hi all,
I wanted to post an update of how i'm doing since i haven't. I had my first infusion on 11th jun, 1 on 18th jun, 1 on 2nd jul and last one on 16th Jul, and then i was supposed to have one on 30th Jul but missed it bc I was so bedridden and sick, and i haven't had any more since. Because I didn't react to the first three and also bc of the testimonies of ppl I'd read who tolerated Vis well, I assumed I was fine, but it seems now i'm one of those who're not... can anyone tell me of anyone they might know or have heard of who reacted as badly to it as I do? I don't know what to do now because my doctor frankly isn't experienced in giving Vis and dosage is calculated by weight, so neither he nor I have any clue as to how to, say, lower dosage, or if that may produce viral resistance. I haven't left my home in six weeks so i'm not having any more infusions in the near future, that's for sure, totally bedridden. I know there's a chorus of ppl who were uncomfortable with the fact that i'm taking vis from a doc here (Hong kong) who's not well versed in its use but I wanted to point out that it wasn't an easy thing to decide--if you were me and lived in Asia, so far away from the US, would you expend the huge sum of money required to go and live in the US to get infused--if you knew someone in ur hometown willing to do it? I'd already spent tons of money on living in nyc last year and doing ampligen. Sorry to rant but just so desperate. anyway i'd be real grateful if anyone cld tell me anything abt anyone they know who's had a similar reaction, or if they know by some means (say through something that dr Peterson might've said) about what they do in such a situation, i'd be real grateful. specifically if anyone knows whether vistide "builds up" in the system, since even when I was on the full protocol dose of ampligen back in NYC, I NEVER had such problems.
THank u!