Showing posts with label Immunity. Show all posts
Showing posts with label Immunity. Show all posts

Tuesday, March 15, 2016

WHO WANTS TO SHARE THE CHICKENPOX????




https://nvnin.wordpress.com/2016/03/15/who-wants-to-share-the-chickenpox/

Chickenpox is one of several minor childhood illness nearly every child experiences in their early years, or at least they used to. Mild fever, a few days of itchy spots, and that was it. What remained was a strengthened immune system and possibly a few minor scars. Since the introduction of a vaccine, chickenpox has become a thing of the past...... or has it? What consequences are there for changing the natural course of a benign childhood disease?
The chickenpox vaccine was introduced in the United States in the mid 90's, and was soon thereafter added to the CDC vaccine schedule. Initially, it was recommended anyone under age 13 receive one dose of the vaccine while anyone over 13 receive two doses, claiming two doses would incur lifetime immunity. Following its implementation, children under 13 continued to contract chicken pox, so in 2006 the CDC recommended that younger children also receive 2 doses of the vaccine. The CDC also claims the vaccine makes this mild disease somehow less dangerous, but this isn't always the case. So, how safe is this vaccine really?

SOME FACTS ABOUT THE CHICKENPOX VACCINE
There are two live virus vaccines for chickenpox licensed in the U.S.: Varivax and ProQuad (MMRV), both manufactured by Merck.
  • The CDC recommends children receive a chickenpox vaccination at 12 months and a booster dose between 4 and 6 years of age;
  • Reported complications from the chickenpox vaccine include: shock, seizures, brain inflammation (encephalitis), thrombocytopenia (blood disorder), Guillain-Barre Syndrome, death, and infection with vaccine-strain chickenpox including possible transmission of vaccine-strain chickenpox to others;
  • Chickenpox vaccine effectiveness is reported to be 44 percent for any form of the disease and 86 percent for moderate to severe disease;
  • Mass use of the chickenpox vaccine in the U.S. has removed the opportunity for the natural boosting of immunity in the population by re-exposure, which provides protection from shingles occurrences. Due to this, adults as well as vaccinated children are now experiencing shingles outbreaks;
  • In 2006, the CDC recommended an additional dose of the chickenpox vaccine for all children under age 13, and a shingles vaccine was licensed and recommended for all adults over age 60 in an attempt to combat the rising occurrence of shingles outbreaks.
  • As of September 1, 2015, there had been 122 claims filed in the federal Vaccine Injury Compensation Program (VICP) for injuries and deaths following chickenpox or varicella vaccination, including 8 deaths and 114 serious injuries.
  • Using the MedAlerts search engine, as of September 30, 2015 there have been 3,358 serious adverse reactions reported to the Vaccine Adverse Events Reporting System (VAERS) in connection with chickenpox varicella-containing vaccines since 1990. Over half of all reported serious chickenpox vaccine-related adverse events occurred in children six years old and under. Of those, 161 were deaths, with over 60% of the deaths occurring in children under six years of age.
    http://www.nvic.org/Vaccines-and-Diseases/Chickenpox.aspx

WHAT ABOUT SHINGLES?
Chickenpox cannot thoroughly be discussed without also mentioning shingles: the reactivation of the varicella virus due to stress or a compromised immune system. The chickenpox vaccine is not used in the UK and many other countries around the world because it is known that re-exposure to the chickenpox virus is required to prevent waning immunity in older individuals, i.e. shingles outbreaks. “If there is less chickenpox in children then there will be no boosting of immunity by exposure to chickenpox for middle and older aged people and thus there will be more shingles, at least until all the elderly have been vaccinated as children but this assumes that immunity conferred by vaccination is lifelong.”

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2563790/

Studies have shown that the chickenpox vaccine does increase the risk of shingles, but even that fact is being distorted: “Vaccinating one-year-olds against chickenpox could temporarily nearly double the incidence of shingles in the wider population, but in younger adults than previously thought.”
https://www.sciencedaily.com/releases/2015/08/150811103555.htm
It should be mentioned that MERCK is maker of both the vaccine for shingles and chickenpox.

WHAT ARE THE CHICKENPOX LIKE?
Many parents still opt for natural infection. This is due to vaccine failure as well as the unknown duration of effectiveness this vaccine may offer. I will be keeping this blog post updated with stories, videos, and pictures of real people from around the world who have experienced chickenpox. I personally did not have chickenpox as a child, and am therefore also attempting to gain exposure as part of my documentary entitled “SPOTTING THE TRUTH!”
https://nvnin.wordpress.com/2016/03/01/what-i-need-to-finish-my-non-vax-natural-immunity-documentary/
CHICKENPOX CASE #1
Here is what the chickenpox were like for a family from the Midwestern United States that opted for natural immunity, as you can see everything is fine, just an award winning case of the chickenpox.









CHICKENPOX CASE #2
The next chickenpox experience comes from New Zealand, this family was kind enough to give full details of their chickenpox experience.




I will be doing similar blog posts for other childhood diseases, including mumps, measles, and rubella. I recently did a blog post regarding mumps, which can be seen here:

If you, or someone you know, currently has a childhood disease and is open to considering my exposure, please contact me. If anyone has had a childhood disease and is open to sharing their personal experiences, please consider giving an interview. Any/all identifying information will be kept strictly confidential at your request. Whether you support natural immunity, have personal experience with vaccine injury, or just want to help with my project, please feel free to contact me:

Or privately
at forcedanarchy@gmail.com

Thursday, February 12, 2015

THE M-M-R VACCINE WEARS OFF / DOES NOT WORK????

I was just looking the frequently ask questions from the NHS about the MMR (MUMPS, MEASLES, RUBELLA) VACCINE and I REALLY have to ask HOW F#CKING STUPID DO THEY THINK WE ARE???? The logic being used is absolutely ABSURD!!!! BELOW ARE A FEW HIGHLIGHTS OF THE STUPIDITY!!!!

How long does protection from MMR last?

It seems to be very long lasting. Virtually everyone (more than 99%) will be protected against measles and rubella for more than 20 years after two doses of MMR.

Protection against mumps after two doses of MMR is a little lower (90-95%) and appears to gradually decline. Mumps in vaccinated people is, however, much less likely to lead to complications such as meningitis or orchitis (painful swelling of the testes) and vaccinated people are less likely to require admission to hospital.

WTF??? MUMPS IS A SELF LIMITED DISEASE AND IS MILDER THE YOUNGER YOU ARE! THE SAME GOES FOR MEASLES! Natural measles gives you life long protection BUT if you notice they claim the MMR protects for over 20 years. I call bullshit on this and think many of the recent outbreaks are from the vaccine wearing off. Yet another reason to seek out the childhood diseases and have them over and done with! Natural immunity is the ONLY immunity!
Take a look at their contradictions on the NHS website and notice that the UK has ONLY the MMR since 1988!!!! Prior to this MUMPS was NOT seen as a big deal, funny how that changes when you can push a vaccine...  ADDING TO THE INSULT IS THE CONTINUED DENIAL OF VACCINE INJURY, I MEAN REALLY WTF... :-( :-( :-(
http://www.nhs.uk/Conditions/vaccinations/Pages/mmr-questions-answers.aspx#long

HAMPSTER DEAD

Wednesday, January 28, 2015

NEW NON VAX NATURAL HEALTH DOCUMENTARY "SPOTTING THE TRUTH"

So THIS is what I need to do the documentary that I am doing titled "SPOTTING THE TRUTH". This is a near impossible documentary but if people step up and help me I can do this! The most critical things is I need are to connect with people who are non vaxers and are seeking natural immunity to the various childhood diseases for their families. I need interviews before, during, and after they have had the childhood diseases (chickenpox, mumps, measles, rubella).
I am also seeking exposure to all of the childhood diseases not only because I have never had any childhood disease (not even chickenpox) but because I would never ask anyone to do something that I am not willing to do myself. I plan on keeping a video diary of the experience and use that as part of the documentary.
I also need to talk to many of the countless people who have been vaccine injured. Vaccine injuries are far to common and in my opinion happen 100% of the time when you vaccinate.
After this I will try to talk to medical experts who are against vaccines and get their take on this. I am not even sure if anyone will speak with me.
Finally, I will use the CDC and Pharmas own information against them. I will also be using the propaganda of the media and pro vaxers against them. IF PEOPLE HELP ME I CAN DO THIS!!!!

For those wondering WHY the documentary I am doing is not just focusing on vaccine injury and is spotlighting natural immunity it is because proving and showing on film that they are lying about the severity of the childhood diseases will shut down one of the biggest arguments the pro vaxers use to justify poisoning humanity. This is why I am seeking out the childhood diseases for myself, and it is why I need to find non vaxing families who are willing to be interviewed before, during, and after the childhood diseases. With that being said talking with the families of the vaccine injured is just as important and will play a huge role in this film.

Feel free to message me privately on facebook https://www.facebook.com/NATURALIMMUNITY or email me forcedanarchy@gmail.com if you can help.

To Protect His Son, A Father Asks School To Bar Unvaccinated Children

I AM VERY SORRY THIS KID HAS CANCER, I AM SORRY WE LIVE IN A WORLD WHERE EVEN THE FOOD SUPPLY IS TOXIC, BUT I FEEL IF THIS IS KID IS THIS SICK HE SHOULD BE THE ONE REMOVED FROM SCHOOL! All of this fear over what used to be not a big deal, a week or so with spots and you were done with it...

www.npr.org/blogs/health/2015/01/27/381888697/to-protect-his-son-a-father-asks-school-to-bar-unvaccinated-childrena

Saturday, September 24, 2011

HPV VACCINE & POSSIBLE MANDATED CIRCUMCISION FOR BOYS!

This is just sick! Next the CDC will be using the HPV excuse as a way to push and possibly mandate circumcision of males. Mark my words on this, they are going to try it! They will use HPV, HIV, or some other hair brained excuse.

This is not the 1st time that a vaccine protecting females was later pushed on boys--They did it with the rubella vaccine.
PLEASE NOTE: While the safety of the HPV vaccine is generally established and still remains recommended by the government health agency, it has been shown in some studies to be associated with anaphylaxis, blood clots and fainting, and linked with some deaths.

*****

HPV Vaccine For Boys? CDC Considers Recommending Vaccinations For All

Vaccinating just half the population against human papilloma virus (HPV) only solves half the problem.

Now that the Centers for Disease Control and Prevention recommend that girls and young women be vaccinated against the disease that can lead to cervical cancer, the treatment's effectiveness with regard to the male population is beginning to come into the limelight. In fact, the CDC is now considering recommending the shot for boys as well, according to Health Day.
From Health Day:
A debate that's been simmering over whether males also should be vaccinated for human papillomavirus, or HPV, could come to a head in October at a meeting of a key advisory committee of the U.S. Centers for Disease Control and Prevention, said CDC spokesman Tom Skinner.
Previous studies have shown that the HPV vaccine could even have a more powerful effect than simply immunizing males against the disease and protecting women. According to Science Daily, one study showed that giving the vaccine to men could prevent as many as 90 of genital warts cases.

A study published in March also said that almost half of the male population of the US could be infected with HPV.

The issue of immunizing girls to the virus has returned to the limelight recently amidst the GOP Presidential debates. Notably, Texas Governor Rick Perry's 2007 mandate to require young girls to be vaccinated against the disease has drawn criticism from fellow conservatives.

According to Everyday Health, the measure was overridden in 2008.
While the safety of the HPV vaccine is generally established and still remains recommended by the government health agency, it has been shown in some studies to be associated with anaphylaxis, blood clots and fainting, and linked with some deaths.

Monday, April 13, 2009

INFO NEEDED! Measles in MD & PA possibly other states

Does anyone have any information on the measles cases in Maryland and Pennsylvania? There could be cases in other states these are just the ones I have read about on Google news. I am seeking exposure as a part of the anti vaccine documentary I am doing and if anyone could give me any information that would be really great.

Please no nasty or rude emails regarding this as I know what I am doing. Feel free to email me off of my blog if you want forcedanarchy@aol.com or reply here Thanks and Take Care

Tuesday, May 27, 2008

Emergency measures are being implemented to halt UK measles outbreak

When will they stop injecting children with this poison?

*****

Emergency measures are being implemented to halt a measles outbreak.

Health chiefs in London have ordered NHS trusts to offer MMR jabs in quick succession amid a surge in measles.

There have been over 200 cases in south east London in the first five months of this year. It comes after a record 1,000 were recorded nationally in 2007.

The Health Protection Agency said it hoped that offering the two jabs within months instead of two years apart would help stem the rise.

Similar steps were taken when there was a high concentration of cases in north London last year.

MEASLES

Measles is a highly infectious virus. It starts with a fever and conjunctivitis before a rash develops

The rash often lasts about a week and other complications can include pneumonia and diarrhoea

The MMR jab is used to immunise children against the disease

Before the triple vaccine was introduced in the late 1980s, there were 20 deaths a year on average in the UK

But since the early 1990s there has just been one in total

It is not known exactly what has caused the rise in cases, but take-up of MMR has struggled to recover from being linked to autism in the 1990s.

At least 95% of children need to have the triple-jab to create herd immunity to stop the disease spreading, but London in particular has struggled to reach that.

About three quarters of children across London have had the first jab which is given to babies at 13 months of age.

The second jab, offered to capture the one in 10 who do not get immunity by the first vaccination, is normally given before children start school.

But the Health Protection Agency has told the six trusts in south east London - Lewisham, Lambeth, Southwark, Bexley, Bromley and Greenwich - to give the second jab one to three months after the first.

Concern

HPA disease control expert Diana McInnes said: "The increase in measles cases is of concern and we know that large numbers of children are still not fully protected.

"In south east London we are encouraging parents to give the second MMR between one to three months after the first dose to protect their children.

"Children's immune systems have a huge capacity and overloading them with the vaccination is not an issue.

"Our main focus is to remind people that they need two doses of the MMR vaccine to be fully protected."

Health officials in Lewisham, which has had some of the highest rates of infection, is running special clinics to get every child under five immunised.

Parents of children between five and 16 who have not had the second jab are also being urged to go to their GP to get the jab.

A Lewisham PCT spokesman warned: "The disease is still spreading, particularly among school-age children."
Story from BBC NEWS:
http://news.bbc.co.uk/go/pr/fr/-/2/hi/health/7408278.stm

Published: 2008/05/19 11:55:59 GMT

© BBC MMVIII

Friday, May 2, 2008

ABC HOW DARE YOU!

How dare ABC run a pro vaccine story and label it "Protecting Your Child From Improper Vaccination" This shows a true lack of ethics :( Improper vaccination would be a story on those poor kids who died in India from the MMR vaccine, not this one sided garbage.

*****

http://www.abcnews.go.com/WN/Germs/story?id=4751184&page=1

ABC News
Protecting Your Child From Improper Vaccination
Government Study Finds 1 in 4 Children Are Improperly Vaccinated
By JOHN McKENZIE

April 29, 2008—

Vaccinations are a childhood ritual and provide vital protection against diseases like measles, mumps, rubella and polio, which can be extremely dangerous for young children. But a report, issued today by the Centers for Disease Control and Prevention, found an alarming 28 percent of toddlers have not been vaccinated according to U.S. guidelines.

Elizabeth Luman of the CDC said, "It's not acceptable to have any child improperly or incompletely vaccinated, because that increases their risk of disease and also increases the risk of outbreaks in the community."

RECOMMENDED TIMES FOR YOUR CHILD'S VACCINES: Input your child's age, and this interactive vaccine scheduler will give you a list of recommended dates for all your child's vaccinations.

Earlier this year, measles outbreaks were reported in San Diego, Arizona and Wisconsin. Health officials said the problem was caused by people who had never been vaccinated, usually out of fear of vaccines. But this government survey is surprising because it affects children whose parents actually intended to have them vaccinated and believed that they had been fully vaccinated.

Government guidelines call for toddlers to get a series of at least 17 injections, protecting them against 15 different diseases. But the survey found that one in five children was actually missing one or more doses.

Do you know which vaccinations your child is missing? CLICK HERE for a step-by-step guide to obtaining and understanding your child's immunization records.

And according to Dr. Lara Danziger-Isakov of the Cleveland Clinic, "Missing even a single dose may impair your immunity."

But mis-timing vaccination doses is also a problem. The government has an exact schedule for when each shot needs to be given. But the study found that one in twelve children got at least one vaccination too early in life.

"If you give them the vaccine at the wrong time, their immune system may not be developed enough to respond to that vaccine, and they may not develop immunity," Danziger-Isakov said.

Want to learn more about childhood vaccines? CLICK HERE for a backgrounder.

Pediatricians say giving vaccines earlier than recommended is often done out of convenience.

Some researchers said today's report should serve as a wake-up call to parents and pediatricians because much more needs to be done to ensure children get the full benefits and protection of these lifesaving vaccines.

Did you know an immunization registry can keep track of your child's records? CLICK HERE for more information.

Copyright © 2008 ABC News Internet Ventures

Monday, April 21, 2008

How Vaccines Can Damage The Brain

Vaccines, Depression and Neurodegeneration After Age 50: Another Reason to Avoid the Recommended Vaccines.

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

It has been estimated that 14.8 million Americans suffer from major depressive disorder and of this number 6 million are elderly. If we include anxiety disorders, which commonly accompany depression, the number jumps to 40 million adults. At a cost of $44 billon dollars a year just for care of the seniors, this impacts the national budget as well. 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 pr! ocess ca lled 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-a). 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 e! ven high er 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 mo re 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 last 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 experience this when suffering from a viral illness -- such things as restlessness, irritability, a need to get away from people, trouble sleeping, fatigue! and dif ficulty 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 destructi! ve.

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 ris! k of dev eloping 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 th! at accom pany each of these vaccines.

Lets, 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 (w! hich 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 dose of immune adjuvant. Compelling studies, using many animal species as well as humans, have shown that this overactivates brain inflammatory mechanism 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 d! isease. 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.

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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 infec! ted 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-1a 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 m! RNA in a utopsied 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. Blaylock RL. Chronic microglial activation and excitotoxicity secondary to excessive immune stimulation: Possible factors in Gulf War Syndrome and Autism. J Amer Phys Surg 2004; 9: 46-51.

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

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


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

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

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


27. 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.


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


29. 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.


30. Perry VH e! t al. Th e impact of infection on the progression of neurodegenerative disease. Nature Rev Neuroscience 2003;4: 103-112.

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


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

Sunday, April 20, 2008

CHEMICALS AND TOXINS IN OUR MODERN WORLD

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CHEMICALS AND TOXINS IN OUR MODERN WORLD
by: Dr. Gary Young

Dr. Gary Young is a leading researcher of essential oils in North America and founder and president of Young Living Essential Oils Company. Dr. Young is one of the world's largest producers and distributors of organically grown therapeutic-grade essential oils. On his farms in Idaho and Utah, he grows and distills his own essential oils. He designed all the harvesting, cultivating and planting equipment himself and has the largest privately owned distilleries in the world, producing the finest quality oils that have been produced in the world bar none. After an injury confined him to a wheelchair, he entered a search for natural healing methods and not only healed himself, but discovered life-changing principles, which have opened up healing doors to countless others.

TOXINS IN VACCINATIONS DOCUMENTED RESEARCH ON TOXIC EFFECTS OF VACCINES
Most children are vaccinated three times by the time they enter grade school, the first in infancy, the second before kindergarten and then re-vaccination before entering Grade 1. The accumulation of these vaccines is what is killing our children and suppressing their immune systems. Are children dying of vaccinations? Absolutely.

My research team has gone to the courts in various states with court orders under the Freedom of Information Act to get information on vaccine contamination that the universities would not release. These documents show that vaccines reduce our immunity in many important ways because they contain many chemicals and heavy metals like mercury and aluminum which are themselves immune suppressing. Mercury actually causes changes in lymphocyte activity. Epidemics and increase in death rates follow vaccinations in every country.

This information is not unknown to our government agencies. The pharmaceutical companies push these vaccines so they can line their pockets with billions and billions of dollars while these vaccinations are injuring and killing people. Five drug companies made nine vaccines given to millions of American children - they used materials with possible Mad Cow links, and this continued for seven years before they even investigated it! It is terrible what's going on and they are claiming that this is necessary to protect your children. It is nothing but a fraudulent activity against the people.

PROTECT YOUR CHILDREN We must begin to take a stand for our rights and our freedoms. If the people of America knew the truth about vaccines, there would be a great war waged against the medical system for forcing children to be vaccinated. If you love your children, form a coalition and start fighting this. The Consumer Health Organization of Canada is a non-profit organization, and could possibly put a lobbying group together and you folks could donate some money to help this group go to Ottawa and start lobbying for your rights. If you don't start rising up and standing up for your rights, it's only going to get worse. There is nothing I would love to see more than a coalition of people rise up and file a class action suit against these pharmaceutical companies until we take them out.

Show me one place in the Bible where it says, "Go thou unto the pharmacists and be vaccinated!"

There are options or alternative ways to prevent these diseases. There is no reason for vaccinations. If your immune system were not capable of defending you against these diseases, you wouldn't be here in the first place. You have an immune system. God gave it to you and God knew what you were going to deal with when he created this world and created us.

PROGRESSION OF INFECTIOUS DISEASES BEFORE AND AFTER VACCINES I have charts and graphs which show that the many of the infectious diseases we're dealing with today were basically dead in the world until vaccines were re-introduced in the twenties, and vaccines have reawakened many of these diseases and brought them back with a vengeance. After the introduction of a vaccine for any particular disease, after a period of about 5 to 8 years, that particular disease mutates and develops a resistance to the vaccine, and then the disease rate begins to climb.

TUBERCULOSIS Graphs show that the tuberculosis virus itself was on a steady and gradual decline. It was eliminating itself from the world, until they introduced vaccines, and now it's on the rise.

TETANUS The Tetanus vaccine was introduced in the Dominican Republic in l975, and graphs showed a rise in the death rate along with inflammations and immune suppression. Tetanus was on a steady decline until they re-introduced the vaccine.

MEASLES The same thing. Measles eradicated itself and declined steadily until they re-introduced the vaccine for measles and now it's starting to climb again.

DIPHTHERIA Here we see the same thing again. Diphtheria went way up and then it slowly started declining until they introduced the vaccine again and then there was a steady increase. Going back in time, we see that the disease was basically eradicated before the vaccine was introduced.

WHOOPING COUGH When the whooping cough vaccine was introduced, we see a delay period of 5 to 10 years where it has to accumulate in the body, starts suppressing immune function and then the next generation of children are born and whooping cough is on the rise again. This happens in every single case, not just 1 out of 10, but every case.

SCARLET FEVER had declined before the introduction of immunization.

DPT (Diphtheria, Pertussin, Tetanus) This vaccine is given to children within a year after they are born. Almost 50 years ago in 1948 two Harvard Medical School scientists, Randolph Byers and Frederick Moll, along with the FDA, carried out tests on DPT vaccines at Children's Hospital in Boston and concluded that severe neurological problems followed administration of DPT vaccines. The results of the tests were published in Pediatrics, a respected medical journal. They were ignored by the medical and pharmaceutical community, who had a vested financial interest in continuing the practice. In 1976, Charles Manclark, an FDA scientist, remarked that "the DPT vaccine had one of the worst failure rates of any product submitted to the Division of Biologics for testing." In 1992, the Institute of Medicine concluded that evidence is consistant with a casual relationship between DPT and acute encephalopathy. The neurological disorders that we now see are definitely increasing, as are death rates of children under 15 years from vaccines.

Avoid Flu Shots! - ALZHEIMER'S AND THE FLU VACCINE Research by Dr. Hugh Fudenberg, M.D., the world's leading immunogeneticist and 13th most quoted biologist of our times (author of nearly 850 papers in peer reviewed journals), shows that individuals who had five consecutive flu shots between 1970 and l980 (the time of the study) have a ten times higher chance of getting Alzheimer's disease than if they had only one or two or no shots. How much clearer does it have to be? Is Alzheimer's on the rise? How many of you who are 50 and older can remember hearing about Alzheimer's 25 years ago? What happened? When did they start giving flu shots? It's all in the documentation. Dr. Fudenberg claimed that the problem was due to the mercury and aluminum in every flu shot (and most childhood shots as well). The gradual mercury and aluminum buildup in the brain causes cognitive dysfunction. Flu shots contain 25 micrograms of mercury. One microgram is considered toxic. (NVIC International Vaccine Conference, Arlington, VA September, 1997. Hugh Fudenberg, MD, is Founder and Director of Research, Neuro lmmuno Therapeutic Research Foundation.) The Johns Hopkins newsletter, l998, also predicted that Alzheimer's could quadruple in coming years.

ANTHRAX VACCINE sold by BioPort. Documented research shows that the anthrax vaccine is contaminated and in fact it doesn't work. It just destroys your immune system. Everyone gets panicky about anthrax. Have you ever been around a cow or a horse or on a farm? Anthrax is on every farm that exists in the world. So if you have ever been around a cow or a horse and you don't have anthrax, you have a natural immunity to it. So, why worry about being vaccinated? The best and the greatest safeguard you've got in the world is building a strong body and keeping it pure and clean. God said, "My spirit will not dwell in an unclean house."

VACCINE INGREDIENTS The list of ingredients which are the base substances in most vaccinations will make your blood start to boil. Mercury and aluminum, pus and sores of diseased animals. horse serum, calf serum, fecal matter, urine, and macerated cancer cells! Formaldehyde (embalming fluid), a preservative for the vaccine, a known carcinogen; a synthetic phenol, also a carcinogen, that may cause paralysis, convulsions, coma, necrosis and gangrene; Simian monkey virus No. 40 in polio vaccines. These are the major base ingredients that are used to formulate every vaccine. This is what they're putting in you when you get a flu shot and when your children get their vaccinations.

Why would anyone want to put this into their blood?

MERCURY POISONING By age two, American children have received 237 micrograms of mercury through vaccines alone, which far exceeds the EPA safe levels of 1/l0th of a microgram per kilogram per day. It is particularly toxic to infants. At birth they are given Hepatitis B containing 12 micrograms of mercury, 30 times safe levels. At four months, DPT containing 50 micrograms of mercury, 60 times safe levels. At six months, Hepatitis B and polio with 65.2 micrograms of mercury, 78 times above safe levels, and at 15 months another 50 micrograms, 4l times above the safe level. These figures are calculated for an infant's average weight in kilograms for each age. These one-day blasts of mercury are called bolus doses. There has never been any research conducted on the toxicity of such doses. My son is not vaccinated and he will never be. I will fight to the death before I allow it to happen if I have to take him to some foreign island in the South Pacific.

AUTISM is related to mercury poisoning. Mercury is found in every vaccine. Mercury is a potent neurotoxin and infants and young children are very vulnerable to the impacts of mercury because it can affect the developing brain. Dr. Candice Pert, internationally recognized pharmacologist, said that there has been an increase in autism of 500% to 600% in the last ten years. Compared to 20 years ago, there is an increase of 1,000%! And the disease is appearing in certain new forms such as regressive forms of autism where the children are initially fine, but regress when they're about a year and a half old, around the time they get the vaccines. Many mothers believe that the vaccines are responsible.

Editor's Note. WASHINGTON, March 27, 2003/U.S. Newswire. A new study of mercury in childhood vaccines demonstrates that the doses are in excess of the Federal Safety Guidelines and show alarming evidence for a link between these excessive doses of mercury from thimerosal-containing vaccines and neurodevelopment disorders such as autism and speech disorders as well as heart disease. Those are the findings of the study published in the current issue of the peer-reviewed Journal of American Physicians and Surgeons authored by Mark Geier, MD, PhD, President of the Genetic Centers of America and David Geier. The authors also conclude that the U.S. should ban the use of thimerosal in all vaccines. The authors point to exploding rates of autism since introduction of thimerosal in vaccines.

TRAVEL VACCINES I have travelled to just about every country in the world. I haven't been vaccinated yet, and I've never brought a disease back from any of those countries. There are some countries that say they require a vaccination in order to go there, but folks, it's a lie. For example: three years ago, you couldn't get a visa to go to Pakistan as an American unless you were vaccinated, but no vaccination is required from the land of Saudi Arabia , so we flew to Oman and got a visa from Oman to Pakistan.

Your body is a temple of God and when you vaccinate it, you have just violated it with the worst sin on the planet.

How can you be a vessel when you put that deadly poison inside God's temple?

TOXINS IN COSMETICS AND BODY CARE PRODUCTS

Your skin is the largest absorbing organ of the entire body. What you put on your skin will be on it all day long absorbing and going into your blood stream. Folks, if you're not going to eat it, then don't wear it.

Do you brush your teeth with a toothpaste from the drug store? It's cheap, only $l.49. Then you spend the rest of your life going to the dentist paying thousands of dollars, and you wonder why you get flu, head colds, head congestion, failing eyesight and polyps in the nose. A major ingredient in a common standard toothpaste is sodium laurel sulfate which was created for degreasing engines on automobiles. It's a deadly toxic substance. Every single common toothpaste, shampoo, bar soap, shaving foam, after-shave, and lipstick contains sodium laurel sulfate. It is a very cheap material that is the base for most of the other ingredients. Researchers have linked sodium laurel sulfate with major allergies in children.

Another chief ingredient in skin and hair products is propylene glycol. Every single agent in these hair conditioners and other products are deadly chemicals with severe side effects. It's the same thing with shampoo. Sodium laurel sulfate is at the top of the list, and then propylene glycol, and yellow #5, SD&C Red artificial colourings. These are all known allergens. How many people go to the doctor every year and have allergy shots because they have allergies and they don't know why.

Allergies are not a disease. Allergies are nothing more than your body saying, "I'm saturated with all these chemicals! Would you please just take me out and shoot me. I can't deal with it anymore". So it has a reaction. It hopes that you will just stop putting this crap on and into your body. Detoxify your body and your allergies are history.

Diaper ointment contains benzyl alcohol, paraffin, glycerol and propylene glycol. Are these not petrochemicals? Has anybody ever had anti-freeze on their hands? It burns like crazy. Propylene glycol is cheap. It's a stabilizer, a preservative, and it takes up anywhere from 50 to 60% of the ingredient volume! That's what's in your diaper ointment.

Don't put chemicals on your children. Love your children enough to either give them something pure or don't give them anything more than water. Don't let your body get chemicalized and the receptor sites impeded so that you can't replicate healthy living cells.

Become label readers. Start educating yourselves. We don't need chemicals, and we don't need drugs. We need what God created when he created this Earth. He gave us all the tools that we need to sustain life and protect us from these marauding diseases and viruses that have been created by man for money.


ESSENTIAL OIL PRODUCTS ARE EDIBLE I made a hand and body lotion, and every single one of the ingredients can be eaten. You may not like the taste of it, but it may be the healthiest thing that you ingest all day. I use milk protein and phospholipids and amino acids and methionine with amino acids, gluco-proteins and essential oils, lavender, clary sage, lemon, and jasmine, herbal extracts and vitamins in my aroma silk conditioner. You could eat every single item there individually or collectively. I made Tender Tush for our children and for my son Jacob. In reality, I made it for mommies to prevent stretch marks. Women don't have to have stretch marks just because they have babies. When my son was born the first thing I did was cover his little body with frankincense oil and the entire umbilical cord with myrtle oil.

LONGEVITY IN TRADITIONAL CULTURES

Old people in certain primitive countries like Hunza Land, Azerbaijan and Vilcabamba in Equador, were able to live to l40 and l60 years of age because they knew a few secrets. These people don't vaccinate their children. They don't take flu vaccines. They don't run to the doctor and the hospital every time the wind blows sideways. They do the things that they were taught by their ancestors. If they start feeling a little sick, they go off some food. Ever watch a dog when he gets sick? What does he do? He quits eating and he goes and starts eating grass. But what do we do when we get sick? Go to the hospital and get treated with jello and ice cream and 7-Up with seven teaspoons of sugar.

I visited these cultures and met people 100, 140, 160 years of age without a single thing wrong with them, still able to read the newspaper without glasses. All the people I met in these countries were farmers. They work and labour in the fields, chopping wood, milking cows, scrubbing clothes, moving the lymphatic fluid. They're still farming the old way, with a hand scythe, with horses or donkeys or oxen and they don't use chemicals. Chemicals are what's killing all of us. They're exercising, not a half-hour a day at the gym, but all day long, and the exercise stimulates the production of Human Growth Hormone. These people never had colds or coughs in their entire lives. Their eyes are bright, their skin is clear. They go mountain climbing at 130.

There are no secrets but there are lost and forgotten ways of life. In every country that I have visited, these old people all practiced fasting every year in the springtime for 30 days. It's not a total fast. They fast from daylight until dark and then they drink juices or eat fruit or vegetable soup during the evening.

During fasting, Human Growth Hormone secretes more than at any other time of your life. The only exception is during strength training where your body will produce even more Human Growth Hormone. Human growth hormone is the modulator for the immune system to keep you healthy and vital.


The other thing that is really critical is they eat foods that contain phos-phatidylserine compounds that are found in soy and foods that are high in Vitamin C.

The Inner Mongolian people actually have the longest history of continual longevity. One thousand years ago, their life expectancy was 120 years. Today their life expectancy is 120 years. It is the only country left in the world where the life expectancy has not declined with the introduction of the American diet. In Hunza Land, their life expectancy has dropped from 160 years to under l00 years. When I was there last year, all of the old people that I had met years ago were all dead. There are no more old people in Hunza Land and never will be ever again. The children had runny noses and were drinking soda pop. The great-great- great grandparents had never tasted soda pop in their lives. They wouldn't touch it, and it tore their hearts out to see their grandchildren and great-grandchildren eating these things they knew would kill them.

* * * ESSENTIAL OILS:

NATURAL IMMUNE BOOSTERS WITH ANTI-INFECTIOUS PROPERTIES

Essential oils were man's first medicine and they were used thousands of years ago. For many years, I believed that herbs were man's first medicine, but recent discoveries from Egyptian and Chinese scrolls show that oils were actually our first medicine. Herbs evolved as medicine when the peasants and slaves observed royalty using the oils with great success. Since they were restricted from using the oils, they started boiling and steeping the herbs and making teas and poultices.

Open your Bible to the book of Exodus and read about essential oils. Throughout the Bible it talks of these various oils and how they were used to protect the people. Hyssop is anti-viral and was used for cleansing the lepers and healing leprosy. Over 40 biblical references are written on hyssop alone. The garments smelled of myrrh and aloe which was sandalwood, not aloe vera. These oils contained anti-viral, anti-fungal and immune stimulating properties.

STIMULATING THE IMMUNE SYSTEM Breathing an essential oil is very effective and can stimulate the immune system. Less volatile oils with heavier molecular weights like myrrh and frankincense remain much longer in the nasal cavity. Many oils, particularly those containing sesquiterpenes and phenols that are high in oxygen, will increase the oxygen around the pituitary and pineal glands as much as 28%.

ANTI-INFLAMMATORY Essential oils like methyl salicylate found in birch and wintergreen are highly anti-inflammatory.Thymol found in thyme bulgaris is 20 times stronger than phenol. Phenol carries one oxygen molecule and is found in many of the oils, but methyl salicylate carries two more.

ESSENTIAL OILS ARE ANTIBACTERIAL, ANTIFUNGAL AND ANTIVIRAL The essential oil works solely as the plant's immune defense-mechanism. They fight infection; they are antibacterial, antifungal and antiviral. Because essential oils have such a strong action against bacteria, viruses and fungus, they are highly effective against the viruses that are facing us today. Research in universities around the world has never found a virus that can mutate in the presence of certain essential oils, particularly oils high in limonene and phenols. Grapefruit has the highest amount of limonenes. Also orange, tangerines, mandarin, lemon and white fir. Limonene which is a very potent anti-viral is now being studied at the University of Wisconsin as a cancer fighting agent by Dr. Michael Gould. Results show that it reversed breast cancer and reduced tumour growth by as much as 40% in laboratory animals. (Haag, J.D. and Gould, M.N. 1994. Mammary carcinoma regression induced by perillyl alcohol, a hydroxylated analog of limonene. Cancer Chemother. Pharmacol. 34:477-483.)

HUMAN GROWTH HORMONE The anterior pituitary secretes two hormones that are very important for immune function: TSH (Thyroid Stimulating Hormone) and HGH (Human Growth Hormone). Deprivation of oxygen reduces the secretion of TSH and HGH by the anterior pituitary and increases depression. TSH and HGH play a joint role in modulating the immune function, which is very critical.

Lavender Oil Our lavender field in St. Mary's produces the greatest lavender oil in the world. Lavender oil contains phenols which contain oxygen molecules which increases the Human Growth Hormone outlets in the anterior pituitary. All you have to do is just breathe it. Very, very simple.

Peppermint oil contains phenols. All you have to do is breathe it to increase the secretion of Human Growth Hormone. Human Growth Hormone is produced by the anterior pituitary, is converted in the liver to IGF-l and then goes to the pancreas to support immune function. Peppermint oil also contains sesquiterpenes which increase oxygen activity in the brain. European research shows that sesquiterpenes increase brain oxygen by as much as 21 to 28%.

Lemon oil is anti-infectious and anti-bacterial and has Vitamin P-like action for circulation. It is calming to the nerves and stomach. It is good for diabetes because it helps regulate pancreatic function and insulin production. It is a great disinfectant and should be in the medicine cabinets in all hospitals. It can be used for respiratory infections, insufficient liver function and digestive conditions.

Thyme Oil is a mono-terpene and is very, very high in thymol which contains oxygen molecules that increase oxygen output in the brain. It's anti-microbial, anti-bacterial, anti-fungal and anti-viral and has a wide spectrum of action against fungus and virus. It's a uterine tonic and cardiotonic. Thymol can be used for sinus, osteoarthritis, bronchitis, cystitis, vaginitis, acne, cardiac fatigue, just simple little things.

Cloves have the highest known anti-oxidant properties.

Longevity oil I created this because of its anti-oxidant properties. People in countries that have great longevity eat foods high in anti-oxidants. This oil blend contains thyme, a powerful anti-oxidant which prevents degeneration in the brain, eyes and heart according to research in Scotland and Austria.

Longevity kit - This kit contains ingredients that are essential to supporting Human Growth Hormone output, conversion and assimilation, maintenance of proteins and the activity of enzymes in the body.

Wolfberry Juice is a natural anti-oxidant that has preserved the longevity of people in Inner Mongolia who today have maintained the most consistent life expectancy free of disease. The Natural Science Institute in Beijing, China began a study in 1982 and researchers who went there did not find cancer, arthritis, diabetes, heart disease, MS, or any degenerative disease amongst the people in the villages where Wolfberry was consumed on a daily basis. Wolfberry contains 15% protein by weight and three times as much vitamin C as oranges.

Berry Young Juice One ounce is equivalent to 1/4 to 1/2 a pound of berries. When I went to Inner Mongolia to do my research, people who ate between one-quarter to one-half a pound of Wolfberries daily were disease free and had never experienced disease in eleven generations that we could research.

Ultra Young - is a spray for the bucal cavity with the Wolfberry Lycium Polysaccharide which stimulates the production of Human Growth Hormone.


CORTISOL gets rid of waste. The common factor that allows people to live to be 150 years old disease-free is cortisol and the foods that produce cortisol. But when you're under stress, the cortisol levels increase, and when cortisol is too high it blocks the HGH receptors and therefore depresses the immune function. Three cups of coffee a day will raise your cortisol levels to a high point for 18 hours and suppress your immune system during that time. Seven teaspoons of sugar will increase your cortisol levels by 300 to 400 times. The latest research in the U.S. shows that the average child consumes 40 tsp. of sugar per day. One can of soda pop contains seven to 12 tsp. sugar. Chocolate does the same thing in any form. One 30 mg. tablet of Prozac will double your cortisol levels. Vaccines increase cortisol. Phos-phatidylserine, a compound found in vitamin C in citrus and fruits high in vitamin C works as a natural cortisol blocker.

HOW TO USE THE OILS MOST EFFECTIVELY There are multiple ways. You can diffuse them in the air and inhale them. But the simplest and most effective way is to put one to two drops on the bottom of your feet. morning and night when you get out of bed, after your shower and before you go to bed. You don't need more than three drops of any one of those oils on the bottom of your feet. Peppermint oil can be diffused or you can rub a drop in your nose. Peppermint oil is fantastic for reducing fevers. Nothing that you can find in a pharmacy will break a fever quicker than peppermint oil. Peppermint oil has also been studied as a weight loss control mechanism. It smells good and it's yummy. Breathing peppermint will decrease the desire to eat, because it creates a sensation of being full.

DETOX The chemicals that we put into our bodies interfere with the conversion of cholesterol into hormones. Our research has shown that essential oils, particularly the phenol and thymol families, will literally digest the petrochemicals and clean up those receptor sites so that the hormone can fit into the receptor site and carry out its normal function. Thyme, mountain savory, oregano, lavender, peppermint and lemon oil are very high in phenols.

You may order Young Living Oils and Products by contacting Consumer Health at 416-490-0986.

BOOK REVIEWS:

K9 Kitchen by Monica Segal.

Is it time to give up that canned and dry pet food from the grocery stores? These commercial products usually contain "animal by-products" - another name for diseased meat not fit for human consumption and partly responsible for the rising incidence of cancer, arthritis and other diseases in our beloved pets. In this excellent book, Monica describes a variety of healthy diets to suit your pet's individual needs. She explores the benefits of feeding a raw food diet, raw bones, home-cooked meals, vitamins and minerals. A whole chapter of scrumptious recipes for cooked dinners, leftover dinners, raw meals and directions for starting a new diet will help you prepare nutritious meals for your pet.

$35

Cancer Cover-Up: An Indictment of Big Medicine and their Suppression of the Cesium Cancer Therapy by Kathleen Deoul.

This book is written from the heart and is an important book for anyone who wants to know what is going on in our health system today and what we can do about it. An extensively documented book, it explains in shocking detail how medical powers have suppressed authentic and effective treatments for cancer and other diseases, like the Hoxey herbs, Burzinski's antineoplastons, krebiozen, hydrazine sulfate, laetrile, oxygen therapies, and Cesium treatments. A number of excellent chapters on vaccines provide essential information about the side-effects of vaccinations and the relationship of the MMR and DPT vaccines to autism and other autoimmune disorders.

$30

***SPECIAL NEWS BULLETIN*** ORGANIC FOOD STANDARDS GUTTED WITH ONE STROKE OF THE PRESIDENT'S PEN

In a week when news of the war eclipsed all other news, a small inconspicuous article reported a HUGE change in organic food laws. The article reports that in February, 2003, United States Congress voted to gut the nation's organic food standards, NO LONGER REQUIRING that organic livestock be given feed that is 100% organic.

How could this happen? It took one request by Tom Hensley, vice-president of Fieldale Farms, a large poultry grower in Georgia who found the all-vegetable diet to be "extremely burdensome for chicken producers". He complained that organic grain was too expensive.

The new law allows producers to give their animals conventional feed with antibiotics and pesticides and STILL LABEL THE MEAT ORGANIC.

President Bush signed the measure into law. No discussion, no debate, no consumer input, all for the sake of one large poultry grower wanting to take advantage of the higher prices he could charge for the "organic" label without actually providing anything organic.

Thursday, April 17, 2008

Marketing Poison To Children

I am outraged that these people have the nerve to try and market vaccines to "tweens" Only in America could people create such a stupid marketing term for children, then use it to sell everything from cancer causing "fast food" to cancer and injury inducing vaccines.

I would say more but this sickens me, and when I 1st saw it on several email list the other day I actually thought it was a hoax, I mean I know big pharma and the government is evil but I never thought they would stoop quite this low. What angers / sickens me the most is the fact I actually gave these monster credit for being "human".

*****

http://cdlhn.com/create_frameset.cfm?id=66&CFID=1499001&CFTOKEN=55461110

Tweens are defined as young people, usually aged 9-12, those IN BETWEEN childhood and teenhood.

In Marketing Vaccines to Tweens, Susan Kirby, of Kirby Marketing Solutions, discusses social marketing and disease prevention that’s specifically directed at “tweens”, and how to empower them to get the immunizations they need.

The presentation features:
# The “4 Ps of Marketing” and the Social Marketing Model
# Tween demographics, facts, and trends
# Behavioral objectives aimed at creating a successful vaccination campaign
# What motivates and inspires your target audience to action
# Barriers to address that might prevent action
# Developing and communicating the message
# How to adapt effective existing campaigns

Dr. Kirby is president of Kirby Marketing Solutions, and has more than 25 years of senior-level experience in public health project management, marketing, and communication campaign development, including six years as Director of the Marketing Research Resource Center at the national Centers for Disease Control and Prevention.

Sometimes the vaccine has a good memory and sometimes it doesn't---WTF???

I love how the vaccine for mumps has been shown not to work, yet they are still making excuses for people to take it. I think these idiots think we are all stupid too to notice so they just make it up as they go along.

Below is one of the worst excuses I have seen so far pushing the mumps vaccine and I am posting it partly as a joke because of how stupidly written it is, I mean you would think if they wanted to convince people they would come up with something better than "Sometimes the vaccine has a good memory and sometimes it doesn't" I mean really, WTF???

*****

http://media.www.easternprogress.com/media/storage/paper419/news/2008/04/17/News/Vaccinated.College.Students.May.Not.Be.Immune.To.Mumps-3329813.shtml

Vaccinated college students may not be immune to mumps

By: Kristen Miller
Posted: 4/17/08
You might remember getting that physical examination before you could start middle school. You might have images of a white-shirted nurse with unpleasantly cold hands, or still be able to taste the tongue depressor shoving your mouth open as you said "aah."

But when you think back to the medical tests you had to take before advancing to middle school, you might not think about getting your MMR shot-because once you have been vaccinated for measles, mumps and rubella, you never have to think about them again.

However, after a mumps outbreak struck a college campus in Iowa and spread to other midwestern states, people might have a good reason to start thinking again.

The Centers for Disease Control and Prevention found that, of the 6,600 people who came down with the virus, the majority of infected were college students, according to the Associated Press. Further, 84 percent of college students who developed mumps received the two required mumps shots when they were younger, according to the article.

Dr. Pradeep Bose of Health Services said the shot is required twice, once at 15 months of age and one more dose before middle school.

Mumps is a virus that mainly affects the ovaries and testicles and may lead to infertility, Bose said. The virus can display symptoms such as swollen salivary glands, abdominal pain, nausea and vomiting.

So why would a vaccine designed to stave off such a serious virus simply stop working by college?

Bose said it doesn't necessarily mean the vaccine was bad. The immune system might respond to the vaccination - which introduces manageable amounts of the virus into the body - very quickly and then wear off, he said.

When the immunity fades and the body doesn't recognize the virus, it's called a wild virus, Bose said.

Memory is important when it comes to the immune system fighting off a virus. Sometimes the vaccine has a good memory and sometimes it doesn't, Bose said. It all depends on the virus and vaccine.

Also, Bose said, the mumps virus is not some random sickness that strikes out of nowhere.

"The mumps virus is not dead; It's there," he said. Even though you may not see many cases of it, people still get the virus.

The mumps outbreak in 2006 started on an Iowa campus, according to the Associated Press article, and was a new viral strain that wasn't targeted by the original vaccine. Bose said Eastern is prepared to deal with an outbreak on campus if it happens.

Right now, Health Services offers MMR shots. But it isn't a requirement in Kentucky that college students get the shots before coming to school unless they are going into programs such as nursing or physical therapy where students have to be in close contact with people on a daily basis.

Bose said right now there are faculty members working to make it a requirement for college students to get the two shots before coming to school.

"I would recommend that strongly," Bose said.

One reason the virus may have spread quickly on the Iowa campus - and why college students are more susceptible to the virus-is because of the way college students live, Bose said.

"Lifestyle makes them at high risk," Bose said. College students live in close proximity to each other in dorms and are likely to share items such as drinking glasses, make-up and cigarettes.

But Bose said if the majority of college students are vaccinated, it creates "herd immunity" and the virus won't be as widespread.

Right now Dr. Bose doesn't know when - or if - there will be a requirement for students to get the vaccine for mumps before college. He is working with other faculty to get the proposal approved by the "higher up."

"It goes through a winding process," Bose said.

The MMR vaccine is offered in health services for $45.

Sunday, April 13, 2008

Early Life Infections Improve the Function of the Immune System

http://www.chiro.org/Immunity/

Early Life Infections Improve the Function of the Immune System
by Daniel J. Murphy, DC, FACO
Vice President of the ICA


A 1998 article published in the journal THORAX titled:
Early Childhood Infection and Atopic Disorder [ 1 ] notes:

1) Atopic diseases (asthma, hay fever, and eczema in this study) are rapidly rising in westernized communities.

2) The mechanism for this increase in atopic diseases is reduced exposure to microbes.

3) Atopic diseases were significantly statistically linked to immunization with the Pertussis vaccine and to treatment with oral antibiotics in the first two years of life.

4) The authors conclude that exposure to certain infections repress atopic disorders.


A 1999 article published in the journal THE LANCET titled Atopy in Children of Families with an Anthroposophic Lifestyle notes [ 2 ]

1) The increased prevalence of atopic disorders in children may be associated with changes in childhood infections as related to vaccination programs and antibiotics that alter intestinal microflora.

2) Children who use antibiotics restrictively and have few vaccinations have lower levels of atopic diseases.


Another 1999 article published in the journal CLINICAL EXPERIMENTAL ALLERGY titled Antibiotic use in early childhood and the development of asthma notes [ 3 ]

1) Antibiotic use is significantly associated with a history of asthma.

2) If antibiotics are used in the first year of life there is a 305 percent increased risk of developing asthma when compared with children who had never used antibiotics.

3) If antibiotics are used only after the first year of life there is a 64 percent increased risk of asthma when compared with children who had never used antibiotics.

4) The greater the number of courses of antibiotics given to children, the greater the risk that they will develop asthma.

5) “Early childhood infection may have a protective role against the subsequent development of asthma.”

6) The treatment of infant infections with antibiotics could play a role in the development of childhood asthma.

7) Antibiotics increase the risk of asthma by “reducing the intensity and duration of acquired bacterial infections.”

8) There is a “temporal association between the increasing prevalence of asthma and the increasing use of antibiotics throughout the developed world.”


A 2000 article published in the journal ALLERGY titled The immunology of fetuses and infants: What drives the allergic march? notes [ 4 ]

1) Atopy refers to allergic conditions which include hay fever, asthma, and eczema, and are associated with the production of IgE antibodies to common environmental allergens.

2) The risk of atopic disease early in life is particularly high in Western industrialized countries.

3) The critical period that influences the development of atopy is the first years of life.

4) “A decline in certain childhood infections or a lack of exposure to infectious agents during the first years of life could have caused the recent epidemic of atopic disease and asthma.”

5) Recovery from natural measles infection reduces the incidence of atopy and allergic responses to house-dust mites to half that seen in vaccinated children.

6) Bacterial infections are modulators of the atopic march.

7) The use of antibiotics during the first two years of life increases the risk of asthma.


Another 2000 article published in the journal THE NEW ENGLAND JOURNAL OF MEDICINE titled Siblings, Day-Care Attendance, and the Risk of Asthma and Wheezing during Childhood notes [ 5 ]

1) Young children with older siblings and those who attend day care are at increased risk for infections, which in turn may protect against the development of allergic diseases, including asthma.

2) Exposure of young children to older children at home or to other children at day care protects against the development of asthma and frequent wheezing later in childhood.

3) The incidence and the prevalence of asthma among children have increased dramatically in the past three decades, making it the most common chronic disease of childhood in the United States, and a decrease in infections during early childhood may be responsible.

4) “The incidence of asthma among children who had two or more older siblings or who attended day care during the first six months of life was significantly lower than that among children who had one sibling or no siblings and who did not attend day care.”

5) Bacterial or viral infections occurring during infancy may provide important signals to the newborn’s maturing immune system.


This article generated an editorial titled Day Care, Siblings, and Asthma — Please, Sneeze on My Child , that included the following comments: [ 6 ]

1) “Parents generally agree that children who attend day care or who have older siblings have more frequent infections. They may be surprised to learn, however, that this tendency may protect their younger children from asthma.”

2) “A common factor underlying the increased prevalence of asthma and atopic disease may be a reduction in early exposure to microbes, with a lasting influence on immune development.”

3) An important signal for normal postnatal immune system maturation is exposure to microbes. Deprivation of these signals in infants may allow a change that increases the risk of eventual asthma and atopic disease.


A 2001 article published in the journal ALLERGY titled The causes of the increasing prevalence of allergy: Is atopy a microbial deprivation disorder? [ 7 ]

1) “The atopic diseases, i.e., primarily, bronchial asthma, atopic dermatitis, and allergic rhinoconjunctivitis, were rare a few decades ago, but constitute today an increasingly severe public health problem.”

2) “The increase in the prevalence of the allergic diseases, especially in those born after 1960, is almost explosive, and there are now epidemics of allergic diseases in many countries.”

3) “The prevalence of asthma in children and young adults has tripled and quadrupled in many industrialized countries during the last two decades.”

4) Allergic sensitization may occur in utero. [Important, as noted below.]

5) Allergic sensitization that occurs early in childhood tends to persist throughout life.

6) The very first months of life are of crucial importance in allergy development.

7) “The more children in the family, the more infections they encounter” and this may help to prevent allergy.

8) Viral infections protect against allergic disease.

9) “If the assumption that early viral or bacterial infections protect against the development of allergic diseases is correct, vaccination should lead to an increase of allergic disorders.”

10) Atopy is correlated to MMR vaccination (measles, mumps, rubella) and with the administration of antibiotics.

11) There is a significant relationship between treatment with antibiotics during the first two years of life and later development of allergy.

12) “Multiple courses of antibiotic treatment are associated with higher allergy prevalence, and the finding that treatment with broad-spectrum antibiotics appears to be more likely associated with allergy development than is ordinary penicillin.”

13) “Microbial agents do indeed play a protective role in the development of allergic disease.”

14) Childhood infections lower allergy prevalence, especially bacterial infections.

15) “From an evolutionary perspective [INNATE], it is perhaps not unexpected that the immune system, which over millions of years has adapted to a heavy microbial load, may react in an ‘inadequate’ way upon a sudden, radical decrease of this load, caused by vaccinations, antibiotics, and especially improved hygienic conditions.”

16) “A change in the ‘microbial load’ seems to be the most probable cause of the increase in the allergic diseases.”


A 2002 article published in the journal ALLERGY titled The rise of atopy and links to infection notes [ 8 ]

1) This article explores the evidence that “exposure to certain antibiotics and public health immunizations in early life” are the cause of atopic disorders.

2) This article also explores the evidence that “certain microbial exposures [infections] can inhibit experimental allergy.”

3) “Certain natural infections promote immune regulatory processes that can restrain atopy.”

4) 45 percent of children in some countries may be suffering from atopic disorders.

5) “Antibiotic receipt in early life is associated with more subsequent atopy and asthma.”

6) Antibiotics given early life (<24 months of age) for any clinical indication “predicted substantially more subsequent atopic disorder.”

7) 80 percent of children who subsequently display atopic disorder received antibiotics at two months.

8) There is a “direct promotion of atopy by antibiotic receipt.”

9) Certain immunizations may also increase subsequent atopy, including pertussis in the DPT vaccine and the measles/mumps/rubella (MMR) vaccine.

10) The limited microbial exposure caused by hygiene, antibiotics, and vaccinations may also explain the rising of inflammatory disorders, such as insulin dependent diabetes, in developed countries.

11) Microbial exposure “may play a key role in allowing the immune system to develop protective responses.”


Another 2002 article published in the NEW ENGLAND JOURNAL OF MEDICINE titled Environmental exposure to endotoxin and its relation to asthma in school-age children notes [ 9 ]

1) “Asthma is the most common chronic disease in childhood and accounts for substantial morbidity and health care costs.”

2) One can have exposure to microbes or to nonviable parts of microbes and not become infected.

3) “Environmental exposure to microbial products may have a crucial role during the maturation of a child ‘s immune response.”

4) Exposure to microbial products is “associated with a significant decrease in the risk of hay-fever, atopic sensitization, atopic asthma, and atopic wheeze in childhood.”

5) “The innate immune system responds [favorably, for ones entire life] to a high microbial burden.”

6) Exposure to microbial products strongly affects the development of atopy and childhood asthma.


This article generated an editorial titled Eat Dirt—The Hygiene Hypothesis and Allergic Diseases , that included the following comments: [ 10 ]

1) There is an epidemic of both autoimmune diseases and allergic diseases.

2) “One theory proposed to explain this increase in the prevalence of autoimmune and allergic diseases is that it results from a decrease in the prevalence of childhood infection.”


Another 2002 article published in the same issue of the NEW ENGLAND JOURNAL OF MEDICINE titled Mechanisms of Disease: The effect of infections on susceptibility to autoimmune and allergic diseases notes [ 11 ]

1) Infectious agents can suppress allergic (asthma, rhinitis, and atopic dermatitis) and autoimmune (multiple sclerosis, insulin-dependent type 1 diabetes, and Crohn’s disease) disorders.

2) The incidence of these disorders began to increase in the 1950s [coincidentally with the availability of antibiotics and vaccinations] and continues today.

3) There has been a significant decrease in the incidence of many infectious diseases in developed countries as a result of antibiotics, vaccination, and improved hygiene.

4) Early childhood infections change immune system maturation.

5) The administration of antibiotics to children increases the risk of asthma and allergy.

6) Decreased exposure of women to viruses before pregnancy may subsequently reduce the degree of protection against these viruses afforded to their newborns.

7) “Vaccination strategies should be examined in the context of the hygiene hypothesis.”

8) Vaccinations may prevent ‘protective’ infections and thus have an unfavorable effect.

9) “In addition to the problem of antibiotic resistance, unnecessary treatment with antibiotics could reduce the degree of physiological immunostimulation afforded by commensal bacteria.”

10) “There is a certain irony in the fact that we must now search for new ways to reproduce the infectious diseases against which we have been fighting with great success over the past three decades.”

11) These mechanisms might extend to other immune disorders, like non-Hodgkin’s lymphomas [cancer], which is also increasing in developed countries.


Another 2002 article published in the AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE titled The Importance of Prenatal Exposures on the Development of Allergic Disease notes [ 12 ]

1) A decreased exposure to infection may play an important role in the etiology of allergic disease, but there is little data on the impact of change in microbial exposure during pregnancy on the child’s risk of developing allergic disease.

2) Exposure to antibiotics in utero is associated with an increased risk of asthma, eczema and hay fever in a dose-related manner.

3) Exposure to antibiotics in utero is a important risk factor in the development of allergic disease.

4) Because the immune system develops in utero, exposure to antibiotics during pregnancy is associated with an increased incidence of allergic diseases.

5) “This effect did not appear to depend on the type of antibiotic prescribed or the trimester the antibiotics were prescribed.”


A 2005 article published in the BRITISH MEDICAL JOURNAL titled Day care in infancy and risk of childhood acute lymphoblastic leukaemia notes [ 13 ]

1) Reduced exposure to infection in the first few months of life increases the risk of developing acute lymphoblastic leukaemia.

2) Several other investigators have reported reduced risks of acute lymphoblastic leukaemia in children with many infections.

3) Reduced infections in the first year of life provides “inadequate priming of the naïve immune system” and “may precipitate a highly dysregulated immune response.”

4) “Similar associations have been reported for type 1 diabetes and allergies in children.”

5) “Some degree of early exposure to infection seems to be important for child health.”



PUBLISHED RESPONSES THAT FOLLOWED THIS ARTICLE INCLUDE:

“Striking the right balance between protecting our children from damaging or life threatening infections whilst exposing them to a ‘sufficient dose’ of milder infections to prime their immune systems, has far-reaching social and behavioural connotations.”

— Roger C Parslow, Senior Research Fellow, Paediatric Epidemiology Group, University of Leeds


[This was my favorite response, by a chiropractor, Dr. Richard Lanigan]

“Gilham et al’s findings should not come as a surprise, however they have stopped short of questioning the possible benefits to the immune system of what were once called ‘normal childhood infections’ and now, are extremely rare.”

“Prevention of infectious diseases is seen universally as beneficial to the health of society. However few have considered the possibility that natural selection and these diseases, played a role in the development of the immune system to fight more deadly diseases.”

Dr. Lanigan then cites references to support the following points:

1) Children who take fewer antibiotics and a lower rate of immunization also have a lower prevalence of asthma, eczema and hay fever than the controls.

2) Children who contract measles are less likely to develop asthma, a disease that was rare thirty years ago and now kills 2000 people per year in the UK.

3) DPT vaccination increases the risk of allergy.

4) There is a specific inverse relationship between contracting measles and atopic diseases.

5) Children who did not have the DPT or polio immunization did not suffer from asthma or other allergic illnesses while 23 - 30 percent of the control group did.

6) Children who suffered infections in the first year of life are less likely to develop insulin dependent diabetes.

7) Immunized children have twice the incidence of type-1 diabetes.

—Richard Lanigan, Chiropractor


“The study by Gilham et al. confirms the hypothesis that reduced exposure to infection early in life has effects on the maturing immune system that increase the risk of acute lymphoblastic leukaemia (ALL) and possibly other malignancies.”

“The immunological basis of this increased risk is uncertain but it could be the result of the inadequate development of immune surveillance mechanisms that detect cancer-specific antigenic determinants.”

“Gilham et al. postulate that the inadequate priming of the immune system due to a lack of exposure to infection permits subsequent infections by unknown exogenous agents, probably viruses, to cause immune dysregulation leading to acute lymphoblastic leukaemia.”

— John M.Grange
Centre for Infectious Diseases
and International Health,
University College London.

— Bernd Krone
Klaus F. Kölmel
Departments of Virology and Dermatology, University of Göttingen, Germany


“Before 1920, acute leukemia among children was a rare event. A significant peak-age incidence (2-5 years) appeared after 1940. Since then, the incidence rate of childhood leukemia has been more or less remarkably stable. This means that some leukemogenic factor must have been introduced in children’s lives some time around 1940.”

“It is a highly striking coincidence that at the same year the introduction of immunization against diphtheria was began on a national scale.”

— Petar I. Ivanovski, pediatrician
University Childrens Hospital, Belgrade


“I wonder if our friends at the CDC, NIH, WHO etc. have considered adding leukemia in addition to diabetes, Guillian-Barre’, Autism, SIDS, Arthritis, Thrombocytopenia, Encephalitis, Death, SBS, Distressed Breathing, Thimerosal Accumulation in Brain (TAB), delayed speech, tics, seizures, hallucinations, dizziness, Hemorrhagic Vasculomyelinopathy etc. etc. etc. to ‘highly coincidental’ adverse reactions from the long list of mass immunizations.”

“Do you think parents would be informed during their child’s well visit of any of the above?”

“In particular, MMR advice from WHO is to jab unless the child is in serious risk of dying. And the only reason given not to jab in this instance is that the death may “incorrectly” be attributed to the MMR. And we wonder why most all serious adverse vaccine reactions are attributed to ‘coincidence’. As clearly seen in this WHO advice—take great lengths to disclaim any adverse vaccine reaction.”

— L. Travis Haws, Dentist
Lakewood CO 80228


“I draw attention to a letter entitled ‘Immunization and Childhood Leukaemia’ in which it was shown that Leukaemia in children in Brisbane Children’s Hospital from 1958 to 1964 showed a significant statistical association with immunization against diphtheria, tetanus and whooping cough.”

In view of Dr Ivanovski’s observations that the incidence of childhood leukaemia increased with the introduction of DPT vaccination it is virtually certain that, if investigated, they will find the group with Leukaemia also shows a statistically significant increase in immunization with DPT vaccine.

— Michael Innis, Director Medisets International


KEY POINTS FROM THIS ARTICLE INCLUDE:

1) A number of studies going back nearly two decades propose that a deficit of exposure to infectious agents in infancy delays immune system development and is consequently responsible for the childhood peak of acute lymphoblastic leukaemia at age 2-5 years.

2) Sending infants to day care increases the incidences of infections, which plays an important role in immune system development, and reduces the incidence of acute lymphoblastic leukaemia.

3) In this study, infants in day care without older siblings had a 39 percent reduction in acute lymphoblastic leukaemia.

4) Infants in day care with older siblings had a 62 percent reduction in acute lymphoblastic leukaemia.

5) “The greatest reduction in risk of acute lymphoblastic leukaemia was seen in children who attended formal day care during the first three months of life.” [Very Important: this indicates that the first 3 months of life are a critical time for infants to actually get infections so that their immune system develops appropriately and strongly, which reduces the incidences of acute lymphoblastic leukaemia and other diseases]

6) Not being infected (“immunological isolation”) in infancy increases the risk of acute lymphoblastic leukaemia.

7) Nine other case-control studies of childhood leukaemia suggest a reduction in risk of around 30-40 percent for day care attendance and increased infections.

8) Not being infected (“immunological isolation”) in the first year of life provides “inadequate priming of the naïve immune system” and “may precipitate a highly dysregulated immune response.”

9) Increased infections in the first few months of life reduce chances of developing acute lymphoblastic leukaemia.

10) “The most plausible interpretation is that this protection comes from exposure to common infections.” [This means that exposure to common infections is a good thing in terms of immune system development and reduced incidence of acute lymphoblastic leukaemia.]

11) Exposure to common childhood infections also reduces incidence of type-1 diabetes and allergies.

12) “Some degree of early exposure to infection seems to be important for child health.” [Very Important]


KEY POINTS IN THE RESPONSES TO THIS ARTICLE INCLUDE:

1) The prevention of infectious diseases [with antibiotics and vaccinations] impairs the development of the immune system so that it is less capable of fighting more deadly diseases, including cancer.

2) Antibiotics and vaccination of children (especially DPT) increase asthma, eczema, hay fever, allergies, atopic disorders, insulin dependent diabetes.

3) Immunized children have twice the incidence of type-1 diabetes.

4) Mass immunizations have been linked to leukemia, diabetes, Guillian-Barre’, Autism, SIDS, Arthritis, Thrombocytopenia, Encephalitis, Death, SBS, Distressed Breathing, Thimerosal Accumulation in Brain, delayed speech, tics, seizures, hallucinations, dizziness, Hemorrhagic Vasculomyelinopathy etc. etc. etc.

5) There is a significant statistical association with immunization against diphtheria, tetanus and whooping cough and acute lymphoblastic leukaemia.


SUMMARY POINTS FROM DAN MURPHY, D.C.

These articles, published in the world’s finest medical journals by many individuals from multiple continents, have several common points of agreement:

1) A person’s immune system begins to develop and mature in utero.

2) The first years, and especially the first few months, of a persons life are also critical times in the lifelong development and maturation of the immune system.

3) The most important factor directing the proper development and maturation of the immune system so that it will best serve a person for life is exposure to bacteria and actually being infected with a variety of bacteria and viruses.

4) Antibiotics, beginning in utero, and certain vaccinations against common childhood diseases received in the first few years of life deprive the developing and maturing immune system of the stimulus required for optimal lifelong function.

5) The consequences of the microbial depravation are increased incidences of allergies, hay fever, eczema, asthma, multiple sclerosis, type-I diabetes, and leukemia.


Dan Murphy graduated magna cum laude from Western States Chiropractic College in 1978, and has more than 20 years of practice experience. He received Diplomat status in Chiropractic Orthopedics in 1986. Since 1982, Dr. Murphy has served part-time as undergraduate faculty at Life Chiropractic College West, currently teaching classes to seniors in the management of spinal disorders.

Dr. Murphy is on the post-graduate faculty of several chiropractic colleges. His post-graduate continuing education classes include “Whiplash and Spinal Trauma” and “Pain Neurology.” Dr. Murphy is the coordinator of a year-long certification program in “Chiropractic Spinal Trauma,” now (2000) in its twelfth year of being offered. This year, the program is being offered through the International Chiropractors Association of California. He has taught more than 700 post-graduate continuing education seminars.

Dr. Murphy is a contributing author to the book Motor Vehicle Collision Injuries, published by Aspen, 1996; and to the book Pediatric Chiropractic, published by Williams & Wilkins, 1998. He writes a quarterly column in the Journal of Clinical Chiropractic.

In 1987, 1991 and 1995 Dr. Murphy received the Post-graduate Educator of the Year award, given by the International Chiropractic Association. In 1997, he received The Carl S. Cleveland, Jr., Educator of the Year award, given by the International Chiropractic Association of California.


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