Is Your Watch Predicting Your Death?What Biologic Age Really Means — and What It Doesn’tMy Whoop tells me I’m eight years older than I actually am.Naturally, that raises a question.Does that mean I’m going to die eight years sooner?Is my watch quietly chiseling a new date onto my tombstone?Fortunately, the answer is no.Still, confusion around biologic age has exploded.Wearables promise insight.Apps offer scores.Some even whisper about your future health, as if destiny lives on your wrist.So let’s slow this down and talk about what biologic age really is — and why it matters far less than you think.The Two Numbers and the DashEvery tombstone has two numbers.One marks when you were born.The other marks when you died.However, the most important part isn’t either number.It’s the dash in between.That dash represents your life.It reflects your health, mobility, independence, and curiosity.When we talk about longevity, we shouldn’t obsess over the second number.Instead, we should focus on making those two numbers far apart — and keeping the dash strong for as long as possible.That’s healthspan.Why Biologic Age Sounds Scarier Than It IsBiologic age is not a prophecy.It isn’t a death clock.It doesn’t predict how long you’ll live.Instead, biologic age is a model.It estimates how your body is functioning right now based on things like:resting heart rateheart-rate variabilitysleep duration and consistencyactivity and recovery patternssometimes weight or blood pressureDifferent devices use different inputs.As a result, they often give different answers.In other words, biologic age reflects recent stress and behavior, not your destiny.Think of it as feedback — not fate.Why Your Watch Isn’t Measuring “Real” AgingEarlier in the Fork U longevity series, we talked about telomeres.Those shorten slowly over decades, one cell division at a time.Your wearable isn’t tracking that.Instead, devices like Whoop measure physiology, not DNA.They detect how hard you’ve been living lately, not how much time you have left.A bad week of sleep, travel, stress, or alcohol can push your biologic age higher.A calm, consistent routine can bring it back down.That’s not aging.That’s load management.A Simple Experiment That Tells the Whole StoryHere’s a trick I tried.I told Whoop I was younger than I actually am.Guess what happened?Suddenly, my biological age dropped below my real age.That alone tells you everything.Whoop isn’t predicting where you’re going.It’s comparing how you’re doing relative to the age you told it you are.Once again, that’s feedback — not destiny.Why I Prefer WithingsI use multiple devices because, frankly, I’m a nerd.However, I tend to prefer Withings for one simple reason.They don’t try to scare you.Instead of telling you how old you “really” are, Withings focuses on things that actually improve your life today:blood pressure trendsbody weight and compositionheart rhythmsleep durationlong-term consistencyMore importantly, they ask better questions.Are you sleeping better?Is your blood pressure improving?Are your habits trending in the right direction?That’s medicine.Not numerology.And no — Withings didn’t pay me to say that.The Biggest Mistake People...

GLP-1 Drugs, the Mediterranean Diet, and the Science of Living LongerFor years, anti-aging has been hijacked by supplements, hacks, and promises that never hold up. Meanwhile, real science has quietly moved forward. Today, the most compelling anti-aging story does not come from a powder, a cold plunge, or a fasting app. Instead, it comes from metabolism.A class of medications called GLP-1 receptor agonists started as diabetes drugs. Over time, clinicians discovered something bigger. These medicines now play a major role in obesity treatment, and they produce effects that reach far beyond the scale. Because obesity shortens lifespan and damages nearly every organ system, it makes sense that drugs that treat obesity could also improve healthspan—the years you live with strength, clarity, and independence.However, weight loss alone does not explain what researchers are seeing. These drugs reduce inflammation, protect the heart, lower biological stress, and may even delay cognitive decline. Importantly, many of these effects occur independent of weight loss. That fact has forced scientists to ask a serious question: could GLP-1 drugs represent a new class of anti-aging medicine?Even longevity-focused clinicians, such as Peter Attia, have publicly discussed using GLP-1 drugs at lower doses in select patients—not for weight loss, but for metabolic health and long-term disease prevention.Why Metabolism Matters for AgingAging is not just about time. Instead, it reflects how well your body regulates key systems over decades. Blood sugar control, inflammation, oxidative stress, and cellular repair all shape how fast—or how slowly—you age.GLP-1 receptor agonists influence all these pathways. Originally designed to mimic a gut hormone that signals fullness, these drugs turned out to do much more. Research shows they lower systemic inflammation, improve mitochondrial function, and reduce oxidative stress. As a result, organs function better for longer.In simple terms, when metabolism runs smoothly, cells behave younger.Retatrutide and the Next Generation of GLP-1 DrugsNewer drugs have taken this concept even further. Retatrutide, a triple-agonist medication, targets three hormonal pathways simultaneously: GLP-1, GIP, and glucagon.In Phase 3 trials, participants lost nearly 29% of their body weight, or more than 70 pounds on average. Yet weight loss only tells part of the story. Retatrutide also lowered inflammation, improved blood pressure, improved lipid profiles, and reduced joint pain.Each hormone plays a role. GLP-1 reduces appetite and inflammation. GIP improves insulin sensitivity and nutrient handling. Glucagon increases energy expenditure and fat oxidation. Together, these pathways keep metabolism active, not slowing down during weight loss.That combination does more than shrink waistlines. It restores metabolic flexibility, which declines with age.Inflammation: The Engine of AgingFor decades, scientists blamed aging on simple wear and tear. Modern research tells a different story. Chronic, low-grade inflammation—often called inflammaging—drives many diseases of aging.Heart disease, stroke, arthritis, fatty liver disease, and cognitive decline all share this inflammatory background. In clinical trials, GLP-1 drugs reduced markers such as C-reactive protein, triglycerides, and blood pressure. These changes signal reduced biological aging risk, not just better lab numbers.When inflammation falls, fewer senescent cells accumulate. Blood vessels stay healthier. Organs function longer.Heart Disease and...

The Holiday Party That Turned DeadlyIt started at a holiday party.Laughter, champagne, a toast — then a collapse.A fifty-two-year-old, active and healthy, suddenly lost consciousness.Paramedics did CPR and shocked her heart twice.She survived — barely.Doctors called it Holiday Heart Syndrome: an alcohol-triggered arrhythmia that can kill.​What Is Holiday Heart?Holiday Heart arises after binge or even moderate drinking, especially around celebrations. Alcohol irritates heart cells, disrupts electrolytes, and scrambles electrical signals, which can trigger atrial fibrillation — an erratic rhythm that raises the risk of clots, stroke, and sudden death. Even a single heavy night can set it off, and repeated use amplifies inflammation and structural damage long after the hangover fades.​Alcohol and Your HeartFor years, the “French paradox” suggested red wine protects the heart, but newer evidence points instead to lifestyle patterns rather than wine itself. Ethanol and its metabolite acetaldehyde directly injure heart muscle, disturb calcium handling, damage mitochondria, and can lead to Alcoholic Cardiomyopathy — an enlarged, weakened heart. Harm shows up even in relatively low intake, and improvement typically requires reducing or stopping alcohol.​Alcohol and CancerAlcohol is a proven carcinogen that promotes DNA damage, inflammation, oxidative stress, and hormonal shifts that favor tumor growth. At least seven cancers — including those of the mouth, throat, larynx, esophagus, liver, colon, and breast — are directly linked to alcohol, with risk beginning above zero and rising with each additional drink. Even up to one drink a day meaningfully increases breast cancer risk, and the combined use of alcohol and tobacco multiplies risk even further.​Blue Zones, Not Blue WineYou’ve probably heard this one:People in Sardinia or Ikaria drink wine every night and live to 100.What’s missing is the math.They sip 3 to 4 ounces — not a glass, not a typical American glass, but a tasting. The flight of wine.Their rustic wines are 10–11 percent alcohol, not the 16 percent bombs from Sonoma.And they don’t live long because of the wine.They live long because of everything else:walking hills, eating beans, taking naps, sleeping well, and belonging to a community.Their wine is cultural, not clinical.If you want their healthspan, copy their diet, movement, and purpose — not the nightly pour.Weight, Metabolism, and AgingAlcohol hijacks metabolism by forcing the liver to prioritize ethanol breakdown, pushing fat and sugar processing aside. Drinks can add substantial hidden calories, promote fatty liver, and stall fat loss, even when the rest of a diet looks reasonable.​Why “Detox” Fixes FailPopular “alcohol detox” supplements promise faster clearance or hangover prevention, but research points to ethanol itself and the inflammatory response as the main drivers of symptoms. Blocking acetaldehyde alone does not prevent mitochondrial damage, immune activation, or the residual effects that follow a night of heavy drinking.​The Longevity HypocrisyModern wellness culture often warns about “toxins” while normalizing regular drinking, even framing certain spirits or wines as health tools. Yet, when viewed through a longevity lens, alcohol stands out as one of the most potent, fully optional biological stressors in the modern lifestyle.​When You StopOnce drinking stops or drops sharply, the body begins to repair: blood

Muscle is Medicine: Why Lifting Weights is Your Best Longevity InvestmentClearly, your body changes as you age. I learned this lesson years ago when my son was three years old. We started him skiing, and he loved every minute of it. When he fell, he tumbled onto his behind, jumped right back up, and skied down the hill like nothing had happened. He was pure rubber and resilience.However, I was 53 years his senior that year. I did an inadvertent 360-degree twirl on the slopes myself. His mother saw me and immediately asked if I had broken my wrist, wondering when I could return to surgery. The difference between a flexible young body and an older body is critical. Consequently, I retired from skiing that season and now enjoy the lodge, where I write and make them great dinners.Indeed, your older body desperately needs work to stay flexible, strong, and balanced as time goes on. I have seen too many independent seniors lose everything after a simple fall in their own home. They go from living on their own to spending their last days in a care center, sometimes never leaving bed. This outcome is not healthspan. Instead, you want a fall to be like my son’s—just on your butt and back up. Sadly, too many fall and cannot get up. This isn't a commercial for a safety pendant, but a sincere plea for you to start working your muscles.Section 1: The Enemy is Muscle Loss (Sarcopenia)Specifically, we talk frequently about heart health and clear arteries in longevity. Those things are unquestionably crucial. Nevertheless, the biggest threat to functional independence as we age is a condition called sarcopenia. This is the medical term for age-related muscle loss.Unfortunately, we start losing about 3 to 8 percent of our muscle mass every decade after age 30. That loss accelerates quickly once you hit 70. This problem is not just about looking less toned; fundamentally, it is about losing the ability to stand up from a chair, carry groceries, or, most importantly, catch yourself when you trip. The falls that result are often catastrophic.Section 2: Big Things Help Small Things—The Cellular ConnectionAmazingly, resistance training is effective at the microscopic level, too. We have talked extensively about the tiny, complex mechanisms of the cell, but here is the key takeaway: small things benefit from big things.In fact, increasing muscle mass through training has direct, positive effects on two major microscopic drivers of aging: mitochondrial function and telomere health.To elaborate, when you challenge your muscles, you signal your cells to create more energy. This signal forces your mitochondria—the cellular powerhouses—to become both more numerous and more efficient. Better mitochondrial function equals more energy and less cellular stress.Moreover, studies show that resistance training actually increases the activity of the enzyme telomerase in some cells. Telomerase helps maintain the protective caps on your DNA called telomeres.Therefore, you don’t need to buy fancy, expensive supplements like NAD or telomere boosters. Picking up a dumbbell costs less money but yields more results. You gain muscular strength, better metabolism, stronger bones, and the cellular benefits all at once.Section 3: Muscle is Your Metabolic PowerhouseLet's consider how muscle mass influences your diet. Your muscle is actually your body’s largest organ for glucose disposal. Think of it like this: when you eat, your body releases glucose (sugar) into your bloodstream....

🧬 Telomeres and Time: Can We Really Rewind Aging?The Lowest Hemoglobin I’ve Ever SeenThe lowest hemoglobin I’ve ever seen belonged to a young woman who was still standing. Her blood count was one-fourth of normal. She was pale, short of breath, and strong enough to walk into the clinic.Doctors soon learned her bone marrow had stopped making new blood cells. The diagnosis was aplastic anemia — a true telomere disease.She survived thanks to her fitness, modern science, and a bone marrow transplant from a generous donor in Germany. Two years later, she’s in law school, healthy, and full of life.What Are Telomeres?Each cell in your body carries chromosomes — long strands of DNA. At the ends of those chromosomes sit telomeres, tiny caps that keep the DNA from unraveling, like plastic tips on shoelaces.Every time a cell divides, its telomeres shorten a little. When they get too short, the cell can no longer divide. Scientists call that stage cellular senescence — cellular retirement.In 2009, researchers Elizabeth Blackburn and Carol Greider won the Nobel Prize for discovering telomerase, an enzyme that can rebuild telomeres. Their discovery sparked dreams of reversing aging. But there’s a catch: cancer cells also use telomerase to live forever. Turning that enzyme on everywhere might turn back time — or turn on tumors.Why Everyone Talks About TelomeresTelomeres became the poster child for longevity marketing.Social media ads promise to “measure your biological age.” Supplement companies claim to “lengthen your telomeres” for hundreds of dollars a bottle.The problem? Telomere tests vary between labs. Results can change by 20 percent depending on the method. They show trends, not destiny.What’s Being StudiedReal scientists are studying how telomeres behave under different conditions.Danazol — a synthetic sex hormone that slows telomere loss in people with inherited marrow failure. It works but brings side effects, so it’s not an anti-aging trick.Henagliflozin — a diabetes drug that increased telomere length in one small study. Whether that helps humans live longer is still unknown.Aripiprazole — an antipsychotic that repaired telomeres in cells after oxidative stress. That’s a Petri dish result, not a prescription for youth.These drugs show that we can nudge biology, but they’re for disease, not for vanity.Vitamins and Compounds That Might HelpNutrients influence telomere health, too.Vitamin D supports telomerase. Long-term studies show it slows telomere shortening.Vitamins C and E help reduce chemical stress that wears telomeres down.Gamma-tocotrienol, a form of vitamin E, may reverse telomere loss — so far only in lab work.TA-65, from the Astragalus plant, may activate telomerase but carries risk. Turning on telomerase could also fuel cancer.Telomir 1 is experimental and not available outside research.None of these is proven to extend life. They’re promising ingredients, not miracles in a capsule.What Lifestyle Still Beats EverythingLifestyle matters more than any supplement.A large study at UCSF showed that people who ate a Mediterranean diet, exercised, and managed stress boosted telomerase activity within months.No powder required.Telomeres respond to care. They’re markers of how you live, not the cause of how long you live.Longer telomeres don’t guarantee longer life — they reflect how your body has handled time, inflammation, and stress.What Scientists Agree

The Mitochondria Problem: Why These Tiny Powerhouses Shape How We AgeMany people suddenly talk about mitochondria. You hear them in political speeches, on podcasts, and across social media. RFK Jr said he can “see” kids with weak mitochondria just by watching them walk through an airport. Others claim special diets or powders can “fix” aging by supercharging these organelles.However, most of that chatter misses the actual science.This post breaks down what mitochondria do, why they matter for aging, and how you can keep them healthy. No hype. No detox teas. Just biology you can use.What Are Mitochondria?Every cell in your body contains tiny structures called mitochondria. They act like miniature cells living inside your larger cells. Each mitochondrion even has its own DNA.Mitochondria divide independently from your regular cells.They manage your energy, converting glucose to ATPFinally, mitochondria keep your organs working.You inherit all your mitochondria from your mother, which is why scientists use mitochondrial DNA to trace ancestry.How Did We Get Mitochondria? (A Very Old Story)About 1.5 billion years ago, a simple cell swallowed a bacterium and refused to digest it. Instead, they formed a partnership.The bacterium supplied energy.The host cell provided safety.That partnership became the mitochondrion. Every person alive today runs on that ancient deal.What Do Mitochondria Do All Day? Mitochondria take glucose from your food and convert it into ATP — the energy your body uses to move, think, heal, and grow. This process runs every second of your life.You cannot swallow ATP and get more energy. ATP supplements don’t work. Only your mitochondria make the usable fuel your body needs.Why Young Mitochondria Work So WellYoung mitochondria act like teenagers. They run fast, bounce back quickly, and handle stress with ease. Cells constantly recycle old mitochondria through a process called mitophagy. This system works beautifully in childhood.Fresh mitochondria power:strong musclessharp thinkingfast recoveryhealthy metabolismWhen mitophagy runs smoothly, you feel energetic and resilient.What Happens When Mitochondria AgeAging slows everything down. Mitochondria begin to leak more “exhaust,” build up mutations, and lose efficiency. Damaged ones don’t get removed as well, because mitophagy weakens with age.Unfortunately, mitochondria do something worse than slow down:They fuse with healthy mitochondria.Imagine pouring spoiled milk into a fresh gallon. The whole jug goes bad. Aging mitochondria do the same thing inside your cells. They spread dysfunction to the healthy ones.How Aging Mitochondria Cause TroubleAs mitochondria fail, they change how cells function. They send distress signals back to the nucleus that alter gene expression. These messages push cells toward inflammation, stress, and survival pathways that your body normally keeps quiet.Even more concerning, changes in mitochondrial shape — too much splitting (fission) and not enough merging (fusion) — appear in both aging and cancer. These shifts support tumor growth, help cancer cells spread, and make some treatments less effective.Aging mitochondria increase the risk of:brain fogmuscle fatigueslower recoveryheart strainmetabolic slowdowncancer-friendly environmentsMitochondria sit at the center of how we age.Why “Mitochondrial Booster” Supplements...

Urolithin A: What It Is, How It Works, and Why Your Gut Decides EverythingBy Dr. Terry SimpsonMost people hear the name Urolithin A and think it belongs in a commercial about prostate health. It sounds like something a man named “Gary, 62,” would talk about while fishing. But Urolithin A has nothing to do with plumbing. Instead, it sits at the center of a new wave of longevity science focused on how our cells clean up old, broken parts.As we age, our mitochondria—the tiny power centers inside our cells—start to slow down. They build up damage and stop working well. Eventually, this pile-up makes us lose strength and energy. That’s where Urolithin A comes in. It helps switch back on a process called mitophagy, which is basically the cell’s recycling program for old mitochondria.Where Urolithin A Really Comes FromYou cannot eat Urolithin A directly. Instead, your body makes it when your gut bacteria break down special plant compounds called ellagitannins. These are found in foods like:pomegranateswalnutsberriesgreen tea (yes, really)Green tea is usually known for its catechins, but it also contains ellagitannins like strictinin. After you drink it, your gut bacteria break these tannins apart and create ellagic acid, which can later turn into Urolithin A.However, this only works if you have the right microbes. And here’s the surprising part:Most people do not.Studies show that only 12% to 40% of adults naturally produce Urolithin A from food. Everyone else makes little to none because their gut bacteria simply aren’t built for the job.How Your Gut Decides EverythingYour microbiome—the community of bacteria living in your digestive system—decides whether you make Urolithin A or not.People who produce Urolithin A usually have:more diverse gut microbesspecial bacteria like Enterocloster and Gordonibacterthe right genes inside those microbes to do the chemical conversionPeople who don’t produce it (called “metabotype zero”) lack those bacteria or the gene pathways needed. Eating more pomegranates or drinking more green tea does not fix this. No diet, including keto or Mediterranean, has been shown to turn a non-producer into a producer.This is why two people can eat the same food, and only one makes Urolithin A.What Urolithin A Does in HumansIn older adults, researchers have tested Urolithin A supplements for up to 4 months. These studies show several encouraging results:muscle endurance improvesinflammation markers decreasemitochondrial health markers look betterEven so, there are limits. Trials show no meaningful improvement in:walking distanceATP (cellular energy) productionoverall physical functionSo the biology looks better, but major clinical outcomes have not changed.What Happens in the Lab (But Not Yet in Humans)Scientists also study Urolithin A in senescent cells—cells that have stopped dividing but still cause inflammation. In the lab, Urolithin A can:reduce senescence markerscalm inflammatory signalsrestore mitophagyimprove oxidative stresseven strengthen circadian rhythms inside aging cellsAll of this sounds exciting. However, these findings are from cell culture, not humans. They give us clues, not guarantees.Food vs SupplementsYou

🧬 NAD: The Molecule of Life — and the HypeHow a lab coenzyme became the latest anti-aging obsessionWhat We Mean by Longevity and HealthspanWhen people talk about longevity, they usually mean how long we live.But healthspan — the years we live well — matters far more.That’s the time before disease steals our energy, mobility, and independence.Modern medicine has already doubled our lifespan in the last century.Now the goal is to extend the healthy part — without falling for pseudoscience along the way.When Marketing Meets MedicineLongevity has become a booming business.Some gurus, like Dr. Eric Topol, do real science.Others, like Peter Attia, sell access: $150 000 per patient for lab tests, a VO₂ max treadmill run, and a few “optimized” workouts.He’s also an investor in AG1 — the influencer’s green drink of choice.Andrew Huberman promotes similar ideas under studio lights bright enough to sterilize a petri dish.Both are clever, credentialed, and caught between data and drama.Then there’s Dr. David Sinclair, who helped discover how cells age — and then helped turn that discovery into a supplement empire.His company tried to patent NMN, an NAD precursor, as a drug.The FDA briefly removed NMN from the supplement market, sending Reddit into meltdown.It’s back now, but the episode showed how quickly science slides into sales.And finally, we have the shirtless salesmen:Paul Saladino, who went from carnivore crusader to “fruit influencer.”Liver King, whose real secret wasn’t liver — it was injectable.And Gary Brecka, who claims to predict your death date (for a fee).These are subscription services disguised as sages.What NAD Actually IsNicotinamide adenine dinucleotide (NAD⁺) is a molecule found in every living cell.It helps convert food into energy and repair DNA.As we age, NAD levels fall — metabolism slows and damage builds up.So scientists asked: If we raise NAD again, can we slow aging?In mice, the answer looks promising.NAD precursors like nicotinamide riboside (NR) and nicotinamide mononucleotide (NMN) increase average lifespan by 5–15 percent and improve energy, insulin sensitivity, and activity.That’s great for mice — but we don’t live in cages or eat lab chow.Can You Get NAD from Food?Not directly — but your body makes NAD from dietary precursors:tryptophan and niacin (vitamin B₃).You’ll find them in fish, poultry, beans, milk, and whole grains — basically, a Mediterranean-style diet.So before spending $90 on capsules, you can spend $9 at the farmers' market.What the Human Studies ShowHuman trials of NR or NMN (usually 500–2000 mg per day for 6–12 weeks) show they are safe and well-tolerated.They modestly raise NAD levels and sometimes improve lipid profiles and blood pressure.But the effects are small and inconsistent, especially in healthy adults.NAD precursors do not reverse aging.They don’t prevent heart attacks or extend lifespan in people — at least, not yet.NAD vs Statins: A Reality CheckMeta-analyses show NAD precursors, especially niacin, can lower LDL (“bad”) cholesterol by about 8–12 percent.That’s fine, but compare it to rosuvastatin (Crestor):DoseAverage LDL Reduction5 mg≈ 45 %10 mg≈ 52 %20 mg≈ 55 %40 mg≈ 63 %That’s the difference between...

🎙 Celebrating 100 Episodes of Science, Sanity, and a Little SarcasmThis is it — our 100th episode of FORK U.Over the last hundred episodes, we’ve gone from goat-gland hucksters to the microbiome, from Kellogg’s enemas to cholesterol chemistry, and from Blue Zones to bird flu.Today, we look back — not just to celebrate the great scientists who shaped modern medicine, but to expose the modern influencers who sell that same science back to you in a bottle.Welcome to The FORK U Hall of Fame and Shame.🧠 The Hall of Fame🩺 Dr. Ancel Keys — The Misunderstood ScientistDr. Ancel Keys didn’t make guesses — he made measurements.He and his team built one of the most detailed long-term studies in the history of medicine.They went village by village across seven countries.They collected what people ate, sent food samples back to labs, recorded EKGs, drew blood, and reviewed medical charts — not for a few months, but for decades.That’s what science looks like: patient, precise, persistent.Critics like Gary Taubes claim Keys “left out countries.”That’s false — and it only proves they never read his work.Keys studied cohorts of men within small villages, followed them carefully over the years to learn how diet and disease connected.Without today’s molecular tools, he still discovered the pattern that modern science later confirmed:ApoB — the protein attached to LDL cholesterol — is transported into the arterial wall, starting the process of atherosclerosis.Keys didn’t chase fame. He chased truth.His data became the foundation of preventive cardiology.If you want to honor him, drizzle olive oil instead of conspiracy.And a personal note — my thanks to Dr. Harry Blackburn, who worked with Keys and has kindly shared insights from those pioneering days.💉 Dr. Frederick Banting and Charles Best — The Children Who Woke UpIn 1922, Banting and Best discovered insulin.Before that, children with diabetes slipped into comas and died.After the first injections, they woke up.Their parents fed them well, but diet alone couldn’t save them.Good science did.It was one of medicine’s greatest moments — and still saves lives every day.🧬 Dr. Kanehiro Takaki — The First VitaminBefore anyone even knew the word vitamin, Japanese surgeon Dr. Kanehiro Takaki saw sailors dying from beriberi.Using early ideas of epidemiology, he realized the problem wasn’t infection but nutrition.He changed their diet — adding barley and vegetables — and the disease vanished.Takaki brought Japan into modern medicine.Even Dr. Charles Mayo admired him.Had he lived longer, he would likely have shared a Nobel Prize.🧫 Dr. Leonard Hayflick — The Original Longevity DoctorIn 1961, Dr. Leonard Hayflick discovered something remarkable:Human cells divide about fifty times, then stop — the Hayflick Limit.He proved aging isn’t mystical. It’s biological.Every division shortens a cell’s life clock until it retires.His research wasn’t about nutrition, but it changed everything about how we understand aging and regeneration.He was the first true longevity doctor — without supplements, slogans, or selfies.❤️ The DASH and Portfolio Diet TeamsThe DASH Diet — Dietary Approaches to Stop Hypertension — came from a dream team of researchers.Dr. Lawrence Appel at Johns Hopkins led the NIH...

Thanksgiving is more than a meal — it’s a worldwide celebration of gratitude built around foods that started here in the Americas. Corn, beans, potatoes, and turkey didn’t just feed a nation; they changed global cuisine. Today, we blend culinary history with medical sense to show how to enjoy the feast without the nap.🍁 A Holiday for the WorldOur Canadian friends already finished their celebration. For their Thanksgiving, I roasted a chicken with Swiss Chalet sauce — if you know, you know. Thank you, Canada, for giving us Tim Hortons, Swiss Chalet, and the perfect excuse for early gravy season.In the United States, we wait for the fourth Thursday in November to celebrate. And while Thanksgiving began as a survival story between settlers and Native Americans, it’s become a global holiday. Whether you’re in Edinburgh, London, or Los Angeles, if there’s a turkey on your table, you’re part of it.🦃 The Turkey TruthTurkey is a ridiculously large bird. Cooking one whole is like putting a cow in the oven and hoping all the parts turn out right — it just doesn’t work.That’s why I separate mine. The breast goes into a sous vide bath until juicy and tender, and the legs roast separately until golden brown. This approach keeps everyone happy and the meat perfectly cooked.Another reason to love turkey: it’s naturally low in saturated fat, especially compared to red meat. So, when prepared well, it’s one of the healthiest centerpieces for your table.🥖 Cornbread Stuffing — Cook It SafelyStuffing the bird might seem traditional, but it can also be dangerous. Baking bread inside raw poultry turns your dinner into a bacteria incubator. Instead, bake it separately.My favorite? Cornbread stuffing — a true dish of the Americas. Combine cornbread cubes, sautéed onions, celery, herbs, mushrooms, and broth. For extra flavor, crisp up some turkey skin like “poultry bacon” and crumble it on top.(You’ll find the full recipe at terrysimpson.com)🥔 Potatoes — From the Andes to Every PlateLong before Europeans knew what a potato was, Indigenous farmers in the Andes were cultivating hundreds of varieties. Those humble tubers crossed the ocean and reshaped diets from Dublin to Delhi. Yes, the Italians perfected Gnochi - and the Irish love of the potato brought many of our finest folks to the United States.At my table, I keep mashed potatoes simple — Yukon Golds, butter, olive oil, milk, salt, and pepper. No truffle oil. No mountain of bacon. Just creamy, honest comfort food.🥗 Green Beans and the Three SistersGreen beans are another gift from the Americas. Native farmers grew them with corn and squash — the Three Sisters that nourished generations. The beans climbed the corn stalks while enriching the soil — the original regenerative farming.In Culinary Medicine, we love beans for their fiber, plant protein, and heart-healthy nutrients.If you’re remaking the classic green bean casserole, skip the canned soup. Use fresh mushrooms, milk, and a touch of cornstarch. Or, sauté the beans in olive oil and garlic for a lighter, Mediterranean twist.(Full recipe posted at terrysimpson.com)🥣 Cowboy Caviar — A Smart StarterBefore the main event, try Cowboy Caviar — a colorful bean salad from the American Southwest. It’s bright, high in fiber, and helps you eat more slowly (and more sanely).Mix black beans, black-eyed peas, corn,...