U.S. Supreme Court Holds for Allowing Good-Faith Defense in Prosecutions for Pain Management, as Urged by AAPS

U.S. Supreme Court Holds for Allowing Good-Faith Defense in Prosecutions for Pain Management, as Urged by AAPS

In a stunning reversal of two Courts of Appeals, the U.S. Supreme Court unanimously overturned their decisions in prosecutions of physicians who were denied a full good-faith defense in connection with their prescription of pain medications. One of the physicians had been sentenced to 21 years in prison, while the other physician received a 25-year sentence.

The Supreme Court agreed with the position taken in the amicus brief filed by the Association of American Physicians and Surgeons (AAPS), which urged allowance of a good-faith defense. “Physicians should not be placed in a Catch-22 of denying patients pain relief or facing decades in prison if prosecuted for it,” stated AAPS General Counsel Andrew Schlafly.

“Lengthy incarceration without proving criminal intent is tyrannical,” states the AAPS amicus brief in Ruan v. United States, No. 20-1410. “A 21-year imprisonment for medicating pain deters all physicians against fully treating patients who suffer.”

On Monday the Supreme Court held that “the Court of Appeals in both cases evaluated the jury instructions under an incorrect understanding of” the requirement of proof of criminal intent by the physicians. The Supreme Court concluded that “the Government must prove beyond a reasonable doubt that the defendant knowingly or intentionally acted in an unauthorized manner.”

This ruling reversed the decision of the 11th Circuit in the Ruan case and the 10th Circuit in Kahn v. United States, No. 21–5261.

“It is rare for the Supreme Court to simultaneously reverse the decisions of two Courts of Appeals,” Mr. Schlafly observes. “Perhaps the shocking sentences without proof by the government of criminal intent by the defendants compelled the Supreme Court to take its extraordinary action,” he added. “The Justices unanimously agreed that this process for punishing physicians went too far and needed to be reined in.”

Next the Courts of Appeals receive these cases back on remand in an opportunity for them to correct their errors.

The Association of American Physicians and Surgeons (AAPS) is a national organization representing physicians in all specialties since 1943. Its motto is omnia pro aegroto (everything for the patient).


Supreme Court Makes Right Decision on Dobbs, Says AAPS

Supreme Court Makes Right Decision on Dobbs, Says AAPS

The issue in Dobbs v. Jackson Women’s Health Organization, which overturned Roe v. Wade, is whether the Supreme Court of the United States has the authority to repeal medical-practice-related laws of 50 States, says the Association of American Physicians and Surgeons (AAPS).

“The federal government has no constitutional authority to regulate the practice of medicine,” states AAPS executive director Jane Orient, M.D. “The Constitution has no explicit provision establishing a right to abortion. This supposed right was not ‘found’ until 1973, when Justice Blackmun perceived it to be hidden in emanations and penumbras.”

In its amicus brief, AAPS noted that in Roe the Court relied on scientific presumptions shown to be wrong in the past 50 years of research.

“Starting with Roe, this Court’s abortion jurisprudence has repeatedly pledged allegiance to scientific fact,” AAPS writes. “The Court has a ‘constitutional duty’ to reexamine its jurisprudence given the now-repudiated ‘factual’ underpinnings of Roe’s central holding.”

The brief outlines the now-known facts of fetal development, illustrated with ultrasound images. From the instant of fertilization, development proceeds at a much more rapid pace than previously believed, AAPS notes.

The AAPS brief concludes: “States have a vital interest in protecting the ‘life of the unborn…. This Court should therefore return to the States ‘the right to readjust [their] views and emphases in the light of the advanced knowledge’ available today.”

Following the 1973 Roe v. Wade decision, organizations including the AMA weakened their ethical positions on the sanctity of life. AAPS, in contrast, remains a strong supporter for life. The Principles of Medical Ethics of AAPS state, “The physician should not condone the taking of human life in the practice of his profession, but at all times respect the sanctity of human life and seek to preserve or improve the quality of life.” In addition, AAPS resolution 2003-2 affirms, “that the Association of American Physicians and Surgeons supports the right to life of human beings from the moment of conception to natural death.”

The Association of American Physicians and Surgeons (AAPS) is a national organization representing physicians in all specialties since 1943. Its motto is omnia pro aegroto (everything for the patient).


AAPS Announces Support for Physician Who is to Be Imprisoned for Making a Speech in the Capitol

AAPS Announces Support for Physician Who is to Be Imprisoned for Making a Speech in the Capitol

Association of American Physicians and Surgeons (AAPS) announces its support for emergency physician and founder of America’s Frontline Doctors (AFLDS) Simone Gold, M.D., J.D.,who  has been sentenced by Judge Christopher (“Casey”) Cooper to 60 days in federal prison, a year’s supervised release, and a fine of $9,500, the largest fine ever imposed on Capitol demonstrators, for the misdemeanor charge of entering a restricted building on Jan 6.

Dr. Gold was in Washington, D.C., by invitation to speak about COVID-19 at a Rally for Health Freedom on the East side of the Capitol. After all the speeches were canceled without explanation, she entered the Capitol building along with a crowd, and attempted to deliver her message there while a police officer stood by without objecting.

AFLDS explained the events of Jan 6 and the subsequent armed invasion to arrest Dr. Gold at her California home in a press statement. The Judge disagreed with Dr. Gold’s portrayal of her conduct as peaceful, in lengthy harsh comments during the sentencing. The facts of the situation were not adjudicated at a trial because Dr. Gold had agreed to a plea bargain.

Dr. Gold’s license to practice medicine is threatened because of alleged “misinformation” about COVID-19 early treatment and vaccination. The president of the Medical Board of California, attorney Kristina D. Lawson, wrote a letter to Judge Cooper prior to sentencing, alluding to a popular AFLDS video: “Doc Tracy, Physician Investigator: ‘Lawson’s Hunt.’”

“Dr. Gold put her professional life on the line in her efforts to provide extensive, life-saving information about early out-patient treatment of COVID-19 and adverse effects of mRNA vaccines,” stated AAPS executive director Jane Orient, M.D. “She made reasonable assumptions that are apparently no longer correct about freedom of speech and assembly, and equal application of the law.”

“This should concern every American,” Dr. Orient said. “Also, those who are defining ‘misinformation’ about COVID need to answer: ‘How many of the million Americans who reportedly died from COVID had received inexpensive early treatment, and how many were denied access to such treatment?’”

The Association of American Physicians and Surgeons (AAPS) is a national organization representing physicians in all specialties since 1943. Its motto is omnia pro aegroto (everything for the patient).


COVID-19: Shall You Rush to Inject Your Toddler?

COVID-19: Shall You Rush to Inject Your Toddler?

Many parents are said to be relieved that they can now take their toddler or 6-month-old infant for their COVID shots. The federal advisory committee considering the shots voted 22 to zero to recommend Emergency Use Authorization (EUA) for both Pfizer and Moderna injections for children at least 6 months old, and FDA and CDC approved them with lightning speed. Thus, the shots that the federal government already bought and paid for won’t have to be wasted.

The shots only have an EUA, not FDA approval, and you will need to sign a consent form. Some data you might like to consider: As of May, there had been 60,442 adverse events involving liver damage reported to the FDA’s Vaccine Adverse Event Reporting System (VAERS), including 204 in children under age 12. Some involved death or need for a liver transplant.

Evidently, children under age 12 were being given unauthorized shots.

Observers of the hearings pointed out:

  • The trials in young children enrolled 4,500 subjects, but 3,000 (67%) dropped out.
  • No actual health benefits were shown, so they used “immunobridging”—comparing antibody response to that of older subjects in a previous trial. A number of experts said that antibody response did not correlate well with immunity, especially against the new variants.
  • Committee members received risk: benefit documents (190 single-spaced pages) at most two days before the meeting, so they did not have adequate time to study them.
  • By fall of 2021, 26 high-quality studies from outside the U.S. showed a two- to seven-fold increased risk of myocarditis (inflammation of the heart) from mRNA shots.

While the shots are “free,” children and their parents will pay the costs of any adverse reactions.

Parents need to do due diligence. In particular, they need to be alert to mild symptoms that could warn of myocarditis. Doctors need to have a “high index of suspicion” for checking blood troponin levels and other indicators of heart damage to allow early diagnosis and treatment.


Missouri Enacts Good Law to Protect Prescription of Hydroxychloroquine and Ivermectin

Missouri Enacts Good Law to Protect Prescription of Hydroxychloroquine and Ivermectin

On June 7, the Governor of Missouri signed into law protection of physicians who prescribe hydroxychloroquine or ivermectin to treat COVID-19. This groundbreaking new law will help immensely by removing obstacles to early treatment that is prescribed by many physicians and supported by many studies worldwide, states AAPS.

“The act of lawfully dispensing, prescribing, administering, or otherwise distributing ivermectin tablets or hydroxychloroquine sulfate tablets for human use shall not be grounds for denial, suspension, revocation, or other disciplinary action by the board,” the new Missouri law states. Enacted as HB 2149, this legislation passed nearly unanimously in the Missouri House and Senate before Governor Michael Parsons signed it into law.

“Physicians have been unfairly targeted by many medical boards for prescribing early treatment for COVID-19,” observes Jane Orient, M.D., executive director of AAPS. “It is encouraging to see Missouri stand up for patients’ rights to receive treatment their physicians think is best.”

This new law also prohibits interference with early COVID-19 treatment by the large pharmacy chains: “A pharmacist shall not contact the prescribing physician or the patient to dispute the efficacy of ivermectin tablets or hydroxychloroquine sulfate tablets for human use unless the physician or patient inquires of the pharmacist about the efficacy of ivermectin tablets or hydroxychloroquine sulfate tablets,” this law states.

“Some pharmacists, particularly ones working for large chains, have blocked prescriptions for patients suffering from COVID-19,” Dr. Orient adds. “Lack of early treatment can result in unnecessary hospitalizations.”

Andrew Schlafly, general counsel of AAPS, declared that “more states should enact similar laws. The State of Missouri is taking the lead in helping patients exercise medical freedom.”

The Association of American Physicians and Surgeons (AAPS) is a national organization representing physicians in all specialties since 1943. Its motto is omnia pro aegroto (everything for the patient).


Worldwide Medical Bombshell: COVID Vaccine “Blood Clots” Explained

Worldwide Medical Bombshell: COVID Vaccine “Blood Clots” Explained

by Dr. Ariyana Love, ND

The strange “blood clots” samples found by embalmer Richard Herschman and first aired by Dr. Jane Ruby on Stew Peters Show at Red Voice Media in January, were recently examined LIVE on air by scientist Mike Adams, in the InfoWars studio, in a worldwide medical bombshell.

The samples pulled out of the veins and arteries of COVID vaccinated corpses shocked the world and exposed that something more than just “vaccination” is happening with the COVID vaxx. The fact that mainstream media did not pick up on this story is more proof we’re in dystopian times.

Embalmer Richard Heirschman’s samples published by Dr. Jane Ruby
Embalmer Richard Herischman’s sample published by Mike Adams of Natural News

These images show synthetic tissue is being grown inside humans from the COVID vaxx. This is most likely the cause of “Sudden Adult Death Syndrome.”

Please see the following studies:

Tissue-Engineered Blood Vessels (2005)
Researchers Grow New Blood Vessels In Just Seven Days (2014)
Arterial reconstruction with human bioengineered acellular blood vessels in patients with peripheral arterial disease
From Autologous Flaps to Engineered Vascularized Grafts for Bone Regeneration

China constructing blood vessels (2020)

Bioactive polymeric scaffolds for tissue engineering

Below are images of artificially grown blood vessels by lab scientists.

Artificial blood vessels
Artificial blood vessels

There are synthetic and natural polymers. They are elastic and made from these five different materials:

  1. Polyester polymers PLLA and PGA are among the most commonly used biodegradable synthetic polymers
  1. Silk fibroin protein is extruded from insects and worms. It has biocompatible properties with the human body and ossess relatively high tensile strength. 
  1. Collagen is used for bone construction.
  1. Hyaluronic acid (HA) is a form of hydrogel material for both hard and soft tissue construction. 
  1. Chitosan is biodegradable polysaccharide that comes from chitin via chemical hydrolysis. It’s used in a gel, sponge, or fiber form. 

I believe the below image from the embalmer and published by InfoWars, is a Silk fibroin tissue construct.

Certified embalmer Richard Hirschman’s sample – infoWars


Nanowires are being used for the hybridization of humans. Pharmaceutical companies and world governments are attempting to grow artificial tissue inside humans, using organic matter from cross-species genomics. They appear to be trying to merge humans with electronic devices for internal tracking and remote control.

Nanowires are superconducter batteries used for tissue scaffolding inside the human body. I wrote about tissue scaffolding technology in December of 2021, in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State.

See studies and patent examples:


Nanowire arrays for neurotechnology and other applications

Internalization of ferromagnetic nanowires by different living cells (2010)

Hydrophobic copper nanowires for enhancing condensation heat transfer

Rotational Maneuver of Ferromagnetic Nanowires for Cell Manipulation

Internalization of ferromagnetic nanowires by different living cells

Ultrathin gold nanowires to enhance radiation therapy

The presence of gold nanowires cause elevated lipid peroxidation and intracellular oxidative stress under radiation. This can literally fry people from the inside using microwave frequency. This could explain why vaxxed persons are reporting torture by electrical activity in their head and their body.

I believe the image below that was shared by Mike Adams on InfoWars, shows a gold Nanowire.

Gold Nanowire – InfoWars

This study entitled, Macroporous nanowire nanoelectronic scaffolds for synthetic tissues, reveals electrical sensors made from silicon which are lab-on-a-chip pharmacological platforms and hybrid 3D electronics-tissue materials for synthetic biology and tissue construction for inside the human body. These are planar devices used to probe electrical activity near the surface of the heart, brain and skin, acting as transmitters, transistor and receivers.

“This is nanoelectronics throughout biomaterials and synthetic tissues in 3D using macroporous nanoelectronic scaffolds. They are using silicon nanowire field effect transistor (FET)-based nanoelectronic biomaterials, given their capability for recording both extracellular and intracellular signals with subcellular resolution.”

Nanowires are also called detectors, metal electrode or carbon nanotube/nanofiber or NanoES. They are implantable microelectrodes, nanoscale semiconductors and flexible/stretchable electrodes. The sensor network is flecible, macroporous and 3D. They are used to construct artificial tissue with embedded nanoelectric sensory capabilities.

Below is an image of Nanowires.



Organoids are used to construct a new brain inside humans, for mind control. Organoids and transgenic hydras are being used to build a new neural network inside the body. The studies showing this can be found in my article entitled, Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

Also see: Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.


I wrote about Microspheres, Microbubbles and Microbeads delayed release technology in my article entitled, Quantum Dots, DNA Barcoding, Nano-Razors & The Israeli State.

Microspheres are in the COVID shots. They are also used for tissue engineering and scaffolding, simultaneous drug delivery and for growing cells inside the human body. The technology is externally controlled by EMF transmission. Microspheres can release their payload, weeks, months and even years later.

This tech was developed with the purpose of destroying cancerous tumor cells and now it’s being misused for the Democide of humanity.

The study entitled, Nanostructured injectable cell microcarriers for tissue regeneration, demonstrates that nanostructured microspheres include nanocomposite and nanofibrous microspheres which have been employed as cell carriers for tissue construction. They produce cell attachment and growth, promote cell-carrier interactions and facilitate stem cell differentiation for target tissue construction inside the human body.  

A study entitled, PHBV Microspheres as Tissue Engineering Scaffold for Neurons, demonstrates that Polymeric microspheres are being used to grow artificial neurons inside humans.

A study entitled, Breathing life into engineered tissues using oxygen-releasing biomaterials reveals that the artificial cells feeds on your blood to grow and survive! This may explain the strange blood clots we’re seeing in vaxxed injured persons. Human umbilical vein endothelial cells are used to grow the artificial cells.  

This study entitled, Generation and differentiation of microtissues from multipotent precurser cells for use in tissue engineering, reveals that Microspheres use unrestricted somatic stem cells from human umbilical cord blood.

This technology is truly vampiric and relies on human baby tissue in order to be grown inside humans. This should not be injected into anyone, especially not children.


Congressmen Ask Good Questions of FDA Prior to Meeting on Authorizing COVID Vaccine for Children under Five

Congressmen Ask Good Questions of FDA Prior to Meeting on Authorizing COVID Vaccine for Children under Five

On June 14-15, the Food and Drug Administration’s Vaccines and Related Biological Products Advisory Committee will meet to consider granting Emergency Use Authorization (EUA) for COVID-19 vaccinations for children under age 5. Prior to the meeting, at least 18 congressmen, led by Rep. Bill Posey (R-FL), Rep. Louie Gohmert (R-TX), Sen. Ted Cruz (R-TX), and Sen. Ron Johnson (R-WI), sent a letter calling for answers to a number of questions.

The Association of American Physicians and Surgeons (AAPS) sent copies of the letter to its members, suggesting that they might want to ask their congressional delegation to sign on.

Questions include the following:

  • “Why has the FDA been so slow to release the hundreds of thousands of pages of data from pre-approval manufacturer studies, post-approval adverse events data, other post-approval manufacturer data submitted to the FDA as required by law?”
  • “What is the cardiac risk factor in administering these EUA COVID vaccines to children?”
  • “Why has the FDA recently lowered the efficacy bar for COVID vaccines for youngest children?”

“The vaccines have evidently been procured and paid for already, and availability is being advertised on television and by medical associations, on the presumption that authorization will be granted,” states AAPS executive director Jane Orient, M.D.

“An EUA is not the same as FDA approval,” she notes. “Informed consent is still required. In case of a serious adverse reaction, limited compensation might be available under the PREP Act, which also protects from liability entities that manufacture, distribute, or administer the vaccine.”

“Parents might have the same questions as congressmen ask in this letter,” she adds.

The Association of American Physicians and Surgeons (AAPS) is a national organization representing physicians in all specialties since 1943. Its motto is omnia pro aegroto (everything for the patient).


Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

Pharma Exposed! Autism Spectrum Disorder (ASD) Is Targeted Gene Deletion!

By Dr. Ariyana Love, ND

In my latest interview with Stew Peters, I brought scientific studies revealing that Autism Spectrum Disorder (ASD) is caused by gene deletion in the brain, specifically in the frontal cortex.

The article I referenced from Nature entitled, Epigenetics and cerebral organoids: promising directions in autism spectrum disorders, explains that the inactivation of the X chromosome in the brain is what causes Autism Spectrum Disorder (ASD).

The three regions of the brain being targeted are the temporal cortex, cerebellum, and prefrontal cortex, especially the frontal lobe. These regions were shown to have lower methylation levels of the X chromosome with ASD. The study specifies that X chromosome deletion occurs by “epigenetic dysregulation” (gene deletion) and “DNA methylation” (genetic coding).

“Although the epigenetic mechanisms involved in autism are not yet fully understood, there are findings suggestive of genome-wide dysregulation and epigenetic alterations in ASD (Autism Spectrum Disorder). These studies point to DNA methylation (gene editing) as a likely contributor in the development of the disorder.

There are certain syndromes that have been linked to ASD. DNA methylation in connection to imprinting and X-chromosome inactivation (gene deletion) could be relevant to the field of ASD research. X-chromosome inactivation is a process in which one of the copies of X chromosomes is inactivated and this is also achieved through DNA methylation. It might be associated with autism, as inactivation or removal of inactivation could lead to genetic aberrations.”

Targeted deletion of the X chromosome in other areas of the brain result in ASD conditions such as Angelman syndrome and Prader–Willi syndrome. Deletion of the X chromosome in females causes Turner syndrome which induces mental retardation, developmental delay and effects social reciprocity and communication, a condition of ASD.

Another study entitled, DIA1R Is an X-Linked Gene Related to Deleted In Autism-1 confirms X chromosome deletion explaining, “A DIA1 deletion coincided with a classical autism diagnosis.”

Autism rates have exponentially risen over the last two decades and continues to sharply rise. Belfast, Ireland just reported that one in 14 children have ASD!


In an interview with Maria Zeee, Attorney Todd Callender stated:

“The 1p36 gene deletion is a congenital disease — you’re born with it — and yet that was the number one serious adverse event, and if you look up the symptomology for that, it’s the elimination of your frontal cortex. Your thinking part of your brain, your decision-making part of your brain, is the number one serious adverse event listed by Pfizer.”

Previously, we were told that deletion syndromes as well as the 1p36 Deletion Syndrome, are rare phenomenons. However, now it’s “the most common human disorder” resulting from the deliberate deletion of the X chromosome in the frontal lobe. Not only does the 1p36 gene deletion cause mental retardation but it also causes genital abnormalities in males and females, affecting fertility.

Another study from 2020 reveals that 25% of people affected by “Covid-19” are loosing the electrical activity in the frontal cortex of their brain. Many of my clients, friends and associates have been reporting “brain fog.” Could this be an adverse reaction from transmission (shedding) of vaxxed persons, caused by targeted gene deletion of the frontal lobe?

In addition, the the authors suggest that the infection may have aged people cognitively by around 10 years!

In her recent report, Dr. Stephanie Seneff, a Senior Research Scientist at MIT’s Computer Science and Artificial Intelligence Laboratory in Cambridge, outlined the extensive neurological damage such as PRION, induced by the mRNA “vaccines.” In particular, she highlighted how the mRNA technology is rapidly aging people.

— To view, copy/paste this report link into your url: file:///C:/Users/metan/Desktop/20220612_MD4CE_Dr_Stephanie_Seneff%20-%20Copy.pdf

By the way, the E1 gene is on the X chromosome genetic lineage. I previously documented how pharmaceutical “vaccines” are deleting the E1 gene in my article entitled, EPIGENETICS: Vaccines Are Deleting Human Genes & Transfecting Cells With Ebola/Marburg.

It begs the question. Have pharmaceutical companies been intentionally inducing Autism by deleting genetic codes in the human brain through their vaccination programs? The only way the deletion of the X chromosome is possible is through the use of mRNA nanotechnology.



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