HHS Sheds Some Weight and More!
This week at Health and Human Services - two confirmations, one efficient restructuring, the resignation of a COVID-era bureaucrat, and more!
We did it!! On Tuesday, March 25th the Senate confirmed Dr. Marty Makary to run the Food and Drug Administration and Dr. Jay Bhattacharya to lead the National Institutes of Health. Makary was confirmed as FDA commissioner by a vote of 56-44, while Bhattacharya was confirmed as NIH director by a margin of 53-47.
The team here at MAHA Action is so excited to see what these brilliant doctors will do inside of government to Make America Healthy Again!
Also, in major news, Secretary Kennedy announced a massive restructuring at the Health and Human Services Department. The changes promise to invigorate and move us back to gold-standard science while ensuring that bureaucratic corruption and red tape are minimized.“We aren't just reducing bureaucratic sprawl. We are realigning the organization with its core mission and our new priorities in reversing the chronic disease epidemic. This Department will do more – a lot more – at a lower cost to the taxpayer,” said Robert F. Kennedy, Jr.
Here are some of the big points to come out of the announcement:
The changes will…
- Save taxpayers $1.8 billion per year through a reduction in workforce that results in a total downsizing from 82,000 to 62,000 full-time employees.
- Streamline the department's functions by slimming down from 28 divisions to 15, including a new Administration for a Healthy America, or AHA. The move will centralize core functions such as Human Resources, Information Technology, Procurement, External Affairs, and Policy. Regional offices will be reduced from 10 to 5.
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Implement the new HHS priority of ending America’s epidemic of chronic illness by focusing on safe, wholesome food, clean water, and eliminating environmental toxins. The reorganization of HHS will reflect these priorities.
While discussing these changes in an interview with Chris Cuomo on News Nation, Cuomo asked Secretary Kennedy if there were plans to look at Long COVID or vaccine injury, to which Secretary Kennedy said, “We’re incorporating an agency within CDC that is going to specialize in vaccine injuries. Those are things that are priorities for me…and are priorities for the American people,” while noting the agency would also look into Lyme disease. He continued, “More and more people are suffering from these injuries, and we are committed to having gold standard science and making sure that we can figure out what the treatments are and that we can deliver the best treatments possible to the American people.”
Secretary Kennedy, in collaboration with Elon Musk, has established a transformative infrastructure within the Department of Health and Human Services, designed to ensure that its agencies truly serve the people.
— MAHA Action (@MAHAAction) March 28, 2025
The previous system was rooted in data monetization,… pic.twitter.com/8G3uXxTGOB
For more details, see this handy HHS Fact Sheet and watch Secretary Kennedy’s announcement on X.
The MAHA world was very disappointed when Dr. David Weldon removed himself from consideration as the CDC director. MAHA Action CEO Del Bigtree sat down with him to discuss that and more (read on for exclusive details) on The MAHA Podcast this Tuesday, but still, an appointment had to be made. With that, Secretary Kennedy gave a glowing endorsement of the interim CDC director, Susan Monarez.
The social media world was up in arms when some users began reviewing the official @CDCGov “X” account - finding controversial posts from the Biden era that demonstrated approval of masks and COVID vaccinations, to name a few. That prompted the Secretary to take to social media and reassure MAHA that he had hand-picked Monarez after the Weldon step back, stating, “X posts that erroneously attribute Biden-era tweets supporting masks, lockdowns, vaccine mandates, etc. to my @CDCgov Director nominee, Susan Monarez, have understandably provoked agita within the MAHA movement. I handpicked Susan for this job because she is a longtime champion of MAHA values, and a caring, compassionate and brilliant microbiologist and a tech wizard who will reorient CDC toward public health and gold-standard science. I’m so grateful to President Trump for making this appointment.”
The next bit of news came as Peter Marks, the Director of the FDA’s Center for Biologics Evaluation and Research (CBER), resigned. His last day will be April 5th. As things shift and change at the FDA and Secretary Kennedy brings the department back to gold-standard science, we can expect a few from the old guard to kick some dust on the situation. In his resignation letter, he claimed credit for Operation Warp Speed and the safety and efficacy of the COVID-19 vaccines while expressing concern about questioning anything regarding the adverse effects of any vaccine. He ended off his long letter by stating, "My hope is that during the coming years, the unprecedented assault on scientific truth that has adversely impacted public health in our nation comes to an end so that the citizens of our country can fully benefit from the breadth of advances in medical science.” MAHA agrees, Mr. Marks. MAHA agrees.
On the day that Marks left office, as per OpenVAERS, a website that pulls data right from the CDC VAERS database, in America, there were:
- 19,310 deaths
- 91,037 hospitalizations
- 2,556 cases of anaphylaxis
- 6,415 cases of Bell’s Palsy
- 2,075 miscarriages
- 9,555 heart attacks
- 37,007 severe allergic reactions
- 8,269 cases of shingles
- 15,537 life threatening events
- 5,347 cases of Myocarditis/Pericarditis…
…from the COVID vaccine alone... In a system that is known to only record less than 3% of all adverse reactions… With zero explanation for this from Peter Marks who triumphantly claimed the success of Operation Warp Speed.
In response to the letter, a spokesperson from HHS said, “If Peter Marks does not want to get behind restoring science to its golden standard and promoting radical transparency, then he has no place at FSA under the strong leadership of Secretary Kennedy.” Out with the old, IN WITH THE NEW! In Dr. Marty Makary’s capable hands, there is no doubt that the position will be filled by someone who better aligns with MAHA’s goals.
Legislative News: A Must Read
\A lot is happening in advocacy this week as MAHA Action hits the ground running and works to ensure the MAHA agenda is implemented across all 50 states.
Our team traveled to Florida late last week to partner with a slew of other health freedom organizations and spoke to Florida representatives about a number of bills we are supporting in the Florida legislature (and two we oppose.)
To get a detailed look at what MAHA legislation is on the calendar in Florida, visit our legislative tracking page and click “Florida.” Florida is one of several states with two bills on the calendar that would prevent liability to pesticide companies for harm from their products… That is one of the reasons why MAHA Action sprung to action with a press conference to alert people to this and the harms that could follow if we don’t act now to make our voices heard.
On Tuesday, MAHA Action hosted a press conference to raise awareness about a slew of bills nationwide that seek to indemnify Bayer Monsanto from liability for illness and injury stemming from its products. To truly Make America Healthy Again, American farmers and families must have access to safe, chemical-free food and related products. Bayer Monsanto, despite already paying out $10b to settle nearly 100,000 cases after a jury previously found their product liable for causing cancer in 2018, is currently seeking to escape liability for causing cancer in 20 states and at the federal level.
Participating in the press conference, which you can view here, were Del Bigtree, CEO at MAHA Action, Kelly Ryerson, a public health advocate and founder of Glyphosate Facts, and Will Harris, owner of White Oak Pastures, a holistically managed, regenerative ranch and farm in Georgia.
During the one-hour-long discussion, MAHA Action CEO Del Bigtree said, “Monsanto wants to have liability protection for glyphosate, which is in their product “Roundup,” We will be doing everything we can to expose this outrageous endeavor by Monsanto - by Bayer. If we have to bring lawsuits, we will bring lawsuits, we will be working on legislation to fight back against this, and what we do best at MAHA is obviously media. We will be producing media to warn the world that they are attempting to poison you with indemnification. MAHA is dedicated to stopping Monsanto on this initiative.”
Outside of Georgia, where this bill passed and is awaiting the governor's signature, several other states have ongoing legislation, including North Dakota, Missouri, Iowa, Tennessee, Florida, and Idaho. We urge you to take action and use the tools we provide to contact your legislator.
Also, this week, West Virginia has set a national precedent in public health policy. With the passage of House Bill 2354, West Virginia has become the first state in the nation to prohibit the use of most artificial dyes in food products, a commendable step toward protecting the health and well-being of its residents.
This legislation marks a meaningful advancement in preventive health, particularly for children who face heightened risks of long-term cognitive and physiological effects from synthetic dyes.
West Virginia’s leadership sets a powerful example for the rest of the country. This is a milestone for the state and a call for broader reform as we collectively work to Make America Healthy Again. Secretary Kennedy traveled to West Virginia to celebrate the win with the governor, and the press conference was chock full of fun. Who knew that on top of everything else, Secretary Kennedy was also doing some personal training on the side?
MAHA Action Bills to Watch
Here are some bills we want you to watch and get engaged with! MAHA Action needs you to step up in your state and fight right alongside of us:
Florida -
H0149 “Cody’s Law”: VERDICT: MAHA SUPPORTS
This bill, "Cody's Law: Florida No Vaccine-Injured Patient Left Behind," requires the Agency for Health Care Administration to expedite the review and payment of claims for severe, life-threatening, or lifelong injuries caused by recommended vaccines, immunizing agents, or emergency countermeasure drugs under Medicaid and medically needy programs. The agency must publish a comprehensive list of related medical conditions and potential adverse reactions on its website, update it as new conditions and treatments emerge, and provide information to help healthcare providers assist affected patients. It must also seek federal approval if needed and develop rules for implementation. The bill takes effect July 1, 2025, ensuring faster and more transparent support for patients with serious vaccine or drug-related injuries.
The MAHA “Why?” "MAHA Action supports this bill. Vaccine injuries have a profound impact on many lives. Ensuring that affected individuals receive proper care while improving transparency around adverse reactions would foster greater accountability and trust in vaccination.
HB0129/S0992: VERDICT: MAHA OPPOSES
This bill imposes new legal restrictions on pesticide-related lawsuits in Florida, limiting liability for distributors, dealers, applicators, registrants, and agricultural employers. A lawsuit can only proceed if the defendant exercised substantial control over design or manufacturing, altered the product, mishandled it inconsistently with its label, or if the manufacturer is outside Florida’s jurisdiction. Failure-to-warn claims are barred for pesticides registered under FIFRA if the EPA-approved label aligns with the agency’s health assessments or carcinogenicity classification. The bill provides broad legal protections for pesticide businesses by setting strict conditions for lawsuits. It takes effect July 1, 2025.
The MAHA “Why?” MAHA Action strongly opposes this bill. It is designed to shield Bayer and Monsanto from accountability rather than prioritizing public health, environmental safety, and consumer protection. By granting pesticide manufacturers legal immunity based on EPA-approved labeling, this legislation severely limits the ability of individuals to seek justice for harm caused by pesticide exposure. Given Monsanto's history of legal battles over toxic products like Roundup, this bill appears to be more about corporate protection than genuine safety standards. Regulatory approval does not equate to absolute safety, especially when industry influence over agencies like the EPA is well-documented. Transparency, independent oversight, and the right to legal recourse must precede corporate immunity.
Georgia:
SB 144: VERDICT - MAHA OPPOSES - Take Action to VETO!
This bill protects pesticide manufacturers in Georgia from liability for health risk warnings beyond those required by the EPA. Starting January 1, 2026, any EPA-registered pesticide with an EPA-approved label or one consistent with FIFRA health assessments will be legally sufficient. Legislative findings highlight agriculture’s economic importance, the need for domestic pesticide production, and concerns over supply chain risks from Chinese imports. By limiting liability to EPA-approved warnings, the bill aims to support American farmers, clarify regulatory authority, and reduce barriers to agricultural input production.
The MAHA “Why?” MAHA Action strongly opposes this bill as it is designed to shield Bayer and Monsanto from accountability rather than prioritizing public health, environmental safety, and consumer protection. By granting pesticide manufacturers legal immunity based on EPA-approved labeling, this legislation severely limits the ability of individuals to seek justice for harm caused by pesticide exposure. Given Monsanto's history of legal battles over toxic products like Roundup, this bill appears to be more about corporate protection than genuine safety standards. Regulatory approval does not equate to absolute safety, especially when industry influence over agencies like the EPA is well-documented. Transparency, independent oversight, and the right to legal recourse must take precedence over corporate immunity.
South Carolina
S1023: VERDICT: MAHA SUPPORTS
This bill seeks to prohibit healthcare professionals in South Carolina from administering synthetic mRNA-based gene therapies, primarily targeting vaccines like those used for COVID-19, based on concerns about potential health risks. The legislation defines synthetic mRNA-based gene therapies as medical products that introduce foreign genetic material into human cells to produce a medical effect, and specifically applies to mRNA technologies intended to prevent or mitigate communicable disease transmission. Healthcare professionals who violate this prohibition would face a mandatory minimum one-year license suspension, with potential additional penalties determined by their professional licensing board. The bill provides exceptions for mRNA therapies that treat non-infectious diseases like genetic conditions or cancer, traditional vaccines, FDA-authorized recombinant vaccines, and FDA-authorized genetic therapies that do not use synthetic mRNA technology. The legislation stems from concerns about potential long-term health risks, including possible genomic modifications, inadequate safety studies, undisclosed contaminants, and potential transmission of side effects through "shedding." Professional licensing boards are required to report any violations to the Department of Public Health, which must maintain records for at least seven years and provide annual reports to the General Assembly. The act would take effect upon the Governor's approval.
The MAHA “Why?” MAHA Action supports this bill as it aims to safeguard public health by restricting the use of synthetic mRNA-based gene therapies in South Carolina, particularly in response to concerns about their potential long-term health risks. By providing clear exceptions for certain treatments and ensuring professional accountability through mandatory reporting and penalties for violations, the legislation strikes a balance between patient safety and the advancement of medical technologies. This bill also reinforces the importance of robust oversight and transparency in administering new medical therapies, giving patients and healthcare professionals confidence in their decision-making.
Community and Camaraderie!
Earth Day is on April 22, and in the spirit of MAHA, we would love to see YOU take action in your community to organize events. Earth Day events are a great way to reconnect with your friends and bring new people into the MAHA mission. We encourage everyone to take the opportunity to re-engage and spread the word about MAHA!
Looking for an event in your area? Make sure to check out our events page!
What’s on the Horizon?
April 5th in El Dorado Hills, California
MAHA Action CEO Del Bigtree will give the Keynote address at this event.
MAHA Root and Rise Farm Event
April 6th in New Roads, Louisiana
April 11-13th in San Diego, CA
MAHA will have an exhibition booth, and Del Bigtree will be the headlining speaker. Please consider supporting this important event and visit us if you are attending.
Changing Life and Destiny 2025
April 25th-27th in Plano, TX
MAHA will have a booth at this event, and Del Bigtree will speak!
THE MAHA PODCAST: BOMBSHELL EPISODE
Big Pharma Blocked His Nomination—Now He’s Naming Names
Dr. Dave Weldon was hours away from becoming CDC Director—until his confirmation was abruptly canceled. Why?
Because he asked the one question the government refuses to answer: Why is autism skyrocketing—and why won’t the CDC study the unvaccinated?
In this bombshell episode of The MAHA Podcast, Del Bigtree sits down with Dr. Weldon—a physician, former Congressman, and longtime vaccine safety advocate—to expose decades of corruption, coverups, and opposition to destroy anyone who questions vaccine policy.
“I’d never seen autism in medical school. Now it’s everywhere—and they have no explanation.”
The system is rigged. The science is politicized. And the stakes have never been higher.
🚨 What he reveals:
✔ Why Dr. Weldon’s nomination to lead the CDC was pulled just 12 hours before his hearing
✔ How the CDC refused to investigate autism rates in unvaccinated populations like the Amish and the Somali community
✔ The real reason we inject newborns with a Hepatitis B vaccine meant for IV drug users
✔ What really happens when scientists publish inconvenient data—and how it ruins lives
✔ How the CDC ignored internal warnings that mercury levels in vaccines were “clearly toxic” for infants
Thanks for reading this edition of Well Sourced - your place for everything MAHA!
