There is much to report on today. Sierra Leone has placed a remote district on a two-week lockdown for discoveries of exceptional Ebola transmission and a huge death toll. However, I’d rather discuss what conventional science has to say about where conventional medicine is going. Then, you decide if there is rationality amongst those in whom you have entrusted your health. (USA included).
University of Utah scientists have run biochemical analysis and computer simulations to discover an “exotic” mechanism of Ebola and similar viruses to replicate. Much of the science is technical, so, I’ll summarize.
An enzyme called “polymerase” slides along the protein “beaded” RNA strand of the virus particle. Polymerase is the enzyme that transcribes the RNA (or in our cells, DNA) into productive information, like proteins or perhaps replicas of the DNA or RNA. Somehow, Ebola virus polymerase knows where to begin on the strand. Once polymerase is attached to the RNA beaded strand, it bumps into and attracts other polymerases to join in on the spree. Saveez Saffarian, is senior author of the new study just published by the Public Library of Science journal PLOS Computational Biology. Now considering all the hoopla about vaccines, let’s look at what this “disinterested” [in vaccines] viral researcher has to say. I don’t expect you to believe just me.
The article continues, “Antibodies in vaccines target the proteins to attack and block viral infection. But viruses quickly mutate different exposed proteins, making vaccines less than ideal — as demonstrated by the discovery that this year’s influenza vaccine doesn’t closely match the viruses circulating this flu season.
Saffarian says that some viruses, known as RNA viruses [which include Ebola], have genetic blueprints made of RNA instead of DNA. Creating vaccines is particularly difficult for many RNA viruses — which include HIV, influenza and the group with VSV and Ebola — because RNA viruses are adept at mutating and changing their envelope proteins to evade vaccines. Saffarian adds that the Ebola virus now in Africa “is mutating extremely fast.”
So while promising vaccines candidates against Ebola now are being developed, Saffarian says, “Vaccines are not the most potent way to fight these RNA viruses…….The only way to create stable antiviral therapies against RNA viruses is to target multiple sites within the replication machinery.”
Hello out there. Yoo hooo WHO!! Yoo hooo CDC!!! Yoo hooo governments!!!!!!! Here is a [financially] disinterested world-class researcher telling you that an Ebola vaccine is a CRAP SHOOT!!!!! The virus changes so fast that it can evade the singular effect of a vaccine, which is never a complete and mature immune response. (That’s why we see measles breaking out in vaccinated populations.
So, please note what Saffarian did say: [we need to] “target multiple sites within the replication machinery.” So, he is pushing the development of antiviral drugs to disrupt said machinery. I can assure you that any such drug will have toxicity, even if it works, as it will interfere with DNA and/or RNA metabolism. And, it will be highly expensive, as will chasing ever changing Ebola with ever changing vaccines like we do with influenza, which we know for sure didn’t work this year. So, what happens when next year’s version of Ebola vaccine doesn’t work? I wouldn’t want to be in the area to find out.
However, please stay tuned, “like” this page, share this site with as many people as you can, and help this information go around the world (go “viral”, pardon the pun). I’ll have a post for everyone in the next few days on how the cheapest (and safest) possible medical substance, ozone, does exactly what we want, but only BETTER. I’ll show you, like I did for scores of health professionals in Sierra Leone, how ozone should target “MULTIPLE sites” to stop Ebola from entering into your cells in the first place. That single action alone should neuter this most dangerous of pathogens, and permit an enhanced NATURAL immunity. All I will do is connect dots of viral structure for you. I’ll explain it in layman’s terms and leave it to you to raise “cain” with the press for not looking into this (ozone) matter further (while they cover vaccines), considering the hard science on the matter.
Remember, we won’t know for sure until we see a responsible trial of ozone therapy. Dr. Robins and I admit that we might be all wet. But it’s better to have tried and failed than not tried at all. However, most promising, we have two cases under our belts now, and I am doing everything I can to see that a proper study gets done. I cannot do it without you!!!!!
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