☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 Profile picture
I am a neurosurgeon on a mission to create health from disease by decentralized thinking & BTC! Bitcoin pleb decade club in exile https://t.co/W4I1WtqhJY

Dec 8, 2024, 18 tweets

Photosynthesis uses visible light to separate water.  To effectively utilize visible light for water splitting, the typical band gap of the semiconductor should lie within the range of 2.0 to 3.0 eV.

Visible light covers the range of approximately 390-700 nm, or 1.8-3.1 eV.

So to help those who are GMO organisms post plasmid intercalation we can use a strategy to raise the band gap to augment the lack of mtDNA power they have due to the dramatic loss of redox and then we can use high intensity pulsed light to help lower the burden of damage to the DNA.

I think this is the path that the jab injured will find success based on my work. Now to convince people in bioengineering to start new lines of research to build machines the GMO humans now need. 5-6 billion people need these services.

2. I've been looking hard at the anti parasite drugs and have found some interesting quantum effects I had not seen before.

Right now in our time, repurposed drugs are being suppressed to favor the mRNA platform of the DoD and BigHarma. The decentralized patient needs to know this and do their own due diligence.

3. Because of what I posted before on band gaps and paramagnetism.......if you have a turbo cancer and you have exposure to SV40 the first line treatment should be Ivermectin and maybe add Fenbendazole. I believe the reason why has to do with a magnetic change that these drugs seem to induce to operate.

Dr. Makis has put out some good info on this combo and virally induced cancers. He has not talked about the quantum biology of either drug. I got interesting in Ivermectin because of COVID and it link to a 2012 paper on HIV. HIV, like turnbo cancers, I believe are linked to the SV40 promoter effect. This paper made big waves in the HIV and Dengue communities but barely a ripple in the COVID story. pmc.ncbi.nlm.nih.gov/articles/PMC33…

4. We will never see clinical studies because Ivermectin for turbo cancer, HIV, or Dengue because it is off patent and cheap. Merck, which used to have a patent on Ivermectin, has partnered with Moderna on mRNA Cancer Vaccines, estimated with a massive development cost 400,000 per treatment. Since this is a fixed cost no one will want to study a repurchased drug that does a better job. So the incentive is built in to not study IVERMECTIN on anything when the DoD and BigHarma are pushing expansion of the mRNA platform. For this reason everyone who has been diagnosed with a turbo cancer, Dengue, even HIV should speak to a decentralized MD to consider these options before you agree to any expensive centralized option first.

5. Currently the old debate in the gay community about Fauci's death squads using AZT has subsided due to the use of protease inhibotors for HIV. Protease inhibitors work well for HIV so one has to discuss this with patients during informed consent discussions.

6. In the podcast I did with Danny Jones I shared a slide and story about a Pancreatic cnacer patient to show that decentralized clinicians have a duty to patients who are told to go home and die by the centralized paradigm. I specifically told Calley Means this story because his Mom was one of those patients and he and his sister did not seem to know about any alternative options for a patient diagnosed with a stage 4 Pancreatic cancer in 13 days. I share a slide with them on the podcast that should have gotten them all to think more carefully than any words found in the book they wrote. Ironically their PR people tell the world that this situation their mom was in caused them to write a book about food for a metabolic disease. This was a bad assumption on their part.

Ivermectin studies on mice in cancer include: Pancreatic cancer, Breast cancer, Colon cancer, glioblastoma, glioma and leukemia. I have not seen IVERMECTIN studies on Lymphoma, Testicular Cancer, Sarcomas but that does not mean one should not consider it.

7. IVERMECTIN acts on Cancer mainly by inhibiting signaling pathways involved in cancer proliferation (Akt, Wnt, mTOR) and by inhibiting CANCER STEM CELLS.

More good news with this drug: it’s practically impossible to overdose on ivermectin, as it has a half-life of 18 hours and it’s cleared from your body within 2 days. Fenbendazole was discovered completely accidentally. It was back in 2017, a gentleman in Oklahoma, Joe Tippens, a gentleman in the 60s, I believe, was diagnosed with terminal cancer, Stage 4 small cell lung cancer, and he was sent home to die by his doctors, and he had a veterinary friend of his who said, “Listen, there’s a dog medicine, dog dewormer medicine, that was discovered accidentally to have very strong anti-cancer properties. Why don’t you try it? You have nothing to lose.” And he put together a protocol with this fenbendazole medicine and also with curcumin, CBD oil, vitamin E, and he cured his terminal cancer, that he had basically less than 1% chance of surviving. And so that was back in 2017, and so this has been known for a few years, now. There is a Facebook group called the Fenbendazole Cancer Support Group. It has a hundred and ten thousand members. A lot of them are cancer patients, a lot of some of them are family members of cancer patients, so this is a large community, and it works. In fact, there was a group of Stanford University medical researchers who were so impressed by fenbendazole that they found three patients who had taken fenbendazole, Stage 4 cancer patients, who took fenbendazole, cured their Stage 4 cancers after they had failed every chemotherapy regimen known to mankind, and they published this case series. Now what’s funny is that they were not able to recommend fenbendazole to these patients, because it’s not FDA-approved.

Now, there is an FDA-approved version of it called “mebendazole”, which is virtually identical. Unfortunately, it goes by the brand name of “Vermox”. It’s much more expensive than fenbendazole, but you can now get generic versions of both for, you know, a dollar a pill. Dr. Makis has posted this picture many times on X before.

8. The fact that Ivermectin is a KNOWN broad-spectrum antiviral by not only Fauci but the entire global pharmaceutical industry tells us in no uncertain terms that Ivermectin should have been IMMEDIATELY looked to as a possible treatment and prevention of any authentic and non-weaponized viral outbreak, but that its continued suppression and vilification points to habitual capital-level criminality predating the SV40 laden CoronaScam by decades, namely Fauci’s “Death by AZT” scam, and the WHO’s Dengvaxia crime in the Philippines, where criminal charges were filed.

9. I believe these drugs have novel mechanisms not yet studied by centralized forces and that is why they work. I call this electromagnetic chemogenetics. The drugs induce charge changes to endogenous proteins in humans. These charge changes activate proteins like ferritin that can be targeted to specific organelles like mitochondria in many failing cell types to rescue them from demise.

Using repurposed drugs with high therapeutic indices for chemogenetic action induce mitochondrial and biochemical changes that take several seconds to activate cells.

Ivermectin has been studied and has been shown to be was associated with reduced inflammatory markers (C-Reactive
Protein, d-dimer and ferritin and faster viral clearance by PCR. Ferritin is the key player here. Why? Ferritin makes cells more sensitive to RF and magnetic fields in cells. In fact, increases in ferritin in mice, have been shown to increase their blood glucose powerfully by itself. This is what blue light does to animals as well.
jeffreydachmd.com/wp-content/upl…

10. Few people know that human ferritin has a paramagnetic area buried with in it. If you have been reading my blogs where I hacked the periodic table you would already know why this is a big deal. Well in people with turbo cancers or HIV linked to SV40 intercalation it might be a huge big deal for a reversal.

In 2016, Ali Güler’s lab at the University of Virginia found a new technique, that is not only non-invasive, but can also activate neurons rapidly and reversibly using magnetic fields and charge variation. I have a sense this is how Ivermectin & Fenbendazole are operating in human turbo cancers. youtube.com/watch?v=iHTpJN…

11. If you can limit the effect of ferritin you can make cells less sensitive to calcium influxes that are associated with turbo cancer initiations.

12. Why is this important. It is built on earlier work published in the literature that no one has followed upon. this is the kind of science that I hope @NicoleShanahan and @dralexisjazmyn look deeply into if Nicole decides to start and fund Alexis's new decentralized lab. As a jab injured patient, Nicole should be incentived by this.

Several earlier studies have shown that nerve cell proteins which are activated by heat and mechanical pressure can be genetically engineered so that they become sensitive to radio waves and magnetic fields, by attaching them to an iron-storing protein called ferritin, or to inorganic paramagnetic particles. These methods represented an important advance in our understanding of cell biology but there are has been little to no follow thru – Just how promising was this data? For example, already this technique has been used to regulate blood glucose levels in mice – but involve multiple components which have to be introduced separately. I mentioned this to Calley Means and told him this is why his belief that pancreatic cancer is a metabolic disease only is horribly flawed. It is an electromagnetic disease at is biological core and explains why someone with SV40 in their genome can be a stage 4 cancer patient in two weeks if they are in the wrong magnetic environment that leads to massive calcium influx in mitochondria. He just had a blank stare when I mentioned it to him.

This 2016 technique built on earlier work, around a protein called TRPV4, which is sensitive to both temperature and stretching forces. These stimuli open its central pore (shown in the You Tube video), allowing electrical current to flow through the cell membrane; this evokes nervous impulses that travel into the spinal cord and then up to the brain.

Ali Güler and his colleagues reasoned that magnetic torque caused rotating forces like we see in the F0 head of the ATPAse and it might activate TRPV4 by tugging open its central pore allowing stray electricity to enter the CNS and PNS. This has huge implications for GBM and ALS as well but no one has studied it.

Moreover, they used genetic engineering to fuse the protein to the paramagnetic region of ferritin, together with short DNA sequences that signal cells to transport proteins to the nerve cell membrane and insert them into it. @Kevin_McKernan would probably find this interesting considering what the mRNA jabs are built around.

13. What did these 2016 experiments teach me?

We may have the ability to treat many diseases we are impotent to deal now like Parkinsons disease, ALS, and mRNA collateral damage. WHY?

This lab found that application of a magnetic field, (like your cell phone, fitbit, or chronic glucose monitor emits) can activate an altered ferritin or TRPV1 protein, as evidenced by transient increases in calcium ion concentration within the cells, which were detected with a fluorescence microscope.

In 2016, the researchers inserted the Magneto DNA sequence into the genome of a virus, together with the gene encoding green fluorescent protein, and regulatory DNA sequences that cause the construct to be expressed only in specified types of neurons. They then injected the virus into the brains of mice, targeting the entorhinal cortex, and dissected the animals’ brains to identify the cells that emitted green fluorescence. THEY DID. Using microelectrodes, they then showed that applying a magnetic field to the brain slices activated the magnetically altered protein so that the cells produce nervous impulses (action potentials).

This paper proved how screens and light can cause cancer because light contains magnetic energy. Nobody seems to know it but me. Now you do too.

To determine whether the altered magnetic protein or ferritin can be used to manipulate neuronal activity in live animals, they injected the magnetic altered protein into zebrafish larvae, targeting neurons in the trunk and tail that normally control an escape response. They then placed the zebrafish larvae into a specially-built magnetized aquarium, and found that exposure to a magnetic field induced coiling maneuvres similar to those that occur during the escape response. This was the video you saw above. This experiment involved a total of nine zebrafish larvae, and subsequent analyses revealed that each larva contained about 5 neurons expressing the altered magnetic protein.

14. Why did I mention Parkinson's above?

In one final experiment, the researchers injected the magnetically altered protein into the striatum of freely behaving mice, a deep brain structure containing dopamine-producing neurons that are involved in reward and motivation, and then placed the animals into an apparatus split into magnetised a non-magnetized sections.

Mice expressing the magnetically altered protein spent far more time in the magnetized areas than mice that did not, because activation of the protein caused the striatal neurons expressing it to release dopamine, so that the mice found being in those areas rewarding.

This means that magnetic environments control dopamine levels and dopamine levels can be induced and reduced using electromagnetic signals. I mentioned this to @jonesdanny in our first podcast and his head exploded when I told him just light alone can be used to induce behavior the government wanted in MKULTRA. this paper is what described what the CIA/NSA/DoD found out about blue light in the 1970s.

This shows that magentically altered proteins by a charged environment can remotely control the firing of neurons deep within the brain, and also control complex behaviors. It is not conspiracy theory when there is published research on it and associated patents. END OF LESSON.

15 @threadreaderapp make a thread

16. So many do not know why infection/sepsis and tech abuse are linked. Some of us do and we teach our clients why it happens. It seems that hospitals, DoD, ICU MDs should consider removing WiFi & blue screens from ICUs and ORs to manage infections. Adding in DDW and PBM units would also be wise. europepmc.org/article/PMC/68…

17. No Politician, healthcare bureaucrat, or Federal agency, or lawyer has the right to deny anyone access to life saving medication. And if they do, they are committing a very serious crime.

@threadreaderapp make a thread.

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