Typically those living in the West are annually starved of the life-giving UVB Ultra-violet light rays (which manifest as the steroid hormone Vitamin D3) throughout the entire duration of Winter & early Spring. As a result the Lymphocytes in their lungs cannot process Vitamin C & E, which leads to Respiratory disfunction & increased vulnerability to ALL infections. Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones. The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body.  Vitamin C is required for the synthesis of collagen, the intercellular “cement” substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin E is an antioxidant which intercepts free radicals and therefore prevents lipid destruction chain reactions. It maintains the integrity of cell membranes. After reactions with free radicals the antioxidant function of vitamin E is lost. Vitamin C is able to regenerate Vitamin E levels but not when the Vitamin D3 levels drop off. As you can see, when any primary systems are compromised, a chain reaction occurs, throwing off your entire metabolism.

There is an immediate correlation between Vitamin D3 deficiency and a deterioration in general health. The statistics are glaring: In children, low vitamin D3 levels are associated with an increased risk of developing auto-immune diseases later in life; including Type 1 Diabetes & Multiple Sclerosis. 50 million teens in the United States are Vitamin D deficient or insufficient. They have a 2.4 fold increased risk of having High Blood Pressure, 2.5 fold risk of having High Blood Sugar and a 4 fold increased risk of having pre-Type 2 Diabetes. In adults, it is linked to an increased risk as much as 50% of acquiring Prostate, Colon, Pancreatic & Breast cancer including Leukemia – ‘Vitamin D Receptor Deficiency Enhances Wnt/β-Catenin Signaling and Tumor Burden in Colon Cancer…controls the level of nuclear β-catenin in colon cancer cells and can therefore attenuate the impact of oncogenic mutations that activate the Wnt/β-catenin pathway.‘ Vaccines & antibiotics drastically deplete the body of these, and other, vital nutrients.

According to Dr. John Cannell, “Autism is caused from a quantitative, not qualitative, variation in one of the enzymes that metabolize Vitamin D. That is, there are no structural differences in these enzymes in autism, only agenetically determined difference in the amount present. These enzymes are responsive to estrogen; estrogen protects the brain from being damaged by low Vitamin D, probably by increasing the amount of activated Vitamin D present, explaining why boys are four times more likely to have the disease.”

Common deficiencies amongst children with Autism frequently include:

1. Vitamin A

2. Vitamin B6/B12

3. Vitamin C

4. Vitamin D3

5. Vitamin E

6. Glutathione

7. Selenium

8. Mitochondria (related)

These are the body’s primary antioxidants (excluding Mitochondria), essential to regulating Free Radicals (unpaired Electrons) throughout the body, staving off Cancer, Diabetes, Autism, Schizophrenia & the rapid macro-degeneration of cells.

a. Hyperbetacarotenemia, a form of intestinal disfunction linked to Measles (from the MMR shot) is marked by excessive beta-carotene in the blood & Vitamin A depletion. The characteristic yellow tint of the skin in hypothyroidism is due to hyperbetacarotenemia. Studies conducted in 1958 and 1961 confirmed that the wild measles virus has a severe short-term effect on immunity and the child’s nutritional status, especially vitamin A which is obliterated by the intervention of such a virus. Vitamin A plays a central role in the development & differentiation of white blood cells, such as lymphocytes, which are essential to the immune response. Vitamins C & E are dependent on Vitamin A. Therefore the bedrock of your immunity is compromised.

b. Starved of Vitamin D3: As a result the Lymphocytes in their lungs can’t process Vitamin C & E, which leads to Respiratory disfunction & increased vulnerability to ALL infections. Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones. The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body. When these organs are compromised , it will throw your entire metabolism off.

c. Many autistic children have a deficiency of Vitamin B6/B12, which is vital for the proper functioning of the brain and nervous system. B-12 is ‘a crucial nutrient for nerve health and the construction of red blood cells that carry oxygen throughout your body; deficiency of which can actually cause brain shrinkage – also associated with Alzheimer’s.  Studies now show that up to 40% of the population may be deficient in vitamin B-12.’ Solutions: Avoid cyanocobalamin. Safe, effective B-12 supplement: Methylcobalamin

d. Estrogen protects the female brain from being damaged by heavy metal toxicity (including low Vitamin D). Testosterone, the male sex hormone increases heavy metal toxicity; explaining why Autism is statistically occurring 4-1 in boys over girls.  “Autism is caused from a quantitative variation in one of the enzymes that metabolize Vitamin D.” Dr. John Cannell

e. Vitamin C is required for the synthesis of collagen, the intercellular “cement” substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin C is also able to regenerate Vitamin E but not when the Vitamin D3 levels drop off.

g. Heavy metals rapidly deplete Selenium in the body. Selenium is necessary for Glutathione production (the body’s primary antioxidant). This causes a chain reaction which triggers liver damage, diabetes, cancer & in the long term, heart failure.

h. The Thyroid Gland is key to overall health. Produces T3 & T4 hormones (Iodine Atoms). Iodine helps regulate metabolism in the body. Thyroid synthesizes vital T3 (rare) from T4 (plentiful). Body needs 150 mg per day – 80% comes from T4 conversion to T3 in the Liver. Vaccine derived heavy metal toxicity neutralizes this function.

i. Damage to the Methylation process – Methylation assists in a critical stage of early development involving the viability of cells, ‘an on/off switch that allows the body to learn how to respond to environmental change. It represents the only cellular pathway that effects both adaptability and structural integrity of the body.

j. Anti-mitochondrial antibodies are elevated; which suffocates Eukaryotic cells (complex structures enclosed within membranes). Mitochondria are the battery pack of your cells. “Mitochondria play an important role in controlling the life and death of a cell. Consequently, mitochondrial dysfunction leads to a range of human diseases such as ischemia-reperfusion injury, sepsis, and diabetes.” Most Eukaryotic cells contain other membrane-bound organelles such as mitochondria, chloroplasts & Golgi body. “Primordial eukaryotic cells lacked ability to use oxygen” – excerpt from Autism case file.

These primary antioxidants are all interdependent, without which your fundamental metabolism is seriously compromised; a hallmark of Autism and a wake up call to those of us more fortunate:

Vitamin A plays a central role in the development & differentiation of white blood cells, such as lymphocytes, which are essential to the immune response. Vitamin A deficiency has been shown to increase T3 and this is further increased by an additional deficiency of iodine. “In the A- and A-I- groups, blood levels of retinol fell to one tenth of the control mean and circulating concentrations of total and free T4 and T3 increased significantly. This biochemical hyperthyroidism contrasted with the maintenance of normal TSH plasma values, suggesting a generalized peripheral refractoriness to thyroid hormones.”

Group B vitamins can act individually or in combination with the cellular enzymes to form vitamin B co-enzymes. These vitamin B co-enzymes are crucial to the metabolic pathways that generate the energy from carbohydrates, fat and protein, needed by every cell in the body. Vitamin B6 (pyridoxine) is required for the synthesis of the neurotransmitters serotonin & norepinephrine and for myelin formation.  ‘In some experiments on chick growth with wholly vegetable diets supplemented with pure vitamin B12, a relationship became evident between the growth-stimulating effect of this vitamin and the content of calcium, iron and vitamin D of the diet.’ Vitamin D insufficiency has now reached epidemic proportions and has been linked to increased body fat and decreased muscle strength.

Vitamin C is required for the synthesis of collagen, the inter-cellular “cement” substance which gives structure to muscles, vascular tissues, bones, tendons and ligaments. Vitamin C is also able to regenerate Vitamin E but not when the Vitamin D3 levels drop off. Vitamins C & E are dependent on Vitamin A. Therefore the bedrock of your immunity is compromised.

Vitamin D is required to increase the circulation of calcium and phosphorous, two minerals necessary for healthy bones. The kidneys produce Vitamin D3 & the liver plays a vital role in the functioning of D3 throughout the body. When these organs are compromised , it will throw your entire metabolism off. The Lymphocytes in your lungs depend on Vitamin D3 (steroid hormone derived from sunlight); without which they can’t process Vitamin C & E.

Vitamin E is an antioxidant which intercepts free radicals and therefore prevents lipid destruction chain reactions. It maintains the integrity of cell membranes. After reactions with free radicals the antioxidant function of Vitamin E is lost.

Selenium is necessary for Glutathione production (the body’s primary antioxidant) – the absence of which causes a chain reaction which triggers liver damage, diabetes, cancer & in the long term, heart failure. Heavy metals rapidly deplete Selenium in the body.

Children coping with Autism are stripped of their Mitochondrial efficiency, the result of a premature breach of the 3 primary core “electrical grid” stations encasing the nerve center/brain (the Blood-Brain barrier, Myelin sheath & Meninges), mainly from vaccine derived heavy metal-virus-mycoplasma-excipient toxic “sludge”. There is a direct correlation between Mitochondrial disfunction in children coping with Autism and the presence of gastrointestinal dysmotility or Inflammatory Bowel Disease, ie. Crohn’s Disease & Colitis. Anti-mitochondrial antibodies are elevated; which suffocates Eukaryotic cells (complex structures enclosed within membranes). Mitochondria are the battery pack of your cells (determine cell efficacy & efficiency – associated with Methylation process). “Mitochondria play an important role in controlling the life and death of a cell. Consequently, mitochondrial dysfunction leads to a range of human diseases such as ischemia-reperfusion injury, sepsis, and diabetes.”

Note: Most Eukaryotic cells contain other membrane-bound organelles such as mitochondria, chloroplasts & Golgi body. “Primordial eukaryotic cells lacked ability to use oxygen” – Autism case.

So you’re seeing a chain reaction affecting 7 major antioxidants in the body, all essential to regulating your overall metabolism, Liver, Kidney, Thyroid, Methylation, including Mitochondrial function, generally neutralized in these children with Autism; and all the evidence points to heavy metal toxicity derived from standard Immunization Vaccines (25 injections by 15 months).

Note: All vaccinated children, regardless, are susceptible to this depletion to a lesser or greater extent.

Vaccines, by their composite nature, inherently damage & disrupt the body’s delicate neurological network; hindering the complex functioning of the brain in maintaining all systems of operation (circulatory, digestive, endocrine, immune, lymphatic, muscular, nervous, reproductive, respiratory, skeletal, and urinary). In practical terms, a synergy factor inevitably occurs when multiple ingredients such as heavy metals, live viruses/or strands of DNA-RNA “heat treated virus”, antibiotics, formaldehyde, detergent, diploid cells (aborted fetal tissue), mycoplasma, phenol dye & excipient buffers are combined together in a vial mixture.

Once these toxins are injected into deep muscle tissue or subcutaneously (either route which literally bypasses one’s natural barriers altogether), a cascading degeneration known as Ischemia, a singing of the neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development, often occurs; resulting in a series of what are termed “microvascular strokes”, ‘as large white blood cells rush to attack the foreign particles injected into our bloodstream…surround tiny capillaries where the foreign particles land, clog and collapse the capillaries.’

The viscosity of this build up of “sludge” clogs/singes the vast network of arterial veins & capillaries leading to the brain while accumulating in the organs (ie. heart, liver, kidney), joints, meninges – 3 layers of protective tissue called the dura, arachnoid, & pia mater that surround the neuraxis (axial unpaired part of the central nervous system), intestines (gut area), along the neural pathways interlacing the entire body (resulting from “stagnant” blood) – comparable to the black paste-like build-up found over time in the lining of your drains – especially in terms of its impact on your vital health. Anaphylaxis, a system-wide allergic & functional breakdown, described as ‘a severe, whole-body allergic reaction to a chemical that has become an allergen‘, and Encephalitis, inflammation of the brain & meninges (Meningoencephalitis) manifesting as ‘diffuse and/or focal neuropsychological dysfunction‘, inevitably follow.

Note: The synergy of vaccine derived heavy metal-virus-mycoplasma-excipient toxicity “sludge” targets 3 primary core “electrical grid” stations encasing the nerve center/brain – kin to throwing water over a main keyboard operating system. In the event the Blood-Brain barrier, Myelin sheath & Meninges are breached, particularly at such a critical stage in early childhood development, susceptibility to (otherwise avoidable) neuro-developmental disorders occurring increases exponentially.  

The Flu Vaccine deception ranks as one of the great cover-ups & swindles  of the last century perpetrated against the general population. Not only has the public been systematically lied to by their elected Gov’t for generations (in league with the World Health Organization & a Vaccine Industry Medical Mafia feeding trough), but the entire bedrock of our natural immunity has been put at risk through the collision of forces being pitted against us around the world.

The pattern emerging is clear, in terms of a criteria for determining the severity of seasonal Influenza – The majority of Flu deaths are attributed primarily to Bacterial Pneumonia triggered by the Flu symptoms. The Flu itself cannot kill you. Most victims of the Flu are those 65 years and older.  In almost every instance a compromised immune system and/or a pre-existing medical condition is the key determinant factor in those unfortunate victims (at whichever age) who die from the Flu.

Further, most children who succumb to seasonal Flu, either via death or serious long-term illness (in particular those tracked since 2009), are subsequently found to have been 8 times more predisposed to a Methicillin-resistant Staphylococcus Aureus (MRSA) bacterial co-infection occurring in the lungs. It is also significant that routine prescription anti-bacterials/virals (chiefly Vancomycin Hydrochloride Capsules & Oseltamivir/Tamiflu), widely distributed globally to ostensibly combat flu-like symptoms, have in fact been the tipping point which has worsened such conditions, hastening Kidney failure, Myocarditis (inflammation of the Heart Muscle) & numerous instances of sudden death.

Note: There are other primary factors to consider in terms of Influenza vaccinations, including the mutability of viruses within the shots & the presence of animal cell substrate derived co-infections/cross-contamination, adventitious agents & neoplasms; all associated with a heightened risk of acquiring cancer. Additionally, there is compelling evidence that the routine administering of post Influenza vaccination Prescription Drugs (Vancomycin & Oseltamivir aka Tamiflu) not only hastened the critical conditions of those who sought hospital care, but may, in fact, have triggered the premature deaths of most, if not all children who succumbed to 2009’s laboratory produced “novel” strain of H1N1 (2 parts Swine Flu, 1 part Human Flu, 1 part Avian Flu).

Note: “Trans” Fats (Hydrogenated Vegetable Oil) –  inhibit conversion of T4 hormones to T3 in the liver (Thyroid function), decreasing your metabolism.

Natural sources of essential antioxidants/vitamins (strictly organic) include:

Wild Halibut, Cod, Krill & Salmon Liver Oil, Coconut/Flax/Hemp Oil, Goose/Straw/Blue/Black/Rasp/Goji/Noni/Elderberries , Plums, Raisins, Red Grapes, Banana, Guava, Lemon, Lime, Orange, Cantaloupe, Kale, Cilantro, Coriander, Curcumin (Tumeric), Carrots, Spinach, Celery, Black/Wild/Long Grain Brown Rice, Red Bell Peppers, Spinach, Baked Potatoes, Green Peas, Celery, Yams, Broccoli/Florets, Spinach, Garlic, Asparagus, Turnip Greens, Lentils, Chickpeas, Kidney Beans, Wheat Germ, Sunflower Seeds, Cashews & Hazelnuts,Tomato, Cabbage, Cauliflower, Amaranth, Potato, Radish, Brussels/Alfalfa Sprouts, Beets,  Wild Snapper & Salmon, Sardines, Beef & Kidney Liver, Free-range Eggs.

Natural sources of essential trace minerals (strictly organic) include:

Brazil nuts, Sesame Seeds, Mollusks, Oyster, Lobster, Shrimp, Herring, Liver, Egg, Beef, Oats, Brown Rice, Garlic, Broccoli, Wheat Germ, Whole Grains, Mushrooms, Red Grapes, Pumpkin & Squash Seed kernels, Brazil Nuts, Almonds, Cashews, Peanuts, Buckwheat, Black/White Soy Beans, Brown Rice, Halibut, Probiotic Yogurt/Kefir, Celery, Himalayan Salt, Cabbage. Natural sources of essential Glyconutrient “sugars” (strictly organic) include:   Wild Honey, Maple Syrup, Blackstrap Molasses, Raisins, Aloevera Gel, Ground Fenugreek, Black/Red Currant, Gooseberries, Green Beans, Cabbage, Eggplant, Tomatoes, Turnips, Shiitake Mushrooms, Kelp.   Natural meat sources of essential Iron, ‘Trytophan’ (precursor of serotonin, converts into niacin/vitamin B3 in liver, helps in regulating sleeping patterns, appetite & mood of an individual) type amino acids, trace mineral & B Vitamins (strictly organic) include:   Beef, Poultry, Elk, Bison, Ostrich, Turkey, Eggs – slow cooked at low/medium temperature, Raw/Soy Milk, Cheese (Gruyere).

Natural non-meat sources of essential Iron, ‘Trytophan’ type amino acids, trace mineral & B Vitamins (strictly organic) include:  

Flax Seed (raw), Lentils, Peanuts, Almonds, Asparagus.   In order to reap the rewards of this program it is prudent to minimize/reduce your overall intake of caffeine & consumption of alcohol. Furthermore, the body has zero tolerance for any/all ‘Standard Immunization’ vaccines, cigarettes/cigars, prescription antibiotics/drugs (ditto any/all recreational drugs), including over the counter acetaminophen (Tylenol) …’Data from the U.S. Acute Liver Failure Study Group registry of more than 700 patients with acute liver failure across the United States implicates acetaminophen poisoning in nearly 50% of all acute liver failure in this country.‘ and any/all non-steroidal anti-inflammatory drugs (Aspirin) …‘People who take NSAIDs for prolonged periods of time can develop several GI side effects, such as stomach aches, indigestion, or even ulcers.’

Supplements should be used primarily as a secondary option or compliment to raw, organic ‘soil & sea based’ plants/vegetables//fruits/herbs/oils/meats. Natural sources contain proportional trace amounts of vital minerals & antioxidants; which the body recognizes immediately & harnesses accordingly; distributing them to whichever regions are most deficient. Whenever possible, natural solutions should be your first course of action. Supplements can be taken to excess, resulting in the body being thrown further out of balance (ie. rapid chelation management – which can lead to overt liver damage & ongoing impairment of Thyroid function). That being said, there are many “relatively” safe & effective supplements available, combinations of which are sometimes needed to help rebuild an Immune System crippled by vaccine derived “synergistic” heavy metal toxicity.

See  VRM: The Autism Report http://vaccineresistancemovement.org/?p=10185

See VRM: The Flu Report http://vaccineresistancemovement.org/?p=9226

See VRM: The Tamiflu Report http://vaccineresistancemovement.org/?page_id=11240 

See VRM: PCV Vaccine Exposed – Breeding Ground For Staphylococcus Aureus http://vaccineresistancemovement.org/?p=9431

See VRM: The Problem With Vaccines http://vaccineresistancemovement.org/?p=488

See VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body http://vaccineresistancemovement.org/?p=8787

See VRM: The Problem With Vaccines Part 5A – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8836

See VRM: The Problem With Vaccines Part 5B – Detoxification & Restoration of the Body http://vaccineresistancemovement.org/?p=8847

Please support VRM in our efforts to fight Big Pharma & the Vaccine lobby. Granted no easy task but we’re committed to resist the Medical Dictatorship being set up for us all. We are also strengthened by having the truth on our side. And eachother. Your donations will help us in the legal trenches so to speak, with website management, legal consulting, rally costs, signs, printing, and general expenses. VRM is strictly non-profit for a reason. We rely entirely upon donations & grassroots efforts to move forward with the bolder initiatives planned. To those who have contributed along the way thus far, much thanks for the ongoing support. It is a privilege to be part of this community-wide awakening. Joel Lord, founder of The Vaccine Resistance Movement