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Now that vaccines are a common topic of conversation is important to learn more about them. In this blog, I’ll explore different issues related to vaccines, such as vaccine definition and ingredients, vaccine development, adverse events, as well the children’s vaccine schedule, and pharmaceutical companies’ liability.

What is a Vaccine?

Pre-2020, a vaccine was defined as a product or inoculant that “stimulates a person’s immune system to produce immunity to a specific disease.” However, after the introduction of COVID-19 shots, the definition was changed to “a preparation that is used to stimulate the body’s immune response against diseases.”

According to pre-2020 CDC documents, vaccines provide protection from infectious diseases as indicated by the presence of antibodies. Vaccines aim to provide immunity, which is produced by a person’s own immune system and lasts for many years – often a lifetime. It was also a well know fact that infection from disease, as well as from vaccination, provide active immunity.

Vaccine Ingredients

We have been told for decades that vaccines are “safe and effective”. Unfortunately, vaccines – just like many other pharmaceuticals – have side effects due to the ingredients they contain. A vaccine not only has the virus it aims to prevent, but it also has more additives – many of which can’t be categorized as health products.

  • Vaccines are made with antigens – the virus that causes the disease it’s trying to prevent
  • Cell culture (growth material like eggs, animal cells, fetal cells from aborted babies)
  • Antibiotics (like neomycin)
  • Stabilizers (like sugar or gelatin)
  • Toxic ingredients [adjuvants (substances that stimulate the immune system – like aluminum), preservatives (like thimerosal – mercury), and inactivating ingredients (like formaldehyde and FD&C Yellow #6)] 

Vaccine Development

The typical vaccine development process takes between 8 to 15 years and involves research, discovery, and testing. Vaccine manufacturers must go through several phases of clinical trials, including animal trials and human trials.

  • The preclinical evaluation phase, in-vitro studies dealing with microbial communities and in-vivo studies dealing with animals, take place to search for therapeutic effects as well as toxic effects of the pharmaceutical product. Generally, preclinical results can predict results in humans, which is why animal testing prior to human testing is necessary. This avoids injuring people unnecessarily during human trials.
  • Clinical trials phase 1 consists of evaluating the product/vaccine in a few healthy individuals to determine dosages.
  • Phase 2 tests the method of drug delivery, dosages, and safety in a larger number of volunteers, using a control group.
  • Phase 3 evaluates the efficacy, safety, and immune response in large groups, assigning participants randomly to a treatment or control group in a blinded manner (to prevent biased comparisons).
  • Phase 4 delves into longer-term safety. 

When adverse events arise, they need to be explored and followed to determine if the rate of the event in the treatment group is greater than that of the control group.  Yet, these numbers may not adequately reflect the “adverse event profile” of the pharmaceutical product. We don’t know if these numbers are truly generalizable to the real world since participants may be a healthier population, they receive the product for a shorter period, and they may not have drug interactions to take into consideration.

Children’s Vaccine Schedule

The children’s vaccine schedule has radically changed over the past 40 years:

  • In 1962, the maximum number of vaccines a child received by age five was 3
  • In 1980, children received 3 vaccines for seven illnesses and two combination vaccines (diphtheria, tetanus, pertussis, measles, mumps, rubella, and a polio vaccine) totaling 24 doses by age 18. 
  • After Fauci became the head of NIAID (1984), many more vaccines and doses have been added to the schedule. Currently, states mandate 69 vaccines for 16 diseases that children have to take by age 18 in order to attend school [Measles, Mumps, Rubella, Chickenpox, Diphtheria, Tetanus, Pertussis, Tetanus-Diphtheria-Pertussis (Tdap), Meningococcal Conjugate, Haemophilus Influenzae Type B (Hib), Rotavirus, HPV, Shingles, Pneumococcal Conjugate, hepatitis A, hepatitis B].

As you can see the children’s vaccine schedule, has dramatically changed since the mid-1980s. The mandatory number of vaccines and doses has increased while Americans’ state of health has declined. Now we have higher rates of autism, asthma, respiratory allergies, food allergies, skin allergies, diabetes, and autoimmune diseases.

It’s concerning that some of the vaccines on the recommended routine immunization schedule are not a matter of necessity for children. However, all of them still pose risks. Common sense would say that there is no reason to inject children with Hep A or B, HPV, Shingles, Influenza, Rotavirus, or Pneumococcal Conjugate – unless they have a specific risk.

For instance, the Hepatitis A virus is acquired from a sex partner who has hepatitis A, by putting something in the mouth that has been contaminated with the stool of a person with hepatitis A, or by consuming food or drinks that have been handled by an infected person. And Hepatitis B virus is spread by sexual contact, sharing needles /syringes /other drug injection equipment, or from mother to child at birth.

Why are newborns and children forced to get the hepatitis A and B vaccines since they are not intravenous drug users, prostitutes, or have multiple sex partners? There are no valid reasons to inject children with these vaccines, unless they have been sexually abused by an infected person, eat or drink sewage-contaminated food and water, or are born from an infected mother.

Vaccine Adverse Events

Children’s immunization schedule that we have now is totally different than the schedule that children had in the 1960s or early 1980s. The tremendous amount of mandated vaccines and dosages have brought along an extensive list of adverse events.

Some of the severe conditions seen as a result of several vaccines are:

  • Acute Disseminated Encephalomyelitis
  • Anaphylaxis
  • Arthropathy (Arthralgia and Arthritis)
  • Autism
  • Bell’s Palsy
  • Brachial Neuritis
  • Chronic Inflammatory Disseminated Polyneuropathy
  • Diabetes – Type 1
  • Encephalitis
  • Encephalopathy
  • Fibromyalgia
  • Guillain-Barré Syndrome
  • Multiple Sclerosis
  • Seizures
  • Transverse Myelitis

This is a list of adverse events connected to each vaccine.

Health Conditions Pre-1980 & Now

Americans’ state of health has been declining over the past decades. Children are now sicker and heavier than ever too. In order to see the decline over the years, we should look at some national statistics pre-1980s in comparison to now.

  • In the early 1980s3% of the population had ASTHMA
    • In 20202% of children ages 0-4, 6% of children ages 5-11, 9% of children ages 11-21, 10.3% of people between 20–24 years of age, and 8.2% of people between 25–64 years of age had asthma.
  • In the early 1980s, FOOD ALLERGIES were rarely mentioned in the medical literature. 
    • In 2007, reported food allergies were 18% higher than in 1997 among children. 
    • Now32 million adults and 1 in 13 children have food allergies.
    • In 20187.2% reported hay fever, 10% reported respiratory allergies, and 13% reported skin allergies.
  • In 198011.8% of Americans had a CHRONIC DISEASE
    • Now, it is estimated that nearly 50% of the population suffers from at least one chronic illness. The cases of autism, food allergies, ADHD, sleep disorders, juvenile diabetes, rheumatoid arthritis, and other chronic and infectious diseases have skyrocketed.    
    • Also, currently almost 70% of Americans take at least one prescription medication.
  • Prior to 1984, AUTOIMMUNE DISEASES (juvenile diabetes, rheumatoid arthritis, Grave’s Disease, Crohn’s disease) were practically unknown.
    • By 2017,  7% of the population suffered from autoimmune diseases.
  • In 19852.5% of Americans had DIABETES
    • In 202111.3% of Americans were diagnosed with diabetes and 23% reported presenting all the symptoms.
  • There is not much info about ADHD pre-1997. In 19976% of children were diagnosed with ADHD.
    • In 201611% had ADHD.
  • In the 1970s, 3 out of 10,000 children had AUTISM
    • Now1 in 34 children has autism.

COVID-19 “Vaccines”

We couldn’t talk about vaccines without exploring COVID-19 “vaccines.” First, you must know that these shots are not vaccines per se. As you learned, in a typical vaccine, an inactive virus or protein is administered to stimulate a person’s immune system, which produces immunity to a specific disease. Therefore, protecting that person from that disease. Additionally, the product in the vaccine does not leave the immediate site of vaccination, typically the shoulder muscle. These processes are not taking place with COVID-19 shots.

On the other hand, mRNA “vaccines” are gene modification therapy products. They trick the body [with mRNA (Pfizer, Moderna) or adenoviral DNA (J&J, AstraZeneca)] into making SARS-CoV-2 proteins in an uncontrolled manner, provoking an antibody reaction.

SARS-Cov-2 spike proteins are the ones developed at the Wuhan Institute of Virology, not previously found in nature. These spike proteins attach to the ACE-2 receptors in the heart, brain, intestines, and many organs, but especially the reproductive organs. These shots also contain polyethylene glycols (PEGs) – used to stabilize the lipid nanoparticles. PEGs are toxic for most people and can cause life-threatening reactions like anaphylaxis.

These “vaccines” leave the site of vaccination. The proteins enter the bloodstream, circulate throughout the body, and accumulate in a number of tissues and organs. They cross the blood-brain barrier, being able to affect the neurological and cardiovascular systems, and the brain. They can, also, be transferred to infants through breast milk.

Another alarming point is that these shots were developed in a few months, instead of 8-15 years. The preclinical evaluation phase – animal trials – was skipped, and phase 1 started a few months after the CDC declared SARS-CoV-2 a pandemic. On December 18, 2020, these mRNA shots were authorized by the FDA for emergency use. Learn more about COVID-19 “vaccine” safety and effectiveness.

Pharmaceutical Immunity

Generally, companies are liable for produced products. When companies bring a product to market that injures or kills people, these businesses are liable for that product. However, pharmaceutical companies are immune from liability. These for-profit companies have virtually zero liability status in relation to vaccines.

Since the 1980s, vaccine manufacturers have been protected from liability under the National Childhood Vaccine Injury Act of 1986. This program took place due to the fact that vaccine manufacturers were losing millions of dollars because they were being sued regularly, and rightfully so when vaccinated children got severe adverse reactions. Now under the program’s protection, they are not liable for deaths or injuries anymore.

Additionally, the government passed the Public Readiness and Emergency Preparedness Act (PREP Act) in 2005. The PREP Act further protects these companies from financial risk and shields them from liability when they launch a product, under a public health emergency, that causes injuries.

The only option for compensating injured people is the Countermeasures Injury Compensation Program (CICP). These are benefits that people can claim if they experience a serious injury from a covered countermeasure (vaccination, medication or device recommended to treat a pandemic, epidemic, or security threat). The CICP is a poor solution since it doesn’t cover legal or medical expert fees, lost wages are capped at $50,000, and victims are not awarded compensation due to pain and suffering. Plus, there is no judicial appeal if the claim is found invalidated – Only 8% of petitioners have been awarded compensation since 2010. 

Points to Consider

  • Is it coincidental that the rate of allergies increases as children are growing and declines at age 24 (when people don’t have to take any more allergen-containing vaccines)? 
  • Is there a correlation between autism (a neurological disorder) and vaccines that have neurotoxic ingredients (mercury and aluminum) that affect the neurological system?
  • Is the decline in Americans’ health related to the changes that national institutes have implemented with their overzealous push for more vaccines and doses?
  • Isn’t it critical to address adverse events to keep our population safe and to avoid forcing vaccines in which the harm-to-benefit ratio is too risky?
  • Since pharmaceutical companies don’t guarantee their products, can you trust them? Would you buy a car from a company that produces cars that are defective and that have caused severe injury or death to some consumers? Would you buy a car from a manufacturer that doesn’t give you a warranty and doesn’t take responsibility for their cars and that can put your health and the health of your loved ones in danger?

By analyzing the specific segments of the population that are at risk, as well as the treatment and prognosis for the virus that each vaccine addresses, one may conclude that public health is not what’s driving the continuously growing immunization schedule. Much more when the current system enriches pharmaceutical companies while neglecting those who suffer adverse events.

Since pharmaceutical companies contribute financially to legislators, health bureaucrats, medical boards, medical schools, and physicians, legislation protects big pharma. In turn, these companies have no incentive for concentrating on safety testing or avoid pushing for more vaccines and dosages. These financial entanglements pose numerous conflicts of interest that endanger the health and lives of millions of children and adults.

Now that you have more in-depth information about vaccines, ingredients, adverse events, vaccine development, immunization schedule, and the liability of pharmaceutical companies, you should consider doing your own research before blindly submitting to doctors’ recommendations.

To a Fitter Healthier You,

Adriana Albritton

The Fitness Wellness Mentor

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