Stop touching receipts. They're covered in toxic endocrine disrupting chemicals that stick to your skin and quickly absorb into your blood stream to wreck havoc on your hormones, fertility, cognition, and countless other side effects of exposure.

The EcoCenter did an analysis in 2022 where they tested hundreds of paper receipts from 144 major retailers and stores in 22 different states and found that 80% of receipts tested had BPS, which was a slight improvement from 84% in a prior 2017 study. They also found supposed safer chemical alternatives in 20% of them, up from 2% in 2017, but I think we should always wearer of these "safer" alternatives. We usually find out years later that these aren't safe either, and they're sometimes even more toxic and persistent in the body and passed down to offspring.

EWG and the University of Missouri Bio Science lab have also done a study where they collected 36 receipts comparing the amounts of BPA, and it found that the total mass of BPA used on a receipt is 250x to 1000x greater than the amount of BPA normally found in a can of food. Not only that, the BPA/BPS on the receipts is a free form of BPA that easily rubs off with simple touch, so you are getting a much higher amount absorbed systematically than you would by eating canned food, which has varying amounts based on various conditions like food acidity, temperature exposure, etc.

Considering we have rapidly collapsing fertility rates, skyrocketing autism rates, gender dysphoria everywhere, extreme mental illness, all kinds of cancer, feminized men, and a massively overweight population, you'd think the government and health regulators would be taking easy action against the use of BPA/BPS and other endocrine disrupting chemicals in receipts and other products, but as always it's profit above all else to fulfill the underlying agenda of those at the top to subjugate the population to sick and twisted games of eugenics.

All these corporations could easily afford the switch to back printed paper receipts like it used to be, and yet they don't. It's very important to reflect on why that is, not stopping at just a simple "profit motive" justification...

If you want to combat these exposures and be the 1 in 10 person with no measured BPA in their blood stream, start supporting your detoxification system with a carnivorous diet rich in fat soluble vitamins and amino acids like taurine and glycine to keep glutathione levels high, get adequate hydration with minerals like magnesium, potassium, bicarbonate, etc, daily sunlight whenever possible, earthing when you sleep, reducing EMF/RF exposures as much as possible especially when sleeping, and most importantly, you need exercise or use a sauna multiple times a week to make yourself sweat.

There are several studies on saunas showing the excretion of chemicals like BPA/BPA in your sweat, along with pesticides, heavy metals, and other environmental toxins. Human Excretion of Bisphenol A: Blood, Urine, and Sweat (BUS) Study



Background

Bisphenol A (BPA) is an ubiquitous chemical contaminant that has recently been associated with adverse effects on human health. There is incomplete understanding of BPA toxicokinetics, and there are no established interventions to eliminate this compound from the human body. Using 20 study participants, this study was designed to assess the relative concentration of BPA in three body fluids—blood, urine, and sweat—and to determine whether induced sweating may be a therapeutic intervention with potential to facilitate elimination of this compound. Methods. Blood, urine, and sweat were collected from 20 individuals (10 healthy participants and 10 participants with assorted health problems) and analyzed for various environmental toxicants including BPA. Results. BPA was found to differing degrees in each of blood, urine, and sweat. In 16 of 20 participants, BPA was identified in sweat, even in some individuals with no BPA detected in their serum or urine samples.

Conclusions

Biomonitoring of BPA through blood and/or urine testing may underestimate the total body burden of this potential toxicant. Sweat analysis should be considered as an additional method for monitoring bioaccumulation of BPA in humans. Induced sweating appears to be a potential method for elimination of BPA.hindawi.com/journals/jeph/…

A Guide to the Kefir Art Form

Kefir is one of the greatest foods on earth for healing the gut and ensuring a strong immune system, and ideally should be made from raw milk. If you don't have access to raw milk, using quality brands of pasteurized un-homogenized grass fed organic milk can still be healthy and valuable, just not ideal. Don't let perfect be the enemy of good. There are many people who have experienced tremendous benefits from homemade kefir with pasteurized milk, along with variations like water or coconut milk kefir. Raw milk kefir will always be the best though in my opinion.

Making perfect kefir will take some practice, but once you got it down, you will become so addicted to it and it's flavors. Often times people don't like it at first because it can be sour or tangy, but if they drink it few a few days, they will quickly find that they start craving it and loving it. I think this is the good bacteria populating the gut and sending signals to your brain for more of the goodness.

Supplies you'll need
-> 1/2 gal glass mason jars
-> 1 QT mason jars (store grains)
->Cheese cloth
->Rubber bands or string to hold cheese cloth
->Strainer (Nylon mesh, metal can alter flavor)
->Wooden spoon (again, no metal)
->Kefir grains

Optional supplies for consistency and perfection
->Heat mat or sous vide setup to control the exact temperature (I think the best kefir is made at 68-70F)

Starting and maintaining your grains
-> Before you start making kefir, you need to get some grains and wake em up. When you first get grains, you don't want to try and make kefir with them right away. it's going to take several batches to wake them up and grow enough to make your first batch of 1/2 or 1 gal worth of kefir.

-> All you do to get your grains ready and growing is 3-4 batches where you let them sit in milk at room temp for a couple days, strain them, and then put them in fresh milk again to repeat the process. Do this a few times and they're awake generally.

-> When you're done making kefir and you have grains left over, they'll continue to grow and grow as you make more batches, so you'll need to store them, eat them, or throw them away. You can keep them in a small amount of fresh milk in the fridge for 1-2 weeks or so before you want to replace the milk. Any grains you take out of the fridge for a new batch of kefir, need at least 1 tiny wakeup batch with a small amount of milk if you want to preserve the flavor, but honestly it still works fine straight from the fridge. All I've noticed with that is some inconsistency in the tangy flavor and thickness, but it depends on what time of year it is. If they were frozen, then you should do at least 2-3 wakeup batches bare minimum, or it will be much more yeasty than you will like.

Fermentation
-> The fermentation duration is contingent on the temperature and amount of grains in the milk. The warmer the temperature, the faster the fermentation, with a lesser likelihood of it being thick and separating too fast into cheese and whey. My perfect temperature for thick kefir is 68F for 3-4 days, but I like mine sour and tangy. Your taste preferences may like only 2 days of fermentation, while others like 5 days for it to be extra sour. This will take trial and experimentation to work out.

->For the amount of grains, you want around .5-1tbs per QT of milk, so if you're using 1/2 gal glass jars, you want at least 2-3tbs of kefir grains bare minimum. Make sure not to overfill the jars with milk and grains as well, as the kefir might expand and come out the top and make a mess.

-> Never completely seal the lid on fermenting kefir, or you will bust a jar and make it more alcoholic. Use cheesecloth with a rubber band so it can breath and release gas, or just a lose fitting lid.

-> After a couple days of fermentation, you will start to see streaks of whey throughout. This is a good sign and means it's propagating throughout the milk as it should. I used to shake my kefir lightly once I saw the streaks of whey touch the bottom on day 1.5-2 or so, but now I just tamp/mix the top with a wooden spoon, pressing down the grains and fat that has risen to the top and not disturbing the rest of the jar. If you shake the kefir too hard, it will sperate super fast into curd and whey and lose thickness.

Straining
-> There is some debate on straining immediately after fermentation or after it's sat in the fridge for a bit, and I prefer the latter. I've noticed my kefir ends up a lot thicker when I take it straight from fermentation into the fridge before straining out the grains, leaving it for a few days to thicken up. To do this, you'll need a decent amount of grains on a rotation, so you probably won't be able to do this at first if you want to keep a batch going all the time as you drink it.

-> At the very least after you make kefir, let it spend 24-48 hours in the fridge, with or without grains. It'll thicken up and improve the flavor.

Rules and tips
-> Never wash grains under water unless something is wrong and you want to start over with their culture, requiring more wake up batches to repopulate. Never use tap or well water, distilled only.

-> Avoid storing in plastic, only glass. Kefir is acidic and plastic alters the flavor in my experience, probably leaching microplastics.

-> Once you got your kefir artform down and you are making it on a schedule, you may have the chance to bank some kefir in the fridge to age for longer. Some of the literal best tasting kefir I've ever had, has been from a longer fridge ferment/aging time. Similar to dry aging meat to improve flavor, you can do the same with kefir. Some might find it gross, others love it. Worth experimenting and seeing if you like it. My favorite batch of kefir of all time was a 3 month age. It tasted like liquid parmesan cheese and was insanely umami and delicious.

I will be sharing affiliate links below for supplies if you want to support me, or you can buy most of them locally from the store. The only thing I 100% suggest getting is my link for the kefir grains. It's a really good lineage and everyone I've ever helped make kefir has started with this lineage with great success.

Feel free to DM me if you have any questions.
Affiliate links to supplies. Most of this you should buy at the store because it's cheaper. Only thing you might want to get from amazon is the mason jars with the attached lid for convenience, as well as the nylon mesh strain strainer and kefir grains. The wooden spoon, cheese cloth, 1QT mason jars, you can find easily locally for much cheaper.

->Cheese cloth



->Strainer (Nylon mesh, metal can alter flavor)



->Wooden spoon (again, no metal)



->Kefir grains



-> 1 QT mason jars (store grains)



-> 1/2 or 1 gal glass mason jars

Pick any of these


1/2 gal


1gal

Did you know that your toilet paper is filled inordinate amounts of PFAS forever chemicals?

These chemicals are found in soaps, clothes, packaging, carpets, tampons, soaps, shampoo, cleaning solutions, beds, chairs, literally everywhere, and they're also in your toilet paper that you wipe your ass with.

Considering we've known these chemicals are toxic and absurdly persistent in the body and environment, carcinogenic, horrible for the brain, and very disruptive to the endocrine system and fertility health for decades now (known intimately by both 3M and DuPont in their internal research very long ago), why in the hell is it still being used in so many products?

It's because they're trying to destroy your fertility and hormones, which results in men with low testosterone that are much easier to control and subjugate, and women who are unable to have children, among many other health issues.

We're all getting attacked by a death cult from every vector we can possibly imagine, so it'd be really cool if we could all unite on this again as a first principle, like we were getting close to having before recent conflicts, instead of arguing about which government is the moral authority in murdering people in war.


time.com/6259819/pfas-f…
pubs.acs.org/doi/abs/10.102…

We need to talk about psychiatric drugs being prescribed to babies, young children, and teenagers.

There are doctors and psychiatrists out there right now that are putting 1 year old babies on anti-depressants, benzos, and other crazy mind altering drugs that have the capacity to COMPLETELY destroy any future they might have and forever alter their brain chemistry, behavior, and perhaps even be causal in them becoming a school shooter or some other type of sociopath/psychopath that inflicts harm on others, or maybe even becomes a CEO one day and willfully poisons the environment to make a buck.

This clip is clearly showing child abuse in my opinion and it's bananas that the medical system has the authority to put your 4 year old on a psychiatric drug for any reason at all. These are key brain developmental moments and altering that process with these profoundly powerful drugs will most definitely change their future trajectory and perhaps even alter them negatively for life with no chance at recovery.

RFK is right about the connection to mass shooters and he should not be ridiculed or dismissed by anyone for wanting to investigate the connection adequately, especially knowing how inadequate and corrupt the FDA is at evaluating drug safety.

What if these drugs cause psychopathy, sociopathy, OCD, dysphoria, dissociation, or whatever other divergence later in life after taking as a kid? There are little to no studies on the long term effects of many of these drugs, especially on ages 0-17, and if there are any studies by the pharma industry, they certainly can't be trusted and should be required to provide raw data for independent analysis. You unfortunately will only get that data in a lawsuit via discovery otherwise, and we know the FDA isn't doing their due diligence or actually vetting the raw data for safety. They only look at what the pharma company presents them.

All the conditions these children are being hyper-medicated for can be directly caused by vaccine injuries as well, along with the abhorrent processed junk food diets parents are feeding their children. Mercury has been definitively shown to cause ADHD, ADD, tics, aggression, anxiety, OCD, and countless other symptoms that make pharmaceutical companies billions of dollars. This is why they are so aggressive about defending vaccination.

Vaccinations are basically future investments from pharma with huge upside potential from all the health problems that can arise from them, especially mental health related issues, which have become a huge part of their profit. We're having multiple epidemics at once between autism, depression, anxiety, autoimmune conditions, cancers, and so many other issues, and you can connect each one of those to a vaccine injury with clear biological plausibility with just aluminum and mercury toxicity, not to mention all these other ingredients like the surfactants, food stuffs, antimicrobials, and foreign DNA.

So here are some stats as of 2020 to give you an idea how pervasive this problem is, and how so many kids are drugged out of their mind right now. It's significantly worse after COVID as many of you already know. I wouldn't be surprised if it was at 10 million kids ages 0-17 on psychiatric drugs at this point. COVID mandates destroyed so many children's mental health
-------------------------------------------------------
Overall population size as of 2020
72 million children/teenagers in total from ages 0-17.
23 million ages 0 to 5.

Drug stats
6.1 million ages 0-17 are on psychiatric drugs. Half a million 5 and under. 85,000 1 year old babies.

3.1 million ages 0-17 are on ADHD drugs. 60k ages 5 and under. 310 1 year old babies.

2.1 million ages 0-17 are on antidepressants. 35k ages 5 and under. 7800 1 year old babies.

830k ages 0-17 are on antipsychotics. 30k ages 5 and under. 1,300 1 year old babies.

1.1 million ages 0-17 are on anti-anxiety drugs. 233k ages 5 and under. 60,000 1 year old babies.

800k ages 0-17 on mood stabilizers. 100k ages 5 and under. 21.5k 1 year old babies.
-----------------------------------------------------
The kid in this PBS clip was diagnosed with bipolar/ADHD/etc and put on an reckless cocktail of drugs at age 4.

Focalin Dexmethylphenidate twice a day - Similar to ritalin, an ADHD drug CNS stimulant. Insane to give to a 4 year old developing brain and he will be forever changed.

Clonadine to sleep at night, which is a crazy use of that drug on a child, given it's an antihypertensive.

Risperadol to "quiet his tantrums", which is an antipsychotic that chemically castrates your kid so he's passive and disassociated with himself, which is essentially a hypnotic state where they are more suggestive and willing to do as they're told.

I don't want to overly criticize the parents because they're just naive and listening to their doctor, someone they've been conditioned to trust, but when they said "if he didn't take it though, idk if we can function as a family. It's almost a do or die situation", that shows the true scale of desperation they feel and how they've been convinced by an authority that chemically castrating their child is the only solution. In reality there is so much more they could do beyond drugs, like putting him on a carnivorous ketogenic diet, figuring out if he has any metal toxicities from mercury or aluminum from vaccines or elsewhere, or some other nutritional deficiency.

Considering they show him only eating corndogs, gatorade, cookies, and goldfish, he is assuredly getting a lot of pesticides in his diet like atrazine and glyphosate, which are not helping his issues, nor are they giving him the nutrition he needs to function properly. If they changed his diet to a ton of red meat, eggs, raw dairy, raw honey, and some fruit, I would bet every dollar I have he would improve substantially and be able to ween off the drugs in time to maybe save his brain into adulthood.

The parents then describe how he becomes animalistic, violent, self harming, and every other symptom that can be definitively caused by mercury poisoning that is often seen in autism, along with becoming disassociated and repeating gibberish over and over, before the clip ends with their psychiatrist giving him more drugs and then outright admitting that he's just experimenting on that poor kid and doing what he was trained to do.

As we all know, his training and protocols came from pharmaceutical companies creating all these drugs in the first place, and then they attached those drugs to a diagnosis in the DSM-5 that he was taught to use as a bible in school. It's clearly just child abuse and human experimentation for profit under the guise of " medical treatment".

Pharma is destroying humanity and must be stopped.
Psychiatry is a predatory pseudoscience that destroys minds and captures souls.

It might be the worst field of "medicine" next to vaccinology, oncology, and nutrition.

This is what they give people in hospitals across the world when they can't eat and have to take IV "nutrition".

Soybean oil, rancid oxidized fish oil, purified egg phospholipids, glycerol, and even 25mcg of aluminum per liter, right into your veins. The combination of the aluminum with all these substances is most definitely going to facilitate some autoimmune disease, especially with the purified egg.

You know what's even more horrifying? This is allowed on all ages, including infants from birth to 2 months old. During the clinical trials from the original US approval in 2016, some pre-term infants died, with autopsy findings showing an accumulation of intravascular fat in the lungs.

When you investigate the studies looking into the adverse reaction profile and safety, they did the EXACT same thing they do in vaccine studies.

1 group gets the SMOFlipid injection, and then the comparator group gets just a soybean oil lipid emulsion with no other ingredients. If they compared the lipid emulsion IV to a simple bag of saline, it would be abundantly clear that it's causing inflammation, heart problems, anemia, vomiting, liver problems, diarrhea, and sepsis that they saw in the trials.

This is what people call modern medicine. It's the further thing from medicine and is just barbaric and homicidal, with it being predicated on fraudulent garbage science that is basically just advertising at this point to sell the product to the FDA for approval and then widespread use in hospitals.

Medical error is the 3rd leading cause of death in the US, and that is a very conservative estimate. When you fully factor in treatment protocols like this, in conjunction with how we treat heart disease, diabetes, cancer, etc, it's incredibly easy to understand that the US medical system is BY FAR the leading cause of death.

Welcome to Rockefeller medicine.


editor.fresenius-kabi.us/PIs/US-PH-Smof…
freseniuskabinutrition.com/wp-content/upl…

Regardless if this is genuine evidence of hydrogel being used or it's just an air bubble from improper preparation of slides, I want everyone reading this to ask themselves a very simple question with historical context and precedent in mind.

Is the government and military (like DARPA) capable of doing a secret advanced nano-tech experiments on the population against their will?

The obvious answer is yes, given we have an endless amount of examples of past human experimentation programs, like the St Louis experiment with cadmium sulfide, or Tuskegee, or countless others. They have admitted to a bunch of these experiments, but you HAVE TO KNOW that is just the tip of the iceberg and there are so many more experiments that you will never ever know about.

So with that, I want you to go read the document shown below and ask yourself the question. Could DARPA, who created the mRNA tech and funded Moderna/Biontech, have used the COVID vaccination program to test a new neurotechnology on a small portion of the people being injected?

Also...What was the magnetic phenomenon that literally thousands of people documented and experienced in the first initial round of vaccination? I felt this on someone with my own hands and that memory will be forever burned into my mind. One side of the neodymium magnet repelled, the other side attracted. You can't just ignore and forget this happened to people. I have hours and hours of footage of it.

I know this is a terrifying question to ponder, but you have to think about it seriously with the evidence already available and history/precedent in mind.
You have lived to see man-made horrors beyond comprehension, so now it's time to try and comprehend them without fear or immediate denialism. They are undeniably working on the technology, so now it's a question of if they are actually using it on people.

Here are some quotes from the DARPA doc to help you think about this seriously.
-----------------------------------------------
TECHNICAL AREA 1: NONINVASIVE NEURAL INTERFACE

>TA1 focuses on the ability to noninvasively record neural activity and stimulate neurons with high spatiotemporal resolution. The technologies in TA1 must only use external sensors and stimulators that do not breach the skin. Example technologies for TA1 may include ultrasound, photoacoustics, magnetic fields, electric fields, or radiofrequency. The final solution could also involve a combination of technologies.

>>>>>ultrasound, photoacoustics, magnetic fields, electric fields, or radiofrequency. The final solution could also involve a combination of technologies.

TECHNICAL AREA 2: MINUTELY INVASIVE NEURAL INTERFACE

>TA2 involves the development of a system that includes a nanotransducer placed on or near neurons of interest and an integrated sensor/stimulator device that sits outside the skin. The nanotransducer may include technologies such as, but not limited to, self-assembled/molecular/biomolecular/chemical nanoparticles, or viral vectors.

>These nanotransducers must be delivered in a minutely invasive (nonsurgical) manner, which may include ingestion, injection, or nasal administration, and involve technology that includes self-assembly inside the body. While the major TA2 goals of developing neural read out and write incapabilities are similar to the goals from TA1, creating a nanotransducer with an optimal delivery route to the brain is a major additional component.

>>>>> self assembled/molecular biomolecular/chemical nanoparticles, or viral vectors.

>>>>>must be delivered in a minutely invasive (nonsurgical) manner, which may include ingestion, injection, or nasal administration, and involve technology that includes self-assembly inside the body

https://twitter.com/VigilantFox/status/1706302447356936521

Full DARPA doc, along with a video of someone in the hospital surrounded by doctors and nurses, confirming objects are sticking to her injection site.

How can anyone watch this video and not at least be intrigued and curious how that is happening? What is the mechanism? Why do magnets stick on one side and repel on the other side? THESE ARE LEGITIMATE QUESTIONS. Calling people crazy for asking this legitimate questions is dishonest and bad faith. There is too much footage of the phenomenon and technology disclosed by DARPA to just dismiss the questions.



Conferences on this technology being studied and designed decades ago.



Dr James Giordano has done many lectures on this technology as well and the current publicly known capabilities, along with what's in the pipeline for further development. These are the real weapons of war, not nukes.




DARPA and the Brain Initiative



DARPA is Funding Nanoparticlees That Permeate Brain To Read Neural Signals



DARPA Wants Brain Interfaces for Able-Bodied Warfighters



The Government Is Serious About Creating Mind-Controlled Weapons



First real-time glimpse of nanoparticles self-assembling into crystals

NYC (and other major cities, like Sacramento) have an active and repetitive west nile mosquito control program where they drive through boroughs like Brooklyn and Queens, and they indiscriminately spray pesticides into the air from trucks on the street. You barely get a warning to go inside your home, and if you're on the street or have a window open, you are going to get doused with it.

There was a scheduled spraying last night in Brooklyn that several people on my feed have posted about, and there will be another tomorrow in Brooklyn and Queens.

I cannot believe that we allow health authorities to do this. Have we not learned our lesson from DDT spraying in the 40s/50s? This is absurd and will do absolutely nothing to prevent disease, and will likely cause more illness from the pesticide exposure, which I'm sure they'll blame on COVID.

This is also why everyone should invest in a high quality air purifier in their home. It's insane governments can just spray this shit on your street a few feet from your home without consent.

If you'd like to read up on the pesticides they are spraying into the air, here is a list. Links to the full schedule and pesticide safety sheets in comments.

Adulticide Products

Anvil 10 +10™

DeltaGard™

Duet™

Merus® 3.0

Larvicide Products

VectoBac

VectoLex

VectoMax

VectoPrime


Anvil 10+10 pesticide warnings...

HAZARDS TO HUMANS AND DOMESTIC ANIMALS

CAUTION. Harmful if absorbed through the skin. Avoid contact with skin, eyes and clothing. In case of contact, flush with plenty of water. Wash thoroughly with soap and water after handling and before eating, drinking, chewing gum, or using tobacco. Remove and wash contaminated clothing before reuse.nyc.gov/site/doh/healt…

COVID-19 Respiratory Management and Critical Care Reference Guide for 2020 - Ventilators, Ketamine, Fentanyl, Propofol, Midazolam, and other drugs.

Have you ever wondered what the full medical procedure guidelines were for putting someone on a ventilator during the COVID pandemic in 2020?

Look no further, as I have finally located the document in my archives that details the ENTIRE process, what drugs they give, and how they manage patients on the ventilator with various drugs such as fentanyl, ketamine, and the well known Midazolam, which was often lethal.

This is what the complete capture of medicine by pharmaceutical companies looks like. None of this has the wellbeing of the patient in mind. It's just pharma and medical companies trying to cram in as many drugs and procedures as possible to milk you and the insurance company for every penny, and to keep you in the hospital for as long as possible. Even worse, if this process kills you, they get paid an additional amount from the government via the CARES act.

This is why mortality was so high during the beginning of COVID in 2020.

Combine all these drugs being used to put you to sleep + ventilation + remdesivir = euthanasia.

Image 1: COVID-19 AIRWAY MANAGEMENT ALGORITHM

Image 2/3: UUED COVID-19 Intubation Plan

Image 4: CRITICAL CARE IN COVID-19






Full document here.

docdroid.net/paroK8H/uued-c…

Cult of the Medics - Chapter 1 of 8

This is one of the most impactful and eye opening documentary series ever made in my opinion. It's very long when all chapters are combined, but it's well worth the watch if you want help attaining a better understanding of the occult and esoteric roots of our medical system and the people behind it's inception.

People love to think that science is a separation of religion or spirituality, but that could not be further from the truth. Modern science was birthed in the occult, and still bathes in it in the shadows.

When you think about how vaccines are made, what is your first impression? Take the polio vaccine for example and think of it in the context of some witch in the forest concocting some brew.

First kill some monkeys, extract the kidney, chop up the kidney into small bits, and mix it with calf serum (blood from a fetus), and put it in a jar to rot at 37C for days.

After it's been fermented for long enough and the medium is exhausted, you then take blended/ground up nervous system and brain from a young child that "died from polio" as the "virus" sample, and mix it with the rotted kidney and calf blood.

It then decays for several more days, doing what they call "culturing" or "growing" the virus, before they filter it through multiple layers of ASBESTOS, and then injected into various animals for "safety testing".

Then they "inactivate" it by mixing that disgusting mix of death and rotted tissue from both monkeys, humans, and calf fetus, with formaldehyde for 2-3 days.

Then it's bottled and injected into human beings, including children.

If that isn't some death cult witchcraft occult ritual, I don't know what is.

Now watch this documentary series and learn the true nature of modern medicine. Cult of the Medics - Chapter 2 of 8

If you or your child is being pressured by your doctor, school, or whoever into getting a vaccine of any type, use this book as your weapon of defense and argumentation.

It's the magnum opus textbook on vaccines and autoimmunity that I think is severely underutilized and valued in the vaccine truth community. The amount of references you can garner from this one text is incredibly powerful for making your arguments for why vaccination is a horrible practice from the jump, and it's especially great in pleading your case to doctors to get medical exemptions for school or elsewhere.

In part 1 called "mosaic of autoimmunity", it discusses the role of adjuvants, experimental models used to justify the use of adjuvants, underlying mechanisms, ASIA syndromes from excessive exposure to adjuvants like aluminum, etc.

In part 2, it has studies on autoimmune conditions induced by specific vaccines, so if you or your kid already have a diagnosis of X autoimmune condition, you can use this book to argue for why you should get a medical exemption as vaccines can greatly exacerbate it.

In part 3, it goes really deep into the autoimmune conditions solicited by vaccination, like lupus, vasculitides, arthritis, connective tissue diseases, alopecia, aluminum biodistribution and biopersistence, thrombocytopenic purpura, type 1 diabetes, narcolepsy, celiac disease, encephalomyelitis, chronic fatigue, skin disorders, and several others.

It has the greatest detail on the mechanisms of harm possible with vaccines and will help you further understand how egregious and fraudulent it is to be using adjuvant laden cocktails as a "control/placebo", or even another vaccine that was deemed safe with the same reified fraudulent practices.

It's a must read. Links below.

Full book.



If you want to purchase the hardcover to wield at in-person discussions (affiliate link. it's expensive AF. Better off downloading and printing it off lol)

onlinelibrary.wiley.com/doi/book/10.10…
sci-hub.st/https://online…
amzn.to/3YU0D11

Watch Siri question Plotkin in regards to the Gardasil vaccine study where they used a substance called AAHS in the control group, which is an aluminum adjuvant. Siri gets him to admit it's not inert - meaning that the Gardasil vaccine, like every other vaccine, was not adequately safety tested before mass administration and it's recommendation to young girls, and now even young boys.

The best paper on this fraud is by Dr Peter Doshi titled "Adjuvant-containing control arms in pivotal quadrivalent human papillomavirus vaccine trials:
restoration of previously unpublished methodology" Links in comments below.

This paper assembled a cohort of five RCTs described as placebo controlled by Merck and others, and found that the control was reported as a placebo, when it was not. This control contained what's known as AAHS, amorphous aluminum hydroxyphosphate sulfate.

Across all these sources, it was reported as a placebo, and nor was it mentioned in any trial registry entry, but it was mentioned in the publications and clinical study reports. In 3 of those 5 trials, the consent forms that people signed described the control as an "inactive substance", which aluminum IS MOST DEFINITELY NOT, especially when injected.

3 trials said their reasoning for this as the control was "to preserve blinding and assess the safety of HPV virus-like particles as the ‘safety profile of (AAHS) is well characterized" - when it the trial is supposed to analyzing the safety of the vaccine as a whole in comparison to an inert placebo.

This is yet another example of how criminal corporations like Merck lie and intentionally manipulate their control groups to ensure that the pseudo=placebo groups have a similar adverse event rate as the vaccine group, so they can claim safety comparatively and get approval. It's just fraud, full stop. No debate.

The scale of harm was confirmed in a 2017 peer reviewed study that found evidence of numerous adverse events reported after these vaccines, with severe autoimmune conditions, permanent disabilities, many hospitalizations, and even some died. These trials were done on young teenage girls and of course Merck didn't attribute any of the deaths of severe adverse events to the vaccine, because they happened in the "placebo" too... UNREAL.

Meanwhile we have continual articles being pumped out by the pharma captured MSM right now denying that the HPV vaccine is harmful amid the massive swath of lawsuits, and even articles pushing for young boys to get the shots now too

Words cannot adequately describe just how criminally evil these corporations, news organizations, and government officials are allowing this to continue.

Saline is the only acceptable inert substance to discern the safety of a vaccine. No more adjuvant cocktails with aluminum, polysorbate, or any other toxin. No more vaccines as the control either.

IT HAS TO BE SALINE OR GTFO. Thank you to @AaronSiriSG @delbigtree @HighWireTalk @ICANdecide for all that you do and this illuminating deposition.

Here are the papers mentioned.

Adjuvant-containing control arms in pivotal quadrivalent human papillomavirus vaccine trials: restoration of previously unpublished methodology



Serious adverse events after HPV vaccination: a critical review of randomized trials and post-marketing case series



Aluminum adjuvants of vaccines injected into the muscle: Normal fate, pathology and associated disease



Amorphous Aluminum Hydroxyphosphate Sulfate (AAHS) from @ChildrensHD

"Studies have found 100% of the intramuscularly injected aluminum vaccine adjuvant is absorbed into the systemic circulation and travels to different sites in the body such as the brain, joints and the spleen where it accumulates and is retained for years post-vaccination."

Have you seen the NASA Future of War document?

This was a presentation from the Chief Scientist Dennis M Bushnell at the NASA Langley Research Center in 2001, where he discusses future strategic issues and future warfare, circa 2025. Langley....CIA?

Given we are just a couple years from this supposed date, what better time to share one of the most wild, terrifying, and ominous documents I've ever seen. What's more concerning is that a SPACE AGENCY, NASA, is producing such content like this. If you know the history of NASA, you'd know operation paperclip.

Isn't it weird how often everything ties back to the JFK assassination and operation paperclip? Almost as if it was a coup and the US merged with mad scientist lunatics for world domination.

For those of you who think it's fake, it was published directly on the DTIC military website, along with a schedule where it's referenced. The presentation from Bushnell was not video or audio recorded, but we have the slides. I'm sure if there was video or audio evidence, it would be one of the most horrifying lectures of all time.

The 4th Annual Testing and Training for Readiness Symposium & Exhibition: Emerging Challenges, Opportunities and Requirement



Future Strategic Issues/Future Warfare [Circa 2025]



The primary reason why I find this document so unsettling, is not only because it was given in 2001, but Bushnell from the jump tells you that it "is based in all cases upon existing, data/trends/analyses/technologies (e.g. NO PIXIE DUST)", meaning this is real technology the military already has, and it lists all the agencies that he had involved. See image 1. He's explicitly telling you that this stuff is REAL and the government/military and corporations are actively pushing for such a horrifying future.

In image 2, he talks about the need to "plan differently" now, because the world is in the process of a IT/Bio/Nano technological revolution, and we're advancing in scales of months instead of decades.

He then refers to "spaceship earth", where he lists the crew (humanity, the people, etc) as plundering the ship's supplies, tinkering with the temperature and life support controls, and INCREASING the size of the crew by 2 million per week. There is the population overgrowth narrative again...

As you get further into the document, it gets more and more horrifying. There is discussion of AI nanobot smart dust that is inhaled into the lungs, bores into lung tissue, and "executes various pathological missions". He calls it a wholly new class of weaponry which is legal. HOW IS THAT LEGAL?!?

He also discusses microwave weapons for behavioral control and altering brain function, the use of bioengineering fungi/prions/parasites and other substances as "fingerprintless" bio archipelago, like these are going to be the repertoire of death and war.

Here are some written excerpts. I'll upload some additional images in the comments below.

The first one I want you to see is what they consider "apparently legal" weapons ofo war.

What is Apparently “Legal”

• Microwave/RF Anti-Functional and AntiPersonnel Weaponry

• Chemical Anti-Functional Weaponry • Chemical “Psychological Effects” via Sensory Organs Weaponry (e.g. smell)

• Chemical Personnel Incapacitation Weaponry [“Non-Warfare” (e.g. Hostage/Terrorism) only]

• PSYWAR

• Acoustic Weaponry

• Mechanical Micro Dust

Humans Have “Taken Over” and Vastly Shortened “Evolution”
• Of the Planet
– Global Warming/Pollution/Deforestation
– Huge “Public Work” (e.g. 3 Gorges Dam)
• Of the Human Species
– Genomic Design and Repair
– “Mind Children” (Moravec)
• Products/Life Forms
– Cross Species Molecular Breeding
– “Directed Evolution” (Maxygen etc.)

U.S. “HUMAN BRAIN PROJECT”

• Begun in early 90’s, funded by 16 organizations across 5 agencies (NIH, NSF, DOD, NASA, DOE)

• AKA “Neuroinformatics” (intersection of neuroscience and informatics)

• “Exploding field;” 10,000 individual presentations at annual meeting of Society for Neuroscience (from molecular geneticists to cognitive psychologists)

• Determining detailed neuroanatomy of human brain (“digital brain atlas”) • Use of IT to study brain, use of brain info to aid IT/AI

Inexpensive Motivational Asynchronous Web-Based Distance Education Enables:

• Demise of the U.S. “underclasses”

• Wealth Creation from enabled “Invention” • Stabilization of World Population

• [Even More] Rapid Technology Diffusion • Equalization of “Haves” and “Havenots”

• Altered Political/military outlooks Worldwide - I.E. Changes “Everything”

The “Ultimate” Education Approach

- Plug and Play Direct Silicon (or other such) device connection to brain, (very rapid) uploads, Education in minutes instead of (many) years

Of Particular Concern
Uncontrolled/Uncontrollable SELF-REPLICATION Of
- Brilliant Robots (IT)
- Nano-Replicators (Nano)
- Rampant Recombinant Bio

(Sample) New(er) Sensors

• Lidar w/ 50% efficiency via S-C optical Amplifiers, Also Fempto-second Lasers

• Molec./Bio Sensors • Nanotags • Smart Card Sensors

• Sensors implanted during Manuf./Servicing

• Nano IR (10E-6 Sensitivity) • Smart Dust

Some Sensor “Swarms”

• SMART DUST
– Cubic mm or less
– Combined sensors, comms and power supply
– Floats in air currents

• NANOTAGS
– Placed on everything/everywhere
– Identification and Status Info

• Co-opted INSECTS

Micro Dust Weaponry

A Mechanical Analog to Bio, Micron sized mechanized “dust” which is distributed as an aerosol and inhaled into the lungs. Dust mechanically bores into lung tissue and executes various “Pathological Missions.”

A Wholly “New” class of Weaponry which is legal.

The first case of autism and the smallpox vaccine

Some credit Leo Kanner as being the first to describe what's known today as autism, back in 1943. The video shows the typical autistic symptoms with the head self harm, stimming, resistance to change, isolation, etc. This is the only clip I could find of Kanner anywhere, so if anyone has the BBC report this video was originally apart of, please share.

After doing some digging, I found a document written by Kanner that has a very interesting admission in it.



On page 9 and 10, it says the following.

"Richard was born on Nov 17th, 1937. Pregnancy and birth were normal. He sat up at 8 months and walked at 1 year. His mother began to train him at the age of 3 weeks, giving him a suppository every morning "so his bowels would move by the clock". The mother, in comparing her two children, recalled that while her younger child showed an anticipatory reaction to being picked up, Richard had not shown any physiognomic or postural sign of preparedness and had failed to adjust his body to being held by her or the nurse. Nutrition and physical growth proceeded satisfactorily.

Following smallpox vaccination at 12 months, he had an attack of diarrhea and fever, from which he recovered in somewhat less than a week"

This is where we have to learn about how the smallpox vaccines was made, and you can find that on the LSU doc on page 5/6/7.

This process is so horrific, barbaric, and completely insane, that I'm dumbfounded that ANYONE can look upon this time in history and think it's a good show for vaccination. None of this is science. It's disgusting levels of barbarism and it's no wonder so many people became ill in the late 1800s and early 1900s.

Let's review. I will be doing a SS article on this as well with more detail.




--------------------------------------------------------
Harvest:

The skin was rinsed with warm water, with or without soap, and the pulp was scraped from the skin with a curette, one form of which was made by sharpening the edge of a hemispherical stainless-steel spoon (Plate 7 .1 B) . If the animals were killed, exsanguination before scraping ensured a less blood-stained product; if they were not killed, they were usually anaesthetized before scraping. Harvests from individual animals were kept separately in sterile containers closed tightly enough to prevent drying by evaporation, and stored below 0 °C except when being processed.

Seed virus used for inoculation

With a procedure that had been in use in many countries for over a hundred years, and with no effort at international standardization, it was not surprising that the strains of virus employed for vaccination in different countries differed in their biological properties . The choice of a particular strain was arbitrary, being based on the history of the vaccine production laboratory concerned . An examination of the situation in 1967 showed that many different strains were then in use.

Since different strains of vaccinia virus vary considerably in their biological properties (see Chapter 2) and since the properties of the viral strain were probably important in determining the differences found in the rates of occurrence of postvaccinial encephalitis in different countries (see Table 7 .8), this was not a trivial matter. However, no steps were taken to recommend internationally which vaccinia strain should be used for vaccine production until after 1967, although some countries in which postvaccinial encephalitis had been a serious problem had changed their production to the less pathogenic Lister strain before this.

Preparation of Liquid Vaccine

Traditionally, the vaccine pulp was processed so as to remove some of the extraneous material and reduce the bacterial count, and it was then dispersed as a liquid suspension called vaccine lymph.

Clarification of the vaccine pulp

The semisolid pulp was usually ground into lymph by comminuting it in a grinder, or later by homogenization in a blending machine . For this purpose it was usually mixed with 40-60% glycerol. Storage of the glycerolated homogenate at low temperature over a period of months led to a steady fall in the number of viable bacteria, but it was later found that the same result could be more rapidly achieved by the addition of phenol (see below) . Periodically bacteriological tests were made to determine when the lymph was suitable for distribution.

Use of glycerol

The introduction of glycerol to "stabilize" the vaccine virus and at the same time prevent bacterial multiplication was regarded as a major step forward in lymph production . This procedure made it feasible to change from arm-to-arm vaccination or the use of an itinerant vaccinated cow (see Chapter 6, Plate 6.12) to the distribution of liquid vaccine in capillary tubes.

Glycerol had three advantages : it acted as an antibacterial preservative, it helped to make the vaccine stick to the skin, and it permitted the maintenance of the vaccine in liquid form at -10 ° C and thereby ensured the long survival of active vaccinia virus.

Use of phenol - Insanely toxic

The bacterial count in glycerolated pulp stored in the refrigerator fell off very slowly . Several months were usually required before it was low enough to allow the vaccine to be issued for use, and repeated testing was necessary during this period . The procedure could be greatly accelerated by adding phenol to a final concentration of 0.5%, a procedure originally recommended by Gins (1924) and Lehmann (1937) and popularized by McClean (1949), whose protocol was as follows : Material harvested from the sheep was ground with twice its weight of a 1 % solution of phenol in distilled water . After this had stood at 22 °C for 48 hours, glycerol, equal in amount to the phenol solution, was added, so that the final concentration of phenol was 0 .4%.

Continuing in comments below. Development of Freeze-dried Smallpox Vaccine

"In my field experiments I compared the stabilities of the glycerinated and lanolinated vaccines in current production ; although the latter was the more stable at 22 °C, it completely lost its potency within a month at 37 ° C. I then tried Otten's method of drying crude vaccine from the liquid state over sulphuric acid ; vaccine made in this way was widely used in Indonesia and some batches had survived at ambient temperatures for remarkably long periods. There was however considerable batch-to-batch variation, a finding that I confirmed ; furthermore, the bulk dried vaccine was cumbersome to handle and distribute into ampoules.

"Without further ado I then started to explore the possibilities of drying from the frozen state, using a large centrifugal dryer of the type that had recently been invented by R . Greaves at Cambridge . This machine was made in the Institute's workshops and although primitive in appearance, it worked very well ; the main difficulty was the making of vacuum-tight seals, at that time rather more of an art than a science.

"After much experimentation, a satisfactory method was devised for purifying animal vaccine and freeze-drying it after adding peptone to a concentration of 5 % . Vaccine thus prepared consistently maintained its original potency for at least three months at 37 'C ; in later experiments, batches stored at the high temperature of 45 °C still gave 100% successful primary vaccination after four years . The criterion for the permissible minimum content of vaccinia virus was fixed by determining the amount of virus needed to achieve 100% successful vaccinations ; the final step in the development stage was the devising of a simple and safe method for reconstituting the dried vaccine in the field . It then remained only to scale up all the processes to a point at which full production could begin ; this was accomplished by 1953/"

1999 Hep B Vaccine House Reform Committee Testimony.

Part 1. Part 2

So I've resisted using chat GPT because I feel like we're all just training Skynet to eventually murder us all and take our jobs, but I became curious what it's response would be to some questions on vaccines and aluminum adjuvants, so I signed up.

Here is the first response to… https://t.co/HlUvQsBwLVtwitter.com/i/web/status/1…
Second question.

"Are there any studies on the safety of injected aluminum into infants?"

This is a verifiable lie and the NIH provided no such studies when asked upon request via FOIA. This has also been requested in court, and they were unable to provide studies either.… twitter.com/i/web/status/1…