The Vigilant Fox 🦊 Profile picture
Dec 2, 2025 28 tweets 11 min read Read on X
The Hepatitis B vaccine is mandated for children to attend public schools in 46 states.

Hepatitis B is transmitted via needles or sexual contact, yet this vaccine is pushed on babies on their first day of life.

Why?

We finally have some answers.

Here’s the real reason every newborn is forced to get it—and why that could finally be changing. 🧵
For decades, @MidwesternDoc has tried to answer the question:

Why do we inject a vaccine meant for adult risk groups into every newborn?

The truth reveals a story of shaky science, ignored safety signals, and hidden agendas.
midwesterndoctor.com/p/why-is-every…
@MidwesternDoc The debate isn’t new. The hepatitis B vaccine has been hotly debated for years.

But the debate is getting a little more, shall we say, weird.

Check out this clip from @HighWireTalk featuring none other than Dr. Demetre Daskalakis.
Just weeks ago, former CDC director Susan Monarez seemed unable to explain why we vaccinate newborns for hepatitis B.

The hepatitis B virus is, after all, a bloodborne pathogen with transmission typically occurring through unprotected sex, blood exchanges like shared needles, and mother-to-child transmission during childbirth.

Only one of these risk factors is relevant to a newborn, but expectant mothers are typically screened for hepatitis B during their prenatal care anyway.

So why exactly do we give it to newborns? Does anyone know? Are we protecting them for a lifetime of unprotected sex and drugs? Does any protective effect from the vaccine even last that long?
The many concerns surrounding giving the hepatitis B vaccine to newborns are not unfounded. The concern is not simply a matter of being anti-vax. And concern about this vaccine certainly isn’t anti-science.

Let’s take a look at the science.

The vaccine was first introduced in the 1980s. And early warnings came fast.

Respected vaccine researcher Bohn Dunbar exposed the pattern of autoimmune complications after her own brother was injured by the hepatitis vaccine in 1994.

A 1998 article in the journal Science highlighted the growing concerns surrounding the vaccine, including the fact that attorneys representing more than 15,000 people sued France’s government for downplaying the risks and exaggerating its benefits.

France then suspended hepatitis B vaccination in schools.Image
A 1999 Congressional hearing laid it out:

• Numerous severe adverse reactions including death, seizures, autism, dysautonomia, MS, rheumatoid arthritis, diabetes, and liver cancer.

• Adverse reaction reports were ignored or dismissed, and short trial durations missed delayed reactions.

• Parents were not informed of the risks, newborns were vaccinated without parental consent, and parents were threatened with intervention from social services.

• Vaccinating low-risk newborns for an adult-associated disease is just plain inappropriate.

• The National Vaccine Injury Compensation Program was denying most claims.

That same year, fewer than 100 U.S. children under age 2 got hepatitis B.

The math doesn’t add up. It never has.Image
@MidwesternDoc @HighWireTalk Also in 1999, back when it was actually possible to find a little truth about Big Pharma on TV, ABC News aired an entire program addressing the hepatitis B vaccine.

They even included vaccine-injured patients and parents of severely injured children.
@MidwesternDoc @HighWireTalk The untold history of the hepatitis B vaccine is jaw-dropping.

From contaminated trials to secret CDC rationales—it’s all here in @MidwesternDoc's full report:
midwesterndoctor.com/p/why-is-every…
The science is and has been stacked against this vaccine.

Studies showed hepatitis B vaccination increased the risk of MS, lupus, arthritis, and other autoimmune conditions.

In France, cases of MS spiked 65% after a national campaign. A CDC dataset showed a 12X higher autism risk when given in the first 30 days of life!Image
Why does the hepatitis B vaccine cause so much damage?

Autoimmune conditions caused by the vaccine are likely due to its antigen having a significant overlap with human myelin.

The molecular mimicry of the vaccine was denied because it couldn’t be proven.

A 1994 Institute of Medicine (IOM) report noted that, although preliminary data existed for many of the reactions attributed to the hepatitis B vaccine, no further research had been conducted.

Wow, thanks IOM.Image
@MidwesternDoc @HighWireTalk The trials were a joke.

They monitored “side effects” for a mere 4–5 days. And the placebos they used? No, not saline—they were other vaccines or even aluminum adjuvants!

Are you kidding me??

Serious reactions—sometimes fatal—were reclassified as SIDS or coincidence. Image
If transmission is typically due to adult risk factors, why not give it only to adults at risk? Healthcare workers, IV drug users, and gay men with multiple partners…

Studies have shown that it can dramatically reduce cases in these groups.

Why infants? There is virtually no risk, and immunity does, in fact, wane.

So what is the point?Image
The CDC’s main argument is prevention of mother-to-child transmission.

But nearly all U.S. expectant mothers are screened for hepatitis B during pregnancy. And infection rates are under 0.5%!

By the numbers, millions of babies must be vaccinated to prevent a single severe outcome.

And that’s not an exaggeration.

And if mom’s status is unknown, it’s actually mandated in many states to screen newborns for hepatitis B anyway.Image
So why the universal newborn mandate?

A former ACIP insider revealed the dark truth:

It’s not about maternal transmission. It’s about capturing a “captive audience” in the hospital—before at-risk youth slip through the cracks later in life.

So, because the CDC was failing to reach inner-city teens, they decided to vaccinate every baby in America.

It was never, ever medically justified—it was bureaucratic convenience disguised as science.

Let that sink in.Image
@MidwesternDoc @HighWireTalk The hepatitis B vaccine’s dark history will leave you speechless.

Were you vaccinated for hep B? What about your children?

@MidwesternDoc's full report is a must-read.
midwesterndoctor.com/p/why-is-every…
The history is disturbing.

The first hepatitis B vaccines were plasma-derived—actually using infected human blood. It even involved chimpanzee-human blood exchanges.

This was during the early AIDS crisis in New York, San Francisco, and LA. Remember: HIV is considered to have come from a chimpanzee virus. Sounds risky.

Merck then rushed out the first recombinant GMO vaccine in 1986.
From the start, the hepatitis B vaccine was expensive—about $145 for three doses compared to $2 for other vaccines.

Uptake was low among the high-risk groups it was meant for.

So regulators shifted strategy: add it to the childhood schedule, where government funding guaranteed sales.Image
By 1991, ACIP mandated hepatitis B vaccination for all newborns. By 1999, it expanded to all children and adolescents.

Parents objected. Pediatricians resisted. Even gay activists called it a failure of public health outreach.

But the CDC pressed forward—insisting it was “safe and effective” for day old newborn babies, despite what the science said.Image
Decades later, the outcome couldn’t be more clear.

Acute hepatitis B cases declined—but chronic hepatitis B rates never budged.

The very condition the program was supposed to eliminate hasn’t even changed since 1976.

Severe injuries from the vaccine, however, skyrocketed.

So was it worth it?Image
@MidwesternDoc @HighWireTalk For the first time in decades, the ACIP is actually doing its job and reconsidering the hepatitis B newborn mandate.

This is our chance to demand change.
midwesterndoctor.com/p/why-is-every…
This isn’t just about one vaccine.

It’s about how “safe and effective” became a slogan.

How risk-benefit ratios were buried.

How the human cost was swept aside.

And how bureaucrats forced a medical intervention on every newborn infant—not for health, but for control and profit.Image
@MidwesternDoc @HighWireTalk The hepatitis B saga is a warning.

When government health policy is driven by politics and profit instead of evidence, children always become collateral damage.

For decades, parents were never told the truth. Now, the cracks are showing. Image
This is a once-in-a-lifetime chance to correct the terrible course we’ve been on.

If you care about medical freedom, informed consent, and protecting children, now is the time to act.

Read the full report. Spread the word. Contact your Senators. Watch the ACIP hearings.

This could be the turning point.

For 30 years, America’s newborns were sacrificed to a policy that never made sense.

Will the ACIP finally end it?Image
@MidwesternDoc @HighWireTalk Thanks for reading! This information was based on a report originally published by @MidwesternDoc.

Key details were streamlined and editorialized for clarity and impact. Read the original report here.
midwesterndoctor.com/p/why-is-every…
@MidwesternDoc @HighWireTalk For a deeper dive into what modern medicine has overlooked—or intentionally buried—check out these other eye-opening reports by @MidwesternDoc:

What We’ve Learned from a Year of Vaccine Shedding Data
midwesterndoctor.com/p/what-weve-le…
@MidwesternDoc @HighWireTalk What They Don’t Tell You About C-Sections
midwesterndoctor.com/p/what-the-don…
@MidwesternDoc @HighWireTalk What’s The Healthiest Water To Drink?
midwesterndoctor.com/p/whats-the-he…
@MidwesternDoc @HighWireTalk While you’re at it, give @MidwesternDoc a follow.

No one brings more research, clinical insight, or historical context when it comes to exposing the health myths we’ve all been fed.

This is easily one of the most valuable accounts you’ll ever follow.

--> @MidwesternDoc Image

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More from @VigilantFox

Jul 23
Your nerves don't tell your brain that something hurts.

They send energy, and that energy can be redirected.

A little girl's legs had hurt every day for 7 years. Not one minute of relief. Then her mom stuck a patch on her. Within seconds she was sobbing:

"Mom, it's gone. It's completely gone."

This was no ordinary patch. It's closer to an antenna — and it came out of a military project. 🧵
A five-foot antenna and an 80-pound backpack. That’s what one man on every deployed Navy SEAL team had to haul out of a plane in 2012, and if that antenna broke on the jump, the team couldn’t communicate back.

Mike Hammond wasn’t trying to build a wellness product. He was a serial entrepreneur fresh off a company exit when a friend from business school asked him to invest in a military antenna project out of Utah. The mission: shrink that five-foot rig into something a soldier could actually carry.

They did it. In Mike’s words, “they basically shrunk that five foot antenna down to the size of a credit card by shifting it to work on electrical microcurrents instead of magnetic fields.”

Then came the part that matters for you: your body runs on those same microcurrents. It’s the current keeping your heart beating while you read this. And when something hurts, your nerves fire that same energy up to your brain.

The patch is, quite literally, an antenna for it. Mike explains: “when your nerves create that energy that goes up to your neural pathway to the brain, when it hits our patch, it’s easier for that energy to go into the patch instead of up to the brain.”

You can feel it happening. Put it on and the patch gets warm. “Well, that’s your energy going into the patch. That’s why it warms up.”

No drugs enter your body. Nothing shocks your nerves like a TENS (Transcutaneous Electrical Nerve Stimulation) unit. And after five clinical trials, Mike says the results keep repeating: “it’s going to work on 85% of people, most are going to have results within 15 minutes and the average decrease is going to be over 60%.”

He adds: “It’s actually floored our doctors how similar every single trial’s been, even with different types of elements.”

And the track record at scale, according to Mike: “we’ve sold over 800,000 of these in the last few years and we haven’t had anyone call us with side effects because we’re not putting anything into the body.”
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You’ve got nothing to lose but the ache.

👉 SignalRelief.com/pulse. Code PULSE for 10% off already discounted prices.Image
Read 8 tweets
Jul 17
How many times have you heard someone say: “I got the flu shot, and I still got the flu anyway”?

Bill Maher says he once got the flu shot and “immediately” came down with the flu.

Lara Trump’s mother had an even worse experience. As a nurse, she got the flu shot every year—and “every time [she’d] ever gotten it, [she’d] get the flu immediately after it.”

Now, she doesn’t get it anymore.

Why do so many people get sick after the flu shot?

This thread explores why that happens—and what really happens inside the body right after a vaccine. 🧵
For decades, vaccines have been marketed as “safe and effective.”

No questions. Nothing else to consider. Safe and effective. Full stop.

But a mountain of buried medical research and endless reports from the vaccine-injured show a very different pattern—one that has repeated for more than a century.

In disease after disease, across multiple countries and multiple eras, vaccines have a weird habit of triggering or worsening the very illnesses they are supposed to be preventing.

Strange.

This occurrence isn’t fringe. It’s documented, replicated, and historically well known.

But millions of people—doctors, teachers, parents, friends—pretend it isn’t.

And even when they do offer a protective effect for some disease, they can leave your immune system weakened and vulnerable to other infections that can end up killing you. Just look at what happened in Guinea-Bissau.
This information comes from the work of medical researcher @MidwesternDoc. For all the sources and details, read the full report below.
midwesterndoctor.com/p/why-do-vacci…
Read 30 tweets
Jul 13
You've heard of Flock cameras, but have you heard of NEMA nodes? Those unassuming little plugs on virtually every streetlight in America, silently turning your city's lighting grid into an always-on, AI-powered surveillance mesh that knows exactly where you sleep, drive, and walk... every single night.

What started as 'smart energy saving' has morphed into the backbone of a nationwide tracking system — powering cameras, sensors, and data fusion that governments and tech giants can tap into with a few clicks. No warrants needed when the infrastructure is already watching.

Tonight, @zeeemedia pulls back the socket on NEMA nodes: how they fit into the bigger surveillance grid, and why your local streetlight might know more about you than your own phone. 🧵
Flock cameras became a household name for a reason. The license plate reader network has been tied to documented cases of police officers misusing it to stalk women, and researchers have demonstrated how easily the systems can be hacked and abused, with reports suggesting predators have exploited that weakness.

But while public attention stayed on the cameras, a quieter buildout was happening overhead. Modern LED streetlights across America are being fitted with NEMA control nodes, small modules mounted on top of the fixture. In their simplest form, these are just photocells that turn the light on at dusk and off at dawn. But the newer generation are smart lighting controllers that let a municipality or utility monitor the light, dim it remotely, detect failures, and manage energy use.

The concern being raised is what else they can carry. Modern nodes can include wireless communication, and while the node itself generally does not contain a camera, many are being installed with the ability to add camera capabilities later. The infrastructure goes in first. The sensors come after.

The scale is already significant. In Washington D.C. alone, roughly 75,000 streetlights have reportedly been upgraded with advanced Internet of Things capable nodes. Much of this buildout accelerated during the COVID lockdowns, when infrastructure went up across cities while residents were told to stay home, and most of it went unnoticed.
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Read 10 tweets
Jul 13
A registered nurse with 30 years of experience treating chronic pain says she saw “TEN TIMES” the positive effects after combining DMSO with castor oil for her peripheral neuropathy.

Castor oil already has anti-inflammatory properties.

But adding DMSO is where she says it “got interesting.”

That’s because DMSO “isn’t just a treatment, it’s a carrier,” Danielle Minetti explained.

“It can pull medications and nutrients right through the skin barrier deep into the body.”

When Danielle combined it with castor oil, she says the results increased “ten times.”

DMSO acted as the delivery system, carrying the castor oil deeper into the areas where she needed relief most.

But DMSO’s potential extends far beyond peripheral neuropathy.

And if you’re one of the 5 million Americans living with carpal tunnel syndrome, this is where the DMSO story gets really interesting.

Because it turns out carpal tunnel may not be caused by overuse after all. 🧵
Somewhere between the wrist pain that shows up after years of typing and the keyboard sitting under your fingers right now, there’s a design decision nobody remembers making.

It wasn’t an accident. It was a deliberate engineering choice made to solve a mechanical problem.

But that problem that stopped mattering almost a century ago. And the fix that’s still shaping our hands today has far outlived it.

Early typewriters had a real problem: type two adjacent keys too quickly and the mechanism would jam.

The fix was mechanical, not electronic. Spread the commonly paired letters as far apart as possible so fingers physically couldn’t hit them fast enough to jam the machine.

That layout is the same one you’re using right now.Image
That was over a century ago.

Mechanical jamming stopped being a problem once electric typewriters showed up. Computers can’t jam at all.

But the keyboard never changed. Image
Read 23 tweets
Jul 12
YouTuber Dan Schaeffer says he “completely cleared” his sinuses by combining DMSO, purified water, and colloidal silver into a nasal spray.

One squirt up each nose twice a day, and the results were “amazing.”

“No pressure, no nothing.”

Dan’s experience is not an isolated one.

In 1992, Russian researchers found that treating children with sinusitis using a 10% DMSO solution followed by local oxygenation provided complete relief in 49 of 52 cases.

DMSO is a cheap substance you can typically find online for under $30.

Turns out it can do much more for your respiratory system than just clear your sinuses. 🧵
Most people think respiratory infections are something you just have to “ride out.”

You get congested. Your throat hurts. Your sinuses clog. Maybe it turns into a cough, maybe it doesn’t. Maybe it moves into your chest, maybe it doesn’t.

So you take a decongestant, stock up on tissues, drink fluids, wait a few days, and hope it passes.

But that entire model skips one of the most important parts of the story:

Where many respiratory infections actually begin.Image
Respiratory viruses don’t typically start as deep lung infections.

They often begin in the upper airway—the nose, sinuses, throat, and nasopharynx.

That matters because the early stage of the illness may be happening in areas that are much easier to reach than the lungs.

In other words, by the time people are talking about bronchitis, pneumonia, oxygen levels, and hospital care, they may have already missed the window of opportunity.Image
Read 31 tweets
Jul 10
Are flavor enhancers used by nearly every major food brand being developed with cells derived from an aborted baby?

Tonight’s special report presents shocking evidence tracing the dark history of these additives and the powerful companies operating behind the label.

Most people have never heard of HEK293 cells. And two reassuring words—“natural flavors”—are concealing a disturbing story the food industry hoped you would never uncover. 🧵
HEK293 is a human cell line originally derived in the early 1970s from kidney tissue taken from a single fetus, believed to have come from an aborted pregnancy.

The cells are used as laboratory tools, not food ingredients.

Researchers can engineer them to express human taste receptors. When a chemical compound activates one of those receptors, the cells produce a measurable signal showing whether a person may perceive it as sweet, bitter, salty, or cooling.

That allows laboratories to screen thousands of potential flavor compounds without putting each one through a human tasting panel.

Senomyx, a biotechnology company that developed flavor enhancers and taste modulators, described this process in its patents. The patents shown in the report identify HEK293 as a preferred cell line for assays designed to find compounds that produce or modify sweet taste.

The cells remain in the laboratory.

“The cells themselves were not added to food products,” Maria explained. Senomyx maintained that no fetal cells or tissue entered finished consumer products.

That distinction answers what a food physically contains.

It does not settle whether the process used to develop it is ethically acceptable.

Supporters argue that HEK293 has been reproduced in laboratories for decades and is now far removed from the original abortion. They point to its value in medical and scientific research, especially when no suitable alternative exists.

@zeeemedia rejects that calculation.

“It doesn’t matter how many years it’s been since that point, that child was still murdered.”

For people who share that conviction, the question is not simply whether fetal material remains in a soda, cereal, vaccine, or medication.

It is whether that product was created using knowledge obtained through a cell line they believe should never have existed.

The dispute does not end with the final ingredient list.

It begins inside the research process—and the next problem is where that process disappears.
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Read 9 tweets

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