BREAKING: CIA Operative Gloria Steinem Dead At 92!
Watch Her Boss- Dr. Paul Ehrlich- Lay Out The Forced Depopulation Plan She Helped Promote, "The FCC Should See To It That Large Families Are Always Treated In A Negative Light On TV... If That Doesn't Work, Then The Government Should Legislate The Size Of The Family & Throw You In Jail If You Have Too Many Kids!"
🗺️ NEW: ICAN’s Interactive Vaccine Exemption Map is LIVE
What exemptions are available in your state?
Search all 50 states + D.C. to see where medical, religious, and philosophical vaccine exemptions are recognized.
Find your state. Know your rights.
🔗 https://t.co/wrZWMQlUlh
BREAKING: STUDY FINDS mRNA “VACCINES” COULD INDUCE OR ACCELERATE CANCER VIA 35 DISTINCT MECHANISMS
We conducted the most comprehensive analysis to date examining the link between mRNA “vaccines” and cancer.
The convergent mechanistic, clinical, and population evidence is now clear: TURBO CANCER IS REAL.
We analyzed CDC mortality data and found an estimated 153,000–197,000 EXCESS U.S. CANCER DEATHS since the 2021 mRNA injection rollout.
Here’s a concise breakdown of our findings:
MECHANISTIC EVIDENCE:
35 distinct cancer-promoting mechanisms converge through 4 major routes: (1) protooncogene activation, (2) mutation pressure, (3) protein–protein interaction network interference, and (4) cancer stem-cell clonal acceleration.
Key mechanisms include EGFR/RAS/MAPK and STAT3–MYC activation, p53/BRCA suppression, impaired DNA repair, residual plasmid DNA and SV40 regulatory elements, LINE-1 reverse transcription, m1Ψ-associated frameshifting, chronic LNP inflammation, immune suppression, and cancer stem-cell expansion—pathways capable of promoting genomic instability, uncontrolled growth, immune escape, dormancy reactivation, and metastatic outgrowth.
Our central concurrent-hit model proposes that these processes do not necessarily operate independently or sequentially. Multiple cancer-promoting hits overlap in the same susceptible host, compressing the time required for dormant, indolent, or microscopic disease to become clinically aggressive.
CLINICAL EVIDENCE:
The published clinical literature includes 333 documented turbo cancer cases across 27 countries, involving lymphomas, leukemia, melanoma, breast cancer, lung cancer, glioblastoma and other glial tumors, sarcomas, and pancreatic cancer. The vast majority of these cases occurred following COVID-19 vaccination, with a minority following SARS-CoV-2 infection.
Approximately 86% of the post-vaccination cases occurred after nucleoside-modified mRNA products—about 56% after Pfizer-BioNTech, 25% after Moderna, and another 5% after exposure to both mRNA products across different doses.
Across these cases, recurring patterns include rapid cancer progression, short-latency recurrence, reactivation of previously controlled disease, and tumors involving the injection site or nearby draining lymph nodes.
POPULATION EVIDENCE:
OUR CDC WONDER ANALYSIS: At least 119,130 EXCESS U.S. CANCER DEATHS since 2021, rising to approximately 153,000–197,000 after accounting for mortality displacement
INDEPENDENT CDC WONDER ANALYSIS (@EthicalSkeptic): 154,330 excess U.S. cancer deaths since 2021, closely matching our corrected range
UNITED STATES (SEER): Early-onset cancer incidence surged 6.4% in just 2 years, from 2021–2023, alongside sharp increases in brain and nervous-system tumors (+19.5%), colorectal cancer (+19.4%), small-intestine cancer (+15.5%), ovarian cancer (+12.8%), stomach cancer (+7.3%), and female breast cancer (+3.6%).
SOUTH KOREA: A nationwide cohort of 8.4 million people found vaccinated individuals had an increased 1-year cancer risk across 6 cancer types: thyroid, gastric, colorectal, lung, breast, and prostate cancer.
ITALY: Vaccinated residents had a 23% higher risk of cancer hospitalization
mRNA ONCOLOGY DANGER:
The very mRNA platform now linked in our paper to 35 oncogenic mechanisms is being repurposed to TREAT CANCER ITSELF.
The platform can distribute systemically, forcing vulnerable tissues including the HEART and BRAIN to express mutated tumor proteins—raising the risk of off-target immune attack, cardiac injury, and neurological damage.
Even more concerning, the LNP delivery vehicle itself promoted metastatic outgrowth in mice even without mRNA cargo, suggesting that some oncologic liabilities reside in the platform itself—not only the encoded antigen.
The first randomized test of mRNA as monotherapy in residual cancer has now FAILED: a Phase 2 trial of an individualized mRNA neoantigen therapy given to 327 patients with residual colorectal cancer crossed its futility boundary and was TERMINATED on a numerical overall survival imbalance.
OUR CALL:
We call for IMMEDIATE MARKET WITHDRAWAL of nucleoside-modified mRNA-LNP products from broad preventive use and a halt to their expansion into adjuvant and neoadjuvant cancer treatment.
35 mechanisms. Hundreds of documented turbo cancer cases. Up to ~197,000 excess U.S. cancer deaths by our analysis. A failed randomized mRNA cancer trial. And the same technology is now being pushed deeper into oncology.
It’s time to END this madness.
@P_McCulloughMD@Docjohnc@McCulloughFund@neo7bioscience
She was healthy. A scraped knee. A tetanus shot. Within minutes: anaphylactic shock. Within weeks: her immune system turned on itself. Within years: she lost her colon, endured seven surgeries, and was told she'd never have children.
She had a son anyway.
Then a court took him. A judge removed her medical rights. They gave her healthy, unvaccinated son sixteen vaccines in two visits. He hasn't spoken to her in two years.
This isn't conspiracy. This is documented medical history—court transcripts, hospital records, a human rights complaint, and an 81-page risk assessment they ignored.
She survived the vaccine that nearly killed her. She did not survive losing her son.
Read her story. Ask the questions she was never allowed to ask. How many more must suffer before we listen?
https://t.co/ZuWDdWP0wV
This isn't tricking the immune system once, or ten times, or fifty. We're at 72 vaccines now, and we're starting in infancy. Of everything I've looked into, this is the one and only product designed to alter your immune system for life.
Some of these vaccines are grown on cell lines that carry aborted fetal DNA. Some contain polysorbate 80 and aluminum, added specifically to trigger inflammation and make the immune response stronger. And now we're seeing something happen in the human body that I don't think we've ever seen before, where the immune system starts attacking itself. It attacks the heart. It attacks the pancreas, which shows up as diabetes. It attacks the myelin sheath, which shows up as multiple sclerosis. We're seeing ulcerative colitis and Crohn's disease in infants now, and I keep asking myself why.
BREAKING NEWS: Another mRNA Vaccine Induced Turbo Cancer mechanism just published!
This time, it's the Pfizer and Moderna Lipid Nanoparticles (LNPs) !!! 😮
"LNP administration promotes tumor metastasis by inducing a systemic inflammatory response"
"LNP injection triggered acute neutrophil accumulation in the lungs, driven by the release of mitochondrial DNA (mtDNA) from necrotic muscle cells at the injection site."
"This mtDNA-mediated signaling activated the TLR9-MyD88 and cGAS-STING pathways, leading to neutrophil extracellular trap (NET) formation, which facilitated the establishment of a pro-metastatic niche"
Special thanks to Dr. Seneff @stephanieseneff who is always on top of the Turbo Cancer literature! 🙏
🚨🚨🚨 Just one paragraph in this shocking paper exposes the whole vaccine adjuvant industry.
What it means is that adjuvants were used - deliberately - to transport residual DNA into cells to create an immune response using oncogenic pathways.
I'll say that in more verbose terms.
Every human cell has a DNA sensing mechanism that will activate if foreign DNA gets into the cell, to protect your cells from that foreign DNA. If it is activated if sets off an extreme immune response but that immune response cannot keep getting activated - if it does you risk developing cancer in those cells.
The mechanism is cGAS-STING and it has a sister TLR9-MyD88.
And the vaccine industry KNEW that adjuvants work by activating them. And they KNEW that they are oncogenic. And they didn't care because they also KNEW that activating this pathway will induce antibodies - and the presences of antibodies (irrespective of whether they provide immunity) is what drives the FDA approvals and thereby the cash.
So if you are asking why cancer rates have been skyrocketing in young people and why this has been happening even before COVID, this provides an explanation that every molecular biologist should have been shouting from the rooftops.
And the worst thing?
That every recombinant vaccine (which by necessity contains unknown amounts of residual DNA) is potentially affected. And they have been in use since Engerix B in 1968.
What has this got to do with adjuvants?
Well, while you were all distracted with Aluminium and its neurotoxic effects, what the vaccine industry didn't tell you was that Aluminium, Triton, Saponins, polysorbates and LNPs are all "transfection agents" - literally microscopic carriers that carry DNA (that shouldn't be there) into cells (that shouldn't be subjected to it).
And that process, described in this paper but happening every day in those injected with residual DNA and a transfection agent, is what this paper shows provides rocket fuel to a cancer.
And THAT is why the pharma industry went crazy when we exposed #plasmidgate.
They didn't want anybody to know.
Don't believe me?
Grok this tweet and watch Grok squirm.
https://t.co/raX5d46A8u
@DrJulieSladden@MaryanneDemasi@DrJBhattacharya@stkirsch@RWMaloneMD@JesslovesMJK@weldeiry@Kevin_McKernan@CanningPharm@Nicolina0815@Fynnderella1
#plasmidgate #novagate
A mother testified before Congress that the Hepatitis B vaccine caused her newborn to stop breathing, develop seizures, and eventually regress into severe autism.
Her story is not a one-off. You need to vaccinate roughly 1 million infants to prevent one case of mother-to-infant Hepatitis B transmission. 6.5 million for one chronic case.
Yet every baby born in an American hospital gets this shot within hours of birth. 🧵
Hannah was described as normal, happy and precocious in her first 18 months.
Then, in July 2000, she was vaccinated against nine diseases in one doctor's visit: measles, mumps, rubella, polio, varicella, diphtheria, pertussis, tetanus, and Haemophilus influenzae.
Afterward, her health declined rapidly. She developed high fevers, stopped eating, didn't respond when spoken to, began showing signs of autism, and began having screaming fits.
In 2002, Hannah's parents filed an autism claim in federal vaccine court. Five years later, the government admitted vaccines caused her autism, settled quietly before it could become a landmark case, and had it sealed.
CDC officials continued to call the vaccine-autism link "debunked" and a "quack" theory.
Whitney Webb just said the quiet part out loud.
Flock cameras are only one part of a “constellation” of surveillance tech.
“They can really spy on you … now from space.”
“You can’t cut those down.”
“This is getting extremely dire.”
“The surveillance state has expanded so much.”
“Flock cameras are bad.”
“But they are one of a constellation … of companies.”
“They are private companies.”
“But they are totally in bed with the national security apparatus.”
And that national security apparatus is quickly moving into something worse than just surveillance.
They’re using surveillance tech to build an AI-powered “predictive” crime apparatus.
“That type of power is weaponized to curb and target dissent.”
“If you’re moving to a paradigm where you can target dissent before it happens, that’s terrible.”
“What we’re talking about here with the Merlin constellation and Satellogic and Palantir is literally what you’re worried about with Flock in space.”
Mark Goodwin: “In April 2022, the first Edge AI-enabled satellite in space was launched by Satellogic and Palantir with assistance from SpaceX.”
Webb: “This is about predictive stuff.”
“It’s about what an algorithm thinks you may do in the future.”
“Or, like, you were at this place where a crime happened … so the algorithm is like, people associated with this hotspot could also be criminals.”
“It’s totally insane.”
@_whitneywebb@markgoodw_in
I spent 5 years in undergrad (biology and chemistry, magna cum laude), 5 years in grad school/med school (neuroscience/physiology and medicine, summa cum laude and cum laude, respectively), and almost 3 years in residency.
When I arrived, all they wanted me to to was force COVID shots, support gender mutilation, and shill for pharma.
I walked away.
So don't tell me people have no choice.
I gave up everything, at the finish line, in first place, because the race was corrupt.
You either have integrity or you don't.
General Mike Flynn: “If you dig deep into the AIDS virus, you’ll find it was manufactured by the US Government.”
“Our government manufactures diseases and then manufactures drugs that are supposed to help — when in fact they DON’T help, just like the COVID vaccines we have now.”
“Fauci created the HIV drug AZT which resulted in the deaths of hundreds of thousands of men.”
“Your own government engineered the plague AND the poison cure.”
My office has learned that an illegal alien granted a drivers license by the state of Connecticut killed a 29 year old Ohioan in a reckless driving accident. While one death alone is an inexcusable tragedy, Connecticut has granted over 60,000 such licenses to illegal aliens, putting countless Americans at risk on the roads. This insanity has to stop.
I am calling on Connecticut’s Governor to immediately apologize for his state’s role in this tragedy while also account for exactly how many illegals have been given Connecticut drivers licenses and whether or not they have used them to vote in U.S. elections.