The latest evidence.

Have you been spiked? How can you tell if you’ve been exposed to genetic editing injection person to person transmission? Most likely with blood work that can detect microscopic clotting in tiny blood vessels. D-dimer test or other blood work, oxygen levels and hemoglobin. Graphene nano particle or graphene oxide nano particle presence will not be detected without specialized equipment. Graphenes are toxic and graphene oxide is highly toxic.

Graphene oxide and other intoxicants can combine to form self-assembling proteins that are used to suppress the immune systems in current use medical products…. therefore do you require RNA to express a protein? Answer: No. You merely have to poison cells with an intoxicant/s and ensure delivery via a transport mechanism.

The immune suppression is secondary to the accumulation of free radicals and oxidative stress.

As you can see below no RNA has been found in these current or future injections.

Graphene products can be excreted provided there is enough glutathione production. This production drops substantially with age.

This is the reason for the boosters as graphene oxide has likely been excreted or not injected in sufficient quantity/calibration via batch # + location and radiation may be required to ‘amplify’ the effects to achieve ‘magnetic’ properties.

Only non-denatured whey products (colostrum) enhance gluthathione production in all tissues.


Disregard the beginning, the real information is contained in the TED talk. This is not future science as she insinuates. There has been no discussion prior to this being released on the planet.

This would also provide a current explanation for the person to person transmission of genetic modification products via graphene oxide and amplified by radiation and the current batch # effects of toxicity calibration, dosage and area. According to this video above they know how many ‘subjects’ must be ‘seeded’ to ensure species to species transmission. 

They have achieved this final step in technology. It is now released upon the planet.

Malaria is not caused by a mosquito. It is entirely preventable as is Lyme, both only effect the immune suppressed. 

All virulence factors are caused by blood toxicity levels and do not originate with the organism.



Unless this is another Ponzi scheme in the greatest wealth transfer in history which wouldn’t surprise me at this stage either, above is the latest evidence regarding the death injection. Nothing is out of bounds, including your chromosomes.

Was Your Deathshot Batch A Lethal One?

Death by Lot

How Bad Is My Batch?

Genetically engineered ‘Magneto’ protein remotely controls brain and behaviour

When they introduced this genetic construct into human embryonic kidney cells growing in Petri dishes, the cells synthesized the ‘Magneto’ protein and inserted it into their membrane. Application of a magnetic field activated the engineered TRPV1 protein, as evidenced by transient increases in calcium ion concentration within the cells, which were detected with a fluorescence microscope.

Next, the researchers inserted the Magneto DNA sequence into the genome of a virus, together with the gene encoding green fluorescent protein, and regulatory DNA sequences that cause the construct to be expressed only in specified types of neurons. They then injected the virus into the brains of mice, targeting the entorhinal cortex, and dissected the animals’ brains to identify the cells that emitted green fluorescence. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated Magneto so that the cells produce nervous impulses.

Lest you think this a one off nut job experiment I’ve traced paper after paper in PubMed describing potential applications that are in use today, including the current and future injections. 

About MRNA Injections (all)

Known adverse events and damage which can not be reversed due to genetic editing mechanisms of action:

  • blood cell changes – clotting or bleeding
  • immune system exhaustion (AIDS)
  • production foreign proteins
  • neurological damage
  • multiplication of cells beyond the ability to self regulate or repair – chromosome damage/aneuploidy/cancer
  • uncontrolled inflammatory response syndromes
  • genetic damage
  • infertility
  • heart damage
  • multiple organ damage


According to experts most damage is genetic in nature.


Bio weapon definition is amplifying natural or bio substances for the purpose of causing harm above that which occurs in nature so while protein expression is a natural process it can in no way be described as a bio weapon similar to the amplified injection mechanism which is experimental gene editing under continued emergency use authorization.

Naturally formed ACE proteins can be inhibited via lactic acid bacteria. 

A friendly reminder.

Suppression and injections cause disease.

Currently available treatments which target the systemic immune system, induce immunosuppression, thereby exposing the patient to the risk of infections and malignancy. The interplay between the gut and the systemic immune system determines the final effect on target organs, including the bowel mucosa.  ….. an altered systemic immune response leads to inflammation-mediated damage to the gut and other organs.
Clinical & Translational Immunology (2016)
The WHO recommends that immunization or treatment be orally administered. 
(1998, 2006, 2011).

The Big Steal – Busted.

Laying this fraud and bait and switch to bed right now. Protein expression caused by toxicity. Experiment done with common yeast and intoxicants as seen in video below and confirmed by scientists/virologists provides the exact same genetic sequence done  as original PCR or RT/PCR for SARS.

I am guessing you may recognize that anyone making a diagnostic and/or treating and/or collecting funds based on this test has committed felony fraud and injury which is not protected by any liability shield as can be seen in the current opioid settlements. 


CDC No Longer Recognizes the PCR Test As a Valid Method for Detecting “Confirmed Covid-19 Cases”

The PCR Smoking Gun?
As of  January 1, 2022, the CDC in a request to the FDA withdraws it’s endorsement of the RT-PCR test.  
The CDC acknowledges that the PCR test does not effectively differentiate between Covid-19 and Seasonal Influenza. 
Amply documented and analyzed by numerous scientists, the RT-PCR test does not detect or identify SARS-CoV-2 and its variants.
While the CDC does not officially acknowledge that the RT-PCR test is invalid, it nonetheless calls for it to be withdrawn. 
It is worth noting that almost a year ago, in January 2021, the WHO also questioned the validity of the PCR test which it had itself put forth at the very outset of the covid crisis.
If the PCR test is invalid as suggested by the CDC’s statement, the 260 Million so-called “Confirmed Covid-19 Cases” collected and tabulated Worldwide since the outset of the alleged pandemic are meaningless.
There is no Pandemic. 
In the Course of the Next TWO Days the RT-PCR Test in the US will be Declared Invalid?
In a bombshell decision, the Centers for Disease Control and Prevention (CDC) have withdrawn the insidious PCR test as a valid method for detecting and identifying SARS-CoV-2. 
“After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.”

“The PCR is a Process. It does not tell you that you are sick”. Dr. Kary Mullis, Nobel Laureate and Inventor of the RT-PCR, passed away in August 2019.

Only three people had the knowledge and the public platform/reach to bust this entire charade and all three are dead. Kary Mullis, pneumonia, August 2019. Brandy Vaughn (anti injection Merck whistle blower), blood clot in lung, December, 2020. Andreas Noack, major developer graphene oxide technology, poisoning/heart attack?, November 2021. Only Kary Mullis was over age 70.

A Pandemic Of Not Thinking – Dr. Sam Bailey Interviews Dr. Tom Cowan

With a 99%+ cure rate meant to warp speed via fear porn, a misappropriated use test and an extremely large payout toward injection/s targeting systemic immune, known to cause injury regardless of what is in them (and God help us if they got multi species chromosome destroying CRISPR right)….. one can only conclude, that was the plan.

Alternavita: All you need to know (critical info in a nutshell)..... by focusing exclusively on these foundational health and immune development issues up to 90% of chronic conditions can be eliminated.

WHO STATEMENTS: 2017 Millennium Goal

  1. Breastfeeding,
  2. food (security)
  3. and water security (sanitation)

are major protective factors against malnutrition and critical factors in the maturation of healthy gut microbiota, characterized by a transient bifidobacterial bloom before a global rise in anaerobes. Early depletion in gut Bifidobacterium longum, a typical maternal probiotic, known to inhibit pathogens, represents the first step in gut microbiota alteration associated with severe acute malnutrition (SAM). Later, the absence of the Healthy Mature Anaerobic Gut Microbiota (HMAGM) leads to deficient energy harvest, vitamin biosynthesis and immune protection, and is associated with diarrhea, malabsorption and systemic invasion by microbial pathogens. A therapeutic diet and infection treatment may be unable to restore bifidobacteria and HMAGM.


Researchers found that malnourished children’s microbiota failed to follow the healthy pattern they identified in healthy children. The microbiota of malnourished children is immature, lagging in development behind that of their healthy peers. Supplementing these children’s meals with widely used therapeutic foods that increase calories and nutrient density reduces deaths from malnutrition, but it does not fix their persistent microbiota immaturity.

“Perhaps more insidious than slowing growth is malnutrition’s effect on less visible aspects of health, including impaired brain development and dysfunctional immunity, which follow these children throughout their lives”.

The Father of The Microbiome

Dr. Jeffrey Gordon


SIBO can cause severe malabsorption, serious malnutrition and immune deficiency syndromes in children (non breastfed) and adults. 

Prognosis is usually serious, determined mostly by the underlying disease that led to SIBO.



The WHO recommends that immunization or treatment be orally administered due to economic, logistical and security reasons. Furthermore, this route offers important advantages over systemic administration, such as reducing side effects, as the molecules are administered locally and have the ability to stimulate the GALT immune responses  (Levine and Dougan, 1998Neutra and Kozlowski, 2006Bermúdez-Humarán et al., 2011).



For ANY infectious or parasitic disease to start, it is ALWAYS a requisite that the host suffer IMMUNODEFICIENCY. At the same time, infectious and parasitic diseases themselves cause additional IMMUNE SUPPRESSION and more MALNUTRITION. This immune suppression is SECONDARY to the accumulation of free radicals, especially oxidizing species, that occurs during and after infectious and parasitic diseases.

Clinical Aspects of Immunology and Biochem J.


Current IBD Research 2016

Currently available treatments for IBD, which target the systemic immune system, induce immunosuppression, thereby exposing the patient to the risk of infections and malignancy. The interplay between the gut and the systemic immune system determines the final effect on target organs, including the bowel mucosa. Inflammatory bowel diseases (IBD) are associated with an altered systemic immune response leading to inflammation-mediated damage to the gut and other organs.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel

Most importantly, the immune modulatory agents used today for IBD do not achieve remission in many patients.

Not all IBD patients benefit from currently available drugs. Young people with IBD do not want to be on long-term drug therapy. Oral immune therapy, while not yet studied in large cohorts of patients, may provide an answer to this unmet need.

Clinical & Translational Immunology (2016)
Gastroenterology and Liver Units, Department of Medicine, Hebrew University-Hadassah Medical Center, Jerusalem, Israel


Tolerance is the ability of the immune system to ‘see’ and respond appropriately. Without galactose (a necessary sugar) the immune system can not 'see'. Your immune system would not be able to function without galactose Your body wouldn’t know which cells are “good” and what cells are “bad.” Your body wouldn’t know who the invaders were and which ones should be attacked by antibodies. As you will learn the importance of these ‘sugars’ in gut microbiota health is a rapidly expanding field of research, only recently discovered, including HMO's (human milk oligosaccharides).

Why galactose? Milk sugar aka lactose has been shown to be very beneficial for the human body though unlike sucrose, lactose is made up of glucose and galactose. There is no fructose in lactose. It is a healthy disaccharide sugar. Galactose is known as the “brain sugar” and supports brain development of babies and children. Galactose helps triggers long-term memory formation. Galactose has been shown to inhibit tumor growth and stop its spread, particularly to the liver. This beneficial sugar can also enhance wound healing, decrease inflammation, enhances cellular communication, and increases calcium absorption.
What does immune ‘tolerance’ mean in simple language?
Immune tolerance, or immunological tolerance, or immunotolerance, is a state of unresponsiveness of the immune system to substances or tissue that have the capacity to elicit an immune response in a given organism. The Th1 cytokine profile is vital for clearance of certain organisms and ancillary immune activity, and a limiting effect on this cytokine profile may result in reduced chances for overcoming infections especially intra-cellular organisms residing within macrophages. Effective clearance will depend on appropriate macrophage activation (which occurs through IFN≥ release by Th1 and NK cells) and production of nitric oxide. If this pathway is disrupted IFN≥ secretion is blocked, impairing macrophage activation. Persistent blockade of these inhibitory receptors has lead to the breakdown in immune self tolerance, thereby increasing susceptibility to autoimmune or auto-inflammatory side effects, including rash, colitis, hepatitis and endocrinopathies. Many drugs may cause checkpoint blockade toxicity including pharmaceutical drugs termed ‘immuno therapy’ by pharmaceutical companies, these include Mab drugs and cancer treatments. Checkpoint Inhibitor–Induced Colitis: A New Type of Inflammatory Bowel Disease? Madeline Bertha, MD MS, corresponding author1 Emanuelle Bellaguara, MD, Timothy Kuzel, MD, and Stephen Hanauer, MD ACG Case Rep J. 2017; 4: e112. Published online 2017 Oct 11. doi: 10.14309/crj.2017.112 PMCID: PMC5636906 PMID: 29043290

The Elderly

Mammal milk is required for enhanced phagocytosis as shown by research, especially in the elderly. Whole fat mammal milk can actually restore phagocytosis in senescent cells in the elderly. Phagocytosis, by which immune cells ‘eat’ bacteria or infected cells, is one of the mechanisms that help to resist infections. Lactic acid bacteria strains like acidophilus also increases phagocytosis.