Ukraine Crime List

The Ship Which Never Sunk - Titanic

Facts:

Was the Titanic deliberately sunk by JP Morgan?
The Titanic Conspiracy | The Ship That Never Sank
Titanic Conspiracy is REAL 2021 .. Titanic Never Sank Conspiracy Theory
Olympic’s name on Titanic wreck
Did Titanic Really Sink? | British Pathé

Portholes:

1 – Proponents of the swap theory have pointed out disparities in the number of portholes on the ships. The Olympic had 16 and the Titanic had 14.

2 – Photographs taken of the Titanic in dry dock show it with 14 portholes. But by the time of its doomed maiden voyage it now had 16, just like the Olympic.

3 – Was this evidence that the ships had been swapped or just that they had added two extra portholes as part of aesthetic changes to the Titanic?

Covid-19 masks are a crime against Humanity and child abuse. The following is a transcript of the highlights (by Henna Maria) from Dr. Margarite Griesz-Brisson’s recent extremely pressing video message, that was translated on-air from German into English by Claudia Stauber. Video at the end of the transcript.

Dr. Margarite Griesz-Brisson MD, PhD is a Consultant Neurologist and Neurophysiologist with a PhD in Pharmacology, with special interest in neurotoxicology, environmental medicine, neuroregeneration and neuroplasticity. This is what she has to say about masks and their effects on our brains:

The rebreathing of our exhaled air will without a doubt create oxygen deficiency and a flooding of carbon dioxide. We know that the human brain is very sensitive to oxygen deprivation. There are nerve cells for example in the hippocampus, that can’t be longer than 3 minutes without oxygen – they cannot survive. The acute warning symptoms are headaches, drowsiness, dizziness, issues in concentration, slowing down of the reaction time – reactions of the cognitive system.

However, when you have chronic oxygen deprivation, all of those symptoms disappear, because you get used to it. But your efficiency will remain impaired and the undersupply of oxygen in your brain continues to progress.

We know that neurodegenerative diseases take years to decades to develop. If today you forget your phone number, the breakdown in your brain would have already started 20 or 30 years ago.

While you’re thinking, that you have gotten used to wearing your mask and rebreathing your own exhaled air, the degenerative processes in your brain are getting amplified as your oxygen deprivation continues.

The second problem is that the nerve cells in your brain are unable to divide themselves normally. So in case our governments will generously allow as to get rid of the masks and go back to breathing oxygen freely again in a few months, the lost nerve cells will no longer be regenerated. What is gone is gone.

[..]I do not wear a mask, I need my brain to think. I want to have a clear head when I deal with my patients, and not be in a carbon dioxide induced anesthesia.

[..]There is no unfounded medical exemption from face masks because oxygen deprivation is dangerous for every single brain. It must be the free decision of every human being whether they want to wear a mask that is absolutely ineffective to protect themselves from a virus.

For children and adolescents, masks are an absolute no-no. Children and adolescents have an extremely active and adaptive immune system and they need a constant interaction with the microbiome of the Earth. Their brain is also incredibly active, as it is has so much to learn. The child’s brain, or the youth’s brain is thirsting for oxygen. The more metabolically active the organ is, the more oxygen it requires. In children and adolescents every organ is metabolically active.

To deprive a child’s or an adolescent’s brain from oxygen, or to restrict it in any way, is not only dangerous to their health, it is absolutely criminal. Oxygen deficiency inhibits the development of the brain, and the damage that has taken place as a result CANNOT be reversed.

Photo – Brain Damage from Lack of Oxygen

The child needs the brain to learn, and the brain needs oxygen to function. We don’t need a clinical study for that. This is simple, indisputable physiology. Conscious and purposely induced oxygen deficiency is an absolutely deliberate health hazard, and an absolute medical contraindication.

An absolute medical contraindication in medicine means that this drug, this therapy, this method or measure should not be used – is not allowed to be used. To coerce an entire population to use an absolute medical contraindication by force, there must be definite and serious reasons for this, and the reasons must be presented to competent interdisciplinary and independent bodies to be verified and authorized.

When in ten years, dementia is going to increase exponentially, and the younger generations couldn’t reach their god-given potential, it won’t help to say “we didn’t need the masks”.

[..]How can a veterinarian, a software distributer, a business man, an electrical car manufacturer and a physicist decided on matters regarding the health of the entire population? Please dear colleagues, we all have to wake up.

I know how damaging oxygen deprivation is for the brain, cardiologist knows it for the heart, the pulmonologist knows it for the lungs. Oxygen deprivation damages every single organ.

Where are our health departments, our health insurance, our medical associations? It would have been their duty to be vehemently against the lockdown and to stop it and stop it from the very beginning.

Why do the medical boards give punishments to doctors who give people exemptions? Does the person or the doctor seriously have to prove that oxygen deprivation harms people? What kind of medicine are our doctors and medical associations representing?

Who is responsible for this crime? The ones who want to enforce it? The ones who let it happen and play along, or the ones who don’t prevent it?[..]It’s not about masks, it’s not about viruses, it’s certainly not about your health. It is about much much more. I am not participating. I am not afraid.
[..]You can notice, they are already taking our air to breathe.

The imperative of the hour is personal responsibility.

We are responsible for what we think, not the media. We are responsible for what we do, not our superiors. We are responsible for our health, not the World Health Organization. And we are responsible for what happens in our country, not the government.” source

Brain Damage From Masks CANNOT BE REVERSED

Who Is Dr. Tedros?

Scott Ritter

William Scott Ritter Jr. (born July 15, 1961) is a former United States Marine Corps intelligence officer who served with the United Nations implementing arms control treaties, with General Norman Schwarzkopf in the Persian Gulf during Operation Desert Storm, and in Iraq, overseeing the disarmament of weapons of mass destruction (WMD), as a United Nations weapons inspector, from 1991 to 1998. He later became a critic of United States foreign policy in the Middle East.

Ritter resigned from the United Nations Special Commission (UNSCOM) on August 26, 1998. He had said that the Commission was undermined by infiltration from the CIA and lack of support from Washington and the UN Security Council. At the time of his resignation, he stated the international community was not assertive enough in disarming Saddam Hussein, who he said was obstructing the inspections.^[1]^[2]^[3] In 2000, Ritter stated that Iraq possessed no significant WMD capabilities. The New York Times reported that Ritter was “the loudest and most credible skeptic of the Bush administration‘s contention that Hussein was hiding weapons of mass destruction.”^[2]

Matthew

The Impact of Sanctions

When asked on US television if she [Madeline Albright, US Secretary of State] thought that the death of half a million Iraqi children [from sanctions in Iraq] was a price worth paying, Albright replied: This is a very hard choice, but we think the price is worth it.

John Pilger, Squeezed to Death, Guardian, March 4, 2000

In the 20-year-long Afghanistan war, the US has committed horrible war crimes in the country. But Washington and the Pentagon usually refuse to acknowledge them, and try to cover up the truth. It also shields criminals and deals with them leniently. This is done even when the evidence of wrongdoing is staring them in the face. The US also imposed sanctions on the International Criminal Court (ICC), which started an investigation into US war atrocities in Afghanistan. Washington has shown zero sincerity to reflect upon the crimes it committed against the Afghan people.

In November 2020, a war crimes inquiry found that there was “credible information” to prove that the Australian Special Forces in Afghanistan had unlawfully killed 39 civilians and detainees and cruelly treated two persons. This sparked global outrage. The Afghanistan Independent Human Rights Commission later called on other nations, especially the US and the UK, to also open inquiries to investigate possible unlawful killings by their forces in Afghanistan. Neither the US nor the UK has made moves in this direction. But it’s widely believed that if a systematic investigation is carried out into US forces, the results would be more appalling and horrible.

The Costs of War project by Brown University estimates that over 46,000 Afghan civilians lost their lives during the longest war in US history. The errant drone strike on August 29 wasn’t the first time Afghan civilians have been killed in drone strikes under the broad banner of the war on terror. Data published in May by Action on Armed Violence (AOAV), a London-based charity, showed that 3,977 casualties were caused by US-led airstrikes between 2016 and 2020. Among them, 1,598 were children. ref

Ordinary Afghans say it had happened to them many times, most of which, however, had not been reported. Innocent Afghans might simply be on their way to carry water, graze cattle or collect wood when the drones strike.

In 2010, it was also reported that 12 American soldiers based in Kandahar province in southern Afghanistan formed a secret “kill team” that allegedly blew up and shot Afghan civilians at random and collected their fingers as trophies.

Besides civilian killings, there are also many allegations over the US forces’ torture, mistreatment and killings of prisoners in Afghanistan. In 2016, in response to a Freedom of Information Act lawsuit filed more than a decade ago by the American Civil Liberties Union, the US Defense Department had to release nearly 200 photographs related to prisoner abuse at US military facilities in Iraq and Afghanistan. The photos were a part of a larger set of 2,000.

The Jews Are Responsible For All the Wars In The World

The Swastika

The swastika is one of the most recognizable symbols in India, and is a part of the Indian culture in Hinduism, Buddhism and Jainism, representing an ancient Sanskrit word meaning “well being.” The hooked cross symbol of the swastika has a rich history, dating back thousands of years. But, it was only this past century that the symbol grew a completely different meaning and became the symbol of suppression and inhuman extermination.

The first use of the hooked cross was on ivory sculptures from 10,000 BCE.

From everything including advertising, design and even hockey jerseys, the swastika was soon becoming a popular design among anyone and everyone. In fact, American military units used the symbol as part of their uniform in the First World War and RAF planes had the symbol painted on them as late as 1939. source

The comparison of swastikas:

The Garden of Eden and Nephilim Giants

The Nephilim (Hebrew: נְפִילִים‎, Nefilim) were a race that came to dominate the antediluvian (pre-flood) world, and are referred to in the Bible as the heroes of old, men of renown. They were reportedly the children born to the “Sons of God” by the “daughters of men”, and are described as giants. It is also most important to note that they are mentioned almost simultaneous to God’s statement that He would destroy the earth by flood, and it seems from this association that their effect upon mankind was one of the primary justifications that brought the destruction.

“Nephilim” is rendered fallen, or possibly feller: a tyrant or bully. Several English translations, such as the King James Version rendered the word “giants”. In the Greek Septuagint, the word “Nephilim” was also translated as “Gigantes” (gigantic). This translation is undoubtedly used because the Nephilim later became known as giants to the ancient Hebrews, as illustrated by the manner in which they were referenced when the Israelite spies were sent into Canaan (Numbers 13:33 ) source

COVID Card - MoveOn

Project Veritas

NUREMBERG 2.0 / COVID-19 and Vaccines

Dr Reiner Fuellmich is the public frontman for an international team comprised of hundreds lawyers and medical experts, who have begun legal proceedings over the CDC, the WHO, and the Davos group for committing crimes against humanity.

The protocol for the PCR test given by the WHO and the CDC was knowingly set to a level that guaranteed 100% false positives or false negatives.

So there is no pandemic.

This is all about getting people to take the shot. Their argument is that we are at the very least being subjected to an illegal experiment. And at the worst, global genocide.

Dr Fuellmich points out how the experimental jab is in clear violation of all ten of the Nuremberg Codes, which carry the penalty of death for those who violate them.

Number 1: Voluntary consent is absolutely essential. There should be no intervention or any element of force, fraud, deceit, duress, overreaching, or other ulterior form of constraint or coercion.

By definition, a vaccine must provide immunity to the virus, protect recipients from getting the virus, reduce deaths, infections, circulation and transmission of the virus.

We are told the experimental jab does none of these, yet they fraudulently call it a “vaccine”. As far as duress, restraint and coercion, it’s everywhere: If you want your life back, get the shot.

Number 2: The experiment should be such as to yield fruitful results unprocurable by other methods. The most fruitful method would be a healthy immune system, which can be achieved through good health and natural supplements, such as Vitamin D and Vitamin C and Zinc but the people are not being told this. In fact, those that point it out are being vilified and silenced.

Number 3: The experiment should be designed and based on the results of animal experimentation. This experimental jab skipped animal testing.

Number 4: The experiment should be so conducted as to avoid all unnecessary physical and mental suffering and injury. According to official reports, there are already thousands of deaths and over a quarter of a million injuries from this experiment.

Number 5: No experiment should be conducted where there is an a priori reason to believe that death or disabling injury will occur. Past trials have shown a strong possibility that these new spike proteins will cause a body to attack itself. This is known as Antibody Dependent Enhancement (ADE) and recent doctors have blown the whistle that this could end up killing everybody who’s been vaccinated in the next two years.

Number 6: The risk to be taken should never exceed the benefit. COVID-19 has a 98-99% survival rate, less deadly than the seasonal flu. The experimental jab is already the most dangerous vaccine in VAERS’ 30-year history.

Number 7: Proper preparations should be made and adequate facilities provided to protect the experimental subject against even remote possibilities of injury, disability, or death. There were no preparations made. There are no facilities. The subject shows up for their shot and goes home.

Number 8: The experiment should be conducted only by scientifically-qualified persons. This experiment has been exclusively run by politicians, the media, celebrities and Big Pharma bureaucrats.

Number 9: The subject should be at liberty to bring the experiment to an end. Thousands of medical experts have attempted to end this madness and their voices continue to be silenced.

Number 10: The experiment must be brought to an end, if resulting in injury or death.

source

Project: Storm Clouds Gathering

How the Revolution Begins – Final Messages – Part 2 (Supply Crunch)

The shortages and supply chain collapse that reared their head in 2021 escalate in 2022. This is a logistical certainty. The chain reaction set off by the mandates is just beginning.

The corporate media and the politicians don’t want to talk about the blockades by port workers and truckers or the rebellion brewing among the military and frontline workers. They don’t want you to think about the implications of firing millions of people at the same time. Sending families with children into poverty, while simultaneously withdrawing social safety nets for the non-compliant. Doing so would make it obvious that that the tragedy that about to unfold was neither unforeseen nor accidental.

The Patriarch’s statement all across Russia at the end of Sunday morning service

The Patriarch’s statement was required to be read out in churches all across Russia at the end of Sunday morning service.

TRANSCRIPT

This is the self-perception of the leaders of the world, who have tremendous power, who run entire governments.

They are planning to wipe out most of humanity, 6 billion people, to leave only a small part of us, but not only that.

They are planning and are only held back by the current limits of science to violate man himself, to desecrate the innermost part of man, the image of God within us, and to destroy that image, in order to turn human beings into a cross between a biological, technical and digital being.

They call this “post-human”, they call it “convergence”.

These world leaders are marching under the banner of transhumanism and posthumanism.

What Are Clinical Trials

Explaining Vaccine Clinical Trial Phases (version 1) by Medical Xpress

Clinical trials are conducted in phases, each with slightly different objectives and increasing numbers of volunteers. This is primarily to ensure subject safety but also to make sure the process is as cost-effective as possible. The data from each phase is thoroughly reviewed and must show both safety as well as the desired effect before progressing from one phase to the next. While most vaccine studies are relatively long clinical trials, often around six to 12 months, safety and efficacy can often be established earlier than the end of the study. The later assessments are then used to demonstrate how long the protection from the vaccine is likely to last.

Pre-clinical

Before a vaccine is considered for human trials, it has to have robust data from laboratory and animal studies to make the investigators, as well as an independent ethics committee, confident it is very likely to be both safe, as well as effective. Once this is the case, it can move to phase 1 trials in humans.

Phase 1

Phase 1 trials are relatively small trials, usually around 100 volunteers, with the primary objective of confirming the safety already strongly expected from animal studies. Generally, blood tests are collected from the volunteers for testing of the vaccine’s efficacy in the laboratory. This gives an indication of whether the vaccine has generated an immune response that is likely to be useful but doesn’t guarantee it is going to work. Often multiple doses are used to try and find the ideal dose to take forward in later phase trials. Phase 1 trials are often conducted in a relatively narrow age range of healthy subjects with no comorbidities to reduce the prospect of confounders (something that would influence the result) and to ensure safety.

Phase 2

Phase 2 trials are still mostly focused on safety but now include a greater number of subjects, often in the order of 1000 to 2000. Laboratory studies of effectiveness are also conducted in phase 2 but actual protection from the pathogen in question starts to be looked at. A slightly more diverse population can sometimes be considered for enrolment, such as a broader age range, to begin to more closely resemble the actual target population. While giving the first look at actual protection, these studies are usually not large enough for us to confirm the vaccine actually does what it needs to do, and that is to protect people from the infection it’s designed to provide protection from. This is where the phase 3 trials come in.

Phase 3

Phase 3 trials are the pivotal final trials before a vaccine is approved for widespread use. While safety remains a focus, these trials are primarily about showing that people that have received the vaccine have significantly lower rates of actual infection than those that have not. To show this typically requires large numbers of volunteers, in the order of 10’s of thousands, depending however on many factors including how widespread the infection is that the vaccine is designed to protect from. While vaccines can fail to show sufficient effect and therefore fail to progress through any phase, it is the failure to provide sufficient protection in phase 3 studies where a number of potential vaccine candidates prove unsuccessful.

Phase 4

Once a vaccine is in widespread use, data collection on its safety, as well as how well it is working, continues to be collected in what is known as phase 4.

Length of clinical trials (also redefined to change publics’ concent)

While typically clinical trials take many years, this is largely because of the cost of each step. Therefore, the time and money for each phase is not invested until the prior phase is complete and has demonstrated the desired safety and efficacy.

In the case of COVID-19, we have been fortunate to see sufficient investment that has enabled planning for all phases of clinical trials to take place at the beginning, allowing the next phase of clinical trials to commence quickly, so as soon as the data from the previous phase supports it. This has meant that we are seeing vaccine development happen at a rate much faster than ever before without compromising at all on any of the usual processes required to be certain about the vaccine‘s safety, as well as how well it is likely to work.

“Usually it takes 8 to 10 years to conduct a robust set of clinical trials before approving a vaccine. This does beg the question of how COVID-19 vaccine developers will combine the phases of the trials to deliver a vaccine to the population in record time. We will have to watch this space!”

see article right

source

What Are the Phases of a Vaccine Trial? (version 2) Students 4 Best Evidence

Posted Sept. 23, 2020 by Cathey Saha

In the midst of the COVID-19 pandemic, everyone has a vested interest in the development of a SARS-CoV2 vaccine that can successfully protect the population and prevent further deaths from occurring. The herd immunity of a vaccinated population would ideally allow our society to somewhat return to our pre-pandemic lifestyles, even with the pathogen existing in our environment. Although we are eagerly anticipating its creation, and many companies are racing to be the first to produce and distribute it globally, a vaccine has to first display a safe pharmacological profile, show efficacy in humans, and importantly, have benefits that outweigh the risks before it can receive approval from drug regulatory bodies.

Initially, preclinical research and development is carried out in the laboratory using in vitro techniques or, if necessary, in vivo techniques in animals. Animal models can be given the vaccine to see if an immune response is produced. If the data from preclinical research shows promise, it is then used to justify subsequent clinical studies in humans.

Phase I Clinical Trial

Phase I clinical trials occur in a small group of healthy adult individuals, approximately 20-100 to evaluate safety. They answer the following questions;

* Is this vaccine safe?
* Does the vaccine seem to work? Does it produce an immune response?
* Are there any serious side effects?
* How is the size of the dose related to the side effects?

Phase II Clinical Trial

Phase II clinical trials study the intervention in a larger group of people (several hundred), stratified by age, to determine efficacy and to further evaluate its safety. They answer the following questions;

- * What are the most common short-term side effects?

* How are the volunteers’ immune system responding to the vaccine?

Phase III Clinical Trial

Phase III studies study the safety and efficacy of the intervention in large groups of trial participants (from several hundred to several thousand) over time. They answer the following questions;

* How do people who get the vaccine and people who do not get the vaccine compare?
* Is the vaccine safe?
* Is the vaccine effective?
* What are the most common side effects?

The regulators will then review the trial results and determine whether to approve the vaccine or not.

Phase IV Clinical Trial

Drug companies may decide to conduct Phase IV trials after a vaccine is released. The manufacturer can continue to test the vaccine for safety, efficacy, and other potential uses. In the case of COVID-19, it may be necessary given the variability in the widespread population taking the vaccine.

Therefore, it is clear that each stage of the trial provides important information regarding whether the vaccine works in individuals, and whether there are side effects. Usually it takes 8 to 10 years to conduct a robust set of clinical trials before approving a vaccine. This does beg the question of how COVID-19 vaccine developers will combine the phases of the trials to deliver a vaccine to the population in record time. We will have to watch this space!

Source: Student 4 Best Evidence

I’m a Clinical Lab Scientist, COVID-19 Is Fake, Wake Up America

**** Warning, after unsuccessful searches lately on the DR Dereck Knauss identity, it is possible that the links have been removed to discredit the Dr. or simply that he does not exist. Dr. Michel Chossudovsky is a real doctor, so the 2nd part is verified and verifiable.****

The following statements by Dr. Derick Knauss on the identity of the virus and on the failures of the PCR test are corroborated by numerous scientific studies including the WHO. See the text by Prof. Michel Chossudovsky at the foot of Dr. Knauss’ article

I have a PhD in virology and immunology. I’m a clinical lab scientist and have tested 1500 “supposed” positive Covid 19 samples collected here in S. California. When my lab team and I did the testing through Koch’s postulates and observation under a SEM (scanning electron microscope), we found NO Covid in any of the 1500 samples.

What we found was that all of the 1500 samples were mostly Influenza A and some were influenza B, but not a single case of Covid, and we did not use the B.S. PCR test.

We then sent the remainder of the samples to Stanford, Cornell, and a few of the University of California labs and they found the same results as we did, NO COVID. They found influenza A and B. All of us then spoke to the CDC and asked for viable samples of COVID, which CDC said they could not provide as they did not have any samples. We have now come to the firm conclusion through all our research and lab work, that the COVID 19 was imaginary and fictitious.

The flu was called Covid and most of the 225,000 dead were dead through co-morbidities such as heart disease, cancer, diabetes, emphysema etc. and they then got the flu which further weakened their immune system and they died.

I have yet to find a single viable sample of Covid 19 to work with. We at the 7 universities that did the lab tests on these 1500 samples are now suing the CDC for Covid 19 fraud. the CDC has yet to send us a single viable, isolated and purifed sample of Covid 19. If they can’t or won’t send us a viable sample,

I say there is no Covid 19, it is fictitious. The four research papers that do describe the genomic extracts of the Covid 19 virus never were successful in isolating and purifying the samples. All the four papers written on Covid 19 only describe small bits of RNA which were only 37 to 40 base pairs long which is NOT A VIRUS. A viral genome is typically 30,000 to 40,000 base pairs.

With as bad as Covid is supposed to be all over the place, how come no one in any lab world wide has ever isolated and purified this virus in its entirety? That’s because they’ve never really found the virus, all they’ve ever found was small pieces of RNA which were never identified as the virus anyway.

So what we’re dealing with is just another flu strain like every year, COVID 19 does not exist and is fictitious. I believe China and the globalists orchestrated this COVID hoax (the flu disguised as a novel virus) to bring in global tyranny and a worldwide police totalitarian surveillance state, and this plot included massive election fraud to overthrow Trump.

Dr. Derek Knauss is a clinical lab specialist focussing on virology and immunology. He is based in Southern California. read from source

Vaccine Attorney List

CA: CALIFORNIA

Brian Lee Burchett
Burchett Law Firm
605 C Street
Suite 300
San Diego, CA 92101
(619) 230-8431

Neal Jordan Fialkow
Neal Fialkow Esq
215 North Marengo Avenue
3rd Floor
Pasadena, CA 91101
(626) 584-6060

Marvin Firestone
Marvin Firestone, MD, JD and Associates
1700 South El Camino Real
Suite 408
San Mateo, CA 94402
(650) 212-4900

Michael Avrim Firestone
Marvin Firestone, MD, JD and Associates
1700 South El Camino Real
Suite 408
San Mateo, CA 94402
(650) 212-4900

William I. Goldsmith
Goldsmith & Hull, APC
16933 Parthenia Street
No. 110
Northridge, CA 91343
(818) 990-6600

Paul Adrian Green
Law Office of Paul Green
1055 East Colorado boulevard
5th Floor
Pasadena, CA 91106
626-381-9893

Anthony A. Liberatore
A. LIBERATORE, P.C.
100 Wilshire Blvd., Suite 700
Santa Monica, CA 90401
424-285-8550

Lawrence Steven Paikoff
Law Offices of Lawrence S. Paikoff, M.D., J.D.
1756 Picasso Avenue
Suite F
Davis, CA 95618
(530) 297-1144

Jeffrey S. Pop
Jeffrey S. Pop & Associates
9150 Wilshire Boulevard
Suite 241
Beverly Hills, CA 90212-3429
(310) 273-5462

Lisa Annette Roquemore
Law Office of Lisa A. Roquemore
30021 Tomas Street
Suite 300
Rancho Santa Margarita, CA 92688-2128
(949) 622-5572

Gerald Edwin Rush
Rush Law and Consulting, APC
333 S. Grand Avenue
Suite 3310
Los Angeles, CA 90071
(213) 232-1620

John Leonard Shipley
937 Woodbury Lane
Davis, CA 95616
(415) 235-9310

DC: DISTRICT OF COLUMBIA

Elizabeth Kyla Abramson
Maglio Christopher & Toale, P.A.
1015 15th Street, NW
Suite 1125
Washington, DC 20005
888-952-5242

Leah VaSahnja Durant
Law Offices of Leah V. Durant, PLLC
1717 K Street, NW
Suite 900
Washington, DC 20006
(202) 775-9200

Renee J. Gentry
Vaccine Injury Clinic, George Washington Univ. Law School
2000 G Street, NW
Washington, DC 20052
(202) 994-8161

Renee Ja Gentry
The Law Office of Renee J. Gentry
2020 Pennsylvania Ave., NW
Suite 164
Washington, DC 20006
(202) 505-6435

Michael Patrick Milmoe
Law Offices of Leah V. Durant, PLLC
1717 K Street, NW
Suite 900
Washington, DC 20006
(202) 775-9200

LeeAnne Pedrick
Maglio, Christopher, & Toale PA
1015 15th St. NW
Suite 1125
Washington, DC 20005
888-952-5242

Joseph Alexander Vuckovich
Maglio Christopher & Toale, P.A.
1015 15th Street, NW
Suite 1125
Washington, DC 20005
888-952-5242

FL: FLORIDA

Robert Hanreck
Robert J. Hanreck, P.A.
44 West Flagler Street
Suite 1775
Miami, FL 33130
786-539-4935

Alison H. Haskins
Maglio Christopher and Toale, PA (FL)
1605 Main Street
Suite 710
Sarasota, FL 34236
(888) 952-5242

Erin Adele Juzapavicus
Milam Howard Nicandri Dees & Gillam, P.A.
14 East Bay Street
Jacksonville, FL 32202
(904) 357-3660

Daniel James Leeper
Leeper & Leeper
2532 Fifth Avenue North
St. Petersburg, FL 33713
(727) 328-8788

Altom M. Maglio
Maglio Christopher and Toale
1605 Main Street
Suite 710
Sarasota, FL 34236
(888) 952-5242

Jennifer Anne Gore Maglio
Maglio Christopher and Toale, PA (FL)
1605 Main Street
Suite 710
Sarasota, FL 34236
(888) 952-5242

William Richard McBride
McBride Scicchitano & Leacox, PA
800 N. Magnolia Avenue
Suite 1800
Orlando, FL 32803
(800) 336-6000

Kyle Monroe Moore
Law Office of Kyle Moore
5901 17th Ave N
St. Petersburg, FL 33710
678-316-7318

Diana Lynn Stadelnikas
Maglio Christopher and Toale, PA (FL)
1605 Main Street
Suite 710
Sarasota, FL 34236
(888) 952-5242

Anne Carrion Toale
Maglio Christopher and Toale
1605 Main Street
Suite 710
Sarasota, FL 34236
(941) 952-5242

Joshua Aaron Whisler
The Whisler Law Firm
7777 Glades Road
Suite 100
Boca Raton, FL 33434
(561) 708-0513

GA: GEORGIA

Julius Vincent Cook
Cook & Tolley LLP
P.O. Box 1927
Athens, GA 30603-1927
(706) 549-6111

Susan M. Cremer
Law Offices of Michael Lawson Neff, PC
945 East Paces Ferry Road
Suite 1770
Atlanta, GA 30326
(404) 531-9700

Donald Philip Edwards
Edwards & Hawkins, LLC.
50 Hurt Plaza SE
Ste 910
Atlanta, GA 30303
404-526-8866

Caryn Suzanne Fennell
Caryn S. Fennell, P.C.
2230 Towne Lake Parkway
Building 600, Suite 140
Woodstock, GA 30189
(770) 479-0248

Nathan Pate Powell
Webb, Tanner & Powell, P.C.
P.O. Box 1390
Lawrenceville, GA 30046
(770) 962-0100

David Gregory Rogers
Rogers, Hofrichter & Karrh, LLC
225 S. Glynn Street
Suite A
Fayetteville, GA 30214
(770) 460-1118

PA: PENNSYLVANIA

Paul R. Brazil
Muller Brazil, LLP
715 Twining Road
Suite 208
Dresher, PA 19025
(215) 885-1655

David John Carney
Green & Schafle LLC
2332 S. Broad Street
Philadelphia, PA 19145
215-326-9256

Lawrence R. Cohan
Saltz Mongeluzzi & Bendesky
One Liberty Place
1650 Market Street
Ste 52nd Floor
Philadelphia, PA 19103
215-575-3887

Samuel A. Dion
Dion & Goldberger
1845 Walnut Street,
Set 1199
Philadelphia, PA 19103
(215) 546-6033

Jeffrey A. Golvash
GOLVASH & EPSTEIN, LLC
9 Dewalt Avenue
Pittsburgh, PA 15227
(412) 882-4717

Jerry Allan Lindheim
Locks Law Firm
601 Walnut Street
Suite 720 East
Philadelphia, PA 19106
215 893-3421

Charles W. Marsar
R.J. Marzella & Associates, P.C.
3513 North Front Street
Harrisburg, PA 17110
(717) 234-7828

Rudolph L. Massa
Massa Law Group, PC
401 Liberty Avenue
Three Gateway Center, Suite 1543
Pittsburgh, PA 15222
(412) 338-1800

Maximillian J. Muller
Muller Brazil, LLP
715 Twining Road
Suite 208
Dresher, PA 19025
(215) 885-1655

Kari Elizabeth Panza
R.J. Marzella & Associates, P.C.
3513 North Front Street
Harrisburg, PA 17110
(717) 234-7828

Amy A. Senerth
Muller Brazil, LLP
715 Twining Road
Suite 208
Dresher, PA 19025
(215) 885-1655

Steven Edwards Winslow
Jubelirer Pass & Intrieri, P.C.
219 Fort Pitt Boulevard
Suite FL 1
Pittsburgh, PA 15222
(412) 281-3850

ID: IDAHO

Bradley Ryan Hine
11254 W. Hickory Loop Drive
Boise, ID 83713
(208) 779-0826

IL: ILLINOIS

Kristina Kay Green
Kralovec, Jambois & Schwartz
60 West Randolph
4th Floor
Chicago, IL 60601
(312) 782-2525

Steven K Jambois
Kralovec, Jambois and Schwartz
60 West Randolph
4th Floor
Chicago, IL 60601
(312) 782-2525

Steven H. Jesser
Steven H. Jesser, Attorney at Law, PC
2700 Patriot Blvd.
Suite 250
Glenview, IL 60026-8021
(800) 424-0060

Edward M. Kraus
Law Offices of Chicago Kent
565 West Adams Street
Suite 600
Chicago, IL 60661
(312) 906-5072

Joseph Paul Shannon
Shannon Law Group, PC
3550 Hobson Road
Hobson Professional Center – Suite 203
Woodbridge, IL 60517
(312) 578-9501

IL: ILLINOIS

Kristina Kay Green
Kralovec, Jambois & Schwartz
60 West Randolph
4th Floor
Chicago, IL 60601
(312) 782-2525

Steven K Jambois
Kralovec, Jambois and Schwartz
60 West Randolph
4th Floor
Chicago, IL 60601
(312) 782-2525

Steven H. Jesser
Steven H. Jesser, Attorney at Law, PC
2700 Patriot Blvd.
Suite 250
Glenview, IL 60026-8021
(800) 424-0060

Edward M. Kraus
Law Offices of Chicago Kent
565 West Adams Street
Suite 600
Chicago, IL 60661
(312) 906-5072

Joseph Paul Shannon
Shannon Law Group, PC
3550 Hobson Road
Hobson Professional Center – Suite 203
Woodbridge, IL 60517
(312) 578-9501

MA: MASSACHUSETTS

Nicole Marie Avitabile
Law Offices of Jeffrey S. Glassman, LLC
Suite 1810
Boston, MA 02110
617-367-2900

Heather M. Bonnet-Hebert
ROBERT B. FEINGOLD & ASSOCIATES
700 Pleasant Street, Suite 520
P.O. Box 7822
New Bedford, MA 02742-7822
508-999-1119

Christopher Davidson Fletcher
Rawson, Merrigan & Litner, LLP
185 Devonshire Street
Suite 1100
Boston, MA 02110
(617) 348-0988

Howard Scott Gold
Howard S . Gold
18 Moran Circle
Sudbury, MA 01776
781-239-1000

Randy Mather Hitchcock
Whitfield Sharp & Hitchcock, LLC
196 Atlantic Avenue
Marblehead, MA 01945
(781) 639-1862

Ronald Craig Homer
Conway, Homer, P.C.
16 Shawmut Street
Boston, MA 02116
(617) 695-1990

Russell D. Luiz
Law Office of Russell D. Luiz
66 N 2nd Sreet
New Bedford, MA 02740
774-305-4159

Timothy J. Mason
Law Office of Sylvia Chin-Caplan, LLC
53 State Street
Suite 500
Boston, MA 02109
617-419-7162

Elaine Whitfield Sharp
Whitfield, Sharp & Sharp
196 Atlantic Avenue
Marblehead, MA 01945
(781) 639-1862

NY: NEW YORK

Catherine D. Aughey
HoganWillig, PLLC
2410 North Forest Road
Suite 301
Amherst, NY 14068
(716) 636-7600

Matthew F. Belanger
Faraci Lange, LLP
28 East Main Street
Suite 1100
Rochester, NY 14614
(585) 325-5150

Kathryn Lee Bruns
Faraci Lange, LLP
28 East Main Street
Suite 1100
Rochester, NY 14614
(585) 325-5150

Patricia Ann Finn
Patricia Finn, P.C.
58 East Route 59
Suite 4
Nanuet, NY 10954
(845) 398-0521

William J. Gerken
The Coppola Firm
3960 Harlem Road
Buffalo, NY 14226
716-839-9700

Robert P. Goodwin
Walsh Roberts & Grace
400 Rand Building
14 Lafayette Square
Buffalo, NY 14203
(716) 856-1636

Corey J. Hogan
Hogan, Willing, Esquire
One John James Audubon Pkwy
Suite 210
Amherst, NY 14228
(716) 636-7600

Ryan C. Johnsen
HoganWillig, PLLC
2410 North Forest Road
Suite 301
Amherst, NY 14068
(716) 636-7600

Robert Joel Krakow
Law Office of Robert J. Krakow, P.C.
233 Broadway
Suite 2320
New York, NY 10279-2320
(212) 227-0600

John F. McHugh
Law Office of John McHugh
233 Broadway
Suite 2320
New York, NY 10279
(212) 483-0875

Michael William Pottetti
Law Office of Michael Pottetti
407 East Main Street
Suite 74
Port Jefferson, NY 11777
631-533-3270

Martin Jeffrey Rubenstein
Martin Rubenstein
191 Douglas Road
Staten Island, NY 10304
646-206-1928

Bruce William Slane
Law Office of Bruce W. Slane, P.C.
188 East Post Road
Suite 205
White Plains, NY 10601
(914) 269-2010

Mark Gordon Strauss
107 University Place
Ste 3h
New York, NY 10003
646-647-9091

Jessica Ann Wallace
Siri & Glimstad, LLP
200 Park Avenue
17th Floor
New York, NY 10166
(212) 532-1091

Jimmy A. Zgheib
Zgheib Sayad, P.C.
75 South Broadway
4th Floor
White Plains, NY 11209
(914) 729-1110

NJ: NEW JERSEY

Carol L. Gallagher
Carol L. Gallagher, Esquire, LLC.
822 Shore Road
Somers Point, NJ 08244
(609) 927-2726

Louis P. McFadden
McFadden Law Firm
1800 New Rd.
Ste 100
Northfield, NJ 08225
609-380-2540

Mark Theodore Sadaka
Law Offices of Sadaka Associates, LLC
155 North Dean Street
Suite 4d
Englewood, NJ 07631-2524
800-810-3457

Kenneth W. Thayer
Brandon J. Broderick, Attorney at Law, LLC
850 Bear Tavern Road
Suite 106
Ewing, NJ 08003
609-434-2037

Phyllis Widman
Widman Law Firm, LLC
2312 New Road
Unit 103
Northfield, NJ 08225
(732) 829-3416

NC: NORTH CAROLINA

Dan Wilson Bolton
Bolton Law, PLLC
5000 Centre Green Way
Suite 500
Cary, NC 27513
(919) 228-6484

Nichole Glance Booker
Mast Law Firm
PO Box 119
Smithfield, NC 27577
(919) 934-6187

Leslie Cooper Harrell
Mullins, Duncan, et al.
300 North Greene Street
Suite 2000
Greensboro, NC 27401
336-645-3320

John Alan Jones
Martin & Jones, PLLC
410 Glenwood Avenue, Ste. 200
Raleigh, NC 27603
(919) 821-0005

Nancy Routh Meyers
Turning Point Litigation
300 North Greene Street
Suite 2000
Greensboro, NC 27401
336-645-3324

Allison Overbay Mullins
Turning Point Litigation
300 North Greene Street
Suite 2000
Greensboro, NC 27401
(336) 645-3320

Philip James Roth
Marshall, Roth & Gregory, PC
90 Southside Avenue
Suite 100
Asheville, NC 28801
(828) 281-2100

John Richard Taylor
Zaytoun Law Firm
3130 Fairhill Drive,
Suite 100
Raleigh, NC 27612
(919) 832-6690

Kimberly Wilson White
Wilson Law, P.A.
434 Fayetteville St.
Suite 2060
Raleigh, NC 27601
919-890-0180

TN: TENNESSEE

Robert Deniger Cobb
Nahon, Saharovich & Trotz
488 South Mendenhall Road
Memphis, TN 38117
(901) 683-7000

William E. Cochran
Black McLaren, et al., PC
530 Oak Court Drive
Suite 360
Memphis, TN 38117
(901) 762-0535

Justin Glenn Day
Milberg Coleman Bryson Phillips Grossman, PLLC
First Horizon Bank
800 S. Gay Street
Suite 1100
Knoxville, TN 37929
865-247-0080

Celia Farrar Hastings
Greg Coleman Law, PC
800 S. Gay Street
First Tennessee Plaza, Suite 1100
Knoxville, TN 37929
(865) 247-0080

William Bliss Hicky
William B. Hicky, Attorney at Law
Two American Center
3102 West End Avenue
Suite 400
Nashville, TN 37209
(615) 933-6611

Russell W. Lewis
1019 16th Avenue South
Nashville, TN 37212
615-200-1122

Michael G. McLaren
Black McLaren, et al., PC
530 Oak Court Drive
Suite 360
Memphis, TN 38117
(901) 762-0535

TX: TEXAS

Brian Robert Arnold
Brian R. Arnold & Associates
600 West Campbell Road
Suite 3
Richardson, TX 75080
(214) 739-4216

Michael Adly Baseluos
Baseluos Law Firm, PLLC
4211 Modena Drive
San Antonio, TX 78218
(210) 787-5993

Scharli Sturtevant Branch
Cantey Hanger
600 W 6th st Ste 300
Fort Worth, TX 76102
817-877-2802

Gil L. Daley
Law Office of Gil L. Daley, II, P.C.
201 Main Street
Suite 600
Fort Worth, TX 76102
(817) 763-9553

Sean Franks Greenwood
Greenwood Law Firm
1415 North Loop West
Suite 1100
Houston, TX 77008
(832) 356-1588

Michael Philipp Gross
Howie Law, PC
2608 Hibernia Street
Dallas, TX 75204-6340
(214) 622-6340

Margaret M Guerra
Margaret M. Guerra, Attorney at Law
1000 Macon Street
Suite 300
Fort Worth, TX 76102
(817) 570-9991

Koby Jack Kirkland
Mejias Lindsay, PLLC
4900 Woodway Drive
Suite 750
Houston, TX 77056
832-426-4574

Randal Gilbert Mathis
Mathis & Donheiser, P.C.
1412 Main Street, Suite 2600
Dallas, TX 75202
214-728-0690

Russell Anthony Murray
Lovett Law Firm
619 Arizona Ave
El Paso, TX 79902
(915) 757-9999

Daniel J. Smith
Smith & Smith
6040 Camp Bowie Boulevard
Suite 14
Fort Worth, TX 76116
(817) 877-5750

VA: VIRGINIA

Timothy Paul Bosson
Bosson Legal Group, P.C.
8300 Arlington Blvd., Suite B2
Fairfax, VA 22031
(571) 775-2529

Gary Alvin Bryant
Willcox & Savage, P.C.
440 Monticello Avenue
Suite 2200
Norfolk, VA 23510-2197
(757) 628-5500

Thomas Scott Carnes
Roy, Larsen, Carnes & Romm, P.C.
109-A Wimbledon Square
Chesapeake, VA 23320-4932
(757) 271-0571

Jesse James Johnson
Johnson Gardy & Teumer
3508 Robs Drive
Suffolk, VA 23435
(757) 539-0350

Isaiah Kalinowski
Bosson Legal Group
8300 Arlington Boulevard
Suite B2
Fairfax, VA 22031
571-771-3225

Alexander Laufer
Eisenhower and Laufer, PC
10560 Main Street
Suite 218
Fairfax, VA 22030
(703) 352-9690

Harrison Whitten Long
Rawls Law Group (Richmond)
211 Rocketts Way
Suite 100
Richmond, VA 23231
804-344-0038

Elizabeth Martin Muldowney
Sands Anderson PC
1111 East Main Street – Suite 2400
P. O. Box 1998
Richmond, VA 23218-1998
(804) 783-7227

Nicholas Paul Provenzo
155 Somervelle St.
Alexandria, VA 22304
(703) 625-3295

Ramon Rodriguez
Sands Anderson PC
1111 East Main Street – Suite 2400
P. O. Box 1998
Richmond, VA 23218-1998
(804) 783-7229

Glen Howard Sturtevant
Rawls Law Group (Richmond)
211 Rocketts Way
Suite 100
Richmond, VA 23231
(804) 344-0038

David Alexander Tierney
Rawls Law Group (Richmond)
211 Rocketts Way
Suite 100
Richmond, VA 23231
(804) 782-0617

WA: WASHINGTON

Kelly Danielle Burdette
Burdette Law, PLLC
249 Main Avenue S., Suite 107 #333
98045
North Bend, WA 98045
206-235-5048

Douglas Lee Burdette
Burdette Law, PLLC
249 Main Street, Suite 107
Number 333
North Bend, WA 98045
(206) 441-5597

Theodore J. Hong
Maglio Christopher & Toale (WA)
1325 Fourth Avenue
Suite 1730
Seattle, WA 98101
(888) 952-5242

Jessi Carin Huff
Mctlaw
8816 SE 77th Place
Mercer Island, WA 98040
888-952-5242

Michael Spencer Kolker
Otorowski Morrow & Golden, PLLC
298 Winslow Way West
Bainbridge Island, WA 98110
(206) 842-1000

Matthew N. Menzer
Menzer Law Firm, PLLC
705 Second Avenue
Suite 800
Seattle, WA 98104
(206) 903-1818

Jessica Anne Olins
Maglio Christopher & Toale (WA)
1325 Fourth Avenue
Suite 1730
Seattle, WA 98101
888-952-5242

Danielle Anne Strait
Maglio Christopher & Toale (WA)
1325 Fourth Avenue
Suite 1730
Seattle, WA 98101
888-952-5242

WI: WISCONSIN

Kristin M. Cafferty
Habush, Habush & Rottier, S.C. (Racine, WI)
5439 Durand Avenue
Suite 220
Racine, WI 53406
(262) 554-6200

Jerome A. Konkel
Samster Konkel and Safran
11063 W. Bluemound Rd.
Suite 205
53226
Wauwatosa, WI 53226
414-224-0400

Andrew Mark Krueger
Krueger & Hernandez S.C. (Middleton)
8215 Greenway Boulevard
Suite 590
Middleton, WI 53562
(608) 824-9540

Joseph Michael Russell
Von Briesen & Roper, S.C.
411 East Wisconsin Ave.
Suite 1000
Milwaukee, WI 53202
(414) 287-1414

Scott B. Thompson
Gingras, Cates & Luebke, S.C.
8150 Excelsior Drive
Madison, WI 53717
(608) 833-2632

Stephanie Ann Thompson
Krueger & Hernandez S.C. (Middleton)
8215 Greenway Boulevard
Suite 590
Middleton, WI 53562
(608) 824-9540

Ryan Truesdale
Groth Law FIrm, S.C.
11063 West Bluemound Road
Wauwatosa, WI 53226
414-375-2030

Jason Wendell Whitley
Novitzke, Gust, Sempf & Whitley
314 Keller Avenue N
Suite 200
Amery, WI 54001
(715) 268-6130

Peter M. Young
Habush, Habush & Rottier, S.C.
3100 Eagle Avenue
P.O. Box 1987
Wausau, WI 54402-1987
(715) 842-4444

42 USC Section 1983- Civil Action for Deprivation of Rights

Every person who, under color of any statute, ordinance, regulation, custom, or usage, of any State or Territory or the District of Columbia, subjects, or causes to be subjected, any citizen of the United States or other person within the jurisdiction thereof to the deprivation of any rights, privileges, or immunities secured by the Constitution and laws, shall be liable to the party injured in an action at law, suit in equity, or other proper proceeding for redress, except that in any action brought against a judicial officer for an act or omission taken in such officer’s judicial capacity, injunctive relief shall not be granted unless a declaratory decree was violated or declaratory relief was unavailable. For the purposes of this section, any Act of Congress applicable exclusively to the District of Columbia shall be considered to be a statute of the District of Columbia.

Putin to Biden: Finlandize Ukraine, or We Will

Do Not Comply - Toolbox files:

The Impact of Fasting On High Blood Pressure

A study recently published in the Journal of the American Heart Association confirms: Elevated blood pressure was effectively reduced after an average of 10 days of fasting, as evidenced by a study of 1610 fasting patients at the Buchinger Wilhelmi Clinic in Überlingen, Germany. 690 subjects in this group had high blood pressure before fasting.

Among them 377 people took antihypertensive drugs, the administration of which could in most cases either be stopped or reduced during fasting as blood pressure fell or remained within the normal range. Since antihypertensive drugs often have serious side effects, long-term fasting could be used as a complementary therapy for high blood pressure. In 920 people with normal blood pressure, blood pressure was reduced while staying within the normal range. Low blood pressure values showed a tendency to increase. The results of the study were published in the Journal of the American Heart Association in November 2020 under the title “Blood pressure changes in 1610 subjects with and without antihypertensive medication during long-term fasting” by the authors Franziska Grundler, Robin Mesnage, Andreas Michalsen and Françoise Wilhelmi de Toledo.

High blood pressure is an important and widespread risk factor for life-threatening diseases such as heart attack or stroke and is mainly caused by an unhealthy lifestyle. Risk factors for high blood pressure include obesity, malnutrition, lack of exercise, stress, smoking, and excessive consumption of salt, sugar or alcohol. According to European medical societies, the threshold above which one speaks of high blood pressure is 140/90 mmHg. The study proves that long-term fasting according to the Buchinger Wilhelmi programme has a beneficial effect on blood pressure. Elevated blood pressure fell both in patients who were treated with medication and in those who were not. The longer the fasting lasted, the stronger the effect. The positive effects of fasting on blood pressure can be explained by the reduction in weight due to fasting, a reduction in waist circumference and the interruption of salt, alcohol and carbohydrate intake and, if necessary, smoking. Fasting triggers mechanisms that act in a similar way to antihypertensive drugs: it promotes the excretion of sodium, activates the parasympathetic nervous system and causes vasodilation. The improvement in blood pressure continued for four days after the fasting ended. Closer examination showed that long-term fasting effectively lowers blood pressure, especially in people with high body weight, lipid and glucose metabolism disorders and in older people.

Future studies will investigate whether these positive results can be sustained over the medium and long term, which is likely to depend on lifestyle changes.

Contact: Dr. Françoise Wilhelmi de Toledo E-Mail: francoise.wilhelmi@buchinger-wilhelmi.com Franziska Grundler, Robin Mesnage, Andreas Michalsen und Françoise Wilhelmi de Toledo: „Blood pressure changes in 1610 subjects with and without antihypertensive medication during long-term fasting, Journal of the American Heart Association, (2020;9:e018649). DOI: 10.1161/JAHA.120.018649 : https://www.buchinger-wilhelmi.com/en/publications-of-the-buchinger-wilhelmi-clinics/

Methods of Cleaning Your Arteries

Between 1788 and 1868, about 162,000 convicts were transported from Britain and Ireland to various penal colonies in Australia

Between 1788 and 1868, about 162,000 convicts were transported from Britain and Ireland to various penal colonies in Australia.^[1]

The British Government began transporting convicts overseas to American colonies in the early 18th century. When transportation ended with the start of the American Revolution, an alternative site was needed to relieve further overcrowding of British prisons and hulks. Earlier in 1770, James Cook charted and claimed possession of the east coast of Australia for Britain. Seeking to pre-empt the French colonial empire from expanding into the region, Britain chose Australia as the site of a penal colony, and in 1787, the First Fleet of eleven convict ships set sail for Botany Bay, arriving on 20 January 1788 to found Sydney, New South Wales, the first European settlement on the continent. Other penal colonies were later established in Van Diemen’s Land (Tasmania) in 1803 and Queensland in 1824.^[2] Western Australia – established as Swan River Colony in 1829 – initially was intended solely for free settlers, but commenced receiving convicts in 1850. South Australia and Victoria, established in 1836 and 1850 respectively, officially remained free colonies. However, a population that included thousands of convicts already resided in the area that became known as Victoria.

source

Graphene Face Masks Impact On Health

‘It’s crazy’: Quebec schools were using nanoform graphene masks: expert see article

The term “nanoform graphene” refers to the carbon coating on the masks.

Jim Thomas, research director at ETC Group, has spent the past two decades tracking the toxicity of nanomaterials.

“We were one of the first groups to raise concerns about them back in 2002,” said the Quebecer, who has been based in Nelson, B.C., for the past year.

When he learned from his sister-in-law that masks containing nanoform graphene were being used in Quebec schools, “I hit the roof,” Thomas said. “It’s crazy.” source

Graphene Oxide: a Toxic Substance - Impact on Health

Graphene Oxide: a toxic substance in the vial of the COVID-19 mRNA Vaccine

We bring to the attention of Global Research readers this important interview with Ricardo Delgado Martin, Founder and Director of Quinta Columna. Ricardo is responsible for coordinating the Spanish research team’s analysis of the impacts of graphene oxide nano-particles contained in the vial of the mRNA vaccine.

The results of their analysis by electron microscopy and spectroscopy are far-reaching. Graphene oxide is a toxin which triggers thrombi and blood coagulation. It also has an impact on the immune system. Graphene oxide accumulated in the lungs can have devastating impacts.

The results of the Spanish study suggest, yet to be fully confirmed, that the recorded vaccine related deaths and “adverse events” (e.g. published in the US by the CDC and in the EU) are attributable to the presence of graphene oxide nano-particles contained in the Covid vaccine vial.

Of significance, (acknowledged by national health authorities) graphene oxide is also contained in the face mask.

Graphene has electromagnetic properties which have been detected in people who have been vaccinated. These effects have been amply documented and confirmed. See the study conducted by the European Forum for Vaccine Vigilance. source

Glyphosate - A Global Health Threat

In our ever-increasingly polarized world, there’s one topic of interest in health and wellness that really seems to call out clear differences in opinion. Glyphosate, the herbicide and active ingredient in products like Roundup, has been touted by some as being a wonderful and safe way to rid crops and even homes of pesky weeds. And clearly, those who feel positively about this chemical are being heard as nearly 150,000 tons of glyphosate are sprayed onto American crops every year. That translates to about one pound of glyphosate for every person in our country. And this chemical makes its way into the water we drink, the agricultural products we consume, and even the air we breathe.

On the other side of this debate are those who feel that glyphosate represents a significant threat to our health. Researchers, like our guest today, look at the available science and have concluded that, by a multitude of mechanisms, glyphosate may well be responsible or at least contributory for a vast array of human ailments, from autism to dementia to autoimmune disease, and so many more.

This debate extends to the confusion surrounding the safety of GMO food. For the most part, the genetic modification of plant seeds is undertaken so that the newly developed plant is not damaged by the weed targeting action of glyphosate. This allows farmers to spray GMO crops with glyphosate, kill the weeds, and still harvest the undamaged plant. But while there may or may not be concern about the specific genetic modification of the plant, this whole scenario sets the stage for glyphosate to appear in our foods and throughout our environment.

That said, this is a fundamental nuance to the GMO debate that absolutely must enter the discussion.

Dr. David Perlmutter is on a mission of empowerment as America’s Neurologist – visit site

Mike Yeadon, Ex-Pfizer Scientist We Are Approaching Stage 5

Mike Yeadon, Ex-Pfizer Scientist Sent This Out on Thursday. We Are Approaching Stage 5

By Staff Reporter – Nov. 8, 2021

The pathway to new world order …

From Henry Makow

Phase 1: Simulate a threat and create fear. (December 2019-March 2020)

– Mount a plandemic
– Kill tens of thousands of elderly people.
– Increase the number of cases and deaths
– Position vaccination as the only solution from the beginning.
– Focus all attention on Covid-19.

Result, (almost) general panic

Phase 2: Sow the tares and division. (March 2020-December 2020)

– Impose multiple unnecessary, liberticidal and unconstitutional coercive measures.
– Paralyze trade and the economy.
– Observe the submission of a majority and the resistance of a rebellious minority.
– Stigmatize the rebels and create a horizontal division.
– Censoring dissident leaders.
– Punish disobedience.
– Generalize PCR tests.
– Create confusion between cases, infected, sick, hospitalized and dead.
– Disqualify all effective treatments.
– Hope for a rescue vaccine.

Result, (almost) general panic.

Phase 3: Bring a treacherous and deadly solution. (December 2020-June 2021)

– Offer a free vaccine for everyone.
– Promise protection and return to normality.
– Establish a herd immunization target.
– Simulate a partial recovery of the economy.
– Hide statistics of side effects and deaths from injections.
– Passing off the side effects of the injections as “natural” effects of the virus and the disease.
– Recover the notion of a variant as a natural mutation of the virus.
– Justify the maintenance of coercive measures by not applying the herd immunity threshold.
– Punish health professionals for the illegal exercise of care and healing.

Result, doubts and feelings of betrayal among the vaxx, discouragement among opponents.

Phase 4: Install Apartheid and the QR code. (June 2021-October 2021)

– Voluntarily plan for shortages.

– Impose the vaccination pass (QR code) to reward the vaccinated, punish the resistant.

– Create an Apartheid of the privileged against the others.

– Take away the right to work or study from non-vaxx.– Withdraw basic services to the non-vaxx.
– Impose PCR payment tests on non-vaxx.

Result, First stage of digital control, impoverishment of opponents

Phase 5: Establish chaos and Martial law. (November 2021-March 2022)

– Exploit the shortage of goods and food.
– Cause the paralysis of the real economy and the closure of factories and shops.
– Let unemployment explode.
– Apply a third dose to the vaxx (boosters).
– Take up the murder of the living old men.
– Impose compulsory vaccination for all.
– Amplify the myth of variants, the efficacy of the vaccine and the immunity of the herd.
– Demonize the anti-vaxx and hold them responsible for the dead.
– Arrest opposition leaders.
– Impose digital identity on everyone (QR code): Birth certificate, identity document, passport, driving license, health insurance card …
– Establish martial law to defeat the opposition.

Result, Second stage of digital control. Imprisonment or removal of opponents.

Phase 6: Cancel the debts and dematerialize the money. (March 2022-September 2022)

– Trigger the economic, financial and stock market collapse, the bankruptcy of the banks.
– To rescue the losses of the banks in the accounts of their clients.
– Activate the «Great Reset».
– De-materialize money.
– Cancel debts and loans.
– Impose the digital portfolio. (Digital Wallet)
– Seize properties and land.
– Ban all global medicines.
– Confirm the obligation to vaccinate semi-annually or annually.
– Impose food rationing and a diet based on the Codex Alimentarius.
– Extend the measures to emerging countries.

Result, Third stage of digital control. Extension of the N.O.M. to the whole planet. source

Most Who Have Taken COVID Vax Will Be Dead By the Year 2025

Thanks to the people who participated in this first ever human experiment with a mRNA gene-therapy, fooled into thinking it was a “vaccine” for a phony “pandemic” allegedly caused by the never-isolated “COVID-19,” we now know the following based on fact-based, post-vaccine research:

1.) It’s not a vaccine. The COVID-19 mRNA vaccine does not provide immunity to Covid or it’s variants so you can still catch Covid and transmit it to others making you asymptomatic. You will likely need a booster shot every 6 months, so get ready to roll up that sleeve every six months once that system rolls out.

[link to www.bustle.com]

2.) The 95% efficacy is the RRR (Relative Reduction Risk) where the real reduction rate ARR (Absolute Reduction Risk) is less than 2% as per this scientific Lancet study.
[link to www.thelancet.com]

This means you are really not protected much at all, as the architects of this phony pandemic would like you to ‘believe.’

3.) The lipid nanoparticles in the vaccines do not remain in the intramuscular region of the deltoid muscle. They seep out into the cardiovascular system infecting the entire body with spike-protein. Something the manufacturers claimed would never happen, yet it does and is why the adverse-side effects are so bad with this shot.

[link to www.sciencedirect.com]

4.) The spike-protein itself is toxic and a part of the disease pathology being the cause of inflammation, ACE2 deregulation and opens up immunity pathways. This means Myocarditis (heart inflammation), Encephalitis (brain inflammation ) and hepatomegaly (liver inflammation) are huge risks and confirmed by many adverse-reactions reported to VAERS and EuroVigilance.

Pro-vaccine Canadian researcher warns covid vaccine spike proteins are killing people… “We made a big mistake.”

Dr. Byram W. Bridle, Ph.D. says the he and several colleagues gained access to a first-of-its-kind “biodistribution” study out of Japan showing that even when injected in muscle tissue in the arm, the mRNA (messenger RNA) injections from Moderna and Pfizer-BioNTech cause the production of spike proteins that more often than not get into the bloodstream and cause deadly blood clots, heart and brain damage, and infertility.

“The spike protein on its own is almost entirely responsible for the damage to the cardiovascular system,” Bridle warned during a recent radio interview.

“If you inject the ‘purified’ spike protein into the blood … [there is] all kinds of damage to the cardiovascular system, it can cross the blood-brain barrier and cause damage to the brain.”

Submitted by malterwitty on Thu, 06/03/2021 source

BRITISH MEDICAL JOURNAL No 7070 Volume 313: Page 1448, 7 December 1996.

BRITISH MEDICAL JOURNAL No 7070 Volume 313: Page 1448,
7 December 1996.

CIRP Introduction

The judgment by the war crimes tribunal at Nuremberg laid down 10 standards to which physicians must conform when carrying out experiments on human subjects in a new code that is now accepted worldwide.

This judgment established a new standard of ethical medical behavior for the post World War II human rights era. Amongst other requirements, this document enunciates the requirement of voluntary informed consent of the human subject. The principle of voluntary informed consent protects the right of the individual to control his own body.

This code also recognizes that the risk must be weighed against the expected benefit, and that unnecessary pain and suffering must be avoided.

This code recognizes that doctors should avoid actions that injure human patients.

The principles established by this code for medical practice now have been extended into general codes of medical ethics.

The Nuremberg Code (1947)

Permissible Medical Experiments

The great weight of the evidence before us to effect that certain types of medical experiments on human beings, when kept within reasonably well-defined bounds, conform to the ethics of the medical profession generally. The protagonists of the practice of human experimentation justify their views on the basis that such experiments yield results for the good of society that are unprocurable by other methods or means of study. All agree, however, that certain basic principles must be observed in order to satisfy moral, ethical and legal concepts:

1– The voluntary consent of the human subject is absolutely essential. This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, overreaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment. The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs, or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.

2– The experiment should be such as to yield fruitful results for the good of society, unprocurable by other methods or means of study, and not random and unnecessary in nature.

3– The experiment should be so designed and based on the results of animal experimentation and a knowledge of the natural history of the disease or other problem under study that the anticipated results justify the performance of the experiment.

4– The experiment should be so conducted as to avoid all unnecessary physical and mental suffering and injury.

5– No experiment should be conducted where there is an a priori reason to believe that death or disabling injury will occur; except, perhaps, in those experiments where the experimental physicians also serve as subjects.

6– The degree of risk to be taken should never exceed that determined by the humanitarian importance of the problem to be solved by the experiment.

7– Proper preparations should be made and adequate facilities provided to protect the experimental subject against even remote possibilities of injury, disability or death.

8– The experiment should be conducted only by scientifically qualified persons. The highest degree of skill and care should be required through all stages of the experiment of those who conduct or engage in the experiment.

9– During the course of the experiment the human subject should be at liberty to bring the experiment to an end if he has reached the physical or mental state where continuation of the experiment seems to him to be impossible.

10– During the course of the experiment the scientist in charge must be prepared to terminate the experiment at any stage, if he has probable cause to believe, in the exercise of the good faith, superior skill and careful judgment required of him, that a continuation of the experiment is likely to result in injury, disability, or death to the experimental subject.

Download the PDF

Covid Vaccine Cuts People off Spiritually

I don’t know how else to put this. I had my second dose of Pfizer two weeks ago and I’ve become convinced there is something in these vaccines that cuts people off from spirit.

It’s like my consciousness has been leashed and life has turned the volume down real low. I had an intense spiritual awakening about 2 years ago triggered by psychs and it’s like all the connection I gained has been erased. I think this is some kind of evil alien tech I’m not even joking. Like Law of One Orion type shit, to stop us ascending whatever that means. I can’t describe the change in my awareness, I struggle to believe it myself. Like my Mode of Operation has been changed. I’m lucky I’m even conscious of it, because I feel like most people aren’t really in touch with spirit and wouldn’t notice anything wrong. For me this is hell. And I know some of you know what I’m talking about when I say I feel like I’ve betrayed my soul’s mission. It’s like there is no forgiveness for me, I’ve failed and allowed myself to fail knowing something was wrong, I didn’t have faith. Part of me thinks I did this on purpose because my connection was so painful. But nothing is worse than this, I’d rather be suffering.

I can no longer:

– Feel empathy, or deep emotion, heartfelt emotion. You know that thing in your chest where you feel, physically, not intellectually. It’s gone. No love, happiness, sadness, anger, anything. No compassion.

– Transcend myself in meditation, feel infinity, God and the like. Like I’ve been reduced to my 5 senses, and even those have been diminished.

– Feel my intuition at all, no gut feelings whatsoever, it’s like I’m completely blind.

– Feel music, art, food. Be passionate about anything, have motivation for anything, I don’t even feel hungry or tired, I feel nothing. Not a numbness, not a dissociation (I’ve had both), but a straight up lack, a severance to that spark that animates our inner lives.

– Lucid dream, astral project, even feel my energetic body at all. It’s like it has dissipated.

– Sleep properly at all, and when I do it’s like I can’t enter as deep a sleep as I used to.

– Breathe or yawn as deeply as I used to?? Which may seem unrelated but breath = prana = lifeforce…ygm. Basically I feel like a bot

If anyone knows ANYTHING about this or how to reverse it. I’ve seen all the shit about funvax and whatever, if this is science it has to be reversible somehow. Hopefully if I don’t take boosters and work on my connection I might be able to improve it. If anyone has been through the same or knows anyone who has, DM me. I had an extremely strong intuition (last one I’ve felt) telling me I would basically die if I took this dose, but my mother is my weak spot and I caved to her (doesn’t help that I’m financially dependent on her etc.) but honestly I should’ve become homeless rather than do this. Now I’d rather become homeless than ever take a booster shot. There is no life without love and yet that is the life I’m now living. So yeah. If anyone had their doubts about the vax, here is my theory on what it does, based on personal experience – source 1 source 2 search results

Watch How Graphene Oxide Reacts to a Phone Call

Inedia or Breatharianism

”A Breatharian is a person who can, under the proper conditions, live with or without eating physical food.” Just as the sun is nourishment for plants, this same energy can fuel your body without the need for food.

The practice of breatharian is not doing away with food or water, but more importantly in the synchronization of mind and body with that of the laws of the universe which allows you to be more self reliant on pulling energy from all around you which sustains wellness.

The Breatharians are those who living on light and energies derived from the sun. But it is no magic trick. Prana Yoga as it is otherwise called, was practiced by many a wise person, for centuries, in India.

COVID-19: The Spartacus Letter

– COVID-19 is a blood and blood vessel disease. SARS-CoV-2 infects the lining of human blood vessels, causing them to leak into the lungs.

– Current treatment protocols (e.g. invasive ventilation) are actively harmful to patients, accelerating oxidative stress and causing severe VILI (ventilator-induced lung injuries). The continued use of ventilators in the absence of any proven medical benefit constitutes mass murder.

– Existing countermeasures are inadequate to slow the spread of what is an aerosolized and potentially wastewater-borne virus, and constitute a form of medical theater.

– Various non-vaccine interventions have been suppressed by both the media and the medical establishment in favor of vaccines and expensive patented drugs.

– The authorities have denied the usefulness of natural immunity against COVID-19, despite the fact that natural immunity confers protection against all of the virus’s proteins, and not just one.

– Vaccines will do more harm than good. The antigen that these vaccines are based on, SARS-CoV-2 Spike, is a toxic protein. SARS-CoV-2 may have ADE, or antibody-dependent enhancement; current antibodies may not neutralize future strains, but instead help them infect immune cells.

– Also, vaccinating during a pandemic with a leaky vaccine removes the evolutionary pressure for a virus to become less lethal.

– There is a vast and appalling criminal conspiracy that directly links both Anthony Fauci and Moderna to the Wuhan Institute of Virology.

– COVID-19 vaccine researchers are directly linked to scientists involved in brain-computer interface (“neural lace”) tech, one of whom was indicted for taking grant money from China.

Independent researchers have discovered mysterious nanoparticles inside the vaccines that are not supposed to be present.

– The entire pandemic is being used as an excuse for a vast political and economic transformation of Western society that will enrich the already rich and turn the rest of us into serfs and untouchables.

Fair use excerpt. Read the whole article here.

Who Was Spartacus?

Spartacus was a Thracian gladiator who, along with Crixus, Gannicus, Castus, and Oenomaus, was one of the escaped slave leaders in the Third Servile War, a major slave uprising against the Roman Republic. Little is known about him beyond the events of the war, and surviving historical accounts are sometimes contradictory. Wikipedia

Who is Spartacus which identifies with the article, “COVID-19: The Spartacus Letter” to your left? “Whoever Spartacus is, they have a very elaborate knowledge in “the field”. If you want to know a lot more about the no. 1 issue in the world today, read it. And don’t worry if you don’t understand every single word, neither do I. But I learned a lot.” source www.theautomaticearth.com/2021/09/spartacus/

Federal Govt HHS Whistleblower Goes Public with hidden Recordings

After writing non-stop for over a year about the dangers and the horrors of the genocidal COVID “vaccine”, to now actually hear a Federal nurse from the US Department of Health and Human Services confirming much of it and to see her raw emotions…it had an overwhelming impact on me that I did not expect.

Overwhelming, heart-breaking Evil. It’s the shock of the real – and it’s a small glimpse of things to come. This video, the first of a series of five to be released over the next several weeks was filmed secretly at a Federal hospital and it will be a game-changer in this information war, as the millions of people who see it respond.

STEVE QUAYLE Warns of Imminent Catastrophic Collapse of America As We Know It

Like the British Empire before it, the US was incrementally groomed to become the primary host of the Globalist bankster parasite over the course of the 20th century, signaled by the founding of the Federal Reserve Bank in 1913 and the decoupling of the US dollar from gold in 1971.

Both events undermined US sovereignty while transforming the US dollar into the world’s reserve currency and the US Treasury and US military into the instruments of the Globalists.

Like the British Empire before it, the world was led to believe that America was the most powerful nation on Earth. The truth was that America had been hijacked by the banksters to engage in incredibly stupid war-profiteering adventures, like the invasions of Korea, Vietnam, Iraq and Afghanistan and through the CIA, to covertly undermine untold numbers of Third World nations around the globe.

These actions served the interests of the criminals who had hijacked America, not the interests of the US Taxpayer who unwillingly funded these operations. These wars bankrupted the US, the same way the First- and Second World Wars bankrupted the UK and I’d hazard to guess that this pump-and-dump model did not arise in the 20th century. source

President Offered $20m Bribe to See That The Covid-19 Cure Be Poisoned

The President of Madagascar, Andry Rajoelina has alleged that the World health organization (WHO) offered $20m bribe to see the Covid-19 cure poisoned.

Rajoelina accused the World Health Organisation of a plot to have its COVID-19 Organics, the local African ‘cure’ for the virus poisoned.

According to his claims, WHO offered a $20 million bribe to poisoned their medicine, Tanzania Perspective reported on the front-page of its 14th May edition.

WHO Offered $20M Bribe To Poison COVID-19 Cure says the President of Madagascar as reported by Tanzania Perspective. The President of Madagascar believes the only reason the rest of the world has refused to treat Madagascar’s cure for the coronavirus with urgency and respect is that the remedy comes from Africa.

In an interview with French media, President Rajoelina reportedly said he has noticed what he believes stems from usual condescension toward Africans.

“I think the problem is that (the drink) comes from Africa and they can’t admit… that a country like Madagascar… has come up with this formula to save the world.”

“What is the problem with Covid-Organics, really? Could it be that this product comes from Africa? Could it be that it’s not OK for a country like Madagascar, which is the 63rd poorest country in the world… to have come up with (this formula) that can help save the world?”

“If it wasn’t Madagascar, and if it was a European country that had actually discovered this remedy, would there be so much doubt? I don’t think so,” the President of Madagascar Andry Rajoelina asserted.

The remedy, COVID Organics, is made from Artemisia, a plant imported into Madagascar in the 1970s from China to treat malaria. Artemisia has had proven success against malaria and according to President Rajoelina it can cure COVID-19 patients within ten days.

However, the WHO has criticized such natural therapeutic measures against the coronavirus as blind faith. In response to the skepticism with which the WHO is treating the COVID Organics, Rajoelina said, “No country or organization will keep us from going forward.”

A host of other African countries including, Tanzania, Guinea-Bissau, DR Congo and Niger, have imported the Madagascan made recipe. source

Florida's Surfside Building Collapse Was Possibly Pulled (a controlled demolition)

And according to Surfside mayor Charles Burkett, roof repairs were underway at the building. He also told the news channel: ‘This [building] is from the 80s. There is no reason for this building to go down like that unless someone literally pulls out the support from underneath, or they get washed out, or there is a sinkhole or something like that, because it just went down.’

‘It’s hard to imagine how this could have happened,’ Burkett said. ‘Buildings just don’t fall down… There’s no reason for this building to go down like that unless someone literally pulls the supports out from underneath.’

Above – (A more detailed graphic showing the apparent extent of the Miami/Surfside building collapse and damage.)

A possible a sinkhole or a controlled demolition?

Officials report ‘banging noise’ coming from Surfside building rubble

There is what looks like an intense light glow in the parking structure (building at right) on the 3rd tier down from the top, then yet another one 5th tier down and then on a lower floor as it is collapsing.

go to page (bookmarkable)

If It Ends in .Com .Net or .Org, It's Seizable

2012 from WIRED – If It Ends in .Com .Net or .Org, It’s Seizable – The U.S. government says it has the right to seize any .com, .net and .org domain name because the companies that have the contracts to administer them are based on United States soil, according to Nicole Navas, an Immigration and Customs Enforcement spokeswoman.

When U.S. authorities shuttered sports-wagering site Bodog.com last week, it raised eyebrows across the net because the domain name was registered with a Canadian company, ostensibly putting it beyond the reach of the U.S. government. Working around that, the feds went directly to VeriSign, a U.S.-based internet backbone company that has the contract to manage the coveted .com and other “generic” top-level domains.

EasyDNS, an internet infrastructure company, protested that the “ramifications of this are no less than chilling and every single organization branded or operating under .com, .net, .org, .biz etc. needs to ask themselves about their vulnerability to the whims of U.S. federal and state lawmakers.”

ICANN is also seeking to distance itself from the U.S. government by being more inclusive, including allowing domain names in a range of written, global languages, ending the exclusivity of the Latin alphabet in top-level domains.

Still, many outside the United States, like China, India and Russia, distrust ICANN and want control of the net’s naming system to be turned over to an organization such as the International Telecommunications Union, an affiliate of the United Nations. Last year, Russian Prime Minister Vladimir Putin met with Hamadoun Toure, the ITU’s chief, and said he wanted international control over the internet “using the monitoring capabilities of the International Telecommunication Union.”

“If we are going to talk about the democratization of international relations, I think a critical sphere is information exchange and global control over such exchange,” Putin said, according to a transcript from the Russian government.

Just last week, Robert McDowell, a Federal Communications Commission commissioner, blasted such an idea.

“If successful, these efforts would merely imprison the future in the regulatory dungeon of the past,” he said. “Even more counterproductive would be the creation of a new international body to oversee internet governance.”

But despite EasyDNS and others’ outrage, the U.S. government says it’s gone that route hundreds of times. Furthermore, it says it has the right to seize any .com, .net and .org domain name because the companies that have the contracts to administer them are based on United States soil, according to Nicole Navas, an Immigration and Customs Enforcement spokeswoman.

But it is possible that the U.S. government’s big-footing over dot-com domains in the name of fighting copyright could add more weight to the arguments of those who want to put the U.N. in charge of the internet’s naming system. While that’s not inevitably a bad thing, it could lead to a world where any .com might be seizable by any country, including Russia, Libya and Iran.

Still, don’t expect Uncle Sam to give up its iron grip on .com without a fight.

The Cost of Israel to US Taxpayers

By Richard H. Curtiss
Former U.S. Foreign Service Officer
The Washington Report on Middle East Affairs

For many years the American media said that “Israel receives $1.8 billion in military aid” or that “Israel receives $1.2 billion in economic aid.” Both statements were true, but since they were never combined to give us the complete total of annual U.S. aid to Israel, they also were lies—true lies.

Recently Americans have begun to read and hear that “Israel receives $3 billion in annual U.S. foreign aid.” That’s true. But it’s still a lie. The problem is that in fiscal 1997 alone, Israel received from a variety of other U.S. federal budgets at least $525.8 million above and beyond its $3 billion from the foreign aid budget, and yet another $2 billion in federal loan guarantees. So the complete total of U.S. grants and loan guarantees to Israel for fiscal 1997 was $5,525,800,000.

One can truthfully blame the mainstream media for never digging out these figures for themselves, because none ever have. They were compiled by the Washington Report on Middle East Affairs. But the mainstream media certainly are not alone. Although Congress authorizes America’s foreign aid total, the fact that more than a third of it goes to a country smaller in both area and population than Hong Kong probably never has been mentioned on the floor of the Senate or House. Yet it’s been going on for more than a generation.

Probably the only members of Congress who even suspect the full total of U.S. funds received by Israel each year are the privileged few committee members who actually mark it up. And almost all members of the concerned committees are Jewish, have taken huge campaign donations orchestrated by Israel’s Washington, DC lobby, the American Israel Public Affairs Committee (AIPAC), or both. These congressional committee members are paid to act, not talk. So they do and they don’t.

The same applies to the president, the secretary of state, and the foreign aid administrator. They all submit a budget that includes aid for Israel, which Congress approves, or increases, but never cuts. But no one in the executive branch mentions that of the few remaining U.S. aid recipients worldwide, all of the others are developing nations which either make their military bases available to the U.S., are key members of international alliances in which the U.S. participates, or have suffered some crippling blow of nature to their abilities to feed their people such as earthquakes, floods or droughts.

Israel, whose troubles arise solely from its unwillingness to give back land it seized in the 1967 war in return for peace with its neighbors, does not fit those criteria. In fact, Israel’s 1995 per capita gross domestic product was $15,800. That put it below Britain at $19,500 and Italy at $18,700 and just above Ireland at $15,400 and Spain at $14,300.

source

If Americans Knew (Mission Statement)

In a democracy, the ultimate responsibility for a nation’s actions rests with its citizens. The top rung of government – the entity with the ultimate power of governance – is the asserted will of the people. Therefore, in any democracy, it is essential that its citizens be fully and accurately informed.

In the United States, currently the most powerful nation on earth, it is even more essential that its citizens receive complete and undistorted information on topics of importance, so that they may wield their extraordinary power with wisdom and intelligence.

Unfortunately, such information is not always forthcoming.

The mission of If Americans Knew is to inform and educate the American public on issues of major significance that are unreported, underreported, or misreported in the American media.

It is our belief that when Americans know the facts on a subject, they will, in the final analysis, act in accordance with morality, justice, and the best interests of their nation, and of the world. With insufficient information, or distorted information, they may do the precise opposite.

It is the mission of If Americans Knew to ensure that this does not happen – that the information on which Americans base their actions is complete, accurate, and undistorted by conscious or unconscious bias, by lies of either commission or omission, or by pressures exerted by powerful special interest groups. It is our goal to supply the information essential to those responsible for the actions of the strongest nation on earth – the American people.

Please help!

CDC Members Own More Than 50 Patents Connected to Vaccinations

The following is a partial list of some of the patents that are owned or shared by members of the CDC and/or ACIP committee, including Dr. Paul Offit:

“Nucleic acid vaccines for prevention of flavivirus infection” –
This patent comes into play during the manufacturing process of vaccines for yellow fever, Zika, Dengue, West Nile virus and more. Various vaccination testing methods – When pharmaceutical companies need to test aspects of a new vaccine, they may utilize one of the CDC’s patented testing methods including an artificial lung system for aerosol vaccines and a process that screens new vaccines for human rhinoviruses. Adjuvant patents – Adjuvants are components within vaccinations intended to create an intensified immune reaction; members of the ACIP own patents on adjuvants used specifically in vaccinations created for premature babies and full term newborns. Assays that assist vaccine development – During the vaccine development process, manufacturers will often observe biological samples for specific antibodies; the CDC owns a patent on an assay that facilitates this monitoring system. Vaccine quality control – patents on various aspects of quality control for vaccinations are utilized by pharmaceutical companies on a large scale once a new vaccine is actively distributed to the public. In total, 56 individual patents were found to be owned or shared by one or more members of the ACIP committee or other committees within the CDC.

Members Claim They are Unbiased
When prompted with questions pertaining to their financial connections with pharmaceutical companies, most ACIP members claim they are able to remain unbiased despite the rewards they receive every time a new vaccination is recommended to the public. In numerous instances, vaccines released to the market are later removed after serious side effects are documented. The rotavirus vaccine was one such example; it was pulled from the market in 1999, a year after its initial approval. In 2001, the House Government Reform Committee found that four out of the eight ACIP members who voted to approve the vaccine had direct financial ties to one or more of the pharmaceutical companies who produced the vaccine for public use. Similar situations involving many other vaccinations have been independently documented over the course of nearly 20 years.

A Multi Billion Dollar Industry
The vaccination industry currently generates $30 billion in profit each year, some of which reaches the hands of the very people who create the vaccine schedule. Despite concerns connecting vaccinations to the increase in autism and a host of other disorders, the number of recommended vaccines continues to grow each year. With a new federal administration interested in uncovering the dirty secrets hidden within alliances between CDC members and vaccine manufacturers, we may begin to see a wave of personal injury and wrongful death lawsuits related directly to unethical behaviors which have led to numerous unsafe vaccines being pushed on an unknowing public. If the National Vaccine Injury Compensation Program (NVICP) is amended or repealed, victims of vaccine damage will be legally permitted to file claims directly against vaccine manufacturers and members of the ACIP committee who often have had knowledge of vaccine risks yet continue to recommend their widespread use.

source

Vaccine "Emergency Use Authorization"

B. EUA MEDICAL PRODUCTS

1. Criteria for Issuance

During the effective period of the HHS Secretary’s EUA declaration, FDA may authorize the introduction of a medical product into interstate commerce when the product is intended for use during an actual or potential emergency. EUA candidate products include medical products and uses that are not approved, cleared, or licensed under sections 505, 510(k), and 515 of the FDC Act or section 351 of the PHS Act.

After the requisite determination and declaration have been issued, and after feasible and appropriate consultations, FDA may issue an EUA only if FDA concludes that the following four statutory criteria for issuance have been met. If the product does not meet the statutory criteria for issuance or is not otherwise an appropriate candidate, an alternative regulatory mechanism (i.e., access under an IND or IDE, which can include expanded access protocols20) may be an appropriate means to provide patients access to an unapproved use of a product in a CBRN emergency.

a. Serious or Life-Threatening Disease or Condition

For FDA to issue an EUA, the CBRN agent(s) referred to in the HHS Secretary’s EUA declaration must be capable of causing a serious or life-threatening disease or condition.

b. Evidence of Effectiveness

Medical products that may be considered for an EUA are those that “may be effective” to prevent, diagnose, or treat serious or life-threatening diseases or conditions that can be caused by a CBRN agent(s) identified in the HHS Secretary’s declaration of emergency or threat of emergency under section 564(b). Potential EUA products also include those that may be effective to mitigate a disease or condition caused by an FDA-regulated product (including a product authorized for emergency use under section 564 or an approved product) used to diagnose, treat, or prevent a disease or condition caused by a CBRN agent.

c. Risk-Benefit Analysis

A product may be considered for an EUA if the Commissioner determines that the known and potential benefits of the product, when used to diagnose, prevent, or treat the identified disease or condition, outweigh the known and potential risks of the product. In making this assessment, FDA must take into consideration the material threat posed by the CBRN agent(s) identified in the HHS Secretary’s declaration of emergency or threat of emergency if applicable (section 564(c)).

In determining whether the known and potential benefits of the product outweigh the known and potential risks, FDA intends to look at the totality of the scientific evidence to make an overall risk-benefit determination. Such evidence, which could arise from a variety of sources, may include (but is not limited to): results of domestic and foreign clinical trials, in vivo efficacy data from animal models, and in vitro data, available for FDA consideration. FDA will also assess the quality and quantity of the available evidence, given the current state of scientific knowledge. The types of evidence that FDA may consider and that should be submitted to support a request for an EUA are discussed more fully in section III.D.2 of this guidance.

d. No Alternatives

For FDA to issue an EUA, there must be no adequate, approved, and available alternative to the candidate product for diagnosing, preventing, or treating the disease or condition. A potential alternative product may be considered “unavailable” if there are insufficient supplies of the approved alternative to fully meet the emergency need. A potential alternative product may be considered “inadequate” if, for example, there are contraindicating data for special circumstances or populations (e.g., children, immunocompromised individuals, or individuals with a drug allergy), if a dosage form of an approved product is inappropriate for use in a special population (e.g., a tablet for individuals who cannot swallow pills), or if the agent is or may be resistant to approved and available alternative products.

source of PDF (page 7 and 8)

Pineal Gland Calcification Fluoride

Jenifer Luke Studies on Fluoridation Impact:

“Fluoride is likely to cause decreased melatonin production and to have other effects on normal pineal function, which in turn could contribute to a variety of effects in humans.” (National Research Council 2006).

In the 1990s, a British scientist, Jennifer Luke, discovered that fluoride accumulates to strikingly high levels in the pineal gland. (Luke 2001). The pineal gland is located between the two hemispheres of the brain and is responsible for the synthesis and secretion of the hormone melatonin. Melatonin maintains the body’s circadian rhythm (sleep-wake cycle), regulates the onset of puberty in females, and helps protect the body from cell damage caused by free radicals.

While it is not yet known if fluoride accumulation affects pineal gland function, preliminary animal experiments found that fluoride reduced melatonin levels and shortened the time to puberty. (Luke, 1997). Based on this and other evidence, the National Research Council has stated that “fluoride is likely to cause decreased melatonin production and to have other effects on normal pineal function, which in turn could contribute to a variety of effects in humans” (NRC, 2006, p. 256).

The Pineal Gland Has Highest Levels of Fluoride in Body

As a calcifying tissue that is exposed to a high volume of blood flow, the pineal gland is a major target for fluoride accumulation in humans. In fact, the calcified parts of the pineal gland (hydroxyapatite crystals) contain the highest fluoride concentrations in the human body (up to 21,000 ppm F), higher than either bone or teeth. (Luke 1997; 2001). Although the soft tissue of the pineal does not accumulate fluoride to the same extent as the calcified part, it does contain higher levels of fluoride than found than in other types of soft tissue in the body — with concentrations (~300 ppm F) that are known in other contexts to inhibit enzymes. While the impacts of these fluoride concentrations in the pineal are not yet fully understood, studies have found that calcified deposits in the pineal are associated with decreased numbers of functioning pinealocytes and reduced melatonin production (Kunz et al., 1999) as well as impairments in the sleep-wake cycle. (Mahlberg 2009).

Fluoride and Earlier Puberty in Girls

In the United States, children are reaching the age of puberty at earlier ages than in the past — a trend that carries health consequences, including a heightened risk for breast cancer. Some evidence indicates that fluoride, via its effect on the pineal, could be a contributing cause to this trend. In animal studies, for example, fluoride exposure has been found to cause a decrease in the amount of circulating melatonin and lead to an accelerated sexual maturation in females. (Luke 1997). Similar findings have been reported in two epidemiological studies of human populations drinking fluoridated water. In the first published fluoridation safety experiment in Newburgh, New York, the authors found that girls living in a fluoridated community reached puberty five months earlier than girls living in a non-fluoridated community. (Schlesinger 1956) Later, in 1983, Farkas reported that postmenarcheal girls were “present at younger ages in the higher fluoride town than in the low-fluoride town, although the reported median ages were the same.”

REFERENCES:

Farkas G, et al. (1983). The fluoride content of drinking water and menarcheal age. Acta Univ Szeged Acta Biol. 29(1-4):159-168.

Kunz D, et al. (1999). A new concept for melatonin deficit: on pineal calcification and melatonin excretion. Neuropsychopharmacology 21(6):765-72.

Luke J. (2001). Fluoride deposition in the aged human pineal gland. Caries Res. 35(2):125-128.

Luke J. (1997). The Effect of Fluoride on the Physiology of the Pineal Gland. Ph.D. Thesis. University of Surrey, Guildford.

Mahlberg R, et al. (2009). Degree of pineal calcification (DOC) is associated with polysomnographic sleep measures in primary insomnia patients. Sleep Med. 10(4):439-45.

National Research Council. (2006). Fluoride in Drinking Water: A Scientific Review of EPA’s Standards. National Academies Press, Washington D.C.

Schlesinger ER, et al. (1956). Newburgh-Kingston caries fluorine study. XIII. Pediatric findings after ten years. J Am Dent Assoc. 52(3):296-306.

CNN: Biden Shut Down Trump's Admin Probe into Origins of COVID-19 in China

Exposing COVID-19 As "The Great HOAX"

Testing for Covid-19 was to Intentionally mislead the public by both the CDC and WHO

The Real Time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) test was adopted by the WHO on January 23, 2020 as a means to detecting the SARS-COV-2 virus, following the recommendations of a Virology research group (based at Charité University Hospital, Berlin), supported by the Bill and Melinda Gates Foundation. (For Further details see the Drosten Study)

Exactly one year later on January 20th, 2021, the WHO retracts. They don’t say “We Made a Mistake”. The retraction is carefully formulated. (See original WHO document here as well as in Annex)

While the WHO does not deny the validity of their misleading January 2020 guidelines, they nonetheless recommend “Re-testing” (which everybody knows is an impossibility).

The contentious issue pertains to the number of amplification threshold cycles (Ct). According to Pieter Borger, et al

The number of amplification cycles [should be] less than 35; preferably 25-30 cycles. In case of virus detection, >35 cycles only detects signals which do not correlate with infectious virus as determined by isolation in cell culture…(Critique of Drosten Study)

The World Health Organization (WHO) tacitly admits one year later that ALL PCR tests conducted at a 35 cycle amplification threshold (Ct) or higher are INVALID. But that is what they recommended in January 2020, in consultation with the virology team at Charité Hospital in Berlin.

If the test is conducted at a 35 Ct threshold or above (which was recommended by the WHO), segments of the SARS-CoV-2 virus cannot be detected, which means that ALL the so-called confirmed “positive cases” tabulated in the course of the last 14 months are invalid.

According to Pieter Borger, Bobby Rajesh Malhotra, Michael Yeadon, et al, the Ct > 35 has been the norm “in most laboratories in Europe & the US”.

The WHO’s Mea Culpa

Below is the WHO’s carefully formulated “Retraction”. The full text with link to the original document is in annex:

WHO guidance Diagnostic testing for SARS-CoV-2 states that careful interpretation of weak positive results is needed (1). The cycle threshold (Ct) needed to detect virus is inversely proportional to the patient’s viral load. Where test results do not correspond with the clinical presentation, a new specimen should be taken and retested using the same or different NAT technology. (emphasis added)

WHO reminds IVD users that disease prevalence alters the predictive value of test

results; as disease prevalence decreases, the risk of false positive increases (2). This means that the probability that a person who has a positive result (SARS-CoV-2 detected) is truly infected with SARS-CoV-2 decreases as prevalence decreases, irrespective of the claimed specificity.

“Invalid Positives” is the Underlying Concept

This is not an issue of “Weak Positives” and “Risk of False Positive Increases”. What is at stake is a “Flawed Methodology” which leads to invalid estimates.

What this admission of the WHO confirms is that the estimate of covid positive from a PCR test (with an amplification threshold of 35 cycles or higher) is invalid. In which case, the WHO recommends retesting: “a new specimen should be taken and retested…”.

The WHO calls for “Retesting”, which is tantamount to “We Screwed Up”.

That recommendation is pro-forma. It won’t happen. Millions of people Worldwide have already been tested, starting in early February 2020. Nonetheless, we must conclude that unless retested, those estimates (according to the WHO) are invalid.

An interview with Dr. Mullis – the scientist who invented PCR test.

In recent months an abundance of evidence has shown that the “gold standard” procedure for detecting COVID-19 is unreliable and could be producing untold numbers of false positives. If this is the case, why are health officials around the world calling for more tests? A discussion with Dr. Kary Mullis – Nobel Laureate, Chemistry – source

The scientist which invented the PCR test, Kary Mullis states – the PCR test is a method which amplifies a small segment of DNA hundreds of times to make it easier to analyze.

In recent months an abundance of evidence has shown that the “gold standard” procedure for detecting COVID-19 is unreliable and could be producing untold numbers of false positives. If this is the case, why are health officials around the world calling for more tests? A discussion with Dr. Kary Mullis – Nobel Laureate, Chemistry – source

Reports are streaming in, declaring a Dark Winter for the world due to COVID19. The media rushes to tell the public that case numbers are on the rise again. In response, case numbers are used to support calls for lockdowns, travel and dining restrictions, and the push for compulsory vaccines.

However, in recent months an abundance of evidence has shown that the “gold standard” procedure for detecting COVID-19 is unreliable and could be producing untold numbers of false positives. If this is the case, why are health officials around the world calling for more tests?

This report is a brief look into the history of the polymerase chain reaction (PCR) procedure and the evidence that PCR is unreliable and should not be used as a determinant for the number of COVID-19 cases or as a factor in political decisions. Please share with friends and family to keep them informed, and if someone shared this with you, please watch with an open mind.

In the months since the COVID-19 panic began health authorities around the world have encouraged the public to “get tested” to help track the spread of SARS-CoV-2, the strain of coronavirus that causes COVID19. However, as fear and hysteria subside, the scientific community and public at large are calling into question the efficacy of the test used to determine a patient’s status.

The main test that is used to determine an individual status involves the polymerase chain reaction (PCR) method. This incredibly sensitive technique was developed by Berkeley scientist Kary Mullis, for which he was awarded the Nobel Prize in 1993. The PCR method amplifies a small segment of DNA hundreds of times to make it easier to analyze. For COVID19, a process known as Reverse transcription polymerase chain reaction (RT-PCR) is used to detect SARS-CoV-2 by amplifying the virus’ genetic material so it can be detected by scientists.

PCR is sometimes described as a technique or process, but for simplicity we will refer to it as a test. PCR is viewed as the gold standard, however, it is not without problems. PCR amplifies a virus’s genetic material and then each sample goes through a number of cycles until a virus is recovered. This is known as the “cycle threshold” and has become a key component in the debate around the efficacy of the PCR test.

In late August 2020, I attended a press conference in Houston, Texas to ask Houston Health Authority Dr. David Persse about concerns about PCR.

Dr. Persse says that when the labs report numbers of COVID-19 cases to the City of Houston they only offer a binary option of “yes” for positive or “no” for negative. “But, in reality, it comes in what is called cycle-thresholds. It’s an inverse relationship, so the higher the number the less virus there was in the initial sample,” Persse explained. “Some labs will report out to 40 cycle-thresholds, and if they get a positive at 40 – which means there is a tiny, tiny, tiny amount of virus there – that gets reported to us as positive and we don’t know any different.”

Persse noted that the key question is, at what value is someone considered still infectious?

“Because if you test me and I have a tiny amount of virus, does tha

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