken feathers....Crow has been donating some feathers and of course my pigeon friends have been donating to the collection. Sure I know most city people think of pigeon as a rat with wings, but I have a flock of about 30 that I feed and keep a heated birdbath for on my city back porch and they are fairly intelligent and I've found them to be nice critters. They also have lessons to teach us being the survivors that they are. Actually, I've never met a critter I didn't like. So don't you worry any about how my cape will look...it willl be a gift from the Creator and will be gorgeous! And besides....I'm an old hepper too, but it doesn't run my life! Liefs Tatezi Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2002 Report Share Posted December 23, 2002 Willem, When you look in the mirror behind that hepper in drag is a sensitive, caring and very special person. I don't have to see you in flesh to know that. And besides, my cape will not be chicken feathers....Crow has been donating some feathers and of course my pigeon friends have been donating to the collection. Sure I know most city people think of pigeon as a rat with wings, but I have a flock of about 30 that I feed and keep a heated birdbath for on my city back porch and they are fairly intelligent and I've found them to be nice critters. They also have lessons to teach us being the survivors that they are. Actually, I've never met a critter I didn't like. So don't you worry any about how my cape will look...it willl be a gift from the Creator and will be gorgeous! And besides....I'm an old hepper too, but it doesn't run my life! Liefs Tatezi Willem Hey, I'm comin to Holland! I'll be traveling there the first 2 weeks of Feb while the flight is cheap. Would love to meet you! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2002 Report Share Posted December 25, 2002 Thanks Willem! I'll let you know when I firm up the reservations and all is set! I've never been out of my country before! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2002 Report Share Posted December 25, 2002 Hi.Okido.It is snowing in Texas and we hve a green christmas,it should hve been the other way around.When yre in Holland you should also visit the ancient cities of Belgium,Brugge,Luik etc.It.s only shorts drives,unlike Texas the distances are short here and the highways are safe and sound.Forinstance Amsterdam-Antwerp is a two hour drive.The Ardennes which are beautifull in winter also within a couple of Hrs distance.It was here where General Patton won his epic battle in world war two and said his famous prayer.And don.t worry about the language EVERYBODY here speaks English which is not the same as American let alone that Texan brawl of yours.Lol.Welcome in the old country and discover your roots.Willem. Re: Willem Thanks Willem! I'll let you know when I firm up the reservations and all is set! I've never been out of my country before! Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 25, 2002 Report Share Posted December 25, 2002 No snow in my area! Some of the countryside got snow blowing in the air, but nothing sticks here. Our grass is still green and the sun is shining today and it's quite nice if chilly. I will have to buy more winter clothes for Holland! Shopping spree! Thanks Willem Alley " If you want to be a hero knight, never look directly into the mirror, lest you see that tin pot on your head instead of a glorious plumed helmet! " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2003 Report Share Posted July 1, 2003 Thanks Willem...yep, you're saved from having to see me....and Francina (my twinnie in spirit) won't have me puking at her house in Holland either ;-) I never forgot your offer to get me the meds Willem....that was so super nice of you. I sure hope in one years time I will be clear.....but even if I'm not, I'll know I gave it my best shot (no pun intended)....lol. Huggggs Carol Re: Sure is quiet... Hi Carol.That.s great news and I.am also off the hook,so to speak, since I suggested to come here and I would get you the Peg.Our Doc. really is a wonderfull person.In one year.s time you join the club of responders.Willem. ----- Original Message Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Hi.Pam,I did three treatments and two studies.1.6 months ribavarin with interferon.2.1 year ribavarine with interferon.3 1 year peg-interferon from schering plough,after one year still undetectable.They say the roche peg-interferon,pegasys,is slighter better about 3 % more change of obtaining a SVR but I don.t know if this is true but where there.s smoke there.s fire.Mabye claudine,she knows everything and Tat might comment on that.I.am not good into research sites,archives etc.They are making progress with the protease inhibitors and maby it will sooner on the market then general believed.Goodluck,Willem. Willem Willem, How many and which treatments did you go through before your virus became undetectable? (Also, what genotype are you?) My husband, Philip, has 1a genotypeand has gone through 2 treatments, regular interferon with riboviron & Schering peg interferon & riboviron. His doctor seems has said that it is not worth his going on the other peg interferon with riboviron (I can't remember the brand name right now) because if he didn't respond to the Schering it's unlikely he'll respond to the other. His viral load was temporarily reduced by both treatments but it did not become undetectable. Any feedback is welcome. Thanks, Love & blessings, Pamela Venus Love is all there is Peace is all there is Joy is all there is Om Shanti Shanti Shanti Om Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Hi.Pam,I did three treatments and two studies.1.6 months ribavarin with interferon.2.1 year ribavarine with interferon.3 1 year peg-interferon from schering plough,after one year still undetectable.They say the roche peg-interferon,pegasys,is slighter better about 3 % more change of obtaining a SVR but I don.t know if this is true but where there.s smoke there.s fire.Mabye claudine,she knows everything and Tat might comment on that.I.am not good into research sites,archives etc.They are making progress with the protease inhibitors and maby it will sooner on the market then general believed.Goodluck,Willem. Willem Willem, How many and which treatments did you go through before your virus became undetectable? (Also, what genotype are you?) My husband, Philip, has 1a genotypeand has gone through 2 treatments, regular interferon with riboviron & Schering peg interferon & riboviron. His doctor seems has said that it is not worth his going on the other peg interferon with riboviron (I can't remember the brand name right now) because if he didn't respond to the Schering it's unlikely he'll respond to the other. His viral load was temporarily reduced by both treatments but it did not become undetectable. Any feedback is welcome. Thanks, Love & blessings, Pamela Venus Love is all there is Peace is all there is Joy is all there is Om Shanti Shanti Shanti Om Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Hi.Pam,I did three treatments and two studies.1.6 months ribavarin with interferon.2.1 year ribavarine with interferon.3 1 year peg-interferon from schering plough,after one year still undetectable.They say the roche peg-interferon,pegasys,is slighter better about 3 % more change of obtaining a SVR but I don.t know if this is true but where there.s smoke there.s fire.Mabye claudine,she knows everything and Tat might comment on that.I.am not good into research sites,archives etc.They are making progress with the protease inhibitors and maby it will sooner on the market then general believed.Goodluck,Willem. Willem Willem, How many and which treatments did you go through before your virus became undetectable? (Also, what genotype are you?) My husband, Philip, has 1a genotypeand has gone through 2 treatments, regular interferon with riboviron & Schering peg interferon & riboviron. His doctor seems has said that it is not worth his going on the other peg interferon with riboviron (I can't remember the brand name right now) because if he didn't respond to the Schering it's unlikely he'll respond to the other. His viral load was temporarily reduced by both treatments but it did not become undetectable. Any feedback is welcome. Thanks, Love & blessings, Pamela Venus Love is all there is Peace is all there is Joy is all there is Om Shanti Shanti Shanti Om Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Hi.Pam,I did three treatments and two studies.1.6 months ribavarin with interferon.2.1 year ribavarine with interferon.3 1 year peg-interferon from schering plough,after one year still undetectable.They say the roche peg-interferon,pegasys,is slighter better about 3 % more change of obtaining a SVR but I don.t know if this is true but where there.s smoke there.s fire.Mabye claudine,she knows everything and Tat might comment on that.I.am not good into research sites,archives etc.They are making progress with the protease inhibitors and maby it will sooner on the market then general believed.Goodluck,Willem. Willem Willem, How many and which treatments did you go through before your virus became undetectable? (Also, what genotype are you?) My husband, Philip, has 1a genotypeand has gone through 2 treatments, regular interferon with riboviron & Schering peg interferon & riboviron. His doctor seems has said that it is not worth his going on the other peg interferon with riboviron (I can't remember the brand name right now) because if he didn't respond to the Schering it's unlikely he'll respond to the other. His viral load was temporarily reduced by both treatments but it did not become undetectable. Any feedback is welcome. Thanks, Love & blessings, Pamela Venus Love is all there is Peace is all there is Joy is all there is Om Shanti Shanti Shanti Om Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Pamela, I'm just thinking out loud here... consider also his liver biopsy. The virus is a fairly slow moving thing. It probably won't hurt to take some time and let him recoup between treatments too. I know some people hit it hard and fast and keep on hitting it with treatment until it's either gone or they've taken all they can take, esp people with cirrhosis. Some, who have very little liver damage, take a lighter approach, knowing that they have more time, that better things and hopefully easier treatments are in the future (tho there's no promise haha). Some with little damage decide never to treat, the hep not always as harmful as the treatment might be. I felt quite honored recently to be referred by my shrink to another of her patient who has hep c. She has mild to moderate liver damage, geno 1a and is on her 2nd treatment but is having a much worse time on the peg and her gastro isn't helping her with sides. We never respond the same way twice and our body isn't the same as before. So certainly waiting a bit wouldn't be a bad thing I think for your husband. I agree with Willem that Roche seems to have better stats for geno 1's, however they are still around 50% or less in the SVR, regardless of brand. If he never went undetected on either treatment, then perhaps he never will. It's just difficult to predict. I went undetectable very fast on regular treatment (I'm geno 1b) but relapsed quickly. So go figure lol. I think the B in geno 1b is for Butthead stubborn! Alley Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Pamela, I'm just thinking out loud here... consider also his liver biopsy. The virus is a fairly slow moving thing. It probably won't hurt to take some time and let him recoup between treatments too. I know some people hit it hard and fast and keep on hitting it with treatment until it's either gone or they've taken all they can take, esp people with cirrhosis. Some, who have very little liver damage, take a lighter approach, knowing that they have more time, that better things and hopefully easier treatments are in the future (tho there's no promise haha). Some with little damage decide never to treat, the hep not always as harmful as the treatment might be. I felt quite honored recently to be referred by my shrink to another of her patient who has hep c. She has mild to moderate liver damage, geno 1a and is on her 2nd treatment but is having a much worse time on the peg and her gastro isn't helping her with sides. We never respond the same way twice and our body isn't the same as before. So certainly waiting a bit wouldn't be a bad thing I think for your husband. I agree with Willem that Roche seems to have better stats for geno 1's, however they are still around 50% or less in the SVR, regardless of brand. If he never went undetected on either treatment, then perhaps he never will. It's just difficult to predict. I went undetectable very fast on regular treatment (I'm geno 1b) but relapsed quickly. So go figure lol. I think the B in geno 1b is for Butthead stubborn! Alley Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2004 Report Share Posted February 14, 2004 Good morning everyone. I have reached the point in my " thinking " (having adjusted somewhat to the diagnosis, knowing that I'm grade 3 / stage 2, knowing I've probably been carrying this virus for over 27years, feeling relatively OK at this point) that I am now considering NOT doing the treatment. I was (on diagnosis 8 months ago) extremely eager to treat and be rid of this virus (scared to death actually). I was a candidate for treatment, I was begun in October 2003, (Pegasys / Copegus by Roche), during the second week I had what docs called a " rather dramatic drop in wbcs and platelets: (not low enough for boosters though), I had to come off treatment temporarily to treat an underlying periodontal disease, I am " all fixed up " as far as my mouth is concerned (at a HIGH price), I am still considered a candidate for Hep C treatment (now that my peridontal disease is under control), but I honestly am at the point that I don't know if I want to ever try Hep C treatment again (pegylated inteferon / ribavirin by either Schering Plough OR by Roche!) LOL. I have ALWAYS (since diagnosis) heard the statement " most people with Hep C don't die FROM it -- they die WITH it " . I've also read about all the side effects from treatment. (they can be really bad for some). I've also read that women with HCV tend to do better with this chronic virus than men do. I'm female, I don't drink alcohol; I'm almost 45 yrs old; from what I've heard -- even if the treatment gets rid of the virus -- it doesn't necessarily mean I will FEEL any better, so............ LOL. What the HECK does one do. Decisions decisions. lol. I'm still undecided and can surely sympathize with any and all who have HCV and with those who are undecided about treatment. Best of luck to all. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2004 Report Share Posted February 14, 2004 Good morning everyone. I have reached the point in my " thinking " (having adjusted somewhat to the diagnosis, knowing that I'm grade 3 / stage 2, knowing I've probably been carrying this virus for over 27years, feeling relatively OK at this point) that I am now considering NOT doing the treatment. I was (on diagnosis 8 months ago) extremely eager to treat and be rid of this virus (scared to death actually). I was a candidate for treatment, I was begun in October 2003, (Pegasys / Copegus by Roche), during the second week I had what docs called a " rather dramatic drop in wbcs and platelets: (not low enough for boosters though), I had to come off treatment temporarily to treat an underlying periodontal disease, I am " all fixed up " as far as my mouth is concerned (at a HIGH price), I am still considered a candidate for Hep C treatment (now that my peridontal disease is under control), but I honestly am at the point that I don't know if I want to ever try Hep C treatment again (pegylated inteferon / ribavirin by either Schering Plough OR by Roche!) LOL. I have ALWAYS (since diagnosis) heard the statement " most people with Hep C don't die FROM it -- they die WITH it " . I've also read about all the side effects from treatment. (they can be really bad for some). I've also read that women with HCV tend to do better with this chronic virus than men do. I'm female, I don't drink alcohol; I'm almost 45 yrs old; from what I've heard -- even if the treatment gets rid of the virus -- it doesn't necessarily mean I will FEEL any better, so............ LOL. What the HECK does one do. Decisions decisions. lol. I'm still undecided and can surely sympathize with any and all who have HCV and with those who are undecided about treatment. Best of luck to all. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2004 Report Share Posted February 14, 2004 Good morning everyone. I have reached the point in my " thinking " (having adjusted somewhat to the diagnosis, knowing that I'm grade 3 / stage 2, knowing I've probably been carrying this virus for over 27years, feeling relatively OK at this point) that I am now considering NOT doing the treatment. I was (on diagnosis 8 months ago) extremely eager to treat and be rid of this virus (scared to death actually). I was a candidate for treatment, I was begun in October 2003, (Pegasys / Copegus by Roche), during the second week I had what docs called a " rather dramatic drop in wbcs and platelets: (not low enough for boosters though), I had to come off treatment temporarily to treat an underlying periodontal disease, I am " all fixed up " as far as my mouth is concerned (at a HIGH price), I am still considered a candidate for Hep C treatment (now that my peridontal disease is under control), but I honestly am at the point that I don't know if I want to ever try Hep C treatment again (pegylated inteferon / ribavirin by either Schering Plough OR by Roche!) LOL. I have ALWAYS (since diagnosis) heard the statement " most people with Hep C don't die FROM it -- they die WITH it " . I've also read about all the side effects from treatment. (they can be really bad for some). I've also read that women with HCV tend to do better with this chronic virus than men do. I'm female, I don't drink alcohol; I'm almost 45 yrs old; from what I've heard -- even if the treatment gets rid of the virus -- it doesn't necessarily mean I will FEEL any better, so............ LOL. What the HECK does one do. Decisions decisions. lol. I'm still undecided and can surely sympathize with any and all who have HCV and with those who are undecided about treatment. Best of luck to all. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2004 Report Share Posted February 14, 2004 Good morning everyone. I have reached the point in my " thinking " (having adjusted somewhat to the diagnosis, knowing that I'm grade 3 / stage 2, knowing I've probably been carrying this virus for over 27years, feeling relatively OK at this point) that I am now considering NOT doing the treatment. I was (on diagnosis 8 months ago) extremely eager to treat and be rid of this virus (scared to death actually). I was a candidate for treatment, I was begun in October 2003, (Pegasys / Copegus by Roche), during the second week I had what docs called a " rather dramatic drop in wbcs and platelets: (not low enough for boosters though), I had to come off treatment temporarily to treat an underlying periodontal disease, I am " all fixed up " as far as my mouth is concerned (at a HIGH price), I am still considered a candidate for Hep C treatment (now that my peridontal disease is under control), but I honestly am at the point that I don't know if I want to ever try Hep C treatment again (pegylated inteferon / ribavirin by either Schering Plough OR by Roche!) LOL. I have ALWAYS (since diagnosis) heard the statement " most people with Hep C don't die FROM it -- they die WITH it " . I've also read about all the side effects from treatment. (they can be really bad for some). I've also read that women with HCV tend to do better with this chronic virus than men do. I'm female, I don't drink alcohol; I'm almost 45 yrs old; from what I've heard -- even if the treatment gets rid of the virus -- it doesn't necessarily mean I will FEEL any better, so............ LOL. What the HECK does one do. Decisions decisions. lol. I'm still undecided and can surely sympathize with any and all who have HCV and with those who are undecided about treatment. Best of luck to all. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2004 Report Share Posted February 24, 2004 Hi Willem I think M. would try to auction it off to raise money for his " defense " . Let's hope he doesn't succeed. I think he's as guilty as sin....but that's just my judgement. Hugggs to you and the hail and rain in Holland Carol Re: Re: side effects--- Sally, you really had a rought time with treatment...which one did you do? Did you respond after going through all that? What genotype are you> Quote Link to comment Share on other sites More sharing options...
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