Insurance mortality data from hundreds of thousands of patients revealed that the more pharmaceuticals a person was on, the more predictable and shorter their life expectancy — and that the majority of early deaths traced back to modifiable nutrient and lifestyle factors, not genetics.
2
Gary Brecka's hierarchy of biohacking starts with zero-cost interventions — morning first light, grounding, breathwork, cold exposure — before any device, because the best biohacking tools mimic what Mother Nature provides: oxygen, light, and magnetism.
3
Red light therapy is Brecka's single highest-leverage device: it displaces mitochondrial nitric oxide, forces oxygen into the aerobic cycle, restores vasomotor microcirculation, and produces broad systemic effects from joint pain relief to improved eyesight.
4
Methylfolate deficiency — driven by the MTHFR gene variant, widespread folic acid fortification, and ultra-processed diets — sits at the root of an enormous range of chronic diseases including hypertension, dementia, depression, and infertility.
Protocols
Concrete recipes — what, when, how much, and why
8 items
Morning first light — 45 minutes outside at sunrise before UVA/UVB appears
WhatGo outside within the first 45 minutes of the day, during first light / sunrise, and expose skin and eyes to natural light without sunglasses. No UVA or UVB rays are present at this time, so there is no skin cancer risk.
WhenDaily, every morning, immediately after waking.
Dose45 minutes at minimum during the first-light window.
For whomEveryone. Especially anyone with mood disorders, sleep disruption, or low vitamin D.
WhyFirst light provides the full therapeutic visible and near-infrared spectrum that regulates circadian rhythm, cortisol signaling, and mitochondrial function — without the UV-driven DNA damage of midday sun. Brecka treats this as his daily antidepressant and nootropic.
Brecka describes his own practice: out on his balcony for first light with breathwork, treating it as a pharmacological intervention — citing enhanced mood, increased focus and concentration as the side-effect profile. He frames this as the free version of red light therapy: you get the therapeutic light spectrum with zero cost and zero UV risk during the first-light window.
Personal experience
Brecka: This morning I just as a joke said I'm taking my morning antidepressant and I was out on the balcony getting just doing some breath work and I listed the side effects of enhanced mood, increased focus and concentration.
I really encourage people to get outside — the first 45 minutes of the day during first light. There isn't any UVA or UVB rays so you don't have a lot of the damaging rays in the first 45 minutes.
Grounding / earthing — direct skin contact with Earth's surface
WhatWalk barefoot on grass, soil, sand, or concrete — any natural surface that conducts the Earth's low-gauss electromagnetic field. Zero cost alternative to PEMF mats.
WhenDaily; any time of day; ideally combined with morning light exposure.
For whomEveryone, especially those who spend most of the day indoors on synthetic floors.
WhyBrecka frames the Earth's surface as a source of free electron transfer that moderates inflammation and cellular charge. The best biohacking devices mimic what nature provides; grounding is the direct delivery of the same electromagnetic signal that PEMF mats try to replicate.
Brecka's framework: humans evolved in direct contact with the Earth's magnetic field (oxygen from air, light from sun, magnetism from earth). Every degree of disconnection from these three inputs correlates with increasing dysfunction. PEMF mats exist for people who cannot or will not spend time outdoors; they emit the same low-gauss current of the Earth. For people who can go outside, grounding is the free equivalent.
Touching the surface of the Earth — grounding — is a very real thing. These are all super expensive things to do. They cost exactly zero.
Red light therapy — near-infrared bed or panel (220V, wavelengths 680–910 nm)
What10–20 minutes daily in a full-body red light bed or in close proximity to a dense panel. Target wavelengths 680–910 nm to capture both visible red (superficial collagen/skin) and near-infrared (deep mitochondrial and microvascular effects). Must be powered by a 220V outlet to generate therapeutic irradiance. Smaller diodes packed tightly are more effective than large bulbs spaced apart.
WhenDaily; can be morning or evening.
Dose10–20 minutes per session. Hard to overdose at this duration.
For whomAnyone with joint pain, age-related vision decline, poor skin, chronic fatigue, or anyone wanting to optimize mitochondrial function. If a full bed is not affordable, clinic memberships and high-quality wall panels are alternatives.
WhyRed/near-infrared light displaces mitochondrial nitric oxide from cytochrome c oxidase, forces the aerobic cycle (16x more efficient than anaerobic), triggers vasodilation, and restores vasomotor microcirculation to joints, the back of the eye, skin, and spine.
CaveatsDevices plugging into a 110V standard outlet are underpowered for deep therapeutic wavelengths. More visible red light does not mean more effective — near-infrared bulbs that appear off are the therapeutic ones. The closer to the device, the deeper the penetration into tissue.
Brecka calls red light therapy his single highest-leverage biohacking device. The mechanism: cytochrome c oxidase in the mitochondrial Krebs cycle can bind either mitochondrial nitric oxide OR oxygen, not both. When it binds nitric oxide the cell runs anaerobic (16x less efficient). Red light physically kicks nitric oxide out, measurable as a post-session spike in serum nitric oxide, and forces the mitochondria back into aerobic metabolism.
Mechanism
Red/near-infrared photons are absorbed by cytochrome c oxidase (the chromophore), displacing mitochondrial nitric oxide. Freed nitric oxide causes temporary vasodilation; simultaneous oxygen docking restores aerobic ATP synthesis. The 70% microvascular component of circulation (vasomotor-powered) is particularly responsive to vasomotor restoration.
Red light therapy in my opinion is probably the most — has the most single as a single device — prolific impact on mitochondrial function.
Also said
“Cytochrome c oxidase will bind with a gas called mitochondrial nitric oxide. And when it's bound to mitochondrial nitric oxide it's sort of like a one-armed man — it can either shake hands with nitric oxide or it can shake hands with oxygen but it can't do both. So in order to bind oxygen... it has to let go of mitochondrial nitric oxide. And one way to do this is to pass red light through the skin and through the wall of the mitochondria — it will literally kick nitric oxide out.”— Verbatim mechanistic explanation that distinguishes red light therapy from a vague wellness tool.
MTHFR-stratified methylfolate protocol
WhatTest MTHFR and companion methylation genes (COMT, MTRR, MTR, AHCY) via a methylation panel or Dutch test. If MTHFR variant is present: eliminate folic acid-fortified foods from the diet entirely and supplement with 5-methyltetrahydrofolate (5-MTHF). Simultaneously check homocysteine: if above 14, add trimethylglycine (TMG) 500 mg/day to drive it toward optimal 6–8.
WhenStart immediately upon confirmed MTHFR variant. For everyone: switch from folic acid to methylfolate supplements regardless of MTHFR status.
Dose5-MTHF: dose per methylated multivitamin product; adjust based on homocysteine response. TMG: 500 mg/day in capsule form.
For whomAnyone with MTHFR variant (estimated 44% of the population has reduced function). Also relevant for anyone with elevated homocysteine, depression, anxiety, ADD/ADHD, fertility issues, autoimmune symptoms, or unexplained fatigue.
WhyMTHFR+ individuals cannot convert folic acid or folate to the active methylfolate form; excess unmetabolized folic acid blocks the receptor. Methylfolate is the rate-limiting cofactor for methylation, which governs DNA replication, mood neurotransmitter synthesis, detoxification, and mitochondrial function.
CaveatsStandard blood folate tests appear normal even when methylfolate is functionally deficient — the relevant test is homocysteine, not serum folate. Folic acid is in nearly all fortified grain products in the US; dietary elimination requires label-checking.
Brecka describes seeing dramatic clinical responses when methylfolate is corrected: peristaltic gut motility restores (constipation resolves), mood lifts, cognitive fog clears, and s-phase arrest in DNA replication restarts. He considers methylfolate — alongside D3/K2 — the single highest-leverage nutrient intervention.
Mechanism
MTHFR converts folate to 5-methyltetrahydrofolate, which donates methyl groups across hundreds of reactions: homocysteine remethylation to methionine, SAM synthesis (the universal methyl donor), neurotransmitter synthesis, DNA methylation, and mitochondrial energy metabolism.
Contrary to popular belief if you have MTHFR you need to avoid folic acid like the plague and you have to supplement with methyl folate, five methyl folate.
Also said
“When you get the folic acid out of the diet and you supplement with methylfolate — magic happens. You see peristaltic activity restored to the gut, you see the normal pace of the gut restore, which in my opinion is one of the most overlooked things in all of modern medicine.”— Specific clinical outcomes Brecka observes in patients after methylfolate correction.
WhatDaily morning supplements: (1) methylated multivitamin (methyl-B12, methyl-B6, 5-MTHF — NOT cyanocobalamin or folic acid); (2) mineral salt (Baja Gold sea salt or Celtic salt) in water; (3) omega-3 fatty acid from black seed oil or fish oil (EPA/DHA); (4) complete essential amino acid supplement (all 8 EAAs, non-caloric, non-fast-breaking); (5) vitamin D3 with K2.
WhenEvery morning; take before or with the first meal.
DoseD3: 5,000–10,000 IU daily; K2 co-administered. Mineral salt: a pinch in morning water. Omega-3: follow product dosing. EAAs: as directed.
For whomEveryone as a baseline. People on statins, corticosteroids, or with MTHFR variants need particular attention to the cholesterol-hormone-D3-methylation chain.
WhyThese cover the three classes of essential nutrients (amino acids, fatty acids, minerals) plus the most pandemic deficiency (D3/K2) and the methylation rate-limiter (methylated B vitamins). All biochemical reactions require these cofactors; deficiency in any one creates a bottleneck expressed as disease.
CaveatsFolic acid in any form (fortified foods, most cheap multivitamins) should be avoided, especially in MTHFR carriers. Collagen supplements are incomplete proteins — the complete amino acid stack matters more for actual tissue-building.
Brecka draws the distinction: there are no essential carbohydrates (the body can synthesize glucose from protein/fat), but there are 8 essential amino acids, 2 essential fatty acid classes, and 12+ essential minerals. Being deficient in even one of the 8 EAAs causes incomplete protein utilization and likely lipogenic conversion.
Personal experience
Brecka confirms he personally takes all four of these supplements daily along with D3/K2.
I take a methylated multivitamin... I take a mineral salt every morning... I take a black seed oil — the omega-3 version from black seed. And then I take something called perfect aminos — it's all the eight essential amino acids.
Boron supplementation to lower high SHBG and free up testosterone
WhatSupplement with boron (a trace mineral) to reduce elevated sex hormone-binding globulin (SHBG), which binds testosterone in the bloodstream and prevents it from exerting biological effect, even when total testosterone appears adequate.
WhenWhen free testosterone is low despite adequate total testosterone, especially if SHBG is confirmed elevated on blood work.
DoseNot specified precisely in this transcript; clinical boron doses typically range from 3–10 mg/day.
For whomMen and women with low free testosterone (men: free T below 4.5–7 pg/mL) but adequate total testosterone, especially those in whom TRT is not yet indicated or desired.
WhySHBG binds testosterone, making it biologically inactive. Many men and women with low free testosterone have normal total testosterone but elevated SHBG. Rather than immediately initiating exogenous testosterone, lowering SHBG with boron can release bound testosterone and normalize free levels without shutting down endogenous production.
CaveatsThis is only one of three main causes Brecka identifies for low testosterone; the others are low LDL cholesterol (substrate depletion from statins) and nutrient deficiencies (D3, DHEA). Check all three before concluding primary hypogonadism.
Brecka's three-cause model for low testosterone: (1) low LDL — the substrate for all steroid hormones; excess statin therapy depletes it; (2) nutrient deficiencies — particularly D3, and low DHEA (often stress-driven and correctable with DHEA supplementation); (3) elevated SHBG — correctable with boron. He emphasizes that primary hypogonadism (true testicular failure) is rare; most low testosterone is secondary or nutritional.
You get sex hormone binding proteins that are actually lowering your free testosterone — you get these things out of the blood or back into normal range taking Boron if you have high SHBG.
Hydrogen water as daily drinking water upgrade
WhatReplace regular filtered water with hydrogen-infused water, which has a negative oxidative-reduction potential (ORP) indicating antioxidant character.
WhenAs daily drinking water, all day.
DoseReplace regular water intake volume; no upper limit stated.
For whomAnyone who already filters their water and wants to further upgrade. Higher priority than any supplement-level intervention.
WhyBrecka demonstrates the ORP difference between tap water (positive, oxidizing) and hydrogen water (negative, reducing). Hydrogen gas is the smallest molecule and penetrates cell membranes freely, reaching mitochondria. His argument: if you have a choice between two water sources and one has antioxidant character, choose the antioxidant option.
CaveatsHydrogen water comes after filtration — tap water containing fluoride, PFAS, polyphenols should be filtered first regardless. Brecka's hierarchy: tap → filtered → hydrogen water.
Brecka views hydrogen water as mimicking the antioxidant character of clean natural running-stream water, which is high in mineral content and negatively charged. Standard municipal tap water, even when rated safe, contains PFAS. He treats water filtration as the non-negotiable baseline and hydrogen infusion as the upgrade.
If you have a choice between drinking regular water or hydrogen water you should be drinking hydrogen water. If you have a choice between drinking tap water or filter water there, you should be filtering your water supply.
PEMF mat — grounding substitute for those who cannot go outdoors
WhatLie on a pulsed electromagnetic field (PEMF) mat that emits the same low-gauss current as the Earth's surface, replicating the electrical environment of grounding for people who cannot spend time barefoot outdoors.
WhenCan be used during sleep, rest, or work.
DoseDaily use; even short sessions contribute.
For whomUrban dwellers with limited outdoor access, those with mobility issues, or anyone wanting to extend the benefit of grounding beyond the time they can spend outside.
WhyAncestrally, humans had continuous contact with Earth's magnetic field. Modern indoor life severs this. PEMF devices are the engineered equivalent of grounding — same signal, delivered indoors. Brecka's rule: the best biohacking tools mimic what Mother Nature provides.
CaveatsThe EMF-blocking tent Brecka uses at night is separate from PEMF — it blocks artificial EMF (Wi-Fi, 5G) during sleep. PEMF delivers beneficial low-gauss Earth-frequency current. These are distinct devices with distinct purposes.
You know my favorite would be PEMF mats — pulse electromagnetic field. These mimic the low gauss current of the earth. So if you don't have time to Earth or ground... come in contact with Mother Earth — you can use a PEMF mat.
What's new
Personal practice updates, fresh positions, predictions
6 items
Insurance mortality data: more drugs = shorter, more predictable life
Brecka spent his career as a mortality expert for life insurance companies, working with data on hundreds of thousands of patients. The single most consistent finding: the more pharmaceuticals a person was on, the shorter and more predictable their remaining lifespan. He could predict time of death to the month.
Why this matters: Life insurance companies have no financial incentive to sell drugs — they just need to know when you will die. Their data is the cleanest possible signal on what actually kills people, and it points squarely at pharmaceutical burden, not cholesterol or other surrogate endpoints.
Background
Brecka worked in insurance actuarial underwriting where companies pull full blood work, medical records, bank statements and demographic data before issuing large whole-life policies. This gave him a decades-long view of how modifiable versus non-modifiable risk factors tracked against actual mortality.
The data revealed that the reason most people were not living healthier, longer lives was modifiable risk factors — diet, lifestyle, supplementation, exercise, mobility, and blood biomarkers — not fixed genetic constraints. The pharmaceutical cascade Brecka describes: chronic vitamin D3 deficiency → symptoms misread as rheumatoid arthritis → corticosteroid prescription → joint degeneration → joint replacement surgery → reduced mobility → cascade of mobility-loss diseases → early death. He could artificially advance someone's actuarial age by six years and one day the moment a corticosteroid was added to their record, then schedule the joint replacement, then watch the ambulatory profile collapse.
The more Pharmaceuticals you were on the easier it was for us to predict your life expectancy. The more you were on the more likely you were to die sooner.
Also said
“I always say that if this database could see the light of day it would permanently change the face of humanity.”— Brecka's framing of how much suppressed mortality intelligence exists in insurance actuarial files that the public never sees.
Vitamin D3 over 50 ng/mL — zero COVID deaths in Israeli data
Brecka cites Israeli population data showing that at functional vitamin D3 levels of 60–80 ng/mL, there was not a single COVID death. He also describes chronically low D3 (7–25 ng/mL) in insurance records as the upstream trigger for a sequence ending in joint replacement and early mortality.
Why this matters: Standard lab reference range bottoms out at 30 ng/mL, which Brecka considers clinically deficient. The Israeli data suggests the protective threshold is roughly double the lab floor — a fact almost never communicated to patients.
Background
Brecka reviewed 20-year medical records on individuals with long-running D3 deficiency and tracked how they progressed to misdiagnosed inflammatory arthritis, corticosteroid prescriptions, and subsequent joint deterioration.
The dose Brecka describes from actuarial inference: 5,000–10,000 IU daily of vitamin D3 with K2. He contends that simply correcting the D3 deficiency — along with adding load to bones — would have prevented the entire downstream cascade in the majority of cases he reviewed. Hyman confirms from Function Health data: 67% of 100,000+ members tested are deficient in one or more nutrients at standard lab reference thresholds, with vitamin D, iron, zinc, B vitamins, and homocysteine among the most common findings.
If your vitamin D was over 50 there was nobody who died. I was actually just going to say that because I was looking at Big Data reporting during that time frame too and in functional ranges of 60 to 80 nanograms there was not a single death.
Also said
“5 or 9,000 IUs 10,000 IUs of vitamin D3 daily with a little K2 and applied a load to their bones — that trajectory would have been completely different.”— Brecka's retroactive actuarial counterfactual: what would have happened if the deficiency had been corrected.
Red light therapy restores vasomotor microcirculation — mechanism behind eyesight and joint pain relief
70% of the body's circulation is microvascular, powered not by the heart but by vasomotor activity — a peristaltic wave in smooth muscle lining small vessels. Red/near-infrared light at the right power and wavelength restores this vasomotor activity, explaining why users report improved vision, reduced joint pain, and better skin — all in tissues that are highly microvascular-dependent.
Why this matters: Most people think red light therapy is a skin tool. Brecka's explanation shows it is a microvascular and mitochondrial tool: the visible effects (skin, hair) are superficial epiphenomena of a deeper circulatory intervention.
Background
The mechanism runs through cytochrome c oxidase: red/near-infrared light displaces mitochondrial nitric oxide from cytochrome c oxidase, forcing oxygen into the aerobic cycle (16x more efficient than anaerobic), triggering temporary vasodilation and then restored oxygen delivery across all microvascular tissue.
Brecka cites Joe Rogan texting him 5 weeks after buying a red light bed: no longer wearing readers; eyesight improved. Brecka himself is 54 with no readers. The mechanism: age-related vision decline is not retinal degeneration — it is loss of microvascular circulation to the back of the eye. Restore vasomotor, restore sight. Same principle for rotator cuff pain, knee pain, low back pain — these structures are all highly dependent on microvascular supply. Structural pathology (cartilage erosion, osteoarthritis) won't reverse, but pain resolves because oxygen delivery improves.
The reason why eyesight begins to degrade in your 50s is not because of something to the rods, the cones, the macula — it's not a degenerative process, it's a lack of microvascular circulation. So if you restore the vasomotor to the back of the eye you restore the eyesight.
Also said
“About 70% of our circulatory system — circulation throughout our body — is actually not done by the heart... the vast majority of our circulation is microvascular. And that's about 70% of our circulatory system that's actually not powered by the heart, it's powered by an activity called vasomotor.”— The anatomical basis for why red light has system-wide effects far beyond skin.
Folic acid (the lab-synthesized form) requires ~10 enzymatic steps to convert to the active methylfolate. People with MTHFR variants cannot complete this conversion — and folic acid may actually block the receptor, competing with the folate they do absorb. Since all US grain products are fortified with folic acid, 44% of the population is functionally methylfolate-deficient even while appearing adequately folated on standard blood tests.
Why this matters: Methylfolate is the central hub of methylation, which governs DNA transcription, mood chemicals, mitochondrial function, detoxification, and fertility. A single widely-distributed genetic variant plus a well-intentioned food policy may be a root cause of an enormous proportion of chronic disease.
Background
Brecka has tested 150,000 patients across 74 biomarkers plus a methylation genetic panel (COMT, MTRR, MTR, AHCY, MTHFR). In his clinical experience methylfolate deficiency is the highest-leverage single nutrient correction he makes.
The s-phase arrest mechanism: when cells replicate DNA and are deficient in methylfolate, they enter s-phase arrest — a checkpoint designed to stop propagation of genetic errors. Supplementing methylfolate can restart replication. Downstream of methylation: homocysteine accumulates when methylfolate is insufficient. Elevated homocysteine (above 14) increases dementia risk 50%. Homocysteine-driven vasospasm causes a majority of the idiopathic hypertension diagnoses in America. Brecka's protocol: eliminate folic acid from the diet, supplement five-methyltetrahydrofolate, and check response via homocysteine (optimal 6–8). TMG (trimethylglycine) at 500 mg/day is the most direct way to lower homocysteine.
Contrary to popular belief if you have MTHFR you need to avoid folic acid like the plague and you have to supplement with methyl folate, five methyl folate.
Also said
“Folic acid... doesn't exist anywhere on the surface of the Earth. You can't find folic acid anywhere naturally in nature. Folate exists naturally in nature.”— Distinguishes the natural substrate (folate) from the industrial compound sprayed on grains (folic acid) — two different things with different metabolic fates.
“If your homocysteine is over 14 you increase your risk of dementia by 50%. This is just simple things you can do to actually — so true.”— Quantifies the clinical stakes of elevated homocysteine — the direct downstream marker of methylation failure.
Sleep medication forces hypoxic suffocation — worsens the problem it claims to treat
Brecka describes how chronically hypoxic patients (low testosterone → low RBC → poor oxygen carrying capacity) cannot achieve deep sleep because the brain wakes them to prevent severe hypoxia. Sleep medications like trazodone, benzodiazepines, and diphenhydramine block the brain's oxygen-monitoring system, allowing entry into deep sleep — but the patient is actually suffocating, not sleeping well.
Why this matters: Explains why people feel worse the morning after sleep medication even when it's been fully cleared from their bloodstream: they were oxygen-deprived for 6–8 hours. This reframes sleep medication from a mild inconvenience to a physiologically dangerous intervention for hypoxic patients.
The fix is upstream: restore testosterone (or correct the reason testosterone is low — low LDL cholesterol from statins, low DHEA from stress, high SHBG, nutrient deficiency, insulin resistance), which restores erythropoietic pressure on bone marrow, which raises RBC and hemoglobin, which resolves hypoxia, which allows normal sleep architecture to return. Brecka is explicit that only 30% of his patients with clinically low testosterone actually need TRT — 70% have a correctable upstream cause.
What happens is trazodone and zum nitrate, diazepam — a lot of these will actually block the brain's view of blood oxygen, essentially shut off the monitoring system and then it allows them to get into a deep sleep but they're not actually sleeping — they're suffocating.
Also said
“That medication's been out of your system for hours. You're not feeling the effects of the Tylenol PM — you're feeling the effects of having suffocated for six hours.”— Reframes next-day grogginess as a symptom of nocturnal hypoxia, not of drug hangover.
LDL is not an independent cardiovascular risk factor — insurance data confirmed it
In Brecka's decades reviewing insurance mortality data, he never processed a single death claim on a centenarian (age 100+) who did not have clinically elevated LDL cholesterol. In addition, the data consistently showed low-LDL individuals on statins had higher incidence of hormone collapse, cognitive impairment, and cardiovascular disease, not lower.
Why this matters: Insurance companies measure LDL but they also measure insulin, glucose, and HbA1c — and metabolic control, not LDL, was the dominant predictor of cardiovascular mortality. The financial incentive structure (not selling drugs) makes their data more reliable than industry-sponsored trials.
The mechanism Brecka describes: LDL cholesterol is the raw material for steroid hormone synthesis (testosterone, DHEA, cortisol). Extreme statin-driven LDL reduction (from 180 down to 57) collapses hormone production → testosterone falls → RBC count falls → hypoxia → cognitive impairment, ED, poor sleep → accelerated mortality. The irony: the therapy aimed at extending life appears in this data to shorten it via this hormonal-hypoxic cascade. Brecka is explicit this is his clinical observation, not a randomized trial.
LDL cholesterol was not a risk factor — an independent risk factor — for cardiovascular disease. That's a big statement... the insurance companies are not selling statins.
Recommendations
Products, supplements, and tools mentioned in the episode
6 items
Vitamin D3 + K2 (5,000–10,000 IU daily)
Supplement
Brecka's highest-priority single supplement based on actuarial data showing chronic D3 deficiency as the upstream trigger for misdiagnosed arthritis, corticosteroid cascades, bone loss, and early mortality. K2 is required to route calcium into bone rather than arteries.
The insurance data Brecka reviewed showed patients with D3 levels of 7–25 ng/mL for years before presenting with joint symptoms. The Israeli COVID data (zero deaths above 60–80 ng/mL functional range) further quantifies the protection at optimal levels. Standard labs consider 30 ng/mL adequate; Brecka considers 30 clinically deficient. At Function Health, 67% of members test deficient by even the standard lab threshold.
5 or 9,000 IUs 10,000 IUs of vitamin D3 daily with a little K2 and applied a load to their bones — that trajectory would have been completely different.
Trimethylglycine (TMG) — 500 mg/day for elevated homocysteine
Supplement
TMG is Brecka's primary tool for lowering homocysteine, which above 14 increases dementia risk 50% and is implicated in idiopathic hypertension via vasospasm. TMG donates methyl groups directly to remethylate homocysteine to methionine, bypassing the MTHFR bottleneck.
Brecka's protocol: check homocysteine (optimal 6–8; standard lab ceiling is 14.9); if elevated, start TMG 500 mg in capsule form daily. He frames this as one of the most underutilized but highest-impact supplements available, given the dementia and hypertension links.
vs alternatives
Methylfolate (5-MTHF) addresses the upstream MTHFR conversion problem; TMG addresses homocysteine remethylation directly via the betaine pathway, which is independent of MTHFR. Both may be needed for fully elevated homocysteine.
The best way to lower homocysteine is 500 milligrams daily in a capsule form of trimethylglycine, TMG. Lots of great manufacturers that make it out there... it's not an expensive nutrient.
Brecka's daily EAA supplement: non-caloric, non-fast-breaking, provides all 8 essential amino acids to ensure complete protein utilization for muscle, natural killer cells, collagen, and connective tissue synthesis.
If even one of the 8 EAAs is missing, protein synthesis cannot complete and the surplus amino acids are likely converted to glucose or stored as fat. Most people do not consider amino acid deficiency when they experience immune weakness, slow wound healing, or muscle loss.
I take one called perfect aminos — it's all the eight essential amino acids. It's non-caloric, won't even break a fast.
Baja Gold Sea Salt (or Celtic Salt) as daily mineral supplement
Supplement
Brecka uses mineral-rich sea salt as his trace mineral and electrolyte source every morning. Standard electrolyte supplements only provide 3–4 minerals; full-spectrum natural salts contain 70+ trace elements including boron, zinc, selenium, manganese — all required as enzyme cofactors.
He frames the mineral need through bone-building: you need 12 essential minerals to synthesize hydroxyapatite (the mineral component of bone), not just calcium. The modern diet and municipal water supply are stripped of most of these trace elements. A pinch of full-spectrum sea salt in morning water is Brecka's lowest-cost mineral intervention.
You need 12 essential minerals to build bone. So if you're not getting the 12 minerals you need to biohack that — you need to add a mineral salt to your morning routine. Maybe it's a Celtic salt, maybe it's a Baja gold sea salt, which is my favorite.
EMF-blocking sleep tent (Faraday-style bed canopy)
Tool
Brecka sleeps under a Faraday-style EMF-blocking tent that screens out Wi-Fi, 5G, and ambient radiofrequency during sleep. He reports improved sleep quality after installation.
His reasoning is precautionary: ancestrally, humans were not exposed to artificial EMF, so the evidence base is not yet settled — but the downside risk is low and the upside (improved sleep from reduced EMF stimulation) is measurable on wearable devices. He treats it as consistent with his biohacking = mimicking nature principle.
I have an EMF tent around my bed. And people were like well you're getting crazy about EMFs... I think that the jury is still out on the implications of 5G and WiFi. Better safe than sorry.
Multi-stage HEPA + carbon + UV air filtration system
Tool
Brecka filters his home air through a HEPA filter, carbon filter, and a UV chamber (UVA, UVB, blue, infrared) before recirculating it. Primary targets: mold, mycotoxins, and HVAC-borne contaminants (particularly relevant in humid climates like Miami).
Brecka's framework: oxygen is one of the three fundamental inputs from nature (alongside light and magnetism). Compromised air quality means compromised oxygen quality, which means compromised mitochondrial function. The Miami mold problem makes this particularly acute but the principle applies everywhere HVAC systems recirculate building air.
It goes through a HEPA filter then through a carbon filter and then essentially it goes into a chamber and it goes through high dose UVA, UVB and blue and infrared light and then it gets sucked up into the chamber in the house.
Lines worth pulling out — contrarian, specific, or perfectly phrased
6 items
The more Pharmaceuticals you were on the easier it was for us to predict your life expectancy. The more you were on the more likely you were to die sooner.
Insurance actuarial finding with no pharmaceutical-industry funding — the cleanest signal available on drug burden and longevity.
Aging is the aggressive pursuit of comfort. The more aggressively people pursue comfort the faster they age.
Brecka's one-line reframe of lifestyle medicine: hormetic stress (cold, heat, exertion, hunger) is not suffering — avoidance of it is the thing that kills you.
Nearly every form of pathology and disease known to mankind is a shift in metabolism — a shift in the mitochondria. The sicker the mitochondria become, the sicker the host will become.
Brecka's grand unifying thesis: all chronic disease is a downstream expression of mitochondrial dysfunction, making the mitochondria the single most important therapeutic target.
I don't believe we have chronic disease in this country. I think we have a chronic expression of nutrient deficiency.
Radical but defensible reframing: most chronic illness is not organ malfunction — it is missing raw material for enzyme pathways that support normal organ function.
Folic acid doesn't exist anywhere on the surface of the Earth. You can't find folic acid anywhere naturally in nature. Folate exists naturally in nature.
Crystallizes the distinction between the synthetic industrial compound used in fortification and the natural nutrient — a distinction with major clinical consequences for the 44% with MTHFR variants.
That medication's been out of your system for hours. You're not feeling the effects of the Tylenol PM — you're feeling the effects of having suffocated for six hours.
Reframes post-sleep-medication grogginess from pharmacological hangover to physiological evidence of nocturnal hypoxia — a completely different problem requiring a completely different solution.
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Educational summary of the cited expert source — not medical advice. Open the source recording linked above and consult a qualified physician before acting on any protocol.