Dangers beyond the spike protein,

… antibodies that result in autoimmunity

Medicine is finally admitting that the spike proteins created by the mRNA in covid shots are pathogenic. Once they are secreted by the cells that make them, they will attach to cellular receptors on normal body tissues. This creates an immune response whereby immune cells will destroy those normal body tissues, creating pathology. This is going to be highly variable from person to person depending on how many spike proteins are made, and what tissues they attach to. In some cases, the spike protein production will continue due to the manmade n1-methylpseudouridines added to the mix, allowing the mRNA to persist, continuously coding for spike proteins to be made. In some people, this results in what is called “long covid”.

There are safe and inexpensive ways to combat spike protein production. First, degrade the spike protein so it won’t attach to receptors. This can be done by consuming nattokinase, bromelain, and curcumin as per the McCollough Protocol. Second, try to prevent the attachment by adding more polyphenols to the diet, or using ivermectin or nicotine to compete with receptors. Third, try to interfere with spike protein production with vitamin C.

The important question is, why would the FDA and CDC continue to push this product, knowing this will happen? The answer is, they want antibodies to be produced. That’s really the goal of any shot called a vaccine… create antibodies. And that’s what they look for to determine if the shot is effective. Surely you must know that any foreign protein you inject into the human body will result in antibody production… that’s what the immune system does. But consider the biological consequences of doing this.

There is only one type of immune cell in your body that will make antibodies, and that is the B-cell. B-cells are unique from all other immune cells because they can immediately react to a foreign protein that was either injected or released from cells that were instructed to make it from injected mRNA. No other immune cells can immediately react to free floating foreign proteins. They can only react to smaller proteins that are shown to them by APCs (antigen presenting cells). Our bodies were designed to work that way so that unsafe antibodies that attach to normal body proteins will not get made. This is why it usually takes two weeks for antibodies to show up in serum: Your immune system is working in harmony to produce safe antibodies that will not create autoimmune issues.

Here's the problem. Some people will make so many proteins that their B-cells will auto-activate and make antibodies against those proteins. What are those proteins that are getting made? They’re supposed to be “the spike proteins”, but we now know (years later) that due to the n1-methylpseuduridines in the mRNA, there can be partial protein production, and these also get released into the bloodstream. The potential for these unknown proteins to resemble normal body proteins, and have B-cells create unsafe antibodies against normal body tissue is real. Then, those B-cells will become memory B-cells that you will have sitting in your bone marrow and lymphoid organs for the rest of your life. The next time they’re called into action, you will get more unsafe antibody production, potentially creating autoimmune conditions like rheumatoid arthritis, lupus, type-1 diabetes, multiple sclerosis, and ulcerative colitis.

How do you combat that? By unsafe and expensive procedures involving therapeutic B-cell reduction, plasmapheresis to remove antibodies, immunosuppressive drugs, or biologics that try to modulate the autoimmune response. Or don’t subject yourself or your loved ones to mRNA injections, because the dangers will be the same, regardless of what protein they tell you it’s supposed to make.

Thanks for reading, and thanks for staying smart.