Category: Vaccines

Vaccinated Koreans suffered a dose-dependent rise in the common cold, infections, pneumonia, and tuberculosis — up to +559%. BILL GATES spent over $100 MILLION on mRNA.

https://x.com/NicHulscher/status/2038026168520073562?s=20

Why this “reassuring” vaccine study may be missing the most important risk pattern

A paper has just been published examining COVID-19 vaccination and sudden death in younger individuals. It has been widely shared because it appears reassuring. The conclusion: no evidence that COVID-19 vaccines increase the risk of sudden cardiac death in healthy young adults.

At face value, that sounds like the end of the discussion. For me, it is the beginning. When a study gives a clean answer to a complex biological problem, it is worth going back into the data to see what has been simplified.

The Finding That Should Have Been the Focus

When I looked at the baseline characteristics, one detail immediately stood out. Individuals who had a recent COVID-19 infection within 90 days were more than twice as likely to be in the group that died compared to those who survived.

This is not a subtle difference. This is a strong signal. And yet, it is not the headline.

Instead, it is adjusted for, controlled, and moved into the background so that the primary question — whether vaccination alone is associated with sudden death — can be answered. But that approach assumes something I do not believe reflects reality.

Abdel-Qadir, Husam, et al. “Association between COVID-19 vaccination and sudden death in apparently healthy younger individuals: A population-based case-control study.” PLoS medicine 23.3 (2026): e1004924.

The study treats vaccination and infection as separate variables. Statistically, that is standard. Biologically, it is incomplete.

We are no longer dealing with a population that has experienced a single exposure. We are dealing with individuals who have been immune primed through vaccination or prior infection, and then repeatedly exposed to the virus. The relevant question is not whether vaccination or infection independently increases risk. It is what happens when they occur in sequence.

The COVID Storm

This is what I have been describing for some time as a “COVID storm.” A subgroup of individuals who have experienced immune priming followed by further infection. In that context, the immune response may not behave in a predictable or balanced way. It may become dysregulated. In the heart, this could manifest as inflammation, altered metabolic function, or electrical instability — and in some individuals, that may translate into clinically significant events.

A Pattern That Doesn’t Sit Comfortably

There is another signal in the study that reinforces this concern. Individuals who received only one dose of vaccination appear less “protected” than those who received multiple doses. That is not a straightforward biological gradient. It is a divergence. And divergence usually means the groups are not the same.

Some individuals continue with further doses. Others stop. In clinical medicine, when someone stops after an initial exposure, it is rarely random. It often reflects intolerance, early symptoms, or a different underlying physiology.

The Question That Wasn’t Asked

What I would have wanted to see in this study is simple. Of the individuals who had a recent infection and then died, what proportion were vaccinated? How many doses had they received? What was the time interval between their last exposure and infection?

That is where the answer is likely to be found. If there is a higher-risk subgroup, it will not sit neatly in “vaccinated” or “unvaccinated.” It will sit in the interaction between exposure and response over time.

We are seeing rising patterns across multiple cardiovascular conditions since 2020 — arrhythmias, heart failure, thrombotic disease, inflammatory cardiac conditions. This is not confined to one diagnosis.

To dismiss these patterns without fully interrogating the underlying mechanisms is not good enough. This is not about ideology. It is not about being pro or anti any intervention. It is about understanding risk properly.

A Lesson From History

I often think about how long it took for the link between smoking and disease to be fully accepted. There were studies that created doubt, arguments about confounding, calls for more data. For decades, uncertainty was enough to delay clarity.

That does not mean the conclusions today are wrong. But it does mean we should be cautious about assuming we already have the full picture.

The conclusion of this study may well be correct in its narrow framing. Vaccination alone may not increase the risk of sudden cardiac death in healthy young individuals. But that is not the full question.

The more important question is this: what is the risk in individuals who are immune primed and then experience a recent infection?

Until that is answered, we are simplifying a complex biological system into variables that are easier to analyse — but not necessarily accurate to reality.

Final Thought

This has never been about proving that one factor is responsible. It has always been about recognising that we may be dealing with a new pattern of disease — one that emerges not from a single exposure, but from the interaction of exposures over time.

If we continue to analyse these events in isolation, we will miss it. And if we miss it, we cannot manage it.

That is the risk we should be paying attention to.

https://open.substack.com/pub/philipmcmillan/p/the-covid-vax-signal-they-didnt-follow

This source article is filled with medical terminology related to the immune system and for most of us would need to be studied in conjunction with a medical dictionary in order to understand it.

A lay person summary of it (thanks to Grok) is that:

• 1. mRNA COVID vaccines work differently from some other types (like certain DNA-based ones mentioned for comparison). After several doses, especially boosters, they can cause the body’s antibody response to change in a specific way—shifting toward antibodies that mainly block the virus from entering cells but are less good at rallying other parts of the immune system to actively destroy infected cells and clear the infection.
• 2. This change means the protection from infection isn’t as strong or complete as what you get right after the first doses or from natural infection. The antibodies still help stop the virus to some degree, but the overall immune defense against catching or spreading the virus may weaken over time with repeated shots.
• 3. Regular antibody blood tests that doctors usually do won’t show this change. Those tests just measure overall antibody levels against the virus spike protein—they don’t reveal how the “style” of those antibodies has shifted or how well they activate the full immune attack. Special, harder-to-get lab tests are needed to spot it.
• 4. Giving boosters too close together makes this immune shift more likely and stronger. When shots are spaced out (like waiting a full year or more), the body has time to reset, and the unwanted change is less pronounced or may even reverse.
• 5. Kids can experience this shift after fewer doses than adults (sometimes just the initial two shots in studies of children). Since children generally have a very low risk of serious COVID illness, any potential downside from this altered immune response could matter more for them than for older or higher-risk adults (where calming down overactive inflammation might actually be helpful in some cases).

https://open.substack.com/pub/rwmalonemd/p/igg4-class-switching-immune-tolerance

For the first time, a former U.S. state funeral directors association president publicly acknowledges the white fibrous clots: “They’ve been the size of the arteries.”

Since 2021, reports of unusual white fibrous clots discovered during embalming have been dismissed as anecdotal or attributed to fringe voices within the profession. That dismissal is no longer credible. The phenomenon is now being confirmed by senior leadership across multiple funeral director and embalmer associations—individuals with decades of experience and responsibility for representing thousands of professionals.

Continue:  https://open.substack.com/pub/petermcculloughmd/p/breaking-former-president-of-the

Continually breaking new ground in integrative and functional medicine, Ann Louise is a top nutritionist who was years before current trends like Paleo and Keto. She is internationally recognized as a pioneer in dietary, longevity, environmental, and women’s health issues. She is an award-winning New York Times bestselling author of over 35 books on health and nutrition including diet, detox, women’s health, men’s health, perimenopause, menopause, beauty and the environment. Described by Self Magazine as one of the Top Ten Notable Nutritionists in the United States, thousands of nutritionists, health coaches, and practitioners have benefited from her work.

Ann Louise Gittleman Website

Meet Ann Louise

About this episode:
In this enlightening conversation, the First Lady of Nutrition sits down with Dr. Ana Maria Mihalcea, board-certified internal medicine physician and award-winning author. Over the past several years, Dr. Mihalcea has been examining the blood of patients suffering from mysterious, unexplained symptoms including long-haul COVID, using dark-field microscopy. She says she has yet to see a truly normal blood sample since the onset of COVID. What she’s observing is raising important questions. In this discussion, she explains how dark-field microscopy differs from traditional blood testing and why it can reveal patterns that standard lab work may miss, including blood clumping, strange self-assembling particles, and other abnormalities that may help explain persistent symptoms. Ann Louise and Dr. Mihalcea also explore possible contributing factors and why some people who never contracted COVID or received the vaccine may show similar findings. They also discuss emerging approaches being explored to support recovery—including EDTA therapy, nattokinase, methylene blue, DMSO, grounding, and more. If you’re someone who is struggling with unexplained symptoms—particularly after COVID infection—this thought-provoking conversation offers insights you won’t want to miss.

Interview: https://open.substack.com/pub/anamihalceamdphd/p/the-covid-effect-when-the-blood-does

Jeff Berwick calls this the most important and probably the most terrifying video he has put out in years. It has nothing to do with nukes, and everything to do with the ticking time bomb in your body – EVEN IF YOU DIDN’T GET THE CLOT SHOT! Don’t miss this one if you want to know the antidote to survive the transhumanist revolution without becoming a hackable human robot.

Click to view the video: https://odysee.com/@DollarVigilante:b/Dr.-Ana-Milhacea-VIDEO-1080p:d

The Spike Protein appears to induce massive release of iron from Ferritin, damaging the microvasculature much like after mini strokes.

I would like to discuss an additional mechanism of microvascular damage today that the Spike Protein may induce. This mechanism can also help to explain the neurological symptoms of Long COVID – and why it resembles post stroke conditions. This mechanism starts with – the Endothelium. Brain endothelial cells contain high amounts of Ferritin.

Iron mediates endothelial cell damage and blood-brain barrier opening in the hippocampus after transient forebrain ischemia in rats
https://pmc.ncbi.nlm.nih.gov/articles/PMC3047193/

SARS-CoV-2 Spike Protein Induces Time-Dependent and Brain-Region-Specific Alterations in Ferroptosis Markers: A Preliminary Study in K18-hACE2 Mice
https://pmc.ncbi.nlm.nih.gov/articles/PMC12897609/

Serum Ferritin Levels Are Associated with Vascular Damage in Patients with Nonalcoholic Fatty Liver Disease.
https://ashpublications.org/blood/article/114/22/5098/77164/Serum-Ferritin-Levels-Are-Associated-with-Vascular

Serum ferritin level during hospitalization is associated with Brain Fog after COVID-19 https://www.nature.com/articles/s41598-023-40011-0

Finish reading: https://open.substack.com/pub/wmcresearch/p/the-spike-protein-ferritin-and-long

If you got multiple COVID-19 booster shots, something happened to your immune system that your doctor probably never mentioned, and that your post-vaccination blood test almost certainly cannot detect.

A growing body of peer-reviewed research published between 2023 and 2025 documents that repeated mRNA boosting causes a progressive shift in the type of antibody your immune system produces against the virus. This shift is not random noise. It follows a well-understood biological pattern. And it has measurable, functional consequences.

This article explains what that shift is, what it means, who it matters most for, and what should be done about it. No prior immunology background is required.

https://open.substack.com/pub/rwmalonemd/p/what-your-covid-booster-did-to-your

The Spike Protein appears to induce massive release of iron from Ferritin, damaging the microvasculature much like after mini strokes.

I would like to discuss an additional mechanism of microvascular damage today that the Spike Protein may induce. This mechanism can also help to explain the neurological symptoms of Long COVID – and why it resembles post stroke conditions. This mechanism starts with – the Endothelium. Brain endothelial cells contain high amounts of Ferritin.

Iron mediates endothelial cell damage and blood-brain barrier opening in the hippocampus after transient forebrain ischemia in rats
https://pmc.ncbi.nlm.nih.gov/articles/PMC3047193/

SARS-CoV-2 Spike Protein Induces Time-Dependent and Brain-Region-Specific Alterations in Ferroptosis Markers: A Preliminary Study in K18-hACE2 Mice
https://pmc.ncbi.nlm.nih.gov/articles/PMC12897609/

Serum Ferritin Levels Are Associated with Vascular Damage in Patients with Nonalcoholic Fatty Liver Disease.
https://ashpublications.org/blood/article/114/22/5098/77164/Serum-Ferritin-Levels-Are-Associated-with-Vascular

Serum ferritin level during hospitalization is associated with Brain Fog after COVID-19 https://www.nature.com/articles/s41598-023-40011-0

Finish reading: https://open.substack.com/pub/wmcresearch/p/the-spike-protein-ferritin-and-long