https://pierrekorymedicalmusings.com/p/newly-published-study-shows-shedding?

Newly Published Study Shows Shedding Of Covid mRNA Vaccine Products

A new study found a strong association of new onset menstrual irregularities with “indirect” exposure to Covid vaccines, i.e. being in proximity with vaccinated persons. Shedding is real.

Article Excerpts:

……after observing shedding phenomena in our patients, I then discovered this illuminating and masterful review paper by French independant researcher Helene Banoun who focused on all the known (but ignored) regulatory issues with GTMP’s and shedding. My work then led to a collaboration with the researcher and physician A Midwestern Doctor (AMD) where we compiled all the evidence showing the mechanisms by which shedding could happen and the evidence that those mechanisms were actually occurring.

AMD then did a herculean job of consolidating and categorizing all the clinical reports of shedding submitted to our respective Substack blogs and Twitter accounts. Our entire comprehensive review follows this review of the study by Peters et al. in case you have not read it yet.

Before I reveal what this troubling study found, know that I was aware of this study (but not its actual findings) for over a year. Why did it take so long to be published? Well, the first journal they submitted to helped to “hold it captive” for over a year before finally deciding to not publish it (per the authors, there were other reasons for the delay as well). In the words of one of the study authors:

After more than a year of censorship from the medical journals, our landmark study and manuscript has been published demonstrating significant circumstantial evidence that something is being shed from the COVID-19 vaccinated population to the unvaccinated population. It is far beyond time for these toxic injections to be withdrawn from the market.

It has been a very long battle to get this article published. Our experience in this process has verified that medical censorship has been in full force during the “pandemic.” The journal editors and publishers fear the potential consequences of publishing anything that contradicts the “safe and effective” propaganda with which the public health authorities have bombarded us.

…..as stated in the documentation of the FDA Design and Analyses of Shedding Studies, “shedding may occur immediately following product administration and again days to weeks later.” (FDA, 2015)

To learn that shedding (i.e. indirect exposure) also induces the same frequency of onset of menstrual irregularities likely explains why a recent FOIA request in Canada uncovered a shocking increase in the rate of stillbirths and miscarriages.

Many other symptoms have been attributed to shedding phenomena as listed below (compiled by A Midwestern Doctor from their analysis of the reports we received):

(See link for article, summary observations of over 1,000 clinical reports and published evidence of shedding)

Go here for a 3 min video of Dr. Kory on shedding.

_________________

https://slaynews.com/news/worm-like-self-assembling-entities-found-bodies-covid-vaccinated-study-warns/

‘Worm-Like Self-Assembling Entities’ Found in Bodies of Covid-Vaccinated, Study Warns

 
A disturbing study has reportedly found evidence of “self-assembling entities” in the bodies of people who received Covid mRNA “vaccines.”

Leading researchers in South Korea and Japan have issued a red alert after their bombshell study discovered the entities they described as “worm-like.”

According to the study, the “self-assembling entities” form “synthetic” nanostructures in the bodies of people who were “vaccinated” with Covid mRNA injections.

The shocking discovery of these “artificial constructions” was revealed in the long-term study’s recently  published paper.

The study was led by South Korean obstetrician Dr. Young Mi Lee and Professor Daniel Broudy of Japan’s Okinawa Christian University.

Following their long-term study of Covid mRNA-vaccinated individuals, Lee and Broudy suggested that their main findings were the direct observation of both “self-assembling entities … of many different shapes,” and of “cellular toxicity” triggered by the Covid injections.

They noted that these discoveries were “especially” observed in blood and sperm cells.

In a Korean laboratory, using flu vaccine and normal saline as controls, the researchers incubated Pfizer and Moderna Covid mRNA “vaccines” in various fluids.

Important detail:

AstraZeneca and Novavax injections did not develop the “self-assembled” structures seen in the Pfizer and Moderna mRNA shots.

The findings resemble objects other doctors have been finding including ‘wires’ with frayed edges around which apparent ‘chips’ often appeared.  These wires were also found in the blood of the ‘vaccinated.’

Each injection was found to have ‘toxic effects on blood cells.’

Each shot had a distinct effect on blood cells:

  • Pfizer triggers “cellular collapse of white blood cells and damaged platelets.”
  • Moderna triggers rouleaux (stacking) of red blood cells.
  • Novavax causes the disintegration of the nucleus of white blood cells and some rouleaux of red blood cells..
  • AstraZeneca triggers “prominent rouleaux.”

Research also shows those who got the clot shot emit a fluorescent orange glow in their faces that is visible under UV light.  Those exposed to shedding emit the glow around their nose.

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https://petermcculloughmd.substack.com/p/sars-cov-2-spike-protein-persists?

SARS-CoV-2 Spike Protein Persists in the Skull-Meninges-Brain Axis and Causes Neurological Damage

New study confirms that the Spike protein is a persistent neurotoxin.

Rong et al has just published a study in the journal Cell Host & Microbe titled, Persistence of spike protein at the skull-meninges brain axis may contribute to the neurological sequelae of COVID-19.

Using optical clearing and imaging, Rong et al observed the accumulation of SARS-CoV-2 Spike protein in the skull-meninges-brain axis of human COVID-19 patients, persisting long after viral clearance.

The authors concluded that persistent Spike protein at the brain borders may contribute to lasting neurological sequelae of COVID-19. These findings corroborate Parry et al and Hulscher et al, who both demonstrated that Spike protein is a persistent, highly toxic substance from both viral infection and vaccination. (See link for article and graphs)

See: Massive Spike Protein Pathogenicity Research Library

For More:

 

 

http://  (Approx. 34 Min)

If the Youtube link is censored, go here:  https://www.dadsavesamerica.com/p/sharyl-attkisson-followed-the-science?

I would say people are familiar with the notion that Big Media is compromised by Big Pharma because of this relationship where they buy billions of dollars in ads. Now the media avoids covering stories we used to cover routinely about medical scandals. I think people have some idea that Big Pharma compromises are political institutions because they donate tons of money to both political parties in order that they be allowed to write laws and bills, to make certain oversight hearings are not held. But I think people are less familiar and put a lot less focus on the medical establishment’s role—how the medical establishment too has been co-opted by Big Pharma interests in ways that are invisible to most people… We’re talking about scientific studies, medical associations, medical schools, and the continuing medical education classes. And it’s important because I think Americans understand, they’ve been watching for 20 years as we’ve grown sicker and sicker and sicker with chronic epidemics of disease.

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**Comment**

Censorship has always been around but the COVID psyop really exposed it for all to see, IF you were willing to see it.  The examples are to infinity:

https://www.midwesterndoctor.com/p/how-dmso-protects-and-heals-the-internal?

How DMSO Protects and Heals the Internal Organs

The evidence behind DMSO’s utility for a myriad of challenging diseases

Story at a Glance:

The therapeutic actions of DMSO make it well suited to treat challenging conditions throughout the body, including many of the internal organs.

•In this article, we will examine how DMSO protects organs from injury (e.g., poisoning or blood loss) and some of the specific diseases DMSO has been proven to treat.

•These include: heart attacks, liver cirrhosis, gallstones, ARDS, lung damage from inhaling smoke, pulmonary fibrosis, pancreatitis, diabetes, nephritis, kidney stones, polycystic kidney disease, cystitis, epididymitis, genital pain, prostatitis, urethral syndrome, enlarged prostates, tubal infertility, endometrial inflammation, and fibrosis.

•This article will review DMSO treatment protocols for those conditions (along with non-DMSO approaches we utilize for them) and provide general DMSO information for those looking to use DMSO for their own health.  (See link for article)

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https://www.midwesterndoctor.com/p/dmso-revolutionizes-skin-care-and?

DMSO Revolutionizes Skin Care and Dermatology

Exploring how skin health goes hand in hand with whole body health

Story at a Glance:

DMSO has a variety of unique therapeutic properties that allow it to address the root causes of many different illnesses—including those of the skin.

•DMSO effectively protects the skin from damage (e.g., radiation, chemotherapy, freezing, blood loss) and rapidly heals skin injuries (e.g., burns, chronic wounds or surgical incisions).

•DMSO addresses many circulatory disorders such as hemorrhoids, varicose veins, venous and diabetic ulcers, and Raynaud’s.

•DMSO also effectively addresses many common (but often challenging) dermatological conditions such as hair loss, psoriasis, shingles, herpes, skin cancer, lichen sclerosis, skin infections, nail issues, acne, eczema, pruritus, mastitis, insect and animal bites, sunburns and skin growths.

•This article will review DMSO treatment protocols for those conditions (along with non-DMSO approaches we utilize for them) and provide general DMSO information for those looking to use DMSO for their own health.

The American medical industry has accomplished a remarkable feat; each year it consumes a greater portion of the national budget (currently over 17.3% of GDP) yet it continues to have some of the worst outcomes in the developed world (despite spending 2-4 times as much on healthcare). This is made possible by a vast medical monopoly that prevents economical therapies from out-competing the medical industry’s cash cows and systemic corruption that makes the government unwilling to confront the sources of illness in our society (e.g., processed food companies or vaccine manufacturers).

The natural therapy I decided to focus on, dimethyl sulfoxide (DMSO), was an ideal choice for this task, as it’s very safe (provided you use it correctly) and rapidly improves a variety of conditions medicine struggles with—particularly chronic pain (discussed here). As such, I’ve received many reports of life-changing benefits from it that left even the reader in disbelief.  (See link for article)

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  • Strokes, traumatic brain injuries, spinal cord injuries, and many circulatory disorders (discussed here).
  • Acute and chronic tissue injuries (discussed here).
  • “Incurable” autoimmune and connective tissue disorders (discussed here).
  • Eye, ear, sinus, and dental conditions such as tinnitus and blindness (discussed here).
  • Internal organ disorders (discussed here).
  • Accelerates wound healing, prevents adhesions, eliminates scars, treats psoriasis and mastitis, insect bites, skin growths and skin cancer (discussed here)

For more:

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/

Question for Aaron Siri, Managing Partner Siri & Glimstad

Carl Tuttle
Hudson, NH, United States
Dec 18, 2024

If antibiotic resistance was acknowledged early on by our Public Health Officials as it was by Dr. Allen Steere in 1977 the focus would have been on developing new antimicrobials (or different combinations) as seen in the treatment of Brucellosis but the potential money grab from a Lyme vaccine was far too lucrative to pass up. Everything about Lyme from that point forward had to support vaccine development. A chronic relapsing SERONEGATIVE disease did not fit the vaccine model. The money orgy produced by vaccines could not be more obvious through recent Covid events. The rest of the world now has a bird’s eye view of what our Public Health Officials are capable of when a false narrative has been dictated. The disabled Lyme community has been shouting from the rooftops for decades and everyone reading this knows of someone severely affected from Lyme disease; shame on you for not speaking up!

The following letter to Aaron Siri, Managing Partner of Siri & Glimstad breaks down the timeline and deception. Attorney Siri recently exposed the truth/facts about childhood vaccines through the depositions of Stanley Plotkin world’s leading authority on vaccines and Dr. Kathryn Edwards world’s leading vaccinologist.

Letter to Attorney Siri:

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: “aaron@sirillp.com” <aaron@sirillp.com>
Cc: “mbarney@sirillp.com” <mbarney@sirillp.com>, “ebrehm@sirillp.com” <ebrehm@sirillp.com>, “ddisabato@sirillp.com” <ddisabato@sirillp.com>, “lconsidine@sirillp.com” <lconsidine@sirillp.com>, “wmoller@sirillp.com” <wmoller@sirillp.com>, “mconnett@sirillp.com” <mconnett@sirillp.com>, “ahaskins@sirillp.com” <ahaskins@sirillp.com>, “cxenides@sirillp.com” <cxenides@sirillp.com>
Date: 12/13/2024 12:29 PM EST
Subject: Question for Aaron Siri, Managing Partner Siri & Glimstad

Siri & Glimstad
Aaron Siri, Managing Partner

Dear Attorney Siri,

When and who ruled out sexually transmitted Lyme disease?

Hold that thought for one moment please….

Weren’t we told by IDSA/Eugene Shapiro that there has never been one case of congenital Lyme? WRONGWRONG!

Weren’t we told by the New York Times that Lyme is “hard to catch and easy to halt”? WRONG!

Weren’t we told by Wormser that persistent symptoms are nothing more than the aches and pains of daily living? WRONG!

Weren’t we told by Mainstream media that LYMErix was taken off the market due to poor sales? WRONG!

Weren’t we told by the CDC/IDSA that the bulls-eye rash appears 80% of the time?  WRONG!

Weren’t we told by the CDC/IDSA Paul Auwaerter that the two-tier Lyme test is a good test?  WRONGWRONG!

Weren’t we told by Wormser that single dose Doxycycline as a prophylaxis after tick bite is sufficient in stopping the disease? WRONG!

Weren’t we told by the CDC/IDSA that there’s no Lyme disease in the south?  WRONG!

Weren’t we told by the CDC/IDSA that it takes 48hrs of tick attachment before the disease can be transmitted. WRONGWRONG!

Weren’t we told by the (CDC/IDSA/ALDF) that there is no toxin involved in Lyme disease? WRONG! Again.

So what else have they gotten wrong??

Getting back to my original question: “sexually transmitted Lyme disease” ...

The 2014 study below found culture positive evidence of Borrelia spirochetes in the genital secretions of these patients:

Culture and identification of Borrelia spirochetes in human vaginal and seminal secretions
https://pmc.ncbi.nlm.nih.gov/articles/PMC5482345/

Conclusions:  The culture of viable Borrelia spirochetes in genital secretions suggests that Lyme disease could be transmitted by intimate contact from person to person. Further studies are needed to evaluate this hypothesis.

Here is the CDC’s stance on sexually transmitted Lyme disease:

About other modes of transmission
https://www.cdc.gov/lyme/causes/index.html

There is no credible scientific evidence that Lyme disease is spread through touching, kissing, or sexual contact. Published studies in animals do not support sexual transmission (Moody 1991; Woodrum 1999), and the biology of the Lyme disease spirochete is not compatible this route of exposure (Porcella 2001).

Carl Tuttle’s comment: ONE SINGLE PUBLICATION 23 YEARS AGO! This is not an actual study proving or ruling out sexual transmission; this is one man’s perspective using the words “suggest/suggests/suggesting.”

Don’t look!  That assures you won’t find!

Isn’t that exactly what you just exposed Attorney Siri in the depositions of Stanley Plotkin and Dr. Kathryn Edwards regarding the vaccine and autism debate? There have been no autism studies for the childhood vaccine schedule to challenge the mantra “Vaccines Do Not Cause Autism because we say so.”

There have been no studies to rule out sexually transmitted Lyme disease so how much sexually transmitted Lyme has been circulating in the public for the past three decades or more?

In 2003 Texas physicians Harvey and Salvato tested their chronically ill patients for Lyme disease via CDC Western blot criteria finding all patients positive for the infection in a state where the prevalence of Lyme infected ticks is only about 1-2%. “No history of bull’s-eye rash or illness following tick bite was reported by these patients.” The CDC defines “Lyme disease” exclusively as a zoonotic illness. Congenital and gestational transfer cases have been disregarded for reasons not evident to us.”

Here is an example of how other infections have been managed:

Chronic Brucellosis and Persistence of Brucella melitensis DNA
https://www.ncbi.nlm.nih.gov/pubmed/?term=Chronic+Brucellosis+and+Persistence+of+Brucella+melitensis+DNA

After acute brucellosis infection, symptoms persist in a minority of patients for more than 1 year. Such patients are defined as having chronic brucellosis. Since no objective laboratory methods exist to confirm the presence of chronic disease, these patients suffer delays in both diagnosis and treatment.

Why haven’t we done this with Borrelia burgdorferi infection…..

1. Administration of a triple versus a standard double antimicrobial regimen for human brucellosis more efficiently eliminates bacterial DNA load.
https://www.ncbi.nlm.nih.gov/pubmed/25246401

The doxycycline-streptomycin-rifampin regimen eliminates Brucella DNA more efficiently than doxycycline-streptomycin, which may result in superior long-term clearance of Brucella.

2. Different Clinical Presentations of Brucellosis.
https://www.ncbi.nlm.nih.gov/pubmed/27284398

It was once believed that rifampin was curative in treating Brucellosis but when symptoms returned doxycycline was added to the mix and when that too failed a third antibiotic, streptomycin was added to the current treatment regimen.

In contrast, oral amoxicillin or doxycycline remains the treatment of choice for treating Lyme disease for over thirty years regardless if debilitating symptoms return. Dr. Allen Steere knew that these antibiotics were not effective for all patients (see 1977 reference) but there has been no change in treatment or research to find more effective ways to eradicate the infection in all stages of disease.

Lyme arthritis: an epidemic of oligoarticular arthritis in children and adults in three connecticut communities. (1977)  https://pubmed.ncbi.nlm.nih.gov/836338/

Steere AC, Malawista SE, Snydman DR, Shope RE, Andiman WA, Ross MR, Steele FM.

Excerpt:

“The best treatment for this illness is not clear. Some physicians have reported that penicillin or tetracycline results in disappearance of the skin lesion (41,42), but others find antibiotics ineffective. Four of the patients with expanding skin lesions received penicillin but still developed arthritis.”

In contrast, the only action item we have in the pipeline after FORTY years for Lyme disease is a vaccine fast-tracked by the FDA in 2017. Since all the eggs have been put into the vaccine basket it would appear that our Health Agencies are in the shot business with annual revenue of $4.3 billion from the sales and patent royalties.

A chronic relapsing seronegative disease DOES NOT fit the vaccine model because you cannot prove vaccine efficacy in a disease where we don’t know who has or does not have the infection! So, deny the chronically infected by suppressing all evidence of antibiotic resistance, claim that the infection is easily treated because newer curative treatment for all stages of disease would give the public an excuse not to take the vaccine, reject all direct-detection methods that prove chronic infection and voila! move forward with patent royalties, vaccine development and pharmaceutical profits. The federal watchdog is no more. People suffering and dying and for what? Lyme for Profit.

The CDC has propagated this false Lyme disease narrative for decades and to this day refuses to recognize the disabling stage of the disease exposed in the documentaries Under our Skin and The Quiet Epidemic.

Suppressing evidence of antibiotic resistance for the sake of a vaccine is a crime Attorney Siri!

This is a criminal case that must be exposed as you have done with the childhood vaccine mantra; “Vaccines do not cause autism because we say so.”

Chronic Lyme does not exist because we say so! DO NOT QUESTION OUR PUBLIC HEALTH NARRATIVE, PERIOD!!! Or else…

We need your help Attorney Siri! We need your help!

Respectfully submitted,

Carl Tuttle
Independent Researcher
Lyme Endemic Hudson, NH

PS. Publication from our public health officials of Vector Borne Division of the CDC:

Post-treatment Lyme borreliosis in context: Advancing the science and patient care
Grace E. Marx*, Alison F. Hinckley, Paul S. Mead

Published 27 June 2021
https://www.thelancet.com/pdfs/journals/lanepe/PIIS2666-7762(21)00130-7.pdf

Tuttle’s comment:

This is the same old garbage (junk science) regurgitated by the CDC/IDSA year after year, decade after decade while avoiding the elephant in the room.

Conclusion: “Fortunately, safe and effective vaccines for Lyme disease may be on the horizon which could both reduce LB incidence on a population scale while averting long-term patient suffering”  Voila and there you have it folks!!!!

_________________

**Comment**

Our case is a perfect example of sexual transmission.  For our story:   https://madisonarealymesupportgroup.com/2017/02/24/pcos-lyme-my-story/

Lida Mattman was able to culture spirochetes from tears, sweat, urine, CSF, blood, plasma, fleas, mites, mosquitoes, etc. and UW researcher Elizabeth Burgess could infect cats orally, ocularly, via IV, and via contact transmission in dogs:  https://madisonarealymesupportgroup.com/2019/04/02/transmission-of-lyme-disease-lida-mattman-phd/  She almost lost her job over these findings because they didn’t want them found.

https://petermcculloughmd.substack.com/p/congos-health-ministry-confirms-disease?

Congo’s Health Ministry Confirms ‘Disease X’ is Malaria

Outbreak began shortly after Congo’s rollout of the novel R21 virus-like particle malaria vaccine.

The Democratic Republic of Congo’s health ministry announced today that the previously unidentified illness coined as ‘Disease X’ by the media and Africa CDC circulating in the Panzi health zone has been confirmed as a severe form of malaria:

“The mystery has finally been solved. It’s a case of severe malaria in the form of a respiratory illness,” the health ministry said in a statement, adding that malnutrition in the area had weakened the local population, leaving them more vulnerable to disease.

This confirms our observations made last week, where we expected this to be malaria based on early testing. However, health agencies continued to ignore that possibility until now….

This entire situation reinforces how the mainstream media consistently attempts to generate as much fear as possible. They were caught propagating severe malaria coupled with malnutrition as the ominous ‘Disease X,’ fueling unnecessary panic….

In an emailed statement to USA TODAY, the World Health Organization (WHO) still claims it hasn’t conclusively determined the cause of the illness yet and lab testing is ongoing. This is similar to when the WHO falsely claimed that an individual in Mexico died of H5N2 bird flu. Soon after the claim, the Mexican government clarified:

“A team of experts from the Health sector ruled that the person identified with influenza A (H5N2) did not die because of this virus, but as a result of chronic conditions that generated septic shock.” They added, “The diseases he suffered were long-term and caused conditions that favored the failure of several organs, specialists concluded.” The individual suffered from kidney disease, type 2 diabetes, and systemic arterial hypertension for more than 14 years.

Right before this malaria outbreak began, in late October, the Congo introduced the novel R21 malaria vaccine into their national immunization program. “R21 is a virus-like particle comprising the central repeats of Asn-Ala-Asn-Pro (NANP) and C-terminal sequence of circumsporozoite protein fused to the hepatitis B surface antigen (HBsAg).”  It would not be surprising if this new vaccine played a significant role in triggering or exacerbating the severe malaria outbreak.

(See link for article)

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For more: