The whole basis for vaccinations is unphysiological. The vast majority of infections enter the body through the nasal passages & the Gastro-Intestinal Tract or the guts. 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.
Many vaccines are laced with the adjuvant salt form of Aluminum (directly linked to early onset Alzheimer’s Disease, Macrophagic Myofasciitis, Chronic Fatigue Syndrome) & Thimerosal Mercury, a devastating neurotoxin implicated in the explosive spread of autism, until recently at 1 in 67…then 1 in 60…now at a rate of 1 in 38 in some regions – ‘individuals born in 2003 have 16.6 times the odds of an autism diagnosis compared with those born in 1992.‘, (which translates to 1 in 30 – as boys are 4 times more susceptible).
Officially, the rate of Autism amongst children has risen to as high as 1 in 50, based on the glaring testimony of 100,000 parents in the US. By 2015, the statistics will conservatively match that of 1 in 38.
Either neurotoxin is linked to psychological, neurological & immunological problems. Heavy metals & live viruses eventually collect in areas of fatty tissue throughout the body, notably including the brain, and linger there for decades, upwards of a lifetime. Is it any wonder so many children have succumbed to Autism during the earliest, most vulnerable stages of development?
A newborn lacks sufficient protection to guard against premature damage to the blood barrier on the brain. The Myelin Sheath, an insulator which protects the cells, is under-developed. Any exposure to heavy metals during the first 2 years is deadly and unwise.
Aluminum causes brain swelling and interferes with the immune system directly. The MMR shot, typically given at 12-18 months is overwhelming and many children have suffered irreversible brain damage from its impact. And remember – children have already accumulated metals in the brain from earlier shots, (Hep B, HIB, HBPV, OPV, DPT), so there is a threshold limit.
Vaccines are the main cause of Autism primarily due to accumulative damage from the Hep B, MMR & DPT shots (multiple live viruses + heavy metal build-up) – leading to Ischemia, a singing of the neural pathways from toxic overload which prevents vital oxygen from reaching the brain, literally inhibiting normal development. Anaphylaxis, a system-wide allergic & functional breakdown, and Encephalitis, inflammation of the brain resulting from vaccine derived heavy metal sludge toxicity, inevitably follow.
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.” Vitamin D3 is not strictly a vitamin in the traditional sense. It acts as a steroid type hormone with uniquely beneficial properties; critical to overall respiratory function.
A mother with several Autistic children sent me her own analysis of the overall Autistic condition,
“Vaccines & Antibiotics kill good bacteria in the intestines leaving room for yeast overgrowth. Prolonged root growth perforates the walls of the intestines. Bad food choices, ie. those containing gluten & milk products cause proteins to leak through these holes & attach to the Opiate Receptors in the brain. Children with Autism literally become addicted to this ‘Heroin’.”
ALUMINUM: Currently children are getting 17 shots containing aluminum, a quadrupling of the amount given since the 1970′s. It is found in Hepatitis A, Hepatitis B, DTaP (diphtheria, tetanus, pertussis), MMR, Hib, Pneumococcal & Gardasil (HPV) vaccines.
Based on Dr. David Ayoub’s findings children, on average, receive 2-400 micrograms per vaccine, over a milligram of Aluminum; a concentration & dosage that is 10 – 20 times more toxic than Mercury. Multiple vaccines are far worse, over a 1000 micrograms on average for a triple set shot. Compounding the problem even more aluminum gets in during the manufacturing process. An indicator that the tools and/or machinery used are not properly monitored for safety.
Acute exposure to heavy metals can lead to a host of auto-immune disorders: Downs Syndrome, Autism, Schizophrenia, ALS, Lupus, Parkinson’s & Alzheimer’s Disease, cognitive disfunction.
“Heavy metals & viruses in vaccines cause abnormal development in brain, long-term changes that put a child at high risk of neuro-degenerative diseases ie. Parkinson’s & Alzheimer’s for the rest of their life; also they become hyper-sensitive to environmental toxins (Pesticides, Herbicides). Live viruses in vaccines are incorporated into your genetic material & passed on to your children. Many rare forms of cancer are now very common ie Pancreatic cancer. Lymphoma is now the number one malignancy in 30 year olds and rising. Asthma has seen a ten fold increase over last 2 decades. Type 1 Diabetes has also been linked to auto-immune disorder caused by vaccines.” Dr. Russell Blaylock
Dr. Christopher Shaw, Canada’s leading Neuro-Scientist released a stunning Peer Review Study in 2009 linking Aluminum in Vaccines with motor neuron degeneration found in victims of Amyotrophic Lateral Sclerosis (ALS) & in those of Gulf War Syndrome. It followed another similar groundbreaking study begun in 2007. Dr. Shaw was a keynote speaker for VRM at our September rally & later in November during our Town Hall event. His contributions to the entire subject are vital.
ALUMINUM TOXICITY IN VACCINES ‘Research indicates that patients with impaired kidney function, including premature neonates, who receive injections of Aluminum greater than 4 to 5 micrograms (mcg) per kilogram of body weight per day, accumulate aluminum at levels associated with central nervous system and bone toxicity.’ Food & Drug Administration Report
This means that for a 6 pound baby, 11-14 mcg would be toxic. The Hepatitis B vaccine given at birth contains 250 mcg of aluminum – 20 times higher than safety levels allow. Babies weigh about 12 pounds (5.5 kg) at 2 months of age when they receive 1225 mcg of aluminum from their vaccines – 50 times higher than safety levels.
‘The results for aluminum were almost identical to ethyl mercury (Thimerosal) because the amount of aluminum in vaccines goes almost exactly with the mercury.’ Dr. Tom Verstraeten/Epidemiologist http://www.vacinfo.org/Aluminum%20in%20Vaccines,%20Free%20ebook.pdf
THIMEROSAL (MERCURY): A neurotoxin linked to psychological, neurological & immunological problems. Nervous system damage, kidney disease, birth defects, dental problems, mood swings, mental changes, hallucinations, memory loss, nerve damage and inability to concentrate can occur. Symptoms also include tremors, loss of dermal sensitivity, slurred speech and, in rare cases, even death and paralysis. This additive alone was the catalyst for another recent Class Action Lawsuit organized by mothers of children who “inadvertently” developed Autism & the many related behavioral disorders associated with it. Autism is now occurring at levels never seen before in history, 1 in 67 conservatively. The average used to be 1 in 20,000. Thimerosal Mercury is added to vaccines austensibly to sterilize the giant multi-dose vats containing the serum.
“Mercury, when exposed to normal human brain tissue homogenates, is capable of causing many of the same biochemical aberrancies found in Alzheimer’s diseased (AD) brains. Also, rats exposed to mercury vapor show the same major protein aberrancy as AD brains. Specifically, the rapid inactivation of important brain enzymes occurs following the addition of low levels of mercury or exposure to mercury vapor, and these same enzymes are significantly inhibited in AD brains. Also, mercury exposure to neurons in culture by other researchers, at a concentration lower than that found in many human brains, has now been shown to produce three of the widely accepted pathological diagnostic hallmarks of AD.
First, in human brain samples the exposure to mercury dramatically reduced the viability of a major brain protein called tubulin, but had little if any effect on another major protein, actin. Both tubulin and actin are critically important for the growth of dendrites or maintenance of axon structures of neurons. Exposing neurons to mercury rapidly results in the stripping of tubulin from the axon structure, leaving bare neurofibrils that form the tangles that are the diagnostic hallmark of AD. Thimerosal, like mercury, also rapidly reduces the viability of tubulin; in addition, however, it abolishes the viability of actin. This likely represents a major difference in the mechanism of mercury versus organic-mercury (more neurotoxic) toxicity. However, both mercury and organic-mercury inhibit tubulin viability and would work in concert to damage neurons of the central nervous system.
Using his cultured neuron system, we studied the extent of neurotoxicity of pure thimerosal and of vaccines with and without thimerosal present. The experiments were done as follows: Neurons were grown in culture for 24 hours. Then pure thimerosal or vaccines were added to test cultures. The death of neurons was observed for the next 24 hours and compared to the death of neurons in the absence of toxicant.
The results were almost identical to the results observed with brain tissues: vaccines with thimerosal present were much more toxic than thimerosal-free vaccines. Pure thimerosal was toxic at the low nanomolar level–an extremely low concentration, about 10,000 times less than the thimerosal concentration found in most vaccines. These results leave little doubt about thimerosal being the toxic agent in the vaccines. However, many vaccines contain aluminum ions that have neurotoxic properties, and aluminum was once considered a factor in AD etiology. So we tested aluminum in the same system.
Aluminum is not nearly as toxic to neurons in culture as is thimerosal. However, we had earlier observed with mercury that the presence of other metals would enhance toxicity. Experiments were done to determine if aluminum would increase the toxicity of very low levels of thimerosal. The results were unequivocal: the presence of aluminum dramatically increased the rate of neuronal death caused by thimerosal. Therefore, the aluminum and thimerosal combination found in vaccines produces a toxic mixture that cannot be compared to situations where thimerosal alone is the toxic exposure.” Dr. Boyd E. Haley http://mothering.com/print/2736
DAVID AYOUB M.D.- Mercury and Autism 1 of 10
“Ethyl Mercury: Organic mercury attached to short carbon chain, converts to inorganic mercury quicker than Methyl Mercury – in about 7 days. Once entered into the brain it becomes trapped. The timing makes the poison. Thimerosal in vaccines: 0.01% = 50,000 micrograms/litre (50% mercury content, 250 times higher than the EPA safe limit). Amount of Hazardous wastein vaccines: 25,000 times higher than EPA safe limit (200 parts per billion = hazardous waste. Drinking water: 2.5 billion parts per billion = toxic waste).”
“One nanomolar levels ‘of Thimerosal’ in the baby will prevent the macrophages from going through phagocytosis (vaccines using Thimerosal as a preservative contain 125,000 nanomolar level of mercury). In other words, they will lose their ability to eat viruses and bacteria that are in the blood that shouldn’t be there, and so Thimerosal suppresses the immune system. This is well known and has been well described in the literature for a long time; that mercury is an immune system suppressor and you see that these autistic children have a truckload of immune problems. So you would prevent that from occurring. That is documented research and I don’t know how the government can even ignore it, or the agencies of the government can ignore it.” Dr. Boyd Hayley
‘Mercury is known to be neurotoxic and has effects on the immune system as well. Mast cells are involved in allergic reactions, and also in inflammation, and innate and acquired immunity. Autistic individuals have a 10-fold greater number of hyperactive mast cells in most tissues. Mercury stimulates vascular endothelial growth factor and interleukin (IL)-6 release from mast cells. These mediators could disrupt the blood–brain barrier and cause brain inflammation (Kempuraj et al., 2010)’ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850891/
‘Theoretical aspects of autism: Causes—A review’ by Helen V. Ratajczak http://www.soundchoice.org/Images/Immunotoxicology_Ratajczak_2011_Review.pdf
Mike Wagnitz, PhD. discusses levels and types of mercury toxicity in vaccines. http://www.autismmedia.org/wagnitz1f.html
MERCURY-AUTISM STUDY 2008: Emerging evidence supports the theory that some autism spectrum disorders (ASDs) may result from a combination of genetic/biochemical susceptibility, specifically a reduced ability to excrete mercury (Hg), and exposure to Hg at critical developmental periods. Elemental/inorganic Hg is released into the air/water where it becomes methylated and accumulates in animal tissues. The overwhelming preponderance of the evidence favours acceptance that Hg exposure is capable of causing some ASDs.
Studies have shown that mercury is taken up in the periphery by all nerve endings and rapidly transported inside the axon of the nerves (axonal transport) to the spinal cord & brainstem. Unless actively removed, mercury has an extremely long half-life of somewhere between 15 and 30 years in the central nervous system. Hair analysis showed mercury levels to be 20,000 higher in those with cardiac abnormalities.
“The search for the association between mercury and cardiovascular disease reveals 358 scientific papers exemplifying the relationship; between mercury & cancer we find 643 scientific papers. The association of mercury with neuro-degenerative diseases is the most significant, with the references numbering 1,445.
It has been shown that mercury rapidly depletes the immune system. Mercury has also been shown to induce auto-immune diseases. Anything that depletes and disturbs the immune system will increase one’s chances of contracting cancer. Mercury binds with hemoglobin, which is responsible for oxygen transport to the tissues. This results in less oxygen reaching the tissues when the body is polluted with mercury. We don’t have to look far in understanding how a heavy metal like mercury can eventually lead one to cancer’s door.” Dr. Rashid Buttar/Center for Advanced Medicine & Clinical Research http://winningcancer.com/index.php/2010/03/heavy-metals-mercury-and-cancer/#arrive
‘Cadmium & mercury deplete selenium in the body (essential for their removal). Selenium atoms combine with cadmium & mercury atoms and escort them out of the body via the bile system. When selenium is depleted by cadmium and/or mercury, there is less selenium to form the deiodinase enzymes that convert T4 to T3, resulting in low T3 and hypothyroidism. Also there is less selenium to form glutathione peroxidase, one of the body’s prime antioxidants.’
‘Melatonin is known to bind heavy metals (Limson et al., 1998REF15) and to increase intracellular GSH levels through an up-regulation of GSH-synthesizing enzymes (Todoroki et al., 1998REF3). It is thus possible to speculate on two mechanisms for melatonin’s antioxidant action, namely, (a) melatonin as a chelating agent binding mercury, thus eliminating its cytotoxic properties, or (b) melatonin causing production of increased levels of intracellular antioxidants such as glutathione (Todoroki et al., 1998REF30). It is not excluded that both these mechanisms could be operating simultaneously. mercury as an inducer of oxidative stress, and the resultant effect on ß-Amyloid (Aß) production and phosphorylated tau levels in neuroblastoma cells. Furthermore, we demonstrated that these effects are reduced and/or reversed by the pineal indoleamine melatonin.’
Pregnant women are at a heightened risk of adverse reactions to vaccines. Thimerosal Mercury is added to the H1N1 series ostensibly to sterilize the giant multi-dose vats containing the serum. Mercury is such a fine neuro-toxin it gets absorbed into the Placenta thereby exposing the fetus, regardless of which trimester, to the potential of serious trauma & long-term side effects including asthma, allergies, chronic fatigue, autism, schizophrenia; unfortunately in certain cases, even death.
‘Injecting mercury into pregnant women and children is absurd. Examine studies which suggest otherwise, and you will find the funding for the study came from those who directly or indirectly profit from, or fear liability from, the use of mercury-containing vaccines.’ CoMed Inc, 09/15/2010
‘Studies of the organs and tissues of the first generation progeny revealed mercury in the stomach and intestine at birth and in the first week of life, apparently on account of the entry of mercury through the placental barrier and by way of their mother’s milk. Subsequently, it was noted that the first-generation progeny of mothers that had been previously exposed to the ethyl mercury compound had significantly reduced fertility in comparison to controls. The second generation progeny had low viability, lagged in their weight growth, and were retarded with respect to ossification in several cases. Finally, it was then observed when mating the second generation progeny that there was a significant decrease in fertility in comparison to the control group.’ David A. Geier/The Institute of Chronic Illnesses, Inc., Lisa K. Sykes/CoMeD, Inc., Mark R. Geier/The Genetic Centers of America, Silver Spring, Maryland, USA – Journal of Toxicology and Environmental Health, Part B, 10:575–596, 2007
The trivalent influenza vaccine contains 3 sets of either ‘killed’ or ‘heat-treated DNA/RNA strands, ostensibly a safe variant blueprint of the live virus itself. Adjuvants are designed to jump-start or supercharge the immune system – to induce a robust immune response; thus immunizing the body against the likelihood of succumbing to the flu while avoiding the direct spread of infection. In truth no virus is fully killed during the vaccine manufacturing process. Typically the vaccinee is left more susceptible to catching the seasonal flu (twice a likely to catch swine flu). Depending on the degree of compromised immune system &/or pre-existing medical condition involved, a vaccine induced Cytokine Storm can rapidly trigger complete auto-immune failure throughout the individual’s body.
‘A cytokine storm is the systemic expression of a healthy and vigorous immune system resulting in the release of more than 150 inflammatory mediators (cytokines, oxygen free radicals, and coagulation factors). Both pro-inflammatory cytokines (such as Tumor Necrosis Factor-alpha, InterLeukin-1 & InterLeukin-6) and anti-inflammatory cytokines (such as interleukin 10, and interleukin 1 receptor antagonist) are elevated in the serum, and the fierce and often lethal interplay of these cytokines is referred to as a “Cytokine Storm”.
The primary contributors to the cytokine storm are TNF-a (Tumor Necrosis Factor-alpha) and IL-6 (Interleukin-6). The cytokine storm is an inappropriate (exaggerated) immune response that is caused by rapidly proliferating and highly activated T-cells or natural killer (NK) cells. These cells are themselves activated by infected macrophages. The cytokine storm must be treated and suppressed or lethality can result.’ http://www.cytokinestorm.com/
Manifestations of a vaccine triggered Cytokine Storm can range from high fever & extreme vomiting to Bronchitis, Hemorrhagic fever (drowning of lungs with fluid), Anaphylaxis (severe allergic reaction), Guillain–Barré syndrome (form of paralysis), Encephalitis (brain inflammation), Acute Respiratory Distress Syndrome, Sepsis (overwhelming immune response/inflammation/organ failure linked to bacterial infection), Bacterial Pneumonia, Febrile Convulsions, Sub-Clinical Epileptic Seizures, Grand Mal Epileptic Seizures, Narcolepsy, organ failure, blindness, coma & death.
Note: an overabundance of T-Cells, Microphages & oxygen free radicals flood the body – attacking the lungs, kidneys, liver, brain, impeding Endocrine, Lymphatic, Immune & Nervous system function.
‘The flu virus causes immune cells to produce cytokine molecules that increase inflammation. Normally this is controlled, but in extreme cases, a “cytokine storm” occurs. This can cause tissue and organ damage, and even death. When you’re fighting the flu, you feel bad not because of the virus but rather because of the “cytokine storm.” But get this: All vaccines trigger their own cytokine storms. And researchers now know that increased inflammation is at the heart of most illness and disease. Which means the vaccines themselves are hazardous to your health. The solution is to avoid flu shots, and if you’ve had them in the past, to take nutrients that will strengthen your immune system and reduce inflammatory cytokine activity.’ Dr. Russell Blaylock http://w3.newsmax.com/blaylock/62b.cfm
Babies as young as 6 months old are now routinely being inoculated for influenza at 6 months; a drastic intervention in early development; by the Medical purveyors’ own admittance, one intended to boost general rates for vaccine uptake. The strategy seems to be in provoking a wider swath of vaccine uptake, thus inevitably opening the floodgates to a greater exposure of the herd.
“We hope that the new recommendations promulgated by the Advisory Committee on Immunization Practices (ACIP) will help. Rather than focus on “high-risk groups,” as has been done in the past, the ACIP now recommends annual influenza vaccination for everyone 6 months of age or older.” http://www.nejm.org/doi/full/10.1056/NEJMp1012333
‘Influenza vaccine (seasonal). (Minimum age: 6 months for trivalent inactivated influenza vaccine [TIV]; 2 years for live, attenuated influenza vaccine [LAIV]) • Administer annually to children aged 6 months through 18 years.’ CDC Standard Immunization Schedule age 0-6 yrs http://www.cdc.gov/vaccines/recs/schedules/downloads/child/2010/10_0-6yrs-schedule-pr.pdf
“But from all of the other studies of toxic substances, the earlier you work with the central nervous system, the more likely you are to run into a sensitive period for one of these effects, so that moving from one month or one day of birth to six months of birth changes enormously the potential for toxicity. There are just a host of neuro-developmental data that would suggest that we’ve got a serious problem. The earlier we go, the more serious the problem.” Dr. Weil, CDC closed door meeting, 2000
In 2 recent landmark Canadian Studies researchers found that seasonal flu vaccination was associated with a 68 percent increased risk of getting swine flu. ‘Estimates from sentinel & 3 other observational studies, involving a total of 1,226 laboratory-confirmed pH1N1 cases and 1,505 controls, indicated that prior receipt of 2008–09 TIV (trivalent inactivated influenza vaccine aka regular flu shot) was associated with increased risk of medically attended pH1N1 illness during spring–summer 2009′ http://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1000258
MUTABILITY OF VIRUSES “Because the influenza virus genome is segmented, co-infection of a single host cell with two or more different influenza viruses can result in a re-assortment (or shuffle) of their genetic material. The antigenic shift can lead to a pandemic if the resulting progeny virus contains an HA protein (clumping of Glycoprotein red blood cells) to which humans have no preexisting immunity, if it has an efficient replication-competent set of internal genes, and if it can readily spread from human to human.” Dr. Antony Fauci, director of the National Institute of Allergy & Infectious Diseases
Early onset autism occurs anywhere from 12-18 months, potentially even earlier. It is significant that autism coincides precisely with most intense period of standard immunization. According to the CDC’S ‘Recommended Immunization Schedule for Persons Aged 0 Through 6 Years—United States • 2010′ by 15 months the average child has received 25 injections including: 3 doses of Hepatitis B, Rotavirus, HIB (Haemophilus Influenzae Type b), IPV (Inactivated Polio Vaccine) & Hepatitis A, 4 doses of DPT (Diphtheria, Pertussis, Tetanus) & PCV (Pneumococcal Conjugate Vaccine), 1 dose of Varicella & Meningococcal and 2 doses of MMR (Measles, Mumps, Rubella).
GIRLS 4 TIMES LESS PRONE TO AUTISM. POTENTIAL REASONS: Girls are developmentally ahead of boys early in life (undoubtedly a species survival mechanism). The female Myelin Shealth & blood-brain barrier may also be stronger. The connective tissue that allows communication between the two hemispheres of the brain tends to be thicker. Estrogen is also believed to decrease Thimerosal’s toxic affects; versus testosterone which greatly increases the toxicity. Autism symptoms appears at 12-15 months, precisely when the MMR vaccine is administered.
X & Y CHROMOSOME: ‘Every DNA molecules is composed of two strands. When a cell detects a DNA duplex with a difference between its two DNA strands, that duplex is “repaired” by the rather Draconian expedient of chopping out the entire region, on both strands of the DNA molecule. No effort is made by the cell to determine which strand is correct — both are discarded. The gap that this creates is filled by copying off the sequence present at that region on the other chromosome. All this editing happens when the two versions of the chromosome are paired closely together in the early stages of gamete (egg and sperm) formation, the process we biologists call meiosis.
All females have two copies of the “so-called” X chromosome. The X chromosome is about the same size as other 22 human chromosomes, which also occur in pairs, and like them is packed with some 1000 genes. The reason there are two copies of the X and other chromosome is to allow for the repair of the inevitable damage that occurs over time to individual genes because of wear-and-tear, chemical damage, and mistakes in copying. Because this sort of damage is passed on to offspring, it tends to accumulate over time. For this reason, genes must be edited every so often to repair the accumulated mutations (biologists call damage to genes mutation).
Males, by contrast to females, have only one copy of this X chromosome, not two. The other chromosome of the pair in males is called the Y chromosome and is much smaller than the X. Biologists thought until very recently that the Y chromosome had only a few active genes. Because there is no other Y to serve as a pairing partner in meiosis, most of its genes had been thought to have decayed, the victims of Muller’s ratchet, leaving the Y chromosome a genetic wasteland with only a very few active genes surviving on it.’ http://www.txtwriter.com/Onscience/Articles/ychromosome.htm
“Experiments using this system have also demonstrated, in agreement with published literature, that many antibiotics, other heavy metals and chemicals increase the toxicity of mercury and thimerosal (ethyl mercury). Additionally, in this same system the female hormone estrogen decreases thimerosal’s toxic effects. In contrast, the male hormone testosterone greatly increases the toxicity. This may explain the 4 to 1 ratio of boys to girls that become autistic and the observation that boys represent the vast majority of the severe cases of autism.” Boyd Haley, Ph.D. (Testimony Before the House Government Reform Committee)
“One of the conundrums of autism is why there is an approximate ratio of four boys to every girl who gets this disease. Dr. Lovell therefore tested the possibility that this could be hormone related. The latest results were quite marked in their effects. Neurons that were pre-incubated with estrogen demonstrated substantial protection against thimerosal-induced neuron death. In contrast, the addition of testosterone caused a very large increase in thimerosal-induced neuron death. A low nanomolar level of thimerosal that gave less than 5 percent neuron death in three hours could be increased to 100 percent cell death by the addition of one micromolar level of testosterone. Testosterone alone at this level also showed less than 5 percent cell death. The opposing effects of estrogen and testosterone may explain the gender-based four-to-one ratio.” Dr. Boyd E. Haley
AUTISM RATE NOW AT 1 IN 50 (1 IN 38 FOR BOYS): Far more children have autism than previously thought, a study of British school pupils has found. Researchers now believe as many as one in 60 children has some form of the condition. The disturbing findings, which are due to be made public within weeks, mean that up to 216,000 children in the UK could suffer from an autistic condition, although many have not yet been diagnosed. http://www.dailymail.co.uk/news/article-1163606/One-child-60-suffers-form-autism.html
AMISH COMMUNITY: NO VACCINATIONS = NO AUTISM – Despite relentless efforts by the Medical Establishment to suggest Autism occurs amongst the non-vaccinated Amish (1 in 10,000 claim) there are in fact no proven cases to show for it – “Unfortunately our autistic daughter — who’s doing very well, she’s been diagnosed with very, very severe autism — is adopted from China, and so she would have had all her vaccines in China before we got her, and then she had most of her vaccines given to her in the United States before we got her.” http://www.whale.to/vaccine/olmsted.html http://imfar.confex.com/imfar/2010/webprogram/Paper7336.html
NEW PEER REVIEWED STUDY CONFIRMS DIRECT VACCINE-AUTISM LINK: ‘The incidence/prevalence of data indicate the timing of introduction of vaccines & changes in the type & increasing number of vaccines given at one time implicate vaccines as a cause of autism. The MMR II vaccine is contaminated with human DNA from the cell line. This human DNA could be the cause of the spikes in incidence.’ Journal of Immunotoxicology
Journal of Immunotoxicology, 2011; 8(1): see pages 68–79 http://www.rescuepost.com/files/theoretical-aspects-of-autism-causes-a-review1.pdf
New Medical Journal Review: Vaccine Injury is a Documented Cause of Autism http://www.ageofautism.com/2011/02/new-medical-journal-review-vaccine-injury-is-a-documented-cause-of-autism.html
40% of children with Autism wait 3 years for a diagnosis. 25% of them are excluded from schools.
“Autism was not a known, described illness until about 1941-3, 8 to 10 years after the introduction of thimerosal and similar organicthiol-mercury compounds in biological mixtures used in medicine and other areas. This argues against autism being a genetic illness. The study of non-vaccinated populations is a very obvious experiment that the CDC and its supporters refuse to consider.” Dr. Boyd Hayley
‘The number of vaccines given before age two has risen from 3 in 1940, when autism occurred in perhaps one case per 10,000 births, to 22 different vaccines given before the age of two in the year 2000.’ Building Wellness with DMG by Roger V Kendall PhD p.104
INCIDENCE OF AUTISM IS EXPLODING EXPONENTIALLY: ‘The incidence and prevalence of autism have dramatically increased over the last 20 years. Decomposition of autism incidence rates into age, period and cohort effects disentangle underlying domains of causal factors linked to time trends. We estimate an age-period-cohort effect model for autism diagnostic incidence overall and by level of functioning…Compared with those born in 1992, each successively younger cohort (generational group as defined in demographics) has significantly higher odds of an autism diagnosis than the previous cohort, controlling for age and period effects. For example, individuals born in 2003 have 16.6 times the odds of an autism diagnosis compared with those born in 1992 [95% confidence interval (CI) 7.8-35.3]. The cohort effect observed in these data is stronger for high than for low-functioning children with an autism diagnosis.’ Keyes KM, Susser E, Cheslack-Postava K, Fountain C, Liu K, Bearman PS/Department of Epidemiology, Columbia University, New York, NY, USA, New York State Psychiatric Institute, New York, NY, USA & Paul F. Lazarsfeld Center for the Social Sciences, Columbia University, New York, NY, USA. http://www.ncbi.nlm.nih.gov/pubmed/22253308
Note: ‘Each successively younger cohort (generational group as defined in demographics) has significantly higher odds of an autism diagnosis than the previous cohort, controlling for age and period effects. For example, individuals born in 2003 have 16.6 times the odds of an autism diagnosis compared with those born in 1992.’
Common deficiencies amongst children with Autism frequently include:
1. Vitamin A
2. Vitamin B6/B12
3. Vitamin C
4. Vitamin D3
5. Vitamin E
10. 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.
f. 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.
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/Autistic 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). This causes a chain reaction which triggers liver damage, diabetes, cancer & in the long term, heart failure. Heavy metals rapidly deplete Selenium in the body.
‘In this metallomics analysis study, we have determined human scalp hair concentrations of 26 trace elements for 1,967 children with autistic disorders aged 0–15 years and showed that many of the patients, especially in infants aged 0–3 year-old, are suffering from marginal to severe zinc- and magnesium-deficiency and/or high burdens of several toxic metals such as aluminium, cadmium and lead. These findings suggest that there is a critical term “infantile window” in neurodevelopment and probable for therapy of autistic disorders.‘ Estimation of autistic children by metallomics analysis – Hiroshi Yasuda, Masahiro Kobayashi, Yuichi Yasuda & Toyoharu Tsutsui, 02/04/2013
Mitochondria are the battery pack of your cells which determine your body’s inherent ability to function efficiently, without which none of these connections are possible. Anti-mitochondrial antibodies are elevated in children with Autism; a process which suffocates Eukaryotic cells (complex structures enclosed within membranes). Vaccine derived heavy metal-antibiotic-detergent-virus sludge targets the Mitochondria while neutralizing major anti-oxidants in the body, causing Ischemia. “Primordial eukaryotic cells lacked ability to use oxygen” – excerpt/Autistic case file.
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.
Unlocking the keys to natural immunity requires a holistic approach to the complex functioning of the body. Every major organ & gland are entirely interdependent, a magnificently delicate apparatus of interconnections, without any one of which, the entire system of operations will inevitably fail, leading to a chain-reaction of adverse metabolic breakdown & compromised immunity. Case in point, the Liver converts Vitamin D3 (cholecalciferol) into Calcidiol (25-hydroxycholecalciferol – aids in prevention of chronic Liver disease, Thyroid disorders, Diabetes, Cancer), from which the kidneys generate Calcitriol (active form of Vitamin D designed to increase calcium levels in the body in order to treat skeletal and tissue-related calcium deficiencies caused by kidney or thyroid disorders).
‘The liver and kidney have important enzymes that change vitamin D from the sun or food to the biologically active form of vitamin D. People with chronic kidney and liver disease are at increased risk of low vitamin D because they lack these enzymes.’
‘Calcitriol (1,25-dihydroxyvitamin D or 1,25(OH)2D3): Calcitriol is made from calcidiol, in the kidneys as well as in other organs, and is the most potent steroid hormone in the human body. Referred to as “activated vitamin D,” calcitriol is said by the experts to “unlock” a cell’s DNA library. Acting through the vitamin D receptors (VDR), calcitriol controls the expression of genes, activating about two-thirds of the ones it controls, suppressing the rest.’ Vitamin D Council
‘Once out of the lysosome (the cells’ garbage disposal system – degrades the products of ingestion & worn out organelles such as mitochondria, handles the products of receptor-mediated endocytosis such as the receptor, ligand and associated membrane) , calcidiol binds to intracellular vitamin D binding protein (IDBP) which facilitates the localization of vitamin D metabolites in the cell.’
‘The liver plays a unique role in controlling carbohydrate metabolism by maintaining glucose concentrations in a normal range over both short and long periods of times. In type 2 diabetes, alterations in hepatic glucose metabolism are observed, i.e. increased postabsorptive glucose production and impaired suppression of glucose production together with diminished glucose uptake following carbohydrate ingestion. The simultaneous overproduction of glucose and fatty acids in liver further stimulates the secretion of insulin by the pancreatic cells, and elicits further peripheral insulin resistance thereby establishing a vicious circle.’ C Postic, R Dentin, J Girard
’Low vitamin D levels and bone disease are well-recognized complications of “cholestatic” liver disease, which decreases the production or flow of bile. More recently, studies have confirmed low vitamin D levels in noncholestatic liver disease.‘ Satheesh Nair, MD, FACP
‘VDBP (vitamin D-binding protein/Gc-globulin) is converted to macrophage-activating factor by the action of either b-galactosidase from B lymphocytes or sialidase from T lymphocytes on carbohydrate side chains of the protein…VDBP-binding sites are upregulated on activated neutrophils (’plays an important role in the inflammatory response to Gram-negative bacterial infections‘), suggesting that changes in its circulating concentration might occur in inflammatory conditions. Consistent with this, in vitro work has shown that GC transcription is enhanced by proinflammatory cytokines (those which make disease worse).’ British Medical Journal
‘Recent Kidney Disease Outcomes Quality Initiative guidelines have raised concerns of 25-hydroxyvitamin D, or calcidiol, insufficiency and deficiency in patients with chronic kidney disease (CKD) not yet on dialysis therapy…a high prevalence of calcidiol deficiency and insufficiency in patients with moderate and severe CKD not on dialysis therapy regardless of geographic location.‘ Department of Medicine, Indiana University School of Medicine, Indianapolis, IN
The Lymphocytes in your lungs also depend on Vitamin D3 (steroid hormone known as “cholecalciferol” derived primarily from direct exposure to sunlight & via fatty fish, egg yolks, and dairy products) in order to process Vitamins C & E, while regulating proinflammatory cytokines (those which make disease worse); thus staving off infections, ie. colds, influenza, asthma, bronchitis, pneumonia.
‘Vitamin D’s metabolic product, 1,25-dihydroxyvitamin D (calcitriol), is actually a secosteroid hormone that is the key which unlocks binding sites on the human genome. The human genome contains more than 2,700 binding sites for calcitriol; those binding sites are near genes involved in virtually every known major disease of humans’.…’The liver converts vitamin D3 (cholecalciferol) to calcidiol…those with CLD ( chronic liver disease) have reduced vitamin D blood levels because the liver’s ability to convert vitamin D3 (cholecalciferol) to circulating vitamin D (calcidiol) is reduced…risk of bone diseases such as osteoporosis which often accompanies chronic liver disease because of the liver’s reduced function.’
Systemic Intracellular Bacterial Infections (Mycoplasma, Chlamydia, Borrelia species) in Neurodegenerative (MS, ALS) and Behavioral Disorders (ASD): ‘Patients with neurodegenerative & behavioral disorders (ie. Autism Spectrum Disorder) often have systemic bacterial, viral and/or fungal infections that may play an important role in their pathogenesis…evidence for systemic intracellular bacterial and viral infections in a majority of patients. For example, examination of blood leukocytes for evidence of ‘Mycolplasma spp.’, ‘Chlamydia Pneumonia’, ‘Borrelia Burgdorferi’ and other infections on the polymerase chain reaction revealed high incidences of systemic co-infections…most common co-infection found was ‘Mycoplasma’ species. The results suggest chronic intracellular bacterial infections are common features of neuro-degenerative and behavioral disorders.’ Garth L. Nicholson, Institute for Molecular Medicine
Note: ‘Commercial vaccines have been examined containing microorganism, and one study found that approximately 6% of commercial vaccines were contaminated with Mycoplasmas.’ http://www.immed.org/NeuroDiseases/SIBI.Myco.Clam.Borr.NeuroMS.ALS.BhavDis.pdf
Mycoplasma: ‘A genus of aerobic to facultatively anaerobic bacteria (family Mycoplasmataceae) containing gram-negative cells that do not possess a true cell wall but are bounded by a three-layered membrane; they do not revert to bacteria-containing cell walls or cell wall fragments. The minimal reproductive units of these organisms are 0.2–0.3 mcm in diameter. The cells are pleomorphic, and in liquid media appear as coccoid bodies, rings, or filaments. Colonies of most species consist of a central core, growing down into the medium, surrounded by superficial peripheral growth. They require sterol for growth. They also require enrichment with serum or ascitic fluid. These organisms are found in humans and other animals and can be pathogenic. The type species is Mycoplasma mycoides.’ http://www.medilexicon.com/medicaldictionary.php?t=58173
Note 1: Mycoplasma are inherently resistant to a vast majority of antibiotics on the market. Children coping with Autism already have a compromised immune system, made worse by the presence of Mycoplasma bacteria in the gut. And remember, vaccines & antibiotics kill good bacteria in the intestines leaving room for yeast overgrowth. Prolonged root growth perforates the walls of the intestines – a critical determinate in all cases of Autism.
Note 2: Children coping with Autism suffer from systemic bacterial (Mycoplasma series), viral (vaccine derived live viruses &/or attenuated strands of DNA/RNA material) and/or fungal infections (yeast overgrowth caused by prolonged use of vaccines & antibiotics) in the gut. Mycoplasma require sterol (cholesterol) for growth & enrichment with ascitic fluid (accumulation of fluid in the abdomen…may be a direct result of a malignant process or secondary to an unrelated comorbidity’).
‘Mycoplasmas are the smallest free-living microorganisms, being about 300 nm in diameter. They are bounded by a triple-layered membrane and, unlike conventional bacteria, do not have a rigid cell wall. Hence, they are not susceptible to penicillins and other antibiotics that act on this structure. They are, however, susceptible to a variety of other broad-spectrum antibiotics, most of which only inhibit their multiplication and do not kill them. The tetracyclines have always been in the forefront of antibiotic usage, particularly for genital tract infections, but macrolides are also widely used for respiratory tract infections.
Apart from the penicillins, mycoplasmas are innately resistant to some other antibiotics, for example the rifampicins. In addition, some may develop resistance, either by gene mutation or by acquisition of a resistance gene, to antibiotics to which they are usually sensitive. Resistance of mycoplasmas to tetracyclines is common and due to acquisition of the tetM gene. The antibiotic susceptibility pattern may be influenced greatly by the source of the mycoplasma; for example, one recovered from a contaminated eukaryotic cell culture that has been subjected to extensive antibiotic treatment may have an antibiotic profile quite different from the same mycoplasmal species that has been recovered directly from a human or animal source. Mycoplasmas may be difficult to eradicate from human or animal hosts or from cell cultures by antibiotic treatment because of resistance to the antibiotic, or because it lacks cidal activity, or because there is invasion of eukaryotic cells by some mycoplasmas. Eradication may be particularly difficult in immunosuppressed or immunodeficient individuals, particularly those who are hypogammaglobulinaemic. The regimes that are most likely to be effective in the treatment of respiratory or genitourinary mycoplasmal infections are presented.’ http://jac.oxfordjournals.org/content/40/5/622.abstract
ANOTHER SIDE EFFECT OF ANTI-PSYCHOTIC DRUGS (TYPICALLY PRESCRIBED TO CHILDREN WITH SEVERE AUTISM): ‘Tardive dyskinesia is characterized by repetitive, involuntary, purposeless movements. Features of the disorder may include grimacing, tongue protrusion, lip smacking, puckering & pursing, rapid eye blinking. Rapid movements of the arms, legs, trunk may also occur.’
TARDIVE DYSKINESIA & AUTISM: ‘Stereotypies and tardive dyskinesia: Abnormal movements in autistic children – Baseline stereotypic movements in 224 autistic children were studied as well as their relationship to certain demographic variables and measures of overall symptomatology and severity of illness. Prediction of haloperidol-related (Anti-psychotic drug) dyskinesias with measures of stereotypies and demographic variables was also attempted. Stereotypies were present in at least mild form in most children, with most showing moderate severity. Most stereotypies were in the orofacial area. I.Q. was found to be negatively related to stereotypies. Furthermore, across methods of assessment, severity and frequency of stereotypies were found to be positively related to overall symptomatology and severity of illness. No significant predictors of development of dyskinesias were found.’ http://www.ncbi.nlm.nih.gov/pubmed/2236468
MAYO CLINIC ON AUTISM MANAGEMENT: ‘No medication can improve the core signs of autism, but certain medications can help control symptoms. Antidepressants may be prescribed for anxiety, for example, and antipsychotic drugs are sometimes used to treat severe behavioral problems.’ http://www.mayoclinic.com/health/autism/DS00348/DSECTION=treatments-and-drugs
Note: Genetics play a significant (but not central) role in determining the early onset Autism & other conditions so prevalent today. Our parents & their parents before them suffered chronic long term exposure to heavy metals & live viruses via similar mass vaccination programs given in their era. The Salk/Sabin Polio shot passed on inter-generational viruses & cancers: “Post-Polio Syndrome”, “Chronic Fatigue Syndrome”, “Myalgic Encephalomyelitis” & “Cerebral Palsy” (known as “Aseptic/Viral Meningitis”). This generational aspect of mineral depletion, which is passed on via the placenta & colostrum, strips a baby of its most vital guard during the earliest, critical stages of development.
As children we inherit a varyingly compromised system based on this legacy. It’s Russian Roulette. Your immune system enters this world with a certain vulnerability. The tipping point comes sooner for some than others.
Further what is categorized as SIDS or Sudden Infant Death Syndrome has nothing to do with bad parenting ie. shaking your baby too aggressively. The child is in agony due to massive brain swelling.
Parents who have been maligned unfairly should take courage from this knowledge.
“Some vaccines, including the MMR, smallpox, and chickenpox vaccines, contain live viruses. By giving three and sometimes four live viruses together, the risk of developing a lifetime viral infection (a persistent viral infection) increases tremendously. This is especially so with the MMR vaccine, which contains two live viruses known to suppress the immune system for months.” Dr.Russell L. Blaylock M.D.
“Cancer was practically unknown until compulsory vaccination with cowpox vaccine began to be introduced. I have had to deal with at least two hundred cases of cancer, and I never saw a case of cancer in an unvaccinated person.” Dr. W.B. Clark of Indiana/1936
Graphic video – live virus shedding from MMR shot given to her child spreads to mother triggering Acute Disseminated Encephalomyelitis (ADEM) & eventual Multiple Sclerosis (MS) http://www.youtube.com/watch?v=PIXluhu4AoU
Vaccine related injuries: Short list of Auto-Immune Diseases/Disorders include –
1) Chronic Fatigue Immune Dis-function 2) Fibromyalgia 3) Lupus 4) Multiple Sclerosis 5) Amyotrophic Lateral Sclerosis (Lou Gehrig’s Disease) 6) Rheumatoid Arthritis 7) Adult & Juvenal Type 1 Diabetes 8) Crohn’s Disease & Colitis 9) Guillaine-Barre Syndrome 10) Bells Palsy 11) Stevens-Johnson Syndrome
Vaccine related Injuries: Childhood afflictions include –
1) Chronic Draining Ear Infections 2) 600% increase In Autism 3) ADHD 4) Asthma 5) Hay-fever 6) Chronic Allergies
Vaccine related injuries: Cancers include –
Pancreatic cancer, Mesothelioma (fatal tumor of the membrane surrounding the lungs), Brain cancers (Primarily Ependymomas & Choroid Plexus Tumors, Astrocytomas, Glioblastomas, Medulloblastoma, Meningiomas), Bone cancers (Primarily Osteosarcomas, Chondrosarcoma & Giant Cell Tumors), Post-Polio Syndrome, Myalgic Encephalomyelitis, Aseptic Meningitis & Non-Hodgkin Lymphoma.
Note: These Cancer Epidemics were never seen before or very rarely before 50-60 years ago.
LUPUS: Detox Treatment Leading To Cure – “I took water from the well plus salt from the Himalayas, added organic superfood, injections of high dosage of vitamin B12 and C, detox meds (German branch mane = To-Ex), Methionine and tried to take care of the amount of acids in my system, got my mercury and gold teeth fillings removed, algae, DHEA, Bach Flower Remedies etc. What helped most was organic superfood such as “ALEN” from Ecuador” VRM Member
Note 1: Acute exposure to heavy metals can lead to a host of auto-immune disorders including Autism, Schizophrenia, ALS, Lupus, Parkinson’s & Alzheimer’s Disease & cognitive disfunction. Lupus is now recognized as an auto-immune disorder triggered primarily by vaccine trauma & related environmental factors. This testimonial is chock full of sensible health choices. Himalayan Salt contains Iodine in proportional trace amounts with other 70 + trace minerals. Iodine helps regulate metabolism in the body. Vitamin B12 stimulates Melatonin in the body, critical to maintaining the immune system. Vitamin C further empowers this system. CQ10 (Co-enzyme q10) is an enzyme produced in the Liver which regulates vitamin C & E & fights Free Radicals, helping to restore energy balance in the body by repairing damage done to the Mitochondria. Algae contain high concentrations of Iodine (0.5–8.0 mg/gm); which fights cancer. Bach Flower Remedies are a powerful source of anti-oxidants.Methionine is a sulfur-containing proteinogenic amino acid vital in the function of metabolism, the prevention of cardiovascular disease, as well as liver (detoxifier) & cognitive function. A significant correlation has been found between risk of Alzheimer’s disease and high plasma levels of homocysteine (due to a lack of re-methylation cofactors), as well as low levels of folic acid, vitamins B6 & B12 An example here of nature working for you, not against you; which unfortunately results when we rely on Western Medicine for solutions.
Note 2: Even if you’ve already received numerous vaccines you can still purge a lot of the damage done. Start with Vitamin D3, Niacin, Omega 3 Fatty Acids, Selenium, Vitamin C, Colloidal Silver, Oil of Oregano, Coconut Oil, Noni Juice, Magnesium, Zinc, Curcumin, Spirulena, Activated Charcoal, Chlorella, Zeolite Powder & Cilantro (last 4 absorb heavy metals accumulated in the body).
“Heavy-metal overloads can effectively be treated using oral supplements of zinc, manganese, cysteine, serine, and vitamins B6, C, and E. The initial treatment must be gradual to avoid a sudden dumping of metal toxics from tissues, which could cause kidney damage and a worsening of symptoms.” Dr. Wm. Walsh.
I would also recommend adding organic Kale, Celery & Beets, Red Grapes with seeds & Apples (both eaten whole) to your diet. A daily swig of Organic Apple Cider Vinegar is also vital to help restore the Alkaline balance in your body. This list is really just a primer for total health regeneration. There are more steps to take but this is the road that will ultimately begin the natural process; a gathering of all the material I’ve found useful along the way gleaned from multiple sources. Find creative ways to add it to your regime. You can do this. Time to be proactive!!!
See original here: http://vaccineresistancemovement.org/?p=488