Sharing my stock up advice, the items you definitely should not be without. 

  • Colostrum
  • Kefir
  • Yogurt
  • Whole Fat Mammal Milk
  • Cod Liver Oil (Winter) Salmon or Fish Oil (Summer)
  • Zinc
  • Sodium Ascorbate
  • GSE (Grapefruit Seed Extract)
  • Salt with iodine
  • Taurine
  • CBD – I use Real Scientific when necessary, comes in a syringe, only takes about a rice size portion under tongue, great for dry cough. (keep refrigerated). 
  • *Salmon DNA drops 
    Mucolyxir® …. Bronchitis, asthma, pulmonary emphysema and acute sinusitis. Patients with the non-productive cough type of emphysema also improved. These persons began to cough up sputum, breathing tests improved, oxygen levels in the blood increased. Persons with acute and chronic ear infections were greatly improved. The microdoses of DNA worked well in all these diseases and did not produce any side effects. Ear infections not helped by antibiotic therapy. Microdose DNA appears to decrease allergies. Mucolyxir® provides a small amount of DNA from wild Pacific salmon, which may help balance mucus levels via a regulatory mechanism.* Based on pre-clinical investigations and clinical trials, Mucolyxir® appears to support liquification and elimination of mucoid substance.

I haven’t tried Mucolyxir®, it is from Nutricology but it appears to have a high efficacy rate. Follow directions carefully, it may be powerful. It appears doctor recommended, check doctor use reports.

Help for a toxic world.
Sodium ascorbate and whole fat mammal milk is a rapid detoxer without having to guess the toxin. Decrease sugar intake for greater benefit.

Phagocytes need NADPH to create superoxide and other reactive oxygen species. In addition to creating NADPH ascorbic acid has the ability to deactivate excess quantities of NADPH and oxidative substances that could harm normal tissues.

The hexose monophosphate shunt produces 5 carbon sugars (ribose and deoxyribose). These 5 carbon sugars are needed to make DNA and RNA. When the immune system signals for production of new immune cells that need these genetic materials DNA and RNA, if the body has too much glucose and too little ascorbic acid there will be a lack of genetic material and inadequate DNA and RNA for creation of needed new leukocytes. High sugar intake will reduce the potential health benefits of this pathway.

Graphene oxide in a thin oil will not mix with water, it will clearly separate. Graphene oxide nano particles can be highly aerosolized. Chloroquine naturally attenuates the effects of graphene oxide toxicity as shown by studies with graphene oxide as a single factor intoxicant. Quinine is safer but still can not be taken long term. What that means in both UV and chloroquine recommendation Trump knew that he was speaking of an environmentally acquired ‘intoxicant’. Same as Debra Birx, who now sells air ‘filtration’ and ‘purification’ products.
It appears some sulfur compounds (H2S) disperse and/or degrade graphene oxide products but don’t appear to reduce toxicity of graphenes. They must be excreted with glutathione (GSH master detox molecule). Bovine colostrum dramatically improves production of glutathione in all tissues. Only non denatured whey products increase GSH production in all tissues.
Organically acquired symptoms:
Sudden loss of taste or smell and fast onset bilateral pneumonia is the result of an intoxicant, possibly inhaled, possibly absorbed, possibly injected. Possibly a gas or chemical reaction or combustion. Possibly an aerosol, possibly an airborne pollutant (dust, mold spores, filaments, metals, shavings etc.) Possibly a radioactive effect. It always was.
See library.
For deadly H2S and toxic byproduct symptoms including those that can be the result of ‘bio sludge’ which is a bio hazard.

I haven’t chased ‘magic bugs’ in a long time since the advent of modern multi organism anti microbials (FtSz inhibitors – Rifaximin – Turmeric – Berberine -Cinnamon (natural FtSz inhibitors) that are relatively safe and produce no ‘resistance’ or mutations so I wasn’t about to go down another rabbit hole with this one as just as a general rule a long time ago I rejected ‘pathogenic’ cause from a particular organism as did the leaders in oral natural immune therapy and SIBO/gut/immune health. FtSz is an ancient cell division protein highly conserved in ‘pathogens’ known to be harmful to humans. It is not found in humans/mammals and it has never crossed species.

Not to mention the WHO also rejected the theory as first cause risk factors for chronic disease by 2017. SAM affects the greatest number of people but I never ruled out toxicity or injections as a major contributing factor for severe outcomes regarding gut/immune health issues. 

Bat lab WuHan? 

I’ll say it again for anyone who thinks bat lab WuHan is true using a ‘virus’ as a biological agent. Zero risk of flu or SARS with a healthy microbiome. I hate using that term ‘virus’ as with autophagy and phagocytosis (macrophage activation) it is a mischaracterization and misrepresentation of the ‘condition’ or mechanism of action which are necessary cellular functions that rid (digest) the body of cellular debris which produce zero side effects or harmful effects. Apoptosis (cell death) is another necessary cellular function unless it is done via poisoning/toxins (see below). Otherwise 2 tons of bone marrow, lymph debris and intestinal cells would accumulate in a person by age 80. This process can decline with age. Necrosis is uncontrolled cell death. It’s a shame people are so uneducated you have to parse every paragraph to a second grade level but you do. That’s why I wrote a book that will never become obsolete regarding fundamental health that only gets shown to be more accurate by the day. 

“Autophagy” the new/old buzzword.

NO BIO WEAPON CARRIES A ZERO RISK FACTOR. Otherwise it can not be termed a ‘weapon’.

The only bio weapon is the death injection, a chemical weapon or an ‘advanced technology weapon’, (above that which occurs in nature for the purpose of causing harm – definition of a bio weapon). All injections cause harm, immune suppression, risk of malignancy and risk to other organs.

Castle Guards

As per usual with Fauci & Co. and their never let a crisis go to waste/ red herring operations they definitely knew they had a major environmental disaster looming in graphene & graphene oxide. Their only job and function is akin to protecting the arsonist (the perpetrators and the underwriters) once the smoke begins to rise and then shift the burden on to the taxpayer. They are covert military operators. 

I would suggest reading the papers on your own after a short search. Some sites have compiled tons of information about graphene and graphene oxide from PubMed.

I personally will not go down any more rabbit holes regarding Fauci & Co. as their syndicate has been in business since 1984 in the modern era as a criminal protection racket. The fraud playbook has been in existence since the days of smallpox.

Their only purpose for existence is to protect criminals and hide/obscure criminal behavior to shield them from liability. You can be sure every ‘agency’, legislature, most courts and media are working toward that end to prevent justice because that is who funds them.

Low-dose exposure to graphene oxide significantly increases the metal toxicity to macrophages by altering their cellular priming state

4 Conclusions
To summarize, the present study clearly uncovers the previously unknown detrimental effects of GO in com-
bination with non-essential metals on macrophages. Our data demonstrate that even at low-dose non-toxic
concentrations, GO can significantly interact with the plasma membrane and undermine its permeability, leading to a compromised cytoskeletal meshwork and membrane integrity. Due to these changes, low-dose
GO pre-treatment can elevate cellular uptake of non- essential metal ions, resulting in increased oxidative stress, and eventually cell death via apoptosis upon exposure to metal ions at non-toxic concentrations.
Overall, our data underscore a new aspect in assessing the impact of ENMs on EHS—the importance of understanding the secondary and synergistic effects of these materials, in addition to assessing direct
Low-dose GO exposure compromised the structure of plasma membrane

Even in one of their usual poison concoctions containing toxic metals the addition of SIX toxic metals would be unheard of as shown below.

Any ‘vaccine’ is an effort to induce ‘tolerance’ to greater and greater levels of toxins or allergens as you can see as demonstrated in alternavita critical info this is foundational error as all injections produce the same toxic effects.
So why do they persist in error?
Obviously it’s their nature.

If graphene oxide is not toxic why are the Chinese looking for an antidote to poisoning?

Due to heavy chemical pollutants the Chinese regularly wear masks from October thru April. In addition tons of these chemicals like cyanide are stored in heavily populated areas. The Chinese are poisoned by default and have been for centuries.

Chinese Researchers Discover Holy Grail of Graphene Oxide Detox

Humic and fulvic acids are not preventing the fish from being poisoned as they are naturally present in the environment which would make graphene oxide not a ‘toxin’ when clearly it is. ‘Sulfur’ compounds apparently disperse and degrade GO but there is no evidence they reduce toxicity of graphene.

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.


Any ‘vaccine’ is an attempt to induce ‘tolerance’ to greater and greater levels of toxins or allergens; fundamental error as all injections produce the same toxic effects by degrees.


What mAbs are made of
Monoclonal antibodies are man-made proteins that act like human antibodies in the immune system. There are 4 different ways they can be made and are named based on what they are made of.

Murine: These are made from mouse proteins and the names of the treatments end in -omab.
Chimeric: These proteins are a combination of part mouse and part human and the names of the treatments end in -ximab.
Humanized: These are made from small parts of mouse proteins attached to human proteins and the names of the treatments end in -zumab
Human: These are fully human proteins and the names of the treatments end in -umab.
Types of mAbs used to treat cancer
Naked monoclonal antibodies
Naked mAbs are antibodies that have no drug or radioactive material attached to them. They work by themselves. These are the most common type of mAbs used to treat cancer. Most naked mAbs attach to antigens on cancer cells, but some work by binding to antigens on other, non-cancerous cells, or even free-floating proteins. Naked mAbs can work in different ways.

Some boost a person’s immune response against cancer cells by attaching to them and acting as a marker for the body’s immune system to destroy them. An example is alemtuzumab (Campath®), which is used to treat some patients with chronic lymphocytic leukemia (CLL). Alemtuzumab binds to the CD52 antigen, which is found on cells called lymphocytes (which include the leukemia cells). Once attached, the antibody attracts immune cells to destroy these cells.
Some naked mAbs boost the immune response by targeting immune system checkpoints. (See Immune Checkpoint Inhibitors and Their Side Effects.)
Other naked mAbs work mainly by attaching to and blocking antigens on cancer cells (or other nearby cells) that help cancer cells grow or spread. For example, trastuzumab (Herceptin) is an antibody against the HER2 protein. Breast and stomach cancer cells sometimes have large amounts of this protein on their surface. When HER2 is activated, it helps these cells grow. Trastuzumab binds to these proteins and stops them from becoming active.

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


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.