As you increase your understanding of the mechanisms of injuries from ModeRNA, Pfizer, AstraZeneca, and J&J shots, you become sharpened to deliver facts that oust medical disinformation. 

Injections can lead to death through a life-threatening allergic reaction called anaphylactic shock. Did you know that the allergic reaction is suspected to be caused by previous exposure to PEG?

Anti-spike-antibodies skew the macrophage response toward pro-cytokine (M1) dominance by inhibiting the inflammation-resolving macrophages called M2, during the SARS infection.

Did you know that spike proteins cause cardiac damage? What are ACE2 Receptors, how do spike proteins bind tight to ACE2, and how does the binding of spike proteins to ACE receptors trigger multiorgan system failure?

Spike proteins cause pulmonary hypertension, pulmonary thromboembolism and thrombosis, lung tissue damage and possible pulmonary fibrosis, which can affect men and women at any age – even children.

Spike proteins can attach to reproductive cells, especially in the ACE2 receptor on the surface of sperm and ovaries. There may be reproductive consequences in young males affected by the COVID-19 infection.

Spike proteins cause loss of Blood-Brain Barrier integrity and breaking down the BBB means particles can easily and directly pass into the brain tissue, which can lead to neuropathology and brain degeneration.

Spike proteins can cause ALS or Amyotrophic Lateral Sclerosis. Keep these questions in mind:

Spike proteins cause frontotemporal lobe degeneration of multiple types and frontotemporal dementia, a chronic, degenerative neurological disease, per the Association for Fronto-Temporal Dementia.

Spike protein can cause the mutations of the FUS gene and cancer. The amino acid sequence of the Pfizer spike protein can cause the FUS gene to create pathologic conformations which can lead to cancer.

Did you know that the adenoviruses used both in the Johnson & Johnson and the AstraZeneca shots increase the risk of developing cancer? These adenoviruses are known to cause tumors that are linked to various forms of cancer.

Anti-Spike-antibody causes damage that are linked to lung damage. The autoimmune antigens target proteins that include skin, gastrointestinal, pancreas, liver, heart, muscle, joint, thyroid, brain and enteric nerve, tight junction proteins and cellular components.

Having previous exposure to coronavirus and the concept called “original antigenic sin” stops true protection against the SARS-CoV-2 if a person has been ill before with a common coronavirus infection.

There is an increased risk of COVID infection and COVID-related death in people who have had a previous influenza vaccine. Getting a flu shot can increase your risk of contracting and suffering from SARS-CoV-2.

The highly elevated and larger SARS-CoV-2 antibody response from a COVID infection or from a COVID shot results in a prolonged illness with severe symptoms, which increases the risk of death.

COVID vaccine can lead to enlarged lymph nodes that may have long term ramifications. Additionally, according to the Society of Breast Imaging, swollen lymph nodes can have long-term axillary adenopathic effects.

Widespread use of COVID shots results in non-neutralizing antibodies, especially in people who have already had a COVID infection. This can lead to virulent mutant viruses that can emerge in the injected population.

Injected persons experience antibody-dependent enhancement (ADE) on re-exposure. ADE is a phenomenon that occurs when a person is re-exposed to the virus, which accelerates its replication and leads to a more severe disease.

Johnson & Johnson and AstraZeneca shots release a transgene that can lead to

potentially deadly side effects from injecting raw genetic material that can induce anti-DNA antibodies, which can integrate into human DNA.

Both Johnson/Johnson and AstraZeneca shots carry a snip of double stranded DNA

(dsDNA) or transgene that is wrapped in an adenovirus outer “shell” and 50-billion particles are injected with each injection.

The AstraZeneca shot has been known to be associated with potentially deadly blood

clots, a condition named Vaccine-Induced Prothrombotic Immune Thrombocytopenia (VIPIT).

MOI # 21 - Circulating S1 spike protein and brain damage
Circulating spike protein leads to diffuse microvessel endothelial damage in lung, liver, brain, and skin. It also leads to microencephalopathy in the brain with marked neuronal dysfunction and a reduction of key neuronal proteins.

MOI # 22- Spike protein binds to the acetylcholine receptors (AChR)
Binding disrupts the transmission of nerve impulses to muscles, possibly resulting in tremors, spasms, seizures, irregular heartbeats. Dysregulation of these receptors could be a possible cause for the uncontrolled inflammatory response in COVID19. It could also explain other clinical manifestations of COVID-19 such as anosmia (loss of smell) and thromboembolic complications (blood clots).

MOI # 23 - Immune response to stimulate spike proteins against brain cells
The biodistribution of ChaAdOx1 (AstraZeneca) in mice confirmed the delivery of vaccine into the brain tissues. The vaccine may therefore spur the brain cells to produce Covid spike proteins that may lead to an immune response against brain cells, or it may spark a spike protein-induced thrombosis.

MOI # 24 - Fatal Pulmonary Hypertension
Promotes growth of human lung vascular cells, leading to thickened pulmonary vascular walls and fatal disease pulmonary arterial hypertension (PAH).

MOI # 25 - Myocarditis
CDC: "The FDA update followed a review of information and discussion at the CDC’s Advisory Committee on Immunization Practices (ACIP) meeting on June 23, 2021. The committee acknowledged 1,226 cases of heart inflammation in 16- to 24-year-olds and said mRNA COVID vaccines should only carry a warning statement."

Montgomery: "In this case series of 23 male patients, including 22 previously healthy military members, myocarditis was identified within 4 days of receipt of a COVID-19 vaccine. For most patients (n = 20), the diagnosis was made after the second dose of mRNA COVID-19 vaccine."

Shay: "The striking clinical similarities in the presentations of these patients, their recent vaccination with an mRNA-based COVID-19 vaccine, and the lack of any alternative etiologies for acute myocarditis suggest an association with immunization.”

Kim: “7 patients with acute myocarditis were identified, of which 4 occurred within 5 days of COVID19 vaccination: All 4 had received the second dose of a mRNA vaccine (2 received Moderna, and 2 received Pfizer) between 1 and 5 days before hospitalization.”

MOI # 26 - A long list of autoimmune diseases
Ehrenfeld: Autoimmune disease linked to SARS-CoV2 illness, implicating the spike protein:ACE2 association as the cause

MOI# 27 - Associated with anti-spike antibody
Antibodies with a high binding affinity to SARS-CoV-2 spike also have a high binding affinity with tTG (associated with Celiac Disease), TPO (Hashimoto’s thyroiditis), myelin basic protein (multiple sclerosis), and several endogenous proteins.

MOI # 28 - Spike protein cross-react with 60 human proteins
Kanduc: “Thromboses and Hemostasis Disorders Associated with Coronavirus Disease 2019: The Possible Causal Role of Cross-Reactivity and Immunological Imprinting.”

60 pentapeptides are shared between the SARS-CoV-2 spike protein and human proteins that— when altered, deficient, mutated, or improperly functioning— cause vascular diseases, thromboembolic complications, venous thrombosis, thrombocytopenia, coagulopathies, and bleeding

MOI # 29 - Lipid nanoparticle accumulation in ovaries

MOI # 30 - Genetic modification of human DNA
Zhang: SARS-CoV-2 RNA and perhaps spike proteins can be reverse transcribed in human cells by reverse transcriptase (RT) – MORE PROOF OF GENETIC MODIFICATION BY THESE SHOTS

MOI # 31 - Concerns about male infertility
Bhattacharya: The testicular effects may impair Leydig cell, Sertoli cell, and sperm functions.

Wang: "These findings provide evidence that the human testis is a potential target of SARS-CoV-2 infection (and hence, spike protein)."

Navara: "ACE2 human testes, epididymis, Leydig cells (testosterone production), Sertoli cells, and sperm. The expression of ACE2 is age-related, with a higher expression in patients aged 20–30 compared to 60yo+ patients that have reduced expression.

Basourakos: "The effects of SARS-Cov-2 (spike protein) on spermatogenesis may linger months after clinical recovery from active infection."

MOI # 32 - Visual disturbances
"The signs and symptoms of our patient were consistent with acute macular neuroretinopathy (AMN) in a 27yo female. An association between AMN and COVID-19 vaccination raises the question: is there a common immune-mediated pathway that can trigger this peculiar macular disease?

MOI # 33 - Miller Fisher Syndrome (MFS) – variant of GBS
Ehrenfeld: "Acute onset of external ophthalmoplegia (paralysis of eye muscles) is a cardinal feature. Ataxia (unsteady gate) tends to be out of proportion to the degree of sensory loss in feet and legs. Patients may also have mild limb weakness, ptosis (unable to open upper eyelid), facial paralysis, or bulbar palsy (cranial nerve disfunction). Occasionally generalized muscle weakness and respiratory failure may develop.

MOI # 34 - Facial paralysis
Renoud: As of March 2021 in the WHO pharmacovigilance database, identified among 133,883 adverse events 844 facial paralysis-related events were reported:
• 683 cases of facial paralysis,
• 168 cases of facial paresis,
• 25 cases of facial spasms, and
• 13 cases of facial nerve disorders (some co-reported in the same case).
The breakdown included:
• 749 cases after the Pfizer-BioNTech vaccine
• 95 cases were reported with the Moderna vaccine

MOI # 35- Multiple sclerosis
Havla: Initial onset of MS with brain lesion

MOI # 36 - Chemical poisoning
MODERNA: Contains SM-102, used to develop lipid nanoparticles for delivery of mRNA
Safety Data Sheet:
• Generic name: 8-[(2-hydroxyethyl)[6-oxo-6-(undecyloxy)hexyl]amino]-octanoic acid
• Trade name: SM-102 in Chloroform
o Chloroform is trichloromethane.
o Suspected carcinogen
o Suspected to damage fertility; known teratogenicity and developmental toxicity in the unborn child
o When exposed to light and/or air, converts to phosgene, a highly poisonous gas
o May cause anemia, cough, CNS depression, drowsiness, headache, heart
damage, lassitude (weakness, exhaustion), liver damage, narcosis,
reproductive effects, teratogenic effects.
• For Research Use Only. Not for human or veterinary diagnostic or therapeutic use.

MOI # 37 - Chemical poisoning
HBCD JOHNSON & JOHNSON: Contains 2-hydroxypropyl-β-cyclodextrin (HBCD)
• HBCD is used for easier diffusion across biological membranes.
• Toxicological effects of this product have not been studied
• Carcinogenicity potential of this product has not been studied
• For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

MOI # 38 - Magnetic poisoning
Graphene is an extremely thin two-dimensional layer of the graphite used in pencils. The graphene-family of nanoparticles (GFN) can penetrate through the physiological barriers or cellular structures by different exposure ways or administration routes and enter the body or cells, eventually resulting in toxicity in vivo and in vitro.
GFNs can induce acute and chronic injuries in tissues by penetrating through the blood-air barrier, blood-testis barrier, blood-brain barrier, and blood-placenta barrier etc.
GFNs can accumulate in the lung, liver, and spleen etc. They can be inhaled and deposited in the respiratory tract and travel to the lower lung airways. The result may be granuloma, lung fibrosis or even cancer. The toxicological mechanisms include inflammatory response, DNA damage, cellular death, tissue necrosis etc.

ACCORDING TO LA QUINTA COLUMNA, in Spain:
• The COVID vaccines in all their variants, Pfizer, Moderna, Johnson & Johnson, AstraZeneca, Sinovac, etc., contain a considerable dose of graphene oxide nanoparticles.
• The masks being used contain graphene oxide.
• PCR swabs for swabs and antigen testing contain graphene oxide nanoparticles.

Graphene oxide is toxic:
• Causes blood coagulation
• Can cause collapse of the immune system and subsequent cytokine storm
• Can lead to inflammation of mucous membranes, loss of taste and partial loss of smell. In the lungs, can lead to bilateral pneumonia
• Depletes glutathione reserves

MOI # 39 - Magnetic poisoning
Magnetite - Magnetic nanoparticles (MNPs) for biomedical applications are typically composed of a magnetic core. One of most commonly used MNP is magnetite (Fe3O4).

The major advantage of magnetic manipulation is ‘‘remote control.’’ Magnetic labeling of cells with magnetic nanoparticles enables the manipulation of cells and also the control of cell functions by applying an external magnetic field. ‘‘Functional’’ magnetite nanoparticles were developed for cell manipulation using magnetic force, and the magnetite nanoparticles were applied to tissue-engineering processes, which are designated as magnetic force-based tissue engineering (Mag-TE).

Here are four uses of magnetite nanoparticles:
o Magnetic force-based gene transfer technique (magnetofection)
o Creating cell patterns using functional magnetite nanoparticles
o Micro-patterned magnetic field gradient concentrators
o Applications for creating of tissue-like constructs in skin, liver, and muscle tissue engineering.

MOI # 40 radiofrequency: Effect of 5G
Rubik, Brown: This is the first scientific paper documenting a link between the detrimental bioeffects of radiofrequency radiation (RFR) from wireless communication in particular 5G, and COVID-19. We conclude that RFR exacerbated the COVID-19 pandemic by weakening host immunity and increasing SARS-CoV-2 virulence by:
• Causing morphologic changes in red blood cells that may be contributing to hypercoagulation.
• Impairing microcirculation and hemoglobin levels exacerbating hypoxia.
• Amplifying immune dysfunction, including immunosuppression, autoimmunity, and hyperinflammation.
• Increasing cellular oxidative stress and the production of free radicals, exacerbating vascular injury and organ damage.
• Augmenting intracellular Ca2+ essential for viral entry, replication, and release; and
• Inducing heart arrhythmias and cardiac disorders.

Dr. Sherri J. Tenpenny is an osteopathic medical doctor, board certified in osteopathic medicine, with a proficiency certification in Integrative Medicine. She was board certified in Emergency medicine from 1986 to 1998, when worked as a full-time Emergency Medicine physician and served as Director of a Level II Trauma center.  

The founder of Tenpenny Integrative Medical Center, a clinic located near Cleveland, Ohio that provides natural, holistic approaches to getting well. Their success has attracted patients from all 50 states and at least 17 countries.  

Dr. Tenpenny has invested 21+ years and far more than 40,000 hours researching, documenting, and exposing problems associated with vaccines. She is a frequent speaker at national and international conferences and a regular guest on radio shows, podcasts and on TV, sharing her highly researched information on why we should just say no to vaccines.