Hi everyone!
I thought I would post this summery I wrote down for my clients to try and concisely communicate why the strategy for working on vaccine damage varies with TKM and why it matters.

This is all just my opinion, please feel free to look any of it up yourself.

The first thing to consider is there are many different technologies we call vaccines that are not all the same thing.
Here’s an overview.

Live attenuated vaccines
Measles, mumps, rubella (MMR combined vaccine)
Rotavirus
Smallpox
Chickenpox
Yellow fever

Inactivated viral vaccines
Hepatitis A
Flu (shot only)
Polio (shot only)
Rabies

Subunit, recombinant, polysaccharide, and conjugate vaccines
Hib (Haemophilus influenzae type b) disease
Hepatitis B
HPV (Human papillomavirus)
Whooping cough (part of the DTaP combined vaccine)
Pneumococcal disease
Meningococcal disease
Shingles

Toxoid vaccines
Diphtheria
Tetanus

Messenger RNA (mRNA) vaccines and viral vector vaccines

Let’s talk about Live attenuated vaccines first.
These vaccines are a product of a process called serial passaging in a lab environment.
Serial passage is the process of growing bacteria or a virus in iterations. For instance, a virus may be grown in one environment, and then a portion of that virus population can be removed and put into a new environment. This process is repeated with as many stages as desired, and then the final product is studied, often in comparison with the original virus. If it is more pathogenic it is said to be “gain of function” and if it becomes less pathogenic it becomes a candidate for vaccine research.

There is significant risk of becoming ill from the pathogen using these types of vaccines, especially if taken through injection and not orally, they are quite hard on the immune system and even conventionally there are populations that shouldn’t take them (immunocompromised people and the elderly)
TKM wise the priorities are straight forward. Support the immune and lymphatic systems. E.S.15, E.S. 3, Mediator, E.S. 26, Spleen, are all good starting options.

Next, we’re going to talk about a bunch of different categories that are similar.
Inactivated vaccines use the killed version of the germ that causes a disease.
Inactivated vaccines usually don’t provide protection that’s as strong as live vaccines. So, one needs doses over time (booster shots) to get ongoing immunity against diseases.
Subunit, recombinant, polysaccharide, and conjugate vaccines use specific pieces of the germ—like its protein, sugar, or capsid (a casing around the germ).
Because these vaccines use only specific pieces of the germ one would need booster shots to get any kind of ongoing immunity.
Toxoid vaccines use a toxin (harmful product) made by the germ that causes a disease. They create immunity to the parts of the germ that cause a disease instead of the germ itself. That means the immune response is targeted to the toxin instead of the whole germ.
Like the other types of vaccines, we’ve been going over one would need booster shots to get ongoing protection against diseases.

ALL these vaccines require the use of an adjuvant for the vaccine to work
An adjuvant is an ingredient used in these vaccines that helps create a stronger immune response in people receiving the vaccine.
There are many different adjuvants used, generally they are toxic substances (notably often aluminum salts) that cause the bodies immune system to respond to the content of the vaccine, they are not targeted however and also cause the immune system to start responding to anything and everything ubiquitous in the environment (I.E. Foods, pollens, clothing fibers, cleaning chemicals, ANYTHING a person is being exposed to regularly during their vaccine schedule)
The amount of adjuvant exposure is responsible for a lot of harm, especially how many adjuvant-based vaccines are recommended for children.
With these types of vaccine complications, the priorities for these vaccines are more complicated than a live attenuated vaccine as the adjuvant needs to be flushed out of the body so detox becomes extremely important in addition to supporting the immune system.
A few good places to start with TKM, E.S. 22, Palming Calves, Bladder sequence, Large Intestine sequence, 5,6,7,8 combo sequence.
I am convinced that these adjuvants are responsible for a lot of allergies and sensitivities that many suffer from childhood and are a large toxic burden on our society.

Messenger RNA (mRNA) vaccines and viral vector vaccines
These vaccines are not a vaccine at all. They are derived from a gene therapy platform based on CRISPR technology, this uses a nano lipid to deliver modified RNA into the genetic material of the body post injection (especially cells that are very electrically active like the heart brain and reproductive system.) one of the modifications to this RNA was the substitution of Pseudouridine for uracil. Pseudouridine stabilizes the mRNA and attempts to force the cells to produce what the vaccine is trying to accomplish (in the case of covid-19, production of spike protein) even worse than that, pseudouridine is not just specific to the covid-19 affected gene sequences which means it can cause any other genetic mutations ones cells are going through to stabilize and become more permanent. (99% of which are very detrimental, and the body would discard as an unhelpful genetic mutation.) on top of that these nano lipids have no targeting mechanism and can adhere to many different types of tissue depending on the electrical attraction forces of the tissue.
TKM wise it’s very important that we attend to the DNA/RNA that could be affected. 6th stratum is primarily responsible for our genome so we would include E.S. 26, 24,26 combo sequence, Median Sequence, Diaphragm, Umbilicus and Third MOC sequences.

Thanks for taking the time to read this, I hope it was helpful! It’s a complicated topic to try and summarize, please feel free to drop your questions in the comments!

PS. If you have been doing the TKM daily suggestions by new years day we will have addressed everything covered in this summary!

Merry Christmas!
-Evan