Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 Read closely , viral kinetics and study Mike ,that study is ok but ya have to read that stuff really close and pick it appart ,we used to do these studies at work with animals and its hard for someone who hasent been around this game to seperate the wording and get to the real meat ,its seems valid for how the study was done .But it was not a real world study there are alot of other variables they forgot about . They say low base line viral ct ,what was their low baseline 1 million per cc/ml 500,000 per ,hi platelet count give me a number alot of those studies are so vague. In general the study is probably valid for that criteria and group but in the real world this virus and many viruses are constently re schuffling the genetic deck ,i had 1b but also many many varients of 1b some strong ,some week thats why i started with 750,000 copies per cc/ml and 4 months later had 69,000 copies per cc/ml this 69 ,000 was of a slightley differnt make up or gena type still 1b but a sub type of 1b . Thats one of natures tricks genetic diversity, and viruses like this have extreme divirsity that 69, 000 was beginning to learn how to out smart the inf and or riba either by random luck [re suffeling genitics randomly , genetic divirsity] or by good ol learning, thease things learn how to out smart the meds ,you know if something is trying to get the combination to this virus it knows and will take counter mesures by re schuffeling its genetics at the attack point where the meds hit the virus. Viruses like this go through so many generations it expressed as an exponent its like time T = g generations and over weeks months years it was always expressed as an exponet . This is 1 reason why you gotta get this the 1st time before it gets a good tast of the meds and starts its counter mesures or by random luck genitic diversity once it finds that combo the meds are locked out. Some people are unlucky and just by chance they have some subtypes that allready have a lock out on meds .Thats why you see some people get an inital drop but on their next pcr the virus is on its way up ,the meds killed the ones that hadent changed but the ones thad had changed locked out the meds .Genetic divirsity, lock out, and the virus can go about its mary way and mutiply back up .And then you have the multi tx ers from my observations after 2nd falure this virus gets its thing togther and locks out meds even if its only a fraction of a fraction of the virus that has mutated its gonna be right back in the game. If your resistant to inf 1a your resistant to inf 1b alot of docs havent figured this out yet and torture their patents with another worthless tx .One reason infergen works is its a synthetic inf with a differnt structure and the virus has never seen this so in most cases it works, of course this gives many one more shot but as usually the meds have to be prescribed correctly and for the right length of time but too many docs have little understanding of this ,Michele had svr snached right from her hands ,thats why i say as long as you have insurance have that pcr done after tx stops 2nd week 1st month ect. That way if you convert to pos you can get back on tx right away with out much ground lost, hell whats another4 , 6 months after a year. 72 weeks is almost a guarentee 1 shot then you know if it does not work no meds of this generation are gonna work. Course if ida converted pos at end of 18 months my plan was to do 4 month of hi dose infergen like i said when i saw my 4 month pcr i had straped in for 2 yrs . I knew that 69,000 could have meant a major problem thats when i droped my ph to 4.5 and they took their good ol time leaving 4 months but they left with 1 month to spare i was just about ready to pull the infergen but at month 6 i hit 11,000 and month 8 neg so i stayed the course with the pegintron even after the converson to neg .Me and doc kicked around the infergen thing but we agried if its working lets leave well enough alone ,doc said it will be your luck you have spun off a random sub type immune to infergen and you will shoot back up to a million ,and i shook my head and said that would be my luck ,leave well enough alone. I always thought all that weight loss and staying on the 180 lb dose factored in some where. Maybe for your last month or two see if doc will give you ,as you put it an off the richter scale dose of riba if your blood can take it .I told you i did some dose reductions with the riba sometimes for a week or two ,it was not getting my blood it was kicking my ass but i alaways did my full shot of peg and took my extra 20 mics and injected at end of week . All in all it was a lovely vaccation , it really wasent that bad you kinda get used to it ,i did have a few days where i thought i was gonna drop dead but then i thought i couldnt be that luckey ,it was that riba kicking my ass and i had to cut back for a spell but allways went back up after a week or two .I dont even remember the 18 months now its like it never happined. Like i said it was never that bad and i even worked many days . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 Read closely , viral kinetics and study Mike ,that study is ok but ya have to read that stuff really close and pick it appart ,we used to do these studies at work with animals and its hard for someone who hasent been around this game to seperate the wording and get to the real meat ,its seems valid for how the study was done .But it was not a real world study there are alot of other variables they forgot about . They say low base line viral ct ,what was their low baseline 1 million per cc/ml 500,000 per ,hi platelet count give me a number alot of those studies are so vague. In general the study is probably valid for that criteria and group but in the real world this virus and many viruses are constently re schuffling the genetic deck ,i had 1b but also many many varients of 1b some strong ,some week thats why i started with 750,000 copies per cc/ml and 4 months later had 69,000 copies per cc/ml this 69 ,000 was of a slightley differnt make up or gena type still 1b but a sub type of 1b . Thats one of natures tricks genetic diversity, and viruses like this have extreme divirsity that 69, 000 was beginning to learn how to out smart the inf and or riba either by random luck [re suffeling genitics randomly , genetic divirsity] or by good ol learning, thease things learn how to out smart the meds ,you know if something is trying to get the combination to this virus it knows and will take counter mesures by re schuffeling its genetics at the attack point where the meds hit the virus. Viruses like this go through so many generations it expressed as an exponent its like time T = g generations and over weeks months years it was always expressed as an exponet . This is 1 reason why you gotta get this the 1st time before it gets a good tast of the meds and starts its counter mesures or by random luck genitic diversity once it finds that combo the meds are locked out. Some people are unlucky and just by chance they have some subtypes that allready have a lock out on meds .Thats why you see some people get an inital drop but on their next pcr the virus is on its way up ,the meds killed the ones that hadent changed but the ones thad had changed locked out the meds .Genetic divirsity, lock out, and the virus can go about its mary way and mutiply back up .And then you have the multi tx ers from my observations after 2nd falure this virus gets its thing togther and locks out meds even if its only a fraction of a fraction of the virus that has mutated its gonna be right back in the game. If your resistant to inf 1a your resistant to inf 1b alot of docs havent figured this out yet and torture their patents with another worthless tx .One reason infergen works is its a synthetic inf with a differnt structure and the virus has never seen this so in most cases it works, of course this gives many one more shot but as usually the meds have to be prescribed correctly and for the right length of time but too many docs have little understanding of this ,Michele had svr snached right from her hands ,thats why i say as long as you have insurance have that pcr done after tx stops 2nd week 1st month ect. That way if you convert to pos you can get back on tx right away with out much ground lost, hell whats another4 , 6 months after a year. 72 weeks is almost a guarentee 1 shot then you know if it does not work no meds of this generation are gonna work. Course if ida converted pos at end of 18 months my plan was to do 4 month of hi dose infergen like i said when i saw my 4 month pcr i had straped in for 2 yrs . I knew that 69,000 could have meant a major problem thats when i droped my ph to 4.5 and they took their good ol time leaving 4 months but they left with 1 month to spare i was just about ready to pull the infergen but at month 6 i hit 11,000 and month 8 neg so i stayed the course with the pegintron even after the converson to neg .Me and doc kicked around the infergen thing but we agried if its working lets leave well enough alone ,doc said it will be your luck you have spun off a random sub type immune to infergen and you will shoot back up to a million ,and i shook my head and said that would be my luck ,leave well enough alone. I always thought all that weight loss and staying on the 180 lb dose factored in some where. Maybe for your last month or two see if doc will give you ,as you put it an off the richter scale dose of riba if your blood can take it .I told you i did some dose reductions with the riba sometimes for a week or two ,it was not getting my blood it was kicking my ass but i alaways did my full shot of peg and took my extra 20 mics and injected at end of week . All in all it was a lovely vaccation , it really wasent that bad you kinda get used to it ,i did have a few days where i thought i was gonna drop dead but then i thought i couldnt be that luckey ,it was that riba kicking my ass and i had to cut back for a spell but allways went back up after a week or two .I dont even remember the 18 months now its like it never happined. Like i said it was never that bad and i even worked many days . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 Read closely , viral kinetics and study Mike ,that study is ok but ya have to read that stuff really close and pick it appart ,we used to do these studies at work with animals and its hard for someone who hasent been around this game to seperate the wording and get to the real meat ,its seems valid for how the study was done .But it was not a real world study there are alot of other variables they forgot about . They say low base line viral ct ,what was their low baseline 1 million per cc/ml 500,000 per ,hi platelet count give me a number alot of those studies are so vague. In general the study is probably valid for that criteria and group but in the real world this virus and many viruses are constently re schuffling the genetic deck ,i had 1b but also many many varients of 1b some strong ,some week thats why i started with 750,000 copies per cc/ml and 4 months later had 69,000 copies per cc/ml this 69 ,000 was of a slightley differnt make up or gena type still 1b but a sub type of 1b . Thats one of natures tricks genetic diversity, and viruses like this have extreme divirsity that 69, 000 was beginning to learn how to out smart the inf and or riba either by random luck [re suffeling genitics randomly , genetic divirsity] or by good ol learning, thease things learn how to out smart the meds ,you know if something is trying to get the combination to this virus it knows and will take counter mesures by re schuffeling its genetics at the attack point where the meds hit the virus. Viruses like this go through so many generations it expressed as an exponent its like time T = g generations and over weeks months years it was always expressed as an exponet . This is 1 reason why you gotta get this the 1st time before it gets a good tast of the meds and starts its counter mesures or by random luck genitic diversity once it finds that combo the meds are locked out. Some people are unlucky and just by chance they have some subtypes that allready have a lock out on meds .Thats why you see some people get an inital drop but on their next pcr the virus is on its way up ,the meds killed the ones that hadent changed but the ones thad had changed locked out the meds .Genetic divirsity, lock out, and the virus can go about its mary way and mutiply back up .And then you have the multi tx ers from my observations after 2nd falure this virus gets its thing togther and locks out meds even if its only a fraction of a fraction of the virus that has mutated its gonna be right back in the game. If your resistant to inf 1a your resistant to inf 1b alot of docs havent figured this out yet and torture their patents with another worthless tx .One reason infergen works is its a synthetic inf with a differnt structure and the virus has never seen this so in most cases it works, of course this gives many one more shot but as usually the meds have to be prescribed correctly and for the right length of time but too many docs have little understanding of this ,Michele had svr snached right from her hands ,thats why i say as long as you have insurance have that pcr done after tx stops 2nd week 1st month ect. That way if you convert to pos you can get back on tx right away with out much ground lost, hell whats another4 , 6 months after a year. 72 weeks is almost a guarentee 1 shot then you know if it does not work no meds of this generation are gonna work. Course if ida converted pos at end of 18 months my plan was to do 4 month of hi dose infergen like i said when i saw my 4 month pcr i had straped in for 2 yrs . I knew that 69,000 could have meant a major problem thats when i droped my ph to 4.5 and they took their good ol time leaving 4 months but they left with 1 month to spare i was just about ready to pull the infergen but at month 6 i hit 11,000 and month 8 neg so i stayed the course with the pegintron even after the converson to neg .Me and doc kicked around the infergen thing but we agried if its working lets leave well enough alone ,doc said it will be your luck you have spun off a random sub type immune to infergen and you will shoot back up to a million ,and i shook my head and said that would be my luck ,leave well enough alone. I always thought all that weight loss and staying on the 180 lb dose factored in some where. Maybe for your last month or two see if doc will give you ,as you put it an off the richter scale dose of riba if your blood can take it .I told you i did some dose reductions with the riba sometimes for a week or two ,it was not getting my blood it was kicking my ass but i alaways did my full shot of peg and took my extra 20 mics and injected at end of week . All in all it was a lovely vaccation , it really wasent that bad you kinda get used to it ,i did have a few days where i thought i was gonna drop dead but then i thought i couldnt be that luckey ,it was that riba kicking my ass and i had to cut back for a spell but allways went back up after a week or two .I dont even remember the 18 months now its like it never happined. Like i said it was never that bad and i even worked many days . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2006 Report Share Posted January 8, 2006 Read closely , viral kinetics and study Mike ,that study is ok but ya have to read that stuff really close and pick it appart ,we used to do these studies at work with animals and its hard for someone who hasent been around this game to seperate the wording and get to the real meat ,its seems valid for how the study was done .But it was not a real world study there are alot of other variables they forgot about . They say low base line viral ct ,what was their low baseline 1 million per cc/ml 500,000 per ,hi platelet count give me a number alot of those studies are so vague. In general the study is probably valid for that criteria and group but in the real world this virus and many viruses are constently re schuffling the genetic deck ,i had 1b but also many many varients of 1b some strong ,some week thats why i started with 750,000 copies per cc/ml and 4 months later had 69,000 copies per cc/ml this 69 ,000 was of a slightley differnt make up or gena type still 1b but a sub type of 1b . Thats one of natures tricks genetic diversity, and viruses like this have extreme divirsity that 69, 000 was beginning to learn how to out smart the inf and or riba either by random luck [re suffeling genitics randomly , genetic divirsity] or by good ol learning, thease things learn how to out smart the meds ,you know if something is trying to get the combination to this virus it knows and will take counter mesures by re schuffeling its genetics at the attack point where the meds hit the virus. Viruses like this go through so many generations it expressed as an exponent its like time T = g generations and over weeks months years it was always expressed as an exponet .. This is 1 reason why you gotta get this the 1st time before it gets a good tast of the meds and starts its counter mesures or by random luck genitic diversity once it finds that combo the meds are locked out. Some people are unlucky and just by chance they have some subtypes that allready have a lock out on meds .Thats why you see some people get an inital drop but on their next pcr the virus is on its way up ,the meds killed the ones that hadent changed but the ones thad had changed locked out the meds .Genetic divirsity, lock out, and the virus can go about its mary way and mutiply back up .And then you have the multi tx ers from my observations after 2nd falure this virus gets its thing togther and locks out meds even if its only a fraction of a fraction of the virus that has mutated its gonna be right back in the game. If your resistant to inf 1a your resistant to inf 1b alot of docs havent figured this out yet and torture their patents with another worthless tx ..One reason infergen works is its a synthetic inf with a differnt structure and the virus has never seen this so in most cases it works, of course this gives many one more shot but as usually the meds have to be prescribed correctly and for the right length of time but too many docs have little understanding of this ,Michele had svr snached right from her hands ,thats why i say as long as you have insurance have that pcr done after tx stops 2nd week 1st month ect. That way if you convert to pos you can get back on tx right away with out much ground lost, hell whats another4 , 6 months after a year. 72 weeks is almost a guarentee 1 shot then you know if it does not work no meds of this generation are gonna work. Course if ida converted pos at end of 18 months my plan was to do 4 month of hi dose infergen like i said when i saw my 4 month pcr i had straped in for 2 yrs . I knew that 69,000 could have meant a major problem thats when i droped my ph to 4.5 and they took their good ol time leaving 4 months but they left with 1 month to spare i was just about ready to pull the infergen but at month 6 i hit 11,000 and month 8 neg so i stayed the course with the pegintron even after the converson to neg .Me and doc kicked around the infergen thing but we agried if its working lets leave well enough alone ,doc said it will be your luck you have spun off a random sub type immune to infergen and you will shoot back up to a million ,and i shook my head and said that would be my luck ,leave well enough alone. I always thought all that weight loss and staying on the 180 lb dose factored in some where. Maybe for your last month or two see if doc will give you ,as you put it an off the richter scale dose of riba if your blood can take it .I told you i did some dose reductions with the riba sometimes for a week or two ,it was not getting my blood it was kicking my ass but i alaways did my full shot of peg and took my extra 20 mics and injected at end of week . All in all it was a lovely vaccation , it really wasent that bad you kinda get used to it ,i did have a few days where i thought i was gonna drop dead but then i thought i couldnt be that luckey ,it was that riba kicking my ass and i had to cut back for a spell but allways went back up after a week or two .I dont even remember the 18 months now its like it never happined. Like i said it was never that bad and i even worked many days . Quote Link to comment Share on other sites More sharing options...
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