Spartan Health

02/19/2026

02/15/2026

Repeal the protections given to vaccine manufacturers in the 1986 Childhooed Vaccine Injury Act.

For 40 years vaccine manufacturers have been immune to liability for any issues with their products/issues caused by their products.

For 40 years, pharmaceutical companies have been held liable for issues with any/all other products they create that cause issues. Issues like baby powder tainted with asbestos, baby food tainted with heavy metals, the op**te epidemic, and many other products whether they were contaminated, lied about or whether they did what they were supposed to do while causing other damage/disease/side effects. These companies have been sued, fined, shutdown, etc.. for how they marketed products and/or what those products did to people…. Except for vaccines.

For 40 years, if a vaccine had issues and caused injury or death; the injured party would have to sue the US Government. The injured party would have to go against the best federal attorneys that government can buy to prove beyond the shadow of a doubt that the vaccine harmed them/their loved one. If successful, the victim would then be compensated by the government with taxpayer dollars and nothing would happen to the manufacturer.

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🚨 Senator Rand Paul Introduces Landmark Bill to End Federal Liability Shield for Vaccine Manufacturers

I am genuinely celebrating this development.

On February 11, 2026, Senator Rand Paul (R-KY), with cosponsor Senator Mike Lee (R-UT), introduced S.3853—“A bill to amend the Public Health Service Act to end the liability shield for vaccine manufacturers, and for other purposes.”

This legislation directly targets the broad civil liability protections granted to vaccine manufacturers under the National Childhood Vaccine Injury Act of 1986.

That law established the National Vaccine Injury Compensation Program (NVICP / “Vaccine Court”) and largely immunized manufacturers from design-defect lawsuits in both state and federal courts—protections no other pharmaceutical category in the U.S. enjoys.

If passed, S.3853 would remove these special immunities, holding vaccine manufacturers to the same product-liability standards that apply to every other drug and medical product company.

Injured individuals and families would once again have access to traditional civil courts and the ability to seek full accountability through the normal judicial process.

The bill is now before the Senate Committee on Health, Education, Labor, and Pensions (HELP) for review.

For 40 years, the 1986 framework has been defended as necessary to maintain vaccine supply and manufacturer participation.

At the same time, many—myself included—have long argued that this unprecedented shield has reduced incentives for safety improvements, limited public scrutiny of product risks, and left affected families with restricted recourse, especially when adverse-event reporting systems are widely acknowledged to capture only a small fraction of actual incidents.

Today’s introduction of S.3853 marks a serious, substantive step toward restoring transparency, market-based accountability, and equal access to justice.

It’s exactly the kind of principled, long-overdue reform I’ve hoped to see.

If you care about medical freedom, informed consent, parental rights, or simply believe no industry should operate above the law, now is the time to pay close attention.

Read the bill.

Contact your senators.

Follow its progress.

This is a moment worth celebrating, and worth fighting for.

🔗 Full bill text and status: https://www.congress.gov/bill/119th-congress/senate-bill/3853

🔗 Full article: https://jonfleetwood.substack.com/p/rand-paul-introduces-federal-bill

01/24/2026

12/03/2025

Measles is getting media attention again so let’s cover the truth behind it all.

The decline in mortality from measles was LONG before the 💉 vaccine. It was motivated by financial incentives from the government. Furthermore, the vaccine spreads the virus, and it contains female cells from an aborted baby. This is all right in the research:

“With the exception of some isolated population groups, almost all children contracted measles before they reached adolescence.

By 1960, thanks to the use of antibiotics and improvements in living conditions, measles mortality was declining steadily in industrialized countries (although not in the developing world). For example, in the United Kingdom deaths from measles had fallen from 307 in 1949 to 98 in 1959. Parents largely came to see measles as an unpleasant, although more or less inevitable, part of childhood. Many primary care physicians shared this view.”1

“In the United States and Western Europe, which did, measles mortality was low and declining and parents seemingly accepted it as an unpleasant part of childhood. What reasons could there be for introducing a measles vaccine? There seemed to be no reason to begin a mass immunization program…”1

Cue the financial incentives…

“In 1962 Congress passed the Vaccine Assistance Act, which authorized financial assistance to states specifically for vaccination programs against polio, diphtheria, whooping cough, and tetanus.”1

The introduction of a mass measles vaccination campaign was not based on a need for this intervention in developed countries like the U.S. as mortality had long been down before the vaccine. It was based solely on financial incentive from the government.

Columbia University even reported that there were other factors that were much more responsible for the decline in diseases than vaccinations:

“The main influences on the decline in mortality were improved nutrition. . . reduced exposure (from better hygiene). . . and, less certainly, immunization and therapy on the large number of conditions included in the miscellaneous group. Since these three classes were responsible respectively for nearly half, one-sixth, and one-tenth of the fall in the death rate, it is probably that the advancement in nutrition was the major influence.”2

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In developed countries with access to proper sanitation and nutrition, naturally-acquired measles is very mild and provides lifelong immunity as well as other benefits.

“In the pre-vaccine era, when the natural measles virus infected the entire population, measles — “typically a benign childhood illness,” as Clinical Pediatrics described it — was welcomed for providing lifetime immunity, thus avoiding dangerous adult infections. In today’s vaccine era, adults have accounted for one quarter to one half of measles cases; most of them involve pneumonia, one-quarter of them hospitalization.

Also importantly, measles during pregnancies have risen dangerously because expectant mothers no longer have lifetime immunity. Today’s vaccinated expectant mothers are at risk because the measles vaccine wanes with time and because it often fails to protect against measles.”3

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The high risk of death and complications of wild measles is because of one missing nutrient. And that missing nutrient is generally only a problem in third world countries.

The World Health Organization has it listed right on their website that measles is more prominent in areas where the population is deficient in Vitamin A and that they recommend treating measles with vitamin A.

We have access to beef, beef liver, cod liver oil, butter from grass-fed cows, etc. that are absorbable protective sources of Vitamin A. Nourishing our children with these nutrients is more effective than any injection, especially one that carries serious risks and contains cells from an aborted baby.

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The MMR vaccine is made from and contains DNA from aborted fetal cells.

The rubella portion of the vaccine was developed after an American researcher at the Wistar Institute cultured rubella virus from a fetus aborted because the mother was infected with rubella. This vaccine is called RA 27/3 because the rubella virus was isolated from the 27th aborted baby and sent to the Wistar Institute in the 1964 rubella outbreak. Researchers were unable to culture rubella from the tissues of the first 26 fetuses sent to Wistar, which had been aborted by doctors because the mothers had rubella during pregnancy.

WI-38 in this vaccine is derived from lung tissue of a 3-month-gestation female fetus.

(Note: There are serious implications for injecting female cells into a male baby…)

Note: These women were told their babies would die due to the mother having rubella, so they agreed to abortion for "medical research." The first 26 babies were found to not even be affected by rubella, meaning they would have been born perfectly healthy.

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Furthermore, the vaccine actually spreads the disease in a mutated form. Measles virus is passed around by secondary transmission from newly-vaccinated people as well:

“Measles virus RNA has been detected in the urine of the vaccinees as early as 1 day or as late as 14 days after vaccination. Measles virus RNA was also detected in the urine samples from all four of the young adults between 1 and 13 days after vaccination.”4

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REF:

1. https://pmc.ncbi.nlm.nih.gov/articles/PMC4007870/

2.http://www.columbia.edu/itc/hs/pubhealth/rosner/g8965/client_edit/readings/week_2/mckinlay.pdf

3. https://financialpost.com/opinion/lawrence-solomon-the-untold-story-of-measles

4. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC228449/

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