Vaccine News – VAXXED TV – It only takes one & Study – Effect of immunization against rubella on lactation products

US National Library of Medicine
National Institutes of Health – May 1982

Study – Effect of immunization against rubella on lactation products.
I. Development and characterization of specific immunologic reactivity in breast milk.

Abstract
The development of an immune response to rubella virus in milk, serum, and nasopharyngeal secretions was studied in lactating postpartum women after immunization with HPV-77 De5 or RA 27/3 live, attenuated rubella virus vaccine administered subcutaneously or intranasally. Over 69% of the women shed virus in milk after immunization. A predictable nasopharyngeal IgA and serum IgG antibody response to rubella virus was observed after subcutaneous or intranasal immunization with RA 27/3 vaccine. Little or no nasopharyngeal antibody response was seen after subcutaneous immunization with HPV-77 DE5 vaccine. A virus-specific IgA antibody response in milk was seen in all women. The presence of rubella virus in breast milk seemed to potentiate the peak levels of virus-specific antibody in the milk. Cellular immune reactivity to rubella virus in milk was observed in all vaccine groups. Thus, the virus-specific immune response induced in human milk after immunization with rubella virus vaccine may be intimately linked with the reactivity in bronchial lymphoid tissue.

US National Library of Medicine
National Institutes of Health – May 1982

Study – Effect of immunization against rubella on lactation products.
II. Maternal-neonatal interactions.

Abstract
The transmission of rubella virus to newborn infants via the process of breast-feeding was studied after immunization of 16 breast-feeding and 10 non-breast-feeding mothers with HPV-77 DE5 live, attenuated rubella virus vaccine administered subcutaneously or RA 27/3 live, attenuated rubella virus vaccine administered intranasally or subcutaneously in the immediate postpartum period. Infectious rubella virus or virus antigen was observed in the breast milk of 11 (68%) of the 16 vaccinated, breast-feeding women studied. After maternal immunization, infectious rubella virus or virus antigen was recovered from the nasopharynx and throat of 56% of the breast-fed infants and from none of the non-breast-fed infants. Of the breast-fed infants, 25% showed transient seroconversion to rubella virus but without any clinical disease. No rubella virus-specific seroconversion was observed in the non-breast-fed infants. These observations provide strong support for the communicability of rubella virus to neonates via the process of breast-feeding.

US National Library of Medicine
National Institutes of Health – Jul 1991

Study – Effect of prior immunity on the shedding of virulent revertant virus in feces after oral immunization with live attenuated poliovirus vaccines.

Ogra PL, Faden HS, Abraham R, Duffy LC, Sun M, Minor PD.
Author information
Department of Pediatrics, School of Medicine and Biomedical Sciences, State University of New York, Buffalo.

Abstract
Groups of infants were immunized with one or two doses of orally inoculated live attenuated Sabin poliovirus vaccine (OPV group) or with one or two doses of enhanced-potency inactivated poliovirus vaccine (EIPV) administered parenterally followed by one or two doses of OPV (EIPV-OPV group). The fecal specimens from both groups were tested for poliovirus shedding 1-2 months after OPV. The virus isolates were examined for nucleic acid sequences in the 5′ noncoding regions (bases 480, 481, and 472 for serotypes 1, 2, and 3, respectively) to determine whether the viruses shed represented nonattenuated revertants, attenuated parent vaccine strains (nonrevertants), or both. In the OPV group, 4 of the 6 virus isolates recovered 30-60 days after the first immunization dose and 1 of the 3 isolates obtained after the second dose were found to be nonrevertants (parent vaccine strain). In contrast, 11 of the 12 isolates in the EIPV-OPV group were of the nonvaccine revertant virus types. The frequency for reversion appeared to differ for different poliovirus serotypes. However, all revertant type 3 isolates were recovered from subjects previously immunized with EIPV.

 

 

VAXXED TV – The vitamin with a black box warning

 

 

 

 

 

 

 

I said please give him everything

 

 

 

I wish she could go to school and show everybody how healthy she is

Three days after his first birthday

 

 

 

 

Both of their husbands are pastors

From that day on

 

 

 

 

 

It’s called an encephalitic cry

It only takes one

 

 

 

 

 

 

Cyclic Vomiting Syndrome

The ALex Jones Channel – Vaccine Damage Is Now A Global Pandemic
Infowars reporter Rob Dew interviews Lori Gregory, vaccine researcher and editor of The Mom Street Journal on the now global crisis that has resulted from vaccine injury.

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ONE FOR ISRAEL Ministry – Jewish Johnathan Ben-David forgave his killer and you would not believe why!!!

How to accept Jesus Christ as your personal Saviour

Testimony by Phil Robertson from Duck Dynasty

1 Corinthians 15 Authorized (King James) Version (AKJV)
1 Moreover, brethren, I declare unto you the gospel which I preached unto you, which also ye have received, and wherein ye stand;
2 by which also ye are saved, if ye keep in memory what I preached unto you, unless ye have believed in vain.
3 For I delivered unto you first of all that which I also received, how that Christ died for our sins according to the scriptures;
4 and that he was buried, and that he rose again the third day according to the scriptures:

Hebrews 6 Authorized (King James) Version (AKJV)
1 Therefore leaving the principles of the doctrine of Christ, let us go on unto perfection; not laying again the foundation of repentance from dead works, and of faith toward God,
2 of the doctrine of baptisms, and of laying on of hands, and of resurrection of the dead, and of eternal judgment.
3 And this will we do, if God permit.
4 For it is impossible for those who were once enlightened, and have tasted of the heavenly gift, and were made partakers of the Holy Ghost,
5 and have tasted the good word of God, and the powers of the world to come,
6 if they shall fall away, to renew them again unto repentance; seeing they crucify to themselves the Son of God afresh, and put him to an open shame.
7 For the earth which drinketh in the rain that cometh oft upon it, and bringeth forth herbs meet for them by whom it is dressed, receiveth blessing from God:
8 but that which beareth thorns and briers is rejected, and is nigh unto cursing; whose end is to be burned.

Isaiah 53 – Old testament Prophecy about Jesus

1 Who hath believed our report? and to whom is the arm of the Lord revealed?
2 For he shall grow up before him as a tender plant,and as a root out of a dry ground:he hath no form nor comeliness;and when we shall see him,there is no beauty that we should desire him.
3 He is despised and rejected of men;a man of sorrows, and acquainted with grief:and we hid as it were our faces from him;he was despised, and we esteemed him not.
4 Surely he hath borne our griefs,and carried our sorrows:yet we did esteem him stricken,smitten of God, and afflicted.
5 But he was wounded for our transgressions,he was bruised for our iniquities:the chastisement of our peace was upon him;and with his stripes we are healed.
6 All we like sheep have gone astray;we have turned every one to his own way;and the Lord hath laid on him the iniquity of us all.
7 He was oppressed, and he was afflicted,yet he opened not his mouth:he is brought as a lamb to the slaughter,and as a sheep before her shearers is dumb,so he openeth not his mouth.
8 He was taken from prison and from judgment:and who shall declare his generation? for he was cut off out of the land of the living:for the transgression of my people was he stricken.
9 And he made his grave with the wicked,and with the rich in his death;because he had done no violence,neither was any deceit in his mouth.
10 Yet it pleased the Lord to bruise him;he hath put him to grief:when thou shalt make his soul an offering for sin,he shall see his seed, he shall prolong his days,and the pleasure of the Lord shall prosper in his hand.
11 He shall see of the travail of his soul, and shall be satisfied:by his knowledge shall my righteous servant justify many;for he shall bear their iniquities.
12 Therefore will I divide him a portion with the great,and he shall divide the spoil with the strong;because he hath poured out his soul unto death:and he was numbered with the transgressors;and he bare the sin of many,and made intercession for the transgressors.

 

The Only Sin That Leads To Hell – Kenneth E Hagin

 

Why I won’t vaccinate

If you choose to read this, please read the whole thing.

So here it is, a little bit of why we no longer vaccinate, with reasoning for each particular vaccination before 12 years old:

As of 2016, a child in America is scheduled to received 74 vaccinations by the time they turn 18. With each shot, you are taking the risk of your child suffering the side effects, even as severe as SIDS, paralysis, deafness, blindness, and death. That’s 74 times… I just personally can’t agree to roll those dice with the lives and lifelong health of my children. With most shots, you are also allowing heavy metals to accumulate in their body.

I am extremely uncomfortable with the notion that as a duty to society, I must choose to inject known poisons into my child’s body. I will never be convinced again to stick a needle into my child containing recognized carcinogens, neurotoxins, and other poisons that can cross the blood-brain barrier and build up in my child’s body. When you put something like aluminum into the body by way of injection, it bypasses the protective mechanisms of the gastrointestinal tract, circulates in your body, and is deposited in your body tissues. *There are NO STUDIES that prove that the amount of aluminum in vaccines is safe to inject into an infant or a toddler (or human for that matter).*

Aluminum IS however known to cause neurological harm, degenerative problems, autoimmune disorders, and inflammatory conditions. Conditions that fall under these categories are: Lupus, Graves’ Disease, Lupus, Celiac Disease, Chronic Fatigue Syndrome, Chron’s Disease, Endometriosis, Fibromyalgia, Arthritis, Scleroderma, Vitiligo, Multiple Sclerosis, Muscular Distrophy, Cancer, Parkinson’s, Diabetes, Asthma, Irritable Bowel Syndrome, and more. These are debilitating ailments that a child can develop at any time and face for the rest of their lives. How can someone tell me as a mother that I need to do this to my child because “it’s best for everyone else?”

Other harmful ingredients and additives whose toxic effects have NEVER been examined by injecting them into small children are Formaldehyde, MSG, 2-Phenoxyethanol, and others.

Formaldehyde is a carcinogen, that is a fact. It can cause genetic damage and kidney damage if inhaled, but no one has bothered to study the effects of shooting it into our children with needles. Glutamate, a component of MSG, is an excitotoxin which is a chemical that affects brain function. They’ve taken MSG out of baby food, but left it in vaccines… 2-Phenoxyethanol is a chemical preservative used in perfumes, insect repellents, germicides, solvent for dyes, plasticizers, and antiseptics. It is harmful and can cause reproductive defects and severe skin and eye irritation if inhaled, swallowed, or absorbed through the skin. Again, despite this, it’s still in vaccines and the harm hasn’t been studied by way of injection. But let’s just assume they’re all safe, right?

Also to be considered is the use of any sort of human DNA such as aborted fetal cells. This can trigger autoimmune reactions. The immune system will attack the foreign human DNA, and this attack can then in turn become an attack against the child’s own body because it can’t tell the difference between same-species DNA. The injected human DNA inserts itself into the genes of the child and alters their genetic function. Animal substances are concerning as well, because when they are screened for disease, there is a possibility of missing animal viruses there are no tests for. This has happened before.

I can’t fathom routinely injecting poisons that I know are harmful and toxic into my child and taking the risk of life-long ailments. Yes, that means I am taking a bit of a higher risk of her catching a disease that vaccines may offer some protection against, but the risks are low, and *vaccinated children catch them too.* It is a FACT that certain toxic ingredients are cause harm, while it is only a possibility that my child may catch diseases we could vaccinate against. There are healthy ways to prevent and combat these diseases, and contracting and managing most of them will result in lifelong immunity.

What I’ve written below this are the chances of my child catching the diseases vaccines are supposed to protect against, and the risks that I feel outweigh the benefits of each vaccination. This includes the side effects of the shots and the harmful chemicals that they contain.

HIB: HIB is NOT a common disease. A breastfed child who does not attend daycare is at an even lower risk of catching it. The fatality rate of those who do catch it is 5%, usually when it is not caught soon enough. There are about 25 cases per year in the US, meaning the risk for my child to catch it in their first 2 years of life is about 1 in 200,000. After age 2, it’s nearly 0. It is also treatable. Concerning adverse reactions include seizures, encephalitis (brain swelling), autoimmune reactions, nervous system dysfunction, anaphalaxis, angiodema, apnea, hives, Guillain-Barré syndrome (GBS), convulsions, renal failure, and severe allergic reactions. The vaccine contains aluminum and formaldehyde, which I’ll explain the issues about later.

PC (Pneumococcus): 1/3 of severe cases of Pc are caused by strains NOT covered by the vaccine. The chances of a child by age 2 having a severe case is 1 out of 2850. Pc is treatable. Again, a breastfed child not in daycare is at low risk for catching this. Most infants suffer one or more systemic or local reactions with this shot. The more concerning adverse reactions in infants and toddlers during clinical studies included: DEATH (SIDS), bronchiolitis, gastroenteritis, pneumonia, SIDS, apnea, decreased limb mobility, arthritis, GBS, seizures, heart failure, pancreatitis/myocardial infarction resulting in death. This vaccine contains aluminum.

DTaP (Diphtheria, Tetanus, Pertussis): Diphtheria is extremely rare, at 5 cases per year and not a single one since 2003 in the US. The risk is basically 0. Tetanus is virtually unheard of in people under 5 years old, and there are only 10 cases per year in people 5-25 years of age. The risk is 1 in 500,000. Pertussis (Whooping Cough) is more common, but in my child’s first 12 years of life, their risk of having a severe case is 1 in 3333. Pertussis is rarely problematic after 1 year of age. Infection is likely to create life-long immunity. It is treatable. The fatality rate is 1% for infants and toddlers and adults do not die from it in the US. Reactions to this vaccine include: death, brain injury, coma, severe seizure disorders, GBS, Brachial neuritis (dysfunction of nerves in the arm), Cyanosis, anaphylactic shock, grand mal seizures, bronchitis, pneumonia, hypotonia, encephalopathy, apnea, SIDS, and autism. This contains aluminum, formaldehyde, polysorbate 80, glutaraldehyde, and 2-phenoxyethanol.

Hep B: This disease is also rare in children under 12. Virtually all cases of Hep B in infants each year are results of transmission by the mother at birth. Vaccinating for this actually began with attempts to control the disease by stopping it within high risk groups. When this didn’t work, they started vaccinating all newborns for it instead. There’s really no reason for an infant to get this shot if the mother is not infected. In the first 12 years of life, chances of contracting Hep B are 1 in 40,000, almost all passed on from the mother. SOME known reactions of this shot are: lupus, blood vessel inflammation, Stevens-Johnson Syndrome, liver damage, wheezing, hair loss, bruises, GBS, eczema , liver damage, asthma, heart palpitations, arthritis, anaphylaxis, severe nerve dysfunc. Paralysis, GBS, seizures, spinal cord inflammation, optic nerve inflammation, multiple sclerosis. This contains aluminum and formaldehyde.

Rotavirus: Most children who gets this don’t even know and recover from it just like any other common virus. When it becomes severe, it’s usually due to dehydration. Fatalities are rare. This vaccine is a live virus, meaning a child who gets the shot can pass the virus on to others or become infected themselves with Rotavirus (Rotavirus infection is a possible side effect). Common side effects mimic the virus itself. Worse reactions include: seizures, Kawasaki disease, intussusception (requiring emergency surgery), DEATH, SIDS, pneumonia, bleeding from low platelet counts, and hives. This vaccine contains monkey kidney cells, fetal cow blood, Polysorbate 80, and pig virus contaminants.

Polio: Polio doesn’t exist in the US, so in all reality my child is not in need of any protection this may offer. The vaccine can cause allergic reactions, anaphylactic shock, lymphadenopathy, convulsions, and other mild reactions. This shot contains baby cow blood serum, human proteins, Glutamate, formaldehyde, 2-phenoxyethanol, and monkey kidney cells.

MMR (Measles, Mumps, and Rubella): Severe cases of these diseases are so extremely rare that the risk is basically 0 for my child. Measles is not common, at 300 cases in the US per year (all ages of people) and complications are uncommon. Mumps is just as rare, and severe complications are almost nonexistent before puberty. Rubella does not cause severe illness in infants and children. There are only 20 cases per year. This is a live virus, so the vaccinated can spread Rubella following the shot. Known reactions include: Measles infection, aseptic Meningitis, arthritis, pancreatitis, pneumonia, severe eye inflammation that can permanently affect vision, nerve deafness in the ear, Stevens-Johnson Syndrome, panniculitis, vasculitis, pneumonia, pneumonitis (nonbacterial lung inflammation), and neurological reactions like brain swelling, GBS, ataxia (balance problems with difficulty walking), multiple nerve inflammation and dysfunction. This vaccine contains cow fetus serum, chick embryo proteins, DNA and protein fragments from human fetal cells, and Glutamate.

Varicella (Chickenpox): Chickenpox is not common, is treatable, and severe complications occur in less than 1% of cases. In my child’s first 12 years of life, their chance of having a severe case is 1 in 25,000. Adverse reactions to this vaccine include: chickenpox-like rash, pneomonitis (severe lung inflammation that can require intensive care), bleeding problems, neurological reactions, stroke, encephalitis, spinal cord inflammation and dysfunction, GBS, seizures, facial nerve paralysis, meningitis, pnemonia, Stevens-Johnson Syndrome, bacterial skin and tissue infections, and more. This vaccine contains Gelatin, which is against my religion to consume, as well as MSG, DNA and protein from human cells, cow fetus serum, and animal cells. This vaccine sheds the Chickenpox virus in the vaccinated for 6 weeks.

Hep A: Hepatitis A is harmless to young children and preventative measures can be taken if they are exposed. Severe cases are extremely rare, and virtually all cases happen in teens and young adults. The risk in these ages is about 1 in 25,000 in teen and adult years of life. Adverse reactions to the shot include: Hepatitis, seizures, bleeding problems, GBS, encephalitis, difficulties with walking and balance, multiple sclerosis, severe anaphylactic allergic reactions, jaundice, fainting, spinal cord inflammation, vasculitis, nerve dysfunction, rashes, and flu-like symptoms.

Influenza (Flu): While the flu may be common, it’s treatable and VERY rarely are there complications from severe cases. There is a wide debate and some evidence that this shot doesn’t even work for children under 2 and the rate of side effects is unusually high, so that alone makes this not worth the potential side effects to me. The nasal mist is a live virus, so those who receive this are contagious with the flu for 6 weeks and are likely have a mild case of the flu after receiving this. Adverse reactions to the flu shot include: tonsillitis, asthma, arthritis, limb paralysis, tremors, difficulty swallowing, febrile seizures, GBS, bleeding from low platelet count, severe allergic reactions, seizures, inflammation of the brain and spinal cord, encephalopathy, dysfunction of nerves in the face, eyes, or arm, fainting, inflammation of blood vessels, Stevens-Johnson syndrome, chest pain, rapid heart rate, eye infection and redness/swelling, and more. There are many different flu vaccinations, so the list of harmful chemicals varies between them and is quite long. These include formaldehyde, MSG, and Mercury or Thimerosal which is incredibly harmful and toxic and has been removed (almost completely) from all other vaccines because of this.
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I hope that people will understand that not all parents who choose not to vaccinate their children are quacks who based their decisions off of Google searches, illegitimate sources, biased information, opinions, or conspiracy theories. While there are some people like that, most of us are not. I urge you to seek out peer reviewed investigatice research and consider its source, funding, and the factors that solidify or vindicate it such as amount of test subjects, presence of control groups and size, or factors that were overlooked. This is important in any research, whether it supports or opposes vaccinations. I encourage you to make the decision whether or not to vaccinate each of your children individually and that you with the risks and benefits specific to your child.