Autoimmunity and Treatment

What They Don’t Tell You About Autoimmune Disorders

and the dangers of conventional rheumatologic approaches to disease

•Treating illnesses by suppressing symptoms frequently precipitates far more severe diseases which have rippled out throughout our society.

•The primary management for most autoimmune conditions is through symptom suppressing drugs, which frequently have significant toxicity.

•In most cases, autoimmune disorders and inflammatory joint conditions have an underlying cause, such as a chronic undiagnosed stealth infection or food allergy, which when addressed significantly improve the condition.

•Many factors in life that we can control and do not require prescriptions to address (e.g., diet, stress or sleep) directly contribute to autoimmunity and, when addressed, improve it.

•This article will review some of the key steps which can be taken to improve autoimmune disorders and reduce one’s reliance upon toxic medications.

Autoimmune conditions have become one of the most common and stubborn health challenges of our time. While conventional medicine often treats them as mysterious immune system malfunctions—managed primarily with harmful steroids and other immunosuppressants —there’s increasing evidence that many of these diseases are not random. Rather, they’re signals of deeper dysfunctions in the body—many of which are tied to the modern lifestyle we’ve come to accept as normal.

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Lifestyle Contributions to Autoimmunity

Many things in our lives that we have control over significantly affect our predisposition to autoimmunity:

Sleep—I have previously written about the profound importance of sleep and how many different illnesses are linked to poor sleep. In practice, we frequently find that patients with autoimmune conditions also have disrupted sleep cycles, and these improve once that is addressed (e.g., by improving sleep hygiene and avoiding blue light).
Note: the treatments for sleeping issues like insomnia are discussed further here.

Sunlight—Since the sun has no commercial lobby to advocate for it, the medical field demonizes sunlight as a cause of cancer despite a deficiency of the sun and sunlight being tied to a wide range of medical conditions (including cancers) and making individuals 60% more likely to die. A loss of sunlight exposure is also tied to many autoimmune conditions (e.g., multiple sclerosis). As such, we frequently find autoimmune patients improve from resuming healthy sunlight exposures (likewise, I suspect this partly explains why ultraviolet blood irradiation benefits so many different autoimmune conditions).
Note: appropriate sunlight exposure (e.g., going outside early in the morning and having the sunlight touch your face without being obstructed by glass) is also very helpful for reestablishing the circadian rhythm and restoring healthy sleep.

Exercise—Many of the benefits of exercise arise from the fluid circulation it creates in the body (as fluid stagnation underlies many illnesses—many of which we suffer from due to our sedentary lifestyle. This perspective in turn, is corroborated by the Chinese Medical viewpoint that blood stasis causes autoimmunity and that either treating blood stasis or zeta potential (which underlies both microclotting and lymphatic stagnation) frequently improves autoimmune conditions.
Note: exercise and eliminating fluid stagnation frequently improve insomnia. Likewise, sunlight exposure is a critical driver of fluid circulation throughout the body, all of which illustrates how intertwined many of the key lifestyle factors we routinely ignore are to our health.

Diet—Food allergens such as wheat, dairy, and nightshades frequently contribute to autoimmune conditions (particularly arthritis), and many have found food elimination diets that identify the reactive allergen to improve their condition significantly. Additionally, in many cases, allergies arise from deficient stomach acid, as without sufficient stomach acid, proteins are often not fully broken down (allowing intact allergens to enter circulation) and triggers acid reflux (due to top of the stomach only closing when sufficient stomach acid is present), which then irritates the lungs.
Note: many of the issues with gluten (e.g., autoimmunity or weight gain) are not experienced in countries like Italy that use more natural forms of wheat.

Stress—is well known to predispose one to autoimmune disorders and flares (e.g., 80% of autoimmune patients report an unusually stressful situation prior to their disease onset, while stress disorders increased the risk of autoimmune disorders by 46%-129%).
Note: some patients will not respond to a rheumatologic drug, until they eliminate the stress in their lives.

The Global Loss of Vitality

If you review the early history of medicine, it is striking:

•How profoundly damaging many of the early western medical remedies were (e.g., the smallpox vaccine or mercury).

•How much healthier people were and how much more effective many natural therapies were in the past than they are now.

This second point prompted me to ask older doctors (from various medical schools) if they had observed a general decline in human vitality in the patients they saw at the start of their careers compared to the end, and all of them shared that they had. Additionally:

•They noted that beyond patients becoming much sicker and having conditions they’d never seen before, it was also much harder to treat them as each therapy they used had shifted from making a dramatic improvement to a more minuscule one, which required numerous successive treatments to bring about an improvement.

•They typically attributed this shift to a loss in human vitality. They cited a variety of correlates (e.g., the average human body temperature dropping, people becoming less able to mount fevers, infants being less able to produce a brisk cry, or increasing degrees of fluid stagnation in their patients).

Note: typically this decline in vitality proceeds in a linear fashion and then spikes at certain times (e.g., after the introduction of the smallpox vaccine, the 1986 law which granted immunity to vaccine manufacturers and led to a rapid proliferation in the vaccine schedule, and after the COVID vaccines). In each case, this increase in disease gets normalized and forgotten by the next generation of doctors (who entered practice after the last wave of sickness had become the “new normal”).

Likewise, many datasets corroborate this steady decreasing vitality in humanity over the decades (e.g., we’ve witnessed a continual increase in autoimmune disorders). Having extensively explored this topic, we believe much of it is due to modern technology (e.g., vaccines, chronic chemical exposures or heavy metal toxicity, dentistry and surgical scars, EMFs, and widespread circadian rhythm disruption). Many of these, in turn, share a common thread—creating fluid stagnation throughout the body.

Note: After thousands of years, around 1830, blood stasis suddenly came to be viewed as a primary cause of disease in Chinese Medicine, which occurred shortly after the smallpox vaccine (which caused many severe injuries resembling blood stasis), which was introduced in China in 1805.

Systemic Suppression

One of the central criticisms of Allopathic (Western) medicine by natural schools of medicine has been that anytime an external agent is used to forcefully change a process which is unfolding within the body (rather than aiding the body’s ability to resolve it) you run the risk of a minor temporary issue being exchanged for a severe chronic one—especially when this is repeatedly done throughout the course of someone’s life. In some cases, this risk is very justified (e.g., in a life-threatening emergency or with a relatively safe drug that has limited long-term complications). At the same time however, a general unwillingness to acknowledge this issue pervades Allopathic medicine.

I’ve thus never forgotten a conference in the 1970s at which one of the world’s leading homeopaths convened a panel to discuss the likely consequences of modern medicine routinely suppressing symptoms (e.g., aggressively using fever suppressing medications or preventing childhood febrile illnesses with vaccination).
Note: studies have repeatedly linked preventing measles, mumps, and chickenpox to severe cancers later in life.

At that conference, building upon the recent mass introduction of suppressive steroids, they correctly predicted that if this suppression continued to increased, in the decades to follow:

•We would see a global shift from less severe illnesses to more severe ones.

•That this suppression would cause physical illnesses to be pushed deeper into the body and be replaced with psychiatric illnesses, and in time spiritual ones (particularly when the psychiatric illnesses were also suppressed with medications)—all of which would dovetail with people being willing to do crazier and crazier things.

Now, everyone has gradually become habituated to patients “just being” sicker and sicker, and that not much can be done about it.

Suppressive Antibiotics

While steroids are one of the medications most associated with “suppressing” illness, many others are too. For example, for years, many natural medicine practitioners (e.g., homeopaths) also told me they’d frequently seen antibiotics “treat” an acute infection but turn it into a chronic one. I wasn’t sure what to make of this (as microbiome disruption could partially but not fully explain it), then I discovered something similar existed in Chinese Medicine:

The concept of Latent Heat is very old in Chinese medicine, having been mentioned for the first time in the ‘Yellow Emperor’s Classic of Internal Medicine’. Latent Heat occurs when an external pathogenic factor penetrates the body without causing apparent symptoms at the time; the pathogenic factor penetrates into the Interior, and ‘incubates’ there, turning into interior Heat. This Heat later emerges with acute symptoms of Heat: when it emerges, it is called Latent Heat.

Note: in modern Chinese Medicine, antibiotics and vaccines are now proposed as sources of latent heat.

Much later, when I read Cell Wall Deficient Forms: Stealth Pathogens all of this finally made sense. This book argued that when bacteria are exposed to lethal stressors, particularly cell wall destroying antibiotics, while most will die, some will instead enter a primitive survival mode and transform into misshapen cell wall deficient (CWD) “mycoplasma like” bacteria which can radically change their size or morphology (and hence look very different). While these bacteria are hard to detect (and when seen, due to no one knowing they “exist,” are often mistaken for cellular debris and ignored), with the correct techniques they can be detected. In turn, the book provides a wealth of evidence that CWD bacteria:

•Are found within many “aseptic” tissues undergoing an autoimmune attack, with specific CWD bacteria associated with many different autoimmune disorders which have no known cause.

•Once the environment is “safe” can transform back into their normal form and cause a sudden recurrence of an infection—suggesting chronic infections are due to antibiotics creating a dormant CWD population rather than continual reinfection.

Note: many popular alternative schools of medicine (e.g., those of RifeNaessens, and Enderlein) came from microscopes which could directly observe these pleomorphic bacteria continually shifting into new morphologies, and that diseases states (e.g., cancer) correlated to specific morphologies, while other morphologies resulted in a symbiotic state of health. Since the morphologies adopted correlated with the internal state of the body, this gave rise to the belief that treatments should aim to create “healthy terrains” within the body, which would give rise to non-pathogenic forms of the bacteria rather than antibiotics that provoked pathogen transformation.

Addressing Autoimmune Diseases

When autoimmune disorders are treated in conventional practice, we feel five errors repeatedly occur:

1. Frequently, autoimmune disorders have a cause (e.g., a chronic infection) that goes unrecognized, resulting in powerful immune-suppressing drugs being used instead, while the underlying issue progresses.

2. In many cases, lifestyle factors significantly exacerbate autoimmune conditions. If these factors were focused on, the symptoms of the autoimmune condition would significantly reduce, and the amount of medication required to manage the condition in tandem would as well.

3. Those lifestyle factors (e.g., diet) can also prevent conventional treatments from working. Because of that, in many cases where a medication that “should work” but does not, focusing on the unaddressed lifestyle factors for a patient is often what’s needed for a remission. Unfortunately, in those instances, rather than the doctor taking a step back and asking, “What am I missing here,” the reflex often is to simply give more immune-suppressing medications. In short, if a patient has been on multiple potent rheumatologic drugs, something important was most likely missed.

4. As many of the safer autoimmune drugs with the best risk to benefit ratio are relatively new, most doctors in practice are not aware they exist (e.g., that side-effect free alternatives to methotrexate exist) or that they can be used to treat many challenging issues in rheumatology (e.g., corticosteroid pills suppressing endogenous steroid production or large rheumatoid nodules). As such, drugs that should not be used for extended periods (e.g., steroids and NSAIDs) are instead frequently the mainstay of treatment.
Note: in some cases (e.g., for a dangerous and rapidly progressing autoimmune disease or in instances where it is not feasible for a patient to implement a natural treatment plan), immune-suppressing medications, even with their side effects, are necessary.

5. Many highly effective non-standard treatments for autoimmune conditions remain fairly unknown despite extensive scientific evidence demonstrating their efficacy (e.g., ultraviolet blood irradiation or DMSO). Likewise, since there are so many natural therapies for autoimmune conditions, it’s often so difficult to sort out which work that they all get cast under the same umbrella and ignored.
Note: many of those therapies are both anti-inflammatory and highly effective at treating mycoplasma bacteria.

Because of these issues, the management of autoimmune conditions remains less than satisfactory for many patients—which is particularly unfortunate given that these conditions are becoming increasingly common (e.g., extensive evidence ties increasing vaccination to autoimmunity).

Conclusion

Since our medical system focuses on treating isolated symptoms with patentable pharmaceuticals rather than attempting to identify the root cause of a permanent illness, patients suffer, particularly those with chronic disorders. In this regard, autoimmune diseases are particularly unfortunate as they force patients to choose between having a debilitating and sometimes fatal illness or a lifetime of fairly toxic immune-suppressing drugs (e.g., steroids have a wide range of severe side effects, particularly when used systemically for a prolonged period).

But here’s the hopeful part: when we start looking at the body as a whole system and work to restore its natural balance—whether through better sleep, movement, diet, or managing stress—people often feel dramatically better. Healing isn’t always fast or easy, but it’s absolutely possible when we stop chasing symptoms and start supporting the body’s own wisdom. Likewise, while very little focus is given in mainstream medicine for producing safe treatments for autoimmunity or arthritis, many natural treatments have been developed (such as DMSO) which no longer force patients to accept a lifetime of toxic therapies to survive and be free of pain.

Author’s note: This is an abridged version of a longer article which goes into more detail on the safest natural and conventional treatments for autoimmune disorders and musculoskeletal disorders like arthritis, the dangers of steroids and the ways to safely utilize or withdraw from steroids. That article can be read here.

from:    https://www.midwesterndoctor.com/p/what-they-dont-tell-you-about-autoimmune?publication_id=748806&post_id=170415402&isFreemail=true&r=19iztd&triedRedirect=true&utm_source=substack&utm_medium=email

New Info on Just What is in those Jabs

Green Monkey DNA Found in COVID-19 Shots

Analysis by Dr. Joseph MercolaFact Checked
May 31, 2023
Link for Video of Sucharit Bhakdti dscussing this issue:   https://rumble.com/v2owij0-why-the-covid-mrna-vaccines-are-actually-dna-gene-therapies-that-must-be-re.html

STORY AT-A-GLANCE

  • Microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project — has discovered massive DNA contamination in the mRNA COVID shots, including simian virus 40 (SV40) promoters
  • SV40 has been linked to cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone. In 2002, the Lancet published evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to 50% of the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year
  • The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S. The highest level of DNA contamination found was 30%
  • The finding of DNA means the mRNA COVID shots may have the ability to alter the human genome
  • Even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself. Partial expression could occur, or it might interfere with other transcription translations that are already in the cell. Cytoplasmic transfection can also allow for genetic manipulation, as the nucleus disassembles and exchanges cellular components with the cytosol during cell division

In the video1 above, Dr. Steven E. Greer interviews microbiologist Kevin McKernan — a former researcher and team leader for the MIT Human Genome project2 — and Dr. Sucharit Bhakdi about the DNA contamination McKernan’s team has found in the Pfizer and Moderna mRNA shots.

As it turns out, spike protein and the mRNA are not the only hazards of these injections. McKernan’s team have also discovered simian virus 40 (SV40) promoters that, for decades, have been suspected of causing cancer in humans, including mesotheliomas, lymphomas and cancers of the brain and bone.3 The findings4,5,6,7 were posted on OSF Preprints in early April 2023. As explained in the abstract:8

“Several methods were deployed to assess the nucleic acid composition of four expired vials of the Moderna and Pfizer bivalent mRNA vaccines. Two vials from each vendor were evaluated … Multiple assays support DNA contamination that exceeds the European Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose requirements …”

As noted by Greer,9 this means that governments and drug companies “have misled the world to a far greater extent than previously known.” If these findings are correct, it would also mean that “the so-called ‘vaccines’ are actually altering the human genome and causing permanent production of the deadly spike protein,” and this internal production of spike protein would, in turn, “trigger the immune system to attack its own cells,” Greer says.

In the interview, McKernan explains how the DNA contaminants found in the COVID jabs can result in the genetic modification of the human genome, and Bhakdi reviews how and why the shots can trigger autoimmune diseases.

Background: What Is SV40?

In 2002, the Lancet published10 evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin’s lymphoma. According to the authors, the vaccine may be responsible for up to half the 55,000 Non-Hodgkin’s lymphoma cases diagnosed each year.

How did this simian (monkey) virus get into the human population? According to the late Dr. Maurice Hilleman, a leading vaccine developer, Merck inadvertently unleashed the virus via their polio vaccine.11 It’s unclear exactly when SV40 was eliminated from the polio vaccine. The timing also varies from country to country. For example, SV40-contaminated polio vaccines were administered in Italy as recently as 1999.12

As reported in a Lancet book review of “The Virus and the Vaccine: The True Story of a Cancer-Causing Money Virus, Contaminated Polio Vaccine and the Millions of Americans Exposed”:13

“By 1960, scientists and vaccine manufacturers knew that monkey kidneys were sewers of simian viruses. Such contamination often spoiled cultures, including those of an NIH researcher named Bernice Eddy, who worked on vaccine safety … Her discovery … threatened one of the USA’s most important public-health programs …

Eddy tried to get word out to colleagues but was muzzled and stripped of her vaccine regulatory duties and her laboratory … [Two] Merck researchers, Ben Sweet and Maurice Hilleman, soon identified the rhesus virus later named SV40 — the carcinogenic agent that had eluded Eddy.

In 1963, U.S. authorities decided to switch to African green monkeys, which are not natural hosts of SV40, to produce polio vaccine. In the mid-1970s, after limited epidemiological studies, authorities concluded that although SV40 caused cancer in hamsters, it didn’t seem to do so in people.

Fast forward to the 1990s: Michele Carbone, then at NIH, was working on how SV40 induces cancers in animals. One of these was mesothelioma, a rare cancer of the pleura thought in people to be caused mainly by asbestos. The orthodoxy held that SV40 didn’t cause human cancers.

Emboldened by a 1992 NEJM paper that found DNA ‘footprints’ of SV40 in childhood brain tumors, Carbone tested human mesothelioma tumor biopsies at the National Cancer Institute: 60% contained SV40 DNA. In most, the monkey virus was active and producing proteins.

He published his results in Oncogene in May, 1994, but the NIH declined to publicize them … Carbone … moved to Loyola University. There he discovered how SV40 disables tumor suppressor genes in human mesothelioma, and published his results in Nature Medicine in July, 1997. Studies in Italy, Germany, and the USA also showed associations between SV40 and human cancers.”

mRNA COVID Jabs Contaminated With Double-Stranded DNA

With that background, let’s get back to McKernan’s findings, which in addition to the featured video are also discussed in Daniel Horowitz’s podcast above. In short, his team discovered elevated levels of double-stranded DNA plasmids, including SV40 promoters (DNA sequence that is essential for gene expression) that are known to trigger cancer development when encountering an oncogene (a gene that has the potential to cause cancer).

The level of contamination varies depending on the platform used to measure it, but no matter which method is used, the level of DNA contamination is significantly higher than the regulatory limits in both Europe and the U.S., McKernan says. The highest level of DNA contamination found was 30%, which is rather astounding.

As explained by McKernan, when using a typical PCR test, you’ll be considered positive if the test detects the SARS-CoV-2 virus using a cycle threshold (CT) of about 40. In comparison, the DNA contamination is detected at CTs below 20.

That means the contamination is a million-fold greater than the amount of virus you’d need to have in order to test positive for COVID. “So, there’s an enormous difference here with regards to the amount of material that’s in there,” McKernan says.

In his Substack article,14 he also points out that people who argue that double-stranded DNA and viral RNA is a false equivalency because viral RNA is replication competent, are wrong.

“The majority of the sgRNA you are detecting in a nasal swab in your nose is NOT REPLICATION COMPETENT as shown in Jaafar et al.15 It is just an RNA fragment that should have lower longevity in your cells than dsDNA contaminating fragments,” he writes.

In that Substack article, McKernan has also copied a 2009 study discussing how DNA in vaccines can cause cancer and highlighted the most relevant parts. It’s a helpful resource if you want to learn more.

Quality Control Is Sorely Lacking

As for how SV40 promoters ended up in the mRNA shots, it appears to be related to poor quality control during the manufacturing process, although it’s unclear where in the development SV40 might have sneaked in. Quality control deficiencies may also be responsible for the high rate of anaphylactic reactions we’ve been seeing. McKernan tells Greer:

“It’s in both Moderna and Pfizer. We looked at the bivalent vaccines for both Moderna and Pfizer and only the monovalent vaccines for Pfizer because we didn’t have access to monovalent vaccines for Moderna. In all three cases, the vaccines contain double-stranded DNA contamination.

If you sequence that DNA, you’ll find that it matches what looks to be an expression vector that’s used to make the RNA … Whenever we see DNA contamination, like from plasmids, ending up in any injectable, the first thing people think about is whether there’s any E. coli endotoxin present because that creates anaphylaxis for the injected.

And, of course … there’s a lot of anaphylaxis going on, not only on TV but in the VAERS database. You can see people get injected with this and drop. That could be the background from this E. coli process of manufacturing the DNA …”

Regulatory Agencies Knew There Was a Contamination Problem

In a May 20, 2023, Substack article,16 McKernan points out that Pfizer itself submitted evidence to the European Medicines Agency (EMA) showing sampled lots contained vast differences in the levels of double-stranded DNA contamination.

The arbitrary limit for dsDNA that the EMA came up with was 330 nanograms per milligram (ng/mg). Data submitted to the EMA by Pfizer shows sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA. McKernan adds:17

“This limit likely did not consider the potency of this dsDNA contamination if it was packaged in an LNP [lipid nanoparticle]. Packaged dsDNA is more potent as a gene therapy. We now know this DNA is packaged and transfection ready.18 Even lower limits should be applied if the DNA is packaged in transfection ready LNPs …

Even with Pfizer being able to cherry pick the data they provided to the EMA for 10 lots, they see a 1 to 815ng/mg variance. If you were to expand this study to 100 or 1000 lots, you’d likely see another order or two of magnitude variance.”

Double-Stranded DNA May Integrate Into Your Genome

The presence of double-stranded DNA also brings up another major concern, and that is the possibility of genomic integration.

“At least on the Pfizer side of things, it has what’s known as an SV40 promoter. This is an oncogenic virus piece. It’s not the entire virus. However, the small piece is known to drive very aggressive gene expression.

And the concern that people, even at the FDA, have noted in the past whenever injecting double-stranded DNA, is that these things can integrate into the genome,” McKernan says.

While McKernan’s paper does not present evidence of genome integration, it does point out that it’s possible, especially in the presence of SV40 promoters:19

“There has been a healthy debate about the capacity for SARs-CoV-2 to integrate into the human genome … This work has inspired questions regarding the capacity for the mRNA vaccines to also genome integrate. Such an event would require LINE-1 driven reverse transcription of the mRNA into DNA as described by Alden et al.

dsDNA [double-stranded DNA] contamination of sequence encoding the spike protein wouldn’t require LINE-1 for Reverse Transcription and the presence of an SV40 nuclear localization signal in Pfizer’s vaccine vector would further increase the odds of integration.”

Manifold Risks

That said, even if genetic modification does not occur, the fact that you’re getting foreign DNA into your cells poses a risk in and of itself, McKernan says. For example, partial expression could occur, or it might interfere with other transcription translations that are already in the cell.

Bhakdi also points out that the SV40 promoters do not need to be present in the nucleus of the cell for problems to occur. Cytoplasmic transfection can, in and of itself, allow for genetic manipulation, because the nucleus disassembles and exchanges cellular components with the cytosol during cell division.

In addition to having DNA floating around and causing potential problems, the RNA in the COVID jab is also modified to resist breakdown. “So, we have TWO versions of the spike protein floating around that can persist longer than anticipated,” McKernan says, and the spike protein, of course, is the most toxic part of the virus that can cause your body to attack itself.

Both McKernan and Bhakdi are adamant that ALL mRNA “vaccines” must be immediately stopped, whether for human or animal use, due to the magnitude of the risks involved.

‘Alarming Problems’

In the video above,20 Yusuke Murakami, a professor at Tokyo University, expresses alarm over the finding of SV40 promoters in the COVID jabs. The interview is in Japanese but has English subtitles. I’ve included it because I think he does a good job of putting the problem into layman’s terms:

“The Pfizer vaccine has a staggering problem,” Murakami says. “This figure is an enlarged view of Pfizer’s vaccine sequence. As you can see, the Pfizer vaccine sequence contains part of the SV40 sequence here. This sequence is known as a promoter.

Roughly speaking, the promoter causes increased expression of the gene. The problem is that the sequence is present in a well-known carcinogenic virus. The question is why such a sequence that is derived from a cancer virus is present in Pfizer’s vaccine.

There should be absolutely no need for such a carcinogenic virus sequence in the vaccine. This sequence is totally unnecessary for producing the mRNA vaccine. It is a problem that such a sequence is solidly contained in the vaccine.

This is not the only problem. If a sequence like this is present in the DNA, the DNA is easily migrated to the nucleus. So it means that the DNA can easily enter the genome. This is such an alarming problem.

It is essential to remove the sequence. However, Pfizer produced the vaccine without removing the sequence. That is outrageously malicious. This kind of promoter sequence is completely unnecessary for the production of the mRNA vaccine. In fact, SV40 is a promoter of cancer viruses.”

Resources for Those Injured by the COVID Jab

The more we learn about the COVID jabs, the worse they appear. While they suck as vaccines, they’re truly masterful bioweapons, as they’re capable of destroying health in any number of ways, through myriad mechanisms.

If you got one or more jabs and are now reconsidering, first and foremost, never ever take another COVID booster, another mRNA gene therapy shot or regular vaccine. You need to end the assault on your body. Even if you haven’t experienced any obvious side effects, your health may still be impacted long-term, so don’t take any more shots.

If you’re suffering from side effects, your first order of business is to eliminate the spike protein that your body is producing. Two remedies that can do this are hydroxychloroquine and ivermectin. Both of these drugs bind and facilitate the removal of spike protein.

The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER. Since the protocol is continuously updated as more data become available, your best bet is to download the latest version straight from the FLCCC website at covid19criticalcare.com21 (hyperlink to the correct page provided above).

For additional suggestions, check out the World Health Council’s spike protein detox guide,22 which focuses on natural substances like herbs, supplements and teas. To combat neurotoxic effects of spike protein, a March 2022 review paper23 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.

from:    https://articles.mercola.com/sites/articles/archive/2023/05/31/dna-contamination-mrna-covid-shots.aspx?ui=f460707c057231d228aac22d51b97f2a8dcffa7b857ec065e5a5bfbcfab498ac&sd=20211017&cid_source=dnl&cid_medium=email&cid_content=art1ReadMore&cid=20230531&cid=DM1408714&bid=1815660384

Physician to Presidents, Nobel Prize Nominee Speaks Out

Dr Vladimir Zelenko risks his life by saying this – [Must See!]

vladimir zelenko

The world renowned Physician of Presidents, and nominee for the Nobel Peace Prize, Dr. Vladimir Zelenko takes a BIG RISK by speaking out fearlessly about the devastating destruction the current vaccinations are causing worldwide. Before a Rabbinical court in Jerusalem he testifies how millions may have died and possibly billions may lose their lives in the coming years. Dr. Zelenko helped make the Vaccine Death Report that shows all the scientific evidence for the shocking claims he is making in this video. Make sure to download this revealing report, after watching this video.

Few medical experts have the courage to speak out
 as freely as this hero of humanity. 

Watch and share!

from:   https: //www.stopworldcontrol.com/zelenko/

 

The Mind & Gut

Evidence for the Gut-Brain Connection

By Nikki Harper

Staff Writer for Wake Up World

It has been known for several decades that gut health appears to have an effect on mental health and brain health – the so-called gut-brain axis. For example, autoimmune diseases such as inflammatory bowel disease have been linked with mood disorders, anxiety and depression. However, the precise mechanism by which the gut-brain axis functions has been largely unknown – but now, new research is starting to shed light on this matter.

According to research published in Nature and carried out by Weill Cornell Medicine, depleted microbiota in the gut can cause altered gene expression in microglia, which are immune cells found in the brain [1]. This effectively interferes with the connections of brain synapses which should occur during a learning process.

The breakthrough was made during a study of mice. Researchers found that mice treated with antibiotics, which depletes the levels of gut microbiota, showed impaired ability in fear extinction, ie they were slower to learn that a threat was no longer present than mice with normal levels of gut microbiota. When researchers sequenced the RNA in the mice microglia, the altered gene expression was discovered.

The same study also examined mice which had been bred to be ‘germ-free’ (ie without gut microbiota). These mice were found to have altered concentrations of metabolites which have been associated with schizophrenia and autism. Researchers were able to mitigate this by restoring gut microbiota in these mice, but only if they did so immediately following birth – an interesting finding, given that the types of psychiatric and mental health disorders associated with autoimmune disease in humans are often those which are also linked to problems with early brain development.

This research is the first time that a potential mechanism for the gut-brain axis has been scientifically described. The gut-brain axis impacts every single human being, every day of their lives,” said Dr David Artis, director of the Jill Roberts Institute for Research in Inflammatory Bowel Disease. We are beginning to understand more about how the gut influences diseases as diverse as autism, Parkinson’s disease, post-traumatic stress disorder and depression. Our study provides a new piece of understanding of how the mechanisms operate.”

The findings of this study open up potential new avenues for treatment of some autoimmune and psychiatric disorders. With a clearer picture of how diet, infection, and lifestyle influence brain health and subsequent susceptibility to neuropsychiatric disorders, we could potentially gain unique insight into how to treat or prevent debilitating, physically and emotionally painful conditions which are becoming increasingly common. The study authors are hopeful. “”We don’t know yet, but down the road, there is a potential for identifying promising targets that might be used as treatments for humans in the future,” said Dr Conor Liston, an associate professor of psychiatry at Weill Cornell Medicine. “Brain chemistry essentially determines how we feel and respond to our environment, and evidence is building that chemicals derived from gut microbes play a major role,” adds Dr Frank Schroeder, a professor in the Chemistry and Chemical Biology Department at Cornell Ithaca [2].

Article sources:

from:    https://wakeup-world.com/2020/02/14/evidence-for-the-gut-brain-connection/