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a.k.a. GARDASIL SYNDROME
a.k.a. CERVARIX SYNDROME
a.k.a. VACCINE INDUCED AUTISM SYNDROME (VIAS)
a.k.a. VACCINE INDUCED GULF WAR SYNDROME (VIGWS)
PATHOLOGY for the Layman: Under certain conditions, the (aluminum) adjuvant in vaccines initiates inflammation that may cause certain pathogens such as Epstein Barr Virus , Bartonella, Babesia, etc., to incubate inside pro-inflammatory cells called cytokines, and become virulent. Mononucleosis (Glandular Fever) and or Lyme Disease in any family member's medical history has proven to be a 100% predictor that a life-threatening reaction will occur. These viruses, enteroviruses, and vector-borne pathogens, together with the HLA-DRB1 genotype, especially the HLA-DR15 allele, combines with a Glutathione S-Transferase deficiency, form a perfect storm for a life-threatening vaccine reaction in adults, and Autism and possible sudden infant death in infants and toddlers. On a second front, vaccine hyper-activated immune cells in the lining of an inflamed gut will cause the gut to become raw in spots and expose antibody-producing immune cells to food proteins. This exposure will result in increasingly new or enhanced food allergies to food proteins such as casein (dairy), gluten (wheat), etc. The patient eventually becomes increasingly Histamine Intolerant, and will fail to thrive due to malabsorption. Histamine is increasingly produced when food protein allergins trigger Mast Cells. Elevated Histamine results in Postural Orthostatic Tachycardia Syndrome (POTS) because histamine dilates blood vessels and lowers blood presssure. The body then attempts to increase blood pressure by cutting off blood flow to extremities. The person typically feels cold, and may present with purple fingertips or toes (Reynaud's). The Stellate Ganglion is triggered to increase blood flow to the brain, which results in poor regulation and cranial hypertension, resulting in debilitating head pressure. Continued inflammation will trigger the "Fight or Flight" response, and the person will excrete magnesium, causing the blood to thicken as it becomes more acidic. This continued response to inflammation causes the body to draw excess magnesium from bone and tissue, resulting in irritability, panic attacks, and possible heart palpitations and arrhythmias. If the inflammation is not stopped, pathogens will continue to become virulent. Irritable Bowel will result, followed by connective tissue disorders, Gastroparesis, demyelinating disorders, organ failure, and death.
The Aluminum adjuvant in a vaccine, especially the Gardasil HPV vaccine, has been found to remain in the body of EVERYONE who receives it. The maximum amount of time (months or years) has not been determined, but multiple autopsies have uncovered aluminum nanoparticles after 6 months, some of which had formed a genetic mutation of the Consensus Primers that now allow them to to stick (bind) to many structures in the body, including the brain. These inflammation-causing aluminum nano-particles will typically cause the HPV vaccine recipient to excrete (pee out) magnesium and calcium, due to the triggering of INFLAMMATION and the FIGHT OR FLIGHT RESPONSE. The (depleted) magnesium is a necessary co-factor for the production of over 300 different enzymes in the human body, including Serotonin. This results in a young adult who can become highly aggressive and combative (temper), where parents or friends must "walk on eggshells" with the individual. The person's ability to remember things may also be noticeably diminished, along with their ability to concentrate. The person will typically become a "night owl," and may find it difficult to fall asleep or stay asleep. An "A" student will often become a "C" or "D" student. Depression can also occur, and a subset of these children will experience thoughts of suicide. A significant number of severely affected young adults may experience "advanced phase symptoms" which may include, but are not limited to: Autoimmune Disease, Gastroparesis, Gallbladder and Thyroid disorders, cancer, Chronic Fatigue Syndrome, allergies and eczema, seizures, or Death. Seizure have been reported more than two years after the last Gardasil HPV vaccination. The first signs are typically 1) a quick temper, 2) lowered blood pressure, and 3) dizziness upon standing. Achy joints and stomach problems may soon follow. Seizures may develop years later. MERCK has turned these children and young adults into walking time-bombs. (ref1) (ref2) (ref3)
RISK FACTORS: Our studies noted that the HLA-DRB1 (especially HLA-DR15) Genotype was of prime importance, along with a compromised liver function, such as caused by a Glutathione S-Transferase deficiency (GSTM1 mutation, etc.), previous Epstein Barr Virus or Mononucleosis, Eczema, Acne, Joint Hypermobility, and exposure to Bunyaviruses (Lyme Disease and its co-infections), especially Bartonella and Babesia, put the patient at a high risk for a life-threatening reaction, especially to the Gardasil HPV vaccine, with Mononucleosis being a 100% predictor of a life-threatening event.
NOTES 2: Enteroviruses, pathogens, gene mutations, and aluminum vaccine adjuvants may contribute and inhibit the body's ability to regulate pro-inflammatory cytokine production and proliferation, resulting in inflammation that fails to self-limit. This abstract describes the pathology of this condition, which may result in cognitive and motor skill disorders, plus life-threatening events, including death, which may result from the administration of a vaccine that contains a pro-inflammatory adjuvant, such as Amorphous Aluminum Hydroxyphosphate Sulfate. Common Pathogens found in these patients included enteroviruses, especially Epstein Barr, plus Arboviruses (especially Bunyaviruses), such as Bartonella and Babesia. Bartonella, which affects Toll-Like Receptor 4 (TLR4), was the most common vector-borne pathogen found in the majority of our patients upon testing. Evidence of Bartonella antibodies were recently found in the blood of 1 out of 4 National Park Employees at Rocky Mountain and Great Smokey Mountain national Parks. Because of these Federally Published and Peer Reviewed Medical findings, we can no longer claim that Vector-borne (transmitted by biting insects) infectious diseases, such as Bartonella, are rare. Reference.
Simplified Version, by Lloyd W. Phillips,
Copyright© Lloyd W. Phillips, September 14, 2013 - Working Copy; Publication Pending
ABSTRACT: PHILLIPS OFFIT WAKEFIELD Syndrome is a progressive, inflammatory condition that fails to self-limit, initiated by trauma to the immune system, such as a motor vehicle accident, surgical procedure, or vaccination. The Gardasil HPV vaccine has been found to be capable of staying in the body for months, by Dr. Sin Hang Lee, who discovered traces of HPV16-L1 gene DNA fragments in the blood and spleen samples from autopsy of a deceased teen(reference)(reference2). In a similar investigation into the unexpected deaths of two teenage girls who became fatally ill after receiving the Gardasil HPV vaccine, University of British Columbia researchers, Chris Shaw and Lucija Tomljenovic identified proprietary antigens from the Gardasil HPV vaccine in central nervous system samples from these children.
Recent 2013 published findings by Kahn et Al disclosed that ALL aluminum-containing vaccines may directly cause sustained inflammation by remaining in the body(reference). We pose the question: Why don't all children suffer serious vaccine reactions? From our study we conclude or hypothesize that the length and severity of inflammation caused by the vaccine adjuvant, and therefore the severity of the potential for vaccine injury, is inversely proportional to the body's ability to neutralize inflammation, and bind to and remove inflammatory aluminum or other vaccine adjuvant(s), immediately after vaccination. In the case of aluminum adjuvants, serum levels of compounds such as silicon (found in bananas, bell peppers, etc.), malic acid (found in apples), glutathione and lack of a Glutathione S-Transferase deficiency (no GSTM1/P1/T1/-or- Z1 genetic abnormality associated with kidney filtering efficiency), may reduce vaccine adverse reaction risks. In several cases we observed that if a person drank coffee on a regular basis, they did not suffer the sever debilitating conditions as their siblings that did not drink coffee, and attribute this to caffeine stimulating Glutathione production. We observed that conditions that may impair Interleukin 10, such as Acne Vulgaris or Eczema, or consumption of sweets (or possibly phosphorous? [found in sodas]), acetaminophen (Tylenol), lithium, and other medications that affect glutathione and magnesium, including, birth control pills, or elevated or unusual body burden and pathogen load, especially Epstein Barr Virus (EBV), Bartonella, Borreliosis, Babesia, FL1953, and pneumonia, may greatly contribute to an adverse vaccine reaction. Multiple systems are disrupted by this inflammation, but one of the most serious disruptions occurs with Opioid Growth Factor production and cell receptor regulation (OGFr), resulting in respiratory depression, reduced GI Tract secretions and peristalsis, often causing constipation, plus dysregulation of thermoregulation, hormone secretion, and immune function(reference). Sustained inflammation may then signals dormant or active Arboviruses, Enteroviruses, or other pathogens (host's pathogen load) to become virulent, and use fast-growing inflammatory cytokines as incubators to multiply and disperse throughout the body by way of infected leukocytes, infecting tissue and organs, plus the CNS and skeletal system. With sustained inflammation, mast cells may proliferate as they become increasingly more sensitive, causing waves of inflammation as an increasing number of antibodies are produced in response to food proteins contacting immune cells in the lining of an inflamed gut. Mature pro-inflammatory cytokines IL-1b and IL-18, may also trigger pathogens to become virulent by initiating inflammation in blood vessels and organs, especially lymph nodes, where many pathogens inhabit. ALL subjects tested showed low 25 Hydroxy vitamin D, which we suspect contributed to the retention of cell which may have normally undergone apoptosis had vitamin D levels been sufficient (apoptosis). Oral supplementation of 5000iu vitamin D3 was sometimes insufficient to restore normal serum vitamin D levels in a significant number of children. It was further observed that while serum magnesium levels were typically low (4.2 to 4.6), intracellular magnesium was virtually depleted, and required an additional 400 to 600 milligrams of Magnesium Glycinate to restore somewhat normal enzyme levels, especially serotonin. We further observed that this inflammation appeared to trigger the "Fight or Flight Response" and was forcing the host to excrete magnesium in urine, which lowered blood ph, causing the blood to thicken (increase viscosity) in preparation for "Battle." This lowered body pH, as observed using pH strips in the first urine after awakening, typically indicated a pH of around 5.0, indicating that the body appears to be depleting bone, tissue, and muscle of minerals to keep the blood at the proper pH. We further observed that this sustained inflammation may also result in varying degrees of cognitive, memory, and motor (skill) disorders, an enlarged Cisterna Chyli, Splenomegaly, intracranial hypertension, which may cause severe head pain that may last 24/7 (which may account for head-banging in autistic children), a protruding fluid pouch at the base of the skull on the back of the neck (two patients), Ankylosing Spondylitis (HLA-B27 present), neuritis (including optic neuritis), cerebral vasculitis, and gut inflammation, which may become self-sustaining in otherwise formerly healthy children and adults. In those tested, we obsered NK-CD57 Counts typically below 30, with the majority falling between 8 and 25. Seizures appeared in a significant number of these children, including an 18 yr old female with an NK-CD57 count of 51, and a 16 yr old male with an NK-CD57 Count of 100. Also present was increased mast cell activity and decreased eosinophils (due to elevated cortisol), which may elevate histamine and contribute to Postural Orthostatic Tachycardia Syndrome (POTS), which may leave the host with alternating high but mostly low blood pressure, fatigue, irritability, irregular heartbeat, and sometimes feeling lightheaded, dizzy, or disoriented upon standing or climbing stairs. A combination of low 25 Hydroxy Vitamin D plus low intracellular magnesium has been observed in all children and adults tested, and was responsible for many symptoms of Osteomalacia and Connective Tissue Disorders in these children, even though serum magnesium typically tested between 4.2 and 4.6. Because of undetected long-term and sustained pathogenic inflammation that can be detected by observing LPS Stimulated cytokines from a 'Comprehensive Cytokine Panel,' it was necessary to administer 5,000 to 10,000iu Vitamin D3 daily to these patients, in addition to 500 to 800mg of magnesium malate to help correct the effects of this condition, and prevent/reverse Parathyroidism. The condition may be more frequent or aggravated in families with a history of genetics or pathogens which inhibit or modify the anti-inflammatory cytokine known as Interleukin-10, such as Acne Vulgaris or eczema(reference). The group demographics appears to parallel humans who are not predominantly Southern European (had little or no inherited Human Leukocyte Antigen (HLA) genes), who appear more likely to host self-sustaining inflammation because of their increased susceptibility to viral pathogens such as Epstein Barr, Mononucleosis, etc., which may act as incubators for pathogens related to autoimmunity, such as Epstein Barr Virus, Bartonella, Babesia, Borrelia burgdorferi, and FL1953, all of which were found by lab tests in virtually all children and adults who were tested, and strongly suspected in the majority of the remainder. However, the small minority that did present with HLA-B27 appeared to have little or no headaches, food allergies, or POTS, but one person of this sub-group did have problems processing both oral vitamin D3 and fish oil. Because Bartonella can infect erythrocytes, endothelial cells, and various macrophage-type cells, including brain derived dendritic cells, the symptoms and severity of pathological manifestations of Bartonellosis have been extremely diverse in this group of children and adults we observed. [note: Vector-borne diseases are NOT rare. 2008 and 2009 published reports of Smokey Mountain and Rocky Mountain National Park Employees revealed that 26.7% had serological evidence (antibodies) of past infection of Bartonella henselae, and 5.7% had active infections during a 1 year period. 31.9% of these park employees also had antibodies against Bunyaviruses (can be spread by mosquitoes), which includes Mouse-Like Viruses (MLVs), and also appeared in the group of children and adults we observed.(reference)]. One way Bartonella may suppress the immune system is by inhibiting TLR4 from producing certain cytokines that target certain viruses and pathogens(reference), but when a vaccination is administered, the vaccine adjuvant violently force the immune system to become fully active, and these pathogens appear to be aggressively targeted once again. Many deceased children, whose families were interviewed post-mortem, had lifestyles with a high probability of exposing them to Bartonella and similar vector-borne pathogens. Much of the inflammation and frothy mucus seen in the lungs and airways at autopsy, may have been driven by Interleukin-13, which can directly cause the overproduction of mucus in airways and lungs(cytokine storm), which could have also resulted in sudden death in a significant number of other children who received the Gardasil HPV vaccine(reference). The sustained inflammation may signal the activation and virulence of dormant pathogens and enteroviruses by tearing apart biofilms, persister cells, and VAULTS within the nucleus of cells, in order to feed inflammation, while exposing the pathogens contained therein. The reaction may become more violent if one of the formerly dormant pathogens happens to be the target of the antigen and adjuvant in the vaccine, such as HPV-16 in stored in a VAULT portion of a cell, persister cell, or biofilm, being targeted by the Gardasil HPV vaccine, and made worse by the administration of multiple inflammation-causing adjuvants from closely spaced or concomitant vaccinations. The majority of the boys and girls tested had NK-CD57 counts far below below lab-normal. If Borrelia burgdorferi (Lyme Disease) is also present, it can induce additional mast cell activation, and release additional inflammatory cytokines (reference). We found a significant number of children had a previous history of pathogens which contributed to, or enhanced T-Cell activation, or resulted in increased mast cell sensitivity and proliferation, such as Epstein Barr, or the vector-borne pathogen(s) Borrelia burgdorferi, Bartonella, Babesia, pneumonia, etc., or acute exposure to, or inhalation of mold or other environmental toxins, especially dried airborne feces particles from rodents, dogs, cats, or other animals, as evidenced by teens who became ill after exposure to (airborne) contaminants from sealed or undisturbed areas occupied by rodents or wild animals, including ferule cats, such as working in a normally closed 100 yr old cloister; autistic twins who were never vaccinated, but whose father had a life-threatening case of Epstein Barr and needed to return to the U.S. from the Dominican Republic, and who were exposed to mold during infancy; or the case of two girls from different countries, one crawling through a formerly undisturbed crawl space under a house, the other, an eleven year old girl, who entered a basement where her mother was sweeping, and inhaled a "cloud" consisting of dirt, mold, and pet feces from a house that had not been occupied for two years. Both girls became ill for about two weeks, and both girls received the Gardasil HPV vaccine about a year later, and suffered severe and life-threaten adverse reactions, including difficulty breathing and severe asthma, which neither girl had prior to their vaccination. In addition to newly-acquired airway inflammation, gut inflammation was observed to become self sustaining due to old and new allergies challenging a heightened immune system, in which histamine-producing eosinophils and mast cells appear to have become increasingly more sensitized and abundant. Gut involvement typically results in malabsorption and may negatively down-regulate many metabolic cycles and enzymes, such as H3K4 trimethylation, which can ultimately result in impaired SEMA5, which controls AXON growth, proliferation, and cone guidance, which may then negatively affect the development of brain structures relating to cognitive abilities, in addition to the direct affects of inflammation upon cells and structures of the brain, such as the myelin-producing oligodendrocytes. Children who are teething are at a higher risk of damage to the brain due to the large amount of histamine that is released to soften the gums, but which also permeates the Blood Brain Barrier. Memory in the adult brain may also be affected by impaired methylation and the body's demands for producing histamine, while dealing with systemic inflammation. Oxidative stress and inflammation rapidly deplete Magnesium, Vitamin D, and other nutrients, resulting in low enzyme production, which together with a GSTM-1, GSTT-1, GSTP-1, or similar genetic Glutathione S-Transferase disorder, which appeared to mimic a defective AGA Gene on Chromosome 4, and ultimately resulted in symptoms similar to Lysosomal Storage Disorder (LSD), which was seen as rapid and sustained weight gain by a significant number of children. Symptoms associated with elevated histamine was observed and attributed to overly sensitized and /or abundant mast cells and eosinophils, typically triggered by newly acquired allergies to foods, resulting from newly-formed food allergies as the result of food proteins coming into contact with immune cells in the lining of an inflamed gut, which then produced antibodies to that food. An unexpected discovery was the presence of vector-borne (biting insect) pathogens, such as Bartonella, Babesia, Borrelia burgdorferi, or FL1953, which was typically present in the family's medical history. Mononucleosis, with exposure to a fungus, with or without a vaccination, has also proven to be virtually a 100% predictor for this inflammatory event. Sustained cerebral vasculitis may be aggravated by mold, but more commonly is initiated by vaccination, resulting in cognitive disorders in infants and toddlers in this subgroup of people. Insomnia, nausea, fatigue, irritability, and head pressure (head banging in toddlers) are often the first signs, along with lightheadedness upon arising from a sitting position. In rare cases, sudden death (SIDS in infants) may result. A Glutathione S-Transferase deficiency was observed in a significant number of these children, along with elevated levels of aluminum, and some had indications of Pyroluria. Virtually all had indications of Postural Orthostatic Tachycardia Syndrome. Except for LPS Stimulated Cytokine Testing, this condition typically remains undetectable by common lab tests. Inflammation may actually increase in later stages, possibly due to IL-10 suppression by a Chron's Disease and gastroparesis-like condition. SANEVAX, a vaccine watchdog group, performed post mortem testing on tissue removed from various structures and vasculature of two deceased teenage girls with unremarkable medical histories, who died suddenly and unexpectedly after receiving the Gardasil HPV vaccine. The proprietary HPV16-L1 Protein Fragments were found firmly attached to the endothelial lining of blood vessels in the brain, and also to other structures, including the hippocampus. Also noted was the HPV16-L1 protein fragments were still bound to the amorphous aluminum hydroxyphosphate sulfate substrate/adjuvant, where it was causing inflammation, and causing immune cells to produce antibodies in that area of the brain, where no vaccine should go. We further hypothesize that the Polysorbate 80 emulsifier (TWEEN), together with Histadide, may have aided the vaccine's passage through tissue into the bloodstream (bullet protein), then through the blood brain barrier. Using Polysorbate 80 to deliver medication through the blood brain barrier has already been proven with other medications in the lab. We document the immune system dysregulation that we observed, which resulted in cascades of potentially life-threatening events, ranging from Autism and autoimmune disease, to death.
CONCLUSION: In a growing subset of the population, especially in those subgroups of the population exposed to vector-borne pathogens, vaccines have now been observed to trigger and actually participate in cerebral vasculitis and other inflammatory disorders. These may become acute or life threatening in the presence of active infections which may have already evoked an inflammatory immune response, particularly those pathogens which inhibit the immune system, such as Bartonella, and/or those pathogens that cause blood viscosity to increase or coagulate, such as Babesia. Vector-borne pathogens have been detected or suspected in the majority of the children in this study, including the FL1953 protozoan, which was found together with Bartonella and Babesia in two teens who presented with seizures. If, however, an adolescent girl becomes pregnant (as observed in the Gardasil contingent), the high levels of Anti-Inflammatory Interleukin 10, released as the result of pregnancy, has been observed to down-regulate and arrest this inflammatory condition.