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Vaccine makers spend millions every year pushing the public to believe that vaccines create immunity and save lives… but do they?

FACT: Vaccines create temporal (short-term) antibodies ONLY. This is the sole requirement from the FDA in order to get approval to sell the vaccine. If you read the vaccine product insert written by the pharmaceutical company that creates the vaccine, it clearly states the increase in temporal antibodies as the basis for proof the vaccine works.

It also gives the percentage of people that had an increase in antibodies after the vaccination. Sometimes this number is quite low in the 50% range, defying any real herd immunity protection theory (more on the myth of herd immunity below).

Antibodies do NOT equal immunity

But science has long known that antibodies alone do NOT create real immunity. Some people with high levels of antibodies can be exposed to an illness and still get sick, while others without antibodies can be exposed and not get sick. Dr. Merrill Chase, nicknamed the Grandfather of Immunology for his pioneering work, did clear-cut research on this issue back in the 1950s. His results are clear: antibody levels don’t determine immunity. More on his work below.

The immune system is a highly complex system and science is still in its infancy understanding how it functions. In fact, immunology textbooks were completely rewritten recently after a University of Virginia study finally proving the link between the gut and the brain through the lymphatic system. Before this 2014 study, immunology books were adamant there was no link.

Doctors are never taught the ingredients in vaccines, the way they disrupt the immune system or the research proving antibodies do not create immunity.

But doctors, who are only trained to promote vaccines and not in the science of vaccination, will never tell you this. In fact, most doctors don’t know since their main sources of vaccine information come from pharmaceutical company representatives paid to sell the vaccine, or the CDC, a government agency that has been called out many times for taking pharmaceutical industry money and collects royalties on vaccines sales.

If vaccines create immunity, why are there multiple cases of outbreaks in vaccinated populations?

Since vaccines are given by injection, they bypass the normal immune pathway and therefore do not trigger the cellular immune system, which science shows to be the main component necessary to create immunity.

As a result, there are numerous reports of outbreaks in fully vaccinated populations, with booster shots not making a difference (studies here). Since there is no benefit of immunity with vaccines, yet the very real risk of side effects and reactions, the question is who really benefits from an outdated vaccine program?

Clearly, vaccines only benefit the pharmaceutical and medical industry, which uses vaccines to create health issues and customers for its prescription drug market and medical treatments. The global vaccine market is worth around $58 BILLION a year with an almost doubling expected in the next decade. As usual, the industry puts profits before patients.

This recent report published by the CDC proves that outbreaks occur in those that are vaccinated…

Click here to read the full report

Merrill W. Chase, 98, Scientist Who Advanced Immunology: NY Times. 

This is an article in the NY Times on the man who was behind the discovery originally, a man considered the
grandfather of immunology and who won a Nobel prize for his discoveries.

Dr. Merrill W. Chase was an immunologist whose research on white blood cells helped undermine the longstanding belief that antibodies alone protected the body from disease and micro-organisms. In the 1940s experts believed that the body mounted its attacks against pathogens primarily through antibodies circulating in the bloodstream, known as humoral immunity.

But Dr. Chase found that antibodies alone cannot orchestrate the body’s immune response.

‘This was a major discovery because everyone now thinks of the immune response in two parts, and in many instances, it’s the cellular components that are more important. Before Chase, there was only humoral immunity. After him, there was humoral and cellular immunity.” – Dr. Michel Nussenzweig, professor of immunology at Rockefeller.

Must-watch video! Brandy Vaughan, founder of Learn The Risk & former pharmaceutical insider, on how vaccines do not create immunity.

VACCINES ARE A BLOCKBUSTER: $60 BILLION BY 2020

Creating future customers

So if vaccines don’t create immunity, what do they create? They create future customers for pharmaceutical companies. How? Because the toxic ingredients create health issues and these toxins accumulate in the body causing more issues the more vaccines are received. This is one reason the US vaccine schedule is constantly increasing and now requires 72 vaccines before a child goes to school.

See the current recommended schedule for vaccines here or refer to the CDC website.

Viruses reduce later health issues 

Before childhood vaccines became a huge moneymaker for pharmaceutical companies, these issues were considered “normal” and there was no fear around catching them. Any long-lasting complications were extremely rare (99.9% of cases recovered within a few days with no lasting issues). In fact, many experts argue that childhood illnesses are good for our immune system.

Recently science has discovered that having a childhood illness REDUCES later health issues, like cancer (Studies here). More of the benefits of viruses here.

The Myth of Herd Immunity

Herd immunity can only come from naturally caught illnesses — NOT from vaccines. Some people may be old enough to remember that just 20 years ago, measles and chicken pox were benign illnesses that, for centuries, were a rite of passage for children.

Herd immunity is only proven in groups where the population was exposed to an illness through the natural immune pathway and has NEVER been proven to exist within vaccinated populations.
Plus, as vaccine inserts clearly state: not all people vaccinated develop an antibody response, which as we now know is not immunity anyway. Therefore the idea of herd immunity through vaccination is pure theory and myth.

Just because it’s contagious doesn’t it mean it’s deadly. In fact, lot of research (studies here) shows a health benefit of these typical childhood illnesses — like reducing cancer risk, lowering risk of heart disease and reducing dementia risk.

The Deadly Impossibility Of Herd Immunity Through Vaccination

By Russell Blaylock MD, neurosurgeon

In the original description of herd immunity, the protection to the population at large occurred only if people contracted the infections naturally. The reason for this is that naturally-acquired immunity lasts for a lifetime. The vaccine proponents quickly latched onto this concept and applied it to vaccine-induced immunity. But, there was one major problem – vaccine-induced immunity lasted for only a relatively short period [if at all] and then this applies only to humoral immunity.

This is why they began to suggest boosters for most vaccines, even the common childhood infections such as chickenpox, measles, mumps, and rubella.

What this means is that at least half the population, have had no vaccine-induced immunity against any of these diseases for which they had been vaccinated very early in life. In essence, at least 50% or more of the population was unprotected for decades.

We have all lived for at least 30 to 40 years with 50% or less of the population having vaccine protection. So even in theory, herd immunity has not existed in this country for many decades and no resurgent epidemics have occurred. Vaccine-induced herd immunity is a lie used to frighten doctors, public-health officials, other medical personnel and the public into accepting vaccinations.”

Click here to read the full article

Do you ever wonder why some children are affected negatively by vaccines while others seem to be fine?

Short answer…

They are not “fine,” their health issue is just lurking in the background and will appear later than others because they are genetically stronger in terms of detox abilities. But because toxins accumulate in the body, if the vaccines or pharma drugs continue, a health issue will arise at some point.

Longer answer…

We are seeing more and more health issues in children than back in the 1980s because dozens more vaccines are being given to children. So the health issues will arise earlier now than they did back then.
So many people born in the 1980s (who had far less vaccines) are just now developing issues like cancer, lupus, chronic fatigue, MS, etc. in their late 30s. It took longer for this age group because they were given less vaccines as children, but it will catch up with nearly everyone at some point.

Studies proving vaccines do not create immunity

These studies indicate that outbreaks do occur in populations that are heavily vaccinated…

Transmission of measles among a highly vaccinated school population–Anchorage, Alaska, 1998.

“During August 10-November 23, 1998, 33 confirmed measles cases were reported to the Anchorage Department of Health and Human Services and the Alaska Department of Health and Social Services (ADHSS). Of these, 26 cases were confirmed by positive rubeola IgM antibody test, and seven met the clinical case definition. This was the largest outbreak of measles in the United States since 1996. This report summarizes results of the epidemiologic investigation conducted by ADHSS and underscores the importance of second-dose requirements for measles vaccine.”
https://www.ncbi.nlm.nih.gov/m/pubmed/9921727/


Risk factors for measles vaccine failure among immunized students.

“An outbreak of measles occurred in a municipal school system which had reported 98% of students immunized against measles.”
https://www.ncbi.nlm.nih.gov/m/pubmed/4047794/


Outbreak of measles among persons with prior evidence of immunity, New York City, 2011.

Report of measles transmission from a twice-vaccinated individual with documented secondary vaccine failure.
https://www.ncbi.nlm.nih.gov/m/pubmed/24585562/


Pertussis epidemic despite high levels of vaccination coverage with acellular pertussis vaccine. 2015 

“Despite high levels of vaccination coverage, pertussis circulation cannot be controlled at all. The results question the efficacy of the present immunization programmes.”
https://www.ncbi.nlm.nih.gov/m/pubmed/24216286/


Challenges in Interpretation of Diagnostic Test Results in a Mumps Outbreak in a Highly Vaccinated Population. 2017 

“This is the first published report of an outbreak of mumps in Ontario in which all confirmed cases had been vaccinated against the disease.”
https://www.ncbi.nlm.nih.gov/m/pubmed/28003216/


Pertussis outbreak in US elementary school with high vaccination coverage.

This investigation demonstrated the potential for pertussis outbreaks to occur in well-vaccinated elementary school populations.
http://www.ncbi.nlm.nih.gov/pubmed/11740314


Major measles epidemic in the region of Quebec despite a 99% vaccine coverage

“Vaccination coverage for the total population was 99.0%. Incomplete vaccination coverage is not a valid explanation for the Quebec City measles outbreak.”
https://www.ncbi.nlm.nih.gov/m/pubmed/1884314/


An outbreak of varicella in elementary school children with two-dose varicella vaccine recipients–Arkansas, 2006.

“Varicella vaccination coverage was 97%.”
https://www.ncbi.nlm.nih.gov/pubmed/19593254


Pertussis epidemic despite high levels of vaccination coverage with acellular pertussis vaccine. 2015 

“Despite high levels of vaccination coverage, pertussis circulation cannot be controlled at all. The results question the efficacy of the present immunization programmes.”
https://www.ncbi.nlm.nih.gov/m/pubmed/24216286/


38% of measles cases that were tested in the 2015 US outbreak were vaccine strain measles. 2015

“During the measles outbreak in California in 2015, a large number of suspected cases occurred in recent vaccinees (3). Of the 194 measles virus sequences obtained in the United States in 2015, 73 were identified as vaccine sequences”.
https://jcm.asm.org/content/55/3/735?fbclid=IwAR3cOmYWV4eUIby6-vMNPnY_ghxxQw372W96th5EzBOHL_eCG-zIoziyERY#sec-2

Studies questioning vaccine-induced immunity

These studies indicate that vaccines don’t always create immunity…

Induction of secretory immunity and memory at mucosal surfaces

There is a considerable disparity with regard to migration of memory/effector cells from mucosal inductive sites to secretory effector sites and systemic immune organs. Also, although immunological memory is generated after mucosal priming, this may be masked by a self-limiting response protecting the inductive lymphoid tissue in the gut. The intranasal route of vaccine application targeting nasopharynx-associated lymphoid tissue may be more advantageous for certain infections, but only if successful stimulation is achieved without the use of toxic adjuvants that might reach the central nervous system.
https://www.ncbi.nlm.nih.gov/m/pubmed/17067945/


The innate immune response differs in primary and secondary Salmonella infection.

These studies provide a coherent view of innate immunity to oral Salmonella infection, reveal novel sources of IFN-gamma, and demonstrate that immune status influences the nature of the innate response.
https://www.ncbi.nlm.nih.gov/m/pubmed/12370380/


Immune Response That Begin Within Cells Lining Our Mucous Membrane Are Fighting Off More Illnesses Than We Know on: ‘An innate antiviral pathway acting before interferons at epithelial surfaces’

Suggests an unfamiliar layer of defense begins its work even before your first immune response becomes active. The newly discovered mechanism protects you with little fanfare or fuss, and occurs within the cells of your mucous membrane — the moist tissues lining your nose, mouth, lungs, and urinary and digestive tracts.
In other words, your immune system begins its fight at the point where viruses normally get in.

https://www.medicaldaily.com/immune-response-begin-within-cells-lining-our-mucous-membrane-are-fighting-more-363992
https://www.nature.com/articles/ni.3319


Normal structure, function, and histology of mucosa-associated lymphoid tissue.

“The mucosa-associated lymphoid tissue (MALT) initiates immune responses to specific antigens encountered along all mucosal surfaces. MALT inductive sites are secondary immune tissues where antigen sampling occurs and immune responses are initiated.”
https://www.ncbi.nlm.nih.gov/m/pubmed/17067945/


Chemokines and the Tissue-Specific Migration of Lymphocytes

Constitutively expressed epithelial chemokines may help determine the character of local immune responses and contribute to the systemic organization of the immune system.
https://www.sciencedirect.com/science/article/pii/S1074761301002618


Variability in Humoral Immunity to Measles Vaccine: New Developments.

Despite the existence of an effective measles vaccine, resurgence in measles cases in the USA and across Europe has occurred, including in individuals vaccinated with two doses of the vaccine. [This study further shows that humeral immunity (antibodies) don’t equal immunity.]
https://www.ncbi.nlm.nih.gov/m/pubmed/26602762/


Failure of inactivated influenza A vaccine to protect healthy children aged 6-24 months.

“Inactivated influenza vaccine did not reduce the attack rate of influenza A infection in 6-24 month old children.”
https://www.ncbi.nlm.nih.gov/m/pubmed/15056235


Haemophilus influenzae Type b Meningitis in the Short Period after Vaccination: A Reminder of the Phenomenon of Apparent Vaccine Failure.

“We present two cases of bacterial meningitis caused by Haemophilus influenzae type b (Hib) which developed a few days after conjugate Hib vaccination. This phenomenon of postimmunization provocative time period is reviewed and discussed. These cases serve as a reminder to clinicians of the risk, albeit rare, of invasive Hib disease in the short period after successful immunization.”
https://www.ncbi.nlm.nih.gov/m/pubmed/22953084/


Severe tetanus in immunized patients with high anti-tetanus titers.

Severe (grade III) tetanus occurred in three immunized patients who had high serum levels of anti-tetanus antibody. The disease was fatal in one patient.
https://www.ncbi.nlm.nih.gov/m/pubmed/1565228/


Specific T cell frequency and cytokine expression profile do not correlate with protection against tuberculosis after bacillus Calmette-Guérin vaccination of newborns.

Critical components of immunity against Mycobacterium tuberculosis, such as CD4 T cell IFN-γ production, may not necessarily translate into immune correlates of protection against TB disease.
https://www.ncbi.nlm.nih.gov/m/pubmed/20558627


Tuberculosis II: the failure of the BCG vaccine.

“Despite the questioning of its innocuousness and efficacy, the BCG vaccine was imposed worldwide in 1950 by medical and political organizations that showed no concern for these questions.”
https://www.ncbi.nlm.nih.gov/m/pubmed/10499822


Specific T cell frequency and cytokine expression profile do not correlate with protection against tuberculosis after bacillus Calmette-Guérin vaccination of newborns.

The frequency and cytokine profile of mycobacteria-specific T cells did not correlate with protection against TB. Critical components of immunity against Mycobacterium tuberculosis, such as CD4 T cell IFN-γ production, may not necessarily translate into immune correlates of protection against TB disease.
https://www.ncbi.nlm.nih.gov/m/pubmed/20558627


Tuberculosis II: the failure of the BCG vaccine.

“Despite the questioning of its innocuousness and efficacy, the BCG vaccine was imposed worldwide in 1950 by medical and political organizations that showed no concern for these questions.”
https://www.ncbi.nlm.nih.gov/m/pubmed/10499822T


Severe tetanus in immunized patients with high anti-tetanus titers.

Three people vaccinated with the tetanus vaccine had extremely high antibody responses (“immunity” according to vaccine research) but didn’t become immune to tetanus. Two became severely ill and one died.
http://www.ncbi.nlm.nih.gov/pubmed/1565228?dopt=Abstract

Every single one of us that has been vaccinated needs to detox

Did you know childhood illnesses can reduce health issues later in life?

NOPE, because vaccines just do NOT work!

Vaccines do not create immunity, which requires natural exposure through the proper immune pathway (and that is not the arm). You have to actually get the disease and fight it off to create real immunity. Only catching the real natural-strain illness through the proper immune pathways (eyes, ears, mouth, nose) will trigger the complex immune process. And then sometimes additional exposures are necessary — again through the proper pathway and to the natural strain.

Vaccines do NOT have to prove any level of immunity to be approved for market. Again: NO VACCINE HAS EVER BEEN PROVEN TO GIVE IMMUNITY — EVER! The facts are there, right in the vaccine product inserts.

Vaccines raise anti-bodies, but mostly to the toxic additives, they have never been proven to give you immunity, ever!

That’s why there are known toxins in them — to stimulate minimal antibodies because the body does not create an immune response to live or dead viruses injected into the arm or leg. This bypasses the majority of the immune system therefore not creating real immunity.

The best vaccine possible is your body’s own immune system — without added toxins and chemicals.

By Brandy Vaughan, ex-pharmaceutical rep turned natural health advocate & founder of Learn The Risk

Why? 

Because almost all diseases and disorders stem from inflammation in the body from toxic exposures (synthetic chemicals, radiation, etc). Our bodies can only process and filter a certain amount of toxins before a health issue will develop — what health issue develops is determined by genetics and how much toxicity we can handle is also determined by genetics.

We all have weak links that are specific to our genes, but genetics CANNOT cause a disease in a once-healthy person. We are not just born healthy and then our genes just somehow turn on us — there has to be a toxic trigger.

Vaccines are often that trigger because of the high level of toxins injected into the body at one time. Why is that a very bad idea? The main reason being that the body cannot handle the huge load and goes into an autoimmune state — meaning it will react to everything in the needle and cause inflammation both directly after the injection, but also upon other exposures.

For example, there are dairy components in vaccines (casein, bovine serum, etc) and when children are further exposed, some will have an allergic inflammatory response (labeled as dairy allergies). But not all children are genetic weak in that area, so for some it will be a reaction to other things in the vaccine or a different health issue will develop.

The toxins in the vaccine, particularly heavy metals like mercury, barium and aluminum, usually head straight to the brain causing neurological damage like autism, speech delays, Alzheimers, etc. Although once in the brain, they travel down the lymphatic system to the gut. And sometimes they end up elsewhere as well. For example, aluminium has been found in muscle tissues causing myopathy and in arthritic joints and in bones causing osteoporosis.

Vaccines are not the only toxic exposure that causes health damage. There are other factors of course, like polluted water, pesticides, radiation, etc. But vaccines are by far the MOST POTENT exposure because anything injected is far more damaging than anything ingested (eaten, drunk or inhaled).

Why? Because injections bypass our bodies’ natural filter process (meaning we cannot filter the toxins out) and therefore toxins go straight into the blood stream (after the muscle tissue) and then to vital organs. On their way through the body, they cause an autoimmune inflammatory reaction that can lead to autoimmune disorders. Hence the skyrocketing autoimmune disorders seen now (lupus, MS, asthma, allergies, type-1 diabetes, arthritis, CFS, gut issues like IBS/IBD).

Hope this helps people see why vaccines cause so much damage, but why the damage is different for every person.

Childhood Illnesses & Disease

Natural viruses protect from disease later in life: And we now know many of these illnesses protect against cancers later in life.

Sometimes the most powerful remedies happen unknowingly. Thankfully now in the 21st century, we understand that certain vitamins and nutrition really play the biggest role in illness protection and symptom minimization, like vitamin A for the measles, and vitamin C and D overall. Illness can seem scary sometimes, but are there benefits if it does happen?

Humanity lives synergistically with pathogens (Bacteria and Viruses). They actually have a purpose.

MEASLES:

Febrile infectious childhood diseases in the history of cancer patients and matched controls. Medical Hypotheses, 1998

Albonico found that adults are significantly protected against non-breast cancers — genital, prostate, gastrointestinal, skin, lung, ear-nose-throat, and others — if they contracted measles (odds ratio, OR = 0.45), rubella (OR = 0.38) or chickenpox (OR = 0.62) earlier in life. [Med Hypotheses 1998; 51(4): 315-20].

Do childhood diseases affect NHL and HL risk? A case-control study from northern and southern Italy.  Leukaemia Research, 2006

Infections by most common childhood pathogens may protect against HL (Hodgkin lymphoma) or, at least, be correlated with some other early exposure, which may lower the risk of HL in adulthood.

Risk factors for Hodgkin’s disease by Epstein-Barr virus (EBV) status: prior infection by EBV and other agents. British Journal of Cancer, 2011

Alexander found that infection with measles during childhood is significantly protective — it cuts the risk in half — against developing Hodgkin’s disease (OR = 0.53) [Br J Cancer 2000; 82(5): 1117-21].

Measles to the Rescue: A Review of Oncolytic Measles Virus. Viruses, 2016

MV Clinical trials are producing encouraging preliminary results in ovarian cancer, myeloma and cutaneous non-Hodgkin lymphoma, and the outcome of currently open trials in glioblastoma multiforme, mesothelioma and squamous cell carcinoma are eagerly anticipated.

Exposure to childhood infections and risk of Epstein-Barr virus–defined Hodgkin’s lymphoma in women. International Journal of Cancer, 2005

Glaser also found that lymph cancer is significantly more likely in adults who were not infected with measles, mumps or rubella in childhood.

Measles virus for cancer therapy. Current Topics in Microbiology Immunology, 2009

Our bodies are amazing. Even getting an illness is part of our bodies journey to transformation and total health. Dr. Stephanie Seneff (Senior Research Scientist MIT) made this fairly new discovery in regard to the flu virus.

She says we live in a symbiotic relationship with all the other species, even the pathogens. The Flu virus goes into the muscles cells and reprograms them to hand over their sulfate. The flu virus delivers the sulfate to your blood. The sulfate cleans your blood by killing off the weak cells allowing growth for new cells. In effect, the flu virus is rescuing your blood from a future meltdown (more serious illnesses, perhaps cancer).

The potential meltdown was there before getting the flu. It’s much like an overcrowded forest that catches fire to thin and clear out the debris and weak trees. It’s a natural process. Depending on what we eat, if we exercise, and if we take supplements to fortify our forest (blood) keeping only the strongest trees (cells) to begin with. Getting sick with the flu isn’t bad, it’s actually good for your body. You are cleaning house.

MUMPS:

Researchers investigated whether mumps might engender immunity to ovarian cancer through antibodies against the cancer-associated antigen MUC1 abnormally expressed in the inflamed parotid gland.

Mumps and ovarian cancer: modern interpretation of an historic association. Cancer Causes Control, 2010

INFLUENZA: 

Influenza virus infection elicits protective antibodies and T cells specific for host cell antigens also expressed as tumor associated antigens: a new view of cancer immunosurveillance. Cancer Immunology Research, 2014

Influenza-experienced mice control challenge lung tumour better than infection-naive control mice.

CHICKEN POX:

Review of the United States universal varicella vaccination program: Herpes zoster incidence rates, cost-effectiveness, and vaccine efficacy based primarily on the Antelope Valley Varicella Active Surveillance Project dataVaccine, 2013

In 2000, varicella incidence dramatically declined to 70% of the prevaccine rate. Herpes Zoster (HZ) reports significantly increased among adults aged 20–69 years from 2000 to 2001. Children with a prior history of varicella demonstrated HZ rates similar to adults. By 2002, the efficacy of the varicella vaccination had declined well below 80%. HZ morbidity costs have exceeded the cost savings from varicella-disease reductions.

Chickenpox in childhood is associated with decreased atopic disorders, IgE, allergic sensitization, and leukocyte subsets. Pediatric Allergy Immunology 2012

Silverberg et al. also reported that wild-type VZV infection up to 8 years of age was found to be protective against atopic disorders that are thought to be “mediated by suppression of IgE production and allergic sensitization, as well as altered leukocyte distributions. Chicken Pox references taken from Goldman, King STUDY

COMMON INFECTIONS:

Day care in infancy and risk of childhood acute lymphoblastic leukaemia: findings from UK case-control study. Biomedical Journal, 2005

Gilham found that infants with the least exposure to common infections have the greatest risk of developing childhood leukemia.

Early life exposure to infections and risk of childhood acute lymphoblastic leukemia. Epidemiology, 2010

Urayama et al also found that early exposure to infections is protective against leukemia.

Why Is China Having Measles Outbreaks When 99% Are Vaccinated?

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Outbreak of Measles Among Persons With Prior Evidence of Immunity

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Persistent Outbreak of Measles Despite Prevention and Control Measures

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