The president of a major medical organization made wild claims about the benefits of transgender procedures on kids during a conversation with a Michigan lawmaker before falling back on so-called “experts,” according to video footage <a href="https://www.dailywire.com/episode/ep-2267-trump-protects-the-american-flag-plus-we-break-a-major-story?elementPosition=3&amp;row=2&amp;rowHeadline=Latest+Episodes&amp;rowType=Horizontal+Show+Episodes+Carousel">published</a> by the Ben Shapiro Show on Tuesday. 
During a video call earlier this year, American Medical Association (AMA) President Bobby Mukkamala defended his organization’s support for transgender procedures on kids by saying they relied on what “experts” had told them. Mukkamala also claimed that puberty blockers were reversible and cited other questionable statistics about transgender regret and suicide rates. 
Mukkamala made the comments during a call with Michigan Rep. Brad Paquette and Dr. Eithan Haim, the <a href="https://www.dailywire.com/news/a-doctor-blew-the-whistle-on-his-hospitals-transgender-clinic-now-the-feds-are-trying-to-ruin-his-life">doctor who exposed</a> Texas Children’s Hospital for doing transgender procedures on kids.  When pressed on the American Medical Association’s <a href="https://www.ama-assn.org/press-center/ama-press-releases/ama-states-stop-interfering-health-care-transgender-children">advocacy</a> for transgender procedures on kids, Mukkamala said that the association effectively rubberstamps whatever “the experts” tell them. 
“Neither one of us spent an hour working on transgender care, neither one of us,” Mukkamala told Haim in the footage obtained by Shapiro. “So we have no business discussing the science that&#8217;s brought to the American Medical Association from people that spent years in training for this, and years taking care of patients for this.”
The call was arranged by Paquette, a Republican who represents the southwest corner of Michigan, who was looking to discuss the AMA&#8217;s endorsement of transgender procedures on kids. Paquette supports shielding kids from transgender procedures and introduced a bill in May that would have banned them in Michigan.
The American Medical Association is the largest association of medical professionals in the United States and plays a powerful role in medical education, ethics, and advocacy.
&#8220;This footage is pretty catastrophic for the AMA,&#8221; Shapiro said. &#8220;It proves beyond any doubt that their support for trans &#8216;healthcare&#8217; is based on fake science, willful blindness, and a total abandonment of all evidence-based medicine — all of which are supposed to be antithetical to the existence of their organization, a violation of the Hippocratic Oath.&#8221;
WATCH BEN&#8217;S FULL EPISODE ON AMA: 
<iframe loading="lazy" title="LEAKED FOOTAGE: American Medical Association Exposed" width="500" height="281" src="https://www.youtube.com/embed/J2hsAz7h07U?feature=oembed" frameborder="0" allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share" referrerpolicy="strict-origin-when-cross-origin" allowfullscreen></iframe>
Throughout the call, Haim pressed Mukkamala to provide evidence that transgender procedures don&#8217;t have damaging long-term impacts on kids. When he brought up the flawed studies frequently cited by WPATH and other proponents of transgender procedures, Mukkamala said that he relied on the interpretations of others and didn’t look at them himself.
“I don&#8217;t look at them. I rely on a specialty society to look at them and then give us their opinion of them. I&#8217;m not an expert at all. And honestly, I don&#8217;t think you are either,” he said. “I&#8217;m not an expert at all. I&#8217;m not an expert at all in the science that you&#8217;re talking to me about. I defer to the experts.”
At one point, Mukkamala clearly mocks Haim for even asking questions about the issue.
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<blockquote class="twitter-tweet">
EXCLUSIVE: Secretly recorded call with American Medical Association President, Dr. Bobby Mukkamala, reveals an alarming abdication of responsibility on &#8220;gender-affirming care&#8221; at the highest level of medicine.
Confronted with &#8216;puberty blocker&#8217; side effects, Dr. Bobby evades: <a href="https://t.co/PCqHqNpjts">pic.twitter.com/PCqHqNpjts</a>
— Ben Shapiro (@benshapiro) <a href="https://twitter.com/benshapiro/status/1960403515999690972?ref_src=twsrc%5Etfw">August 26, 2025</a></blockquote>
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Commenting on Mukkamala&#8217;s repeated claims that he was not an expert,  Shapiro said that he should at least be aware of the ethical issues surrounding transgender medicine.
&#8220;And sure, he’s not an expert in endocrinology or plastic surgery,&#8221; Shapiro said. &#8220;But as the President of the AMA, he’s meant to be an expert in the AMA’s code of ethics, and at the bare minimum, the Hippocratic Oath.&#8221;
Mukkamala also claimed during the call that puberty blockers were reversible. Studies have shown that puberty blockers can cause permanent damage to fertility and loss of bone density, especially in the hips and spine. 
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3/ CLAIM: The AMA’s Dr. Bobby asserts that so-called “puberty blockers” are “reversible,” dismissing Dr. Haim’s attempts to correct him—despite Dr. Haim having worked with patients who need puberty blockers for actual endocrine disorders and being well versed in their harms. <a href="https://t.co/nHYvgnBiQr">pic.twitter.com/nHYvgnBiQr</a>
— Ben Shapiro (@benshapiro) <a href="https://twitter.com/benshapiro/status/1960403521141887136?ref_src=twsrc%5Etfw">August 26, 2025</a></blockquote>
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He also suggested that between 50-70% of transgender individuals commit suicide and that only 2% of those who have medical transgender procedures regret those procedures. Both numbers are suspect, as even the most extreme studies only say that up to 40% of transgender identifying people have attempted suicide. 
&nbsp;
<blockquote class="twitter-tweet" data-media-max-width="560">
5/ CLAIM: Dr. Bobby insists there is only a 2% regret rate among those who medically ‘transition,’ and cites his source as the doctors who perform the transing of the kids. An unbiased group if ever there was one… <a href="https://t.co/kLDFzHAByd">pic.twitter.com/kLDFzHAByd</a>
— Ben Shapiro (@benshapiro) <a href="https://twitter.com/benshapiro/status/1960403528066707955?ref_src=twsrc%5Etfw">August 26, 2025</a></blockquote>
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The 2% regret rate comes from a <a href="https://pubmed.ncbi.nlm.nih.gov/33968550/">study</a> that only measured after surgery, not the tens of thousands of kids who have been placed on puberty blockers or cross-sex hormones. It also did not measure regret past two years after the initial surgery. 
After Paquette told Mukkamala that he was upset by what he was hearing about kids being pushed to transition, he said that “the way to not be distraught is to talk to experts.”
Mukkamala also appeared to claim that sex change surgeries were not happening on kids in Michigan. This conflicts with data <a href="https://stoptheharmdatabase.com/state/michigan/">compiled</a> by Do No Harm that shows that there have been at least 186 kids who have undergone a transgender surgery in Michigan. 
The American Medical Association has been a staunch defender of transgender procedures on kids for years. In April 2021, the organization sent a <a href="https://www.ama-assn.org/press-center/ama-press-releases/ama-states-stop-interfering-health-care-transgender-children">letter</a> to governors across the country urging them not to protect kids from transgender procedures. 
“Empirical evidence has demonstrated that trans and non-binary gender identities are normal variations of human identity and expression,” the organization wrote. “It is imperative that transgender minors be given the opportunity to explore their gender identity under the safe and supportive care of a physician.”
Then, in a 2022 speech, then-American Medical Association President Jack Resneck Jr. claimed that opposition to transgender procedures on kids was driven by “misinformation.” 
“Drivers of disinformation say that gender-affirming care clinics are performing genital mutilation surgeries on teens, not involving families in care decisions, or using medical treatments on young children who show up after wondering for one day if they are trans,” he said.
Advocates of radical gender ideology will frequently cite organizations like the American Medical Association for reasons why the procedures should remain legal. Over two dozen states have acted in the last few years to ban transgender surgeries on minors.
WATCH THE FULL CONVERSATION:
<iframe loading="lazy" title="The AMA’s Dr. Bobby Mukkamala on “Gender Affirming Care”" width="500" height="281" src="https://www.youtube.com/embed/Mxb1qG-yvzY?start=4&#038;feature=oembed" frameborder="0" allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture; web-share" referrerpolicy="strict-origin-when-cross-origin" allowfullscreen></iframe>

MixCollage-26-Aug-2025-02-06-PM-282

Leaked Footage Exposes Top Med Org’s Support For Trans Procedures On Kids: ‘I’m Not An Expert At All’

American Medical Association

Ben Shapiro

Medical Research

Michigan

The Ben Shapiro Show

Transgender

transgender surgery

In another example of Israeli scientists changing the world for the better, experts at Tel Aviv University (TAU) are preparing to perform the world’s first spinal cord implant.
Unlike most other bodily injuries, spinal cord injuries do not allow for cell regeneration. But the TAU scientists took blood cells and reprogrammed them through genetic engineering so they acted like embryonic stem cells. They took the cells and inserted them into a gel formed from collagen and sugars derived from fat tissue to “mimic the embryonic development of the spinal cord,” Prof. Tal Dvir, of TAU’s Sagol Center for Regenerative Biotechnology, head of the Nanotechnology Center, and Chief Scientist of the biotech company Matricelf, <a href="https://english.tau.ac.il/research/engineered-spinal-cord">explained</a>.
He continued:
<blockquote>
The spinal cord is made up of nerve cells that transmit electrical signals from the brain to every part of the body. When the spinal cord is torn due to trauma — from a car accident, a fall, or a battlefield injury — this chain is broken. Think of it like an electrical cable that’s been cut: if the two parts don’t touch, the electrical signal can’t pass. The cable won’t carry electricity, and in the same way, the person can’t transmit the signal beyond the site of the injury.
Neurons are cells that do not divide and do not renew themselves. They are not like skin cells, which can repair themselves after injury. They are more similar to heart cells: once damage occurs, the body cannot restore them.
</blockquote>
“At the end of the process, we don’t just turn the cells into motor neurons — because cells alone won’t help us — but into three-dimensional tissue: neuronal networks of the spinal cord,” he said. “After about a month, we obtain a 3D implant with many neurons that transmit electrical signals. These 3D tissues are then implanted into the damaged area.”
<a href="https://get.dailywire.com/subscribe/plus/?utm_campaign=summer&amp;utm_content=editorialsummersale&amp;utm_medium=website&amp;utm_source=editorial" target="_blank" rel="noopener">End of Summer Sale – Get 40% off New DailyWire+ Annual Memberships</a>
“About six months ago we received preliminary approval to begin compassionate-use trials with eight patients,” Dvir recalled. “We decided, of course, that the first patient would be Israeli. This is undoubtedly a matter of national pride. The technology was developed here in Israel, at Tel Aviv University and at Matricelf, and from the very beginning it was clear to us that the first-ever surgery would be performed in Israel, with an Israeli patient.”
The first implant should happen within a year. “Once we prove that the treatment works — everything is open, and we’ll be able to treat any injury,” says Prof. Dvir.
“Our goal is to help paralyzed patients rise from their wheelchairs. The animal model trials showed extraordinary success, and we are hopeful that the results in humans will be just as promising,” Dvir <a href="https://www.jpost.com/israel-news/article-864808">concluded</a>.
The list of Israel’s contributions to medicine is a strong reminder of the cutting-edge nature of Israeli science. Here are some noteworthy examples:
<blockquote>
Copaxone, a drug for multiple sclerosis developed by Teva Pharmaceuticals.
Rasagiline (Azilect): developed at Israel’s Technion to treat Parkinson&#8217;s disease.
Doxil: The first FDA-approved nanotechnology-based cancer drug, developed at the Hebrew University. It delivers chemotherapy directly to cancer cells.
Exelon: A medication for Alzheimer&#8217;s disease.
PillCam (Given Imaging) – A swallowable capsule camera that takes images of the digestive tract, revolutionizing endoscopy.
BrainsGate – A device that uses electrical stimulation to enhance drug delivery to the brain, helping stroke patients.
IceSense3 (IceCure Medical) – A cryoablation device used to freeze and destroy tumors, particularly in breast cancer treatment.
ElMindA – a brain-mapping system using EEG and machine learning to diagnose brain-related conditions (e.g., ADHD, concussion).
MeMed – a diagnostic platform that distinguishes between viral and bacterial infections within minutes, helping reduce antibiotic misuse.
V-Wave – A heart failure treatment device that regulates pressure inside the heart.
</blockquote>

Inflamed spine, illustration

Hope For Paraplegics As Israel Plans First Spinal Cord Implant

Health

Israel

medicine

Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. announced on Tuesday that his department is canceling 22 mRNA vaccine development contracts, totaling about $500 million.
Kennedy said mRNA vaccines, including the most widely used COVID-19 immunizations, have been ineffective, so his department is instead shifting this funding toward &#8220;safer, broader vaccine platforms that remain effective even as viruses mutate.”
&#8220;After reviewing the science, and consulting top experts at [National Institutes of Health] and [Food and Drug Administration], HHS has determined that mRNA technology poses more risks than benefits for these respiratory viruses,&#8221; RFK said in a video posted to X.
Kennedy said that mRNA vaccines used during the pandemic &#8220;only code for a small part of the viral protein, usually a single antigen.&#8221;
&#8220;One mutation, and the vaccine becomes ineffective,&#8221; he said. &#8220;This dynamic drives a phenomenon called antigenic shift, meaning that the vaccine paradoxically encourages new mutations and can actually prolong pandemics as the virus constantly mutates to escape the protective effects of the vaccine.&#8221;
Millions of people, RFK noted, caught the Omicron variant, despite being vaccinated. This is due to the nature of the mRNA vaccines. &#8220;A single mutation can make mRNA vaccines ineffective,&#8221; the secretary emphasized.
“Let me be absolutely clear: HHS supports safe, effective vaccines for every American who wants them,&#8221; Kennedy told the public. &#8220;That’s why we’re moving beyond the limitations of mRNA for respiratory viruses and investing in better solutions.&#8221;
Biomedical Advanced Research and Development Authority (BARDA), an HHS agency, is terminating 22 mRNA vaccine development investments &#8220;because the data show these vaccines fail to protect effectively against upper respiratory infections like COVID and flu,&#8221; a press release from HHS reiterates.
<blockquote class="twitter-tweet">
We reviewed the science, listened to the experts, and acted. BARDA is terminating 22 mRNA vaccine development investments because the data show these vaccines fail to protect effectively against upper respiratory infections like COVID and flu. We’re shifting that funding toward… <a href="https://t.co/GPKbuU7ywN">pic.twitter.com/GPKbuU7ywN</a>
— Secretary Kennedy (@SecKennedy) <a href="https://twitter.com/SecKennedy/status/1952851097019633766?ref_src=twsrc%5Etfw">August 5, 2025</a></blockquote>
BARDA will now focus on &#8220;platforms with stronger safety records and transparent clinical and manufacturing data practices,&#8221; HHS said. &#8220;Technologies that were funded during the emergency phase but failed to meet current scientific standards will be phased out in favor of evidence-based, ethically grounded solutions – like whole-virus vaccines and novel platforms.&#8221;
Related: <a href="https://www.dailywire.com/news/more-maha-wins-12-states-cutting-soda-candy-from-food-stamps?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=0&amp;row=0&amp;rowType=Vertical+List&amp;title=More+MAHA+Wins%3A+12+States+Cutting+Soda%2C+Candy+From+Food+Stamps">More MAHA Wins: 12 States Cutting Soda, Candy From Food Stamps</a>

RFK Jr

RFK Jr. Shuts Down $500M In mRNA Vaccine Research: ‘More Risks Than Benefits’

Robert F. Kennedy Jr.

vaccine

Vaccines

A pre-born life frozen since 1994 has finally been welcomed into the world, in what is believed to be the oldest embryo ever brought to birth.
Tim and Lindsey Pierce utilized embryo adoption to grow their family, per the <a href="https://apnews.com/article/baby-embryo-30-year-birth-ohio-129926d4456dcba4781f155898aca7d8">Associated Press</a>. The Ohio-based couple is part of a small movement of people who focus on frozen embryos currently suspended in time.
For many Christians who believe life begins at conception, it is unthinkable to “dispose of” these fully unique human persons even at their very early stages of development. But embryo adoption remains an underutilized option, especially considering estimates that more than 1.5 million frozen embryos are currently being stored in the United States today.
The Pierces adopted the frozen embryo from Linda Archerd, 62. 
She said she had four frozen embryos after undergoing an IVF procedure more than 30 years ago and gave birth to one daughter. But then she and her husband divorced, stalling her plans to expand her family further. Still, Archerd thought about her embryos and believed they deserved a chance at life, too.
“I felt all along that these three little hopes, these little embryos, deserved to live just like my daughter did,” Archerd told AP.
She found the Pierces through an embryo adoption agency. One embryo did not survive the thaw, Archerd told the outlet. Two embryos were transferred, but only one implanted, resulting in the live birth of one little boy on Saturday.
The biological mother of the donated embryos said she looks forward to meeting her son, named Thaddeus Daniel Pierce, which was one of the stipulations she put forth for the adoption.
Archerd said she already sees the family resemblance. “The first thing that I noticed when Lindsey sent me his pictures is how much he looks like my daughter when she was a baby,” Archerd said. “I pulled out my baby book and compared them side by side and there is no doubt that they are siblings.”
“I’d love to meet them some day,” she said. “That would be a dream come true to meet — meet them and the baby.”
Lindsey Pierce told <a href="https://www.technologyreview.com/2025/07/29/1120769/exclusive-record-breaking-baby-born-embryo-over-30-years-old/#:~:text=The%20embryos%20were%20created%20in,Christian%20%E2%80%9Cembryo%20adoption%E2%80%9D%20agency.&amp;text=A%20baby%20boy%20born%20over,for%20the%20%E2%80%9Coldest%20baby.%E2%80%9D">MIT Technology Review</a> that she and her family are doing fine. “We had a rough birth but we are both doing well now,” the new mom told the outlet. “He is so chill. We are in awe that we have this precious baby!”
“The baby has a 30-year-old sister,” she said. The outlet also noted that she and her husband, Tim, who are 34 and 35 respectively, were only toddlers when their future son was conceived.
“We thought it was wild,” Lindsey said. “We didn’t know they froze embryos that long ago.”
“We didn’t go into it thinking we would break any records. We just wanted to have a baby,” she added, noting how her family thinks the whole thing is “like something from a sci-fi movie.”

Three Decades Later, Life Begins: Ohio Baby Boy Born From 1994 Frozen Embryo

Ohio Baby Conceived, Frozen In 1994 Becomes 'Oldest' Embryo Ever Born

Adoption

babies

Ohio

Pro-Life Movement

Science

Scientists at the University of Florida in Gainesville are developing a universal cancer vaccine designed to target cancer cells already forming in the body. The vaccine could be especially effective against some of the deadliest cancers, including pancreatic and ovarian cancer.
The problem in the past has been that because cancers tend to be specific to each person, a cancer vaccine would have to be tailored for that specific individual rather than a one-size-fits-all vaccine, and in the time spent to create a personal vaccine, the cancer could mutate.
“It can be months from the time you get a patient&#8217;s specimen to when they actually have a personalized therapy,” study senior author and pediatric oncologist Dr. Elias Sayour said, as Live Science <a href="https://www.livescience.com/health/cancer/universal-cancer-vaccine-heading-to-human-trials-could-be-useful-for-all-forms-of-cancer">reports</a>. “The idea that something could be available immediately, albeit in a nonspecific way … could be revolutionary for how we bridge therapy and how we manage patients.”
The experimental vaccine was discussed in the journal <a style="font-style: inherit; font-weight: inherit;" href="https://go.redirectingat.com/?id=92X1590019&amp;xcust=livescience_us_1632594187414033690&amp;xs=1&amp;url=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41551-025-01380-1&amp;sref=https%3A%2F%2Fwww.livescience.com%2Fhealth%2Fcancer%2Funiversal-cancer-vaccine-heading-to-human-trials-could-be-useful-for-all-forms-of-cancer" data-analytics-id="inline-link" data-url="https://www.nature.com/articles/s41551-025-01380-1" data-hl-processed="skimlinks" data-placeholder-url="https://go.redirectingat.com/?id=92X1590019&amp;xcust=hawk-custom-tracking&amp;xs=1&amp;url=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41551-025-01380-1&amp;sref=https%3A%2F%2Fwww.livescience.com%2Fhealth%2Fcancer%2Funiversal-cancer-vaccine-heading-to-human-trials-could-be-useful-for-all-forms-of-cancer" data-google-interstitial="false" data-merchant-name="nature.com" data-merchant-network="SkimLinks" data-mrf-recirculation="[Livescience] Article - Inline Link" data-mrf-link="https://go.redirectingat.com/?id=92X1590019&amp;xcust=livescience_us_4664427368791827916&amp;xs=1&amp;url=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41551-025-01380-1&amp;sref=https%3A%2F%2Fwww.livescience.com%2Fhealth%2Fcancer%2Funiversal-cancer-vaccine-heading-to-human-trials-could-be-useful-for-all-forms-of-cancer" data-custom-tracking-id="1632594187414033690" data-hawk-tracked="hawklinks" data-label="Nature Biomedical Engineering">Nature Biomedical Engineering</a>; the abstract stated, “Our findings show that the resistance of tumors to immunotherapy is dictated by the absence of a damage response, which can be restored by boosting early type-I interferon responses to enable epitope spreading and self-amplifying responses in treatment-refractory tumors.”
The experimental vaccine is built on mRNA that triggers cells to produce new proteins, and hopes to strengthen the body to create more type-I interferons, which can locate cancerous tumors.
Sayour explained that cancer can impede interferon signals and block anti-cancer immune responses, so the experimental vaccine could catalyze an immune “reset.”
“I personally think this can be used for all forms of cancer,” Sayour stated. “I believe this is a universal paradigm that can be used to treat cancer,” adding that the vaccine could stop a relapse of the cancer after remission.
“This exciting and novel paper shows promising evidence that giving the immune system a short, targeted boost at just the right time can help previously unresponsive tumors respond to immunotherapy,&#8221; Diana Azzam, from the Center for Advancing Personalized Cancer Treatments at Florida International University, said. “This approach could be especially helpful for ‘cold’ tumors — types of cancer that usually don&#8217;t trigger a strong immune response, like pancreatic, ovarian, and some types of breast cancer.”
“Sayour and his colleagues have <a style="font-style: inherit; font-weight: inherit;" href="https://clinicaltrials.gov/study/NCT05660408" data-analytics-id="inline-link" data-url="https://clinicaltrials.gov/study/NCT05660408" data-hl-processed="none" data-mrf-recirculation="[Livescience] Article - Inline Link" data-mrf-link="https://clinicaltrials.gov/study/NCT05660408" data-custom-tracking-id="3743527965317849267" data-hawk-tracked="hawklinks" data-google-interstitial="false" data-label="launched a human trial testing a two-hit approach">launched a human trial testing a two-hit approach</a>: an off-the-shelf cancer vaccine followed by a personalized one,” Live Science noted. “This approach saves valuable time needed for personalized vaccinations and may induce rapid immunity that can be further seized upon by personalized therapy,&#8221; Sayour asserted.

Gainesville, University of Florida, campus entrance with students

Breakthrough Cancer Vaccine In The Works At University of Florida

Cancer

Florida

University of Florida

A child born in Iowa is celebrating his first birthday and was declared the youngest premature baby ever by Guinness World Records. 
Nash Keen weighed just 10 ounces, about the same as a bar of soap, when he entered the world at 21 weeks of gestation on July 5, 2024. The formerly tiny newborn, nicknamed “Nash Potato,” is now thriving and hitting milestones after spending six months in the neonatal intensive care unit (NICU) at the University of Iowa Health Care Stead Family Children’s Hospital, per the <a href="https://apnews.com/article/premature-birth-guinness-world-record-22d4092b92af131a3efeea96aeb120e3">Associated Press</a>. 
“Nash is so full of personality,” his mom Mollie Keen told the outlet. “He’s a happy baby.” 
“Being in the NICU as long as he was, you’d think that he would be, you know, more fragile and stuff,” she added. “And he’s not. He’s a very determined, curious little boy, and he’s just all smiles all the time.”
Upon reaching his first birthday, Guinness World Records declared Nash the world’s most premature baby, beating out the organization’s previous record holder, born in 2020 in Alabama, by a single day.
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Guinness World Records named Nash the world’s most premature baby after he reached his first birthday. The previous record holder was born in Alabama and was older than Nash by just one day. 
These incredible stories help to turn the pro-abortion argument for “personhood” being linked to viability on its head as increasingly younger premature babies are able not just to survive, but to thrive, even when they are born very early. This is thanks to advancing technology and a commitment to delivering exceptional medical care to fragile newborns.
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Mollie reportedly said that she had a previous miscarriage and was concerned she would also lose Nash when she went into preterm labor. However, she and her husband, Randall, discovered that the University of Iowa Health Care Stead Family Children’s Hospital was capable of caring for extremely premature babies.
“One of the things I noticed about the medical team is that they were very calm,” she told AP of the staff there. “You never really saw them, like, get anxious or anything. And so we kind of just learned to, like, watch them. If the doctors and the nurses weren’t freaking out, there was no reason for us to freak out.”
“We wanted to give Nash a chance,” Molly told Guinness World Records during an interview.
Despite being born so early and therefore being at risk for a slew of medical complications, Nash is developing in what his doctor says is the best outcome possible for him.
Although he is still on oxygen and using a feeding tube, his parents plan to introduce solid food soon. He is rolling over, and they hope he’ll crawl soon, too. 
“He’s truly the best thing to ever happen to us,” Mollie said.
The Guttmacher Institute, a pro-abortion organization, “<a href="https://www.guttmacher.org/node/26263/printable/print">updated</a>” its definition of viability in August 2022, stating, “A fetus generally reaches viability between 24 and 28 weeks LMP (gestational age).”
This definition is out of date, considering the increasing number of cases like Nash’s, where very premature newborns survive and thrive. These kinds of cases prove that viability is not a fixed gestational point in time, and more broadly, does not determine the humanity of an unborn baby.

NICU

Most Premature Baby Ever Celebrates First Birthday, Declared Guinness World Record Holder

Abortion

baby

Iowa

Medical

Pregnancy

FDA Commissioner Marty Makary has committed to reviewing the abortion pill&#8217;s safety, according to Sen. Josh Hawley (R-MO).
Hawley posted a letter he received from Makary on social media, noting the FDA head promised to review the safety of mifepristone, the popular abortion drug.
&#8220;As the Commissioner of Food and Drugs, I am committed to conducting a review of mifepristone and working with the professional career scientists at the Agency who review this data,&#8221; Makary wrote in his letter to Hawley.
<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
FDA chief Marty Makary just committed to me to do a full review of the chemical abortion drug’s safety: “As Commissioner of Food and Drugs, I am committed to conducting a review of mifepristone” 👇 <a href="https://t.co/nMxUhE18UA">pic.twitter.com/nMxUhE18UA</a>
&mdash; Josh Hawley (@HawleyMO) <a href="https://twitter.com/HawleyMO/status/1929696353010987013?ref_src=twsrc%5Etfw">June 3, 2025</a></blockquote>
<script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script>
&#8220;As with all drugs, FDA continues to closely monitor the postmarketing safety data on mifepristone for the medical termination of early pregnancy,&#8221; Makary wrote.
Makary also noted that mifepristone is currently enmeshed in legal battles.
&#8220;FDA generally does not comment on matters that are the subject of pending litigation and therefore is unable to provide further information on this topic at this time,&#8221; the FDA chief said.
&#8220;FDA is committed to safeguarding public health by ensuring the safety, efficacy, and quality of the products it regulates,&#8221; Makary wrote. &#8220;The Agency carefully evaluates the scientific data, leveraging rigorous science to make informed decisions.&#8221;
The two-pill chemical abortion regimen — mifepristone, usually followed by misoprostol — aims to end the life of the unborn baby and expel it from the woman’s uterus. However, the drugs sometimes fail to expel all the fetal tissue, which can cause life-threatening complications.
An <a href="https://www.dailywire.com/news/abortion-pill-22-times-more-dangerous-than-fda-claimed-new-study-says?author=Mairead+Elordi&amp;category=News&amp;elementPosition=7&amp;row=0&amp;rowType=Vertical+List&amp;title=Abortion+Pill+22+Times+More+Dangerous+Than+FDA+Claimed%2C+New+Study+Says" target="_blank" rel="noopener">analysis</a> released in April found that more than one in 10 women experienced a “serious adverse event” after taking the mifepristone abortion pill in 2023. This can include hemorrhaging, needing a blood transfusion, an emergency room visit, and even deadly conditions like sepsis.
That is about 22 times higher than what the FDA listed on its label for the brand Mifeprex in 2023. The FDA <a href="https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/020687Orig1s025Lbl.pdf" target="_blank" rel="noopener">cited</a> clinical studies saying less than 0.5% of women suffered “serious adverse reactions” to mifepristone.
Meanwhile, more than one in 20 women need a second abortion attempt after the abortion pill fails, another analysis of insurance claim data <a href="https://www.dailywire.com/news/more-than-1-in-20-women-need-second-abortion-attempt-after-abortion-pill-fails?author=Mairead+Elordi&amp;category=News&amp;elementPosition=0&amp;row=0&amp;rowType=Vertical+List&amp;title=More+Than+1+in+20+Women+Need+Second+Abortion+Attempt+After+Abortion+Pill+Fails" target="_blank" rel="noopener">released</a> this week showed.
Last month, Robert F. Kennedy Jr., head of the Department of Health and Human Services, told lawmakers he had requested the FDA do a “complete review” of the abortion pill in the wake of the new data.
“It’s alarming,” RFK Jr. told Hawley during a Senate committee hearing.
“Clearly, it indicates that at the very least the label should be changed,” he said. “I’ve asked Marty Makary, who’s the director of the FDA, to do a complete review and to report back.”
A few months before Roe v. Wade was overturned, the FDA scrapped the requirement that women must obtain abortion pills in person from a healthcare provider, allowing them to get them online through the mail.

President Trump Signs Executive Orders At The White House

FDA Chief Commits To Full Review Of Abortion Pill

Abortion Drug

Josh Hawley

Pro-Abortion

On the latest episode of “Michael &amp; …” Daily Wire host Michael Knowles sits down with Dr. Andrew Wakefield, a highly-controversial figure who has called for more research into the safety of vaccinations, especially the Measle, Mumps, and Rubella (MMR) vaccination, which is typically given to children around 12-15 months of age.
Wakefield has been stripped of his medical license and accused of being a fraudster, allegedly falsely claiming in a 1998 study that the MMR vaccine causes autism in children and sparking a dangerous anti-vaccine movement.
WATCH: 
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<a href="https://www.dailywire.com/episode/andy-wakefield-member-exclusive?elementPosition=0&amp;row=0&amp;rowType=Vertical+Show+Episodes+Carousel">Speaking to Knowles</a>, however, Wakefield said that study, which focused on children whose parents thought their child was vaccine-injured, never made such a claim.
“This was a case series just reporting what the parents had told us, what the doctors had told us, who referred them, and what we found on the clinical investigation,” Wakefield says. “We could not leave out the parents&#8217; reference to the MMR [vaccine]. But we said at the conclusion of the study, this study does not prove an association, let alone a causal association with the MMR vaccine.”
“So hold on, hold on,” Knowles interjects. “This is the part that&#8217;s the craziest in the story to me.”
“You are blamed for creating vaccine skepticism. You are blamed for measles outbreaks. You are blamed and called a terrible fraudster and a horrible practitioner of medicine because you said in your 1998 study that the MMR vaccine causes autism. Except you didn&#8217;t say that?”
“Quite the opposite,” Wakefield says. “And we said what we do need is further research into this matter. And that was it. And, the study was really a report of bowel disease [symptoms] in combination with this regressive developmental disorder.”
Knowles then asks Wakefield if he believes the MMR vaccine causes autism.
“Does this vaccine cause autism? Are you willing to say, ‘Yes, it does?&#8217;” Knowles asks. “Or do you say, ‘Look, I just think this should be investigated, as I said in my 1998 study.’ And how concerned should parents be?”
“I wouldn&#8217;t change my position,” Wakefield says. “In my personal belief, there is a very strong indication that it causes autism. But that&#8217;s not good enough. You don&#8217;t make public policy based on Andy Wakefield&#8217;s belief — it needs the science that we advocated for all those years ago.”
During the discussion, Wakefield says he never retracted his study, and disputes the media’s claim that his colleagues did.
“Nine of my colleagues were persuaded to sign the retraction of an interpretation — the interpretation being that the MMR vaccine causes autism,” Wakefield says. “I said, we never made that claim. How can you retract something that doesn&#8217;t exist?”
“You know, they were under pressure,” he says of his colleagues. “I don&#8217;t judge them, but they fell in line and did that.”
Wakefield and two other colleagues “just refused to do that,” he says. “It was a retraction of an interpretation that was never made. And that&#8217;s the truth behind it.”
Knowles also asks Wakefield about a number of accusations made against him.
“So they accused you of misconduct in the methods of the study,” Knowles said. “They accused you of taking money from other interests — they had this whole litany of accusations in the popular media. Was there any truth to the allegations?”
“The lawyers had come to me at some point during this, the conduct of this work, not the research, not the Lancet paper, and I had agreed,” Wakefield says. “This is very common practice to undertake a study to determine whether there was a link between the vaccine.”
“People work for both defendants and for plaintiffs in medical litigation,” he continues. “But I was singled out as, ‘Oh, Wakefield was doing this to undermine the MMR vaccine and launch his own vaccine onto the market and make a fortune.’”
Wakefield says he disclosed that he was working on behalf of these children in litigation, as was proper protocol, despite accusations that he did not.
“It&#8217;s totally transparent, but the allegation was that it was a cover-up, that…was all a big secret,” he says. “No, it wasn&#8217;t…but what do you do about that when you don&#8217;t control the editorial you write?”
During the lengthy discussion, Wakefield also gives his thoughts on separating out the MMR vaccine, delaying the shot on the vaccination schedule, his film “Vaxxed: From Cover-Up to Catastrophe,” his ties to HHS Secretary Robert F. Kennedy Jr., and much more.

MK&-Show-2 (2)

Knowles Sits Down With Andy Wakefield, Former Doctor Pinned As Man Who Sparked ‘Anti-Vaxx’ Movement 

COVID-19 Vaccine

Measles

Michael Knowles

Robert F. Kennedy Jr., head of the Department of Health and Human Services, told lawmakers on Wednesday that he has requested the Food and Drug Administration (FDA) do a &#8220;complete review&#8221; of the abortion pill.
The announcement was welcomed by pro-life conservatives, who previously wondered how RFK Jr., a former Democrat, would respond to abortion-related issues, having previously said that while he believes every abortion is a “tragedy,” the issue is “more nuanced and complex.”
During Wednesday&#8217;s Senate committee hearing, Senator Josh Hawley (R-MO) asked RFK Jr. if he was aware of a new analysis from the Ethics &amp; Public Policy Center indicating that mifepristone is many times more dangerous than the FDA says on the label for the abortion pill, and he said he was.
&#8220;It&#8217;s alarming,&#8221; RFK Jr. told Hawley.
&#8220;Clearly, it indicates that at the very least the label should be changed,&#8221; he said. &#8220;I&#8217;ve asked Marty Makary, who&#8217;s the director of the FDA, to do a complete review and to report back.&#8221;
RFK Jr. also said that he did not yet have a sense of the timeline of the review.
<blockquote class="twitter-tweet" data-width="500" data-dnt="true">
RFK Jr. says he has asked FDA to do a thorough review of mifepristone in light of a study indicating serious side effects could be 22x more common than the FDA says <a href="https://t.co/kHLNGqsdeA">pic.twitter.com/kHLNGqsdeA</a>
&mdash; Emily Kopp (@emilyakopp) <a href="https://twitter.com/emilyakopp/status/1922739876417445997?ref_src=twsrc%5Etfw">May 14, 2025</a></blockquote>
<script async src="https://platform.twitter.com/widgets.js" charset="utf-8"></script>
An <a href="https://www.dailywire.com/news/abortion-pill-22-times-more-dangerous-than-fda-claimed-new-study-says?author=Mairead+Elordi&amp;category=News&amp;elementPosition=7&amp;row=0&amp;rowType=Vertical+List&amp;title=Abortion+Pill+22+Times+More+Dangerous+Than+FDA+Claimed%2C+New+Study+Says" target="_blank" rel="noopener">analysis</a> released last month found that more than one in 10 women experienced a “serious adverse event” after taking the mifepristone abortion pill in 2023. This can include hemorrhaging, needing a blood transfusion, an emergency room visit, and even deadly conditions like sepsis.
That is about 22 times higher than what the FDA listed on its label for the brand Mifeprex in 2023. The FDA <a href="https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/020687Orig1s025Lbl.pdf" target="_blank" rel="noopener">cited</a> clinical studies saying less than 0.5% of women suffered “serious adverse reactions” to mifepristone.
Meanwhile, more than one in 20 women need a second abortion attempt after the abortion pill fails, another analysis of insurance claim data <a href="https://www.dailywire.com/news/more-than-1-in-20-women-need-second-abortion-attempt-after-abortion-pill-fails?author=Mairead+Elordi&amp;category=News&amp;elementPosition=0&amp;row=0&amp;rowType=Vertical+List&amp;title=More+Than+1+in+20+Women+Need+Second+Abortion+Attempt+After+Abortion+Pill+Fails" target="_blank" rel="noopener">released</a> this week showed.
&#8220;We&#8217;re very thankful for this announcement from Secretary Kennedy. We encourage the FDA to conduct its own study to best ensure that women are given an honest and clear presentation of the dangers of the abortion pill,&#8221; Ryan Anderson, President of the Ethics and Public Policy Center and one of the authors of the analysis told The Daily Wire.
The two-pill chemical abortion regimen — mifepristone, usually followed by misoprostol — aims to end the life of the unborn baby and expel it from the woman’s uterus. However, the drugs sometimes fail to expel all the fetal tissue, which can cause life-threatening complications.
A few months before Roe v. Wade was overturned, the FDA scrapped the requirement that women must obtain abortion pills in person from a healthcare provider, allowing them to get them online through the mail.
“We applaud Robert F. Kennedy Jr. for his swift directive to FDA for a thorough study of the dangerous chemical abortion pill,” Doug Truax, founder of Foundation for the Restoration of America, which put out another report on the abortion pill&#8217;s &#8220;serious adverse events&#8221; told The Daily Wire.
“The health and safety of women is at risk and we can’t allow ideology to trump science,” Truax said.
Last year, Daily Wire Editor Emeritus Ben Shapiro <a href="https://www.dailywire.com/news/ben-shapiro-challenges-rfk-jr-on-abortion" target="_blank" rel="noopener">challenged</a> Kennedy Jr. on abortion during an interview, telling him that abortion is “not just a tragedy. It’s a crime against the child because the child has an independent interest. What do you say to that?”
“I say that I understand that position, and I don’t agree with it,” Kennedy responded, adding that he believes “the solution of having the state come in and dictate choices that a woman is making is not a good solution.”
RFK Jr. appeared before both Senate and House committees on Wednesday to defend President Donald Trump&#8217;s proposed budget cuts to the HHS, which RFK Jr. <a href="https://www.nytimes.com/2025/05/14/us/politics/rfk-jr-hhs-overhaul-hearing.html" target="_blank" rel="noopener">said</a> would be &#8220;painful&#8221; but would save money “without impacting critical services.”

HHS Secretary RFK Jr. Testifies On Budget During House And Senate Hearings On Wednesday

RFK Jr. Wants ‘Complete Review’ Of Abortion Pill, Says Prescription Label Downplays Risks

RFK Says He Has Asked FDA For 'Complete Review' Of Abortion Pill After Data On Dangers

Department of Health and Human Services

Health and Human Services

Health Care

A new study of ultraweak photon emission, the process in which organisms exhibit a spontaneous emission of light without an external excitation, used a technology to demonstrate that the glow from that process ends upon death, a technology that may be <a href="https://www.newscientist.com/article/2479590-all-living-things-emit-an-eerie-glow-that-is-snuffed-out-upon-death/">used in the future</a> to aid in the detection of human disease.
University of Calgary Professor Dan Oblak and his colleagues studied rats using digital cameras while the temperature remained steady and light was excluded.
“The fact that ultraweak photon emission is a real thing is undeniable at this point,” Oblak stated. “This really shows that this is not just an imperfection or caused by other biological processes. It’s really something that comes from all living things.”
A 2024 <a href="https://westminsterresearch.westminster.ac.uk/download/f35a0e7ae5d24dc4263db3032e8abe8f41ae87a1c852d83a8a8f13f0fa44c4ce/2292116/fphys-15-1348915.pdf">study</a> from Great Britain of ultraweak photon emission spoke of the link between reactive oxygen species (ROS), which are &#8220;reactive molecules and free radicals&#8221; produced during cellular metabolism, and ultraweak photon emission. The study stated: “Sustained exposure to high levels of ROS, via elevated production or the failure of antioxidant defenses, is associated with the pathophysiology of multiple diseases, Furthermore, the failure to produce ROS effectively in response to stressors is also indicative of metabolic dysfunction. The intrinsic link between ROS production and biophoton release means that monitoring UPE in living organisms represents a real-time, non-invasive method of early-state disease diagnosis.”
“The nice thing about ultraweak photon emission is it’s a complete passive monitoring process,” Oblak asserted.
“According to literature, the UPE seems to be influenced by some diseases (including diabetes, hemiparesis, Protoporphyria, or a typical cold), and even by the cerebral intention/relaxation (brain activity/meditation),” a <a href="https://www.sciencedirect.com/science/article/pii/S1011134421000191">2021 study</a> claimed. “These allow to consider UPE as a natural and promising non-invasive spectroscopic tool for helping during the diagnosis of a variety of illnesses or stress-/mood-state disorders.”
Ultraweak photon emission should be differentiated from bioluminescence, which has greater light intensities and is connected to specific biochemical reactions. Bioluminescence is exhibited in fireflies and jellyfish, for example. Ultraweak photon emission, conversely, results from oxidative stress reactions.

A futuristic woman exploring outer space

‘Glow’ From Humans Stops At Death, Study Says. Here’s Why Understanding It Could Save Lives.

Detection of disease

Photons

The Department of Health and Human Services (HHS) is investing half a billion dollars into a project that seeks to develop universal vaccinations for numerous viruses, according to a <a href="https://www.wsj.com/health/healthcare/rfk-jr-bets-500-million-on-universal-vaccines-in-shift-from-covid-19-funding-0299d927" target="_blank" rel="noopener">report</a> from The Wall Street Journal.
The project is called &#8220;Generation Gold Standard.&#8221; It seeks to use chemically inactivated whole viruses, which is how flu vaccines were created decades ago. Currently, flu vaccines contain synthetic viral proteins or pieces of viruses.
The goal is to create these vaccines with such technology that are &#8220;universal,&#8221; meaning they will protect against multiple strains of a virus, like the flu, coronavirus, and RSV.
The new project would shift HHS from its current COVID projects and use funding from larger <a href="https://www.dailywire.com/news/doge-meets-hhs-rfk-jr-to-terminate-20000-bureaucrats-restructure-department" target="_blank" rel="noopener">cuts</a> the department has already made.
For example, The Journal noted that under former President Joe Biden, HHS developed a $5 billion project called NextGen, which studied new COVID vaccines. Under HHS Secretary Robert F. Kennedy Jr., NextGen has been deemed &#8220;wasteful,&#8221; and several of the projects within NextGen have been given stop-work orders.
Generation Gold Standard will give the American public &#8220;a cost-effective, accountable alternative&#8221; to COVID vaccines and therapeutics, an HHS spokesperson told the Journal.
Next year, the project aims to begin trials for a universal flu vaccination, which would protect against numerous strains. Another goal is for trials for a universal coronavirus vaccine to start by 2026, “with FDA approval targeted for 2029.&#8221;
Two scientists with senior roles in the project are Dr. Matthew Memoli, the principal deputy director of the National Institutes of <a href="https://www.washingtonpost.com/health/2025/03/10/vaccines-nih-rfk-research-canceled/" target="_blank" rel="noopener">Health</a> (NIH), and Dr. Jeffery Taubenberger, acting director of NIH&#8217;s infectious-diseases institute.
“Our commitment is clear: every innovation in vaccine development must be grounded in gold standard science and transparency,” Secretary Kennedy said in a statement.
Under Kennedy, HHS has already made shifts in funding for vaccinations. For example, NIH will <a href="https://www.dailywire.com/news/maha-in-100-days-how-trump-and-rfk-are-transforming-american-food-healthcare" target="_blank" rel="noopener">stop</a> spending money to determine why Americans hesitate to get vaccines. NIH is terminating or scaling back more than 40 related grants and has said that such spending no longer aligns with NIH priorities.
Related: <a href="https://www.dailywire.com/news/maha-in-100-days-how-trump-and-rfk-are-transforming-american-food-healthcare" target="_blank" rel="noopener">MAHA In 100 Days: How Trump And RFK Are Transforming Food And Healthcare In America</a>

RFK Jr.

HHS Investing $500 Million To Develop Universal Vaccines

Director of National Intelligence Tulsi Gabbard on Wednesday called for the United States to stop funding gain-of-function research at biolabs around the world.
Gabbard made the comments during an interview with podcast host Megyn Kelly, as they discussed the likelihood that the United States directly funded the research that led to the creation of COVID-19 and the state of the ongoing probe into the lab leak that released the virus. It is now widely accepted by American officials that a lab leak stemming from gain-of-function research triggered the 2020 pandemic.
“The reason why this is so important is not just what has happened in the past, it&#8217;s because this gain-of-function is happening in biolabs around the world,” Gabbard <a href="https://www.youtube.com/watch?v=rMKTSYxto_Y" target="_blank" rel="noopener">said</a>, pointing to her previous warnings about U.S.-funded biolabs in Ukraine.
“In order to prevent another COVID-like pandemic or another major health incident that could effect us in the world, we have to end this gain-of-function research and provide the evidence that shows exactly why and how it’s in our best interests, the American people’s best interest, to bring an end to it,” she added.
Gain-of-function research is a process in which scientists genetically alter an organism to study how it responds under specific conditions. It can involve increasing transmissibility, virulence, and other characteristics of a pathogen.
Gabbard did not specifically name which American-funded labs she said were performing gain-of-function research.
Gabbard told Kelly that she still had an intelligence team working with National Institutes of Health Director Jay Bhattacharya and Health and Human Services Director Robert F. Kennedy Jr. to investigate direct links between U.S.-funded gain-of-function research in Wuhan, China, and the pandemic.
Kelly asked when the public could expect to find out the &#8220;exact experiment&#8221; that led to COVID. Gabbard replied that her team was working on it with Bhattacharya and would release the information &#8220;hopefully very soon.&#8221;
Based on the increasing consensus that the lab leak was the cause, Gabbard said she was not surprised that Dr. Anthony Fauci had been pardoned preemptively as President Joe Biden left office. “Is it any wonder that he sought a preemptive pardon for anything during a certain period of time by President Biden before he left office?” she said.
In May 2021, Fauci <a href="https://www.cnbc.com/2021/07/20/if-anybody-is-lying-here-senator-it-is-you-fauci-tells-sen-paul-in-heated-exchange-at-senate-hearing.html">said</a> that the NIH “has not ever and does not now fund gain-of-function research in the Wuhan Institute of Virology.” However, later evidence from the House Select Subcommittee on the Coronavirus Pandemic determined that the EcoHealth Alliance used NIH dollars to fund gain-of-function research in Wuhan. EcoHealth is currently under investigation by the Justice Department and has been barred from receiving any further federal grant dollars.
Gabbard said that much of the research her team has conducted can be found at <a href="https://www.whitehouse.gov/lab-leak-true-origins-of-covid-19/" target="_blank" rel="noopener">COVID.gov</a>, where the Trump administration has compiled a page explaining how the coronavirus is believed to have originated in a Chinese lab.
In addition to the COVID investigation, Gabbard said that her team was looking at other instances of the United States funding &#8220;dangerous&#8221; gain-of-function research that &#8220;in many examples has resulted in either a pandemic or some other major health crisis.”

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