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Health

Cancer drug pioneer praises RFK Jr., suggests link between childhood cancer and COVID shots

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From LifeSiteNews

By Calvin Freiburger

Trump nominee for Secretary of Health and Human Services Robert F. Kennedy Jr. received a ringing endorsement from an acclaimed medical expert on Tuesday who said the country needs to take seriously a possible link between the COVID-19 shots and childhood cancer.

Dr. Patrick Soon-Shiong is a billionaire who pioneered the cancer drug Abraxane and has owned and led multiple medical companies. In 2018, he purchased the Los Angeles Times (which he blocked from endorsing Democrat Kamala Harris for president in 2024), and his ImmunityBio was among the companies recruited by the Trump administration to contribute to Operation Warp Speed.

On Tuesday, Soon-Shiong appeared on the 2WAY podcast, where he shared his thoughts about some of the big medical policy questions of the next four years.

“I think people misunderstand Bobby Kennedy, Robert F. Kennedy. He’s really all about the science,” he said. “I’ve sat down with him, met with him for the first time. I’ve not known him until I sat down with him, because I wanted to understand what he was thinking. And after hours of sitting down with him, I was so impressed. He knows more about the science than most doctors.”

Soon-Shiong went on to say “we’re going to have to address the rising incidence of cancer. For the first time in my career, I’ve seen an 8-year-old, 9-year-old, 10-year-old with colon cancer. The first time in my career, I’ve had a 13-year-old child in our clinic die of metastatic pancreatic cancer. We have to face this effectiveness and reality.”

The doctor ended on an optimistic note, saying that “there are effective therapies because we understand the science in such an immense way,” and adding that he is “excited about this next four years of bringing this information across and not to scare the population to say, look, we could lead the world in our innovation and using healthcare as a foreign policy around the world.”

large body of evidence identifies significant risks to the COVID shots, which were developed and reviewed in a fraction of the time vaccines usually take under Operation Warp Speed.

The federal Vaccine Adverse Event Reporting System (VAERS) reports 38,264 deaths, 219,594 hospitalizations, 22,134 heart attacks, and 28,814 myocarditis and pericarditis cases as of December 27, among other ailments. CDC researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.

An analysis of 99 million people across eight countries published in February in the journal Vaccine “observed significantly higher risks of myocarditis following the first, second and third doses” of mRNA-based COVID shots, as well as signs of increased risk of “pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” and other “potential safety signals that require further investigation.” In April, the CDC was forced to release by court order 780,000 previously undisclosed reports of serious adverse reactions, and a study out of Japan found “statistically significant increases” in cancer deaths after third doses of mRNA-based COVID-19 injections and offered several theories for a causal link.

Earlier this month, a long-awaited Florida grand jury report on the COVID shot manufacturers found that there were “profound and serious issues” in pharmaceutical companies’ review process, including reluctance to share what evidence of adverse events they found.

All eyes are currently on Trump and his health team, which will be helmed by Kennedy at HHS. As one of the country’s most vocal critics of the COVID establishment and vaccines more generally, his nomination brought hope that the second Trump administration will take a critical reassessment of the shots that the returning president has previously embraced, although most of Kennedy’s comments since joining Trump have focused on other issues, such as conventional vaccines and harmful food additives.

Censorship Industrial Complex

Celebrity Doctor says YouTube removed videos about vaccine discussions, insisted he take reeducation

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Dr. Drew condemns YouTube’s demand for “reeducation” after video takedowns, calling it a threat to free speech and medical dialogue.

Dr. Drew Pinsky, widely known as Dr. Drew, has publicly criticized YouTube for removing two of his videos over alleged violations of the platform’s medical “misinformation” policy. On January 14, 2025, Pinsky took to X to challenge YouTube’s decision, highlighting concerns about free speech and the suppression of open dialogue on health-related topics.

In order to get the flags removed from his video, YouTube told Dr. Drew that he would have to attend a form of reeducation training and have no violations for 90 days, or else it would delete his entire channel and all of his videos. Pinsky has over 1,000 videos on the platform.

In one of his posts, Pinsky expressed frustration over the platform’s actions: “This weekend, @YouTubeCreators accused me of spreading ‘medical misinformation’ & took down 2 videos with an MD & a lawyer. I’ve been a board-certified physician for over 40 years – 2x @YouTube’s existence.”

The flagged videos featured discussions with Dr. Kelly Victory, a board-certified physician, and attorney Warner Mendenhall. Pinsky elaborated that these conversations centered around the side effects of mRNA vaccinations, a topic he argues warrants open discourse rather than censorship. In his discussion with Dr. Victory, she stated that the “vast majority of the people who have been injured are young, healthy people who were under the age of 50 who had fundamentally zero risk from COVID itself. They all got COVID. These are people who would have been fine if they were just left alone.”

Pinsky defended the content, asserting that sharing professional perspectives and personal beliefs in a public forum should not be equated with spreading misinformation. He emphasized that their dialogue was an exchange of viewpoints rather than a promotion of falsehoods.

In a separate video with Warner Mendenhall, the attorney discussed legal cases involving individuals who suffered severe reactions following vaccination. Pinsky highlighted that Mendenhall shared client experiences and expressed personal beliefs—not medical advice. Pinsky wrote, “It is not medical misinformation for someone to state their belief that a large number of people were harmed by a medical product or study.”

This isn’t the first time YouTube has targeted Dr. Drew’s content. He noted that previous strikes were resolved after discussions between his production team and YouTube officials. Despite the latest removals, Pinsky confirmed that the videos remain accessible on X, suggesting that alternative platforms may offer more space for unrestricted conversations.

A prominent internist and addiction medicine specialist, Dr. Drew Pinsky has been a notable media figure for decades. His career includes hosting television shows like Dr. Drew On Call on HLN and Lifechangers on The CW.

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FDA bans highly used food dye

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FDA Finally Bans Cancer-Linked Red No. 3 Food Dye

By Nicolas Hulscher, MPH

The Food and Drug Administration (FDA) announced on Wednesday that it is banning the use of Red No. 3, a synthetic dye responsible for the vibrant cherry red color in foods and beverages, citing its association with cancer in animal studies:

The dye is still used in thousands of foods, including candy, cereals, cherries in fruit cocktails and strawberry-flavored milkshakes, according to the Center for Science in the Public Interest, a food safety advocacy group that petitioned the agency in 2022 to end its use.

Food manufacturers will have until Jan. 15, 2027 to reformulate their products. Companies that make ingested drugs, such as dietary supplements, will get an additional year.

This ban was LONG overdue. Unfortunately, the other synthetic food dyes that have also been linked to serious deleterious health effects still remain on the market. A few months ago, I summarized the harm linked to synthetic food dyes — outdated FDA standards expose Americans to toxic food dyes linked to cancer, neurobehavioral issues, and other health risks, demanding urgent regulatory action:

Synthetic Food Dyes: A Half-Century of Harm

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November 25, 2024
Synthetic Food Dyes: A Half-Century of Harm
 

by Nicolas Hulscher, MPH

 

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Batada et al found that nearly half (43.2%) of grocery store products contained artificial food colorings (AFCs), with Red 40 (29.8%), Blue 1 (24.2%), Yellow 5 (20.5%), and Yellow 6 (19.5%) being the most common. Candies (96.3%), fruit-flavored snacks (94%), and drink mixes/powders (89.7%) had the highest prevalence of AFCs, while produce contained none.

Oliveira et al summarized the deleterious health effects linked to synthetic food colorings in children: neurobehavioral disordersallergic reactionscarcinogenic and mutagenic potentialgastrointestinal and respiratory issuestoxicitydevelopmental and growth delays, and behavioral changes.

Sultana et al illustrated the specific health hazards associated with particular synthetic food dyes:

Miller et al conducted a systematic review of the potential neurobehavioral impacts (activity and attention) of food dye consumption. They included 27 clinical trials of children exposed to synthetic food dyes and found that 16 of 25 challenge studies (64%) demonstrated evidence of a positive association, with 13 studies (52%) reporting statistically significant findings. The authors concluded, “Current evidence from studies in humans, largely from controlled exposure studies in children, supports a relationship between food dye exposure and adverse behavioral outcomes in children, both with and without pre-existing behavioral disorders.” They also noted that:

“Animal toxicology studies were used by FDA as the basis for regulatory risk assessments of food dyes [25]. All current dye registrations were made between 1969 and 1986 based on studies performed 35 to 50 years ago. These studies were not designed to assess neurobehavioral endpoints. Dye registration was accompanied by derivation of an “acceptable daily intake” (ADI) based on these studies. FDA ADIs have not been updated since original dye registration, although there have been several reviews of specific effects since then, the latest in 2011.”

Synthetic food dyes, widely prevalent in U.S. products and lacking nutritional value, rely on outdated FDA approvals despite evidence of widespread toxicity, carcinogenicity, and adverse neurobehavioral effects, strongly warranting urgent regulatory action to protect public health.

While the FDA has finally made a decision that will benefit public health, they are still allowing the dangerous COVID-19 genetic injections to be administered to all individuals aged 6 months and older despite far exceeding criteria for a Class I recall. The immediate removal of unsafe and ineffective gene therapy injections should be the first priority before anything other product bans.

Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

www.mcculloughfnd.org

Please consider following the McCullough Foundation and Nicolas Hulscher on X (formerly Twitter) for further content.

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