please your latest result ?
interferon?not peginterferon?
16weeks is too little it cannot be used such a short time, the time to know if one responds is 24 weeks by 16weeks you dont even know if there is response or not, some genotypes may use 12 weeks
the only short time i know is staggered use by pisa research hospital
No, I only took 3million iu of Alfa interferon weekly for 16weeks, I will be testing the hbsag quantitative very soon.
what is hbsag level?it goes up before a possible hbvdna reactivation
if hbsag less than 400iu/ml it is possible to keep inactive carrier state or have a flare to clear hbsag
is this a therapy stop after pegintf add on to tdf?
my viral load test today is 35 iu/ ml. have not taking any medicine since January this year.
you must reach at least 24weeks then go with high dose vit d3 and tenofovir and pegintf response might be sustained after peg is finished especially because hbsag is already low
go buy generic tenofovir online then
unfortunately, that is where I will stop, $75 per injection of 3 million iu of Alfa interferon has really drain and taking away most of my assets.
osteocare is absoltely not good for you unless you have bone problems, it has no vit d
take vit d3 10.000iu pills, look for the biggest vit d3 dose per pill, this will allow better response to peg (low vit d have no response or worst response), do not look for pills like 400iu or 1000iu, that s nothing
surely continue and do not even think to stop! My hbsag stayed stable and even went up in W24 but dropped rapidly later.
weekly injection of 3 million iu of Alfa interferon for sixteen weeks, hbsag result stable at 745 iu/ ml.
thanks, I will start the inf. injection soon, but is the oesteocare good for
Ur doctor is completely ignorant to recommend Lamivudine. With this you have a big risk of resistance. Pls dont accept.
Well, shes real ignorant. To say there is no day you can get negative. a lot of members on this forum have cleared. The best regime: TNF with Inf add on. And your hbsag is less than 1000. You have the highest chance to clear. I suggest you look for another doctor.
Ur doctor is completely ignorant to recommend Lamivudine. With this you have a big risk of resistance. Pls dont accept.
Well, shes real ignorant. To say there is no day you can get negative. a lot of members on this forum have cleared. The best regime: TNF with Inf add on. And your hbsag is less than 1000. You have the highest chance to clear. I suggest you look for another doctor.
stef, I am currently taking osteocare which comprises :
vitamin d3 200 iu
calcium 800mg
magnesium 300 mg
zinc 10mg
what I want to ask is , is it good for me.
Stefan, I will b meeting the Dr. today, I am thinking of going for tenofovir and vitamin d, before I add peginf, or I should just go straight to peginf and vitamin d
joc2011, thank you very much, but may I also hear from Stef2011
look at the statements from my Dr. today.
1. she is only going to put me on lamivudine, because that is what is good for me.
2. there is no day I will ever be negative for hbsag, even those who are not infected have a trace of it.
3. peginterferon and vitamin d3 have no effects on hbsag
I could not talk much to her because a mate in my area who did not know of my condition was her record taker, I resisted, so treatment discussion is adjourned to tomorrow.
peging since hbsag is less than 1000 iu/ml. high chance to clear
pls, I want to start medication, but I don't know which one to start with, kindly give ur valuable advice base on my results.
pls, I need your valuable advice on my results.
pls what treatment option should i discuss with the dr. concerning my
hbsag value 795.27 iu/ml
viral load 513 iu/ ml
AST. 23 u/ l. expected value 5 - 34 u/ l
ALT. 17 u/l. expected value 10 - 36 u/l
thanks for always there for me
regards: waschool
my viral load results today is 513 iu/ ml. what can I do now.
haemoglobin is 15.6 g/ dl, viral load results will be ready soon.