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Health Matters's avatar

The weak link that is not mentioned is vaccines. Those children coming from other countries, often rural...come to Canada or US...and forced into the toxic vaccine schedule. This is huge and nobody is asking or looking at the vaccines people with these diseases have been subjected to.

Vinu Arumugham #MAHA's avatar

"ASCA recognizes mannan, a fungal cell-wall glycan

Anti-OmpC and anti-CBir1 target outer membrane porin C from E. coli and commensal bacterial flagellin

Anti-glycan ALCA, ACCA, and AMCA target carbohydrate epitopes of fungal cell walls

None of them, the authors conclude, are autoantibodies in the classical sense."

Sorry, there seems to be a fundamental misunderstanding here. The human immune system is highly unlikely to directly attack self tissue due to self tolerance. Most autoimmunity is due to cross-reaction by the immune response directed at vaccine antigens that are similar to self antigens. Basically autoimmunity is anti-cancer defense. It works best against antigens that are slightly different from self (cancer neoantigens).

Cancer immunology, bioinformatics and chemokine evidence link vaccines contaminated with animal proteins to autoimmune disease: a detailed look at Crohn's disease and Vitiligo

https://zenodo.org/records/1407617

Why do we have an immune response against fungal antigens as you point out? Yeast protein contaminated HepB and HPV vaccines. Vaccines can also be contaminated with E. coli proteins and all injections involve the injection of skin commensal bacterial antigens at the injection site.

Lymeland's avatar

Thank you for including this paper, Vinu. Very helpful. Many are connecting Alpha Gal Syndrome (AGS) with vaccines as well, which makes a lot of sense since they prime the body to react later when exposed. The proof on tick transmission of AGS is sketchy at best, although tick bites can also serve as a trigger for a body that is already primed. The COVID gene therapy shot proved this pathogenic priming perfectly.

Health Matters's avatar

Thank you, exactly! I have no scientific background, just personal experience and after hearing Sasha talk about exactly what you mentioned above, it explains my immune system - it was killed by multiple vaccines as a child. The food issues of gluten, corn, milk, etc, the UC diagnosed at 30-- proteins in all in vaccines.

Vinu Arumugham #MAHA's avatar

Sorry to hear that. I went down this path because my son developed multiple life-threatening food allergies and the doctors had no answers.

Vaccines and Biologics injury table based on mechanistic evidence – Feb 2020 Covering over 125 conditions

https://zenodo.org/records/3647593

Health Matters's avatar

Thank you. I hope your son was helped by your research.

Thank you for the link you provided. I am now helping to take care of my 98 yr old Mom- injured by the 3 jabs my sibling took her to get- against our wishes. Dementia started soon afterwards. So sad.

Trent's avatar

Vinu can’t get a study peer reviewed. He lacks science literacy and has been wrong on every single point.

Trent's avatar

Vinu has no idea what he is talking about.

JimmyD's avatar

Terrain is better than the false germ theory!

Chemicals are not for human consumption.

Only good nutrition is needed!

Masaki Fujii's avatar

https://sashalatypova.substack.com/p/vaccine-induced-food-allergies-turning

According to Sasha Latipova, the polio vaccine increases the risk of Crohn's disease by 2.28 times and ulcerative colitis by 3.48 times in vaccinated children compared to unvaccinated children.

Dr. Coleen Boyle, Director of a research division within the CDC, concealed the following findings:

(1) The MMR vaccine (measles, mumps, and rubella) increases the risk of Crohn's disease by 3.01 times.

(2) The MMR vaccine increases the risk of ulcerative colitis by 2.53 times.

https://link.springer.com/article/10.1007/s12328-024-01926-x?fromPaywallRec=true

Ulcerative colitis can also be triggered by m1Ψ-mRNA vaccination.

Even if the mechanism is unknown, mathematically speaking, "correlation implies causation in terms of probability."

Statement by Dr. William Makis:

"I have a daughter taking TOFA (tofacitinib) for UC (ulcerative colitis).

Her baseline CRP level was 15, but it dropped to 11 by the fourth day.

She started taking Ivermectin, and now—48 days later—it has reached <0.5 [undetectable].

Ivermectin produces a unique anti-inflammatory response that TOFA cannot explain.

With TOFA alone, one would expect a reduction from baseline to 0.5 times the level.

This result is 0.05 times the level."

A book by Dr. Satoshi Omura, the discoverer and developer of Ivermectin, states that "Ivermectin exerts an anti-inflammatory effect via TLR4."

Dr Efevretis's avatar

Really clear breakdown, and the distinction you draw that the antibodies in IBD target microbial antigens rather than self-tissue is the part most write-ups flatten into "autoimmune" and lose.

It matters more than a technicality: if the immune system is reacting to the microbial community rather than the body, then the ~25% heritability isn't loading a gun aimed at the gut, it's setting how tolerant someone is of a shifting microbiome. That quietly moves the lever from the genome, which you can't touch, to the exposures you can.

John The Visionary's avatar

Water dilutes stomach acid literally causing IBD. Don't drink water with meals. Wait 30 minutes before eating after drinking water and up to 90 minutes after meals before drinking water. The rest is pure bullshit that detracts from diluted stomach acid. If you must drink with meals, drink acidic drinks like tomato, orange or apple juices.