Interview with Dr. Gary Mezo
Questions by Sander Olson. Answers Dr. Gary Mezo.
Gary Mezo, PhD, ARNP, PAC, is a medical researcher who has spent the last decade doing groundbreaking work in the field of nanobacteria. Nanobacteria were discovered a decade ago, and are responsible for many human diseases. Dr. Mezo has developed a safe, effective method to destroy nanobacteria, called NanobacTX. You can find more information about him by going to the website: www.nanobaclabs.com.
Question 1: Tell us about how and when you discovered
nanobacteria. Our
colleagues and Nobel Prize Nominee Medical Researchers, Neva Ciftcioglu, PhD and
Olavi Kajander, MD, PhD,
(Microbiology Department-University of Kuopio, Finland) were working on several
medical research projects in 1992 using mammalian cell cultures. They became
frustrated because their mammalian cell cultures kept dying. Mammalian cell
cultures and most all human biologicals are normally grown in fetal bovine serum
(FBS) and cell culture death is a common problem in medical research that forces
researchers to start entire projects over again and again. Well, this time
instead of just discarding the dead mammalian cell cultures, they just left them
in the incubator and subsequently forgot about them. Approximately four months
later finding the old cultures, they realized that an unusual thin slimy film
had developed on the culture surfaces. Well, since scientists are by nature as
inquisitive as cats, Drs. Ciftcioglu and Kajander they couldn’t resist full
evaluation of this unusual slime. They were not able to determine the nature of
the film using the highest power light microscopes, so they used Scanning
Electron Microscopes and Transmission Electron Microscopes from lowest to
highest magnification (100,000X). Lo and behold! They found these
20-200nanometer sized nanobacteria in calcified shells: The bacteria in the
stone! They had never seen anything like them, and nothing like them had ever
been seen or described in the microbiology world. These nanobacteria are
structurally and physiologically unique in many ways: they are 20-200 nanometers
in size, they have a unique “cellular” structure and membrane structure like
nothing else on earth, they replicate very slowly (every 3-5 days) and by
different methods, they are pleomorphic meaning that they assume different life
forms for different phases and activities of their lives, they can go dormant in
a self-made calcium shell, they are saprophytic in humans, they are “the
toughest of bugs” resistant to being killed both In-Vitro and In-Vivo and they
are the cause of many human diseases. They are structurally and functionally
simplistic, unbelievably small and genetically unique. Although nicked-named by
one reporter as “Conan the Bacterium”,
Drs. Ciftcioglu & Kajander formally named this novel pleomorphic
nanobacteria that thrives in our blood, Nanobacterium sanguineum. Question 2: How long have you been studying nanobacterium
sanguineum? Has there been any gene sequencing? This
serendipitous and huge discovery
was the beginning of what was to become life-dedicated research on nanobacteria.
Because of the fundamental uniqueness of these nanobacteria, the basic science
on it continues today, with involvement of nanobacterial researchers all over
the world at prestigious universities and research facilities. Today, after 10
years of intensive and exhausting research, we know a great deal about these
unique pathogenic disease-causing nanobacteria and how they cause human
diseases. The gene-sequencing done originally by Drs. Ciftcioglu and Kajander
has been successfully replicated by 5 nanobacterial research groups that I am
aware of and there are definitely unique findings (new peptides) involved in the
genetic sequence. Question 3: How many
different types of nanobacteria are there? In what ways do nanobacteria differ
from larger bacteria? NanobacLabs
Researcher, Dr. Neva Ciftcioglu
is currently at the NASA Johnson Space Center on a 1 year sabbatical doing
nanobacterial research on the astronauts. It appears that nanobacteria “go
wild” in zero gravity and the astronauts have an unusually high incidence of
kidney stones, calcified coronary artery disease, arthritis and other disorders
involving pathological calcification. NASA is more than just casually interested
in finding out about these nanobacteria, especially since the geological
discovery of finding nanobacteria in the martian Allende rock. For the purposes
of this interview, I would like to downplay this aspect of research at this
time. It is clearly “good press” and sensational, but the research is not
done yet and we need to focus on the eradication of the human disease caused by
these nanobacteria: Heart Disease, Kidney Disease and many others……. Question 4: How much do we currently know about
nanobacteria? What
is most important at this time is that
Nanobacterium sanguineum has been shown by multiple researchers to be a unique
organism that causes pathological “disease” calcification in humans. In
other words, it is the calcification that we find in the human body that we were
not “born with“. These nanobacteria secrete a slimy calcium biofilm around
themselves that subsequently hardens, creating a calcium shell “igloo”
around them. They are able to build upon themselves in this calcified form like
coral formation. When we look at pathological calcification in humans (coronary
artery heart plaque, vascular plaque, soft tissue calcifications, kidney stones,
PKD, arthritis and others) what we are actually seeing is calcified nanobacteria
in concretion-like colonies. No human tissue is resistant to nanobacteria…..they
easily cross the blood-brain barrier to cause brain calcification disorders and
“brain sand”. They cause “apoptosis” or cell-death in any and all
tissues they contact. They alter RNA and DNA and transcription expression. To
our knowledge, they are ubiquitous and are everywhere. We have no defense
mechanism against them. They cause production of human antibodies in response to
their biofilm, but when our cellular defense systems arrive, they cannot
“see” anything because the nanobacteria are too small…..it’s like
fighting a war against invisible men. Our immune hyperalert process resultant
from nanobacterial biofilm causes chronic inflammation in our tissues affected
by the nanobacteria. Most human degenerative disease processes have been
associated with chronic pathological calcification, but they were misunderstood
by physicians and medical researchers as a natural process of human degeneration
or aging. Now we know better. Because
of the fact that nanobacteria only replicate every 3 to 5 days and their nano
size, it takes approximately 35-40 years for a human to become symptomatic from
them, even if infected at birth. These factors have led us to not discover these
pathogens for all of this time: incredibly small nano size, undetectable with
light microscopes and incredibly slow growth rate……..from our myopic
viewpoint, if we were unable to detect it with medical light microscopes, we
assumed there were no pathogens present…..the blood was sterile. Wrong. Question 5: When did you make the connection
between human calcification related diseases and nanobacterial treatment? NanobacLabs’
medical research work on
human calcification disorders and nanobacterial treatment began after learning
about nanobacteria. It was my hypothesis that Nanobacterium sanguineum caused
all pathological calcification in humans that let me to develop a prescription
medication to eradicate nanobacterial calcification. I personally designed the
medical treatment based on the properties I learned were necessary to eradicate
nanobacteria in culture form outside of the body. Our Nobel Prize Nominee
Researchers, Drs. Ciftcioglu and Kajander have been collaborators for many
years. One of their most recent published discoveries is that nanobacteria are a
contaminant in IPV polio vaccines that we give our children. They suspect that
all human biologicals developed in fetal bovine serum are contaminated, as cows
are one of the known vectors of nanobacteria. They continue to work on the basic
science associated with the nanobacteria organism, while NanobacLabs works on
the medical research and treatment side. Question 6: What is NanobacTX? How effective is
it? Our
human nanobacterial research and the discovery of how to safely and effectively
eradicate pathologically calcified nanobacteria is literally forging new medical
frontiers. We have scientific proof that we are eradicating the calcified and
soft plaque that cause heart disease with our prescription NanobacTX. We
anticipate that the results from our Western IRB Monitored NanobacTX-ACES
Cardiology II Study done by Board-Certified Cardiologists will be published in
the Cardiology Journals in Mid-2002. Additionally,
the core technology of NanobacTX is currently being used in other formal medical
research studies to eradicate the pathological calcification associated with
Kidney Stones, Polycystic Kidney Disease (PKD), Chronic Prostatitis, Benign
Prostatic Hyperplasia (BPH) and associated with neurodegenerative disorders such
as Autism, Alzheimer’s and Multiple Sclerosis. Our safe & effective
prescription treatment is called “NanobacTX”. Our medical diagnostic blood
tests for nanobacterial antigen and antibodies is called “NanobacTEST”. Both
are currently available by physician prescription from our participating medical
clinical researchers throughout the world. Learn more at our website: www.nanobacLabs.com
To
find a doctor near you call toll-free 1-877-676-2241. Question 7: What are your plans
for the future? This
is what I see for our future: ∙
Recognition of Nanobacterium sanguineum as the #1 cause of degenerative
diseases. ∙
Widespread use of our NanobacTX in the treatment of heart disease. ∙
Heart Disease becomes a rare cause of death. Heart Surgery done only for
emergencies. ∙
NanobacLabs development of treatment and protocols for most degenerative disease
states. ∙
Proactive/preventive use of NanobacLabs regimens in middle-aged asymptomatic
populations. ∙
Routine annual blood testing with NanobacTEST for Nanobacteria at birth and at
all ages. ∙
Development of synthetic mammalian culture media for research.
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