Posted 7/28/2015 2:31 PM (GMT -5)
Thanks for this interesting thread, OP.
Apparently most chronic Lyme victims have VERY HIGH Nagalase levels--- above 2.5-- which is very bad because nagalase disables our macrophage cells!! One chronic Lyme patient shared that his Nagalase level was 2.9.
A normal nagalase level for a healthy college student should be around 0.5-- the lower the better. We Lymies should not have such high nagalase levels.
No one knows whether borrelia produces Nagalase, but we do know that high levels of Nagalase impairs/weakens the immune system and sets a person up for chronic infection and even cancer. Why on earth the FDA has shut GcMaf companies down -- after so much research shows that GcMaf can cure both early stage cancer, autism, alzheimers and chronic fatigue-- is beyond me. And now "they" are apparently murdering the doctors who successfully treated people with GcMaf... Hmmm...
Lyme victims with high nagalase levels should be allowed to use GcMaf to bring down their levels, if only so that they have properly functioning macrophages. The medical community seems to be insane.
Nagalase is a chemical that is produced by both cancerous tumors and by viruses to boost their own survival rates by dampening the ability of immune system macrophage(scavenger) cells to vacuum up cancer cells, viruses and bacteria. Nagalase disables GcMaf, thereby stopping our macrophages from attaching to vitamin D3, a vitamin which activates the macrophages so that they can devour both cancer cells and viruses or bacteria. Nagalase stops this process by inhibiting the body's natural production of GcMaf. In short, Nagalase prevents vitamin D receptors on a macrophage from being activated by lowering the body's natural Gcmaf stores. When a macrophage is not able to attach to Vitamin D3 and wake up properly--- it gets cranky and it spews out inflammatory cytokines, known as a cytokine storm. Cytokine storm is what killed so many victims of the spanish flu--they literally died by drowning on the inflammation liquid in their lungs, not from the flu virus itself.
As a destroyer of the immune system, Nagalase **could*** be part of a stealth biological weapons or population control strategy --- in that it weakens the immune system by disabling macrophages which then sets a person up to die or become very ill the next time they contract a virulent organism, since macrophages require d3 to be able to mobilize properly. This is called "binary biowarfare," meaning that a softening agent is first introduced into a population (such as nagalase), after which a flu or other virus could be introduced, through the food supply or via vaccination--- which normally does not kill, but which would be made much worse by the presence of high levels of nagalase. Children who later develop autism supposedly showed very high nagalase levels after they had been vaccinated at 18 months--- Meaning that the nagalase was introduced directly by the vaccine, or that it was manufactured by a live virus carried inside the vaccine. (Or that all the children had high nagalase levels due to having cancer, which they did not have.) The doctors who died ostensibly had clear evidence to show that nagalase was somehow being introduced to children through their vaccinations. Almost all of 400 autistic children tested by one of the murdered doctors had high nagalase levels.
I truly hope that the medical research community gets to the bottom of this tragedy, and that the perpetrators are held accountable. America cannot allow big pharma and their paid flunkies at the FDA to devour our young people.