|* live virus * the microbes * the vaccines|
3 Main Recipes
VIDEO: 'First Autism'
Antitoxin for Toxin
Flu shot brands
My son was paralyzed by the DPT shot when he was 4 yrs old. He was only able to blink, swallow, and breathe for 3 days, finally softening up, and dragging a leg for weeks.
He was paralyzed from the Tetanus toxin in the DPT whooping cough shot, because the lethal dose of Tetanus Toxin for 50 lb ('Universal Doses') in his shot didn't have enough anti-toxin and it paralyzed him. Luckily he weighed 50 lb, so he was able to survive the 50 lb dose, or he would have been yet another mysterious SIDS death. That was in 1984, and I've been tracking vaccinations ever since, which has led me down the autism trail...
Adult doses (age 7 up) are 4-10x LESS toxic than child doses.
The Amish do not vaccinate,
and have no autism.
Allison Jones on 'The Panel'
with Dr Andrew Wakefield (2016).
DEDICATED to my brother,
Dr Ronald Conrad Jones,
PHD in Toxicology,
whom taught me early on
about human physiology
& the nature of cancer!
how they work,
how they cause Autism...
Tetanus... Salmonella... Diphtheria's Phage
VIDEOS = visit my YouTube Channel: 'Allison Jones vaccines'
1 - How the Whooping Cough Vaccine is Made.
2 - Endotoxin, Exotoxin, & Gardasil.
3 - Polio Vaccines.
4 - The Broken Polio Cycle.
5 - Only Smallpox.
6 - The First Autism.
Starting in 1890, horses were injected with diphtheria toxin,
to produce antibodies. Doctor offices were had stables in the back.
Notice the tubes taking blood from their necks (serum of their antibodies).
How the first Diphtheria Vaccine with Aluminum caused Autism
Horse 'Antibody Serum' (blood) was called the "antitoxin" to deadly diphtheria toxin, but antibody shots are not vaccines. The shot was for Diphtheria, a bacteria that colonized the throat and its necrotic toxin caused a pseudo-membrane to form and quickly kill the youngest.
By 1913, Diphtheria Toxin began to be injected into people, along with antibodies to counter the lethality of the toxin. This shot did not work and by the early 1920s there was an epidemic, partially due to the horrendous sanitation problems in burdgeoning cities.
Then in 1931, Glenny added Aluminum to the current Diphtheria Toxin + antibody product, increasing antibody production 1000x (thousand), turning the first babies autistic seen by Dr Kanner by 1943. He called them Autistic because they were in their own world and didn't speak.
current Diphtheria Toxin + antibody product,
increasing antibody production by 1000x (thousand),
turning the first babies autistic seen by Dr Kanner by 1943.."
Autistic children are the survivors of Diphtheria toxin exploding cells and their DNA coating the attached Aluminum, which is then attacked by antibodies too, in what I call a "Teratomic Effect" because this DNA is foreign. After birth the antibodies of the mothers circulate for two years as the childs immune system leading the charge and saving the day. Her antibodies will attack the DNA-aluminum-diphtheria-toxin combo, especially in boys because every cell in their body as XY chromosomes, something foreign.
During the pregnancy her body wanted to attack the foreign fetus but her placenta is the only thing preventing that from happening by sending "quieting" signals. But a shot is like a bomb, inwhich the foreign DNA of the child (half is the fathers), this DNA is now attached to Aluminum that's adsorbed to Diphtheria Toxin and its percieved as the enemy and attacked too. If neuron cells explode then the immune system can track them into the brain and destroy irreplaceable neurons that have not made all their connections, which is why autism is Age-Dependent.
Aluminum is not free in nature,
its always bound in rock,
The first diphtheria shot used Alum (potassium + aluminum), today it purified and amplified with a favored mercury catalyst
to produced a hydroxide of this metal that does NOT belong in our bodies.
Even mercury is spewed from volcanoes and excreted better by the body,
and was used as an anti-microbial for centuries, and is not the cause of autism.
Injections of aluminum attached to Diphtheria toxin was the first cause,
just the beginning, the first way to destroy budding neurons and their pathways in the Limbic System and Pre-frontal Cortex.
1) Tetanus Toxin, #2 deadliest, is Paralytic. 2) Diphtheria Toxin, #3 deadliest, is Necrotic.
Astrocytes get inflamed protecting neurons.
Microglia cells are the Macrophages of the brain, the janitors.
Childhood Vaccine Microbes
Diphtheria & Tetanus Toxins need equal amounts of Antitoxin to keep the MLD (Minimum-Lethal-Dose) of them that's in all the whooping cough vaccines from killing the recipients (tetanus toxin) or destroying neurons in the limbic system (diphtheria toxin). They’re flocculated together (Lf), and called Toxoids.
LPS (lipo-poly-saccharides) are 'Endotoxins' of Gram-negative bacteria from their outer membranes.
Just one molecule of LPS makes 100 million fibrinogen (that make normal blood clots) tangle into amyloid plaques that are not normal, starting a chain reaction of the body repairing perceived damage through the perceived threats from so many adjuvants, like LPS, in successful vaccines going for high antibody titers.
Astrocytes get inflamed protecting neurons from LPS.
Amyloids prevent the brain from draining toxins (flushing out toxins that build up during the day) during sleep at night.
LPS (endotoxin) of Gram-Negative Bacteria in Vaccines:
MPL = Mono-Phosphoryl-Lipid.
OMPC = Outer Membrane Protein Complex.
Phenol is extremely lethal, only 1,000 ppm will kill a human within 5 minutes when injected. It's made from paraffin, which is coal tar (petroleum).
Shots with Phenol (lethal dose 1,000 ppm 5 mins in human):
a) Fluzone (popular flu shot) has 300 ppm.
b) Adacel & Daptacel have 6,600 ppm.
c) Pneumovax (strep shot) has 2,500 ppm.
d) Pentacel has 6,600 ppm.
e) IPOL (polio shot) has 5,000 ppm.
Neuron development ("brain cell") in the Cerebral Cortex,
Newborn - 1mo - 3mo - 6mo - 12mo - 24mo
historically & globally,
do NOT have autism...
Glutamates cause "Chemical Concussions" damaging neurons.
This is suspension material to ensure the product does not settle and leave target germ material in the tip of the syringe, for example, so gelatin is added to some vaccines, mostly the live virus vaccines and Fluzone.
Gelatin is from melting cow skeletons (leftover from slaughterhouse industry), and its ingestion in food and juice is one thing, but injection should not occur in babies.
The excitotoxins (glutamates, MSG) drive energy linked excito-toxicity. They knock magnesium off the NMDA receptors on cells, allowing too much calcium into the cell, which allows Mitochondria to die & break DNA. Broken DNA leads to broken protein fragments and the cell swells with useless proteins, leading to a damaged cell that’s targeted for destruction by the microglia cells. Microglia are the macrophages of the brain, marking these cells for apoptosis and their explosion which can lead to a chain reaction causing other cells nearby to become excitotoxic and explode.
1) Gelatin is Collagen from leftover cow skeletons, etc.
2) Injestion is not invasive like injection.
3) Proquad vaccine (MMR, varicella like viruses) contains 14,500 mcg of gelatin.
Hydrolyzed Gelatin (collagen),
Horses were infected with diphtheria bacteria to produce antibodies that could be used in vaccines (for whooping cough/pertussis) attached to diphtheria antitoxin.
Horses were also infected with tetanus bacteria to produce antibodies that could be used in vaccines (for whooping cough/pertussis) attached to tetanus antitoxin.
Vaccine production: Growing virus inside "immortalized" cells
wrapped around micro-carrier beads in fbs blood in tanks.
Daptacel is a vaccine for Pertussis bacteria (whooping cough),
with Tetanux Toxoid & Diphtheria Toxoid (includes their antitoxins).
Oligodendrocyte cell wrapping around brain Neuron.
Nude Mouse (no immune system)
Large amounts of aluminum are used in many 'inactivated' vaccines.
thus we never find the answers we are looking for...
so viruses become lazy (attenuated).
But, attenuated viruses in vaccines behave differently
such as, measles & polio:
1) Measles can exist in a Quasi-species state.
The crippled 'Edmonston strain' used in all MMR vaccines can not infect human cells thru the normal measles entry called 'CD-150', but instead infects human cells through HHV-6 receptors on cells. HHV-6 is "Human Herpes Virus-6" which is a resident herpes virus inside humans and uses receptor CD-46. And because cancer cells in the human body are loaded with HHV-6 herpes virus with 10x more receptors on those cancer cells, they can use measles to kill tumors!
2) Polio virus reverts back to its original virulent state within 48 hours.
This allows the body only 2 days to prepare for the real thing, which can be a set-up for disaster within malnourished children with their weakened immune systems suffer neuropathies or paralysis (such as, in India & Africa where we see this phenomenon), or, in America where children have greater nutrition and stronger immune systems, yet still shed new mutant strains of polio for months following live immunization, which created many of the EVs that began to appear in the 1960s, (EV-68, EV-71, & now, Hand-Foot-Mouth disease).
"Most strains of H. influenzae (HIB) are opportunistic pathogens; that is, they usually live in their host without causing disease, but cause problems only when other factors (such as a viral infection, reduced immune function or chronically inflamed tissues, e.g. from allergies) create an opportunity." -(wikipedia)
"Interaction with Streptococcus pneumoniae: Both H. influenzae and S. pneumoniae can be found in the upper respiratory system of humans. In an in vitro study of competition, S. pneumoniae always overpowered H. influenzae by attacking it with hydrogen peroxide and stripping off the surface molecules H. influenzae needs for survival. When both bacteria are placed together into a nasal cavity, within 2 weeks, only H. influenzae survives." -(wikipedia)
Beer Yeast: 'S. Cerevisaie' has virus genes inserted
into their genome to sweat out the viral
They are ground up to be the substance
of some HepB and HPV vaccines, up to 5%
or target material containing antigens would be lost,
but this can cause shock & seizures.
Hepatitis-B Virus (HBV) vaccine production diagram.
CERVARIX [Human Papillomavirus Bivalent (Types 16 and 18) Vaccine, Recombinant] is a non-infectious recombinant, AS04**-adjuvanted vaccine that contains recombinant L1 protein, the major antigenic protein of the capsid, of oncogenic HPV types 16 and 18.
The L1 proteins are produced in separate bioreactors using the recombinant Baculovirus expression vector system in a serum-free culture media composed of chemically-defined lipids, vitamins, amino acids, and mineral salts. Following replication of the L1 encoding recombinant Baculovirus in Trichoplusia ni insect cells, the L1 protein accumulates in the cytoplasm of the cells. The L1 proteins are released by cell disruption and purified by a series of chromatographic and filtration methods. Assembly of the L1 proteins into virus-like particles (VLPs) occurs at the end of the purification process. The purified, non-infectious VLPs are then adsorbed on to aluminum (as hydroxide salt). The adjuvant system, AS04, is composed of 3-O-desacyl-4’-monophosphoryl lipid A (MPL) adsorbed on to aluminum (as hydroxide salt).
CERVARIX is prepared by combining the adsorbed VLPs of each HPV type together with the AS04 adjuvant system in sodium chloride, sodium dihydrogen phosphate dihydrate, and Water for Injection.
CERVARIX is a sterile suspension for intramuscular injection. Each 0.5-mL dose is formulated to contain 20 mcg of HPV type 16 L1 protein, 20 mcg of HPV type 18 L1 protein, 50 mcg of the 3-O-desacyl-4’-monophosphoryl lipid A (MPL), and 0.5 mg of aluminum hydroxide. Each dose also contains 4.4 mg of sodium chloride and 0.624 mg of sodium dihydrogen phosphate dihydrate. Each dose may also contain residual amounts of insect cell andviral protein (<40 ng) and bacterial cell protein (<150 ng) from the manufacturing process."
- this quote is from the drug 'Cervarix' formation
listed by manufacturer GSK. (Research grants could start with the
dangerous levels of aluminum, repeated 3x within weeks of each other,
and the dangerous MPL of Salmonella (AS04), a powerful immunogenic LPS.
Because over-stimulation of the immune system can cause destructiion
in the wrong places in the body, for the wrong reasons.)
Salmonella LPS forces a strong immune response,
but one molecule of LPS (gram -negative bacteria) will cause
a million fibrinogens to become tangled into incorrect clots
called Amyloid plaques: malformed bloodclots.
The Vaccine RECIPES
thus each dose is 25 mcg mercury starting at 6 months, then every year.
Neurite Formation in Human Babies
FBS is fetal cow blood, food for the cells hosting virus
being grown inside the tank for vaccine products.
The host cells are either animal (attenuated) or human (non-attenuated)
needing Fetal Bovine Serum for food, hence the red color.
Most flu vaccines are dead virus ("inactivated") shots, but there has been a live flu virus vaccine sprayed up the nose, called Flu-Mist.
Quick means to deliver drugs and live viruses into the brain (before the immune system has a chance to cover cribriform plate openings with mucus). The cribriform plate has numerous holes, like a salt shaker, for the nerves from the Olfactory Bulb to come down through the brain - to figure out what you are smelling. It's leftover from our prehistory as reptiles, which remains by the existence of our brainstem, considered by researchers as the reptile part of our brain.
Despite the good intentions of many doctors, there are "Experts" whom were bought and told to sell us cigarettes. Doctors are told to sell us drugs pushed by pharma companies, while performing cesareans to pay for their medical school. Negative research is not published. Any research on the negative effects of vaccines and the casualties that litter its history have been exempt from research, punishing any doctors that wished to study them, like Dr Andrew wakefield.
The medical institution argued against handwashing back when some brilliant doctors figured out hand washing was a good idea. But it was forbidden, and the medical institution argued against these doctors in the courts for a mind-numbing 70 years, not passing until 1910!
Researchers can NOT get grants to look at vaccine Adverse Events,
thus, there are NO studies looking at vaccine problems.
The Dehradun Plant where vaccines are produced. It's in Uttarakhand, India.
Bad Reactions to TOXIN shot
Manufacturer's Notes on common "adverse events" (bad reactions) from the DtaP (whooping cough), now put in other shots. Super toxic being the MLD (minimum lethal dose) of deadly toxin for a 50lb child, given to babies. It needs to EXACT amount of Anti-Toxin or it will kill (SIDS) or leave them on the Spectrum from loss in the Limbic.
EEG disturbances with encephalopathy,
Serious and acute neurological disorders,
Complicated convulsions (with or without fever),
Persistent and Inconsolable Crying (lasting 3 hrs or more),
Unusual & High-pitched Crying,
Collapse (hypotonic-hyporesponsive episode),
Severe Neurological Complications.
Fretfulness, Vomiting, Anorexia,
Persistent and Inconsolable Crying,
High-pitched and Unusual Cry,
Collapse (hypo-tonic-non-responsive episode),
Convulsions, Acute Encephalopathy,
Permanent Neurological Deficit.
Chronic Neurological Damage, SIDS,
Shock and "Unusual shock-like" state,
Protracted & Inconsolable Cry,
of myelin sheaths in the central and peripheral nervous system
leading to degenerating motor control and loss of sensation."
in sensitive species (e.g. humans, monkeys, rabbits)
as little as 100 to 150 ng per kg of body weight is lethal."
2) Tetanus -"Epilepsy is induced in lab rats by injecting them with Tetanus toxin, creating seismic activity, and their interest in new things disappears, locomotion is the same, but they explored everything less, from the familiar to novelty items."
interest in new things disappear,
locomotion is the same,
but they explored everything less,
from the familiar to novelty items."
The multi-dose bottle (10 dose) bottles contains 250 mcg MERCURY,
thus each dose is 25 mcg mercury starting at 6 months, then every year.
Kain, Del Bigtree, Allison Jones, Shuman, Dr Wakefield, Silvers.
Author Jones (vaccine researcher since 1984),
Dr Andrew Wakefield (physician & vaccine researcher).
Do you know what's in a Shot?
email * the vaccines * live virus
Jones (206-525-0783), PO Box 1683, Topanga, CA 90290
copyright@ 2008-2017 Neoteric, All rights reserved.