DECENTRALIZED MEDICINE #18: JAB RECOVERY PATHWAYS

Sunlight stimulates T lymphocytes in the skin through a mechanism separate from vitamin D production. Sunlight energizes T cells, which play a central role in human immunity.  T cells, whether helper or killer types of lymphocytes, need to move to do their work, which is to get to the site of an infection and orchestrate a response. The study below shows that sunlight directly activates critical immune cells by increasing their movement.  How do they move?  Light in the sun creates H2O2, which makes cells move.  This shows that free radical signaling has a positive connotation, not a negative one.  This is a magnetochemical signal in the sun's light.  

T cells possess intrinsic sensitivity to blue and UV light. Solar light detection is coupled to the generation of H2O2 and activation of Src kinase and PLC-γ1, leading to elevated intracellular [Ca2+]. Non-visual photosensitivity is greater in activated T cells and enhances T-cell motility. 

The majority of T lymphocytes are found in our skin. NK cells come from T lymphocytes. NK cells are cytotoxic lymphocytes that have drawn considerable attention recently as a promising tool for immunotherapy in patients with various refractory hematological malignancies and metastatic solid tumors. I have a sense that the SV40 promotor inactivates T cell motility in turbo cancer formation.  

Why?  Only a partial response has been shown in centralized clinical results of experimental protocols, attributed mainly to the relatively low number of NK cells infused and their short in vivo persistence. A significant challenge, therefore, in advancing the clinical applicability of NK cells is to expand ex vivo NK cells that display increased functionality upon in vivo infusion. Different combinations of cytokines have been studied to induce NK cell expansion. Sunlight, with fasting, increases NAD+ in cells and is active during the leptin-melanocortin pathway.  This might be critical for jabbed patients to avoid oncogenesis due to the presence of 60 billion copies of the SV40 promoter per jab.

SV40 Ori’s normally need T antigen to replicate. This is true unless they have ColE1 and F1 origins, as seen in the Pfizer vaccine.

I also think CBD oil needs to be studied in those who took the jab based on Kevin McKernan's work and our results with people who used it during COVID-19.

WHY?

A lesson on the quantum biology of photosynthesis.

Did you know that we get a 40% higher yield of cannabis plants at 1200 ppm CO2?

Currently, the biosphere is starved of CO2 at 420 ppm.

The architects of our vaccine bioweapons program support lowering CO2 further.

They also want to block the sun, which would keep CO2 emissions lowered.

Might that be because Cannabis and nicotine were an antidote to the designs they employ? Did you know King Charles just announced a plan to ban nicotine products in the UK by 2030? Do you think he knows something?

Cannabis split from Humulus lupulus (hops) 24M years ago.

Why is its photosynthesis optimized for 1200ppm CO2?

ANSWER: It is because of the effect of deuterium on water. Plants grown in D(2)O show a decreased tendency to fractionate carbon-13 during photosynthetic incorporation of carbon dioxide. The isotopic ratio C(13)/C(12) of the tissues of deuterated plants appears to be proportional to the deuterium content of the tissue. This effect was found in specimens of the partially deuterated vascular plant Nicotiana tabacum, cannabis, and in cultures of the fully deuterated alga Chlorella vulgaris.

Another trick BigHarma plays is using an aluminum adjuvant, which allows you to camouflage all the DNA in your shot. Why? Aluminium is a perfect atomic reflector of UV light biophotons, so it blocks the optical signaling from DNA to the ribosomes and mtDNA to stimulate protein translation. This has a massive effect on POMC translation as a dopant contaminant.

When Gardasil was first approved in 2006, Merck assured the FDA in the USA that there was no HPV DNA in the vaccine. However, this was challenged in 2011 when Sin Hang Lee found HPV DNA in a young, sexually naive girl who had never been exposed to the virus but had received Gardasil. This was due to the atomic effects of contaminant atoms. They ruin the semiconductor of cells and destroy optical signaling, making disease generation more likely.

In 2011, the FDA admitted residual DNA in the vaccine but said it was "expected" to be in products manufactured using recombinant technology and that Gardasil posed "no risk to vaccine recipients."

The FDA claimed that the presence of DNA fragments was not a problem without showing any studies to prove it had been investigated or that it was safe for humans.

Is there a risk that residual DNA fragments in Gardasil can enter host cells and integrate into the genome? I believe there is now good evidence that this is the case. All one needs is a "transfection agent," and some studies suggest adjuvants in vaccines can act as transfection agents.

In 1985, the FDA set an upper limit of 10 picograms per dose. In 1987, the WHO increased its recommended limit to 100 picograms and then again to 10 nanograms (i.e., 100 times higher)—a limit now adopted by the FDA.

The paper pictured above argues that it’s difficult to quantify the levels in Gardasil jab, though. HPV DNA is tightly bound to the aluminum adjuvant (AAHS) and forms an insoluble precipitate, which gives it incredible substantivity in a cell and makes genomic intercalation more likely.

Most genomic experts can easily detect the HPV L1 gene DNA in the insoluble precipitate and the soluble DNA in the solution using nested PCR with Sanger sequencing for confirmation.

Genomics expert Kevin McKernan, the first to discover residual DNA in Pfizer’s COVID-19 vaccine, taught me this lesson during our collaborations. He agrees with Dr. Lee's papers above that the FDA’s permissible limit of 10 nanograms is futile because it increases the cancer risk for the compliant.

Kevin has repeatedly pointed out on his X page that the trick the FDA plays with the guidelines is when you ask scientists to measure the residual DNA, you’ll miss most of the DNA because it is all bound up to the aluminum adjuvant. This is why they add Aluminum to the jab to hide the contamination. This is why one should never comply with any jab. All jabs carry this risk now.

The 10-nanogram limit they've created is just smoke and mirrors because they have legal protection now. They say if it’s below that, then they don’t care, but here you have something that hides the DNA in aluminum, and they whistle past the graveyard of patients who took their shots.

Aluminum is one problem, but now mRNA vaccines are known to have 55 different atoms present and SV40 promoters, all of which can perform this task. I also believe mRNA technology in food will pose this EXACT risk to jabbed people.

SUMMARY

I have spoken with Dr. Alexis Cowan about how sunlight, specifically UV light, operates the wiring diagram of the mitochondria. You can find that here.  It essentially shuts it down while increasing skin T lymphocytes to become NK to hunt for cancer cells—people who took the jab need to upregulate their own NK T lymphocyte production. Sunlight with UV light appears to be the best way to do this. It should be the key option discussed with patients to avoid oncogenesis. 

In decentralized medical research, researchers interested in using exogenous nicotinamide (NAM) supplements to help the jabbed should be considered in those who took jabs known to have the SV40 promotor.  I plan on discussing this further with Nicole Shanahan soon after the election.  We need this study for those who complied and took the jab without knowing their risks. The slide below shows why I think 24/7 exposure to daily 380 nm light is the best plan for the jabbed. It directly helps metabolism, but it actually repairs the circadian clock gene dysfunction—the jabs also CAUSE circadian disruption.

What things in the future can be tested for jabbed to help them avoid disease?

NAM is a form of Vitamin B3 and a potent inhibitor of enzymes that use NAD+ for their activity. Hence, NAM might be directly involved in controlling redox-sensitive enzymes, mitochondrial functions, cell metabolism, energy production, and cell motility.  The studies done on NAM by Josh Rabinowitz and Charles Brenner have not been kind to NAM or their analogs, but in post-jabbed patients, the results may be quite different, and I believe this should be studied.  

My perspective on chronic disease creation caused by the jabs is a different perspective for disease modeling than exists today in centralized science. It is far more coherent and discernible to understand when you examine the simplicity of the idea.

Biologic information from the environment must have a connection to its source in cells; that source is mtDNA. The mtDNA then makes a wireless connection using light to the sun and Earth, which is paramount for wellness. Only then can the data from nature remain reliable and pliable for life's uses through all these physical laws I have given you over 15 years.

Only living things sense and seem to know about their connection to "ex-formation" by the mechanisms built into how mitochondria can feel our connection to Mother Nature. That connection is hard-wired into every cell by its mitochondrial genome and copied and pasted into the maternal germ line of all the genomes of life.

In this way, mothers must remain connected to nature to pass information on accurately. The disease can manifest in children when mothers do this. The child does not need to sense this to get a disease because all mitochondrial DNA comes from our maternal line. This is childhood cancer, depression, and suicides have been on the rise since 1900. No one sees what I see, but they will because of what happened with COVID jabs. This is why the jab architects now weaponize the Means siblings on media. They want to rewrite jab history like Bernays taught the Industrial-military complex.

Mitochondria with high heteroplasmy should never be connected with an excellent nuclear genome if one wants to stay healthy. This is obvious during pregnancy when making a child, as decentralized 16 explains. Leptin resistance in a mother is a sign of avoiding pregnancy; it blocks fecundity. It is also why infertility rates are skyrocketing in the Western world, where technology use is rising, ala MKULTA/Brain Health Initiative. The kids born to these parents are now facing mitochondrial diseases like cancer, diabetes, depression, and suicide at unparalleled rates.  

This is akin to putting an Apple computer into a Windows server. Putting insufficient data from mitochondrial DNA into nuclear genomes that are not coherent leads to all disease categories. That is, conditions of existence and natural selection are working in order. They are the Ying and Yang of epigenetics. 

Centralized science of vaccination and light use is now genetically engineering changes to the mitochondrial DNA using excessive blue light and nnEMF to expand their distance, ruining our cell's data processing ability. In this sense, our modern civilization is genetically engineering us to extinction, and the biological information cells continue to receive will get more and more misunderstood until the genome responds with nonsense code. Nonsense code = Chronic disease illness.

The best example of nuclear genome nonsense coding = is cancer. This is how the expansion of the cytochrome proteins over time can lead our cells to oncogenic change. The implication: Might mutations in mitochondria be needed and required from an evolutionary perspective to get us to change what we are doing to remain healthy? Yes, that is my answer. Thus, the most helpful answer for life today is to stay in direct contact with its "ex-formation" to avoid this situation where the disease has to warn us to change our environment. This is why wild animals migrate. They are in tune with nature because they are appropriately connected to the sun and Earth. They do not live indoors as a man does and take BigHarma jabs. The light that regenerates you is the answer. It is never food first unless you are working for the opposition. When you know better, you simply do better.

THE TAKE AWAY: 

Electrons are like glue to light as words are to their meaning. Electrons can catch terrestrial sunlight, like words, and capture meaning to create the world we experience. We need sunlight to produce NK killer cells after SV-induced cancers. We can only hope that our words can capture what we mean, but we know they can't possibly capture that much joy, grief, or wonder.......or can they? I've been telling you ALL for some time to spend less time with food gurus like Calley and Cassie Means and way more time with bio-physics because that is where the treasure is buried. I believe the Means siblings are nefarious in this game as well.

Those are the globalists who are all in on the global vaccination plan I warned about in the Danny Jones podcast.

EXPLAIN centralized PEER REVIEW link to the MOSSAD and the US Federal government LIKE YOU ARE THIRD GRADE

I'll repeat it… “Peer review” is a method used in centralized science to strip you of individual medical sovereignty.

If you outsource your thinking to centralized experts who are controlled by the BigHarma Gutenberg printing press, you will wind up being chronically wallet-biopsied by the industrial healthcare complex. Do you understand the game yet?

Go to minute 3:33:00

https://open.spotify.com/episode/3F72MA1NwSDgmDOG1X7x15

Remember that the PEER review is run by dual passport holder (UK/Israel) Robert Maxwell. His daughter is in jail protecting the Zionist Federation guys and the Royal Family. Maxwell was a primary actor in the MEGA Group. She worked for Epstein, and the MEGA Group employed Epstein.

Epstein has ties to Israeli intelligence and well-documented ties to influential Israeli politicians and the Mega Group. Those guys are layered links to the MOSSAD and Meyer Lansky.

Ronald Lauder, a cosmetic heir who makes billions blocking women from the sun, is a Mega Group member. He has known Trump for close to 60 years because they are both Wharton Alumni in Pennsylvania. He is a former member of the Reagan administration and a long-time donor to Israeli Prime Minister Benjamin Netanyahu. He is very influential in Israel’s Likud Party. He was a long-time friend of lawyer Roy Cohn. Robert Kennedy Sr. was Cohn's assistant to Senator Joe McCarthy in the 1950s during Eisenhower's administration. Cohn's father ran B'nai B'rith as its President. Roy Cohn was one of the first group of Americans who received the Salk vaccine, and he died of AIDS in 1986. Sadly, no one ever checked him for SV40, but if I were in power, I think I'd look at his remains and sample them for SV40.

Lansky and his friends in MEGA lured Cohn to NYC to work for the accounts of MURDER Inc in 1954 and 1955, Cohn reportedly had deep connections in the 1950-80s to Ira Malnick.

Lansky worked on cryptography from 1969 to 1983. That work linked art sales and money laundering through the IRS and Treasury via infiltration of the Executive branch. This work created the PROMIS software program. It was stolen in a bankruptcy conspiracy by the DOJ and Industrial military complex corporations, Wackenhut. This program allowed Lansky and his associates to follow the Fed, Treasury, and IRS's actions while also monitoring Israel's financial movements. This gave Lansky data on all their financial interactions to see how well their programmable money project was progressing. I covered this here: https://kruselongevitycenter.com/djonesqapublic

This code in this software had dual use that allowed the US and Israeli governments to launder money for their intelligence arms. It also allowed Lansky and his syndicate to stay ahead of his partners in the Industrial-military complex by following where money was being moved. This software was critical in setting up the money laundering schemes from cartel smuggling and set the stage for the Iran Contra money laundering schemes that linked the MOSSAD to the Executive Branch. It also linked the drug trade into Mena, Arkansas, where John Gotti and the governor made sure that the project operated undisturbed.

These are the people I think Calley and Casey Means are working for.

CITES

1. https://www.nature.com/articles/srep39479

2.  https://journals.asm.org/doi/10.1128/jvi.68.2.787-796.1994

3. https://anandamide.substack.com/p/sv40-origin-of-replication-in-mammalian