ARTERIOSCLEROSIS IS AN INFECTIOUS DISEASE PROCESS THAT IS LARGELY REVERSIBLE 

By now, you have probably heard about CNPs (Nanobacteria). CNPs have been finally declared as "not-alive" by feuding microbiologists, but nonetheless they do meet criteria as a new form of infectious entity. They have met Koch's Postulates for different diseases by different researchers at prestigious institutions. CNPs, like Prions & Viruses have not met the microbiological definition of being "alive", yet we are acutely aware of the diseases and harm they cause.

CNPs were originally named "Nanobacterium sanguineum" or "Nanobacteria" by their Finnish discoverer & Nobel-Prize Nominee, E.O. Kajander, MD, PhD in 1988. By calling them Nanobacteria, he immediately upset the microbiology gurus, and started quite a furor! Kajander later said that he wished he would have called them something else, because the "bacteria" part of the name, made microbiologists apply their criteria for "living" to the nano-sized self-replicating infectious particles....Now they are referred to as CNPs by most researchers. Research teams at Mayo Clinic Infectious Disease, Cardiovascular Disease & Kidney Disease divisions have decided to call them CNPs or NPs. Our Cleveland Clinic and NASA researchers call them CNPs, but they're all talking about Dr. Kajander's Nanobacteria all the same! All of these researchers give these nano-sized CNPs a great deal of deference and respect....and their research continues today. Our CNP research is also continuing at scores of collaborating universities and private research facilities Worldwide. Nanobiotech Pharma founder Gary S. Mezo invented the anti-CNP patented nanobiotics: NanobacTX, Urobac, Dermabac & RegenurEYES. NanoBiotech Pharma is the only source of his nanobiotics for CNP infections.....shown effective in basic science research & published clinical trials to eradicate CNPs. 

CNPs have been shown to be the active direct cause of pathological calcification in human tissues, joints, osteoarthritis, rheumatoid arthritis, kidney stones, gallstones, cataracts, cancers, microvascular disease, coronary artery plaque, calcified atherosclerotic plaque, calcified pineal glands & neurological (Alzheimer's & MS) plaques and even "brain sand". Research has shown that where NPs reside, you will find pathological calcification & the attendant inflammation.....and vice-versa.

HOW? Coronary Artery Calcification (CAC) plaque grows upon itself at a rate of 44% per year. As these CAC plaques grow, the vaso vasorum cause neovascularization to the area, thereby revving-up the inflammatory responses. When these plaques become a certain size, they outgrow their intimal-medial space in the arterial walls and become inflamed and "unstable". In this state of inflammation and instability these plaques are considered by current endovascular research as "vulnerable plaques", because they are in a state that is primed and poised for plaque rupture. CNPs cause pathological calcification and inflammation wherever they reside.

As you probably remember among the cornerstones of your medical studies: pathological calcification has never been addressed scientifically other than to say it is "idiopathic" and a part of aging. Did you ever wonder WHY? Do you think that we were designed to calcify and turn-to-stone as we age by basic design? Actually, in the absence of an active Mechanism-of-Action, pathological calcification of tissues is quite impossible at normal (physiologic) levels of calcium & phosphate (remember your physiology, organic & biochem?). The mechanism-of-action of pathological calcification is, in fact, an active biological process of CNP infection. CNPs utilize and oxidize serum LDL, VLDL, calcium & phosphate (and many other blood & serum components) to form a slimy lipopolysaccharide (LPS) biofilm endotoxin that revs-up and chronically stimulates our immune reaction. They also form calcium phosphate (apatite) shells "igloos" around their resident 25-200 nanometer-sized colonies.....and they can, over time, aggrigate to become as large as kidney stones or gallstones.

Our discoveries have led to the invention & development of unique multiple disease-targeted nanobiotics that have been shown in peer-reviewed, published clinical studies to safely and effectively dissolve/eliminate pathological calcification as well as the associated inflammation and plaques......

"Arteriosclerosis is not a symptom of aging.....it is the other way around! It is the root cause of aging of tissues & organ systems head-to-toe. By reversing the existing effects & presence of arteriosclerosis, we are DIRECTLY addressing the effects of aging. Think of what arteriosclerosis does, as an example, to the endocrine system: over time microvascular disease affects tissue beds and as it progresses....the process causes end-organ atrophy and subsequent hormonal hypo-function. If by reversing arteriosclerosis, we resupply the tissue with adequate bloodflow again....we can then challenge & stimulate that endocrine system to reproduce those hormones at a pre-arteriosclerotic level. All tissues and end-organs can benefit from improved bloodflow! Reverse arteriosclerosis and you reverse tissue & organ aging!"

We want to hear from you if you are interested in becoming a participating physician in our upcoming clinical trials or want to discuss more, then please EMail us at: physicians@nanobiotech.us  Please include your pertinent practice information, address and EMail/contact information. We will be happy to refer patients to your practice for therapy with NanobacTX, Urobac, Dermabac & RegenurEYES.

Our Nanobiotics are only available directly from us at NanoBiotech Pharma and cannot be obtained anywhere else. If anyone but us says that they have NanobacTX, Urobac, Dermabac or RegenurEYES, it's an illegal knockoff and not the real thing...