All vaccines are designed to target the under-developed areas of the brain & central nervous system in babies & young children (comprising the Blood-Brain barrier, Myelin Sheath & Meninges).

The most serious damage incurred by vaccines, leading to neuro-developmental difficulties and neurological damage, is typically associated with demyelination, the breaching of myelin (protective casing around nerve cells).

“Almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.” Charles Posner, Harvard Medical School Department of Neurology, 1947

In a growing number of cases this will leave them stricken with life-long debilitating diseases, such as Multiple Sclerosis. The Vaccine Industry has termed this toxic synergistic response to vaccines in the body as“multifocal or atypical demyelinating syndromes”: in a deliberate attempt to obfuscate the genuine facts from our communities.

Is it any wonder, given the accumulative barrage of vaccine ingredients interfering with early childhood development, across the spectrum, from as early as 12 hours old (Hepatitis B Vaccine)? 

The HPV vaccines, Gardasil & Cervarix, which target teenagers and young adults (both male & female), contribute to “immune-mediated reactions to the nervous system” resulting in “Motor Neuron Disease” throughout the brain; and for those young teens whose threshold cannot withstand the toxic assault, due to a prolonged, compromised immune system (coupled with pre-existing medical conditions) stemming from the long-term accumulation of vaccine/anti-biotic/bad food choices inflicted erosion/saturation of the brain & gut, the eventuality of “multifocal or atypical demyelinating syndromes” (ie. Multiple Sclerosis).

Gardasil cervical cancer vaccine syringe. This vaccine protects against human papillomavirus (HPV). HPV causes a number of cancers, including cervical and penile cancers, and genital warts. Vaccination is mainly aimed at teenage girls.

Gardasil cervical cancer vaccine syringe. This vaccine protects against human papillomavirus (HPV). HPV causes a number of cancers, including cervical and penile cancers, and genital warts. Vaccination is mainly aimed at teenage girls.

Destruction of myelin and oligodendrocytes leading to the formation of large demyelinated plaques is the hallmark of multiple sclerosis (MS) pathology.‘ Journal of Neuropathology and Experimental Neurology

Multiple Sclerosis (like Amyotrophic lateral sclerosis/ALS, Lupus, Parkinson’s & Huntington’s Disease) is one of the most debilitating neuro-developmental disorders resulting from this breach of the body’s delicate nerve center (Blood-Brain barrier, Myelin sheath & Meninges). There is a scientifically verifiable link between vaccine derived sludge-toxicity related damage to these vital centers (in addition to post-vaccination ‘prescribed’ drug adverse reactions) & onset of MS.


About 250,000 to 350,000 Americans have multiple sclerosis (MS), and women are affected almost twice as often as men. MS is characterized by scarring of the myelin in the brain and spinal cord, causing varying degrees of neurological impairment depending on the location and extent of the scarring. Although the cause of MS is unknown, scientific evidence increasingly suggests that genetics may play a role in determining a person’s susceptibility to MS. There are several treatments to alleviate the symptoms of MS but no cure.

Physically, the brain and the spinal cord are involved. Specifically, degeneration of myelin, a material which is composed mainly of fats and serves as an insulation for the nerves, much like the covering of an electric wire, degenerates. This fatty insulation allows a nerve to transmit its impulses with lightning-like speed, enabling people to move almost without thinking. The loss of this myelin insulation causes what is, in effect, a short-circuiting so that a person loses the ability to make smooth, rapid, and coordinated movements.

Thus, MS is a demyelinating disease. With multiple sclerosis, the loss of myelin appears to the naked eye as a hardened sclerotic (scar) area. These areas are multiple within the central nervous system, thus the term multiple sclerosis. Different areas of the brain and spinal cord are responsible for different kinds of movements. For example, the cerebellum, an out-pocketing of the brain, is responsible for making coordinated movements. When an area of demyelination occurs in the cerebellum, coordinated movements become difficult. The neurological deficit is quite dependent on the region of the brain or spinal cord that has been affected.


The road to repairing this trauma incurred by vaccines:

A protein activated by vitamin D could be involved in repairing damage to myelin in people with multiple sclerosis (MS), according to new research from the University of Cambridge.

Researchers, from the MS Society Cambridge Centre for Myelin Repair, identified that the ‘vitamin D receptor’ protein pairs with an existing protein, called the RXR gamma receptor, already known to be involved in the repair of myelin, the protective sheath surrounding nerve fibres.

By adding vitamin D to brain stem cells where the proteins were present, they found the production rate of oligodendrocytes (myelin making cells) increased by 80%. When they blocked the vitamin D receptor to stop it from working, the RXR gamma protein alone was unable to stimulate the production of oligodendrocytes.

In MS, the body’s own immune system attacks and damages myelin, causing disruption to messages sent around the brain and spinal cord; symptoms are unpredictable and include problems with mobility and balance, pain, and severe fatigue. The body has a natural ability to repair myelin, but with age this becomes less effective.

“This work provides significant evidence that vitamin D is involved in the regeneration of myelin once the disease has started.” Professor Robin Franklin from the MS Society Cambridge Centre for Myelin Repair.’

See: VRM: Gardasil/Cervarix Part 2 – Demyelination, Multiple Sclerosis & the Copaxone Connection 



The ultimate, most heinous crimes in history have been committed with impunity, without regard for human life, or with any vestige of humanity. Think on this, the Vaccine Industry has such over-reaching power now. They are impacting our communities and destroying an entire generation of children, for seemingly nothing more than profits. That and more.

Their goal, those who wield power behind the curtains, is to completely restructure & re-engineer the human species, such that, in one generation, our capacity for self-determination of the body will be null & void, ineffectual. Cancer will be commonplace at 20-30. Autism will be 1 in 2 in most households.

Eventually, the species will be brought down by those Elites perched in their high towers, isolated and secure, coveting all the research knowledge to which we, the common people, will never be privy.

So the questions is, what are we going to do about this looming threat, while we still have the capacity to rise up and fight back? Vaccine Resistance Movement


The brain is an electrical field, a massive electrical grid complex which regulates the entire operation of life for the body.

The human body is hard-wired to the brain, an intricate bio-electric network; analogous to a tree deeply rooted into this matrix of highly electrical “soil”.  

Tree roots 

The vast majority of infections enter the body through the nasal passages (mucous membrane) & the Gastro-Intestinal Tract or the guts (gut flora). Accordingly 80% of the body’s immune system is situated at these junctures; the natural first line of defence.  

Vaccines are injected into deep muscle tissue/subcutaneously, either route which literally bypasses one’s natural barriers altogether. Thus the body is left vulnerable to live viruses & heavy metals.

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 singeing 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, spleen), 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). 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.

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, the risk of neuro-developmental disorders ie. Autism occurring, increases exponentially.


The lymphatic system, which produces White Blood cells (Lymphocytes), crucial to determining the capacity of your Immune system to fight off (adapt to) incoming viral, bacterial & fungal infections, is similarly hard-wired to the brain, intertwined, buried in the Meninges layering of tissue. Not only is the lymphatic system interconnected with the brain, but clearly, all systems of functionality are also intricately linked to the primary core of the brain.

The Meninges layering is designed to insulate the brain & spinal cord from injury – notwithstanding the accumulative barrage of synergistic toxicity associated with early childhood vaccines. “Probably no field in embryology has been less explored than that relating to the meninges.” Lewis H. Weed

The discovery was made possible by the work of Antoine Louveau, PhD, a postdoctoral fellow in Kipnis’ lab. The (lymphatic) vessels were detected after Louveau developed a method to mount a mouse’s meninges – the membranes covering the brain – on a single slide so that they could be examined as a whole. “It was fairly easy, actually,” he said. “There was one trick: We fixed the meninges within the skullcap, so that the tissue is secured in its physiological condition, and then we dissected it. If we had done it the other way around, it wouldn’t have worked.”

After noticing vessel-like patterns in the distribution of immune cells on his slides, he tested for lymphatic vessels and there they were.’

Lymphatic system

This is further confirmation of my entire thesis on Vaccine toxicity and its effects on a child’s brain & central nervous system.

 It also explains the resulting sinkhole effect: where-by vaccine-injured children are typically unable to acquire, and in turn, unable to harness their vital supply of trace minerals & anti-oxidants; which ultimately cripples their Immune system.  

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, if these levels are depleted, the bedrock of your immunity is undermined. All vaccines straightjacket the immune system, by stripping the body of its ability to harness vital trace minerals & antioxidants; the essential arsenal that any child requires to successfully overcome the symptoms of any incoming infection.

Children coping with Autism are typically starved of Vitamin D3. As a result, the Lymphocytes in their lungs can’t process Vitamin C & E, which leads to Respiratory dysfunction & 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. 

Children with Autism Spectrum Disorder have had the rug pulled out from under them at a critical stage of early development, depleted of their vital mineral & antioxidant base, stripped of Mitochondrial & Thyroid efficiency/functionality, their vulnerable “electrical grid” nerve center violated prematurely – which significantly inhibits the capacity of the body to carry out its normal systems of operation; and all the evidence points to heavy metal toxicity derived from standard Immunization Vaccines (25 injections by 15 months conservatively).

The gut level “plumbing” crisis, a hallmark of Autism, is the end result of a “house” in crisis; ground zero for neurological & neuro-developmental dysfunction. VRM 

See: VRM: The Autism Report

See: VRM: The Problem With Vaccines Part 4 – Primary Aspects of Vaccine Toxicity Affecting The Body


Bradstreett1Dr. Jeffrey Bradstreet, M.D., of Melbourne, Florida was a warrior, fighting on behalf children with Autism, exposing the link between heavy metal-containing vaccines and resulting neurological & neuro-developmental degeneration, leading to early onset Autism. Bradstreet also represented thousands of families in the U.S. Court of Federal Claims, which tried to brandish him a pariah in the Medical community. He was also a preeminent healer, able to restore the health and well-being of countless vaccine-injured children through holistic protocols.

Dr. Jeffery Bradstreet identified the gut-brain connection in all children coping with Autism, the critical ink between vaccine-derived oxidative stress on the body, brain inflammation and ensuing inflammatory bowel disease (Crones, Colitis). His treatment protocols focused on a key determinant factor, which aids in regulating brain-gut functionality, a neuro-peptide G-protein-coupled receptor located in the duodenum (small intestine) known as Secretin.

Individuals coping with Autism have a marked decrease in levels of Secretin, upwards of a 50% drop. Without this versatile & powerful hormone, neural capacity in the brain is drastically hindered, which cripples the body’s overall metabolism. causing a chain reaction of problems, including ‘visceral inflammation’, uncontrollable seizures, ‘stress-responsivity/adaptation’, ‘learning and memory’, ‘behavioral and autonomic reflex control’. and ”pathology in the gastrointestinal tract.’ – linked to yeast overgrowth and toxic bacterial build-up.
For many of these Autistic children & young adults under Bradstreet’s care (upwards of 900 case files), the administering of Secretin, combined with potent anti-oxidants saw dramatic results, from improved motor skills in the brain to an overall marked increase in communication, sensory awareness, social adaptability, the stabilizing of the gut.

Consequently, his work represents the missing link, the final piece in the Autism puzzle. Secretin operates/functions as short-cut conduit or super-highway, between the brain & gut. This factor is critical in clearing a path toward ultimately overcoming and reversing the myriad symptoms of Autism.

Vaccine researchers in the field have long recognized that gut dysfunction and premature (vaccine-derived) damage to the brain & central nervous system are intrinsically related. Bradstreet, however, has gone further, identifying the actual linchpin, a measurable (non-genetic) marker, drastically depleted in those individuals suffering from Autism Spectrum Disorder.

Why would a doctor so dedicated to inspiring the lives of children, a devout family man devoted to his patients, loved by everyone, seek to end his own life, turning a pistol on himself and pulling the trigger?

Perhaps the answer to this question is buried in the Medical system he found himself at odds with, particularly the U.S. Court of Federal Claims, the bottomless pit of Vaccine-Industry fallout. Bradstreet was a constant thorn in their side, high on the Vaccine Industry black-list; and his ongoing defiance of the FDA, in utilizing alternative treatment protocols, only fueled the fire of controversy.  

Bradstreet’s treatments included a wide variety of dietary supplements, secretin infusions, immunoglobulin therapy, chelation, glutathione, and prednilisone. He ordered numerous laboratory tests, many of which were non-standard tests not approved by the FDA, or ones performed outside the U.S.

[Bradstreet] began with a diagnosis of autism, yeast overgrowth, and a fungal infection in July, 1999. Subsequent diagnoses included autoimmune encephalopathy; autoimmune disease not elsewhere classified and immune mechanism disease not elsewhere classified); allergic gastroenteritis and autoimmune disease; unspecified urticaria, unspecified encephalopathy, and allergic gastroenteritis; encephalopathy unspecified, unspecified disorder of immune mechanism, gastroenteritis, and colitis; disturbance of sulphur-bearing amino acid metabolism, unspecified disorder of immune mechanism, unspecified disorder of metabolism, and encephalopathy unspecified; the same diagnoses in July, 2004, with the addition of “rule out epilepsy, unspecified”; autoimmune disease not elsewhere classified, unspecified disorder of metabolism, unspecified disorder of immune mechanism, and encephalopathy not elsewhere classified; and toxic effect of mercury and its compounds, autoimmune disease not elsewhere classified, and unspecified disorder of immune mechanism.‘ Special Master Vowell

Dr. Jeffrey Bradstreet, M.D. joins a growing list of alternative medical practitioners & researchers who have defied the code of silence & blind faith surrounding the Vaccine Industry, and paid the highest price for that virtuous commitment to the truth. Dr. Andrew Moulden, Dr. Boyd Graves, Dr. Mayer Eisenstein…who will be next to suddenly die under mysterious circumstances?

Bradstreet & RFK Jr