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Let the people do what they want, you get Woodstock. Let the government do what it wants, you get WACO!....Mary.

 

 

 

 

297A- (X) HTML - DR GARY KOHLS - 20081013-0330

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FOR RESEARCH AND EDUCATIONAL PURPOSES ONLY

 

(FINAL REVISION)

 

DR G A R Y K O H L S

BY JACQUES HARDY

 

I don't usually write articles about a person but, as you are about to see, this is a very special case. I am reproducing below four articles received from Dr. Gary Kohls. These articles add up to a long and complicated reading time but as you will see, it is worth the effort and it may actually save your and your family's life. So, please read it all very carefully and draw appropriate conclusions. Next, you may want to start a world revolution and save the world from itself !

 

In what follows, you can see that things are not the way we think they are. Think about it all, learn and live 20 years or more longer. It is that simple.

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This is dated March 6th 2008 (18:37):

 

 

Preventive Psychiatry E-Newsletter # 329

50 Things Your Doctor Failed To Tell You About Vaccines

 

“All the available evidence shows that the decline of the infectious diseases was due (not to the vaccines but) to social factors, hygiene, sanitation, housing, nutrition, etc.”

 

http://www.eurosolve.com/charity/bava/vaccination.html Smallpox Smallpox would have disappeared around 1870 if Jenner's cronies had not persuaded Parliament to force the smallpox vaccine onto children in 1867, causing the largest epidemic of smallpox ever with a peak of 42,000 deaths in 1872. To test the effectiveness of natural immunity versus vaccination, the non-vaccinated Kingston Clinic staff challenged six vaccinated doctors to join them, in 1936, in a smallpox isolation unit. The doctors had the very good sense not to accept the offer.

The degree of AIDS incidence in Brazil, Haiti, Burundi, Rwanda, Tanzania, Zaire Zambia, Uganda and Malawi coincides with the degree of smallpox vaccination intensity.PolioAmerican health authorities are considering a complete change of policy in the face of strong evidence that all cases of polio are caused by the polio vaccine. Bernard Reis, English professor at Cornell University and an "energetic, athletic achiever" was paralyzed by polio a month after his baby was, by law, polio-vaccinated. 1.1 million dollars damages were awarded to Kay McNeary after she was crippled by polio alter changing her baby's nappy.

Millions of children, in the fifties and sixties, were given the Salk vaccine contaminated with the cancer-causing virus SV40. Dr F Klinner stated, "Many here voice a silent view that the Salk and Sabin vaccines, being made of monkey tissues, have been directly responsible for the major increase of leukemia in this country." The Lancet reported an outbreak of paralytic polio in Oman in fully vaccinated children. The vaccine lobby said what was needed was an increase of the vaccine dose at birth, 6, 10 and 14 weeks, and at times of other vaccines being given.Tuberculosis The World's largest vaccine trial, in Southern India, of the BCG vaccine, resulted in more TB in the vaccinated group than in the control group.DPT The whooping cough vaccine is made from the mucus of infected children, mixed with formaldehyde, aluminum and mercury. In a recent study of 540 Dutch babies, 512 had adverse reactions to the DPT vaccines. Thirty-thousand cases of diphtheria have occurred in recent years, in the UK, amongst diphtheria vaccinated children. A University of California study showed that 1,000 SIDS (cot deaths) per year are caused by the DPT shots. Dr Robert Mendelsohn, pediatrician, said, "...nearly 10,000 SIDS each year" (in the USA) " are related to the vaccines routinely given to children." In 1986 Dr Michael Weiner

PhD. stated, "More die each year from SIDS than the total number of all AIDS cases since 1981, yet little research money has been allocated to study the possibility of a relationship between these deaths and the DPT vaccine."MMROver a period of four years, in the UK, 66% of all measles cases were in vaccinated children. In a 1986 measles outbreak in Corpus Christi, Texas, 99% of the children had been vaccinated. 26% of children rubella-vaccinated developed arthralgia or arthritis. (US Science magazine.) Trials on the rubella vaccine, in the USA and Australia, show a failure rate of between 80 and 93%. Dr Glen Dettman found that one third of rheumatoid arthritis sufferers had live rubella viruses in their joints. The Lancet reported that West German authorities had listed 27 neurological reactions to the mumps vaccine, including meningitis, febrile

convulsions and epilepsy. There are 30,000 new cases of epilepsy; 10,000 of which are children, in the UK alone, each year.Hepatitis B The hepatitis B vaccine is made from the blood of human beings infected with hepatitis B; ie someone at high risk of developing AIDS. A Lancet study of 1991 showed a 20% hepatitis infection rate in 358 hepatitis-vaccinated Gambian children.HIB A. Minnesota study showed that the American Hib "polysaccharide" vaccine increased the risk of Hib-induced meningitis five-fold. The Lancet, August 1991, reported 9 cases of Hib-induced meningitis in vaccinated children. A study on the least useless Hib vaccine - the PRP-OMPC - in Los Angeles found a lowering of antibody response as vaccine dosage increased.Influenza The Post

Office dropped influenza vaccine promotion after it failed to show any reduction in absenteeism. The "Influenza Monitoring and Information Bureau" is funded by the influenza vaccine manufacturers. Six hundred elderly, influenza-vaccinated Birmingham people showed over double the respiratory disease than a similar non- vaccinated group. Dr Robert Mendelsohn stated that any influenza vaccine could cause Guillain-Barre Syndrome and paralysis. Influenza vaccines are made from material taken from 'flu victims; material then processed with mashed chick embryos, taken from disease-ridden intensive battery sheds. In November 1991, a Chesterfield man died within hours of being injected with the vaccine.Typhoid The typhoid vaccine is made from the excrement of typhoid-infected people.Cholera The World Health Organization has finally admitted, after countless cholera jabs, that the vaccine is useless, and has advised that, "It is not worth having."In General Known and suspected effects of vaccines include, asthma, eczema, increased allergies, encephalitis, cancer, leukemia, cot death, meningitis, lower motor neuron disease, juvenile diabetes, violent behavior, and so on. American medical historian, Harris Coulter, writing in 'Vaccination, Social Violence and Criminality' states, "A large proportion of the millions of US children suffering from autism, seizures, mental retardation, hyperactivity, dyslexia and other shoots and branches of the hydra-headed entity called "developmental disabilities", owe their disorders to one or another of the vaccines against childhood

diseases." According to Dr R de Long, "Since 1981 we have been immunizing the human population with attenuated (live) viral vaccines en mass. Such unparalleled use. . . may be the reason for the appearance of new diseases." We now have 20,000 new diseases, and rising. Vaccine makers, acting through corrupt bureaucrats, politicians and mass media agents, have always been able to pass off their wares after fraudulent animal testing; the human being is the real guinea-pig. Dr J A Morris, leading US infectious disease expert declared, "We only hear about the encephalitis and the deaths, but there is an entire spectrum between fever and death, and it's all those things in between that never get reported." - Dr R Mendelsohn said, "There now exists a growing theoretical concern which links immunization to the huge increase, in recent decades, of

auto-immune diseases, eg rheumatoid arthritis, multiple sclerosis, lymphoma and leukemia. "According to Dr Duperrat, "...vaccination causes, furthermore, an explosion of leukemia." A report in the Revue de Pathologie et de Physiologie Clinique, stated, "The vaccine modifies the terrain of the vaccinated, driving it towards alkaline and oxidized terrain; the terrain of cancer, the fact can no longer be ignored." Dr R Moskowitz, writing in the Journal of the American Institute of Homeopaths stated that vaccination could arouse latent, cell- bound, antibody immune viruses, leading, through stress or shock to "autonomous multiplication of cells, ie. cancer." Professor R Simpson, of the American Cancer Society, said that vaccines may cause rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus, Parkinson's Disease, and cancer.

 

All the available evidence shows that the decline of the infectious diseases was due to social factors, hygiene, sanitation, housing, nutrition, etc. Dr Moskowitz suggests that there are "fewer greater insults one can offer the immune system of a young child than to introduce, directly into his/her bloodstream, the foreign proteins or live viruses that compose modern Vaccines." And finally, if doctor, his receptionist, nurse and the "health visitor" cannot bully, threaten and arm-twist 90% of mothers on doctor's list into having their offspring permanently damaged with

vaccines, doctor will not get his annual bonus - on top of everything else -- of £1,737. + + + + +

 

This is dated August 30th 2008 (00:33)

The Military/Industrial/Congressional Complex’s

“Blow-It-Up Then Fix-It-Up” Scam

 

Where the World’s Vanishing and Unaffordable Oil is Actually Going

 

On Wed, 13 Oct 2004 19:20:38 -0400 Peter Tocci writes:

 

Somebody's getting a big chunk of the $200 billion in Iraq (the blow-it-up/fix-it-up game, sponsored by John Q).

Carlyle Group's stock shot up after 9/11. Two wars based on 9/11 bring tremendous profit to suppliers--especially the oil industry, but also weapons, vehicles, hi-tech, and materiel.

 

Do me a favor - -try to find out how many gallons of fuel have been used up to now in just the two Gulf wars by our military.

 

Hint: in peacetime (which we never get) the military uses enough fuel in one year to run the entire mass transit system of the US for 14 years!! An M-1 Abrams tank gets 252 gallons per hour.

 

An aircraft carrier gets 5,628 gallons per hour,

 

while a B-52 uses only 3,612 GPH.

 

The F-4 fighter-bomber averages 1,640 GPH,

 

but the F-15 sips along at 1500...until the afterburner cuts in, when it goes to 14,400 GPH.

 

More than 300 F-16's (1,052 GPH--getting more fuel-efficient!) were stationed in the Gulf with four carrier groups,

 

and an additional 725 assorted jets were in Saudi Arabia

 

(if your mind ain't boggled yet, it never will be). War, chaos, terror, disease, etc - - all means of transferring wealth, achieving genocide.

 

If they achieve no other goal than getting a war started, they've already done plenty for profit margins. What better product to sell than one that blows up?

 

(Cruise missile = $1 million each). But, the idea is, you gotta GET the things to blow up for there to be any profits for the investors, work for the workers and prestige for the CEOs...

Peter

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This is dated September 4th, 2008 (15:29)

Hunger and Militarism

By Gary G. Kohls, MD

 

Years ago I read a story about an elderly man, a loner, who lived in an impoverished area of Cleveland. Neighbors had noticed his mail piling upon his porch. When they received no response to phone calls or knocks on the door, they called the police, who broke into the man’s house. What they found is an allegory for our time

 

The old man was dead in his bed, surrounded by hundreds or thousands of dollars worth of rifles, pistols and guns of every type. Boxes of bullets and cartridges were stacked on the floor. He had a knife in his hand and an actual harpoon was leaning against his refrigerator, which was empty. In a nation of plenty and with grocery stores in the man’s neighborhood, he had died of starvation.

 

He had ignored his health and starved while “defending” himself and his property against “evil enemies” who never came to rob him. He had spent all of his money – his Social Security check, his pension, everything – on guns and ammunition but had spent nothing on food. He was afraid of burglars, perhaps justifiably, but had developed an obsessive fear of “the other” that had cost him his life.

 

It is the same in our world. The arms race that financially bankrupt the Soviet Union (“The Evil Empire”, as we called them) and morally and (nearly) financially bankrupt the United States of America (“The Great Satan”, as they called us) during the Cold War occurred at the expense of starving, unemployed, unhealthy and desperate people all around the world, including many in our own backyard and in the local ghettos on the other side of the tracks. Mutual fear caused the superpower nations and their allies to spend obscene amounts of money on inedible weapons systems in the name of “security”.

 

Amazingly, the five permanent members of the United Nations Security Council, that body that is supposed to promote world peace, accounted for, in the Reagan years, 87% of all weapons sales world-wide, and the United States was by far the worst one. Over the past three decades, approximately $1,000,000,000,000 (one trillion dollars) annually has been spent for war-making and war preparation. During the Cold War, the saber-rattling superpowers each spent $12 trillion dollars on troops, weapons development and weapons production, while thoughtful people helplessly watched the escalating injustices of poverty, hunger and homelessness. Our so-called leaders were worried enough about budget crises to cut social spending but cowardly enough to never question the budget requests of the warmongers in the Pentagon who wanted more and more

money.

 

The unrestrained arms buildup was contagious. Even starving third world nations led by dictators, military juntas, corporations and corrupt “presidents-for-life” were pawns of the superpowers and bought weapons of all types. This immoral arms dissemination was largely responsible for human rights disasters in countries like this post-WWII short list: Korea, Vietnam, Cambodia, Rwanda, the Congo, South Africa, Guatemala, El Salvador, Panama, Honduras, the Balkans, East Timor, Lebanon, Palestine, Israel, Iraq, Afghanistan, Pakistan, the Philippines, Darfur, Chechnya and other states of the former USSR, with predictable long-term consequences of famine, poverty and refugeeism.

 

The legacy of militarism is like chickens that have come home to roost. In the midst of our military power and “glory”, funded by essentially blank check federal borrowing that we taxpayers and our progeny will eventually have to pay for, we have masses of hungry, sick and poor who are conveniently hidden in inner city or on the reservation ghettos that most of us don’t see. We wonder why there is unaffordable health care, deteriorating infrastructure and escalating violence when military budgets dwarf programs of social uplift. But we shouldn’t have to wonder why there is so much hopelessness, ignorance, desperation, poverty and anger at a system of government that denies opportunities, represses, oppresses and then shows no remorse or shame for having done so.

 

Are we going to continue starving people, without any pangs of conscience, while cheering our #1 Military Superpower status? Are we going to continue to waste scarce resources on unaffordable military programs while ignoring investments to foster a sustainable peace and a sustainable economy? Are the Pentagon, the CIA and the dozens of other intelligence agencies (whose “black box” budgets and operations are well-hidden from public scrutiny) turning into expensive make-work jobs programs? Are we going to continue to ignore the fact that defense industry jobs cost taxpayers at least twice as much to generate and fund as any domestic job, such as green technology jobs? Are we going to continue to allow obscene military spending at the expense of the disappearing middle class and the burgeoning lower class?

 

For the last 30 years, the people who have been in positions of political and economic power in this nation have answered those questions with a resounding “yes”. There are still many in America today who recall fondly the “trickle-down economics” of the corrupt corporate capitalism put in place by Ronald Reagan in the early 1980s.

 

Those policies were ultimately disastrous for the vast majority of Americans, and the so-called “Reagan Revolution” of the 1980s started the process that resulted in America’s unsustainably bloated military budgets, the disappearance of the family farm and other small businesses, the fouling of the environment with hundreds of thousands of unregulated, lethal industrial pollutants and the dramatic increase in the disparities in wealth that are manifested all around by grinding poverty for the many, excess luxury wealth for the few, unsustainable credit card debt for tens of millions and increasing personal bankruptcies, home mortgage foreclosures and unaffordable and/or inaccessible health care.

 

America, and the world, needs to wake up before we all starve (spiritually as well as nutritionally), armed to the teeth, but with empty stomachs and refrigerators and no political will to solve the problems before it is too late.

 

Gary G. Kohls, MD, Duluth, MN

 

Checked by AVG. Version: 7.5.524 / Virus Database: 270.6.14/1645 - Release 9/1/2008 7:19 AM

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This is dated September 5th, 2008 (13:39)

Fellow healthcare givers and others concerned: Please read the following carefully because there are serious implications in it from an excellent and courageous research physician, Dr. Blaylock and other scientists that cannot be refuted by the various BigPharma industries in whose interest it is to continue pushing their highly profitable vaccines on trusting, unsuspecting physicians and their equally unsuspecting, trusting patients. If for no other reason than for the medical community to avoid future lawsuits from damaged patients or their families, we must understand the risks of these substances. Gary.

 

“Stimulating the immune system with a vaccine is far different than contracting an infectious illness naturally. Vaccines are made of two components–the agent you wish to vaccinate against–for example, the measles virus; and an immune system booster called an immune adjuvant. These adjuvants are composed of such (neurotoxic) things as aluminum compounds, MSG, lipid compounds and even mercury. Their job is to make the immune system react as intensely as possible and for as long as possible.

Studies have shown that these adjuvants, from a single vaccine, can cause immune over-activation for as long as two years. This means that the brain microglia remain active as well, continuously pouring out destructive chemicals. In fact, one study found that a single injection of an immune activating substance could cause brain immune overactivation for over a year. This is very destructive.”

Vaccines, Depression and Neurodegeneration After Age 50:

Another Reason to Avoid the Recommended Vaccines

By Russell L. Blaylock, M.D., CCN

http://www.russellblaylockmd.com/

It has been estimated that 6 million elderly Americans suffer from major forms of depressive illness at a cost of $44 billon dollars a year. Depression later in life tends to last longer and be more severe than at younger ages. It is also associated with a high rate of suicide.

Previously, it was thought that major depression was secondary to a deficiency in certain neurotransmitters in the brain, particularly the monoamines, which include serotonin, norepinephrine and dopamine. While alterations in these important mood-related neurotransmitters is found with major depression, growing evidence indicates that the primary culprit is low-grade, chronic brain inflammation. In addition, we now know that inflammatory cytokines can lower serotonin significantly and for long periods by a number of different mechanisms.

Researchers have also discovered that most people with major depressive disease (MDD) have higher levels of the neurotransmitter glutamate in their spinal fluid (CSF) and blood plasma. This is the same glutamate found as a food additive-for example, MSG (monosodium glutamate), hydrolyzed proteins, calcium or sodium casienate, soy protein isolate, vegetable protein concentrate or isolate, etc. Much of the free glutamate in the brain of depressed people comes from within, that is it escapes from special cells within the brain itself (microglia and astrocytes). Free glutamate, that is, existing outside the neurons, is very toxic to brain connections and brain

cells themselves - mainly by a process called excitotoxicity.

This connection between high brain glutamate levels and major depression was discovered quite by accident, when researchers observed that the anesthetic drug ketamine could relieve depression for a prolonged period. Ketamine is a powerful blocking drug for a class of glutamate receptors (NMDA receptors).

For quite some time it was known that depression could cause a loss of neurons in the hippocampus of the brain-the area most important for recent memory (declarative memory or working memory), the form of memory most affected in Alzheimer’s disease. This shrinkage of the brain usually occurred with long-term depression, yet it was shown, using sophisticated testing, that even without brain shrinkage, memory could be adversely affected. Some antidepressants could not only reverse the memory loss but could reverse the shrinkage as well.

The implication was that the elevated brain glutamate, via excitotoxicity, was destroying brain connections and later killing brain cells in the hippocampus and that the antidepressants were lowering brain glutamate levels. Subsequent studies have confirmed that drugs that block excitotoxicity also reduce depression and that some antidepressants reduce brain glutamate levels.

The Link Between Elevated Brain Glutamate and Inflammation

A tremendous amount of research has now demonstrated the link between chronic low-level brain inflammation, elevated brain glutamate levels and major depression. We know that as we age, the level of inflammatory immune cytokines increase (such as interleukin-1ß (IL-1), IL-6 and TNF-). That is, the level of inflammation in our body increases, with high levels being seen at the extremes of life –the 80s and 90s.

This progressive elevation in the body’s inflammation increases our risk of a number of inflammation-linked diseases, such as cancer, arthritis, muscle weakness, fatigue, sleep disturbances, memory loss and confusion. People with Alzheimer’s and Parkinson’s disease have even higher levels of these inflammatory cytokines –much higher.

When inflammatory chemicals are elevated in the brain it makes brain cells more vulnerable to a number of toxins, many of which are in the environment. One study demonstrated, using a series of sophisticated techniques, that if brain cells were exposed to low levels of a pesticide there was little toxicity seen and that if you exposed these same brain cells to an immune stimulant alone, little damage occurred. But if you first exposed the brain cells to the immune stimulant, the same low dose of pesticide could destroy a great number of brain cells.

The importance of this observation was that the vaccine made the brain cells hypersensitive to the toxin so that even in concentrations that normally would do not cause harm, could wiped out most of the neurons. One of the strongest connections between an environmental toxin (pesticides) and a neurological disorder is with Parkinson’s disease. The reason it is more common in the elderly is that they have the highest levels of inflammatory cytokines. This also explains the high incidence of Alzheimer’s disease, which reaches

incidences of 50% after age 80.

The link depression was also by accident. Doctors using immune cytokines to treat patients with cancer or hepatitis found that one third of the patients developed major depressive illness within days of the treatment and that it resolved only when the treatment was terminated. Other studies, in which inflammatory cytokine levels were measured in people with major depressive illness, also found most had high levels of these inflammatory chemicals.

To their surprise, they found that many of the antidepressant medications commonly used lowered inflammatory cytokines levels and that patients who failed to respond had the highest level of the cytokines.

So, how is this linked to excitotoxicity? Neuroscientists have known for some time that inflammatory cytokines cause the brain to release higher levels of glutamate –the more intense the inflammation, the higher the brain glutamate level. The highest levels are found in the prefrontal lobes and limbic system, the areas most related to mood control. MSG also increases brain inflammation.

Vaccination and Brain Inflammation

A great number of studies have shown that when you vaccinate an animal, the body’s inflammatory cytokines not only increase dramatically, but so do the brain’s inflammatory chemicals. The brain has its own immune system that is intimately connected to the body’s immune system. The main immune cell in the brain is called a microglia. Normally, these brain cells are lying throughout the brain in a resting state (called ramified). Once activated, they can move around, traveling between brain cells like amoeba (called amoeboid microglia).

In the resting state, they release chemicals that support the growth and protection of brain cells and their connections (dendrites and synapses). But when activated, they secrete a number of very harmful chemicals, including inflammatory cytokines, chemokines, complement, free radicals, lipid peroxidation products, and two excitotoxins –glutamate and quinolinic acid.

In essence, these brain immune cells are out to kill invaders, since the body’s immune system sent an emergency message that an invasion had occurred. With most infections, this phase of activation lasts no more than a few days to two weeks, during which time the immune system successfully kills off the invaders. Once that is accomplished, the immune system shuts down to allow things to cool off and the brain to repair what damage was done by its own immune system.

What researchers knew was that during this period of activation, people generally feel bad and that what they experience closely resembles depression –a condition called “sickness behavior”. Most of us have experienced this when suffering from a viral illness –such things as restlessness, irritability, a need to get away from people, trouble sleeping, fatigue and difficulty thinking.

Studies have shown that there are two phases to this “sickness behavior”; one in which we have the flu-like symptoms and a later onset of depression-like symptoms that can last awhile. They have also shown that all of these symptoms are due to high levels of inflammatory cytokines in the brain, which come from activated microglia.

A number of studies have also shown that after age 50, people have exaggerated and prolonged “sickness behavior”, much more so than younger people. This is one of the reasons why many elderly hang onto flu symptoms for months after exposure.

There is also another immune phenomenon that plays a major role in vaccine-related brain injury. Researchers discovered that when you vaccinate an animal, the brain microglia immune cells turn on partially (called priming), that is, they are in a state of high readiness. If the immune system is activated again soon after (days, weeks to months), these microglia explode into action secreting levels of their destructive chemicals far higher than normal. This overreaction can be very destructive and make you feel very depressed.

Stimulating the immune system with a vaccine is far different than contracting an infectious illness naturally. Vaccines are made of two components–the agent you wish to vaccinate against–for example, the measles virus; and an immune system booster called an immune adjuvant. These adjuvants are composed of such things as aluminum compounds, MSG, lipid compounds and even mercury. Their job is to make the immune system react as intensely as possible and for as long as possible.

Studies have shown that these adjuvants, from a single vaccine, can cause immune overactivation for as long as two years. This means that the brain microglia remain active as well, continuously pouring out destructive chemicals. In fact, one study found that a single injection of an immune activating substance could cause brain immune overactivation for over a year. This is very destructive.

Flu Vaccines and An Expanding Vaccine Schedule for the Elderly

Public health authorities and physician societies are in an all out campaign to have every elderly person vaccinated every year with the flu vaccine as well as a growing number of newer vaccines. When I was practicing neurosurgery, the hospitals had an automatic written order on all older patients’ charts mandating a flu vaccine, unless it was countermanded by the physician, which I always did. Now, they are giving the shots in malls, tents and every available site they can muster. And worse still, using lies and scare tactics to frighten the elderly onto getting the shots (such as the bold lie of 36,000 elderly dying of the flu every year).

As you age your immune system, including that special immune system in your brain, releases significantly more inflammatory immune cytokines than when you were younger. This serves to prime the microglia, as discussed. So, when you get your first flu shot your microglia overreact and does so for a very long period–perhaps years. Many elderly report that the flu shot gave them the flu. Proponents of vaccines, retort with a condescending laugh, that it is impossible because the flu vaccine contains killed flu viruses. In truth, what these people are reporting is a prolonged, intense “sickness behavior” response to the vaccine. To the body, it is worse than getting the flu. Remember, no one is recording the number of elderly who die after getting the flu shot, especially if

they die months later, which can happen with sickness behavior, especially if they have a preexisting chronic illness or are infirm.

Here is the shocking truth. With the elderly already having increased inflammatory cytokine levels both systemically and in their brain, stimulating these primed microglia so that a chronic overstimulation of the brain’s immune system is triggered, will not only increase their risk of developing one of the neurodegenerative diseases, but will also substantially increase their risk of developing major depression. Remember, this also increases their risk of suicide and even homicide dramatically.

Anxiety is a major problem with depression, and vaccinations will greatly worsen the condition. In fact, vaccination, especially multiple vaccinations, will maintain the brain in a state of inflammation that will be self-perpetuating, because the excess release of glutamate in the brain, as well as glutamate in the diet, will further enhance microglial activation and excitotoxicity.

Those who are prone to developing one of the neurodegenerative diseases, such as Alzheimer’s disease or Parkinson’s disease will be at a drastically increased risk as we have seen experimentally when even animals exposed to subtoxic concentrations of environmental toxins and vaccinated develop neurologic worsening.

Most people use pesticides in their home and studies have shown that the concentrations in homes are sufficient to trigger Parkinson’s disease in susceptible people. Vaccinations, as these studies have shown, will greatly increase risk. Most doctors are completely unaware of this important research.

You must keep in mind that “health authorities” urge the elderly to get the flu vaccine each and every year. This will keep the microglia in a primed and even activated state continuously. Recently, neurologists announced that the incidence of neurodegenerative disease had been grossly underestimated and that neurological diseases of aging were increasing at a frightening rate. They have no explanation. Over the last three decades the number of elderly receiving yearly flu vaccines has risen from 20% before 1980 to over 60% today.

If this were not depressing enough, now the public health authorities and medical specialty societies are adding a whole new set of vaccines for those above 50 years of age, including the pneumococcal and meningiococcal vaccines. What is being completely ignored by the promoters of these vaccines is the effect of multiple doses of immune adjuvant that accompany each of these vaccines.

Let’s say you see your doctor and he talks you into getting the flu vaccine, the pneumococcal and meningiococcal vaccine all during the same office visit. That way, he can save you extra office visits. What your doctor ignores is that he is giving you three doses of powerful immune adjuvant all in one sitting, which means that your body and brain are assaulted by a massive dose of powerful immune activators, which have been proven to activate the brain’s immune system to dangerous levels, even when given as a single dose. Proof of this mechanism exists not only in animal studies, but in humans as well.

Mercury and Aluminum

There are other ways that vaccines can cause havoc in the brain. Most vaccines contain aluminum compounds. A multitude of studies have shown that aluminum, especially if combined with fluoride, is a powerful brain toxin and that it accumulates in the brain. With each vaccine injection, a dose of aluminum is given. These yearly aluminum inoculations accumulate not only at the site of the injection, but travel to the brain, where it enters neurons and glial cells (astrocytes and microglia). A number of studies have shown that aluminum can activate microglia and do so for long periods. This means that the aluminum in your vaccination is priming your microglia to overreact. The next vaccine acts to trigger the enhanced inflammatory reaction and release of the excitotoxins, glutamate

and quinolinic acid.

You must also appreciate that any infection, stroke, head injury or other toxin exposure will also magnify this inflammatory brain reaction initially triggered by your vaccines. Studies have now indicated that the more one’s immune system is activated the more like he or she will suffer from one of the neurodegenerative diseases.

Mercury is also a powerful activator of brain microglia and can do so in extremely low concentrations-in nanomolar amounts. Because of its numerous reactions with sulfhydral compounds in the body (which are ubiquitous), mercury can poison a number of enzymes both systemically and in the brain. Of special concern is the ability of mercury, especially ethylmercury (the kind found in vaccines called thimerosal) to inhibit the regulation of brain glutamate levels. (It does this by inhibiting the glutamate transfer proteins that control the removal of glutamate from outside the neuron, where it does its harm.)

In essence, mercury, in the concentrations being injected with vaccines, triggers excitotoxicity, increases brain free radicals and lipid peroxidation products, inhibits critical brain enzymes, inhibits antioxidant enzymes and impairs DNA repair ability. The flu vaccine contains enough mercury to do all of these things. You must keep in mind that each flu vaccine adds to the mercury supplied by your last vaccine, that is, it is progressively accumulating in your brain.

In addition, the aluminum in the vaccines also primes microglia and when combined with mercury is infinitively more toxic to the brain. Now, if this is not enough, we also have to consider the contamination of vaccines with foreign viruses and viral components. Studies have shown that this is not a rare occurrence, with up to 60% of vaccines being contaminated in one study of several major manufactured vaccines. When confronted with this fact, vaccine proponents just shrug their shoulders and say –“We don’t think these things are harmful.”

Yet, the studies say otherwise. It has been found that insertion of viral fragments, not even the whole virus, is sufficient to trigger the brain’s microglial system and subsequent excitotoxicity, leading to progressive brain degeneration. This is accepted to be the mechanism by which the HIV virus causes dementia in a great number of AIDS victims. Fragments of the virus (gp140 and Tat) are engulfed by the microglia and this triggers chronic brain inflammation and excitotoxicity. The herpes virus and measles virus can do the same thing.

Danger of Live Virus Vaccines

A number of studies have shown that live viruses used in vaccines can enter the brain and reside there for a lifetime. One such study, in which autopsied elderly were examined for the presence of the measles virus, found that 20% of the brains had live measles viruses and 45% of other organs were infected. These viruses were highly mutated, meaning that they could be just as potent as other measles viruses, but could be even more virulent. Worse is that in most cases they cause a smoldering destruction of tissues without the obvious symptoms of infection, which has been shown in a number of studies.

Live virus vaccines are made using a process to attenuate the pathogenic or disease-causing virus by passing it through a series of cultures. The problem is that the reverse can also happen within the body. A number of studies have shown that when we produce free radicals in our body (and we produce tons of such radicals over a lifetime), it mutates the viruses residing in our tissues. This is what was found in the autopsy study I referred to above.

Likewise, these viruses can trigger brain inflammation and degeneration, which has been shown in a number of studies-that is, there exist a chronic degeneration of the brain over years or decades. Because it is so far separated from the time of the original vaccine, physicians just attribute it to old age or heredity, anything but the vaccines.

Virologists are also concerned that such mutated live viruses can also infect other people, leading to outbreaks of disease totally unsuspected by health authorities.

Conclusion

Current recommendations by the CDC for adult vaccinations include a total of 14 separate inoculations with infectious agents and powerful immune adjuvants. To be fair, some of these are for special medical risks and conditions, such as high-risk behaviors, illegal drug use and HIV infected individuals. If we eliminate these, women will be exposed to 10 inoculations and men 7, should they follow CDC guidelines, which doctors follow.

According to CDC recommendations, multiple vaccinations for a single disease are separated by no more than 4 weeks, which is close enough together to produce priming and subsequent hyperactivation of brain microglia. We have seen that this can trigger a smoldering process of brain inflammation and excitotoxicity that can not only result in depression, anxiety and high suicide rates, but can increase one’s risk of developing one of the neurodegenerative diseases as well.

We have also seen that in many cases a person will be injected with several vaccines during a single office visit and that this means their body is exposed to a very large doses of immune adjuvants. Compelling studies, using many animal species as well as humans, have shown that this overactivates brain inflammatory mechanisms that can last for years.

In addition, several additives to vaccines, such as mercury and aluminum, are powerful brain toxins that are known to accumulate in the brain over years and can trigger brain inflammatory/excitotoxic mechanisms. Vaccine contaminants, such as bacteria, mycoplasma and viral fragments can also produce prolonged brain inflammation and neurodegeneration.

Because the elderly already have high levels of inflammatory cytokines, they are at a special risk. The very young (babies and small children) are at a high risk because their brains are undergoing the most rapid development at the very time they receive the greatest number of vaccinations–the first two years of life. In fact, they receive 22 vaccines during the first year of life, one of which contains a full pediatric dose of mercury. Like adults, they receive many inoculations (up to 9 inoculations) in one office visit. This is

insane and in my estimation, criminal.

Nasal flu vaccines are even worse, because they introduce a live virus into the nasal passages, which can then travel along the olfactory nerves, which leads to the very part of the brain first and most severely affected by Alzheimer’s disease. A number of studies have shown that viruses and bacteria can pass along this route to the brain. In fact, in one study scientists sprayed a bacterium into the nose of mice and observed a rapid development of Alzheimer’s type plaques in the mouse’s brain.

So, what should older people do? First, studies have shown that the primary cause of immune deficiency in the elderly is purely dietary. The carotenoids, such as beta-carotene, alpha-carotene, canthaxanthin, lutein and lycopene significantly enhance the immunity of the elderly. Zinc, magnesium and selenium are also essential. One should also avoid omega-6 oils (the vegetable oils-corn, safflower, sunflower, canola, soybean and peanut oils), since they greatly enhance inflammation and depress immunity. The EPA component of fish oils (omega-3 oils) is also a powerful immune suppressant. DHA is not. A healthy immune system means that you can fight infections efficiently and rapidly.

Regular exercise, such as brisk walking or weight exercises three to five times a week also boost immunity, while extreme exercise suppresses immunity. Sugar and refined carbohydrates also suppress immunity and inflame the brain. Exercise protects the brain from aging effects and from degeneration.

Adequate sleep is also vital to both brain health and good immune function. Pubic health officials and spokesmen for the major medical societies are lying to the public concerning vaccine safety. We now possess sufficient information from a great number of studies to halt this disastrous vaccine policy. We are facing a medial disaster in this country, which is already well on its way.

1.McGeer PL and McGeer EG. Local neuroinflammation and progression of Alzheimer’s disease. J Neurovirology 202; 8: 529-538.

2.Tavares RG, et al. Quinolinic acid stimulates synaptosomal glutamate release and inhibits glutamate uptake into astrocytes. Neurochem Int 2002; 40: 621-627.

3.Eastman CL, et al. Increased brain quinolinic acid production in mice infected with a neurotropic measles virus. Exp Neurol 1994; 125; 119-124.

4.Glass JD and Wesselingh SL. Microglia in HIV-associated neurological diseases. Microsc Res Tech 2001; 54: 95-105.

5.Turowski RC and Troozzi PL. Central Nervous System toxicities of cytokine therapy: In: Plotnikoff NP, et al, Eds. Cytokines, Stress and Immunity. Boca Raton, CRC Pres, 1998, pp 93-114.

6.Mrak RE, et al. Glail cytokines and Alzheimer’s disease: Review and pathogenic implications. Human Pathol 1995; 26: 816-823.

7.Klatschmidt C, et al. Stimulation of inotropic glutamate receptors activates transcription factor NFkB in primary neurons. Proc Nat Acad Sci USA 1995; 92: 9618-9622.

8.Gao HM, et al Distinct role for microglia in rotenone-induced degeneration of dopaminergic neurons. J Neurosci 2002; 22: 782-790.

9.Dyatlov VA et al. neonatal lead exposure potentates sickness behavior by Listeria monocytogenes infection in mice. Brain Behav Immun 2002; 16: 477-492.

10.Nakai Y, et al. Apoptosis and microglial activation in influenza encephalopathy. Acta Neuropath (Berl) 2003; 105: 233-239.

11. Anderson T et al. NMDA-receptor antagonist prevents measles virus-induced neurodegeneration. Eur J Neurosci 1991; 3: 66-71.

12. Conner TJ, et al. Depression stress immunological activation: the role of cytokines in depressive disorders. Life Sciences 1998; 62: 583-606.

13. Renault PF, et al. Psychiatric complications of long-term ineterferon-alpha therapy. Arch Internal Medicine 1987; 147: 1577-1580.

14. Adams F et al. Neuropsychiatric manifestations of human leukocyte interferon therapy in patients with cancer. JAMA 1984; 252: 938-941.

15. Broderick PA, et al. Interleukin-1 alters hippocampal and norepinephrine release during open field behavior in Sprague-Dawley animals: differences from the Fawn-Hooded animal model of depression. Prog Neuropsychopharmacol Biology 2002; 26: 1355-1372.

16. Katayama Y, et al. Detection of measles virus nucleoprotein mRNA in autopsied brain tissues. J General Virology 1995; 76: 3201-3204.

17. Nicolson GL et al. High frequency of systemic mycoplasma infections in Gulf War Veterans and civilians with amyotrophic lateral sclerosis. J Clin Sci 2002; 9: 525-529.

18. Blaylock RL. Interaction of cytokines, excitotoxins, and reactive nitrogen and oxygen species in autism spectrum disorders. JANA 2003; 6: 21-35.

19. Blaylock RL. Central role of excitotoxicity in autism. JANA 2003; 6: 7-19.

20. Blaylock RL. Food additive excitotoxins and degenerative brain disorders. Medical Sentinel 1999; 4: 212-215.

21.Pilc A, et al. Mood disorders: regulation by metabotropic glutamate receptors. Biochem Pharmacol 2007; (Epub ahead of print)

22. Palucha A, Pilc A. The involvement of glutamate in the pathophysiology of depression. 2005; 18: 262-268.

23. Paul IA, Skolnick P. Glutamate and depression: clinical and preclinical studies. Ann NY Acad Sci 2003; 1003: 250-272.

24. Pittenger C, et al. The NMDA receptor as a therapeutic target in major depressive disorder. CNS Neurol Disorders Drug Targets 2007; 6: 101-115.

25. Magaki S et al. Increased production of inflammatory cytokines in mild cognitive impairment. Exp Gerontol 2007; 42: 233-240.

26. Gao H-M et al. Synergistic dopaminergic neurotoxicity if the pesticide rotenone and inflammogen lipopolysacchride: relevance to the etiology of Parkinson’s disease. J Neurosciences 2003; 23: 1228-1236.

27. Holmes C et al. Systemic infection, interleukin 1ß, and cognitive decline. J Neurol Neurosurgery Psychiatry 2003; 74: 788-789.

28. Godbout JP et al. Exaggerated neuroinflammation and sickness behavior in aged mice after activation of the peripheral innate immune system. The FASEB J 2005; 19: 1329-1331.

29. Perry VH et al. The impact of infection on the progression of neurodegenerative disease. Nature Rev Neuroscience 2003;4: 103-112.

30. Feiring B et al. Persisting responses indicating long-term protection after booster dose with meningococcal group B outer membrane vesicle vaccine. Clin Vaccine Immuno 2006; 13: 790-796.

31. Vaccine Excepients and Media Summery Center for Disease Control and Prevention. (also source for recommended vaccines for adults and children).

+ + + + +

WHAT NOW?

 

All the above is quite interesting but now, I have something else on my mind and it is that suddenly, there is presently a lot of talk about Armageddon. Why this? Well the way I reason is like this:

 

 

1. Armageddon is an act of God NOT an act of man.

2. The Plutocracy-ruled U.S.A. needs depopulation .

3. They find the present rate of depopulation far too slow.

4. So they plan to cause an Armageddon of their own.

5. For this an all out world war would accomplish the job.

6. And so they will use people's naivety... or stupidity.

7. And create an Armageddon of their own.

8. Claiming all the time that it is God's will.

9. Hence victory for the plutocracy.

10. And universal death for the fools. + + + + +

P.S. 1:

 

 

"Capitalism is a philosophy of failure, the creed of ignorance, and the gospel of envy. Capitalism leads to the enslavement of the sheep citizens by the greedy, selfish plutocratic class" JACQUES HARDY.

 

P.S. 2:

WARNING: Whatever I say is considered anti-plutocratic and unacceptable by the wealthy few (those who rule the world), therefore if you have read this (gasp!), you must hurry up and go to confession or else they will make minced meat or perhaps apple sauce with you. Don't forget your position of plutocratic slave, also called "patriot"... totally FREE to suffer and die so the wealthy few can get wealthier and more powerful.

 

Faithfully yours,

 

 

 

Jacques Hardy, Canada

Proud to have been banned by all the truth-hating media, starting from 1978.

 

 

 

 

These weekly reports covering socio-political subjects are the results

of the joint efforts of an Australian-Canadian-Russian-US team,

with help from other countries.

FOR RESEARCH AND EDUCATIONAL PURPOSES ONLY

THIS IS A PERSONAL OPINION, WHICH YOU CAN REPRODUCE, PUBLISH OR DELETE AS YOU SEE FIT, AND YOU ARE ALSO FREE TO CONGRATULATE ME, IGNORE ME OR CONDEMN ME FOR SUPPORTING THE FEW HONEST AMERICANS WHO WANT TO PUT A STOP TO THE PLUTOCRATIC MURDERING RAMPAGE.

N. B. : My stuff is never copyrighted, so you can use it as you wish FOR the benefit of MANKIND / HUMANITY and AGAINST narrow, selfish, nationalistic interests.

- - - - - -

YOUR NAME WAS REFERRED TO ME AS BEING A PERSON INTERESTED IN THE EVOLUTION AND FUTURE OF HUMAN SOCIETY, BUT IF YOU DON'T WANT ME TO WRITE TO YOU, IF HUMANITY LEAVES YOU INDIFFERENT, PLEASE SAY SO AND I WILL STOP AT ONCE.

To be removed from this list, please kindly reply to this e-mail with the word REMOVE and you will be instantly removed, deleted and forgotten.

When replying, please refer to number in subject line

Email Address = jacques.hardy

Apt. 327, 117 Cartier, Pointe Claire, P.Q.

H9S 5K4 CANADA

PHONE: (514) 697-2576 (If busy, leave message)

FAX: 514-697-2774 (ask first)

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FOR RESEARCH AND EDUCATIONAL PURPOSES ONLY

 

 

* * * * *

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