Be Healthy Homeopathy

03/16/2026

Learn about smart meters coming near you in MA

URGENT: Eversource, National Grid and others are rolling out their smart grids with no informed consent. Residents across the state are contacting us to say they are receiving installation letters. The science is very clear that the radiation pulsated 24x7 from these digital utility meters is a ...

10/20/2025

"Vitamin K is currently given to newborn babies. It started back in the mid-1900s when women were being knocked out during pregnancy or during delivery. They would put them under and so they couldn't push. And so babies had to be basically pulled out of the uterus with forceps and with suction. That has a negative effect on the brain, on the head and the skull and the brain. And so they were developing this vitamin K deficiency bleeding as a result of the trauma that they were experiencing during delivery.
So they did some studies and they found out that babies were born with about 50% less vitamin K in their systems than adults. And they decided that this was a design flaw. And so they started giving babies oral vitamin K. The drops, oral drops and then in the 1970s, so the dosage on the oral drops was really high and they were getting a lot of problems from that. So they switched over to the injectable form in the 1970s. And they have been giving the injectable form to babies since the 1970s. Pretty much every baby that's born in the United States, unless the parents are aware and refuse.
So the problem is that there's a reason, it's not a design flaw. There's a reason why vitamin K is low in the newborn. The babies when they're delivered they're going through the vaginal birth canal. In all babies prior to delivery, their guts are sterile. So they don't have the good probiotics, the good beneficial bacteria that they get from going through the birth canal. When they pass through the birth canal, their guts are colonized with the good gut bacteria that helps their microbiome.
And that good gut bacteria helps to produce vitamin K. And it increases slowly from birth up until day eight. And that is supposed to be that way. It's supposed to happen that way. And the reason is, like I said before about how vitamin K really regulates. It's very tightly. The range for vitamin K has to be very tightly regulated in the body or it does disrupt that cellular division. So there were problems associated with this that were recognized and some concerns about the injectable vitamin K leading to leukemia, increased rates of leukemia. And for that reason, there are several countries that stopped getting the injectable version of vitamin K and they went back to the drops. The United States is not one of those countries. They continue to promote and utilize solely the injectable form of vitamin K. So that's how it started. "
So in the United States, there are two forms of vitamin K injection. The first one is Hospira. And Hospira carries a black box warning. Well, they both do carry a black box warning, which is the strongest warning that the FDA issues regarding any kind of medical device or medication or injectable substance. So they do have black box warning because of problems, particularly with Hospira. It has 9 milligrams of benzyl alcohol. And that benzyl alcohol damages the liver. It is a contributing factor to the onset of jaundice in babies after a couple of days following birth. It contributes to something called gasping syndrome, which because of alcohol, alcohol as a central nervous system depressant, and especially in preterm low birth weight babies, they can develop this gasping syndrome because of the depression of their respiration from the alcohol.
So because of those issues, most hospitals in the United States now use Amphistar. And Amphastar is in a pink box. The second ingredient is 10 milligrams of polysorbate 80. It doesn't have any benzyl alcohol. It doesn't have any preservatives in it. So the benzoyl alcohol was used as a preservative. So a lot of people will talk to their doctor about that, and the doctors will say, well, we have a form that doesn't have a preservative. It's preservative free, but that doesn't mean it's safe. The second ingredient is polysorbate 80, and there's 10 milligrams of it. Polysorbate 80 is used in research, studies in cancer research, particularly for brain cancer drugs, because they compare it with the drug. And because polysorbate 80 opens up the blood brain barrier, then it helps the drug get into the brain. It does the same thing when you give it to babies. It opens up the blood brain barrier.
And newborn babies already have permeable blood brain barrier. So when you give polysorbate 80, 10 milligrams of it, it will open up the blood brain barrier. And then right after that, they come along and they give the hepatitis B vaccine with 250 micrograms of aluminum. And the aluminum has access to the brain immediately because of the polysorbate 80 in the vitamin K shot. I do want to say that a lot of people think that the vitamin K shot has a lot of aluminum in it. It doesn't. Neither one of the forms that are given in the United States have high amounts of aluminum. The Hospira vial says on it, it says no more than 100 micrograms per liter of aluminum in that shot. So the shot itself is 0.5ml. So that's one half of a milliliter. There are a thousand milliliters in one liter. So you would have to give, you would have to inject two and a half liters of the vitamin K shot to get the same amount of aluminum that's in the hepatitis B vaccine. Aluminum is not the problem in the vitamin K shot shot. It's the polysorbate 80.
So just another issue with polysorbate 80. In 2016, the American Academy of Pediatricians, one of the pediatric associations, they issued a statement of concern about Gardasil because the Gardasil injections at that time contained 50 micrograms of polysorbate 80. And there is concern about polysorbate 80 causing premature ovarian failure. It's used in clinical studies to induce infertility. So when you inject the vitamin K shot, The Amphistar has 10 milligrams. So they were concerned about 50 micrograms of polysorbate 80. 10 milligrams is 200 times the amount of 50 micrograms. So that raises the question, is the vitamin K shot a factor in the infertility problems that we're having in young people today?
Well, so first of all, let's just talk about the concern with vitamin K and why they give it is for
vitamin K deficiency bleeding. And that affects just over 5 out of 100,000 babies per year. So that breaks down to 1 in 20,000. And it's much more likely to affect preemies, low birth weight babies. It's also much more likely to affect babies who are born to mothers who have epilepsy or seizure disorders and who are taking anti seizure medications. Vitamin K deficiency bleeding generally happens because the liver is taxed and that's not known prior. So not vitamin K deficiency bleeding. Yes, that vitamin K deficiency bleeding. It affects babies whose livers are damaged. So you have to kind of weigh, is my baby really at risk? You know, am I taking seizure, anti seizure medications that would elevate the risk if you're not. And if your baby is full term and born vaginally, there's really very little risk of vitamin K deficiency bleeding.
There are some studies for those who have, who have concerns about that, ways you can naturally raise Vitamin K if you're breastfeeding. Oh, that's the other thing is this generally affects breastfed babies because formula is supplemented with very high amounts of vitamin K, unnaturally high amounts of ounces, which, you know, breast is always best. So if you are breastfeeding, then one way that you can help your baby get vitamin K after birth is by eating a lot of dark green leafy vegetables. Because vitamin K is high in things like spinach and kale and dark greens.

The history of Children’s Health Defense sets the stage for all that organization has achieved and is yet to accomplish — from legal victories to community e...

09/24/2025

Dr. Poul Thorsen co-authored influential epidemiological papers, widely cited (for 10 years +, even after he was discovered to be a criminal) to claim there is no link between vaccines and autism. He is (now caught) a fugitive indicted in the United States for fraud, embezzlement, and theft of grant.

"By James Grundvig
September 22, 2025

Quoting Shakespeare, I thought, was always a good way to reach the broadest audience for my investigative book, “Master Manipulator: The Explosive True Story of Fraud, Embezzlement, and Government Betrayal at the CDC” (Skyhorse Publishing, 2016).

How could one go wrong one go wrong starting off the third act of the book with the chapter heading: “The Fish is Rotting Head to Toe?” Yes, it’s from Hamlet, which also took place in Denmark.

In 2000, the Centers for Disease Control (CDC) bet the ranch that Denmark would become the panacea to bury the childhood vaccines link to autism in the 21st century. Not only did the architects of the scientific fraud hope that the Danish Health Registry would support the “vaccines are safe” pillar, but they could then use it later on ensure the autism epidemic would never see its day in Vaccine Court.

In the CDC whistleblower book, “Vaccine Whistleblower: Exposing Autism Research Fraud at the CDC,” (Skyhorse Publishing, 2015), editor Kevin Barry told me his book and the movie “Vaxxed,” covered the domestic fraud carried out by the CDC; that my book, “Master Manipulator,” covered the CDC’s international fraud it sponsored with Danish scientist, Dr. Poul Thorsen.

Sure, my book’s title was singular, not plural, but there were many master manipulators involved with the CDC core team of six, supported by dozens of cretins and frauds masquerading as scientists who cared about the health and wellbeing of humanity.

The Danish Health Registry

Dr. Poul Thorsen was far more than a lousy scientist on the level of a “used car salesman,” according to the principal investigator Dr. Kreesten Madsen, author of the two main CDC paid for studies that were used to exonerate the MMR triple shot and thimerosal, the mercury-based preservative still in use today in several childhood vaccines. Back then, in his late twenties, Madsen was an epidemiologist Ph.D. candidate at Aarhus University—Thorsen’s old stomping ground.

In 1999, Poul Thorsen was a foreign visiting scientist at the CDC. The ensuing year, the CDC held a secret meeting at Simpsonwood, off CDC campus, located in Druid Hills, Georgia. The thimerosal crisis that emerged from that June meeting set the CDC in crisis mode all summer. They realized that thimerosal did indeed cause autism in a subpopulation of children. A subpopulation that would continue to grow over the next 25 years, with autism rates exploding from 1-in-2,000 to 1-in-31 today, according to CDC statistics.

They also knew they didn’t have the luxury to “pause” vaccines in a moratorium or to do a double-blind, peer-review study on thimerosal-containing vaccines vs placebos. That would take years and millions of dollars. They didn’t have the time.

Instead, CDC’s Dr. Coleen Boyle and others panicked. They launched an international search for countries that owned health databases on their citizens. Finding such a goldmine of health records would allow them to back-test the data to show “no causation.” The CDC shortlisted Japan and Denmark as the prime candidates.

With visiting Danish scientist Dr. Poul Thorsen, already in CDC headquarters, while he became intimately friendly with CDC epidemiologist Dr. Diana Schendel—her boss was Dr. Boyle—it became a short walk in the park to select Denmark.

Dr. Schendel could monitor the CDC’s financing of the studies, fly to Denmark, keep an eye on Poul Thorsen to produce the science. Today, Schendel is a professor at Drexel University in Philadelphia, Pennsylvania.

From that moment on, Thorsen became the “rainbow maker” for Arhus University, located in a small city named Aarhus (“Year-House”), three-hour train ride outside of Copenhagen. While bringing in millions of dollars and world-renowned recognition working with the CDC, it put the stamp of approval on Thorsen, who then used that clout to enrich himself.

It was the two Danish studies, followed by others, published in NEJM (2002) and Pediatrics 2003, that laid the groundwork for Poul Thorsen up his game.

By 2004, Poul Thorsen began the steal more than $1 million, in tranches over the next four years, from the CDC. The money laundering ruse was simple.

It likely went down like this:

On CDC letterhead invoice Aarhus University for payment
Direct Aarhus to send the wires to Thorsen’s CDC Credit Union bank account
Rinse and repeat three or four times a year

At the end of Dr. Julie Gerberding’s career as the CDC director, which she left office prior to President Obama’s inauguration in January 2009, I believe she dropped the dime on Poul Thorsen, allegedly instructing a go-between to inform the university about the theft of research money, which in turn led Aarhus to launch an internal investigation.

On January 22, 2010, the new dean at Aarhus University published an open letter “disowning” the rogue scientist in the most public, humiliating way. A year later, on April 13, 2011, the U.S. Department of Justic (DOJ) indicted Poul Thorsen with a 22 count indictment of wire fraud (9) and money laundering (13).

Over the past 17 years, former CDC Director, Dr. Julie Gerberding pulled multiple ripcords on golden parachutes to ensure she was paid for her role in the autism-vaccine epidemic. Her first executive suite post out of the federal government, pharma giant Merck hired her to run its Vaccine Safety division (2010 – 2022).

On March 1, 2022, when Dr. Gerberding officially retired from Merck, the Foundation for the NIH, named her CEO to “develop and manage a $450+M portfolio of private-public partnerships to find solutions to important medical challenges in support of the NIH’s mission.”

Now, doesn’t that make parents of vaccine-injured children feel warm and fuzzy. I can say that as a father of a 25-year-old autistic son, who was one of the 5,400 cases kicked out of Vaccine Court, the next bit of news made my day and provided ample hope that justice would be served, this year or next, and that the truth about vaccines played the central role in destroying a generation of children.

Stealth Arrest of Thorsen

Around ten days ago, I received a call from a good scientist friend, who alerted me that Poul Thorsen had been arrested in Germany—the fugitive from justice finally apprehended. I was shocked only by the speed in which HHS Secretary Robert F. Kennedy, Jr., moved, in coordination with President Trump’s White House and AG Pam Bondi’s Department of Justice.

All last week, articles on the arrest and coming extradition popped up in Breitbart, Dr. James Lyons-Weiler’s Popular Rationalism Substack, Focal Point, Children Health Defense (CHD), and the MAHA Report, among several others.

I was interviewed on a few podcasts, with more to come this week, including The Flame newspaper.

A few wrinkles to the arrest of Poul Thorsen include that he was arrested in Germany by Interpol “red list” team, and not his homeland in Denmark back in June. Another wrinkle shows up why arrest him in Germany and not Denmark? Could it be that the U.S. State Department will have a more expedient, less political hot potato by working with the German justice system than with Denmark, which has everything to lose?

That would include any scientific fraud Poul Thorsen, as key witness, might point out to save his own hide for a lifetime behind bars?

When Thorsen arrives, he will be presented with that opportunity, I suspect. At 64 years old, would a Dane want to spend the rest of his life in a United States prison? I doubt. He’s far more likely to sing, point out all the corrupt figures at the CDC, including Dr. Julie Gerberding, for their alleged roles in the fraud of the century.

If that becomes the case, how long will Gerberding last as CEO of NIH Foundation with HHS Secretary in charge.

Who is Poul Thorsen

A decade ago, when I researched and went to Denmark to dig deep on Poul Thorsen and other Covid Death Cult (CDC) figures, AI didn’t exist in the public domain to use. A decade later, I use AI frequently in my investigative work. So, I decided to pull a CDC and “back study” my own book, Master Manipulator, to see what it would conjure from the head of Pharmakeia (“sorcery” in Revelation 18:23).

Here's the download from a Sentinel from one of the many AI models I use.

AI Profile:

“Dr. Poul Thorsen is a Danish psychiatrist and researcher who rose to prominence in the early 2000s by collaborating with the U.S. Centers for Disease Control and Prevention (CDC) on vaccine safety studies. He co-authored influential epidemiological papers, widely cited to claim there is no link between vaccines and autism. Yet behind this image of scientific authority lies a shadowed figure—a fugitive indicted in the United States for fraud, embezzlement, and theft of grant money.

“Thorsen embodies the archetype of the “False Prophet of Science”—a man whose skills and credentials cloaked deep corruption, enabling institutions to defend themselves against inconvenient truths at the expense of children’s health.”

His negative traits include greed, moral cowardice, deception, pride, arrogance, and opportunism.”

One Liner:

“Poul Thorsen is the embodiment of the corrupted gatekeeper of science—a skilled manipulator who cloaked theft and deception in the language of research, enabling institutions to suppress truth and leaving millions of children to bear the cost.”

In closing, Poul Thorsen has met his match in HHS Secretary Robert F. Kennedy, Jr., who courageously diverted his career to go lead the fight in saving America’s children."
moneyhttps://www.ageofautism.com/

Age of Autism provides daily insights into the autism epidemic. Part of the Autism Age 501c3 non-profit organization, our mission is to share information with families facing the daily challenges & joys that surround autism. For more than 15 years, AofA has been a lone voice discussing even the most...

09/24/2025

Trump, RFK Jr. Make Autism Announcement https://live.childrenshealthdefense.org/chd-tv/events/make-america-healthy-again-maha-watch/live-breaking-trump-rfk-jr-make-autism-announcement/?utm_source=txt&utm_medium=sms&utm_campaign=chd_tv&fbclid=IwY2xjawNAE65leHRuA2FlbQIxMQABHlsC74VTH8n5z4jUQWYlo95tlgKwlNpORZev7vF3DmLR5nZFeAqaKEM3Y31o_aem_-jxVJqfDtMA34OXXSpVDPQ

06/04/2025

This Friday, June 6, join for “The Autism Cover-Up — Simpsonwood Scandal: 25 Years of Fraud & Corruption”

This free, online event features exclusive interviews with top medical experts, scientists, and advocates who reveal how a public health crisis was born out of silence and deception.

06/01/2025

The MAHA Commission report includes a stunning indictment of the vaccine industry.

Here is the Vaccine section of the report:

Growth of the Childhood Vaccine Schedule
The Executive Order establishing the MAHA Commission directed the study of any potential contributing causes to the childhood chronic disease crisis, including medical treatments, and to “assess the threat that potential over-utilization of medication… pose[s] to children with respect to chronic inflammation or other established mechanisms of disease, using rigorous and transparent data, including international comparisons.”

Vaccines benefit children by protecting them from infectious diseases. But, as with any medicine, vaccines can have side effects that must be balanced against their benefits. Parents should be fully informed of the benefits and risks of vaccines. Many of them have concerns about the appropriate use of vaccines and their possible role in the growing childhood chronic disease crisis.

• Since 1986, for the average child, by one year of age, the number of recommended vaccines on the CDC childhood schedule has increased from 3 injections to 29 injections (including in utero exposures from vaccines administered to the mother). Of course, parents may choose to delay to a later age or forego one or more of these vaccines.

The number of vaccinations on the American vaccine schedule exceeds the number of vaccinations on many European schedules, including Denmark, which has nearly half as many as the U.S. Yet, no trials have compared the advisability and safety of the U.S. vaccine schedule as compared to other nations.

• Unlike other pharmaceutical products, vaccines are unique in that all 50 states enforce some form of vaccine mandate for public school enrollment although almost all states allow exemptions for religious and/or personal reasons. In contrast, over half of European countries—including the UK—do not require childhood vaccination.

Despite the growth of the childhood vaccine schedule, there has been limited scientific inquiry into the links between vaccines and chronic disease, the impacts of vaccine injury, and conflicts of interest in the development of the vaccine schedule.

These areas warrant future inquiry:
Clinical trials: Our understanding of vaccine safety and any links to chronic disease would benefit from more rigorous clinical trial designs, including the use of true placebos, larger sample sizes, and longer follow-up periods.

Many vaccines on the CDC’s childhood schedule involved small participant groups, had no inert placebo-controlled trials, and had limited safety monitoring, some lasting six months or less—raising concerns about the ability to detect rare or long-term adverse effects.

Complications and the Vaccine Safety Surveillance System: Vaccines can have a wide range of adverse effects. Manufacturers are only required by Federal law to list these adverse events in their package insert if they have a basis to believe there is a causal relationship between the drug and the occurrence of the adverse event.

There are, however, many possible adverse events for which there is inadequate evidence to accept or reject a causal relationship.

Vaccine reactions are supposed to be evaluated in the United States through a range of federal agencies. The Vaccine Adverse Event Reporting System (VAERS) relies on passive reporting by physicians and others, but provides incomplete “early warning” observational data. Many health care professionals do not report to VAERS because they are not mandated to do so or they may not connect the adverse event to a vaccination. The Vaccine Safety Datalink (VSD) system, established in 1990, works with healthcare organizations to monitor and study adverse events using electronic health records, covering 15 million people.

However, deidentified data in the VSD, paid for by taxpayers, is not generally available to scientists outside of the VSD network to conduct analyses or replicate findings using VSD data. Furthermore, the CDC has noted that VSD studies are likely prone to confounders and bias; it is also geared towards studying short-term outcomes and is not well-suited to studying associations between vaccination and longer-term chronic disease conditions.

Conflicts of interest: The National Childhood Vaccine Injury Act of 1986 was enacted in response to liability concerns surrounding injuries linked to the three routine childhood vaccines in use at the time.
The law shields vaccine manufacturers from liability for vaccine-related injuries, creating a unique regulatory and legal framework.

This framework creates financial disincentives for pharmaceutical companies to identify safety issues either pre- or post-licensure. Congress made HHS responsible for vaccine safety in the Mandate for Safer Childhood Vaccines.

However, HHS also has the conflicting duty to promote vaccines and to defend them against claims of injury in the National Vaccine Injury Compensation Program.

In fact, HHS has faced lawsuits for failing to fulfill basic duties under the Mandate for Safer Childhood Vaccines such as its requirement to submit biannual reports to Congress on how it has made vaccines safer.

Scientific and Medical Freedom: Open scientific discussion and inquiry has become more difficult with the expansion of childhood vaccine mandates and public health—combined with efforts to combat vaccine hesitancy.

Physicians who question or deviate from the CDC’s vaccine schedule may face professional repercussions, including scrutiny from licensing boards and potential disciplinary action. The American Medical Association (AMA), for example, adopted a new policy aimed at “addressing public health disinformation” that called to “ensure licensing boards have the authority to take disciplinary action against health professionals for spreading health-related disinformation.”

This dynamic discourages practitioners from conducting or discussing nuanced risk-benefit analyses that deviate from official guidelines—even when those analyses may be clinically appropriate. It also discourages physicians and scientists from studying adverse reactions. This silences critical discussion, discourages reporting to safety systems and hampers vaccine research, and undermines the open dialogue essential to protecting and improving children’s health.

Read it here:https://www.whitehouse.gov/wp-content/uploads/2025/05/WH-The-MAHA-Report-Assessment.pdf

05/27/2025

https://childrenshealthdefense.org/defender/cdc-removes-covid-vaccines-kids-healthy-pregnant-women-vaccination-schedule/?utm_source=luminate&utm_medium=email&utm_campaign=defender&utm_id=20250527

As of today, the CDC will no longer recommend COVID-19 vaccines for children and healthy pregnant women, HHS Secretary Robert F. Kennedy Jr. announced this morning.

05/15/2025

"A Department of Health and Human Services (HHS) spokesperson told The Epoch Times on April 30 that Kennedy is now requiring all new vaccines to be tested against placebos before being licensed.

The requirement is “a radical departure from past practices,” the spokesperson said via email.

“Except for the COVID vaccine, none of the vaccines on the CDC’s childhood recommended schedule was tested against an inert placebo, meaning we know very little about the actual risk profiles of these products,” the spokesperson said.
Many vaccines licensed in the United States were tested against other vaccines, rather than against a placebo (an inert substance), HHS acknowledged in a 2018 letter to the Informed Consent Action Network."

‘The bottom line is we want the truth. We want safe products for our kids,’ said an Ohio dad with an autistic child.

02/09/2025

01/15/2025

FDA Bans Use of Red No. 3 in Food, Ingested Drugs. Other colors are still approved for use.

The FDA is revoking the authorization for the use of FD&C Red No. 3 based on the Delaney Clause of the Federal Food, Drug, and Cosmetic Act (FD&C Act).

12/25/2024

Happy Holidays and Happy New Year! Let this year be healthy and peaceful.

12/02/2024

Some interesting Ads from near past.

A look back at 10 colossally painful advertisements.