reSee.it - Related Video Feed

- First, HHS will act on acetaminophen. - The FDA is responding to clinical and laboratory studies that suggest a potential association between acetaminophen used during pregnancy and adverse neurodevelopmental outcomes including later diagnosis for ADHD and autism. - We have also evaluated the contrary studies that show no association. - HHS will launch a nationwide public service campaign to inform families and protect public health. - HHS wants therefore to encourage clinicians to exercise their best judgment and use of acetaminophen for fevers and pain in pregnancy by prescribing the lowest effective dose for the shortest necessary duration and only when treatment is required. - Some studies have also found the use of acetaminophen in children can potentially prolong viral illnesses. - FDA will drive new research to safeguard mothers, children, families.

Liz Eldon and the speaker are reassessing fluoride rules following the National Toxicity Program's August release. The new science shows a direct inverse correlation between fluoride exposure and IQ loss in children. Utah has become the first state in the country to ban supplemental fluoride. The speaker and Liz Eldon were in Utah this week to announce the ban.

Florida announces the Florida MAHA Commission, a working group that will 'recommend state level integration of these Make America Healthy principles.' Those principles are 'individual medical freedom, informed consent, parent rights, and also market innovation.' The commission will be chaired by First Lady Casey DeSantis and Lieutenant Governor Jay Collins, including Surgeon General Joe Latapo, ACA Secretary Siobhan Harris, DCF Secretary Taylor Hatch, elder affairs secretary Michelle Branham, and department of environmental protection secretary Alexis Lambert, with experts in nutrition, health, vaccine safety. Its objectives include 'promoting clean, safe, and nutritious industry,' 'improving transparency and accountability in health care,' 'working on the causes of chronic diseases to identify and prevent future occurrences,' and 'restoring trust in the medical profession and in public health.' It will 'prioritize reforms that empower Floridians,' 'reduce regulatory burdens,' and 'hold actors accountable for their conduct' while 'fostering incentives for healthy living and innovation.'

If we're gonna make America healthy again, we can't allow public health to be undermined. So could you explain what steps you're gonna be taking to ensure vaccine guidance is clear, evidence based, and trustworthy? We're going to make it clear evidence based and trustworthy for the first time in history. Only one of those 19 vaccines, 92 doses, only one of those vaccines has ever been tested against an inert placebo. And what we're doing now is any new vaccine that before it's approved and licensed will have to show demonstrate safety against inert placebo. And we're going to go back and do observational studies on the existing vaccines to see if they're linked to any of these chronic disease epidemics so that people can understand the risk profile of those products and make good assessments for their own health.

A congressional report reveals that popular baby food products contain high levels of toxic heavy metals, including arsenic, lead, cadmium, and mercury. The report calls for stricter regulation by the FDA. However, one company, Nature's One, takes proactive measures to ensure the purity of its organic baby formula by testing ingredients for heavy metal toxins before they even enter the facility. The company also conducts periodic testing of finished products. Other major brands, such as Gerber and Plum Organics, were found to have heavy metals in their products, with Gerber failing to recall some items. Representative Krishnamoorthy emphasizes the need for stronger federal standards and FDA regulation. Jay Hyman, CEO of Nature's One, believes it is his responsibility to prioritize consumer safety and remove harmful toxins from products. It is advised for parents to maintain a varied diet for their babies and be aware of reports on companies with higher or lower levels of heavy metals.

Research has revealed that folate deficiency in a child's brain can lead to autism. We have also identified an exciting therapy that may benefit larger numbers of children who suffer from autism. Peer reviewed literature has documented that up to sixty percent of folate deficient children with ASD can have improved verbal communications if given Leukavorin. I have instructed NIH, FDA, and CMS to help doctors treat children appropriately. Jay will help tell that story, which started with sound science, the kind that restores faith in government.

Working with governors in 24 states to advance MAHA legislation, aiming to remove soda from the SNAP program. Operation Stork Speed is underway to eliminate harmful chemicals from baby formula. Efforts are focused on improving school lunch programs by removing food dyes and other detrimental chemicals, which allegedly impact academic performance, school violence, and mental and physical health. Collaborating with governors to implement cell to cell legislation, restricting cell phone use in schools to improve academic performance. A significant reduction in animal testing at NIH and the FDA has been announced, transitioning to AI for more precise identification of toxic impacts. Partnering with Elon to streamline operations across health agencies, aligning with the goal of making America healthy again.

The speaker says they want dyes removed from food, noting that products like Froot Loops contain dyes in the US but not in Canada or Europe. They are launching a review of Generally Recognized as Safe (GRAS) standards, which were adopted in 1958 to avoid testing common foods like flour, dairy, and eggs. The speaker claims industry took advantage of GRAS to add chemicals to food without review, resulting in 10,000 ingredients in US food compared to 400 in Europe. They state the US has the worst chronic disease burden globally. The plan is to eliminate GRAS standards for new products, review old ingredients for safety, and encourage companies to remove harmful ingredients.

Speaker announces that the Florida Department of Health, in partnership with the governor, is going to be working to end all vaccine mandates in Florida, Washington. All of them. Every last one of them. Every last one of them is wrong and drips with disdain and and slavery. K? Who am I as a government or anyone else? Or who am I as a man standing here now to tell you what you should put in your body? Who am I to tell you what your child should put in your body? I don't have that right. Your body your body is a gift from God. What you put into your body what you put into your body is because of your relationship with your body and your God. I don't have that right. Government does not have that right. They want you to believe they have that right. And, unfortunately, you know, they've been successful.

Vaccine recommendations typically come from the Advisory Committee of Immunization Practices (an outside consulting committee at CDC) and VRBPAC (within FDA), which recommends vaccine licensure. These committees only adopted evidence-based medicine about twelve years ago. The speaker states that during their administration, they want safety studies prior to vaccine licensure and recommendation. They claim vaccines are exempt from pre-licensing safety testing, and the COVID vaccine was the only one tested in a full placebo trial. They assert that the other 76 shots children receive between birth and 18 have not been safety tested against a placebo, meaning the risk profile is not understood. The speaker intends to remedy this.

After seeing a 2022 study showing 100% of school lunches tested positive for toxic metals, the speaker revisited the work of Dr. Renee Jo Dufault, an FDA whistleblower who claimed there was undisclosed mercury in high fructose corn syrup. The speaker hypothesized that infant formulas, which often contain high fructose corn syrup, might also contain undisclosed mercury. Collaborating with Zen Honeycutt from Moms Across America, the New MDs podcast, and Dr. Stephanie Senov, they tested 20 formulas purchased from various stores, testing each twice. All formulas tested positive for aluminum and lead. Aluminum levels were reportedly 1,000 times higher than the other metals.

Speaker 1 discusses important findings from autism research that families should know when making decisions. The FDA will act on acetaminophen use during pregnancy, with the FDA responding to clinical and laboratory studies that suggest a potential association between acetaminophen used during pregnancy and adverse neurodevelopmental outcomes, including later diagnosis of ADHD and autism. Scientists have proposed biological mechanisms linking prenatal acetaminophen exposure to altered brain development, and the FDA has evaluated contrary studies that show no association. Today, the FDA will issue a physician’s notice about the risk of acetaminophen during pregnancy and begin the process to initiate a safety label change. HHS will launch a nationwide public service campaign to inform families and protect public health. The FDA recognizes that acetaminophen is often the only tool for fevers and pain in pregnancy, as other alternatives have well-documented adverse effects. HHS encourages clinicians to exercise their best judgment and use acetaminophen for fevers and pain in pregnancy by prescribing the lowest effective dose for the shortest necessary duration and only when treatment is required. Thanks to politicization of science, the safety of acetaminophen against the risk of neurodevelopmental disorders in young children has never been validated. Prudent medicine therefore suggests caution with acetaminophen use by young children, given that strong evidence also associates it with liver toxicity. Some studies have found that use of acetaminophen in children can potentially prolong viral illnesses. The FDA will drive new research to safeguard mothers, children, and families. In addition to a possible acetaminophen connection to autism for pregnant women, infants, and toddlers, the research has revealed that folate deficiency in a child’s brain can lead to autism. There are also other confirmation studies. One finding cited is that two studies show children who are circumcised early have double the rate of autism, highly likely because they’re given Tylenol. The speaker notes that none of this is positive, but it is information that should be paid attention to. Speaker 0 comments that there is a tremendous amount of proof or evidence, though he is not a doctor, and that he studied this a long time ago.

Everything regarding vaccine policy will change due to better information. No vaccines given in the first six months of life have been tested, except for the DTP vaccine. According to the Institute of Medicine, the one study done on DTP found a link, but it was thrown out because it was based on the CDC's surveillance system, which they deemed no good. The speaker questions why the CDC lacks a functional surveillance system, especially since vaccines are exempt from prelicensing safety testing. The CDC's system captures fewer than one percent of vaccine injuries, rendering it worthless. The speaker pledges to fix the system and follow the science, including publishing all data sets, replicating studies, and publishing peer reviews, which the CDC has never done. This will provide the public with real answers for the first time.

The speaker states that vaccine policy will change due to better information. They claim that none of the vaccines given in the first six months of life have been tested, except for the DTP vaccine, which a study linked to issues, but was dismissed due to problems with the CDC's surveillance system. The speaker asserts the CDC lacks a functional surveillance system to capture vaccine injuries, with their own study showing it captures less than 1% of injuries. They plan to fix this by implementing a functional surveillance system, using data management, and providing answers to the public. The speaker promises to follow the science, use gold standard science, publish all datasets, replicate studies, and publish peer reviews, which they claim the CDC has never done, to provide real answers.

Florida will end all childhood vaccine mandates, announced by Governor DeSantis and Surgeon General Joseph Ladopo. Question: reaction, and would you recommend the same to your patients? Speaker 1: "I would definitely not have mandates for vaccinations. This is a decision that a physician and a patient should be making together. The parents love their kids more than anybody else. I could love that kid, so why not let the parents play an active role in this? There are some states now where you're seeing an increase in homeschooling because parents are running from the health care system. They can't get health care because doctors are unwilling to take the risk of taking care of children who don't want vaccinations because it might impact, the way their practices are run. They They shouldn't feel pressure from the government to decide what to do with the vaccination schedule. They should do what's the best interest of the person in front of them that sees a child and what those parents desire. That's how the system's supposed to run. But"

Speaker 0 notes a doubling or tripling of baby deaths in the last year, which sparked curiosity. Speaker 1 says their own government told them a medical treatment was safe, and it killed babies. Speaker 2 states they have lost all faith that Health Canada is looking out genuine for the best interests of Canadians. Speaker 1 says doctors made extra money to push vaccines and were given a billing code to do it, and she has pulled all the billing codes. Speaker 3 asserts they’ve purchased the vaccine that hasn’t been approved and distributed it to the provinces, so the second it’s approved they can start jabbing themselves and pregnant mothers with it. Speaker 4 asks why vaccinations were necessary, noting that when going to the hospital for birth, you expect to go home, and then you don’t. Speaker 0 suspects criminal negligence by the government and public health officials. Speaker 2 agrees, saying “Possible.” Speaker 0 contends they pushed a narrative to everybody, including pregnant and breastfeeding women, that the mRNA shots were safe and effective. Speaker 2 recalls wiretapping, harassment, and charges, and that they didn’t allow any expert witnesses to testify. Speaker 1 says Canadian babies died, and police are trying to cover it up by stopping detective Helen Graves from testifying about it. Speaker 3 comments that dominant individuals maintain subordinates’ place through constant aggression. Speaker 5 argues that choosing not to vaccinate is one thing, but being unable to fly or ride trains with vaccinated people and thus putting them at risk is another issue. Speaker 2 says CBC started with a story to implicate her and paint her in an uncomplimentary light to the public. Speaker 6 claims Canada must shift its understanding of CBC, describing it as a state broadcaster pushing the agenda of the Liberal government of Canada. Speaker 3 declares this is the most significant health matter affecting children today, and they are still not investigating. Speaker 2 asserts that everything emanates outward from this case involving law enforcement, the judicial system, the pharmaceutical industry, and health agencies, and how they work together and censored information; all of it ties to this one case, making it dangerous.

Robert F. Kennedy Jr., as HHS secretary, announces decisive steps by the department to defend a fundamental right: a parent’s right to guide their child’s health decisions. He states that this right is non negotiable and will not be ignored under the Trump administration. HHS has launched an investigation into a troubling Midwest incident in which a school administered a federally funded vaccine to a child without the parent’s consent and despite a legally recognized state exemption. He emphasizes that when any institution disregards a religious exemption, it breaks trust, fractures the sacred bond between families and the people entrusted with their child’s care, and that this will not be tolerated. The Health Resources and Services Administration (HRSA) is sending a letter to HRSA-supported health center grant recipients underscoring that federal funding requires compliance with federal and state laws that protect parental rights. Kennedy notes another right every American should know: the right of access to their children’s health records. He references HIPAA as establishing that right of access, and states that if you have legal authority to make decisions for your child, you should have the right to see their records. There will be no delays, no secrets, no excuses. The department is launching compliance reviews of providers and major health care systems to ensure parents have timely access to their children’s information. The Office for Civil Rights has issued a letter reminding healthcare providers of their clear legal duty to give parents access to their children’s medical records. If a provider stands between a parent and their child, HHS will step in. Kennedy makes it clear that schools and healthcare systems cannot sideline parents. If a provider ignores consent, violates an exemption, or keeps parents in the dark, HHS will act quickly and decisively, using every tool available to protect families and restore accountability. The Vaccines for Children program must never become a workaround to bypass parents. The department is reviewing how states and districts process exemptions to ensure the program follows the law, not the other way around. He invites anyone who believes their rights or their child’s rights have been violated to file a complaint with the Office for Civil Rights at hhs.gov/ocr/complaints. Kennedy closes by asserting that parents know their children best, love them the most, and that HHS will defend their voice, authority, and rightful place at the center of their children’s health care decisions. The message ends with thanks and attribution: Produced by the U.S. Department of Health and Human Services.

The speaker states they searched for years for a pre-licensing safety trial of the 72 vaccine doses effectively mandated for American children. They claim that every other medication requires a safety trial comparing health outcomes in a placebo group versus a vaccine group before FDA licensing. The speaker assumed this was also done for vaccines. They state they found out that vaccines were exempt from this requirement.

The Louisiana Department of Health is requested to study the last 10 years of death certificates of infants who died suddenly and without explanation, as defined by statute, and compare this data to the infants' immunization history. This resolution is a strategic move by Health Freedom Louisiana and supporting legislators after failing to mandate vaccine data on death reports. It exemplifies persistence in pursuing alternative approaches to achieve their objectives.

I have instructed NIH, FDA, and CMS to help doctors treat children appropriately. Jay will help tell that story, which started with sound science, the kind that restores faith in government. The announcement, this announcement also represents a historic collaboration between NIH, FDA, CDC, and CMS. We expect this to be the first of many announcements over the coming years that deliver actionable information to parents on underlying cause of autism and the potential paths for prevention and reversal.

The speaker asks a series of yes or no questions regarding the FDA's authority over the safety of baby lotion. The FDA cannot require a safety review before the lotion is sold, nor can they prohibit the use of toxic ingredients like formaldehyde. Manufacturers are not required to register with the FDA before selling their baby lotion. The FDA also cannot require safety information about the lotion once it is on the market, nor can they mandate a recall if the lotion causes bad reactions in babies. Manufacturers are not obligated to report any bad reactions to the FDA.

The speaker states they are "making America healthy again" by banning petroleum-based synthetic food dyes, with the worst two to be banned within two months. They are working with Secretary Rollins on new dietary guidelines to replace the current 453-page guidelines, which they claim are based on "politicized science." The goal is to implement changes in school lunch programs by the next school year. They are also working to remove sodas and candy from the SNAP program, noting that 38% of children are diabetic or pre-diabetic, costing the country a trillion dollars annually. Arizona, West Virginia, Utah, and Indiana have applied for SNAP waivers. Utah was the first state to ban supplemental fluoride, and Florida may follow. They are working to change federal fluoride regulations based on a National Toxicity Program meta-review that found an inverse correlation between fluoride exposure and lowered IQ in children. The speaker says they are revamping GRAS standards to address the 10,000 ingredients in US food, compared to Europe's 400. They are launching Operation Stork Speed to ensure high-quality milk for children and have initiated an autism study, promising definitive answers on autism and other autoimmune diseases within a year.

The speaker asked why the FDA and HHS removed thimerosal from most children's vaccines but left it in a few. They admitted not being vaccine experts and offered to investigate and provide more information later. The speaker expressed interest in sharing the answer with the public.

President Trump asked Speaker 1 to investigate the cause of something. Speaker 1 is approaching the investigation agnostically, looking at everything, and will be transparent in the study designs. The studies will be contracted out to 15 premier research groups from all over the country. They will examine mold, parental age, food and food additives, pesticides, toxic exposures, medicines, and vaccines. Speaker 1 believes they will have preliminary answers in six months, but definitive answers will take about a year after that.

Speaker 0: A child born in a hospital in The United States today, within an hours of coming from source into this body, the first thing that happens to them is pharmaceutical intervention without really asking, barely informed consent. That child's eyes are smeared with erythromycin ointment, and they're given a hepatitis B vaccine in their first day of life. And the hep B vaccine is for hepatitis B, which is a sexually transmitted disease, an IV drug user disease, of course, which babies are not gonna be exposed to, and yet every single baby in America is getting the intervention. So from the literally the day we are born, we're— Speaker 1: I these mean, why not test the pregnant mother for those? Speaker 0: They do. Speaker 1: Okay. Speaker 0: So They give it to the women who even if they have tested negative— Speaker 1: they give majority. Absolutely. So I don't understand why would you treat a child on his first day of life for illnesses you know for a fact he doesn't have, it isn't gonna get? Speaker 2: So a child's born let's just take the sign. The child's born. Hep B is spread by two routes, sexually transmitted disease or intravenous needles. So my one day old isn't going to be having sex or doing heroin right away. So what's the purpose of getting this on the schedule in the first day of life, the first hours of life? Speaker 0: And if you push, and I welcome anyone to do this with their doctor, you get to two things. You get to the American patients are too stupid to remember, so we need to do it right away. That's literally like what they say. And then my doctor told me that that a child at daycare could trip over a needle that has hepatitis B on it. That's literally what they get to. Speaker 2: That a needle could be on the playground that somebody just did heroin or something, threw the needle down, and it has hepatitis B blood on it. I asked the doctor, has there ever been in human history a case of hepatitis B two being transferred that way? They said no. It's only through intravenous needles and sex. So you actually to to just to steel man this, and, again, welcome anyone to respond, there is not actually a scenario absent of intravenous needles or sex, that a person gets hepatitis b. Speaker 0: There is not a reason for this to be given.