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Is there such a thing as an ‘intergenerational curse’?

Published Feb 03, 2026 5:00 am

When a man dies of a heart attack at 49—and his father died at 48 of the same cause, two uncles suffered fatal strokes at the same age, and a brother survived a myocardial infarction at 40 after angioplasty—it is almost inevitable that the surviving family members ask a deeply human question: “May sumpa ba ang pamilya namin?”

Medicine encounters this question often, though it is rarely phrased so starkly in textbooks. Patients may not use the word “curse” in clinic, but they express it in other ways: “Doc, parang sinusundan lang kami.” “Ganito rin ang nangyari sa tatay ko.” “Mukhang pare-pareho ang ending naming pamilya.”

Knowing your family history doesn’t make you doomed. Ignoring it does.

The idea of an intergenerational curse is as old as civilization itself. From ancient Greek tragedies to biblical genealogies, from royal families to modern political dynasties, repeated misfortune across generations has often been interpreted as destiny, punishment, or fate.

But what does science actually say?

The human need to find meaning in patterns
Tracing patterns through generations—family history can reveal inherited health risks, not curses.

The human brain is a pattern-seeking organ. When events repeat themselves—especially tragic ones—we instinctively search for meaning. Randomness feels unbearable; patterns feel explainable, even if frightening.

This is why families with repeated early deaths, cancers, strokes, or heart attacks often describe their history in moral or metaphysical language. It is emotionally easier to believe in a “curse” than to confront the uncomfortable truth that biology, behavior, and environment may be conspiring silently across decades.

Medicine does not dismiss this instinct. Instead, it translates it.

What looks like a ‘curse’ is often genetics

From a scientific standpoint, the most powerful explanation for repeated early cardiovascular events in families is inherited risk.

Early identification of inherited risk can save lives.

Large population studies have consistently shown that:

  • Having a first-degree relative (parent or sibling) who had a heart attack before age 55 (men) or 65 (women) doubles to triples one’s own risk;
  • Certain genetic profiles strongly predispose individuals to early atherosclerosis, abnormal cholesterol metabolism, hypertension, abnormal clotting, and endothelial dysfunction.
  • Conditions such as familial hypercholesterolemia, for example, can cause severe coronary artery disease in the 30s or 40s—even in individuals who appear otherwise healthy.

In families like the one described, the clustering of events at nearly identical ages strongly suggests a shared genetic vulnerability, not a supernatural curse.

Genes do not guarantee disease—but they load the gun.

But genes rarely act alone

If genetics were destiny, identical twins would always die of the same causes at the same age. They do not.

This is where the second layer comes in: shared environment and learned behavior.

Family eatinag habits influence heart health from one generation to the next.

Families tend to share: dietary habits, attitudes toward exercise, smoking or alcohol patterns, stress coping styles, sleep habits, and health-seeking behavior (or the opposite—avoidance of doctors).

A father who normalizes heavy smoking, salty food, long work hours, and avoidance of check-ups unintentionally teaches his children the same script. Not because he wants to harm them—but because culture is transmitted quietly.

Thus, what looks like an inherited curse is often an inherited lifestyle, reinforced over generations.

Genes load the gun. Environment pulls the trigger.

The role of epigenetics: when experience writes on genes

Modern science adds a third, more subtle layer: epigenetics.

Epigenetics refers to changes in gene expression that do not alter DNA itself, but affect how genes are turned on or off. Chronic stress, poor nutrition, trauma, and even in utero exposures can leave epigenetic marks that influence disease risk in offspring.

This means that the lived experiences of one generation—poverty, war, chronic stress, untreated illness—can biologically shape the next.

Still, this is not a curse. It is biology responding to history.

And importantly, epigenetic changes are often reversible.

Famous families and illusion of curses

History is filled with prominent families whose repeated tragedies have been mythologized as curses—oyal houses, political clans, and well-known dynasties. In reality, these families often share: genetic vulnerabilities, intense public stress, dangerous environments, high-risk professions, and relentless scrutiny.

When illness or tragedy is repeatedly visible in the public eye, it appears more ominous. But visibility is not causality.

Illness does not discriminate between famous and unknown families. It only becomes more noticeable when the family is already well-known.

Why the language of ‘curse’ persists

Despite all this evidence, the word curse persists because it captures something science alone does not: the emotional weight of repetition.

When someone grows up expecting an early death because “that’s how it always happens,” that belief itself can become harmful. It may lead to fatalism, neglect of preventive care, unconscious self-sabotage, delayed treatment, and resignation rather than resistance.

In this sense, the most dangerous “curse” is not genetic—it is hopelessness.

Can the cycle be broken?

The most important medical truth to convey is this:

  • A family history is not a family sentence.
  • Modern cardiology has radically altered outcomes for high-risk families. Early identification and aggressive prevention can delay—or entirely prevent—events that once seemed inevitable.

This includes early and regular screening, aggressive cholesterol and blood pressure control, smoking cessation, stress management, dietary change, appropriate medications, and timely interventions like angioplasty when needed.

The brother who survived a heart attack at 40 after angioplasty is not evidence of a curse. He is evidence of interruption—of medicine stepping into a family pattern and changing its trajectory.

He represents the generation where the story can change.

From curse to call to action

Seen through a medical lens, what families call an intergenerational curse is better understood as an intergenerational warning.

It is the body’s way of saying pay attention, intervene early, do not repeat silently. When framed this way, family history becomes not a prophecy—but a map.

A more hopeful language

As physicians, we must be careful with words. Language shapes outcomes.

Instead of “curse,” we should speak of inherited risk, family patterns, biological vulnerability, and preventable trajectories.

Because words like ‘‘curse’’ suggest inevitability. Medicine exists precisely to challenge inevitability.

The final truth 

There is no scientific evidence for an intergenerational curse. There is overwhelming evidence for intergenerational risk—and equally strong evidence that risk can be modified, delayed, and sometimes entirely avoided.

The past explains vulnerability. It does not dictate the future.

In families where tragedy has repeated itself, the most powerful act is not fear—but foresight. Not resignation—but responsibility.

And when one generation chooses awareness over denial, prevention over fatalism, and action over superstition, what was once called a curse quietly becomes something else entirely: a turning point. 

When family history should alarm you
Red flags that require attention

1. Early heart disease in close relatives.

  • Heart attack, angioplasty, bypass surgery, or sudden cardiac death
  • Before age 55 in men or 65 in women
  • Especially if involving a parent, sibling, or multiple relatives

2. Repeated strokes or heart attacks in the family.

  • Two or more close relatives with stroke or heart disease
  • Events occurring at similar ages across generations

3. Known inherited conditions.

  • Familial hypercholesterolemia
  • Early-onset hypertension
  • Inherited clotting disorders
  • Cardiomyopathies or arrhythmias

3. Sudden or unexplained deaths.

  • Death during sleep, exercise, or at a young age
  • “Bigla na lang” deaths without clear diagnosis

Severe risk factors clustering in the family.

  • Very high cholesterol or triglycerides
  • Diabetes at a young age
  • Resistant hypertension
  • Strong family history of smoking-related disease
  • What you shoukd do if you're at risk

If any of the above apply, do not wait for symptoms. Take proactive steps:

  • Have your blood pressure, blood sugar, and cholesterol checked early and regularly.
  • Consider baseline ECGand further cardiac evaluation as advised.
  • Discuss your family historyopenly with your doctor — details matter.
  • Start lifestyle changes early (diet, exercise, smoking cessation, stress management).
  • Follow medicationsconsistently if prescribed.
  • Encourage other family membersto get screened, too.