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Dr. David E. Martin: "Monkeypox" & Sudden "Shingles Outbreaks" Are BOTH COVID Vaccine Injuries—NOT New Viruses! Spike protein shots shatter immunity, reactivating dormant viruses like varicella-zoster (SHINGLES) & mimicking pox lesions. Now they're rebranding vaccine-damaged skin eruptions as "monkeypox" or "shingles surge" to hide the truth! Notice the explosion...

104,313 views • 11 days ago •via X (Twitter)

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There’s a hidden truth beneath the story of the chickenpox and shingles vaccines that no vaccine “expert” will ever tell you. Dr. Suzanne Humphries: “In the old days, we would all get chickenpox.” It was never a big deal. Then came the vaccine. By preventing chickenpox in kids, it created more of a much worse disease. Dr. Humphries: “Chickenpox, we used to get continuously.” “It was very rare for adults to get shingles before the chickenpox vaccine came out, extremely rare.” “But since then, the rate of shingles in adults and children has skyrocketed.” Why? Because adults who were exposed to children with chickenpox received a natural immune boost that kept shingles in check. There’s further evidence that childhood chickenpox prevented other future illnesses, including cancer. Scientists knew that licensing a chickenpox vaccine carried significant risks of worsening other diseases. Before it came out, one of the world’s leading varicella experts also noted that chickenpox was long considered too mild to justify a vaccine. Big Pharma was well aware of all these concerns. But they marched ahead with the chickenpox vaccine anyway. As a result, they’ve reduced a disease that was never even a problem, and worsened other, far more serious, illnesses. These are the kinds of things that you’ll never hear from vaccine “experts,” pharmaceutical companies, or the media. Which is why we launched Shot Week. This week, we have gone through and exposed the lies used to justify Big Pharma’s vaccines, from measles shots to mRNA Covid shots. But the full web of lies that has been spun to justify vaccines is far too much to unravel in a few posts on X. So we’re promoting one book that breaks down the entire decades-long propaganda and censorship campaign. This book is a must-read for every new parent. Order it below:🧵 Joe Rogan Dr Suzanne Humphries

Stand for Health Freedom

231,508 views • 16 days ago

SHINGRIX Shingles Vaccine...Clinical Trials Used No Placebo & 'Safety Tested' For Only 7 Days. Black Box Warning For Guillain Barre Syndrome Causing A 'Polio Like' Paralysis. 50% Of Recipients Experience Severe Systemic Reaction. Vaccine Causes 15X Increased Risk Of Shingles. --- WARNINGS AND PRECAUTIONS --- *⃣ In postmarketing, Guillain-Barré syndrome was observed during the 42 days following vaccination with SHINGRIX & Black Box Warning added in 2021. *⃣ Anaphylaxis & Syncope is associated with SHINGRIX. Emergency procedures & appropriate medical treatment should be administered for cerebral perfusion & anaphylaxis. *⃣ Documented Lupus cases induced by the Shingrix vaccine. ---CLINICAL TRIAL & SAFETY STUDY--- *⃣ GSK Glaxosmithkline Clinical trials for SHINGRIX used diluted SHINGRIX as the placebo. *⃣ Shingrix participants in 'safety studies' were monitored for 7 days post vaccination. Two independent datasets—a general practice dataset (Outcome Health’s Population Level Analysis and Reporting) & a statewide hospital and notifiable conditions linked dataset (Vaccine Safety Health Link)- were analysed. A 15-fold increase in new onset shingles within 21 days post vaccination. ---POST MARKETING ADVERSE EVENTS--- Gout Shingles Arthritis Myalgia Optic Ischemic Neuropathy New onset immune mediated disease Death GI distress Arthralgia Neuropathy Infective pneumonia Influenza Neuralgia Guillain Barre Syndrome Lupus ---DESCRIPTION & INGREDIENTS--- The gE antigen is obtained by culturing GMO genetically engineered Chinese Hamster Ovary cells, the adjuvant suspension component is AS01B. Shingrix contains 5 Phosphates, DOPC, MPL which comes from the cell wall of Salmonella, QS21, Polysorbate 80, Sucrose, Host Cell Protein & DNA. ---NEW NOVEL ANTIGEN USED IN SHINGRIX--- AS01B Adjuvant & QS21 Excipient:Intramuscular injection of free QS21 results in necrosis at the injection site & it is likely that the toxicity of free QS21 that was observed after injection is caused by the binding of QS21 to cellular cholesterol in the membranes of local cells. QS21 binds irreversibly to cholesterol to form a complex, and when QS21 is exposed to erythrocytes it causes pores to form in the lipid bilayer of the cells. Systemic reactions occur in 50% of the recipients. ---NUMBERS NEEDED TO PREVENT NEURALGIA--- The numbers needed to treat to prevent 1 case of neuralgia is 356 patients receiving both doses of Shingrix. ---Waning Efficacy Over Time--- Year 1: 67% Effective Year 2: 50% Effective Year 8: 27% Effective Year 10: 15% Effective Shingles of course is a painful illness, but it can be cured permanently & cleared from the system within 14 days using a natural 3 part protocol. Let me know in the comments or thru DM if you would like my protocol I developed that cured my husband's severe Shingles in 2016. The vaccine is harmful & allopathic antiviral treatments after a shingles diagnosis are toxic to the system & do not heal the root cause as to why you got shingles in the 1st place. Heal, treat the root cause & permanently eradicate the post shingle neuropathy is the best way to deal with shingles. 👇GSK SHINGRIX Package Insert👇 👇SHINGRIX Causes Guillain Barre Syndrome👇 👇SHINGRIX Vaccine Causes Lupus👇 👇SHINGRIX Causes 15X Increase In Shingles👇 Speaker: Dr Jeffrey Barke, MD

Valerie Anne Smith

447,469 views • 1 year ago

A CDC Whistleblower's Story: How a Vaccine "Success" Masked a Public Health Crisis For 8 years, Dr. Gary Goldman was a top epidemiologist on the CDC's Varicella (chickenpox) Active Surveillance Project. His job was to track the vaccine's impact. What he discovered was a pattern of scientific suppression that prioritized a "winning narrative" over public health. Here's the breakdown: 1. The "Success" Story Was Misleading. The CDC was thrilled to publish Dr. Goldman's studies showing an 80% drop in chickenpox cases. What they ignored was his crucial context: the decline began at the PEAK of chickenpox's natural 3-5 year cycle. The initial drop was largely a natural phenomenon, not solely the vaccine's achievement. 2. The Critical Omission: Ignoring Shingles. The same virus that causes chickenpox (VZV) later reactivates as shingles (herpes zoster). From the start, the project REFUSED to surveil shingles, despite FDA warnings. This was a catastrophic oversight. Why? Because natural chickenpox circulation in children provides "exogenous boosting" to adults who had chickenpox, reinforcing their immunity and preventing shingles. Remove chickenpox via mass vaccination, and you remove this protective boost. 3. The Inconvenient Truth Emerges. Dr. Goldman fought to start shingles surveillance in 2000. The results were immediate and alarming: • Shingles rates in children with prior chickenpox infection skyrocketed, approaching the high rates seen in adults. • Adults also showed a statistically significant increase in shingles. A 20-25% increase in adult shingles would offset EVERY benefit from eliminating chickenpox hospitalizations and deaths. The program was creating a new, more severe public health problem. 4. The CDC's Playbook: Suppress and Obfuscate. Instead of acting, the CDC: • Ignored Internal Data: Downplayed Dr. Goldman's alarming, ascertainment-corrected findings. • Published a Flawed Study: Cited a separate study in a non-vaccinated area (which showed no shingles increase) to claim "mixed results," muddying the waters. • Systematically Under-Reported Cases: The CDC published shingles rates that were NOT corrected for under-reporting. Dr. Goldman's capture-recapture methods proved the CDC's published rates reflected only HALF the true number of cases, creating a falsely low baseline. 5. The Revolving Door. The final, stark conflict of interest? Dr. Julie Gerberding, who served as CDC Director from 2002-2009, overseeing this program, later resigned to become the President of Merck's Vaccine Division—the manufacturer of the Varicella vaccine. The conclusion is inescapable. The CDC actively suppressed damaging data on the varicella vaccine's link to a shingles epidemic to protect a "successful" program's image. The scientific process was compromised, and the public has been left with the consequences. This is not an anti-vaccine story. It is a pro-transparency story. It reveals how institutional science can fail when the pressure to prove success overrides the duty to pursue the whole truth.

Camus

52,989 views • 10 months ago

🚨WARNING: The Shingrix shingles vaccine is grown in Chinese Hamster Ovary Cells using an SV40 Promoter—linked to cancer in lab studies. FDA black box warning: Guillain-Barré paralysis risk! New 2025 study: 11X shingles surge within 21 days post-vax. Is this "protection"?...NO Shingrix production raises red flags: Immortalized CHO Chinese Hamster Ovary cells engineered with plasmids containing SV40 promoter to crank out viral antigens. SV40 drives high gene expression but has oncogenic potential—linked to cancerous tumors. Ingredients you won't love: • GMO Chinese hamster ovary cells (host proteins & DNA remnants) • AS01B adjuvant: MPL (Salmonella cell wall toxin), QS-21 (plant saponin), Polysorbate 80 • Phosphates & more chemicals "Clinical trials"? A joke—used diluted Shingrix as "placebo" & only tracked safety for 7 days. Real harms emerge later. Post-marketing horrors (VAERS/CDC data): • Guillain-Barré Syndrome: RR 2.84 (42-day risk window) per 2021 JAMA study. FDA added warning in 2021. • Optic ischemic neuropathy: 3 cases in trials vs. 0 in placebo • Gout flares • Reactive arthritis & polymyalgia rheumatica: Causal links in follow-up studies 2025 bombshell: Self-controlled case series in UK GP data showed 11-fold shingles increase (RI 10.96) in 21 days post vaccination. More red flags: • Anaphylaxis & syncope common • Documented lupus induction cases • Prolonged neuro/musculoskeletal symptoms: Case reports of lasting pain, weakness • Dermatomal rashes mimicking shingles Shingles hurts, but Shingrix vaccine? That's a HARD NO! And Toxic antivirals like Paxlovid don't fix root causes—stress, immunity dips. If you are unfortunate enough to develop shingles, there are natural protocols to clear the virus completely from your system...I used one in 2016, to heal my husband's severe outbreak in 10 days, no nerve pain, no scarring, no permanent damage. Heal root causes: Diet, herbs, heal from within. Protocol linked in replies. Cited research also linked in replies...

Valerie Anne Smith

663,033 views • 8 months ago

Dr Fauci Admits, "We Don't Do True Placebo Trials On Vaccines." Del Bigtree, CEO, I.C.A.N. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. Shocking List Of 'Placebos' Used In Vaccine Clinical Trials. FDA, WHO & CDC Approved Vaccine Trial "Placebo": Thimerosal Mercury & Aluminum Oxide Other Already Approved Vaccines Clinical Trial Vaccines & What Placebo Was Used: HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Hepatitis A Clinical Trial...Placebo Was Aluminum Adjuvant. Prevnar-9 Pneumonia Clinical Trial...Placebo Was DTP-Hib Vaccine. Cholera Vaccine Clinical Trial...Placebo Was K-12 E.Coli Vaccine. Prevnar-23 Pneumonia Vaccine...Placebo Was Hep A & Hep-B Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. Some COVID-19 Vaccine Clinical Trials...Placebo Was Meningitis Vaccine. The Government believes, "Testing a new vaccine against a saline injection is considered unethical." The Government believes, "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." The Government believes, "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." This is the most flagrant violation of human rights. causing harm to both children & adults. Crimes against humanity with no informed consent & no true placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are similar. 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 Speaker: Del Bigtree ICAN - Informed Consent Action Network @MAHAalliance

Valerie Anne Smith

1,082,646 views • 1 year ago

"The Big Problem With 'Trusting The science' Is Who's Behind The science." Dr Eric Berg "When You Test A Drug, It's Against A Placebo." "Vaccines Are Not Tested Against Placebos...They Are Tested Against Another Active Vaccine." "That's Like Testing Whiskey Against Bourbon." 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo used was Aluminum Adjuvant & only safety tested for 5 days. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo used was Aluminum Adjuvant & Hep-A Vaccine. Only safety tested for 14 days. Hepatitis A Clinical Trial...Placebo used was Hepatitis-B Vaccine & participants were monitored for 14 days. Influenza A Clinical Trial...Placebo used was Influenza B Vaccine & clinical trial volunteers were followed for 28 days. Meningitis Vaccine Clinical Trial...Placebo used was the DTaP Vaccine & adverse reactions were monitored for 7 days. Pertussis Vaccine Clinical Trial...Placebo used was the Diphtheria & Tetanus Vaccine. Participants were followed for 14 days. Prevnar-13 Pneumonia Clinical Trial...Placebo used was the Prevnar-7 Vaccine & volunteers were monitored for 7 days. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine & patients were monitored for 2 days. Chicken Pox Vaccine Clinical Trial...Placebo used was diluted Chicken Pox Vaccine & trial volunteers were monitored for 42 days. Shingles Vaccine Clinical Trial...Placebo used was diluted Shingles Vaccine & participants were followed for 7 days. mNEXSPIKE Covid Vaccine Clinical Trial...Placebo used was SPIKEVAX Covid Vaccine & only safety tested 7 days. Without informed consent & without the use of a saline placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are the same. The US CDC Government's belief on placebos as stated on the CDC website... 1⃣ "Testing a new vaccine against a saline injection is considered unethical." 2⃣ "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." 3⃣ "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 👇Vaccine Excipients Used In Vaccines👇 Speaker: Dr. Eric Berg DC Video: @toxins_in_children

Valerie Anne Smith

113,112 views • 10 months ago

The TGA finally admit myocarditis is an autoimmune response which means the vaccine causes autoimmune issues. Given biodistribution studies showed vaccine lipids entered all body organs this means all organs are at risk of autoimmune responses. No wonder Pfizer didn’t test for autoimmune responses in their trials! Is it just me or do others struggle to remember any mention of Covid causing myocarditis before the vaccine rollout. I seem to recall the initial hysteria was around Covid causing cytokine storms and respiratory problems with lots of pictures of people (young people at that) lying in bed with a ventilator struggling to breathe. Not pictures of people clutching hearts. Furthermore and I’m annoyed I didn’t ask this question how do health authorities know that people who had Covid didn’t actually get myocarditis from the vaccine given most of the adult population was vaccinated. It’s all to convenient to blame myocarditis on Covid, yet the authorities never tested the distribution and degradation of the vaccine spike protein so how can they rule out the vaccine having caused myocarditis for those who caught Covid. Let’s not forget the vaccine was codon optimised to increase the expression of spike protein, and the lipids were designed to enter all cells not just those with an ACE receptor. Given these enhancements increased the potency of the vaccine, I fail to see how the vaccine isn’t more toxic and dangerous than the virus. Finally, the TGA claim only 2 in 100,000 doses cause myocarditis from the vaccine. This is rubbish . That would mean only 1,200 people in Australia have myocarditis. I myself have spoken to hundreds of people who got it after the vaccine. #auspol TGA Australia #pfizer #moderna

Gerard Rennick

507,740 views • 3 years ago

Dr. Robert Sullivan, MD—a board-certified anesthesiologist—stood before the U.S. Senate with a devastating admission: "I am vaccine injured." His testimony shatters the myth that COVID vaccine injuries are "rare" or "mild." A Doctor’s Body, Broken - Three weeks post-vaccination, he went from elite fitness to heart failure. - Diagnosed with pulmonary hypertension—a progressive, fatal disease caused by spike protein-induced vascular damage. - 50% lung capacity loss—yet he "looks normal." How many others are silently suffering? The Science They Ignored - December 2020: Georgetown researchers warned spike protein (from infection or vaccines) could destroy lung blood vessels. - Autopsies confirmed it: COVID victims had the same lung damage Dr. Sullivan now lives with. - Peer-reviewed studies show spike protein is directly toxic to the heart, lungs, and brain. The System Failed Him - He filed a VAERS report (a system most doctors aren’t even taught exists). - No CDC follow-up. No FDA investigation. - "If you are harmed, you are on your own." The Silent Epidemic - Athletes post-vaccine saw 5-10 years of aerobic decline in a week. - Long COVID patients show identical vascular destruction. - How many "mysterious" heart and lung cases are actually vaccine injuries? A Demand for Justice 1. ACKNOWLEDGE the injured. 2. END medical mandates—restore INFORMED CONSENT. 3. INVESTIGATE spike protein toxicity NOW. To the thousands suffering in silence: You are not "anecdotes." You are not "anti-science." You are victims of a system that refuses to see you. This is not conspiracy. This is medicine. And medicine must do better.

Camus

366,034 views • 1 year ago

The World Health Organisation (WHO) has declared Monkeypox a global public health emergency, triggering emergency powers to drive vaccine sales that benefit big pharmaceutical companies with ties to the organisation. This decision serves corporate interests rather than public health. Regulatory agencies that are meant to protect the public fall under undue influence from the industries they regulate. The WHO is a corrupt organisation that is designed to funnel taxpayer money to its billionaire donors. Australian taxpayers gave $30 million to the WHO last year, likely as a show of loyalty. Transparency is lacking. Major donors include Gavi, a vaccine alliance funded by corporations tied to predatory giants like BlackRock and Vanguard, who also own large shares in pharmaceutical companies. The WHO's Monkeypox emergency, declared solely by its director-general, Tedros Ghebreyesus, highlights the unchecked power of the position. This decision created a market for four already-approved vaccines linked to companies backed by BlackRock and Vanguard, ensuring massive profits for their shareholders. A new Monkeypox vaccine is expected soon, likely fast-tracked by compromised regulators like Australia's Therapeutic Goods Administration (TGA). The WHO previously tried to raise alarm over Monkeypox but found little public concern, so they rebranded it as "Mpox" to push vaccine sales. This benefits the predatory billionaires who control vaccine companies, funnel money to Gavi and the WHO, and fund political parties, including Australia's Liberal and Labor parties. Recent revelations show Anthony Fauci concealed plans to engineer a more deadly and highly transmissible Mpox virus. This "gain-of-function" research has pandemic potential and should be stopped immediately. It’s troubling that Australia's CSIRO was involved in gain-of-function research for COVID-19, yet faces no consequences. The WHO and the TGA have failed in their regulatory duties, serving political agendas rather than public interest. During COVID, the TGA prioritised government control over public health, and there are concerns the same will happen again with Mpox. Every Monkeypox case should be verified through public lab tests, especially as redacted data was used to justify COVID measures that harmed public health. The time of blind trust in the WHO's narrative is over; it’s now the age of ‘prove it’. #WHO #JustSayNo #MpoxEmergency #Mpox

Malcolm Roberts 🇦🇺

56,521 views • 2 years ago