VACCINATION DEBATE SOLUTION

PROBLEM

Parents are not vaccinating their children for fear of autism

The goal presented here is not to contribute to the vaccine debate, but to end it, by giving parents DNA facts relative to their newborn’s tolerance to vaccine ingredients -- not endless studies and clinical trials on other people’s children and mice. 

Everyone can win. It's clear vaccines are safe for some people. Yet the DNA fact is some of us can metabolize adjuvant toxins and heavy metals out of our bodies and some of us cannot. Only an individual test will tell.  

THIS IS NOW A HUMAN RIGHTS ISSUE

• Studies analyzing other infants is useless to determine individual risk.
• Specific to the vaccine debate about thiomersal and heavy metal adjuvants in vaccines, some of us can metabolize these heavy metals, adjuvants, and excipients out of our bodies. Some of us who are immunocompromised cannot.  
• With the technology available now for decades, and a high-demand for answers, this is a human rights issue. 

NO MORE ROLLING THE DICE 

Given the timing now to harness both genetics technology and the RFJ Jr. Bobby Buzz around the vaccine debate that is self-generating a high-demand for answers, this is an ideal opportunity to deliver a solution to parents, our children, to our front-line doctors, and to the Administration, who are on a MAHA mission to prevent vaccine injury that lasts a lifetime. 

THE HEART OF THE MATTER

Vaccines are emotional for parents on both sides of the debate in defense of their personal choice for their child. 

• It's emotional because potential adverse outcomes are beyond a parent’s control to prevent unknown risk for their child. 

• It's emotional because there are no definitive answers from our doctors, the FDA, and the CDC to avoid individual risk. 

Constant pharmaceutical ads on TV all say, "Do not take this drug if you are allergic to it." OK, but how do we know if we are allergic?  

• Let's replace fear with facts. 

SOLUTION

VAST - VACCINE ADJUVANT SENSITIVITY TEST for Newborns 

To empower parents to choose, VAST is a painless buccal screening test at birth (swab on the inside of the cheek) to determine an infant’s genetic response to vaccines with a 60 second diagnosis before any vaccine is administered.

A SIMPLE ANSWER

VAST provides parents with a simple answer: 

    YES to receive a preservative-free VAST Dx vaccine 

    OK  to receive a standard vaccine

    NO vaccine recommended until immune system matures

Parents will finally have real-time data to 

CHOOSE VACCINATION WITH FACTS NOT FEAR

DNA does not lie. Genetic results for the baby out-of-the womb is critical to determine if detoxification DNA is functioning before any environmental insults are administered to the newborn, such as vaccine excipients and ingredients. If the newborn is genetically unable to detox these toxic environmental insults before the immune system has matured, these chemicals and toxins WILL change DNA for a lifetime. 

Infant Immunocompetence is Important to the Vaccine Provider to Know

"Determination of altered immunocompetence [for every infant born] is important to the CDC and vaccine providers to identify vaccines that are safe for infants with compromised immune systems."

https://www.cdc.gov/vaccines/hcp/imz-best-practices/altered-immunocompetence.html

The vaccine schedule includes 50 immunizations from birth  to 18 years old. VAST at birth covers each inoculation for a lifetime. 

• VAST eliminates emotional fear of risk with individual DNA facts. 
• VAST gives parents a personalized answer for their newborn to choose a standard vaccine or a preservative-free vaccine. 
• In some cases, no vaccine is recommended until the immune system matures.  
• Standard vaccines are manufactured in multi-dose vials with preservatives to prevent contamination using the same vial on multiple people. 

HEAVY METALS

Some autism concerns are focused on heavy metal adjuvants like alum and preservatives like thiomersal / thimerosal that contains mercury. Aluminum salt is an adjuvant added to vaccines to artificially trigger the immune system to react to the injected virus thus creating antibodies to the virus. 

Yet wouldn't the newborn immune system automatically react to a virus without the artificial thimerosal or aluminum triggers?  Yes, the immune system can naturally react to a virus in a vaccine without thiomersal or aluminum salts triggers. 

VAST IS DESIGNED TO PREVENT IMMUNOTOXICITY

IMMUNOTOXICITY refers to the adverse effects that foreign substances, like chemicals or drugs, can have on the immune system that encompasses a range of potential outcomes, including suppression of the immune system (immunosuppression) or overstimulation (immunostimulation). These effects can lead to increased susceptibility to infections, allergies, autoimmune diseases, or other immune-related disorders. 

HOW TO PREVENT IMMUNOTOXICITY

VAST analyzes your infant's methylation status, detoxification, and heavy metals genes functionality to determine genetic response to vaccine adjuvants and excipient ingredients. We ALL require healthy metabolism of these toxins before any vaccination or drug. This is not only about the heavy metal preservative thiomersal. There are many other ingredients in both preservative-free and standard vaccines that can trigger immunotoxicity. 

For SOME newborns, NO vaccine is recommended until the immune system matures after 3 years old. 

Challenges for the Newborn Immune Response to Respiratory Virus Infection and Vaccination

The increased susceptibility to severe disease in newborns following respiratory virus infection is a result of their naïve immune status together with the altered responsiveness of the immune system. The altered response in newborns is in part due to the need to create a permissive environment for establishment of the microbiome. Colonization by the array of microbes that make up the microbiome is an important regulator of immune system development [3]. The inherent bias of the neonatal immune system towards an anti-inflammatory T cell response allows for colonization of the microbiome without generating potent pro-inflammatory signals that can lead to pathogenic, tissue-damaging responses [3]. Although the newborn benefits from an immune state that allows establishment of the microbiome, the trade-off is an immune system that often contributes to increased susceptibility to severe disease following viral infection. Continue reading via link above...

FDA

The food industry manufactures preservative--free food because the market (we the people) demand it. And yes, the FDA APPROVES single dose preservative-free vaccines, and are available RIGHT NOW! BUT ONLY IF YOU ASK FOR IT. 

If you are not sure, a VAST test at birth, will confirm your choice. The VAST goal is to prevent induced immunotoxicity from all vaccine ingredients and excipients. 

Vaccines are medications. They are biological products designed to stimulate the immune system to recognize and fight off specific diseases. They are typically made from weakened or inactivated forms of viruses, bacteria, or other disease-causing agents. As a practical matter for the MAHA healthcare system, it simply makes sense to test first if a newborn with non-functioning detoxification genes (or a human of any age) to be screened for immunotoxicty risk. 

Saliva genetic tests, like VAST, are FDA cleared for use. The FDA has also authorized direct-to-consumer genetic tests that analyze DNA from saliva samples for various purposes, including detecting genetic variants related to medication metabolism (PGx--Pharmacogentics Test ) as well as assessing the risk of certain cancers. Saliva collection devices used in genetic testing have also been FDA cleared. 

YOUR GENES CHOOSE 

The method to gather these facts is validating methylation status and genetic biomarkers of 22 genes and 82 variations. Just ONE compromised variant is enough to say NO to standard vaccines. 

Metallothionein (MT) genes encode a family of cysteine-rich proteins that play crucial roles in metal homeostasis and protection against heavy metal toxicity, DNA damage, and defense against oxidative stress. In humans, there are four main MT isoforms (MT1, MT2, MT3, and MT4), with MT1 having multiple subtypes (MT1A, MT1B, MT1E, MT1F, MT1G, MT1H, MT1M, and MT1X). These genes are located on chromosome 16. Human CPOX is a mitochondrial enzyme that effects susceptibility to mercury toxicity in children and adults. 

Based on individual genetics, some humans excrete heavy metals efficiently from the body, and some do not. Only an individual screening test will tell who’s who, so parents are empowered with facts to choose standard vaccines or single-dose preservative-free vaccines for their child.  

According to FDA.gov:

“All vaccines routinely recommended for children 6 years of age and younger are available in formulations that do not contain the preservative thimerosal”.  And “vaccines that do not contain thimerosal are also available for adolescents and adults”.   

See Key Points stated on this Vaccine Safety FDA.gov page: https://www.fda.gov/BiologicsBloodVaccines/SafetyAvailability/VaccineSafety/UCM096228  

FACTS NOT FORCE

• VAST eliminates fear of vaccines with DNA facts. 
• VAST gives parents a way to eliminate emotional guesswork to choose what is best for their children's health. 
• VAST will naturally increase vaccine use (sales) with facts not force.
• VAST is a method to develop vaccine drugs (and all drugs) based on genotype.
• VAST is an opportunity to manufacture vaccine drugs that work (100%) of the time on 100% of the people.
• What parent would not want the empowering VAST report for their newborn, regardless of their side of the debate.        

INFANT ANTIBIOTIC USE = CHRONIC DISEAE

PROBLEM

64% of newborns are treated with antibiotics out-of-the-womb.

Antibiotics were invented to treat life or death infections. NOT to dole out like candy for a sniffle, and especially not designed for newborns out of the womb. 

The problem is antibiotics kill everything in the gut microbiome, and the first 1000 days after birth represent a critical window for gut microbiome development, which is essential for immune system maturation and overall health.

The neurotransmitters produced by the gut microbiome are dysregulated by antibiotics, setting the stage for long-term excessive inflammation, tissue damage, infections, allergies, asthma, obesity, type 1 diabetes, and other chronic diseases. 

Neurotransmitters:

• Serotonin: Regulates sleep, mood, cognition, learning, memory, and physiological processes such as vomiting (bulimia, binge-eating) and vasoconstriction (higher blood pressure).
• Dopamine: Plays a role in reward, motivation, and movement
• GABA: An inhibitory neurotransmitter that reduces anxiety and stress
• Glutamate: An excitatory neurotransmitter involved in learning and memory
• Norepinephrine: Influences mood, attention, and arousal
• Histamine: Regulates inflammation and gut motility 

In 2024, among 3,622,673 births in the United States, approximately 2,318,510 newborns (64%) were treated with antibiotics. 

64% OF OUR POPULATION ARE AT RISK FOR CHRONIC DISEASE 

Reasons for newborn antibiotics use: 

• Antibiotics are used during and after labor, particularly for 32.4% newborns delivered by cesarean section in the US.
• Antibiotics are used to treat neonatal pneumonia in 1 of 200 live births.
• Antibiotics may also be used prophylactically to prevent infections in infants at high risk, like preemies. In the United States, approximately 1 out of every 10 babies (10%) or roughly 360,000, are born prematurely each year and receive antibiotics.
• During vaginal delivery, 10--20% of newborns come into contact with a mother's fecal matter when meconium, the first stool of a baby, is passed into the amniotic fluid before or during labor and are treated prophylactically with antibiotics.
• 6% of deliveries are born to mothers with infections.
• Common antibiotics used in newborns include amoxicillin, gentamicin, and ceftriaxone.

IS IT LIFE OR DEATH? 

1. Amoxicillin use in newborns causes microbiome disruption and poor immune system development leading to lifetime risk of excessive inflammation, tissue damage, infections, allergies, asthma, obesity, type 1 diabetes, and other chronic diseases. 

Amoxicillin and DNA Damage

Direct DNA Damage to Bacteria:

• While primarily known for inhibiting cell wall synthesis, amoxicillin can induce DNA lesions in bacterial cells. 
• This damage is a result of amoxicillin’s interaction with the bacterial cell, leading to reactive oxygen species (ROS) excessive production and subsequent DNA damage. ROS plays crucial roles in cellular signaling and various physiological processes. 
• ROS can be beneficial at a moderate level.  ROS At excessive levels it can cause diabetes, cancer, and neurodegenerative diseases.

2. Gentamicin carries a risk of kidney dysfunction and hearing loss for babies with a genetic variant in the MT-RNR1 gene. This risk is 1 in 500 people due to the antibiotic's ability to bind to the hair cells in the inner ear, causing damage.

3. Ceftriaxone is neonatal treatment for sepsis and meningitis. It is contraindicated in neonates primarily due to its potential to displace bilirubin from albumin binding sites, leading to increased free bilirubin in the blood. If bilirubin is not bound to albumin, it can cross the blood-brain barrier and cause brain damage (bilirubin encephalopathy) in newborns. This can exacerbate jaundice, a common condition in neonates, and increase the risk of kernicterus, a complication of severe jaundice and a serious brain damage condition caused by high bilirubin levels. Sixty percent of infants experience yellowing of their skin and eyes during the first few weeks of life. Severe complications are rare, but can be life-threatening. Premature infants have lower albumin levels and a higher risk of bilirubin-induced neurotoxicity, so they are particularly vulnerable to the effects of bilirubin displacement. 

THE BIRRTH OF CHRONIC DIEASE

Antibiotics is 1 of 3 underlying causes for the extreme rise in mental health dysfunction and chronic disease in the United States. 

Antibiotics Bleed The Spectrum

Because antibiotic administration often occurs alongside vaccination, it's like a chemical bomb blows up inside the baby, with no guided target for which neurotransmitters the antibiotic destroys, hence the accurate term, 'spectrum disorder.' The various outcomes all manifest from chemical assaults on the human body, however in different degrees. 

Autism spectrum disorders are neurological conditions related to brain development. The spectrum includes Asperger's or Level 1 autism, on the high-functioning end of the autism spectrum, often retaining intelligence throughout life. Low-Functioning autism or Level 3 autism has significant impairments in multiple areas of development and functioning, sometimes for a lifetime. The spectrum also includes limited and repeated patterns of behavior, such as OCD, an anxiety disorder. 

ADD / ADHD (Attention-Deficit/Hyperactivity Disorder)

Today, ADHD (Attention-Deficit/Hyperactivity Disorder) is not considered a form of autism spectrum disorder (ASD) yet also has a spectrum of types. ADD and ADHD are caused by dysfunctional neurotransmitters, particularly dopamine and norepinephrine, that can present with overlapping symptoms.

Dr. Daniel Amen, a psychiatrist and brain imaging specialist, has identified seven distinct types of ADHD/ADD. These types are based on differences in brain function and how they affect attention, impulsivity, and hyperactivity. Each type has specific symptoms and treatment approaches. 

It's common for individuals to have both ADHD and genetic Autism Spectrum Disorders. Yet antibiotics, specifically amoxicillin, disrupt DNA and can silence genes, making them non-functional. 

Gut Bacteria and Neurotransmitters

https://pubmed.ncbi.nlm.nih.gov/36144440/

Dicks LMT. Gut Bacteria and Neurotransmitters. Microorganisms. 2022 Sep 14;10(9):1838. doi: 10.3390/microorganisms10091838. PMID: 36144440; PMCID: PMC9504309.

Gut bacteria play an important role in the digestion of food, immune activation, and regulation of entero-endocrine signaling pathways, and also communicate with the central nervous system (CNS) through the production of specific metabolic compounds, e.g., bile acids, short-chain fatty acids (SCFAs), glutamate (Glu), γ-aminobutyric acid (GABA), dopamine (DA), norepinephrine (NE), serotonin (5-HT) and histamine.  Afferent vagus nerve (VN) fibers that transport signals from the gastro-intestinal tract (GIT) and gut microbiota to the brain are also linked to receptors in the esophagus, liver, and pancreas. In response to these stimuli, the brain sends signals back to entero-epithelial cells via efferent VN fibers. Fibers of the VN are not in direct contact with the gut wall or intestinal microbiota. Instead, signals reach the gut microbiota via 100 to 500 million neurons from the enteric nervous system (ENS) in the submucosa and myenteric plexus of the gut wall. The modulation, development, and renewal of ENS neurons are controlled by gut microbiota, especially those with the ability to produce and metabolize hormones. Signals generated by the hypothalamus reach the pituitary and adrenal glands and communicate with entero-epithelial cells via the hypothalamic pituitary adrenal axis (HPA). SCFAs produced by gut bacteria adhere to free fatty acid receptors (FFARs) on the surface of intestinal epithelial cells (IECs) and interact with neurons or enter the circulatory system. Gut bacteria alter the synthesis and degradation of neurotransmitters. This review focuses on the effect that gut bacteria have on the production of neurotransmitters and vice versa.

It's common for individuals to have both ADHD and ASD, caused by vaccines and antibiotics administered at the same time.

NEWBORN SOLUTION TO REPLACE ANTIBIOTICS

COLOSTRUM -- LIQUID GOLD

Antibiotics also negatively impact the beneficial effects of colostrum in mothers milk released by the mammary glands for 2 to10 days after giving birth. With or without mom’s colostrum, such as infants on formula, antibiotics disrupt the infant's gut microbiome functionality, setting the stage for lifelong chronic disease.

The cure for a newborn infection is mom's colostrum for the first days after birth, not antibiotics. Why? Antibiotics kill everything in the newborn gut microbiome, making neurotransmitter production and regulation dysfunctional, creating the onset of neurotransmitters development disorders on day one. 

Colostrum is full of rich immune factors and beneficial bacteria playing a crucial role in establishing a healthy gut microbiome in infants. 

Some of the benefits of colostrum are:

• Helps strengthen your baby's immune system.
• Helps to establish a healthy gut by coating the intestines. ...
• Offers ideal nutrition for a newborn.
• Has a laxative effect that helps your baby clear meconium (your baby's first poop) and lessens the chance of jaundice.
• Easy to digest.

THE LIQUID GOLD BOBBY BANK 

Colostrum is a concentrated source of nutrition to develop the immune system, especially important for ill or premature babies.  No antibiotic is necessary. 

If the government is giving a $5,000 baby bonus to new mom's, please give $5,000 to stillborn mom's and an additional $5,000 for any mom who can pump more, to give their colostrum to other newborns to grow up healthy. Saved in a 'Liquid Gold Bobby Bank' named after RFK Jr.