William B. Risley, Jr., D.C.

3rd gen. (Palmer) chiropractic physician since 1997. Avid reader of the scientific literature. Consensus is not science.☀️🌘💦🧲

[William B. Risley, Jr., D.C. @risleydc]

In 4 months I’ve critically read ALL the studies that purportedly exonerate #vaccines from causing #ASD & I’m aghast at the (lack of) data. The lack of proper safety studies, true inert placebos, an #unvax group, & over reliance on epidemiological data prone to #confounding

[Rusty ⚡️: Solar Powered ☀️ @ze_rusty]

There’s a cell in your eye that has nothing to do with vision.

It’s called the Melanopsin retinal ganglion cell.

Its job is to measure light and tell your brain what time it is.

Peak sensitivity: 480nm

That's the exact blue your laptop screen and every LED bulb puts out.

Those cells wire straight to the SCN, your master clock, sitting right above where your optic nerves cross.

A burst of 480 nm light hits your retina.

Your brain reads it as daytime.

Every clock in your body adjusts accordingly.

Now imagine that signal arriving at 11:30 PM

Your biology gets a midday message in the middle of the night.

Melatonin production is delayed.

Cortisol stays elevated longer than it should.

You feel exhausted.

But your brain hasn’t been told it’s nighttime yet.

So you end up lying in bed

"TIRED but WIRED"

[Tyler Lawton Ph.D. @tylerlawtonphd]

Science has known about the role that light plays in biology for a long time. This book was published in 1979 and details the scientific data of how light entering our eyes controls

- the pineal gland and melatonin
- growth and development
- body temperature
- kidney function
- red and white blood cell counts
- metabolic function
- thyroid function
- sexual function
- pituitary function

The eyes are the windows to the soul. Block the light and you block one of the most substantial regulators or our biology and health. Wearing sunglasses, seeing glasses, or contacts and sitting in building or cars behind windows filters and blocks vital signals to our brains and disrupts the system. This is not new.

The Influence of Ocular Light Perception on Metabolism in Man and in Animal has a free PDF online: https://t.co/MUIdqsh1lR…

[Dr. Ammous @AmmousMD]

Mitochondria originated from free-living bacteria.

Antibiotics can therefore impair mitochondrial function and our ability to generate energy.

Only use antibiotics when absolutely necessary.

[Roger Seheult, MD @RogerSeheult]

🚨🚨🚨🚨Today the U.S. House passed the Sunshine Protection Act, advancing legislation that would make Daylight Saving Time permanent nationwide.

This is the biggest legislative step this issue has taken in years but it is not law.

The bill now moves to the U.S. Senate, where there is still an opportunity for it to be debated, amended, or rejected. If you care about health and circadian biology, this is the time to speak up.

The scientific case against permanent DST has become increasingly strong:

• Morning light is the most powerful signal for synchronizing the human circadian clock.
• Permanent DST delays sunrise for much of the year, especially in winter, reducing exposure to morning light when our brains need it most.
• Later sunrises are associated with chronic circadian misalignment, sleep loss, poorer mood, reduced alertness, and increased cardiometabolic risk.
• Studies comparing western versus eastern portions of time zones consistently show worse health outcomes where people experience later sunrises despite sharing the same clock time.
• The American Academy of Sleep Medicine and numerous sleep and circadian experts recommend permanent Standard Time, not permanent DST, as the option that best aligns with human biology.

The argument for permanent DST is largely one of convenience and preference for lighter evenings. The argument for permanent Standard Time is one of physiology and public health.

If you believe our laws should reflect the best available scientific evidence, now is the time to respectfully contact your U.S. Senators. Tell them that while ending the twice-yearly clock changes is a worthy goal, permanent Daylight Saving Time is not the healthiest solution. Ask them instead to support permanent Standard Time, which preserves the morning light our circadian system depends on.

Please REPOST this. The Senate has not yet voted, and informed voices can still make a difference.

@LeaderJohnThune is the Senate majority leader that will determine when this legislation comes to the Senate for debate. He should know how you feel.

[William B. Risley, Jr., D.C. @risleydc]

@AmmousMD Paul Masons’ talk on lectins nails it: https://t.co/MabpxENdXV

[William B. Risley, Jr., D.C. @risleydc]

@MaryBowdenMD Been doing Epley and other CRP's for 30 years. I see about 1-2 cases a week in-office. Simple and effective treatment...I get referrals from two Neuro's, NP's, and an ENT. Lets just say I've got plastic liners on my garbage cans for a reason. https://t.co/ZaLL21bhp8

[William B. Risley, Jr., D.C. @risleydc]

It's sad that SAD is happening in high sun places... It's even more sad that these experts dance around the true cause: It's not from a lack of socialization as we all huddle around air conditioning in AZ. It's from a lack of full-spectrum sunlight exposure. Seasonal Affective Disorder is a lack of UV light not activating the POMC gene and our endogenous opiate production. Nature designed you to be addicted to the sun. https://t.co/GH3TNRUEdl @AmmousMD @DrJackKruse @MaxGulhaneMD @zaidkdahhaj

[FOX 10 Phoenix @FOX10Phoenix]

Extreme summer heat is causing seasonal depression as Arizona residents are forced indoors. FOX 10's Taylor Wirtz spoke with an expert, and has more on how the ways summer can take a toll on people's mental health. https://t.co/q23xx9hUX3

[Ethical Skeptic ☀ @EthicalSkeptic]

🚨Cancer Continues its Rise🚨

🔸154,300 excess deaths to date (signals start of a potential 40-year "horror curve")

🔸Inflected exactly with the largest date of mRNA vaccine uptake (panel 1)

🔸Is corroborated by PPI-Neolplasm in Constant-$ (panel 2)

🔸Is corroborated by the 2023 CDC SEER data (demarked on panel 2)

🔸Is corroborated by an alarming uptick in new (younger) cancer patient web chatter (panel 3)

🔸Is arriving in younger ages and in more aggressive forms (panels 3 and 4)

Do NOT let angry trolls lie to you - they are silent on the topic now - take notice of this warning flag of dishonesty.

Our models are proving out in spades.

[Dr. Ammous @AmmousMD]

The benefits of sunlight go far beyond vitamin D:

• Vitamin D (UVB): Bone & immune health
• Nitric oxide (UVA): Vasodilation & lower blood pressure
• Alpha-MSH: Pigmentation, appetite regulation & inflammation control
• Beta-endorphin: Mood & natural pain relief
• Dopamine: Circadian timing, focus & retinal function
• Serotonin → Melatonin: Mood by day, sleep & antioxidant defense at night
• Melanin: Light harvesting, mitochondrial function & redox balance
• Infrared light: Structured (EZ) water, tissue repair & mitochondrial signaling
• Circadian clock genes: Synchronizes metabolism & hormone release
• Cortisol rhythm: Healthy morning cortisol, lower evening cortisol
• Leptin signaling: Supports energy balance & satiety
• Thyroid function: Optimizes metabolism through circadian entrainment
• Mitochondria: Improves redox state & resilience to environmental stress
• Immune system: Helps regulate inflammatory responses

Sunlight is far more than a source of vitamin D, it's the primary environmental signal that coordinates human biology.

[Ethical Skeptic ☀ @EthicalSkeptic]

Good News and Bad News

First the good news... Covid mortality is almost non-existent, with a CFR far below even the common cold. Down 90% from two years ago.

Now the bad news... Cancer weekly EXCESS Mortality is 75 x the rate of all Covid Mortality.

We are paying the piper - and this goes on for decades...

[Dr. Ammous @AmmousMD]

In bones, there's a fine balance between:

-The anabolic, building up, strengthening phase
And
The catabolic, breaking down, cleaning dead cell phase

Loss of circadian rhythm from blue light, EMFs, lack of sunlight shifts that balance heavily towards catabolic side
→ Osteoarthritis

[☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 @DrJackKruse]

When you add atomic mass to the base chain through bad food, supplements, ideas, peptides, exercise, jobs, light, lack of grounding, living in the wrong state you get a hip replacement.

I have both my hips I emerge from the vagina from. I plan to keep it that way too. I might have too much atomic mass in my adipocytes, but thankfully that is not where my colony of mitochondria matters most.

My ideas inbiophysics masterfully targeted the core illusion of centralized orthopedics that Sisson sells you. The "wear and tear" model of osteoarthritis (OA) is a mechanical fairy tale told to protect a multi-billion-dollar joint-replacement pipeline.

Joints do not fail because they are "overused" anymore than an engine fails because it turns over; they fail because the quantum-mechanical pacing system that governs their atomic regeneration has been desynchronized by artificial light and electromagnetic chaos.

The Mark Sisson example is the ultimate cautionary tale of the corporate wellness paradigm he resells. When a lifestyle brand is explicitly predicated on a "food and exercise first" dogma, it cannot absorb a biophysical reality where light dictates the clock, and the clock dictates structural mass.

Sisson's hip failure in California wasn't a failure of his ancestral diet; it was a failure of the local photoelectric environment and the circadian disruption of his chondrocytes' internal pacing. He tried to move to FLA to help but he moved right into the failing magnetic dynamo of NADD+ and singlet oxygen. His hips got Landauer liquidated, as a result of his false beliefs.

By analyzing the decentralized science of the chondrocyte matrix, we can see exactly how the atomic mass and the clock loop connect to keep your original hips right where they belong.

Centralized medicine notes that cartilage is avascular and aneural, relying entirely on synovial fluid for passive diffusion. What they fail to see is how cartilage actually moves nutrients and maintains structure:

The Piezoelectric Collagen Matrix: Type II collagen and highly sulfonated proteoglycans (like aggrecan) form a dense, highly ordered, crystalline lattice. This matrix is structurally bound by a rigid table of polarized ferroelectric water (K=160).

The Compression Pump: When a joint is mechanically loaded under natural conditions, this crystalline, structured water matrix generates a localized piezoelectric current. This current drives the precise, non-thermal transport of ions and nutrients into the avascular cartilage zone.

The Paramagnetic Breakdown: When isolated blue light and nnEMF drop that water table to bulk water (K=78), the cartilage loses its dielectric capacitance. The piezoelectric pump stalls. The joint can no longer generate the organized electrical signals required to guide the chondrocytes.

The BMAL1-CLOCK Loop: The True Master of Joint Anabolism

For my tribe I've identified, the BMAL1-CLOCK heterodimer is not a metabolic option; it is the fundamental temporal gatekeeper of cartilage survival. In a healthy, magnetically pinned environment, the chondrocyte clock cleanly separates the daily cycle into two distinct, non-overlapping phases:

The Anabolic Phase (Sunlight Triggered): Under normal circadian rhythms, BMAL1 upregulates SOX9, the master transcription factor for joint health. SOX9 directly drives the expression of COL2A1 (Type II collagen) and ACAN (aggrecan). The cell uses this phase to actively rebuild the joint's physical matrix using clean, protium-based building blocks.

The Catabolic Phase: At night, anabolic synthesis shuts down, and enzymes like MMP13 and ADAMTS4/5 perform controlled, microscopic pruning to clear out damaged matrix elements.

Circadian Rhythm Disturbance (CRD) and the Catabolic Lock

When you subject the joint to a chronic modern environment, bathed in artificial blue light, ungrounded, and stripped of the planetary geodynamo's pacing, the BMAL1-CLOCK oscillations flatten out.

The Permanent Breakdown: Without the clean, high-amplitude oscillation of BMAL1, the physical separation between building up and breaking down is destroyed. The cell loses its ability to activate SOX9.

The Signaling Cascade: The flattening of the clock genes forces an immediate up-regulation of the Wnt/β-catenin, MAPK/ERK, and PI3K/Akt pathways. In a healthy cell, these pathways are used tightly and rhythmically; in a state of CRD, they run completely uncoupled.

The Enzyme Avalanche: This unchecked signaling tells the chondrocytes to continuously synthesize MMP13 and ADAMTS4/5. The cell is locked into a permanent, non-stop catabolic loop. It degrades its own collagen framework and proteoglycan anchors faster than it can ever replace them. THIS DEFINES A LANDAUER LIQUIDATION. This is why aging humans see a severe drop in BMAL1-positive chondrocytes in their knees, the clock has literally been extinguished.

The WEIGHT IRONY?

The centralized paradigm he believes in and sells into with trainers tell you fatties destroy joints faster than the fit. What he was ignorant of, was the atomic mass of DEUTERIUM in your joints is the weight you should have focused in on.

I still got mine at sixty plus......

The Isotopic Weight Trap he missed: Adding Mass to the JointThis is where your point about adding atomic mass to the base chain completes the biophysical picture.

The Deuterium Infiltration: When the chondrocyte’s IMM capacitor drops below its 30 MV/m threshold due to singlet oxygen and broken intersystem crossing, the cell loses its ability to exclude Deuterium (D⁺).

The Brachistochrone Jam: This heavy hydrogen infiltrates the chondrocyte’s mitochondria, jamming the ATPase nanomotors. The energy required to run the high-fidelity synthesis of complex, heavy proteoglycan structures like aggrecan completely vanishes.

The Structural Failure: Instead of building a highly organized, light-bending, homochiral ECM that can cushion mechanical loads, the energy-deprived chondrocyte can only spin out weak, structurally flawed, heterochiral matrix components.

The joint doesn't fail because it walked too many miles or lifted too much weight. It fails because it was forced to operate in a state of permanent quantum and temporal misalignment.

By treating OA as a mechanical "wear and tear" problem, centralized medicine can blame the patient's lifestyle while selling them a titanium socket. By looking through the decentralized lens of quantum biophysics, we see the truth: protect your light, pin your local magnetic fields, keep your BMAL1 oscillations high, and your biology will preserve the original joints you emerged from the vagina with. Learn how to cut the right weight......DEUTERIUM.

[Ethical Skeptic ☀ @EthicalSkeptic]

If you want to know why 83% of truly ancient megaliths point to one spot on the planet - obtain the book...

If you want to know why mankind forgot this and was forbidden to know it, and what that means - obtain the book...

Be forewarned, you will never be the same person again.

https://t.co/3J6i4jdwSi

[⚡️ The Blue Light Diet ⚡️ @BlueLightDiet]

Wait bruh. Eating a food "out of season" or something flown in from another part of the world can be bad for my health?

Yes.

Your body reads seasonal and light coded signals from the food you eat.

This 2018 study in Nutrients (PubMed 30115853) fed rats the exact same cherries but the cherrys were fed to the rats either “in season” or “out of season.”

What does that mean?

Rats were kept under controlled light cycles that mimic seasons (long day “summer” vs. short day “winter”). They were fed the same cherries (harvested in summer long day conditions) either “in season” (matching the rats’ current light cycle) or “out of season” (a mismatched shorter light cycle). Some rats were also on a high fat obesogenic diet.

So what happened?

Eating the cherries out of season (a photoperiod mismatch) changed gene expression and the physical structure of white fat tissue in a way that made the rats fat cells more prone to storing fat, especially when combined with a junky diet. In season cherries did not have the same effect.

Your ancestors ate with the seasons for a reason.....they didn't have giant cargo planes and ships lol. But that protected them.

Modern grocery stores and fed ex let us eat summer fruit in February and your metabolism pays a bad health toll.

Eat local & in season gets you a better nutrient profile and your body gets the right environmental signals.

Less inflammation and better fat metabolism when your eating habits are aligned with nature instead of modern life.

Now combine this with no eating at night after the sun goes down and you will have a diet approved by the natural force that developed you over millions of years.

[Zaid K. Dahhaj @zaidkdahhaj]

What’s incredible about the circadian clock is that it’s not a human invention

It’s not even a vertebrate invention

The core molecular mechanisms, the CLOCK/BMAL1 transcription-translation feedback loop, is conserved across species that diverged over a billion years ago

Cyanobacteria have circadian clocks. Single-celled organisms that predate multicellular life have circadian clocks. The system is that old

It emerged because the planet rotates, and any organism that could anticipate the 24 hour light-dark cycle rather than just react to it had a survival advantage

What that means mechanically is that the circadian system is THE ORGANIZING LAYER that everything else runs on top of

[☣️ Pleb Kruse = BTC foundationalist in exile 🟩🔆 @DrJackKruse]

Your being sold a centralized lie and the sycophants like Johnson are helping your enemies.

GLP-1s don't solve obesity. They pharmacologically mimic satiety in a Rockefeller built world that manufactures hunger by hiding deuterium in food for profit. That’s NOT a cure. That's a patch on a centralized system that profits from breaking your metabolism with deuterium in the first place.  Few see the game for what it is because the Rockefeller paradigm taught everyone to see the world through biochemical lens and not the biophysical lens.

https://t.co/CKbzg17TVy

Mainstream centralized Rockefeller trained metabolic science and corporate healthcare platforms evaluate GLP-1s through a two-dimensional, chemical-only spreadsheet, labeling them a "cure" for global obesity because they stimulate insulin secretion, delay gastric emptying, and suppress appetite.

They are completely blind to Landauer’s Principle, quantum spin chemistry, and the hard laws of statistical mechanics: GLP-1 receptor agonists do not fix the underlying metabolic breakdown; they are a highly lucrative, top-down pharmaceutical patch designed to manually force open the cell's fluid channels because the centralized technosphere has systematically poisoned the epigenetic landscape with Deuterium.  This is a planned demolition of Chromosome #2 as I mentioned in this podcast below.

https://t.co/AcbIygLCyd

The modern industrial diet is not merely dense in surplus calories; it is an engineered high-mass isotopic trap. Corporate food processing, monoculture agriculture, and the proliferation of synthetic additives alter the natural Deuterium-to-Protium ratio of the food chain.

The Kinetic Isotope Effect (KIE) Jam: When an individual consumes a diet caked in fractionated, high-deuterium mass while living an indoor, un-grounded lifestyle under the artificial flicker of blue LEDs, their internal water lattice undergoes a dielectric collapse (≈160→80).

The Stator Fracture: Because Deuterium possesses twice the atomic mass of normal light hydrogen protons (1H), its inclusion into the mitochondrial matrix delivers a crushing kinetic impact to the sub-nanometer channels of the F0-F1 ATP synthase nanomotors.  The rotors deform, and their optimal 9,000 RPM velocity drops to zero, plunging the cell into chronic pseudohypoxia due to NADD+ as the cause of lowered NAD+.

The Hunger Mirror: Lacking the vital Redox Potential (ΔΨ) needed to maintain cellular structure, the system hits Landauer's Limit (≥ ln2)
To prevent total informational erasure, the brain's reward centers interpret this deep, sub-molecular electron depletion as an emergency calorie famine. The system manufactures a permanent, runaway craving for more substrate (hunger), locking the consumer into a continuous loop of metabolic consumption.

What has my thesis uncovered for humanity?  The paradigm is attacking Chromosome #2 just as a Fabian would do.  People forget what John D. Rockefeller told Congress when Teddy Roosevelt broke up Standard Oil.  He would bankrupt America for ruining what he built.  The human-specific Chromosome 2 fusion megastructure was engineered by Nature specifically to act as an indestructible quantum blockchain to enforce absolute isotopic sovereignty. It clusters the Glucagon (GCG) gene network (2q24.2), the POMC gene (2p23.3), and the EDAR gene (2q12.1) around a central interstitial telomeric loop (ITL) at 2q13–14 to serve as a synchronized thermodynamic engine.

Under normal diurnal solar governance, capturing the morning 0.66 eV solar infrared pulse triggers the Cortisol Awakening Response (CAR), which naturally cleaves the GCG network to unleash the exocrine pancreas's 2-liter sodium bicarbonate fluid flush. This downward fluid vortex is the body's primary exhaust manifold, designed to sweep accumulated Deuterium mass out through the gut before it can back-load up the vagus nerve to freeze the brainstem.  When a patient injects a synthetic GLP-1 peptide like Ozempic, they are bypassing the Sun's chronological text to force an artificial, uncoordinated mass ejection across the system:

The Accelerated Flush: The drug forces the tissues to upregulate a high-velocity variant of the G3P (Glycerol-3-Phosphate) shuttle, manually throwing heavy Deuterium out of the cellular matrix to un-jam the mitochondrial stators.

The Dopaminergic Flattening: As the heavy isotope burden is cleared, the mitochondrial nanomotors return to their 9,000 RPM velocity, generating a massive, localized voltage spike that compresses the internal matrix into a tight 30-million-volt-per-meter event horizon on the IMM.

The Zero-Entropy Sink: This extreme containment creates a biological black hole. It locks down kinetic energy and electron spin fluctuations so completely that no stray energy can escape as noise. The brain's reward center is turned into an absolute zero-entropy sink, dropping the volume on almost every craving, food, sex, work, and the urge to get out of bed, inducing the profound state of clinical anhedonia reported across high-dose users.

What did my podcast warn about?  The coming destruction of the number one protein in man by these drugs.  COLLAGEN.

Failing to naturally fire the Chromosome 2 exhaust valve by relying on a synthetic chemical shortcut introduces long-term atavistic chaos across the cell boundaries. Forcing a permanent, non-circadian fluid manipulation uncouples the liver's microsomal membranes, altering the electron-transport efficiency of the entire Cytochrome P450 (CYP) monooxygenase superfamily.

The iron active sites of the CYP enzymes become congested and stall, leading to the localized accumulation of partially metabolized steroid intermediates. Under the Telomere/rDNA Co-Regulation Model (TRCS), this unresolved structural stasis targets the highly repetitive 45S rDNA arrays.   When the structural fuse blows, it will drive an uncontrolled, asymptotic p53 master switch surge that forces the cell to drop its high-flux mammalian programming, causing an immediate, non-genetic rollback to a loose, hypermobile connective tissue matrix (Ehlers-Danlos Syndrome phenotype) and primitive, low-flux immunity.  This is why people bones are looking like 80 yr old women at 35.  This is why Hollywoods faces look as they do.  Few see the game as I do.  This post is why they really blocked my TED talk.  I discussed this with Adrian D'Amico yesterday in a not yet released podcast.

YOU ARE PAWN IN THEIR MATRIX AND THEIR SYCOPHANTS WILL TRY TO CONVINCE YOU THE NEXT GLP-1A IS BETTER!

The centralized pharmaceutical dynasty markets GLP-1s as a permanent lifestyle necessity because their entire financial matrix relies on keeping you trapped inside an artificial, dual-monopoly loop: one system profits from breaking your metabolism with deuterium-heavy processed inputs, while the other profits from selling you a lifetime patentable patch to clear it.

They design their entire metabolic guidelines on Nocturnal Rodent Models, animals engineered by nature to live in the dark with flat skulls, inverted circadian mechanics, and zero human-scale Chromosome 2 fusion stability, ensuring the population remains completely dependent on top-down system interventions as Earth's global dipole continues its accelerating 5% per decade asymptotic collapse through mid-2026.

Wake up from your retarded thinking before they wipe you out.

CITES

https://t.co/o0kEm7tE3i

[Kevin McKernan @Kevin_McKernan]

This never happens..
Except when it does.

[Ethical Skeptic ☀ @EthicalSkeptic]

💥CANCER INCREASE CONTINUES 💥

Now that the 2023 CDC SEER release has validated this model, we can get on with professional evaluation of our next steps as a society.

➯ Excess Mortality = 9.8%
➯ Diagnosis & Treatment Excess = 28.5%