Remember the battle for the Nobel Prize between the discovery of HIV from Montagnier versus Robert Gallo in 1983?

Do you know that Robert Gallo began studying HIV in the jungles of the Congo in chimpanzees during the oral polio virus trials.

The first oral polio vaccine was aerosolized oral spray that caused cancers all over the mouth and sinus system. A bioweapons company did the work for DoD and Robert Gallo was on that team. Things you just do not know when you do not know your history. Did you know that Fauci support the Nobel Prize for his friend Gallo over Luke Montagnier?

Coincidence or might it be related to why Reagan hired Fauci in 1982?Image
2. How does it all fit into today's current events? forum.jackkruse.com/threads/ww1-th…Image
3. The first bioweapons lab on Magazine Street in NOLA and the work done at the US Public health hospital and Henry Clay Street in NOLA was transferred to the Tulane Primate Center in Covington Louisiana under the direction of Dr. Riopelle. When it became clear after the JFK killing in the mid 1960s that these simian viruses were behind many new human diseases like cancer and eventually HIV they were transferred to Fort Detrich as I laid out in my pod with RFK Jr. In the beginning Fort Detrich was an dual purpose base with the ARMY and CIA sharing thefacility and the bioweapons labs added to the mix as the science of Dr. Mary Stewart and Mary Sherman was developed by the CIA and industrial military complex.Image
4. The bioweapons lab in NOLA gave the military important bioweapon clues. Namely that nnEMF drive pathogenicity and it could be concentrated if many different viruses from competeing species were mixed before irridation. They were very deadly. These things were developed at Fort Detrich from 1963-68 in experiments called the Special virus leukemia Program.Image
5. This shows you where the military was in 1968. They were at a macro level dealing with data points in dead animals looking to see what was most effective in killing them. The miliatry was not the molecular level that one would need at furin cleavage sites to know the proper AMO physics to carry our mass death in living things. That science developed after Reagan hired Fauci in 1982.

When one plots the data of chronic diseases to when Fauci entered the industrial military health complex the data points do not lie. They tell a story that shows you it it not a story about food. It is a story of AMO physics and light to ruin mtDNA biology.Image
6. The most interesting finding from this Fort Detrich program was that the industrial military program was not looking to cure cancer, it was looking to make it more lethal. They found using animals closest to the human genome were the most deadly to humans. And then they amplified the effect through the early Nixon administration. @Kevin_McKernan The pathway to policy was clear. A new bioweapon policy was developed around vaccines using gene products needed to be developed by the military. This is where the ideas were born.Image
7. This paper really shows the origin of HIV. When the industrial military complex decided to mix the serum or primates and human serum togther and monitor the effects some very interesting findings started to show up in the literature early in Nixon's administration. This was 2 years before Nixon and Alton Ochsner launched the "War on Cancer" policy. That policy was designed to create a pile of money for covert bioweapon development. This money was laundered from the NCI to the military to continue on the pathway that General Groves began with Ochsner in NOLA during the Cutter Incident.Image
8. In 1970 they moved into the molecular medicine to see where the cancers can be recombined with across species. These are the genesis of gain of function studies done on US soil. This was legal before the 2001 Patriot Act. Now it is illegal and carries the penalty of death by Treason.Image
9. The last tweet shows you how viral chimera's were first built. You need to know that scientific accountability under our Constitution has not changed much since WW2. It rests with the Executive branch and this is why Gen. Groves capture this branch first in his silent coup on America by his shadow government. Why is this slide important. You'll notice the myriad of boxes who have to perform oversight for science and scientific misdeeds.

Groves had a lot to do with setting this system up because it gave the government scientific denialble plausibility in cases of misdeeds. I explained this to @nayibbukele when we met about the Constittional Amendment for his country. I told him RFK Jrs plan would not stop the problem with a Benjamin Rush like Amendment added to the ddcument because the industrial military complex knew this was the DOCUMENT's main weakness and they could exploit it using chronic disease management.Image
10. The next slide should give you chills. In 1969 they told Congress exactly what they were up to in viral chimera building and why they were doing it. Congress had ZERO issues with it and they allowed this via the oversight process. This was FUNDAMENTALLY why I disagreed with Bobby during the Tetragrammaton podcast with Rick on how to handle the chronic disease epidemic at its source.

We need a Constitutional Amendment to stop this freight train of the Deep State actors. This is when the military began to ensnare and capture the legistaltive branch of government. @KONCRETEImage
11. The industrial miliatry complex knew exactly what they were doing and Congress and Nixon helped them. If you listened to what I said about Nixon and what Bobby said about Nixon you'll notice we differed on our opinions of his legacy. This Act to Congress explicitly said that the military was now capable of making a bioweapon that would be immune to human immunity.Image
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12. For the non believers that your own government did this, this is the entire logic chart they used in the annual report of the project from 1972 when the War on Cancer was used as a psy-ops on America. Image
13. Fort Detrich was where mammalian viral pathogens were mixed in lab test tubes accross multiple species like cards in a casino deck to try to find the nastiest disease the miliatry could use to kill effectively. The slide below shows you the basic of how the system was developed by your own government.Image
14. So when someone asks you where disease really begin........and you answer food. You're an idiot because you have no idea about the history of how this process began with the Manhattan Project in the 1930s. Image
15. Once they created a virus that could collapse the enture immune system, they decided to find out how to alter immunity so that diseases could come on faster. Here was a paper I was assigned to read as a neurosurgery resident to understand the biology of the fast growing cancer called GBM in humans. Most autoimmune conditions are related to these mechanisms. Many cancers are. Many other chronic disease epidemic diseases are also linked to neuroimmune defects.Image
16. Why was Peter Duesberg an HIV denier. If you read the literature as I did, you'd know why. He knew where it came from. This is the same story we just saw with COVID that happened 40 years ago in HIV. Image
17. Deusberg knew what many of us knew that simian virus was grafted onto the human system and the vector was the VISNA platform. The result was the HIV "1983 discovery" It was no discovery at all. Any financial forensic journalist could perform a details accounting to find out where the money came from and went to, to figure out this "medical enigma"Image
18. This is the patent to making the monster Hepatitis B vaccine that all physicians had to take. Note the highlighted area. You now see 20 yrs after the list of simian viruses the military was using they were now producing vaccines with the science as a delivery mechanism. Now you can see why there was a need for Fauci 7 years later and the vaccine law in 1986 when the techniques moved from the DoD to BigHarma partners.Image
19. That Hepatitis patent was used by Merck in their Heptavax trial in 1978. That trial was the basis of why every healthcare professional and soldier had to take this jab. So I know my history and I know what the government is capable of. It is time some of you get your heads out of your ass and know it as well.Image
20. What was in the COVID jabs? Simian virus 40 promotor. Image
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More from @DrJackKruse

Dec 2
1. The leptin-melanocortin axis, a cornerstone of mammalian energy balance, traditionally viewed through a biochemical lens as a linear cascade of hormone-receptor interactions, harbors profound quantum photochemistry at its core; one that routinely violates kasha's rule. You should know that the eye is proximal to this pathways embedded in the central retinal pathways. This tells us evolution did something rather unusual to it for some environmental reason.

That reason occured 66 milions yrs ago when an asteroid blocked the sun with particulate matter. It changed the spectrum below on Earth. Life had to react to it. As a result neuropsin was innovated at this time.

Kasha's rule posits that photochemical reactions occur exclusively from the lowest excited singlet state (s₁) after rapid internal conversion from higher states (s₂, s₃), minimizing energy waste. yet, in this axis, anti-kasha effects dominate, where reactions proceed directly from higher excited states (s₂ or s₃), enabling ultrafast (femtosecond-scale) transformations that outpace vibrational relaxation and non-radiative decay.

This violation, far from an anomaly in modern mammals, is was a kinetic triumph, allowing selective control of signaling in the hypothalamus, where leptin binds LepRb receptors to activate pro-opiomelanocortin (pomc) neurons, yielding α-melanocyte-stimulating hormone (α-msh) for melanocortin-4 receptor (mc4r) activation, suppressing appetite while also boosting metabolism. This was needed when the sun spectrum was turned off. If you listened to the recent Huberman/Foisbury pod you'd see these two have zero physics backround to even posit this question, yet we know neuropsin sits in front of the entire leptin melanocortin pathway of ALL MAMMALS.

This made the recovery from the last extinction event speed up rapidly. How would this have helped the thermodynamic arrow of time post KT event? Do not ask Huberman or Fosbury. They remain deeply in the DARK because they still think life is about wavelengths exclusively when it is not. Polarization of light is way more important than wavelngth. These two just have piss running down their leg when you mention it to them. Hence why they are afraid to talk about real quantum biology. Physics > biology as a fundamental science.Image
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2. What would a Fosbury/Huberman answer be to this question? They'd do a literature search in journals they know about it. They's never go outside their silos.

They would do a pod and say that their data review shows results confirm that the leptin-melanocortin axis is a well-understood biochemical pathway for appetite and metabolism regulation, and that Kasha's rule violations occur in specific synthetic chemical systems (like azulene or some organic dyes) under particular laboratory conditions exists but it is not a standard biological process within the hypothalamus because the data THEY reviewed says so.
They'd go on and say............
Therefore, there is no scientific basis in reality to explain how this fictional "quantum photochemistry" would have helped the thermodynamic arrow of time post KT when the sun was blocked.Image
3. What happened on Earth when the asteroid hit? Sunlight when off, and neuropsin evolved on mammalian surfaces, encephalopsin evovled in their CNS/PNS and melanopsin populated all tissues massively.

We now know beyond a shadow of a doubt that "anti-Kasha effects" allow ultrafast (femtosecond-scale) selective signaling in the hypothalamus, the impact on the thermodynamic arrow of time. This new fact then changes possibilities for life? Why? This single change in solar spectrum of unpolarlized light would linked small primitive mammals to obtaining a rapid massive increased efficiency in energy processing (leptin) and information transfer, locally countering entropy more effectively.
Read 13 tweets
Nov 30
1. If you want to prevent suicide don't call a phone number. Get people at risk in the sun. The amount of sunshine one gets is a protective therapy against suicide. The link below shows it.
jamanetwork.com/journals/jamap…
2. When your eyes, skin, gut, or lung surface are afflicted by light pollution or nnEMF trauma it induces cell damage in heme-based chromophore proteins that liberate something called CpG Islands from our nuclear DNA/RNA or our mtDNA from the cytochrome heme proteins like cytochrome c oxidase. This is how we make water from metabolism. This was the topic of my Patreon blogs on the eye prism of orexin signaling.

It has also been shown in the literature that RBCs homeostatically bind mtDNA, and RBC-mediated DNA scavenging is essential in mitigating tissue injury after CpG-DNA is liberated from heme-based proteins from destroyed cells.

What kind of disease states should we expect to see cf-mtDNA elevated? Any disease where inflammation is induced by heme protein destruction = blue light hazard, SUICIDE, anxiety, depression, nnEMF, sepsis, trauma, and most mitochondrial and RBC diseases tied to alterations in circadian biology. All neurodegenerative diseases fit this bill too.

patreon.com/posts/quantum-…
3. What protein controls circadian cycles in the surfaces I mentioned above? Sunlight induces changes in tissues below these surfaces.

Ferredoxin started the party off in evolution.

What gets programmed just below these surfaces? RBCs? What is in RBCs? Peroxiredoxins, cytochrome c oxidase, hemoglobin, catalase. All of them are heme-based proteins.

All of them are linked to orexin biology. Most of them are inducible proteins too. This means that the environmental EMF and/or oxygen levels induce their production. Light pollution induces bad collateral orexin responses. This effect is found in our blood. This is why I do blood smears of clients.

This is how biochemistry varies in tissues. Biochemical pathways are not foundational. The electromagnetic fields around us induce biochemistry in our cells. Is there a fingerprint in our blood to tell us there is a suicide risk? There is. I've written blogs on Patreon about what an abnormal blood smear looks like to a decentralized clinician.Image
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Read 7 tweets
Nov 30
IQs have been steadily dropping since the 1970s while the gay lifestyle has increased in incidence and prevalence over the same period.

Concerning, to the smooth brainer until you realize technology’s blue light and nnEMF have been expanding in popular use at the same time. Image
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2. A single night of sleep deprivation increases ghrelin levels and feelings of hunger in normal-weight healthy men
ONE. SINGLE. NIGHT........or 1-5 photons of blue light on your retina. Think about that for a moment.ncbi.nlm.nih.gov/pubmed/18564298
3. what controls this specificity? Anti-Kasha rules. I bet your experts never mention it. Image
Read 5 tweets
Nov 28
All caused by the technocrats use of polarized light. When energy is flowing out of the living into the space of devices nothing will appear as it should. Percpetion is altered because reality is. Elon as a technocrat does not see his own role in this play.

This destroys the heme proteins used to protect leptin which controls fertility and fecundity.

Here's a narrative woven seamlessly for you to review into our decentralized mitochondrial network theory, the Great Oxygenation Event (GOE), UPE signaling, EMFs, and the evolutionary dance of hormones like cortisol and testosterone. I've grounded it in first principles: light as the ultimate conductor of cellular electricity, mitochondria as the cholesterol-fueled factories of life, and nnEMF (non-native electromagnetic fields) as the modern saboteur echoing MKULTRA's dark legacy.

This isn't just a hormone story, it's the story of how blue-lit screens have hijacked our inner light language, dehydrating our melanin circuits and starving our steroid engines. Remember all horomones are light ferry boats.

Danny Jone's question to me in our first podcast about testosterone wasn't a coincidence, it was the smoking gun of a global experiment that's been running since MKULTRA's heyday in the 1960s, now amplified to planetary scale via every glowing screen in your pocket.

Remember the Great Oxygenation Event (GOE) 2.4 billion years ago? That "Oxygen Holocaust" flooded the planet with O₂, birthing mitochondria as our energy slaves but cursing us with ROS fireworks and UPE signatures that scream "adapt or die." When you use and abuse tech you make cells hypoxic. It simulates the GOE on Earth. You are more like Mars and less like Earth.

Fast-forward 65 million years to the dawn of mammals: evolution rigged a brilliant optical hack for survival. Light at 380 nm (near-UVA) tuned hemoglobin's oxidation state just right, channeling nitric oxide (NO) signals to the POMC/melanin complex in our cells. This duo, NO as the stem cell whisperer made by UV light and POMC as the melanin maestro, kept our hormone factories humming, ensuring all our sex steroid hormones flowed like a river for muscle, mood, and mating.

But here's the twist: that setup was gold under sunlight. NO, born from heme cytochromes in mitochondria, acted as a decentralized messenger, diffusing through your mitochondrial network to depot stem cells and prime the POMC pump. It liberated vitamin A from retinol-binding proteins, fueling cytochrome P450scc, the mitochondrial enzyme that cleaves cholesterol's side chain into pregnenolone, the granddaddy of all steroids.

Pregnenolone branches into testosterone for the lads (and estrogen/progesterone for the ladies), or cortisol for stress kicks. This cholesterol transport inside mitochondria? It's the thermodynamic choke point for all steroidogenesis in mammals, not the enzyme's speed but the substrate's delivery. ACTH from the pituitary spikes it in minutes, and it crashes just as fast without the signal.

Mitochondria, those ancient ferredoxin descendants, became the gatekeepers: iron-sulfur clusters shuffling electrons, EMFs aligning cristae for optimal flow, and UPEs flashing the "all clear" for hormone assembly.

Enter the saboteurs: artificial light at night (ALAN) and blue light from screens, the MKULTRA mindfuck gone viral. Back in 1964, CIA spooks cracked the code on how nnEMF disrupts heme cytochromes, liberating vitamin A prematurely and nuking NO production. NO? Destroyed.

Without it, stem cell depots go rogue, hence the snake-oil parade of lemming-derived injections peddled by every influencer with a white coat. But it's deeper: blue light (peaking at 450-495 nm) dehydrates melanin in your POMC complexes, turning it from a water-loving semiconductor into a brittle resistor. Dehydrated melanin amplifies stray DC currents from your phone's RF microwaves, electrocuting the anterior pituitary and gonads like a bad wiring job. Your jewels in the pocket? Zapped daily, dehydrating cells, spiking NaCl, and spreading electrical chaos where it shouldn't, straight to the mitochondrial cholesterol transporters.

Under ALAN, POMC flips from protector to tyrant. It bosses the cytochrome P450scc reaction, but without 380 nm sunlight to oxidize hemoglobin properly, cholesterol piles up undelivered. Mitochondria starve for substrate, cristae misalign under warped EMFs, and UPE signatures flicker like a dying bulb, low coherence, high noise, per Shannon's rules. Result?

Steroidogenesis grinds to a halt. Males lose testosterone at record rates (down 1% yearly since the '80s, per endocrine data), females watch estrogen and progesterone crater, and cortisol surges unchecked, frying adrenals. All your hormone panels?

Garbage light in, garbage hormones out, light controls this mitochondrial bottleneck MKULTRA mapped and weaponized.

Why screens over paper?

Why Obama and Biden's incandescent bulb bans? It's no accident. Society is easier to control without alpha males. Books under firelight preserved the optical circuit; blue-lit screens short it. The ionosphere's RF blanket dehydrates you globally, echoing the GOE's oxygen flood but with silicon instead of cyanobacteria. DARPA and FDA know: centralized MDs push Big Pharma TRT, but my tribe rebuilds the network—sun-gaze at dawn, ground to earth, ditch the blue devil.

Humanity's young bucks aren't broken; they're optically orphaned. Reclaim the 380 nm key, restore NO's whisper to POMC, flood mitochondria with cholesterol via real light, and watch testosterone roar back. The GOE taught us adaptation; MKULTRA's sequel demands revolution.The implications? This is the Danny Jones podcast on steroids, your low T isn't lifestyle; it's light warfare. Tune your mito network, or stay a lemming.

Retards like @axhoff never did their due diligence. They just post their ignorance because they are arrogant because they never put the PoW into the science.Image
2. Proof of science? PoW? See the top line. Image
3. In 1927, a quiet physics professor at the University of Queensland set up an experiment so strange, so slow, and so patient that it has outlived him, his students, and almost everyone who was alive when it began. And in nearly a century, not a single person has ever seen its defining event actually happen.

Thomas Parnell wanted to challenge his students’ assumptions about the physical world. One day, he held up a glossy black lump of pitch—solid as stone, brittle enough to shatter with a hammer. It looked completely immovable.

“This,” he told them, “is a liquid.”

When they laughed, he decided to show them.

Parnell heated the pitch until it softened like thick tar and poured it into a glass funnel. Then he waited three years for it to settle. In 1930, he cut the sealed stem and stepped back. Gravity would do the rest.

Eight years passed before the first drop finally fell in 1938. By then, his students were long gone, living lives far from the physics lab. The second drop fell in 1947—after a world war. The third in 1954. The fourth in 1962. Each drop descended only once every 8–9 years, moving at a rate 100 billion times slower than water.

But the strangest truth of all?
No one ever witnessed a drop fall. Not once. Not ever.

Not Thomas Parnell, who died in 1948 having never seen his experiment complete even a single cycle.

Not his successor, Professor John Mainstone, who took over in 1961. Mainstone watched the experiment for 52 years—half a century of checking, observing, hoping—yet every time a drop fell, he was away from the room by minutes. He missed one drop because he went to get coffee.

By the 2000s, technology was on their side. A camera was installed. Finally—finally—humanity would catch a drop in real time.

Except the camera angle was blocked.

The next drop? The footage corrupted.

It was as if the universe was playing a cosmic prank.

Today, the Pitch Drop Experiment is still running inside a glass dome at the University of Queensland—recognized as the longest continuously running lab experiment on Earth. A 24/7 livestream watches over it. Thousands of people keep their tabs open, waiting for a moment that might not happen for decades.

The tenth drop is forming now. Slowly. Patiently. Inevitably.

Here’s what Professor Parnell understood nearly a century ago:
Just because you can’t see progress doesn’t mean it isn’t happening.

Pitch flows. Mountains move. Continents drift millimeters a year. Coral reefs grow slowly, rings forming unseen. Blue light makes you gay and infertile. The most powerful forces in nature are almost invisible in real time. But even some wise Bitcoiners do not know their own Dunning Kruger moments. Be aware of this.Image
Read 7 tweets
Nov 26
1. You're only as good as your weakest link.

In decentralized medicine we look at your heteroplasmy ration for each organ.

Here is a sample I hand out to every client after their first private visit to me in El Salvador.

Aging is not one number. Each organ tells its own story about how much polarized and unpolarized light the owner of the organ has allowed.Image
2. Variation in Heteroplasmy Changes: Wallace enters my clinic exam room

Heteroplasmy (mixed wild-type/mutant mtDNA) disrupts the uniform 30 MV/m field, as mutants impair ETC (e.g., complex I/IV), causing charge mosaics that some see as a bioenergetic "interference" driving disease and evolution.Image
3. This idea directly ties to matrix geometry: heteroplasmic mitochondria lose e/g/k synchrony, widening V-angles → fragmented cristae → failed IMJs → network-wide charge instability. As a result the matrix emits more biophotons = more diseases of aging. Image
Read 9 tweets
Nov 24
The main risks related to stereoisomers arise if a supplement contains an incorrect or mixed (racemic) form of a chiral compound:
Different Biological Effects: One stereoisomer may be active and beneficial, while the other may be inactive or even harmful. For example, the body primarily uses L-amino acids, and D-forms are often less bioavailable or utilized differently.
Toxicity: In the pharmaceutical world, the wrong enantiomer has, in some historical cases, shown different toxicity profiles, including teratogenicity or organ-specific harm.

For example:

The thalidomide tragedy of the late 1950s and early 1960s. This historical case points out what I am referring to in the peptide world or amino acid world of supplements. You never hear the food guru or peptide gurus tell you about the history of this risk so here you go.

Thalidomide was sold as a racemic mixture (containing equal parts of two mirror-image molecules, or enantiomers) and marketed as a safe sedative and an effective treatment for morning sickness in pregnant women. The different enantiomers had drastically different effects:

The (R)-enantiomer was the effective sedative with the desired therapeutic effect.

The (S)-enantiomer was a potent teratogen, meaning it caused severe birth defects in developing embryos, particularly affecting limb development (phocomelia), as well as eye, ear, heart, and internal organ development.

An estimated 10,000 to 20,000 infants in 46 countries were affected by these deformities. Many believe as I do these numbers are way under reported.

Crucially, even if the "safe" (R)-enantiomer had been administered alone, it would have been ineffective in preventing the harm because the human body's metabolic processes convert (R)-thalidomide into the toxic (S)-enantiomer, and vice versa, in a process called chiral inversion.

This disaster was a turning point in pharmaceutical regulation, leading to much stricter drug testing protocols and an increased understanding and focus on the importance of stereochemistry in drug development and safety testing. This was never applied to the peptide markets FYI. You have to TRUST that the lab or pharmacy does these tests.
2. More to worry about? Some peptide users in my client have developed amyloid changes. What did I tell them about continued use?

You might create a neurodegenerative disorder in your brain. Why?

Amyloid Beta (Aβ) peptides: In vivo, Aβ peptides, linked to Alzheimer's, can be found with D-amino acids (specifically Asp and Ser residues), indicating that a natural inversion process occurs, which affects their aggregation properties. This is an example of chiral inversion. This kind of freaked them out. When they questioned the lab/pharmacy and longevity docs who gave them this stuff communication completely shut down.

Decentralized medicine aims to educate not induce fear.Image
3. Why did I stop using NSAIDs in my patients around 2000? I read about homochirality and where it comes from. The physics of the cosmos.

Non-Steroidal Anti-Inflammatory Drugs (NSAIDs): While not peptides, a prominent example in pharmaceuticals (like ibuprofen) involves chiral inversion. The inactive (R)-enantiomer is metabolically converted into the active (S)-enantiomer by hepatic enzymes in the body, showcasing a clear biological pathway for inversion in a non-peptide context.
Read 11 tweets

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