"It is very possible that PATERNAL AGE is the major predictor of(non-familial) autism." Harry Fisch, M.D., author "The Male Biological Clock". Sperm DNA mutates and autism, schizophrenia bipolar etc. results. What is the connection with autoimmune disorders? Having Type 1 diabetes, SLE,etc. in the family, also if mother had older father. NW Cryobank will not accept a sperm donor past 35th BD to minimize genetic abnormalities.VACCINATIONS also cause autism.

Monday, November 30, 2009

Details of Secret German Contract with GSK revealed by BILD

Details of Secret German Contract with GSK revealed by BILD

Monday, 30 November 2009 18:31

Germany signed a secret contract to prepare for a pandemic of deadly flu - in

BILD has revealed the agreement with pharmaceutical firm GlaxoSmithKline (GSK) which was apparently signed from an underlying fear of the bird flu virus. It came into affect when the swine flu pandemic began.

And you can read portions of the 'Agreement between the German government and its states and GSK' regarding the preparation of a vaccine for the killer virus in Germany:

“GSK offers all states... the possibility... to buy 25 per cent of its Dresden-produced pandemic vaccine, to a maximum quantity necessary to supply 50 per cent of the German population.”

Meaning: At most, half of Germany will be provided for.
“The buying price... is €7 plus tax per dose, €1 of which is covers the antigen components and €6... the booster components.”

Meaning: The serum itself only costs €1 per dose; it’s the booster that is expensive.
It is agreed upon that “an obligation does not exist on the part of GSK to supply the theoretically-calculated weekly supply of the pandemic vaccine within a certain timeframe".

Meaning: GSK doesn’t have to uphold any delivery dates.
“The states hold GSK... free of any claim for damages by third parties, losses or financial costs, or any legal actions incurred.”

Meaning: Should any unexpected major side effects arise, the manufacture has only very limited responsibility. In lawsuits the province would take main legal responsibility.
“The parties commit themselves to treat all information which is exchanged in the frame of this contract as confidential.”

The contract... ends with its carrying out in the first case of a pandemic or by Dec 31, 2012 if no acute case has been present.”




Monday, 30 November 2009 14:13

The particle size of AS03 (Pandemrix adjuvant) is 150-155 nm which makes Pandemrix a nano vaccine, according to a report that appeared in the journal Molecules on September 1st, 2009.

The study called Squalene Emulsions for Parenteral Vaccine and Drug Delivery by Christopher B. Fox of the Infectious Disease Research Institute, Seattle, states that the particle size is between 150-155nm, and therefore nano in size. That means that the Pandemrix vaccine can have side effects even on the DNA level.

A recent report of a pregnant woman who became braindead after rececing the swine flu jab in Finland received small molecular heparin for the sake of blood thinning because she had an artificial heart valve.

It is possible that she died because of an interaction between the vaccine and the medicine.

This interaction could, for example, have an impact on very complex system of blood coagulation, says a Finnish expert who found the report.

Mirjaleena Isoaho in Finland contacted doctors but found widespread ignorance about nano vaccines and extremely dangerous effects of these vaccines on people health.

Isoaho has summed up her thoughts by writing a blog entry called: "Finnish people, Pandemrix is a nano vaccine and we've been seriously screwed."


What you don't know can hurt you.

Monday, November 30, 2009

What you don't know can hurt you.

WithoutConsent is about informed consent. We promote transparency in the pharmaceutical industry and the governments that regulate it ... because you can't make good choices with bad information - or no information at all.

Clinical trials with "fast-track" swine flu vaccines that contain an adjuvant - substances that turbocharge the immune system's response to the vaccine - are underway on four continents. The adjuvant is an oil called squalene, which causes incurable autoimmune diseases in animals. Autoimmune diseases occur when the immune system attacks the body instead of defending it.
Over the past 35 years, scientists in laboratories like UCLA Medical Center and the Karolinska Institute, which awards the Nobel Prizes in Medicine and Physiology, have published papers showing how squalene injected into rodents will cripple them. They used squalene to induce diseases like rheumatoid arthritis in animals (the animal version is called "adjuvant arthritis") in order to search for a cure in humans.

Click on this link for a comprehensive list of papers showing squalene's toxicity.] SqualeneReferences-AnimalToxicology.pdf If you go to the National Library of Medicine database called Pubmed, you can search for the papers on the WithoutConsent list and read abstracts of their content. Type in the search terms "squalene, autoimmune" and it'll call up a short list of papers on the subject. Some you can download for free.

Novartis and GlaxoSmithKline - the pharmaceutical companies selling swine flu vaccines with the squalene adjuvants MF59 and AS03 respectively, say the shots are safe. The European Union (EU) and China agree. They've licensed influenza vaccines that contain squalene; and having denied adding squalene to its vaccines for years, the U.S. Department of Defense reportedly adds squalene to "military vaccines," according to the Sept. 28 edition of The New York Times.,%20flu&st=cse Here's what this medical-industrial complex isn't telling you. Small mammals injected with this oil not only develop the animal versions of rheumatoid arthritis, squalene also induces the animal "model" for multiple sclerosis called Experimental Allergic Encephalomyelitis (EAE); as well as the antibodies specific to systemic lupus erythematosus. The morbidity rate is 100 percent.

The European Medicines Agency report on GlaxoSmithKline's new swine flu vaccine called "Pandemrix" says on pg. 17 that it contains 10.69 milligrams of squalene.

An appendix to the report says on pg. 29 that subjects injected with the vaccine suffered "Headache, Tiredness, Pain, redness, swelling or a hard lump at the injection site; Fever, Aching muscles and joint pain." It says these complaints were "very common" - occurring with more than 1 in 10 doses of Pandemrix.

In 1 out of 1,000 doses, subjects reported "Allergic reactions leading to a dangerous decrease of blood pressure, which, if untreated, may lead to collapse, coma and death; Fits, Severe stabbing or throbbing pain along one or more nerves and Low blood platelet count which can result in bleeding or bruising." In 1 in 10,000 doses, volunteers reported "Temporary inflammation of the brain and nerves causing pain, weakness and paralysis that may spread across the body; and Narrowing or blockage of blood vessels with kidney problems."

Can something cause arthritis and MS in animals be safe in humans? Decide for yourself. Our inaugural newsletter reports information that you won't read anywhere else.
We're not going to tell you what to do about this - except to get informed.
Your health could depend on it.


The Goal Of Every H1N1 Swine Flu Vaccine: Immunotoxicity, Neurotoxicity And Sterility

Monday, 30 November 2009
The Goal Of Every H1N1 Swine Flu Vaccine: Immunotoxicity, Neurotoxicity And Sterility

[Prevent | Friday, 30 October, 2009.]
Science dictates that only a randomized double-blind, placebo-controlled study can generate unbiased results in any clinical trial. In the history of vaccine development, no such study has ever been performed. It is only unscientific opinions and pharmaceutical propaganda which have propelled the mythological validity, safety and effectiveness of vaccines. Dozens of controlled studies have scientifically verified the immunotoxicty, neurotoxicity and sterility of common vaccine ingredients which destroy human health, yet they are all ignored by conventional medicine.

There should be a public outcry and challenge to every public health official, medical specialist or scientist (from any country) who justifies the inoculation of their population without providing the evidence of safety and effectiveness of the respective H1N1 vaccine in their country.

The public should be demanding that their governments materialize at least one vaccine trial which is randomized, double-blind and placebo-controlled that can scientifically validate the assertions of public health officials.

Since the pharmacokinetic properties of vaccines are not studied, vaccine manufacturers cannot deny any of the toxic effects listed below. The reason they never analyze the absorption, distribution, metabolism or excretion of these ingredients is because it would eradicate the vaccine industry. However the individual effects of each ingredient and their toxic effects on cells are well documented.

Every Physician, Nurse or medical personnel who administers the H1N1 vaccine (or any vaccine) should be asking themselves why they are injecting the following ingredients into patients that have been scientifically proven to cause immunotoxicity, neurotoxicity, sterility and cancer:

Novartis Focetria Adjuvanted H1N1
Influenza Vaccine Ingredients/Toxicity
Polysorbate 80: Sterilie Agent
Potassium Chloride: Neurotoxin
Squalene: Neurotoxin
Thimerosal: Neurotoxin

Novartis H1N1 Monovalent Influenza Vaccine Ingredients/Toxicity
Beta-Propiolactone: Carcinogen
Polymyxin: Neurotoxin
Neomycin: Immunotoxin
Thimerosal: Neurotoxin

GlaxoSmithKline Arepanrix Adjuvanted
H1N1 Influenza Vaccine Ingredients/Toxicity
Formaldehyde : Carcinogen
Polysorbate 80: Sterilie Agent
Sodium Deoxycholate: Immunotoxin
Squalene: Neurotoxin
Thimerosal: Neurotoxin

GlaxoSmithKline Pandemrix Adjuvanted
H1N1 Influenza Vaccine Ingredients/Toxicity
Octoxynol 10: Immunotoxin
Polysorbate 80: Sterilie Agent
Potassium Chloride: Neurotoxin
Sodium Deoxycholate: Immunotoxin
Squalene: Neurotoxin
Thimerosal: Neurotoxin

GlaxoSmithKline Fluarix 2009-2010
Formula Ingredients/Toxicity
Formaldehyde : Carcinogen
Octoxynol 10: Immunotoxin
Polysorbate 80: Sterilie Agent
Sodium Deoxycholate: Immunotoxin

Sanofi-Pasteur H1N1 Influenza Vaccine Ingredients/Toxicity
Formaldehyde : Carcinogen
Polyethylene Glycol: Systemic Toxin
Thimerosal: Neurotoxin

MedImmune H1N1 Vaccine Ingredients/Toxicity
Monosodium Glutamate: Neurotoxin
Gentamicin Sulfate: Nephrotoxic
Monobasic Potassium Phosphate: Immunotoxin

FLUARIX 2009 Latest Package Insert Ingredients/Toxicity
Formaldehyde : Carcinogen
Gentamicin Sulfate: Nephrotoxic
Polysorbate 80: Sterilie Agent
Sodium Deoxycholate: Immunotoxin
Thimerosal: Neurotoxin

CSL PANVAX H1N1 Vaccine Ingredients/Toxicity
Beta-Propiolactone: Carcinogen
Neomycin: Immunotoxin
Sodium Taurodeoxycholate: Carcinogen/Immunotoxin
Polymyxin: Neurotoxin
Thimerosal: Neurotoxin

CSL Afluria H1N1 Influenza Vaccine Ingredients/Toxicity
Beta-Propiolactone: Carcinogen
Neomycin Sulfate: Immunotoxin
Polymyxin B: Neurotoxin
Potassium Chloride: Neurotoxin
Sodium Taurodeoxycholate: Carcinogen/Immunotoxin
Thimerosal: Neurotoxin

Note: An additional CSL H1N1 Vaccine is Undergoing Trials with AS03 Adjuvant which contains Squalene. (Link.)

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Sunday, November 29, 2009

Under penalty for noncompliance, will we get injected with squalene, an adjuvant that caused Gulf War syndrome?

Under penalty for noncompliance, will we get injected with squalene, an adjuvant that caused Gulf War syndrome?
Sunday, November 29th, 2009 at 12:45 pm
ATTENTION, Please: The WHO has declared swine flu (N1H1) pandemic. This will probably imply governmental demands for universal mass vaccinations under penalty for not complying. Flu vaccine contains squalene oil as an adjuvant.

Micropaleontologist Dr. Viera Scheibner conducted research into the adverse effects of adjuvants in vaccines and wrote: Squalene “contributed to the cascade of reactions called “ Gulf War syndrome. GIs developed arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, deadly Amyotrophic Lateral Sclerosis, Raynaud’s phenomenon with paroxysms of lack of blood in fingers and toes in fingers and toes, Sjorgren’s syndrome with blurred vision, chronic diarrhea, night sweats and low-grade fever.”

‘Swine Flu Vaccination Poses Serious Threat to Your Health":

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Mercury, Autism, Vaccines

David Ayoub, M.D.

Friday, November 27, 2009

In this report, we describe two unrelated Egyptian male infants with limb malformations and constriction rings.

Clin Dysmorphol. 2009 Nov 24. [Epub ahead of print]

Limb malformations with associated congenital constriction rings in two unrelated Egyptian males, one with a disorganization-like spectrum and the other with a probable distinct type of septo-optic dysplasia.
Temtamy SA, Aglan MS, Ashour AM, El-Badry TH.

Departments of aClinical Genetics bOrodental Genetics, Division of Human Genetics and Genome Research, National Research Centre, Cairo, Egypt.

In this report, we describe two unrelated Egyptian male infants with limb malformations and constriction rings. The first case is developing normally but has severe limb anomalies, congenital constriction rings, scoliosis because of vertebral anomalies, a left accessory nipple, a small tumor-like swelling on his lower back with tiny skin tubular appendages, a hypoplastic scrotum, and an anchored penis. The second case is developmentally delayed with limb malformations, congenital constriction rings, a lumbar myelomeningeocele, hemangioma, and tiny tubular skin appendages on the back. The patient also had bilateral optic atrophy. The constellation of features in our patients cannot be fully explained by the amniotic disruption complex. The first patient may represent an additional case of the human homolog of the mouse disorganization mutant. The presence of bilateral optic atrophy in the second case, although without an absent septum pellucidum nor other brain anomalies resembles the infrequently reported disorder of septo-optic dysplasia with limb anomalies. Both cases were sporadic and could be caused by a new dominant mutation because of the high paternal age of case 1 and the history of paternal occupational exposure to heat for both fathers. We draw attention to the phenotypic overlap between the disorganization-like syndrome and septo-optic dysplasia with limb anomalies.

PMID: 19940763 [PubMed - as supplied by publisher]

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Thursday, November 26, 2009

Autism: a Novel Form of Mercury Poisoning

Autism: a Novel Form of Mercury Poisoning
S. Bernard, B.A., A. Enayati, M.S.M.E., L. Redwood, M.S.N., H. Roger, B.A., T. Binstock
Sallie Bernard, ARC Research, 14 Commerce Drive, Cranford, NJ 07901 USA, 908.276.6300, fax 908.276.1301

Summary Autism is a syndrome characterized by impairments in social relatedness and communication, repetitive behaviors, abnormal movements, and sensory dysfunction. Recent epidemiological studies suggest that autism may affect 1 in 150 U. S. children. Exposure to mercury can cause immune, sensory, neurological, motor, and behavioral dysfunctions similar to traits defining or associated with autism, and the similarities extend to neuroanatomy, neurotransmitters, and biochemistry. Thimerosal, a preservative added to many vaccines, has become a major source of mercury in children who, within their first two years, may have received a quantity of mercury that exceeds safety guidelines. A review of medical literature and U.S. government data suggests that (i) many cases of idiopathic autism are induced by early mercury exposure from thimerosal; (ii) this type of autism represents an unrecognized mercurial syndrome; and (iii) genetic and non-genetic factors establish a predisposition whereby thimerosal’s adverse effects occur only in some children.

Autistic Spectrum Disorder (ASD) is a neurodevelopmental syndrome with onset prior to age 36 months. Diagnostic criteria consist of impairments in sociality and communication plus repetitive and stereotypic behaviors (1). Traits strongly associated with autism include movement disorders and sensory dysfunctions (2). Although autism may be apparent soon after birth, most autistic children experience at least several months, even a year or more of normal development — followed by regression, defined as loss of function or failure to progress (2,3,4).

The neurotoxicity of mercury (Hg) has long been recognized (5). Primary data derive from victims of contaminated fish (Japan – Minamata Disease) or grain (Iraq, Guatemala, Russia); from acrodynia (Pink Disease) induced by Hg in teething powders; and from individual instances of mercury poisoning (HgP), many occurring in occupational settings (e.g., Mad Hatter’s Disease). Animal and in vitro studies also provide insights into the mechanisms of Hg toxicity. More recently, the Food and Drug Administration (FDA) and the American Academy of Pediatrics (AAP) have determined that the typical amount of Hg injected into infants and toddlers via childhood immunizations has exceeded government safety guidelines on an individual (6) and cumulative vaccine basis (7). The mercury in vaccines derives from thimerosal (TMS), a preservative which is 49.6% ethylmercury (eHg) (7).

Past cases of HgP have presented with much inter-individual variation, depending on the dose, type of mercury, method of administration, duration of exposure, and individual sensitivity. Thus, while commonalities exist across the various instances of HgP, each set of variables has given rise to a different disease manifestation (8,9,10,11). It is hypothesized that the regressive form of autism represents another form of mercury poisoning, based on a thorough correspondence between autistic and HgP traits and physiological abnormalities, as well as on the known exposure to mercury through vaccines. Furthermore, other phenomena are consistent with a causal Hg-ASD relationship. These include (a) symptom onset shortly after immunization; (b) ASD prevalence increases corresponding to vaccination increases; (c) similar sex ratios of affected individuals; (d) a high heritability rate for autism paralleling a genetic predisposition to Hg sensitivity at low doses; and (e) parental reports of autistic children with elevated Hg.

Trait Comparison
ASD manifests a constellation of symptoms with much inter-individual variation (3,4). A comparison of traits defining, nearly universal to, or commonly found in autism with those known to arise from mercury poisoning is given in Table I. The characteristics defining or strongly associated with autism are also more fully described.

Autism has been conceived primarily as a psychiatric condition; and two of its three diagnostic criteria are based upon the observable traits of (a) impairments in sociality, most commonly social withdrawal or aloofness, and (b) a variety of perseverative or stereotypic behaviors and the need for sameness, which strongly resemble obsessive-compulsive tendencies. Differential diagnosis may include childhood schizophrenia, depression, obsessive-compulsive disorder (OCD), anxiety disorder, and other neuroses. Related behaviors commonly found in ASD individuals are irrational fears, poor eye contact, aggressive behaviors, temper tantrums, irritability, and inexplicable changes in mood (1,2,12-17). Mercury poisoning, when undetected, is often initially diagnosed as a psychiatric disorder (18). Commonly occurring symptoms include (a) "extreme shyness," indifference to others, active avoidance of others, or “a desire to be alone”; (b) depression, “lack of interest” and “mental confusion;” (c) irritability, aggression, and tantrums in children and adults; (d) anxiety and fearfulness; and (e) emotional lability. Neuroses, including schizoid and obsessive-compulsive traits, problems in inhibition of perseveration, and stereotyped behaviors, have been reported in a number of cases; and lack of eye contact was observed in one 12 year old girl with mercury vapor poisoning (18-35).

The third diagnostic criterion for ASD is impairment in communication (1). Historically, about half of those with classic autism failed to develop meaningful speech (2), and articulation difficulties are common (3). Higher functioning individuals may have language fluency but still show semantic and pragmatic errors (3,36). In many cases of ASD, verbal IQ is lower than performance IQ (3). Similarly, mercury-exposed children and adults show a marked difficulty with speech (9,19,37). In milder cases scores on language tests may be lower than those of unexposed controls (31,38). Iraqi children who were postnatally poisoned developed articulation problems, from slow, slurred word production to an inability to generate meaningful speech; while Iraqi babies exposed prenatally either failed to develop language or presented with severe language deficits in childhood (23,24,39). Workers with Mad Hatter’s disease had word retrieval and articulation difficulties (21).

Nearly all cases of ASD and HgP involve disorders of physical movement (2,30,40). Clumsiness or lack of coordination has been described in many higher functioning ASD individuals (41). Infants and toddlers later diagnosed with autism may fail to crawl properly or may fall over while sitting or standing; and the movement disturbances typically occur on the right side of the body (42). Problems with intentional movement and imitation are common in ASD, as are a variety of unusual stereotypic behaviors such as toe walking, rocking, abnormal postures, choreiform movements, spinning; and hand flapping (2,3,43,44). Noteworthy because of similarities to autism are reports in Hg literature of (a) children in Iraq and Japan who were unable to stand, sit, or crawl (34,39); (b) Minamata disease patients whose movement disturbances were localized to one side of the body, and a girl exposed to Hg vapor who tended to fall to the right (18,34); (c) flapping motions in an infant poisoned from contaminated pork (37) and in a man injected with thimerosal (27); (d) choreiform movements in mercury vapor intoxication (19); (e) toe walking in a moderately poisoned Minamata child (34); (f) poor coordination and clumsiness among victims of acrodynia (45); (g) rocking among infants with acrodynia (11); and (h) unusual postures observed in both acrodynia and mercury vapor poisoning (11,31). The presence of flapping motions in both diseases is of interest because it is such an unusual behavior that it has been recommended as a diagnostic marker for autism (46).

Virtually all ASD subjects show a variety of sensory abnormalities (2). Auditory deficits are present in a minority of individuals and can range from mild to profound hearing loss (2,47). Over- or under-reaction to sound is nearly universal (2,48), and deficits in language comprehension are often present (3). Pain sensitivity or insensitivity is common, as is a general aversion to touch; abnormal sensation in the extremities and mouth may also be present and has been detected even in toddlers under 12 months old (2,49). There may be a variety of visual disturbances, including sensitivity to light (2,50,51,52). As in autism, sensory issues are reported in virtually all instances of Hg toxicity (40). HgP can lead to mild to profound hearing loss (40); speech discrimination is especially impaired (9,34,). Iraqi babies exposed prenatally showed exaggerated reaction to noise (23), while in acrodynia, patients reported noise sensitivity (45). Abnormal sensation in the extremities and mouth is the most common sensory disturbance (25,28). Acrodynia sufferers and prenatally exposed Iraqi babies exhibited excessive pain when bumping limbs and an aversion to touch (23,24,45,53). A range of visual problems has been reported, including photophobia (18,23,34).

Comparison of Biological Abnormalities
The biological abnormalities commonly found in autism are listed in Table II, along with the corresponding pathologies arising from mercury exposure. Especially noteworthy similarities are described.

Autism is a neurodevelopmental disorder which has been characterized as "a disorder of neuronal organization, that is, the development of the dentritic tree, synaptogenesis, and the development of the complex connectivity within and between brain regions" (54). Depressed expression of neural cell adhesion molecules (NCAMs), which are critical during brain development for proper synaptic structuring, has been found in one study of autism (55). Organic mercury, which readily crosses the blood-brain barrier, preferentially targets nerve cells and nerve fibers (56); primates accumulate the highest Hg-levels in the brain relative to other organs (40). Furthermore, although most cells respond to mercurial injury by modulating levels of glutathione (GSH), metallothionein, hemoxygenase, and other stress proteins, neurons tend to be “markedly deficient in these responses” and thus are less able to remove Hg and more prone to Hg-induced injury (56). In the developing brain, mercury interferes with neuronal migration, depresses cell division, disrupts microtubule function, and reduces NCAMs (28, 57-59).

While damage has been observed in a number of brain areas in autism, many nuclei and functions are spared (36). HgP’s damage is similarly selective (40). Numerous studies link autism with neuronal atypicalities within the amygdala, hippocampi, basal ganglia, the Purkinje and granule cells of the cerebellum, brainstem, basal ganglia, and cerebral cortex (36,60-69). Each of these areas can be affected by HgP (10,34,40,70-73). Migration of Hg, including eHg, into the amygdala is particularly noteworthy, because in primates this brain region has neurons specific for eye contact (74) and it is implicated in autism and in social behaviors (65,66,75).

Autistic brains show neurotransmitter irregularities which are virtually identical to those arising from Hg exposure: both high or low serotonin and dopamine, depending on the subjects studied; elevated epinephrine and norepinephrine in plasma and brain; elevated glutamate; and acetylcholine deficiency in hippocampus (2,21,76-83).

Gillberg and Coleman (2) estimate that 35-45% of autistics eventually develop epilepsy. A recent MEG study reported epileptiform activity in 82% of 50 regressive autistic children; in another study, half the autistic children expressed abnormal EEG activity during sleep (84). Autistic EEG abnormalities tend to be non-specific and have a variety of patterns (85). Unusual epileptiform activity has been found in a number of mercury poisoning cases (18,27,34,86-88). Early mHg exposure enhances tendencies toward epileptiform activity with a reduced level of seizure-discharge amplitude (89), a finding consistent with the subtlety of seizures in many autism spectrum children (84,85). The fact that Hg increases extracellular glutamate would also contribute to epileptiform activity (90).

Some autistic children show a low capacity to oxidize sulfur compounds and low levels of sulfate (91,92). These findings may be linked with HgP because (a) Hg preferentially binds to sulfhydryl molecules (-SH) such as cysteine and GSH, thereby impairing various cellular functions (40), and (b) mercury can irreversibly block the sulfate transporter NaSi cotransporter NaSi-1, present in kidneys and intestines, thus reducing sulfate absorption (93). Besides low sulfate, many autistics have low GSH levels, abnormal GSH-peroxidase activity within erythrocytes, and decreased hepatic ability to detoxify xenobiotics (91,94,95). GSH participates in cellular detoxification of heavy metals (96); hepatic GSH is a primary substrate for organic-Hg clearance from the human (40); and intraneuronal GSH participates in various protective responses against Hg in the CNS (56). By preferentially binding with GSH, preventing absorption of sulfate, or inhibiting the enzymes of glutathione metabolism (97), Hg might diminish GSH bioavailability. Low GSH can also derive from chronic infection (98,99), which would be more likely in the presence of immune impairments arising from mercury (100). Furthermore, mercury disrupts purine and pyrimidine metabolism (97,10). Altered purine or pyrimidine metabolism can induce autistic features and classical autism (2,101,102), suggesting another mechanism by which Hg can contribute to autistic traits.

Autistics are more likely to have allergies, asthma, selective IgA deficiency (sIgAd), enhanced expression of HLA-DR antigen, and an absence of interleukin-2 receptors, as well as familial autoimmunity and a variety of autoimmune phenomena. These include elevated serum IgG and ANA titers, IgM and IgG brain antibodies, and myelin basic protein (MBP) antibodies (103-110). Similarly, atypical responses to Hg have been ascribed to allergic or autoimmune reactions (8), and genetic predisposition to such reactions may explain why Hg sensitivity varies so widely by individual (88,111). Children who developed acrodynia were more likely to have asthma and other allergies (11); IgG brain autoantibodies, MBP, and ANA have been found in HgP subjects (18,111,112); and mice genetically prone to develop autoimmune diseases "are highly susceptible to mercury-induced immunopathological alterations" even at the lowest doses (113). Additionally, many autistics have reduced natural killer cell (NK) function, as well as immune-cell subsets shifted in a Th2 direction and increased urine neopterin levels, indicating immune system activiation (103,114-116). Depending upon genetic predisposition, Hg can induce immune activation, an expansion of Th2 subsets, and decreased NK activity (117-120).

Population Characteristics
In most affected children, autistic symptoms emerge gradually, although there are cases of sudden onset (3). The earliest abnormalities have been detected in 4 month olds and consist of subtle movement disturbances; subtle motor-sensory disturbances have been observed in 9 month olds (49). More overt speech and hearing difficulties become noticeable to parents and pediatricians between 12 and 18 months (2). TMS vaccines have been given in repeated intervals starting from infancy and continuing until 12 to 18 months. While HgP symptoms, may arise suddenly in especially sensitive individuals (11), usually there is a preclinical "silent stage" in which subtle neurological changes are occuring (121) and then a gradual emergence of symptoms. The first symptoms are typically sensory- and motor-related, which are followed by speech and hearing deficits, and finally the full array of HgP characteristics (40). Thus, both the timing and nature of symptom emergence in ASD are fully consistent with a vaccinal Hg etiology. This parallel is reinforced by parental reports of excessive amounts of mercury in urine or hair from younger autistic children, as well as some improvement in symptoms with standard chelation therapy (122).

The discovery and rise in prevalence of ASD mirrors the introduction and spread of TMS in vaccines. Autism was first described in 1943 among children born in the 1930s (123). Thimerosal was first introduced into vaccines in the 1930s (7). In studies conducted prior to 1970, autism prevalence was estimated, at 1 in 2000; in studies from 1970 to 1990 it averaged 1 in 1000 (124). This was a period of increased vaccination rates of the TMS-containing DPT vaccines among children in the developed world. In the early 1990s, the prevalence of autism was found to be 1 in 500 (125), and in 2000 the CDC found 1 in 150 children affected in one community, which was consistent with reports from other areas in the country (126). In the late 1980s and early 1990s, two new TMS vaccines, the HIB and Hepatitis B, were added to the recommended schedule (7).

Nearly all US children are immunized, yet only a small proportion develop autism. A pertinent characteristic of mercury is the great variability in its effects by individual, so that at the same exposure level, some will be affected severely while others will be asymptomatic (9,11,28). An example is acrodynia, which arose in the early 20th Century from mercury in teething powders and afflicted only 1 in 500-1000 children given the same low dose (28). Studies in mice as well as humans indicate that susceptibility to Hg effects arises from genetic status, in some cases including a propensity to autoimmune disorders (113,34,40). ASD exhibits a strong genetic component, with high concordance in monozygotic twins and a higher than expected incidence among siblings (4); autism is also more prevalent in families with autoimmune disorders (106).

Additionally, autism is more prevalent among boys than girls, with the ratio estimated at 4:1 (2). Mercury studies in mice and humans consistently report greater effects on males than females, except for kidney damage (57). At high doses, both sexes are affected equally; at low doses only males are affected (38,40,127).

We have shown that every major characteristic of autism has been exhibited in at least several cases of documented mercury poisoning. Recently, the FDA and AAP have revealed that the amount of mercury given to infants from vaccinations has exceeded safety levels. The timing of mercury administration via vaccines coincides with the onset of autistic symptoms. Parental reports of autistic children with measurable mercury levels in hair and urine indicate a history of mercury exposure. Thus the standard primary criteria for a diagnosis of mercury poisoning – observable symptoms, known exposure at the time of symptom onset, and detectable levels in biologic samples (11,31) – have been met in autism. As such, mercury toxicity may be a significant etiological factor in at least some cases of regressive autism. Further, each known form of HgP in the past has resulted in a unique variation of mercurialism – e.g., Minamata disease, acrodynia, Mad Hatter’s disease – none of which has been autism, suggesting that the Hg source which may be involved in ASD has not yet been characterized; given that most infants receive eHg via vaccines, and given that the effect on infants of eHg in vaccines has never been studied (129), vaccinal thimerosal should be considered a probable source. It is also possible that vaccinal eHg may be additive to a prenatal mercury load derived from maternal amalgams, immune globulin injections, or fish consumption, and environmental sources.

The history of acrodynia illustrates that a severe disorder, afflicting a small but significant percentage of children, can arise from a seemingly benign application of low doses of mercury. This review establishes the likelihood that Hg may likewise be etiologically significant in ASD, with the Hg derived from thimerosal in vaccines rather than teething powders. Due to the extensive parallels between autism and HgP, the likelihood of a causal relationship is great. Given this possibility, TMS should be removed from all childhood vaccines, and the mechanisms of Hg toxicity in autism should be thoroughly investigated. With perhaps 1 in 150 children now diagnosed with ASD, development of HgP-related treatments, such as chelation, would prove beneficial for this large and seemingly growing population.

Table I: Summary Comparison of Traits of Autism & Mercury Poisoning
(ASD references in bold; HgP references in italics)

Psychiatric Disturbances

Social deficits, shyness, social withdrawal (1,2,130,131; 21,31,45,53,132

Repetitive, perseverative, stereotypic behaviors; obsessive-compulsive tendencies (1,2,43,48,133; 20,33-35,132)

Depression/depressive traits, mood swings, flat affect; impaired face recognition (14,15,17,103, 134,135;19,21,24,26,31)

Anxiety; schizoid tendencies; irrational fears (2,15,16; 21,27,29,31)

Irritability, aggression, temper tantrums (12,13,43; 18,21,22,25)

Lacks eye contact; impaired visual fixation (HgP)/ problems in joint attention (ASD) (3,36,136,137;18,19,34)

Speech and Language Deficits

Loss of speech, delayed language, failure to develop speech (1-3,138,139; 11,23,24,27,30,37)

Dysarthria; articulation problems (3; 21,25,27,39)

Speech comprehension deficits (3,4,140; 9,25,34,38)

Verbalizing and word retrieval problems (HgP); echolalia, word use and pragmatic errors (ASD) (1,3,36;21,27,70)

Sensory Abnormalities

Abnormal sensation in mouth and extremities (2,49; 25,28,34,39)

Sound sensitivity; mild to profound hearing loss (2,47,48; 19,23-25,39,40)

Abnormal touch sensations; touch aversion (2,49; 23,24,45,53)

Over-sensitivity to light; blurred vision (2,50,51; 18,23,31,34,45)

Motor Disorders

Flapping, myoclonal jerks, choreiform movements, circling, rocking, toe walking, unusual postures (2,3,43,44; 11,19,27,30,31,34,39)

Deficits in eye-hand coordination; limb apraxia; intention tremors (HgP)/problems with intentional movement or imitation (ASD) (2,3,36,181; 25,29,32,38,70,87)

Abnormal gait and posture, clumsiness and incoordination; difficulties sitting, lying, crawling, and walking; problem on one side of body (4,41,42,123; 18,25,31,34,39,45)

Cognitive Impairments

Borderline intelligence, mental retardation – some cases reversible (2,3,151,152; 19,25,31,39,70)

Poor concentration, attention, response inhibition (HgP)/shifting attention (ASD) (4,36,153;21,25,31,38,141)

Uneven performance on IQ subtests; verbal IQ higher than performance IQ (3,4,36; 31,38)

Poor short term, verbal, and auditory memory (36,140; 21,29,31,35,38,87,141)

Poor visual and perceptual motor skills; impairment in simple reaction time (HgP)/ lower performance on timed tests (ASD) (4,140,181; 21,29,142)

Deficits in understanding abstract ideas & symbolism; degeneration of higher mental powers (HgP)/sequencing, planning & organizing (ASD); difficulty carrying out complex commands (3,4,36,153;9,18,37,57,142)

Unusual Behaviors

Self injurious behavior, e.g. head banging (3,154; 11,18,53)

ADHD traits (2,36,155; 35,70)

Agitation, unprovoked crying, grimacing, staring spells 3,154; 11,23,37,88)

Sleep difficulties (2,156,157; 11,22,31)

Physical Disturbances

Hyper- or hypotonia; abnormal reflexes; decreased muscle strength, especially upper body; incontinence; problems chewing, swallowing (3,42,145,181; 19,27,31,32,39)

Rashes, dermatitis, eczema, itching (107,146; 22,26,143)

Diarrhea; abdominal pain/discomfort, constipation, “colitis” (107,147-149; 18,23,26,27,31,32)

Anorexia; nausea (HgP)/vomiting (ASD); poor appetite (HgP)/restricted diet (ASD) (2,123; 18,22)

Lesions of ileum and colon; increased gut permeability (147,150; 57,144)

Table II: Summary Comparison of Biological Abnormalities
in Autism & Mercury Exposure

Mercury Exposure


Binds -SH groups; blocks sulfate transporter in intestines, kidneys (40,93)
Low sulfate levels (91,92)

Reduces glutathione availability; inhibits enzymes of glutathione metabolism; glutathione needed in neurons, cells, and liver to detoxify heavy metals; reduces glutathione peroxidase and reductase (97,100,161,162)
Low levels of glutathione; decreased ability of liver to detoxify xenobiotics; abnormal glutathione peroxidase activity in erythrocytes (91,94,95)

Disrupts purine and pyrimidine metabolism (10,97,158,159)
Purine and pyrimidine metabolism errors lead to autistic features (2,101,102)

Disrupts mitochondrial activities, especially in brain (160,163,164)
Mitochondrial dysfunction, especially in brain (76,172)

Immune System

Sensitive individuals more likely to have allergies, asthma, autoimmune-like symptoms, especially rheumatoid-like ones (8,11,18,24,28,31,111,113)
More likely to have allergies and asthma; familial presence of autoimmune diseases, especially rheumatoid arthritis; IgA deficiencies (103,106-109,115)

Can produce an immune response in CNS; causes brain/MBP autoantibodies (18,111,165)
On-going immune response in CNS; brain/MBP autoantibodies present (104,105,109,110)

Causes overproduction of Th2 subset; kills/inhibits lymphocytes, T-cells, and monocytes; decreases NK T-cell activity; induces or suppresses IFNg & IL-2 (100,112,117-120,166)
Skewed immune-cell subset in the Th2 direction; decreased responses to T-cell mitogens; reduced NK T-cell function; increased IFNg & IL-12 (103,108,114-116,173,174)

CNS Structure

Selectively targets brain areas unable to detoxify or reduce Hg-induced oxidative stress (40,56,161)
Specific areas of brain pathology; many functions spared (36)

Accummulates in amygdala, hippocampus, basal ganglia, cerebral cortex; damages Purkinje and granule cells in cerebellum; brain stem defects in some cases (10,34,40,70-73)
Pathology in amygdala, hippocampus, basal ganglia, cerebral cortex; damage to Purkinje and granule cells in cerebellum; brain stem defects in some cases (36,60-69)

Causes abnormal neuronal cytoarchitecture; disrupts neuronal migration, microtubules, and cell division; reduces NCAMs (10,28,57-59,161)
Neuronal disorganization; increased neuronal cell replication, increased glial cells; depressed expression of NCAMs (4,54,55)

Progressive microcephaly (24)
Progressive microcephaly and macrocephaly (175)


Prevents presynaptic serotonin release and inhibits serotonin transport; causes calcium disruptions (78,79,163,167,168)
Decreased serotonin synthesis in children; abnormal calcium metabolism (76,77,103,179)

Alters dopamine systems; peroxidine deficiency in rats resembles mercurialism in humans (8,80)
Either high or low dopamine levels; positive response to peroxidine, which lowers dopamine levels (2,177,178)

Elevates epinephrine and norepinephrine levels by blocking enzyme that degrades epinephrine (81,160)
Elevated norepinephrine and epinephrine (2)

Elevates glutamate (21,171)
Elevated glutamate and aspartate (82,176)

Leads to cortical acetylcholine deficiency; increases muscarinic receptor density in hippocampus and cerebellum (57,170)
Cortical acetylcholine deficiency; reduced muscarinic receptor binding in hippocampus (83)

Causes demyelinating neuropathy (22,169)
Demyelination in brain (105)


Causes abnormal EEGs, epileptiform activity, variable patterns, e.g., subtle, low amplitude seizure activities (27,31,34,86-89)
Abnormal EEGs, epileptiform activity, variable patterns, including subtle, low amplitude seizure activities (2,4,84,85)

Causes abnormal vestibular nystagmus responses; loss of sense of position in space (9,19,34,70)
Abnormal vestibular nystagmus responses; loss of sense of position in space (27,180)

Results in autonomic disturbance: excessive sweating, poor circulation, elevated heart rate (11,18,31,45)
Autonomic disturbance: unusual sweating, poor circulation, elevated heart rate (17,180)

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More Concerns Regarding Needle
Devices Being Used For H1N1 Vaccines

Dr. Tenpenny on Vaccines The reactions are just starting to show up. Please warn your Candian friends. Their Swine flu vaccines contain squalene.The Canadian Press: PHAC confirms 24 cases of anaphylaxis across Canada after H1N1 flu shots
TORONTO — There have been 24 confirmed cases of a type of severe allergic reaction called anaphylaxis in Canadians who have received an H1N1 flu shot, including one person who died after getting vaccinated, the head of the Public Health Agency of Canada said Wednesday.

Squalene? Long-term neurological damage?

News and Views » Letters
November 26, Vaccine facts were not fully investigated
Squalene? Long-term neurological damage? The Georgia Straight really hit the nail on the head with the article [“What’s in your vaccine?”, November 19-26]. Squalene may be natural, but injecting the substance produces an entirely different outcome than ingesting it, as shown by a number of independent studies.

The problem is that for too long, vaccine stats have reflected a “don’t look, don’t find, don’t report” syndrome. Anyone who doubts this should access [TV station] WLWT’s investigative report on vaccine victims in the military, “Secret Shots”.

As for damage-control claims that the anthrax vaccine never had squalene, award-winning investigative journalist Gary Matsumoto has compiled an impressive body of evidence in [his book] Vaccine-A, showing it was, indeed, used in an experimental anthrax vaccine. As retired U.S. army colonel David Hackworth remarked: “Even the Nazis didn’t run medical experiments on their own troops.”

> Darren Pearson / Vancouver


WHO Hid Evidence of Harm Caused by Free UNICEF Jabs in Bosnia

Thursday, 26 November 2009 14:34

News - Latest News

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WHO deliberately helped hide evidence that 117 children in Bosnia and Herzegovina were severely damaged by CSL vaccines, distributed for free by UNICEF in 2002, alleges Jagoda Savic.

As part of a UNICEF immunization project with the CSL vaccine for diphtheria, tetanus and pertussis vaccine, 117 children from 29 cities suffered severe side effects.

The children all suffered the same neurological damage, some of them stopped being able to walk talk and eat, got encephalitis, epilepsy, autism, and psycho-motoric and intellectual delay.

However, in spite of the scientific evidence that the damage was caused by the vaccine, documented by Savic and others in Bosnia, an investigation was blocked by the WHO and the UN mission in Bosnia Herzogovina, which insisted that the vaccines were safe.

The lengths the authorities went to to conceal the damage done by the vaccine included keeping back samples for seven years before sending them for analysis for toxicity.

However, a laboratory analysis done abroad on some children showed mercury poisoning and heavy brain inflammation.

WHO’s Global Advisory Committee for Vaccine Safety (GACVS) stated the vaccine was safe in spite of the evidence and said there was no need to invesigate the case.

According to Savic, a professor of toxicology said a main cause of health damage of all these children was post-pertussis encephalopathy. This blocked the regular elimination of non dangerous mercury from child’s body (ethyl salycilate) while keeping mercury inside the body and transforming it in methyl mercury which acts as neuro- toxin. Post-pertussis encephalopathy also caused brain inflammation, says Savic.

This case shows that the WHO and UN are failing to fulfil their mission to protect the public health.

On the contrary, harmful vaccines are being distriubted free to children as part of UN programmes – but when the damage becomes visible, the evidence is hidden, manipulated or ignored.

This same approach is being repeated with the swine flu jab.

Doctors and patients in Europe are reporting deaths in connection with the swine flu jab to their national medical agencies. But these agencies, which approved the untested drug in the first place, and WHO simply deny there is a link.

That is not surprising when you consider that pharamaceutical companies sit on key vaccine advisory boards of WHO, funded by the World Bank and the Rockefeller Foundation.

The UN has now been caught red handed helping to manufacture false data to support the thesis that global warming is man mande and justify carbon taxes and rule by an autocratic government run by a global „elite“ who control the Federal Reserve, including the Rockefellers.

Man dies in Sweden from the flu shot - now 9 official deaths

Man dies in Sweden from the flu shot - now 9 official deaths

Aftonbladet reports that a man in his fifties died after having received the poisonous Pandemrix "swine flu" shot. He had been through a heart transplant operation and the shot made his body reject the new heart. Authorities in Sweden are now afraid fewer will want to take the vaccine.

"- It can not be said it was wrong to vaccinate this man. We do write on our home page that people who have been through heart transplants belong to the risk group and should get vaccinated. But we have new knowledge now which we can learn from." says Ingemar Persson, case investigator at the Swedish Medical Products Agency. "- The vaccine is the direct or indirect cause of this mans death." he continues.

Several involved agencies and departments will hold a press conference today to try to calm down worried citizens and again claim that the vaccine is "tested and safe".

The official death toll in Sweden is now nine but our sources claim there might be as many as 80 deaths. Then there are also many reports about abortions as a result of the shot, just like in other parts of the world. Officials are desperate to declare any deaths in proximity to the vaccinations as coincidental and therefor the official numbers can not be trusted. In fact, the whole official story regarding the "swine flu" in Sweden can no longer be trusted since it is clear that media together with the Swedish authorities have been and still are engaged in a massive propaganda campaign to vaccinate as many as possible without any clear declared reasons or logic.

The ties between scientists, politicians and the Pharma industry and WHO is also not clarified.

This is by far the biggest medical scandal in modern times in Sweden.

Johan Niklasson

Original article


Wednesday, November 25, 2009

Another Woman Loses Her Baby After Pandemrix Jab in Portugal

Another Woman Loses Her Baby After Pandemrix Jab in Portugal

Last Updated on Wednesday, 25 November 2009 07:02
Tuesday, 24 November 2009 21:05

Another woman who vaccinated with the Pandemrix swine flu jab in Portugal has lost her baby.

The woman from Ponte de Sor lost her baby in the 34th week at the Hospital de Portalegre after getting the jab.

In the space of eight days, at least four women vaccinated with the 'Pandemrix' in Portual have lost babies, two in Portalegre, one in Lisbon and another in Leira.


Tuesday, November 24, 2009

H1N1 Vaccine Deaths in Germany: German doctors issued warning about swine flu jab

Beat the Flu This Winter
I received this e-mail from Nancy Campbell of Above Rubies. Mrs. Campbell asks that her articles be reprinted in their entirety with her web address included. I’ve read Above Rubies for years. It is a wonderfully encouraging magazine for homemakers and mothers who embrace God, home, and family.

Dear friends,

As we approach flu season, it is good to be reminded of ways to prevent it. There are better ways to prevent the flu than being vaccinated. Check out the following points to keep yourself and your family in good health during this winter season.

Foreign Investors Group

Foreign Investors Group
Foreign Investors Group Investment Guide

Scientist Repeats Swine Flu Lab-Escape Claim in Published Study

Scientist Repeats Swine Flu Lab-Escape Claim in Published Study


An Avalanche Of Reports Of Adverse Reactions To The H1N1 Swine Flu Vaccine

An Avalanche Of Reports Of Adverse Reactions To The H1N1 Swine Flu Vaccine – And Yet World Health Authorities Continue To Insist That It Is Safe
Is the swine flu vaccine safe? Only a small portion of the population has been vaccinated in most areas so far, and yet already there is an avalanche of reports of adverse reactions to the H1N1 swine flu vaccine. Reports are pouring in from all over the world even though the mainstream media seems extremely hesitant to report on these cases. You see, most of the time the mainstream media doesn't want to report on a "rare" reaction to the H1N1 swine flu vaccine because they do not want to "alarm" the public. The feeling in the mainstream media is that the benefits of being vaccinated far outweigh the risks. Of course that is a complete load of nonsense. When you read the reports of adverse reactions to the vaccine in this article, keep in mind that the majority of vaccine side effects such as autism, neurological disorders, autoimmune diseases, Guillain-Barre Syndrome, paralysis, infertility and cancer can take weeks or months to show up. To have so many reports of adverse reactions show up so early is a very troubling sign - and yet world health authorities continue to insist that the H1N1 swine flu vaccine is perfectly safe.

Well, if you read our previous article entitled "Shocking H1N1 Swine Flu Vaccine Miscarriage Stories From Pregnant Women", you would already know that the swine flu vaccine is most definitely NOT safe for pregnant women.

But is it safe for the population as a whole?


Even the head of the National Institute of Allergy and Infectious Diseases is openly admitting that "there's no vaccine, there's nothing, that is 100 percent safe".

But do the benefits outweigh the risks?

Consider that question as you read the following reports from the mainstream media about adverse reactions to the H1N1 swine flu vaccine.....

-A 14 year old boy who lives in Virginia is struggling to walk after coming down with a reported case of Guillain-Barre syndrome just hours after receiving the H1N1 swine flu vaccine.

-Although only a very small percentage of the French populaton has been vaccinated, one young woman in France has already been diagnosed with Guillain-Barre Syndrome after taking the H1N1 swine flu vaccine.

-At one school in Sweden where the students were mass vaccinated with the Pandemrix H1N1 swine flu vaccine, 130 of the 233 students at the school called in sick the day after the vaccination.

-Nine students in Mississippi were recently rushed to the hospital after experiencing severe reactions to the H1N1 swine flu vaccine.

-One child in Michigan was recently left paralyzed after taking the FluMist H1N1 swine flu vaccine.

-A 21 month boy in Germany has died a horrible death after getting the H1N1 swine flu vaccine.

-In Canada, one man's 17 month old son developed a fever the day after receiving the swine flu shot and suffered a seizure four days later and was rushed to hospital.

-In Brooklyn, one six year old girl with epilepsy was given the H1N1 swine flu vaccine without permission and she reacted so severely to it that she ended up in the hospital.

-A major German newspaper is actually admitting that at least seven people have died so far in Germany following an injection with the H1N1 swine flu vaccine Pandemrix.

-A 4 year old boy in Sweden was reportedly on the edge of death after taking the H1N1 swine flu vaccine.

-Officially, a total of 8 people have died from the H1N1 swine flu vaccine so far in Sweden.

-A third woman in Portugal has lost her baby after taking the H1N1 swine flu vaccine.

-The Jerusalem Post recently reported on the death of a 75-year-old man two days after he had received the H1N1 swine flu vaccine.

-The Chinese government is admitting that two people have died in China after receiving domestically manufactured H1N1 swine flu vaccines.

-A 42 year old Canadian woman who had been vaccinated for the H1N1 swine flu has now died from the virus.

-Another woman in Canada collapsed and had to be taken to the hospital in a stretcher after getting injected with the H1N1 swine flu vaccine.

-At least 10 people in the Northwest Territories have reported allergic reactions to the H1N1 swine flu vaccine.

-A journalist working for the German news magazine Der Spiegel reported that he became extremely ill with an extremely high fever, chills and severe nausea just days after receiving a swine flu vaccine.

But the reports above are just the tip of the iceberg. There are a whole lot more problems that we aren't hearing about.

For example, the following are actual reactions to the seasonal flu vaccine and to the H1N1 swine flu vaccine as reported by a registered nurse in Nashville, Tennessee.....

*Regular Flu Vaccine- Two hours after administration, the patient had a severe burning sensation in their hands and feet, headache, and nausea/vomiting.

*Regular Flu Vaccine- Numbness of the arm where the shot was administered for two days.

*Regular Flu Vaccine- Increased/abnormal pain with rash at the injection site for two to three days.

*Regular Flu Vaccine- Approximately two to three weeks after vaccination, the patient experienced Bell's Palsy. Bell's Palsy is a condition in which the patient experiences facial drooping/paralysis due to malfunction/inflammation of cranial nerve VII. The patient also experienced body aches, headache, and malaise for 1-2 weeks. Bell's Palsy is idiopathic/ cryptogenic in nature, and a diagnosis is formed after ruling out other possibilities. The patient's physician stated that the Regular Flu Vaccine could have caused the Bell's Palsy.

*Swine Flu Vaccine- Increased Body aches, nausea/vomiting, and headache for 2 weeks for two separate patients.

*Regular Flu Vaccine- I spoke with an older African American male about his grandfather...He stated his grandfather was a perfectly healthy fellow who took no daily medicines and had no medical conditions. The grandfather took his first Seasonal Flu Vaccine at the age of 70 and died two days afterwards. This also happened to my great grandfather as explained to me by my grandmother. Both seasonal flu victims were healthy with no medical conditions, took no daily prescribed medicines, were elderly but phsycially fit and died with 2-3 days of vaccination.

*Regular Flu Vaccine- Chest pain, nausea/vomiting, and severe headache was a complaint of multiple patients...occurring within 3-6 hours of administration.

Not only can the swine flu vaccine cause horrific side effects, but for some people it can even mean potential death. A 4 year old boy from Rochester, Minnesota almost died after getting the H1N1 swine flu vaccine. Just check out the video news report below....

A couple of readers on our sister site, Bird Flu Pandemic, have also reported severe reactions to the H1N1 swine flu vaccine.....


My friend was diagnosed w/GBS today. She had the H1N1 vaccine on Tuesday. She woke up friday morn. with one side of her face paralized, now almost her whole face is paralized. She is starting blood and plasma transfusions tonight. She will be transferred to Barnes hospital soon for more extensive testing. To those who laugh at the severity of this strange, unknown sickness and vaccine I hope you stay informed and not ignorant.


I am a healthcare employee…..the only vaccine offered to employees was the live vaccine. I decided to get it and be the “guinea pig” instead of my toddler. Received the nasal spray on Tuesday, woke up Wednesday with a sore throat and stuffy nose, Thursday had a terrible chest congestion/cough with fever and splitting headache, Friday all symptoms were worse and I couldn’t breathe! I was diagnosed on Friday with H1N1 and pneumonia….. good thing I got the vaccine, huh?

On another blog, one reader reported a very sad H1N1 swine flu vaccine horror story.....


Amy got her H1N1 flu shot today and had a nasty reaction. Just wanted to let everyone know so they can beware if and when you get yours. I am not getting one myself.

She lost her hearing, got diarreah, felt like she was going to pass out, heart heart was very racey, she felt like she couldn't breath, she was slurring her speech, her head felt very blurry/foggy etc.. She really did not want to get it to begin with and the doctor talked her into it. She said she will not get it again that's for sure. She said she thought she was gonna die. And as if she had a stroke. She is fine now but it took awhile for her to feel better. They kept her in the office for a while to keep an eye on her.

The following reports are from one site that has been documenting reactions to the H1N1 swine flu vaccine in Canada.....


So the call Aaron got Wed about the 18 yr. old Scott who had a stroke!!!! I talked to the girlfriends mom Kerrie who is our friend. He is still in a coma. They said it is bacterial, and brought in a specialist from the states. He is bleeding from his brain, and many internal organs. Last night Kerrie left me a message saying the doctors, and specialist have spoken with the parents and admitted it is due to the h1n1 vaccine!!!!!!!!!!!!!


" i heard some of the nurses and staff talking today about kids who have gotten the h1n1 shot….i think a boy under or just 2 died from the shot (I will ask around for confirmation), and a lot of kids have gotten really sick from the shot, some kids have gotten swine flu from the shot. i talked to 4 people today that got the shot and got really super sick. i’ve been here since thursday…i went to my OB’s clinic and they are giving out shots to pregnant women in the clinic, and the place was packed. they have tried to vax me 3 times but i have refused!"


a friend of mine today shared that her daughters friend ( a teenager) had taken the vax, and that same day she was bathing and became instantly ill… she felt light headed to the point of passing out, couldn’t communicate, managed to get her house coat on, head spinning and got down stairs opened the front door so she could yell out for help because she didn’t know what was happening to her. she passed out at the door.

The following reports are from a Facebook group called "h1n1 Vaccine Reactions".....

Pamela Genge-Way:

I had my vacine last friday around 2:00pm and around 10:00 that night, I started breaking out in hives. Have never had hives before this. All the hives started joining together, crazy itchy!!!! I was like I had a sunburn over my whole body. Started to swell in the arm, hands, legs, feet, chin, and lip. My feet is still swollen, but not itchy now. Thank God!!!

Melissa Steinhart:

My 3 yr old got the shot, 2 days later came down with a runny nose, high fever (103) and massive headache. 36 hours later, the fever went away, but the headache remained. No one at her school was sick or is sick, so I know it was this shot. NO WAY am I getting the 2nd one..

Heather Noëll:

I have a friend who's elderly aunt received the H1N1 vaccination and then died of swine flu two weeks ago.

Sheryl Colbourne:

My 10 month old son had his needle on Sat morning... 9 hours later he developed a Fever of 100-102 and very soar leg, didnt want to walk or crawl.

Jennifer Griffith:

My doctor is treating a 4 yr old who was perfectly healthy before he got the Swine/H1N1 vaccination a few weeks ago. His brain swelled, and he was given 2 weeks to live as his body is shutting down. As of today he's alive, but my doctor is not sure if he's going to make it.

Lisa Engle:

ran into a mom who was LIVID after vaccinating her son last week. his arm is still swollen and splotchy, he's had a fever and been vomiting since.
Mona Tannous:

Took my 2 yr and 10 month for shot yesterday. My 10 moths seems ok with no reaction. My 2 yr daughter didnt sleep all night. Started with very sore arm and I think joint pain since she was pointing to her knees. Then she started low grade fever. She vomitted. Then she woke up again complaining of stomach pain and vomitted another time!

After reading these stories, are you sure that you want to get yourself injected with the H1N1 vaccine? Thanks to the U.S. Congress, if you live in the United States and you get the swine flu vaccine you cannot sue anyone if something goes wrong. You alone will be responsible. Are you sure that you want to have a toxic stew that could include mercury, aluminum, formaldehyde, Triton X100 and Polysorbate 80 (among other goodies) injected directly into your bloodstream?

Are you sure?


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