Dissolving Amyloid Fibrils After mRNA Vaccination
I recently came across a post on X about a child whose mother had received 2 doses of the Pfizer mRNA COVID-19 vaccine while pregnant, and now the child, who is 3 years old, has amyloid‑like clumps/microclots in their blood. Here’s the post (embedded below), for anyone interested in learning more, OR you can read the full case study from Kevin W. McCairn Ph.D.’s Substack.
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Amyloids are clumps of proteins that have mis‑folded into rigid β‑sheet “stacked” structures; they don’t dissolve easily and can accumulate in tissues or blood, disrupting normal cell function and blood flow. Because their presence is linked to degenerative conditions such as Alzheimer’s, systemic organ amyloidosis, and micro‑clotting, finding amyloid material in infants signals an abnormal inflammatory or coagulation process at a critical stage of development, raising concerns about impaired oxygen delivery, neurodevelopment, and long‑term organ health.
What Do The Clinical Trials Say?
In the clinical trials for the Pfizer-BioNTech COVID-19 vaccine, women were cautioned that they should not get pregnant and pregnant women were actually supposed to be excluded from the trials. Despite this warning, 270 women did get pregnant after being included in the trials.
In Pfizer’s report, they state that for 238 of the 270 pregnancies “no outcome was provided.” So basically, they only documented the outcome of 32 pregnancies reported out of the 270 total.
In those 32 pregnancies, there were:
23 spontaneous abortions
2 spontaneous abortions with intra-uterine death
So, 25 of the 32 pregnancies with known outcomes resulted in a miscarriage, a rate of 78%. Miscarriage typically occurs in only 12-15% of pregnancies.
2 premature births with neonatal death
1 spontaneous abortion with neonatal death
1 normal outcome
So, basically of the 32 pregnancies they knew the outcome of, 87.5% of them resulted in the death of the fetus or neonate. Hiding this data and choosing to not alert the world to what they found, is criminal. Credit to Pierre Kory MD for his breakdown of these documents on his substack back in 2022.
After emergency use authorization was approved, pregnant women were told that these vaccines were “safe & effective” by their pharma-funded doctors, elected officials and mainstream news. Oh, and Pfizer tried to hide the data from the public (and evidence of their criminality) for these trials for 75 years.
Since the rollout of these vaccines, and also after COVID came on the scene in 2020, we have seen a drastic drop in birth rates in all western nations around the world, and we are finding spike proteins in reproductive organs, and really all over the body, months after vaccination. It really makes me wonder if the birth rate drop was a result of this experimental injection.
Anecdotally, I personally know several people who had a severe adverse reaction to either Moderna or Pfizer’s mRNA vaccine. I also know of 2 women who delivered still-born babies around 2022, when these shots were first being pushed on pregnant mothers.
Below is an excellent video from Dr John Campbell, however he does not discuss the data found in Pfizer’s trials like Dr Pierre Kory did, but mainly focuses on the lack of data overall for pregnant women in these trials. Like me, he is amazed that mRNA injections are still being marketed as safe for pregnant women, and even recommended by health authorities.
Back to Our Case Study Child
Circling back to the case study of the 3-year-old child, even though this single case is anecdotal and un‑replicated, the implications of this case are horrific. I could not find any mention of testing or monitoring done on these babies that were exposed to this treatment in utero, and we know that even with the adults who volunteered to be in the study, they were not monitored for all that long afterwards. We also have heard reports that the trials were often unblinded or that there was no control group. So we really don’t know how widespread the effects could be and what the lives of these children will end up looking like.
Those who have been following this issue will know that this is not the first instance of observed clotting disorders, strokes, and other cardiovascular issues post mRNA vaccination. This product seems to have been drastically misrepresented from the ground up. I feel that the victims deserve some accountability from the people who allowed this to happen.
“Let food be thy medicine.” — Hippocrates
On a lighter note, I now will get into some of the supplements, herbs and lifestyle changes that seem more promising. My regular readers will know that my first approach to healing health issues in my house is to look at what foods and herbal medicines can be added to support healing.
Keep in mind that, since the mRNA platform itself, and subsequent injuries are very new and mainstream, pharma-funded news has largely been covering it up (by calling it “long-covid”) or censoring information altogether, this area of medicine has had very little study.
I am confident as more awareness develops in this space and more people turn to first-hand sources for their information—medical or otherwise, and we will see more helpful nutritional or herbal-based adjunctive therapies emerge that support healing from these injuries.
Other Recent Research Related to the mRNA Platform
The Yale Post-Vaccine Syndrome study (2025) identified circulating spike protein in symptomatic individuals up to 700 days post-vaccination.
Yonker et al. (2023) detected spike protein in serum and exosomes of adolescents weeks to months post-injection.
Swingle et al. (2023) demonstrated delivery of mRNA to the placenta in vivo using ionizable lipid nanoparticles.
Safford et al. (2024) showed that elasticity-tuned lipid nanoparticles enhanced biodistribution to the maternal-fetal interface.
McCairn, Ph.D. et al. (2025) documented Cadaver "Calamari" Amyloidogenic Fibrin Aggregates and Spike Protein Pathology from Cadavers Exposed to Bioengineered SARS-CoV-2
Can diet or supplements really “dissolve” amyloid plaques?
The structural similarities between amyloid plaques from Alzheimer’s patients and those injured by the mRNA platform should be provoking science to try out different adjuctives to see if there is a similar benefit for mRNA injury victims. Alzheimer’s plaques are made from Aβ‑peptide, whereas the infant case report shows fibrils in fibrin(ogen)–spike‑protein micro‑clots. The proteins, diameter, twist and staining can look quite different under the microscope, but they are both broadly referred to as “amyloid” and may respond similarly to therapeutics. Unfortunately, until direct studies are published on vaccine‑ or infection‑related micro‑clots, we have to treat all interventions as experimental and monitor outcomes carefully.
As always, this information is provided for educational purposes only and does not constitute medical advice. Please use common sense and consult with your healthcare provider before you try anything you see online.
Below is a summary of several natural compounds with at least some peer‑reviewed evidence (cell → animal → early human) for destabilising or enzymatically digesting amyloid material. And for parents out there, the fourth column shows which strategies already look reasonably child‑friendly at food‑level or physiologic doses. Again, this is not medical advice, please consult with your child’s healthcare provider before trying anything you see online.
| Compound (🌱 = kid‑friendly at food levels) | What the research shows | Typical adult supportive dose* | Pediatric note |
|---|---|---|---|
| 🌱 Curcumin (turmeric) | Binds Aβ, blocks aggregation; plaque shrinkage in transgenic mice and small human PET pilot study | 0.5 – 4 g/day with fat or piperine | Trials up to 4 g/day for 8 weeks in children (IBD) showed good safety |
| EGCG (green‑tea catechin) | Remodels Aβ into non‑toxic forms; broad anti‑amyloid activity study | 200 – 600 mg/day extract | Tea is fine; avoid > 300 mg/day extract in kids due to rare liver‑injury risk |
| 🌱 DHA (omega‑3) | Lowers blood Aβ and plaque load in animal & early human trials review | 1 – 2 g/day combined DHA + EPA | Essential for neuro‑development; prenatal & infant studies show no serious harms |
| Nicotinamide (vitamin B3) | Reduces APP/presenilin expression in mice; human tau‑targeted trial underway study | 0.5 – 1.5 g/day (divided) | Only RDA levels studied in children; megadoses untested |
| 🌱 Melatonin | Enhances Aβ clearance; cognitive benefit in rodent AD models study | 0.5 – 5 mg at bedtime | Short‑term use (0.5–3 mg) generally well‑tolerated in children |
| Nattokinase | Degrades fibrin/amyloid micro‑clots in vitro; long‑COVID pilot work planned preprint | 2 000 – 4 000 FU/day, empty stomach | Potent blood‑thinner; not recommended under 18 yr without specialist care |
| Lumbrokinase | Earthworm‑derived enzyme mix; clinical micro‑clot trial recruiting trial | 20 – 40 mg/day | Pediatric safety unknown—research use only |
| Serrapeptase | Rat data show fibrin‑amyloid digestion; decades of use in Japan for clot lysis study | 10 – 60 mg/day, empty stomach | No pediatric trials; theoretical bleeding risk |
*Doses reflect ranges used in published studies or common clinical practice; they are not recommendations of what you should take. This information is provided for educational purposes only. I am a researcher, not a doctor.
Sources from the table above:
Curcumin — pubmed.ncbi.nlm.nih.gov
Melatonin — pubmed.ncbi.nlm.nih.gov
DHA — pubmed.ncbi.nlm.nih.gov
Nattokinase — biorxiv.org
Lumbrokinase — polybio.org
Nicotinamide pubmed.ncbi.nlm.nih.gov
EGCG— pubmed.ncbi.nlm.nih.gov
Serrapeptase —pubmed.ncbi.nlm.nih.gov
Comparing Alzheimer’s Amyloids to Post-mRNA Amyloids
You can click on each image for the source and more information about each.
Alzheimer’s Amyloids in brain tissue
Alzheimer’s Amyloids
Post-mRNA Amyloid found in circulating blood
Post-mRNA Amyloid
Alzheimer’s vs mRNA Microclots
A notable difference between amyloids from Alzheimer’s patients and amyloids from post-mRNA exposure (aside from their visual shape, as shown above) is that they are composed of different types of proteins. Also, Alzheimer’s amyloids are found in the brain, whereas mRNA microclots are found circulating in the bloodstream. Because of these differences, it may end up that the approach to treating these two conditions is not at all similar. Like I said earlier on in the article, this is still a developing area of research and we don’t know for sure if these therapies will work for mRNA clots like they do for Alzheimer’s.
Practical Take‑Aways
Again, I am providing this information for educational purposes only. By including dose information I am not, in any way, representing that I think you should try these, especially without consulting with your healthcare provider. I am only reporting on what the current research is saying. That said, here is what I would start with if I had taken the mRNA vaccines.
Test for Microclots - there are a few tests available online, but this is really kind of an unverified/rare test. I only found 2 places that really look like they are offering a real blood test and both are a bit expensive. 1: https://labs.mygotodoc.com/products/microclot-test 2: (possibly only available in Europe) https://apheresiscenter.eu/microclots-test
If these tests are unaccessible for some reason, I don’t know that you necessarily need them, though they would be nice to track progress.
Start with food and lifestyle changes that double as plaque‑fighters
Oily fish or algae‑based DHA (300–500 mg/day for toddlers upward)
Turmeric in meals (¼ tsp ≈ 200 mg curcuminoids)
Solid sleep hygiene—if needed, sleep supportive herbs, or melatonin may be indicated (though I don’t love melatonin because it can be habit-forming).
Reserve the clot‑breaking enzymes (nattokinase, lumbrokinase, serrapeptase) for formal clinical oversight. They can thin blood and are largely untested in children.
Track labs if you go beyond dietary levels. Baseline liver enzymes (for high‑dose polyphenols) and coagulation markers (for proteolytic enzymes) help spot rare adverse effects early.
Remember the evidence is still early‑stage. Most trials referenced here are looking at Alzheimer’s brains or lab‑grown fibrils—not infant blood anomalies linked to maternal vaccination in live humans. Treat anything more than a culinary spice or standard fish‑oil dose as an experiment and keep your pediatrician or other healthcare provider in the loop.
Final Thoughts
While headlines about amyloid “micro‑clots” in post‑COVID or vaccine contexts have ignited public curiosity, the peer‑reviewed science still points to slow‑and‑steady, lifestyle‑first interventions—omega‑3s, anti‑inflammatory spices, and good sleep—as the safest starting point, which pretty much everyone can do, including young children. Targeted supplements and enzymatic clot‑breakers are definitely looking promising but are probably best explored under professional guidance until larger human studies confirm both efficacy and safety.
We are just at the beginning of seeing the harms of this new mRNA platform. I am hopeful we can learn how to undo the damage that has been done to so many.
