Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. Good luck and think positive!! Yes, you CAN hope that it will continue! start Just had my first Pegasys injection last night. So far, NO side effects, all is normal. 5 years ago, when I had Pegintron treatment, after the first injection I felt really bad, with fever, chils, pain. Why this difference? Can I hope/expect it will continue like this? Thank you Mircea Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. Good luck and think positive!! Yes, you CAN hope that it will continue! start Just had my first Pegasys injection last night. So far, NO side effects, all is normal. 5 years ago, when I had Pegintron treatment, after the first injection I felt really bad, with fever, chils, pain. Why this difference? Can I hope/expect it will continue like this? Thank you Mircea Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 > > Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. > > Good luck and think positive!! Yes, you CAN hope that it will continue! > > start > > > Just had my first Pegasys injection last night. > So far, NO side effects, all is normal. > > 5 years ago, when I had Pegintron treatment, after the first injection > I felt really bad, with fever, chils, pain. > > Why this difference? Can I hope/expect it will continue like this? > > Thank you > > Mircea > > > Hi I did the full 48 week TX about 7 years ago and never missed a day of work put was a nonresponder. hope it goes easy for you. I would not take any antidepressants unless I really need them just more drugs you don't need but Doctors push on you. When I found out I had Hep that was the first drug they said to take, so far never have and I'm on the transplant list. rich > > > [ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 > > Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. > > Good luck and think positive!! Yes, you CAN hope that it will continue! > > start > > > Just had my first Pegasys injection last night. > So far, NO side effects, all is normal. > > 5 years ago, when I had Pegintron treatment, after the first injection > I felt really bad, with fever, chils, pain. > > Why this difference? Can I hope/expect it will continue like this? > > Thank you > > Mircea > > > Hi I did the full 48 week TX about 7 years ago and never missed a day of work put was a nonresponder. hope it goes easy for you. I would not take any antidepressants unless I really need them just more drugs you don't need but Doctors push on you. When I found out I had Hep that was the first drug they said to take, so far never have and I'm on the transplant list. rich > > > [ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 > > Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. > > Good luck and think positive!! Yes, you CAN hope that it will continue! > > start > > > Just had my first Pegasys injection last night. > So far, NO side effects, all is normal. > > 5 years ago, when I had Pegintron treatment, after the first injection > I felt really bad, with fever, chils, pain. > > Why this difference? Can I hope/expect it will continue like this? > > Thank you > > Mircea > > > Hi I did the full 48 week TX about 7 years ago and never missed a day of work put was a nonresponder. hope it goes easy for you. I would not take any antidepressants unless I really need them just more drugs you don't need but Doctors push on you. When I found out I had Hep that was the first drug they said to take, so far never have and I'm on the transplant list. rich > > > [ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2007 Report Share Posted October 8, 2007 > > Mircea, you may continue to feel well. I don't know why you would have a difference and I'm not familiar with Pegintron, but I just did my 4th Pegasys shot yesterday and I've been feeling fairly well for the last month. I do have some slight aches, some nausea (more from the Ribavirin I think), some tiredness, etc., but nothing like what I had expected in my mind prior to beginning. > > Good luck and think positive!! Yes, you CAN hope that it will continue! > > start > > > Just had my first Pegasys injection last night. > So far, NO side effects, all is normal. > > 5 years ago, when I had Pegintron treatment, after the first injection > I felt really bad, with fever, chils, pain. > > Why this difference? Can I hope/expect it will continue like this? > > Thank you > > Mircea > > > Hi I did the full 48 week TX about 7 years ago and never missed a day of work put was a nonresponder. hope it goes easy for you. I would not take any antidepressants unless I really need them just more drugs you don't need but Doctors push on you. When I found out I had Hep that was the first drug they said to take, so far never have and I'm on the transplant list. rich > > > [ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 I'm glad you posted that about anti-d's just being more drugs we don't need, I'm going to talk to my fam dr about getting off them. I was on Cymbalta for months before I started tx but I'm past that low point in my life when I needed them so I think it's time to put one less chemical in my body. Thanks! Gayle PS: Good luck with the list. Do they just call you out of the blue should one become available? > Hi I did the full 48 week TX about 7 years ago and never missed a > day of work put was a nonresponder. hope it goes easy for you. I > would not take any antidepressants unless I really need them just > more drugs you don't need but Doctors push on you. When I found out I > had Hep that was the first drug they said to take, so far never have > and I'm on the transplant list. > rich > > > > > > I just did > my 4th Pegasys shot yesterday and I've been feeling fairly well for > the last month. > > > > Good luck and think positive!! Yes, you CAN hope that it will > continue! > > > > > > Just had my first Pegasys injection last night. > > So far, NO side effects, all is normal. > > > > 5 years ago, when I had Pegintron treatment, after the first > injection > > I felt really bad, with fever, chils, pain. > > > > Why this difference? Can I hope/expect it will continue like this? > > > > Thank you > > > > Mircea > > > > > > > > > > > [ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 I'm glad you posted that about anti-d's just being more drugs we don't need, I'm going to talk to my fam dr about getting off them. I was on Cymbalta for months before I started tx but I'm past that low point in my life when I needed them so I think it's time to put one less chemical in my body. Thanks! Gayle PS: Good luck with the list. Do they just call you out of the blue should one become available? > Hi I did the full 48 week TX about 7 years ago and never missed a > day of work put was a nonresponder. hope it goes easy for you. I > would not take any antidepressants unless I really need them just > more drugs you don't need but Doctors push on you. When I found out I > had Hep that was the first drug they said to take, so far never have > and I'm on the transplant list. > rich > > > > > > I just did > my 4th Pegasys shot yesterday and I've been feeling fairly well for > the last month. > > > > Good luck and think positive!! Yes, you CAN hope that it will > continue! > > > > > > Just had my first Pegasys injection last night. > > So far, NO side effects, all is normal. > > > > 5 years ago, when I had Pegintron treatment, after the first > injection > > I felt really bad, with fever, chils, pain. > > > > Why this difference? Can I hope/expect it will continue like this? > > > > Thank you > > > > Mircea > > > > > > > > > > > [ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 Rich Why did you go through the full 48 weeks if it did not work for you? Usually drs can tell at week 12 or 24 if it works or not. From what I've read, chances that a person nonresponding at week 24, is cured at week 48 are slim to none. Good luck anyway > > > > > > I just did > > my 4th Pegasys shot yesterday and I've been feeling fairly well for > > the last month. > > > > > > Good luck and think positive!! Yes, you CAN hope that it will > > continue! > > > > > > > > > Just had my first Pegasys injection last night. > > > So far, NO side effects, all is normal. > > > > > > 5 years ago, when I had Pegintron treatment, after the first > > injection > > > I felt really bad, with fever, chils, pain. > > > > > > Why this difference? Can I hope/expect it will continue like > this? > > > > > > Thank you > > > > > > Mircea > > > > > > > > > > > > > > > > > [ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 Rich Why did you go through the full 48 weeks if it did not work for you? Usually drs can tell at week 12 or 24 if it works or not. From what I've read, chances that a person nonresponding at week 24, is cured at week 48 are slim to none. Good luck anyway > > > > > > I just did > > my 4th Pegasys shot yesterday and I've been feeling fairly well for > > the last month. > > > > > > Good luck and think positive!! Yes, you CAN hope that it will > > continue! > > > > > > > > > Just had my first Pegasys injection last night. > > > So far, NO side effects, all is normal. > > > > > > 5 years ago, when I had Pegintron treatment, after the first > > injection > > > I felt really bad, with fever, chils, pain. > > > > > > Why this difference? Can I hope/expect it will continue like > this? > > > > > > Thank you > > > > > > Mircea > > > > > > > > > > > > > > > > > [ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 > > Rich > > Why did you go through the full 48 weeks if it did not work for you? > Usually drs can tell at week 12 or 24 if it works or not. > > From what I've read, chances that a person nonresponding at week 24, > is cured at week 48 are slim to none. > > Good luck anyway Thanks I went through the full 48 weeks because my Doctor did not take a starting load count, said all he cared was the final number. That and his kick back from the drug company. The first load count he took was at 24 weeks and the virus was still there then after the full TX it was the same. He told me to look at is as I put the outcome off a few years. LOL rich www.rslaserkits.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 > > Rich > > Why did you go through the full 48 weeks if it did not work for you? > Usually drs can tell at week 12 or 24 if it works or not. > > From what I've read, chances that a person nonresponding at week 24, > is cured at week 48 are slim to none. > > Good luck anyway Thanks I went through the full 48 weeks because my Doctor did not take a starting load count, said all he cared was the final number. That and his kick back from the drug company. The first load count he took was at 24 weeks and the virus was still there then after the full TX it was the same. He told me to look at is as I put the outcome off a few years. LOL rich www.rslaserkits.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2010 Report Share Posted August 27, 2010 Hi everybody, Since Marcia wrote her comments on another list, I showed interest in what she said. I do agree with mostly of what is said on this list, but I also agree that some cod fish oil doesn't hurt, I'm afraid of high dose supplements as I'm also afraid of giving valtrex and other hard stuff for ever. At the moment, sadly I'm not able to afford any treatment or foreign doctors or even a nathuropath, don't have insurance to cover drugs, but living in ontario i have doctors visits and some lab test for free. Realy I have no clue where to start to take advantage of my sons developmental time, he is 3.11 yo and 35 lb, has a pdd-nos " pre-diagnose " by a pediatrician, he is been progresing a lot since he started GFCF diet on February and some regular multivitamin and fish oil, but also by seeing the need he has of getting some form of behavioral coaching and speech terapy and things like that, which I started as soon as I noticed his obvious pdd/ocd behaviors, I have to admit that he has improved a lot with the behavioral approach I had been taking. He is not officialy diagnose yet, there is " waiting list " to get diagnose and to get profesional speech terapy and stuff., maybe he'll get it on december, but so far, I wonder where to start. Any comments would be appreciated, so I can make some decitions according to our situation. Thanks a lot to everybody. Sasha. Quote Link to comment Share on other sites More sharing options...
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