SunMoonsStars
Senior Member
- Messages
- 159
Has anyone researched ganciclovir / valcyte mechansism?
It indeed is supposed to suppress replication but why do people have symptoms re-emerge ?
I read a nurses theory that states the drug is taken up by the cells and does inhibit replication but at same time there are virons chased out. Then the other cells of immunity like NK cells are supposed to come and kill those off. If you have poor NK functioning and this doesn’t happen your body is seeing these as increase in virus and same exact symptoms return or get worse.
It makes sense.
I also read an old post here stating that Dr Montoya had changed his approach 2015 on using 1800 a day for 3 weeks down to 900 thereafter. To instead 225 a day and every 2-3 weeks as you can without symptoms increasing toward 900 a day.
Increasing all the immune supports you can during this time as well is a huge plus to tolerate therapy and succeed I assume.
Gcmaf is a big one and there are not any actual medical approaches to stimulating NK cell FUNCTION I can find. I read that Interferon Alfa and IL2 are possibilties even in Genetic NK FNKD Deficiency.
Why aren’t we able to have access to these kinds of immunotherpy possibilities.?
It indeed is supposed to suppress replication but why do people have symptoms re-emerge ?
I read a nurses theory that states the drug is taken up by the cells and does inhibit replication but at same time there are virons chased out. Then the other cells of immunity like NK cells are supposed to come and kill those off. If you have poor NK functioning and this doesn’t happen your body is seeing these as increase in virus and same exact symptoms return or get worse.
It makes sense.
I also read an old post here stating that Dr Montoya had changed his approach 2015 on using 1800 a day for 3 weeks down to 900 thereafter. To instead 225 a day and every 2-3 weeks as you can without symptoms increasing toward 900 a day.
Increasing all the immune supports you can during this time as well is a huge plus to tolerate therapy and succeed I assume.
Gcmaf is a big one and there are not any actual medical approaches to stimulating NK cell FUNCTION I can find. I read that Interferon Alfa and IL2 are possibilties even in Genetic NK FNKD Deficiency.
Why aren’t we able to have access to these kinds of immunotherpy possibilities.?