Hepatitis B is a nonliving virus particle. A discussion about it was not included in the original book published in 1984 because it was not routinely administered at that time.
This shot is now routinely given to babies within 24 hours of birth. This is insane. The idea of injecting this stuff is to have B-cells in the body create serum antibodies. Guess what, the B-cells in newborns can’t do that. The ability of B-cells to communicate with T-cells and make functional antibodies is not possible until between the ages of 9 and 12 months! Why are they doing it then? In my opinion, it is to indoctrinate you into believing that this procedure is normal to “protect” your child on day 1, and have this ideology follow you for the rest of your life.
What keeps newborns protected then, if they can’t make antibodies? The theme running through this book is this: Serum antibodies do not protect you from infections, they can only react to infections after they happen. The true protection of infection is cellular, in those sentinel cells that guard the epithelial layer that separates the inside of you from the outside. This is called “innate” immunity because you were born with it. The innate immune system in babies is very robust, and its job is to learn as much as it can about the environment. While it is learning, it is also protecting the babies from ALL infections because it is broad and non-specific.
This is one of the reasons babies will put anything and everything into their mouths, even when you’re not looking. Their immune systems are getting trained. Babies and children that are exposed to pets, especially dogs that are allowed outside, develop their immune systems faster and stronger and are 30% less likely to develop colds, ear infections, and coughs. https://www.orlandohealth.com/content-hub/get-a-pet-to-boost-your-childs-immune-system So, let your children have pets, play outside, and get dirty so their immune systems get trained.
How does this training and learning work? Simply put, there are octopus like dendritic cells guarding that epithelium. They “taste” everything they come in contact with by engulfing and chopping it up into protein parts. These proteins are called antigens and are then displayed or presented on the surfaces of dendritic cells. Dendritic cells are sometimes called “professional antigen presenting cells” because they are really good at this. They present the antigens to naïve T-cells. These naïve T-cells then become trained in the thymus gland behind the breastbone to recognize these antigens and remember them. After that, the T-cells are no longer naïve, they know what’s going on, become “cytotoxic”, and can now destroy organisms that have these antigens on them.
In fact, it is the T-cells and other cells of the immune system that destroy organisms associated with infections BEFORE antibodies are even produced after the first exposure to the organism. It takes a long time, sometimes weeks to make antibodies, and antibodies don’t destroy organisms anyway. Antibodies simply attach to the antigens on organisms, marking them so that the cells of the immune system can more easily recognize them for destruction the NEXT time infection happens. This paper states “While the humoral antibody response to viral envelope antigens contributes to the clearance of circulating virus particles, the cellular immune response to the envelope, nucleocapsid, and polymerase antigens eliminates infected cells.” https://pubmed.ncbi.nlm.nih.gov/7612225/
So, what is in this Hepatis B shot that results in antibodies that is supposed to react to infections? The first shots that came out in 1981 contained Hepatitis B viral antigens that were obtained from the blood of gay men and intravenous drug users. Why those people? Because they, not babies, are most prone to developing Hepatitis B infections. Remember that the spread of this virus is through direct contact with bodily fluids and infected blood. Hugging, kissing, sharing food, coughing, and sneezing have been found irrelevant in transmitting the disease. Unfortunately, members of this subset of people are also the most prone to developing HIV infections. Even though manufacturing of this shot took measures to keep the HIV out, there was concern that some contamination might happen, so it was pulled from the market. In 1986, they came up with a way to insert part of the genomic sequence of the shell of the Hepatitis B virus into the genome of yeast, and have yeast grow and multiply with this new genetic sequence in it. This is called the genetic recombination method of producing antigens to be used in vaccines. Along with this yeast grown Hepatitis B antigen, they include aluminum as an adjuvant to entice the immune system to react to the antigen. As we’ve discussed previously, the aluminum is toxic, and you can’t possibly know how much of it is in each shot. Some babies cannot naturally metabolically eliminate this toxin, predisposing them to neurological side effects, including autism. There are ways to help eliminate metal toxins by a process called chelation.
Does injection of this antigen prevent everyone from developing chronic infections of Hepatitis B? No. In fact, some people who have been injected multiple times still get infections. In fact, the vaccine package insert for RECOMBIVAX HB clearly states that the shot will not protect everyone. Here’s a link to the package insert: https://www.fda.gov/media/74274/download
There are a few other things disclosed in that package insert that will alert parents if they take the time to read it. Look at the clinical trials section 6.1. This shot got FDA approval because the trial lasted five days looking for adverse reactions. That’s right, FIVE DAYS! But look at what happened in the post marketing experience section 6.2 AFTER the shot was approved. There is evidence of significant neurological adverse events including “Guillain-Barré syndrome; multiple sclerosis; exacerbation of multiple sclerosis; myelitis including transverse myelitis; seizure; febrile seizure; peripheral neuropathy including Bell's Palsy; radiculopathy; herpes zoster; migraine; muscle weakness; hypesthesia; encephalitis.”
Parents, I implore you, please download and read the vaccine package inserts! Here’s a link to all vaccine package inserts: https://www.fda.gov/vaccines-blood-biologics/vaccines/vaccines-licensed-use-united-states
The reason Hep B is given at birth is because the virus was prevalent in the minority community and they historically do not go to he doctor for vaccinations. Someone thought it was wise to vaccinate everyone at birth thus trying to eliminate the virus in people who would not return to the doctor.
Wow.
And of course as with the Covid Vax Injuries... the parents never attribute the damage to their children to these other toxic shots.
We have a friend who is rabidly pro Covid vax.... he has a son who is on the severe end of the spectrum... the irony is that this was likely caused by a vaccine. To suggest this to him would only incite rage... so we'll leave it unsaid.
REJECT ALL VACCINES