A safe alternative to killer vaccines

Where to Find Green Homeopathic SAFE Vaccines

If you are a child of the 50’s, some of you will remember receiving a sugar cube in a paper cup that you needed to take (probably at your elementary school). Everyone told you it wouldn’t hurt, there would be no needle involved, and that eating that sugar cube would keep you safe from catching a disease called polio. If this was you, welcome to human vaccine trials, you’ve earned a place in history. For better or worse.


The Salk polio vaccine originated from Cutter Labs in California and while many were fine, others were not. In fact, that particular vaccine was later found to infect hundreds of children who subsequently became paralyzed and died.

The concept of vaccines, the theory, is accurate. Introducing a “vaccine” to mucous membranes is where human immunity begins and it’s the way nature intended exposure to pathogens to occur. And it’s also more logical to introduce one disease at a time- as opposed to multiple diseases with one injection. That is how Mother Nature tends to work, too.

And these two ideas are the main principles behind a 200-year-old method of disease prevention that is quickly (thankfully) gaining popularity among those who choose not to partake in the conventional vaccine schedule. The method is called homeoprophylaxis, or HP for short.

From the article:

“HP is delivered on tiny sugar pellets, one disease at a time, devoid of adjuvents, preservatives, antibiotics, animal viruses, GMOs or excipients of any kind. It contains only the frequency of the disease. This is how illness occurs in nature. The innate developing immune system recognizes one disease, begins an immune response by producing a fever, then a discharge or eruption, and then resolution by developing lifelong immunity to a specific virus. HP produces a similar response yet in a much milder way. We might observe a very brief runny nose or perhaps a longer nap. However, there is no immune system confusion, no viral competition, no crossed signals, and no system overload like with conventional vaccines!

HP Is made by serial dilution of an original substance, either from a natural disease or from an animal, mineral or vegetable source. It is diluted past Avogadro’s number (remember high school chemistry?), rendering it devoid of any molecules, and thus harmless. It maintains the original energetic frequency, however. It’s this stimulation to the immune system that primes it to recognize a disease when encountered in the environment to effectively mount an immune response in the most natural way. Or, the disease is repelled altogether.”

There are no dangerous side effects and there has never been a death from homeoprophylaxis. In fact, the effectiveness of homeoprophylaxis has proven to be robust and in many cases exceeds the effectiveness of conventional vaccines without all the dangerous and sometimes deadly side effects.

But does it work? Who uses it?

Thanks to our friends at The Healthy Home Economist, we know that it does work and several large-scale observational studies have found:

  • Leptospirosis in Cuba (2.5 million people (Bracho, G, Varela, E, Fernandez, R, et al. “Large-scale application of highly-diluted bacteria for Leptospirosis epidemic control.” Homeopathy. 99 (2010): 156-166))
  • Meningitis in Brazil (85,000 people (Mroninski, Adriano, Mattos. Homeopathic Links, Winter 2001, Vol 14(4))
  • Influenza (International Journal of High Dilution Research 2011; 10(36):174-176)
  • Japanese encephalitis in India (20 million people (Srinivasulu, G.An Open Observational Study on the prevention of Japanese Encephalitis through Miasmatic Prescription, Journal of Homoeopathy,U.K. 2014))
  • HP is also effective for the prevention of childhood diseases as observed in 3500 children (Golden, Isaac. “Homeoprophylaxis-A Fifteen Year Clinical Study: A Statistical Review of Efficacy and Safety of Long Term Homeoprophylaxis. Gisborne. Vic. 2004).

With HP, there is no expected antibody production (that’s not the goal, either) because antibody production isn’t necessarily the gold standard of immunology. People vary greatly in how their immune systems respond to stimulation from pathogens. HP addresses the innate arm of the immune system, unlike vaccines that just boost antibodies in a mechanical way. Truthfully, the artificial stimulation of the immune system can potentially cause damage and paves the way for possible lifelong issues with autoimmunity.

There are 3 applications for HP –

  1. Endemic disease (such as leptospirosis)
  2. Short term epidemics (such as influenza)
  3. Childhood diseases

For short-term epidemics, like flu, you dose for a few weeks/months until the risk is past. Some practitioners give “influenzinum” to their patients at the beginning of flu season and then every 6 weeks until the end of flu season.

More from the article:

“For childhood disease we use a program that contains single monthly doses for a period of about 3 years.  This includes 8 diseases that are on the recommended schedule that parents typically vaccinate for. Protection begins immediately with the first dose and continues for a period of about 10 years. Re-doses can be administered in teen years or young adulthood depending on exposure to disease and risk of the specific disease.”

HP is also safe to use when traveling to foreign countries, because the claim that you mustreceive vaccines to travel, is inaccurate. Actually, the only vaccine required to re-enter the US is yellow fever if you have visited a country where yellow fever is endemic; find that info on the CDC’s site under “travel” where you can click on links for each country and learn about the yellow fever risk. For all other vaccines- like those for hepatitis, dengue fever, typhoid, malaria, and others- HP is more than suitable and can provide protection- many of the studies already conducted have taken place in countries where these tropical epidemics exist.

If you hate the thought of injecting your tiny newborn with conventional vaccines, loaded with neurotoxic chemicals and additives that can damage their health for a lifetime, there IS another way. In fact, to learn more, the second international conference for parents and healthcare practitioners is taking place in St. Petersburg Florida, October 7-9, 2016. For more info, click here

If you want to purchase Green vaccines then please click here to go toWorldWideChoice.org with info on how to obtain them for you and your family!
(I have no affiliation with this group, but hear great things, I make ZERO commissions on it but this doctor does have them available along with a free consult.

Source: The Healthy Home Economist

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Erin Elizabeth


Erin Elizabeth is a long time activist with a passion for the healing arts, working in that arena for a quarter century. Her site HealthNutNews.com is less than 2 years old but has already cracked the top 20 Natural Health sites worldwide. She is an author, public speaker, and has recently done some TV and film programs for some of her original work which have attracted international media coverage. You can get Erin’s free e-book here and also watch a short documentary on how she overcame vaccine injuries, Lyme disease, significant weight gain, and more. Follow Erin on FacebookTwitter, and Instagram.

Vaccines – did your medic show you this?


Jason Christoff
This is what a medical doctor is “supposed” to make any vaccinating parent aware of, before they vaccinate. The law of informed consent is an international medical charter that’s designed to inform a patient of the risks involved with any treatment, if the treatment is proven to cause permanent injury or death. Why do you think you’ve never been informed of the injuries or deaths linked directly to vaccination?

MMR Vaccine Fraud / meningitis and more

June 14, 2014

Dr. Andrew Wakefield Exposes MMR Vaccine Fraud


In this video, Dr. Andrew Wakefield reveals that in the recent “measles outbreak” in Wales earlier this year, records now show there was only one single laboratory confirmed case of measles in March, down from three cases in February.

He also shows proof that he was not the first scientist to show the link between autism and the MMR vaccine, as has been widely reported. In fact, there were so many reported cases of the MMR vaccine being linked to autism prior to 1998, that Dr. Wakefield’s article published in the Lancet was “late” in reporting what was already widely known.

Dr. Wakefield also sets the record straight on the recent N.Y. Times article that praised Dr. Maurice Hilleman, the pioneer vaccine researcher who worked for Merck, regarding the mumps vaccine. (See our earlier story on Dr. Hilleman and the polio vaccine which spread cancer here.) The MMR vaccine, according to statistics provided by the US CDC and British Health Authorities, increases the risk of infertility and testicular cancer more than any other vaccine.

Starting at 10:44 in the video, Dr. Wakefield reveals the fraud and corruption behind the MMR vaccine that allowed it to gain such a wide market in the U.S. and around the world. It will shock you!

Vaccine Epidemic
by Louise Kuo Habakus and Mary Holland J.D.


Vaccine Epidemic bookcover Dr. Andrew Wakefield Exposes MMR Vaccine Fraud


June 14, 2014

Cover-up Scandal:

CDC’s Vaccine Research Exposed as Flawed and Falsified


CDC Headquarters Cover up Scandal: CDC’s Vaccine Research Exposed as Flawed and Falsified


CDC’s Vaccine Safety Research is Exposed as Flawed and Falsified in Peer-Reviewed Scientific Journal

Substantial Scientific Evidence Exists that Vaccine Ingredient is a Developmental Neurotoxin

Watchung, NJ, June 12, 2014
by PRNewswire

Just months after U.S. Congressman Bill Posey compared the Center for Disease Control (CDC)’s vaccine safety studies to the SEC’s Bernie Madoff scandal, malfeasance in the CDC’s studies of thimerosal-containing vaccines has, for the first time, been documented in peer-reviewed scientific literature. While the CDC states on its website that “low doses of thimerosal in vaccines do not cause harm, and are only associated with minor local injection site reactions like redness and swelling at the injection site,” the journal BioMed Research International now provides direct evidence that the CDC’s safety assurances about the mercury-containing preservative are not fact-based, according to the article’s lead author, Brian Hooker, PhD.

The paper opens by citing over 165 studies that have found Thimerosal to be harmful, including 16 studies that had reported outcomes in human infants and children of death, acrodynia, poisoning, allergic reaction, malformations, auto-immune reaction, Well’s syndrome, developmental delay and neurodevelopmental disorders including tics, speech delay, language delay, ADHD and autism. These findings by multiple independent research groups over the past 75+ years have consistently found thimerosal to be harmful. “Substantial scientific evidence exists and has existed for many years that the vaccine ingredient thimerosal is a developmental neurotoxin” says George Lucier, former Associate Director of the National Toxicology Program.

Studies showing harm from thimerosal sharply contradict published outcomes of six CDC coauthored and sponsored papers – the very studies that CDC relies upon to declare that thimerosal is “safe” for use in infant and maternal vaccines. Dr. Hooker, biochemist and vaccine industry watchdog, said of the six CDC studies, “Each of these papers is fatally flawed from a statistics standpoint and several of the papers represent issues of scientific malfeasance.  For example, important data showing a relationship between thimerosal exposure and autism are withheld from three of the publications (Price et al. 2010, Verstraeten et al. 2003 and Madsen et al. 2003).  This type of cherry-picking of data by the CDC in order to change the results of important research studies to support flawed and dangerous vaccination policies should not be tolerated.”

Dr. Boyd Haley, international expert in mercury toxicity and a co-author of the recently published paper said “There is no doubt that authorities in the CDC have initiated and participated in a cover-up of vaccine-induced damage from thimerosal to our children—-and this I consider criminal.” The paper, “Methodological Issues and Evidence of Malfeasance in Research Purporting to Show Thimerosal in Vaccines is Safe,” was published on June 6 and contains eight pages of evidence that the CDC has had knowledge of the vaccine preservative’s neurological risks, yet continues to cover them up.

The paper concludes, “five of the publications examined in this review were directly commissioned by the CDC, raising the possible issue of conflict of interests or research bias, since vaccine promotion is a central mission of the CDC. Conceivably, if serious neurological disorders are found to be related to Thimerosal in vaccines, such findings could possibly be viewed as damaging to the vaccine program.”

Dr. Hooker has submitted over 100 FOIA requests to the CDC over the past 10 years and has amassed thousands of pages of documents showing malfeasance in the CDC’s vaccine safety program.  Hooker revealed that one CDC document quoted a top official instructing CDC employees to “Review all correspondences and documents to see if there is ‘foreseeable harm’ to the agency if they were released” so the documents could be redacted by CDC attorneys prior to release.

Barry Segal, founder of the Focus Autism Foundation and former entrepreneur whose company sales peaked near $2 billion said, “We are in the process of exposing what may be the biggest federal scandal ever with immense damage to our economy and our people, especially our children who are the future of our country. Their health has been compromised by mercury in vaccines. We need Congress to take action now. Thimerosal must be banned.”

A more effective vaccine preservative “2PE” has replaced thimerosal in many other vaccines and possesses a much better safety profile according to Dr. Hooker.

The Focus Autism Foundation is dedicated to providing information to the public that exposes the cause or causes of the autism epidemic and the rise of chronic illnesses – focusing specifically on the role of vaccinations. To learn more, visit FocusAutism.org.  A Shot of Truth is an educational campaign sponsored by Focus Autism

BioMed Research International


Focusautism.org – www.focusautism.org

A Shot of Truth – www.ashotoftruth.org

See Also:

CDC Caught Hiding Data Showing Mercury in

Vaccines Linked to Autism


Vaccine Epidemic
by Louise Kuo Habakus and Mary Holland J.D.


Vaccine Epidemic bookcover Cover up Scandal: CDC’s Vaccine Research Exposed as Flawed and Falsified


Dr Rebecca Carley



Dr carly






mumps vaccine failure Mumps Vaccine Proves Ineffective as Outbreaks Among Fully Vaccinated Increase


By Alliance for Natural Health

But instead of acknowledging the vaccine’s problems, the CDC and mainstream media blame people who don’t vaccinate. Action Alert!­­

Mumps is a nasty virus—it can cause fever, headache, and painfully swollen glands. In serious cases, it can causemeningitis, deafness, and even testicular inflammation. Mumps is also easily spread through mucus: if an infected person sneezes, coughs, or even talks, they can pass it on.

For these and other reasons, most Americans are vaccinated against mumps through the MMR (measles, mumps, and rubella) shot, which is also one of the more dangerous vaccinations. But in the early 2000s, researchers began to notice an alarming pattern: those vaccinated against mumps were still becoming ill with it—at alarming rates.

This worrisome trend is accelerating: in April 2014, the New Jersey Department of Health warned of an outbreak of mumps at the Stevens Institute of Technology. Eight cases of mumps were confirmed—yet all of those infected had been fully vaccinated with two documented doses of the MMR shot.

What’s going on here? Is the vaccine losing its efficacy—or was it never effective in the first place? There are a number of explanations:

  • The effectiveness of the MMR vaccine in preventing mumps is—according to Dr. William Schaffer, a pro-vaccine researcher at Vanderbilt University—“not so good.” A CDC study of a 2009–2010 mumps outbreak in the northeastern US found that a full 77% of those sickened in 2009 outbreak had been vaccinated.
  • The effectiveness of the mumps vaccine depends heavily on the strain contracted. According to a 2008 FDA study, the vaccine is “0 to 33%” effective on the Rubini strain. Even so, this study, like other government studies, blamed outbreaks on low vaccination rates instead of on low vaccine effectiveness.
  • A whistleblower case unsealed in 2012 suggests that Merck, the producer of the MMR vaccine, might have misrepresented the results of research on the vaccine’s efficacy from the start. The case, initiated by a pair of former Merck researchers, claims that Merck manipulated the results of clinical trials in order to keep its exclusive right to manufacture the vaccine. By claiming a fabricated 95% effectiveness rate, Merck allegedly defrauded the US government, causing it to buy 4 million doses of “mislabeled and misbranded” MMRs vaccines. The suit also claims this helped spark two major mumps outbreaks, and that “the ultimate victims here are the millions of children who every year are being injected with a mumps vaccine that is not providing them with an adequate level of protection.”

The Justice Department refused to pursue the case.

Conventional medicine openly acknowledges the dangers of the MMR vaccine, yet still decrees that its benefits outweigh its risks. When the evidence clearly dictates that there is less benefit to the mumps vaccine than thought, the usual arguments at least need to be revised.

Some observers believe that the risks from this vaccine are magnified by giving three shots in one rather than individually. That idea deserves more attention. The usual reason conventional medicine prefers to give a lot of shots all at once is that they worry they won’t be able to get parents to come in more often. This is not a proper justification for exposing kids to unnecessary risks.

When too many vaccines are given within a short period of time, the body may experience an immune system overload, as discussed in J. Barthelow Classen’s evidence review of vaccinations published in the peer-reviewed journal Molecular and Genetic Medicine. In his review, Dr. Classen discusses the data supporting a relationship between an epidemic of inflammatory diseases and vaccine-induced immune system overstimulation, as well as the evidence linking immune overload with epidemics of diabetes (both type 1 and type 2) and obesity. Government officials simply ignore these legitimate concerns and keep adding more vaccinations all together at ever younger ages, as revealed by the CDC’s busy vaccine schedule.

Despite all this evidence, the government still refuses to comment on or conduct further research on the vaccine schedule or the ineffectiveness of the MMR vaccine for mumps. There’s no way to know why for sure, but one possible reason is that— after spending millions on a multiyear contract with Merck—they’re attempting to avoid another embarrassing repeat of the Tamiflu scandal, where the government spent $1.5 billion on flu treatments that were found to be no more effective than aspirin.

Of course, those who choose not to vaccinate their children are still the laughingstock of the mainstream media. Just this month, The Daily Show aired a scathing segment mocking parents who choose not to vaccinate.

Action Alert! Contact the Centers for Disease Control and ask them to do more research on mumps, the MMR shot, and the vaccine schedule.


Take Action112 Mumps Vaccine Proves Ineffective as Outbreaks Among Fully Vaccinated Increase


Neurosurgeon Speaks Out On How Vaccines Harm Child Brain Development

September 5, 2013 BY DAVE MIHALOVIC

Neurosurgeon Speaks Out On How Vaccines

Harm Child Brain Development

 If childhood vaccines are safe, why are well over half a million vaccinated American children afflicted with autism, while non-vaccinated Amish and Mennonite children rarely suffer from the disorder? Why has the incidence of asthma, allergies, autoimmune disease, Type 1 diabetes and neurological conditions also dramatically increased in vaccinated children?

Furthermore, why do obstetricians give pregnant women influenza vaccines that contain a toxic dose of mercury and why are new babies injected with the Hepatitis B vaccine within hours of birth when there is no medical justification for it?

In this informative lecture, Dr Blaylock addresses these and many other vaccine-related issues. If you are concerned about your and your family’s health and want to make an informed decision on behalf of your child or children, this is a really important video for you to watch. You will never look at vaccination and the so-called health care system the same way again.

If you would like a high quality copy of this lecture you can purchase the DVD at:



Dave Mihalovic is a Naturopathic Doctor who specializes in vaccine research, cancer prevention and a natural approach to treatment.


New study on vaccines – what more is there to say?


Sunday, July 14, 2013

A New Study:

Acidic Aluminum Adjuvant In Vaccines

Transfers to the Brain!

Newly published research by Keele Conference scientists shows that aluminum adjuvant in vaccines transfers to the brain. They have documented the path from injection site to the brain, and that once in the brain, it persists. Newborns, the elderly, and people with a certain genetic variation are particularly at risk.


by Heidi Stevenson
A new study adds a major link in the association of aluminum adjuvants in vaccines with neurological disorders. It demonstrates the pathway along which aluminum in vaccine adjuvants is transferred from the injection site to the brain, where it persists indefinitely. They have also identified a likely carrier and a means by which the process occurs.
The study is exhaustive, eliminating a wide array of options that might mitigate against their findings. They also focused on two groups to determine if their findings indicate that they’re at particular risk. They include newborns and people with a certain genetic variant. On top of that, the elderly may be at significantly higher risk for aluminum adjuvant-induced neurotoxic harm.
Please note that variant does not mean defective! We all have genes that are not like those of the majority. That does not indicate a defect, only a distinction. Viva la difference!

Reason for the Study

Nanoparticles are not as new in medicine as generally believed. The study states:
The use of nanomaterials in humans is not as contemporary as is recently portrayed. For decades, alum, a nanocrystalline compound formed of aluminum oxyhydroxide, has been the most commonly used adjuvant in vaccines.
In macrophagic myofasciitis (MMF), “alum-loaded macrophages [are] typically detected at sites of previous injections (up to >12 years later), resulting in a specific granuloma called macrophagic myofasciitis or MMF.” *
CCL2 is a cytokine that recruits monocytes, memory T cells, and dendritic cells to sites of inflammation. Earlier work has shown that 252 ASIA patients had an increase in circulating CCL2, along with a variation in the CCL2 gene. It’s also known that:
  • Danger signals from the CCL2 cytokine draw monocytes, which causes them to convert to macrophages before migrating to lymph nodes.
  • Dendritic cells (DCs) transfer antigens to a large network of distant dendritic cells, also known as antigen-presenting cells (APCs).
  • Alum injections are known to incite “significant changes linked to activation of the innate immune system in distant organs”.
These facts resulted in this study to detemine whether injected nanomaterials, most particularly alum, could be moved to distant organs through phagocytosis and CCL2 signaling.

The Experiments

Experiments were done on laboratory mice. A fluorescent surrogate for alum particles, fluorescent latex beads (FLBs), was used to assess movement and distribution of intramuscularly injected materials. Morin stain and particle induced X-ray emission (PIXE) were used to assess movement of alum hybrids, Al-Rho, which match the particle size of injected adjuvant aluminum. Using graphics from the study, I will attempt to explain what was done, though not all aspects of the study will be covered.
Standard C57BL/6 lab mice were injected in the tibialis anterior muscle (equivalent to a calf muscle in humans) with an alum-containing vaccine at a dose equivalent to that given to humans, with the amount calculated by an FDA standard. As is intended with an adjuvant, an intense localized inflammation ensued, which lasted until day 4 post-injection, when it stabilized. The local aluminum concentration decreased rapidly until day 4, remaining stable until day 21.


Aluminum-loaded macrophages were found encased in granulomas from day 4 post-injection, as shown in this image. The left-hand image shows a photo of a granuloma, and the right-hand image is a PIXE graphic demonstrating the high aluminum load. (Yellow shows the greatest load.)
Signs of aluminum were found in the spleens and brains of these mice, as shown in these graphics:


Photographic images show spleen (left) and brain (right) tissues, with areas of PIXE imagery indicated with bright pink squares. The PIXE images showing aluminum loading are on the right side of each photo.


The graph on the left shows the percent of areas in the brains found to have aluminum spots. Notice the small number in unvaccinated mice. The numbers shown on days 21 and 365, one year post-vaccination, demonstrate that the aluminum does not dissipate. (The authors believe that the bar for day 180 is an anomaly, caused by either “interindividual variations in aluminum handling or to sampling problems related to variable proportions of grey and white matter in the randomly scanned areas”.
The aluminum that makes its way to the brain is persistent.
Movement of Alum Surrogates


The image to the right shows the movement of FLBs by macrophages from the injection site to interstitial spaces in the muscle around it. Notice the bright red slash in the image to the left showing the fluorescing surrogates for alum,  FLBs (fluorescent latex beads) one hour after injection. The right-hand image shows how they’ve been dispersed by macrophages four days later.


The image to the left is a graph of  the number of cells loaded with FLBs (surrogate alum) found in popliteal (knee area) lymph nodes (P-DLN) and inguinal (groin) lymph nodes (I-DLN) at one hour, day 4, and day 21. Notice that movement of FLBs to lymph nodes is dramatic by day 4. Other images (not shown) document that this movement can be accounted for by inflammatory dendritic cells and macrophages that are derived from monocytes.
Another related part of this section of the experiment utilized injection of a compound known to inhibit FLB movement by phagocytes  to popliteal lymph nodes. At day 4 movement to popliteal lymph nodes was down by 32%, and to inguinal lymph nodes by 69%. This treatment resulted in significant reduction of FLB in lymph nodes, further confirming that macrophages are the primary means of transportation to lymph nodes.


After moving to lymph nodes, the FLB alum surrogates moved to the spleen, as shown in the image to the right. The left-hand graph shows the number of FLBs in the spleen peaking at day 21 and decreasing to a little over half that number on day 90. Compare this with the previous graph, which shows FLBs leaving the lymph nodes between days 4 and 21. This increase in FLBs in the spleen between these same dates indicates that they’re moving from lymph nodes to the spleen.
The question then is: How does that happen? There is no connection between lymph nodes and the spleen. However, if you look at the graph on the right, you can see that FLBs are found in the blood, too. The authors surmise that the FLBs must travel in macrophages through the thoracic duct, the largest lymph vessel, which releases most of the body’s lymph into the blood system. Thus, macrophages carrying the alum-surrogate FLBs are transported from lymph nodes into the blood system, and then arrive in the spleen.


The authors wrote, “Cerebral translocation of FLBs was delayed but relentless until the d90 endpoint in C57 mice,” and the graph to the left shows it. Only a small amount of the alum surrogate injected into the standard C57 lab mice reached the brain on day 4, but you can readily see how the pace picks up by day 21, and more than doubles again by day 90, the endpoint of the study on C57 mice.
The CX3CR1GFP/+ mice, indicated by the white bars, have an inserted gene that allows visualization of the microglia, which are a particular kind of macrophage found in the brain and spinal cord. As you can see, the FLBs were still increasing on day 180, the study’s endpoint for these mice.


The image to the right shows FLBs in the brainstem of a CX3CR1GFP/+ mouse. The inset is a photo of a stained slice of brain with their locations indicated by dots. The larger image is of an unstained section on day 21 showing the FLBs located mostly just under the pia membrane, i.e., on the surface of the brainstem.
Preventing FLBs from Transporting to Organs


Some C57 mice were given the FLB injection intravenously into the tail, rather than into the tibial anterior leg muscle. The result is shown in the graph on the left. Notice that hardly any FLBs ended up in the brain by either day 21 or 90. Clearly, little, if any, immune response resulting in macrophages engulfing FLBs is triggered by an intravenous injection.


After ablating (destroying) popliteal and inguinal lymph nodes, the number of FLBs reaching the blood, spleen, and brain was reduced by 60-80%. The graph to the left shows the percentage of FLBs remaining compared to controls. The number that reached the spleen was only about 20% and the number reaching the brain was about 40%. This indicates that movement of FLBs by macrophages to local lymph nodes is part of the process for movement of most FLBs—and by analogy, most alum—from injection site to organs, including the brain.
Blood-Brain Barrier


One of the concerns in clinical procedures involving toxic elements on newborn babies is their weak blood-brain barrier. Mice with a leaky blood-brain barrier, called mdx, were used to see what happens in this situation. The graph to the right shows that, by day 21 the number of FLBs reaching the brain of an mdx mouse with a leaky blood-brain barrier is significantly greater than in a normal C57 mouse, and that this remains a problem over time.
Images from the muscles, spleen, and brain chimeric (genetically engineered) mice with a green fluorescing protein confirmed these findings.


Confirmation: FLBs Correlate with Alum Adjuvant
The Morin stain for aluminum showed  “Al-Rho particles were avidly phagocytosed after i.m. injection and formed intracellular agglomerates similar in size to the vaccine adjuvant”, as can be seen by the clusters in the “Vaccine” and “Al-Rho” images to the left. These images are similar to the first image of an aluminum-induced granuloma shown above.
The graphs below show Al-Rho movement from lymph nodes to spleen, and spleen to brain:


The Al-Rho nanohybrid surrogates for alum showed up prominently in the popliteal and inguinal lymph nodes, which are nearest to the injection site, by day 4, as shown in the left-hand graph. Most have moved by day 21, showing up in the spleen, as you can see by the middle graph. By day 90, you can see that a significant number of Al-Rho have left the spleen. However, from the graph on the right, you can see that they’ve been moving from the spleen to the brain. The movement is strikingly similar to that of the FLBs.
Effect of CCL2 Cytokines in Alum Distribution
The CCL2 cytokine is suspected to be at the center of some ASIA disorders because research has shown that ASIA patients have high amounts in their blood, along with a genetic variant related to CCL2. Mice bred to be deficient in the CCL2 cytokine were used to see what effect they have on distribution of the alum surrogate, Al-Rho, to lymph nodes and organs.


In the left-hand graph of the image to the right, you can see that there is significantly less movement of Al-Rho from the site of an intramuscular injection to organs. Compared with controls, 65% the amount of Al-Rho is found in the nearest lymph node at day 4, and even less, 34%, gets to the inguinal lymph node. On day 21, only 15% as much is found in the blood, 29% in the spleen, and only 18% as much Al-Rho is found in the brains of CCL2-deficient mice compared to controls.
The graph to the right of “CCL2 Deficient Mice” shows the amount of Al-Rho found in the same kind of CCL2-deficient mice after they’ve been injected with rCCL2, a recombinant form of CCL2 that was used because no other version is available. The results are dramatically different. First, note that the y-axis scale is dramatically different, running up to 600%, instead of only 80%. By day 21, the rCCL2 injections increased distribution of Al-Rho to the blood by 274%, the spleen by 180%, and the brain by 341% as compared to controls.
These experiments, along with others not described here, document that more CCL2 cytokines—which draw monocytes and dendritic cells to the site of inflammation—than normal are directly associated with the distribution of alum to the brain.


This study has demonstrated that aluminum adjuvant particles can be transported to the brain through CCL2 signaling that brings monocytes to the site of vaccine administration. The route is shown to be:
  1. First to the nearest lymph nodes.
  2. Through the lymph system’s thoracic duct.
  3. Through the thoracic duct into the bloodstream.
  4. Through the blood to the spleen and possibly partially directly to the brain.
  5. From the spleen to the brain.
This process appears to occur in all mice, though at a slow rate. However, in mice with high levels of CCL2 cytokines, the process is speeded up dramatically. The study also documented that an inefficient blood-brain barrier, as is found in the youngest babies, allows significantly more alum through to the brain.
The toxic potential of aluminum is high. This study has demonstrated that injecting alum adjuvants with vaccines results in transferrence to the brain, where it persists. Most people have a high tolerance to alum. However, there are limits in anyone. In the case of people with high levels of CCL2—such as those with a genetic variant leading to high CCL2 levels, as found in ASIA patients—even small amounts of injected alum can be disastrous.
Consideration needs also to be given to the association of aluminum in the brain with Alzheimer’s disease, which is afflicting an accelerating percentage of people as they age.
As the study’s authors point out:
It is likely that good tolerance to alum may be challenged by a variety of factors including overimmunization, BBB immaturity, individual susceptibility factors, and aging that may be associated with both subtle BBB [blood-brain barrier] alterations and a progressiveincrease of CCL2 production.
With the rapidly increasing number of vaccinations recommended, and even mandated, in schedules, along with the increasing number of people suffering from chronic neurological and autoimmune disorders, surely it’s past time to sound the alarm. At the very least, serious research to investigate these risks must be launched.
The researchers involved with the Keele Conference are doing valuable research aimed at identifying and mitigating these risks. It’s long past time for the agencies supposedly concerned with public health to follow these leaders of science.
Three of the study’s authors, Christopher Exley, Romain Gherardi, and François-Jérôme Authier, attended the 10thKeele Conference titled, “Illuminating and Elucidating Aluminium’s Exposome: From Geochemistry to Neurochemistry, From Microbe to Man”:
  • Dr. Exley was the conference administrator and has published a large number of studies on the topic, not to mention being involved in several of the studies and references of this conference.
  • Dr. Gherardi presented his latest work on macrophagic myofasciitis (MMF), a new vaccine-associated disease, indicating that the cytokine CCL2 is not simply a biomarker of MMF inflammation, but is also associated with its pathophysiology. He suggested that CCL2 should be investigated in relation to other autoimmune/inflammatory syndromes (ASIA).
  • Dr. Authier reported on a new non-invasive method to diagnose MMF, which has hitherto been diagnosable only via muscle biopsy. He also suggested that MMF is probably more prevalent than currently realized.
* Unattributed quotations are from the study.

Source:  Please refer to source article link for graphics linked to above article



The deaths just keep mounting all across the world: Children are collapsing into comas and then dying, just minutes after receiving combination vaccines that have been deceptively marketed as “completely safe.”

Last year, Australia temporarily banned flu vaccines in children after they were found to have causedvomiting, fevers and seizures (http://www.naturalnews.com/029586_A…).

Today the damage from vaccines is emerging in Japan, where the health ministry has suspended the use of vaccines from Pfizer and Sanofi-Aventis following the deaths of four  there who died within minutes after receiving these vaccine shots.

All four children received combination vaccines, where multiple shots are combined into one high-potency injection. MMR is another example of a combination vaccine shot that combines vaccines for measles, mumps and rubella.

There is very strong evidencethat vaccines are far more dangerous when given in combination than when given one at a time (http://naturalnews.tv/v.asp?v=60825…). (http://www.naturalnews.com/030678_M…)




The great vaccine damage cover-up

What will now happen in Japan is that a group of vaccine safety experts will meet to discuss the vaccines, and no doubt most of the members of that group will be paid off by Big Pharma.

Within a day or two, a statement will be issued that states there is “no causal relationship exists between vaccines and child deaths” and the vaccine program will continue as usual. The ongoing deaths of children will be ignored or explained away as “mere coincidence.”

How many coincidences does it take to make a pattern? If you’re one of the brainwashed vaccine zealots,there is never a pattern.

ALL deaths are automatically considered “coincidence,” no matter how many occur or how frequently they appear. A true scientist, of course, would observe the pattern and realize there is a cause-and-effect phenomenon taking place.

But then again, vaccine zealots are nothing like real scientists. They are propagandists.

This is how the vaccine industry operates every day: Lie to the public that the vaccines are 100% safe and effective, then deny any hint of vaccines causing damage to anyone. It’s a double-layer deception.

First, there’s the deception that vaccines are safe (they aren’t, and the vaccine industry refuses to subject them to scientific clinical trials versus non-vaccinated children in order to prevent this truth from coming out), and secondly that vaccines don’t damage anyone.

That’s yet another lie: Vaccines cause untold damage to the neurology of children and adults alike.

Children are routinely killed by vaccines, and vaccines are being pushed in the false context that presumes vaccines are the only way to protect children from infectious disease in the first place.

Nutrition actually works better, and it doesn’t kill children. But that’s not the choice presented to parents.

The choice is either vaccination or non-vaccination.

The choice is never presented as vaccination or vitamin D supplementation, is it?

The real cost in human suffering

If vaccines are so safe, then why do so many healthy young children suddenly collapse into autism in the hours or days following vaccination?

Why is this neurological damage a global phenomenon that almost always occurs in children who are vaccinated?

Why are non-vaccinated children so much healthier, more vibrant, more intelligent and more immune to infectious disease?

The vaccine industry doesn’t want you to ask these questions. You’re supposed to just accept their propaganda, take your shot, and keep coming back for more, year after year.

If your child gets autismit your fault, not theirs (according to them).

If your child collapses into a coma and dies,you have no legal recourse because the U.S. Supreme Court has made it illegal to sue for damages from vaccine companies (http://www.naturalnews.com/031453_S…).

The entire medical system has been configured to suppress vaccine lawsuits and deny the evidence of vaccine damage and death.

The court system denies justice to anyone whose children are damaged or killed by vaccines.

And parents who question the safety of vaccines are ridiculed by doctors and even called “baby killers” by Bill Gates, who has funneled tens of billions of dollars into mass vaccination campaigns despite the fact that vaccines are killing children.

Of course, the vaccine industry claims its vaccines are saving far more children than they are killing (they claim their vaccines kill exactly zero children, by the way — a number that is an obvious lie).

But even this argument falls flat when you consider that using nutrition to enhance immune function is far more effective than using vaccines. Even the Nobel prize winning Luc Montagnier, co-discoverer of the AIDSvirus, says you can cure AIDS with a strong, healthy immune system ( http://naturalnews.tv/v.asp?v=BAFF5… ). Much the same is true with nearly every other common infectious disease: Strong immune function resists infection far better than any vaccine.Vitamin D, for example, also works to prevent tuberculosis.

The CDC has never admitted it publicly, of course, because the CDC is a political organization that protects the profits of the vaccine makers.

When it comes to what’s real versus what’s just corporate propaganda, one thing is certain:Scientific facts have never stood in the way of vaccine profits.

The vaccine industry has becomean unstoppable death machinebased on non-existent science and arrogant quackery. It has become a huge profit center for the medical industry, of course, because much of the damage caused by vaccines results infuture medical care profitst hat feed the drug companies(http://naturalnews.tv/v.asp?v=BAE7F…).

What’s clear from all this is that vaccines are great at one thing: Population control.

“The world today has 6.8 billion people… that’s headed up to about 9 billion.

Now if we do a really great job on new vaccines, healthcare, reproductive health

services, we could lower that by perhaps 10 or 15 percent.”

– Bill Gates (http://www.naturalnews.com/029911_v…)

As of this week, the population of children in Japan has been reduced by four. And more vaccine-induced deaths are no doubt happening all across the world that go unreported or are intentionally censored out the medical records.

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