Same Storm, Different Houses
How trauma may influence gene activity, and what science tells us about resilience
- Trauma & Resilience
- Epigenetics
- Plain-language science
A question I have carried for decades
I grew up in Poland under a communist regime. My grandmother survived the Holocaust and then lived most of her adult life under communism. Her hardship did not end with her. I could feel it in my mother and aunts, and in some ways in my own generation too.
My fascination started with books, long before science. As a young reader I fell in love with Russian literature, especially Dostoyevsky. Later I learned that his own life was a storm. In 1849 he was sentenced to death and led before a firing squad, then spared at the last moment and sent to four years of hard labor in Siberia. He carried that experience into everything he wrote. His characters suffer, break, and sometimes find redemption, and I kept wondering why some collapsed under their pain while others found a way through.
Later I read Viktor Frankl's Man's Search for Meaning. Frankl, a psychiatrist who survived the Nazi concentration camps, observed that people who held on to a sense of meaning often seemed better able to endure. His observation stayed with me, even though it is one man's experience rather than a scientific explanation. James Garbarino's Lost Boys showed me how early trauma and neglect can shape the lives of troubled young men. And Bessel van der Kolk's The Body Keeps the Score argued that trauma is not only a memory, but something that can affect the body and nervous system. Each book asked the same question in a different way, and I have been chasing it ever since.
In three decades of nursing, first in Poland and then in the United States, in ICUs, recovery rooms, and now psychiatry, I kept seeing the same puzzle. Two people go through the same terrible event. One struggles for years. The other heals and moves forward. Sometimes they are siblings, raised in the same home.
Why? That question led me to a field called epigenetics, and it has become a real passion of mine. Epigenetics studies how life experiences, including stress and trauma, may influence the way our genes are used. If that sounds complicated, don't worry. I will explain it in plain words below, along with what the science can and cannot tell us yet.
Same storm, different houses
Imagine a strong storm moving through a neighborhood. Every house faces the same wind and rain. Afterward, the damage looks very different from house to house.
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One house loses its roof.
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Another has a broken window.
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A third barely shows a scratch.
The storm was the same. The houses were not. Each was built with different materials, on different ground, and had been through different weather before.
Trauma works in a similar way. The event is the storm. Each person is a house, shaped by their genes, their childhood, their relationships, and what they have already lived through.
It is also worth knowing that most people who live through trauma do not go on to develop lasting PTSD. Resilience is common. Epigenetics is one piece of this puzzle, not the whole explanation. Our responses to trauma also reflect inherited genetic differences, earlier experiences, relationships, the places we live, ongoing stress, physical health, and the support and treatment available to us. No single biological mechanism can fully explain why one person develops lasting symptoms while another does not.
What is epigenetics?
"Epigenetics" sounds like a big word, but the basic idea is simple. "Epi" means "on top of," so epigenetics means "on top of the genes."
Start with genes. Your genes are instructions you inherited from your parents. Picture a giant cookbook inside every cell of your body, full of recipes for building and running you. The recipes themselves stay the same.
But your body does not use every recipe all the time. A heart cell and a brain cell carry the same cookbook, yet they use very different recipes. Epigenetics is part of the system that helps decide which recipes are used, when, and how much.
A helpful picture is a dimmer switch. The wiring in your home stays the same, but a dimmer can change how bright a light is. In a similar way, epigenetic changes can influence how actively a gene is used, without changing the gene itself. The real system is more complex than a single switch, but the picture is a good place to start.
One of the most studied epigenetic mechanisms is DNA methylation. Small chemical tags, called methyl groups, attach to DNA. You can picture them as sticky notes in the cookbook. Depending on where they land, they can make a recipe easier or harder to use. Their effect depends on the gene, the location, and the type of cell, so it is not always as simple as "more notes, less activity." Methylation is also only one of several epigenetic mechanisms. Others involve the proteins that DNA is wrapped around and certain RNA molecules.
Here is why this matters: these patterns can respond to life. Studies link stress, nutrition, sleep, relationships, and trauma with differences in DNA methylation. This is one way experience may "get under the skin."
What scientists have found so far
First, a little about the stress system. When you face danger, your brain signals your adrenal glands to release stress hormones such as cortisol. This system is called the HPA axis. Once the danger passes, cortisol itself helps signal the system to settle down, a bit like a thermostat. Several genes help fine-tune that feedback. Much of the research on trauma and epigenetics has focused on these genes.
The studies below are early but important. Think of them as clues, not final answers.
A gene, an experience, and how they interact
A gene called FKBP5 helps regulate how the body responds to cortisol. Some people carry a version of this gene linked to higher risk after adversity. In a 2013 study, adults with that version who had been abused as children showed reduced methylation in one specific region of the gene. That change was linked to a more reactive stress-hormone system. People with the same gene version who were not abused did not show it.
The study points to an interaction between genes and experience. It does not show a single biological switch that causes PTSD.
Research at Johns Hopkins
Researchers at Johns Hopkins studied a gene called SKA2, which appears to be involved in how cells respond to stress hormones. In 2014 they reported that methylation of SKA2, together with a common genetic variant, was associated with suicidal behavior across several groups, and they proposed it as a possible biomarker. A later study of Dutch soldiers linked SKA2 methylation and childhood trauma with stress-hormone reactivity and with PTSD symptoms after deployment.
These are research associations. SKA2 cannot reliably predict any one person's risk, and it is not used in clinical care.
Questions across generations
Dr. Rachel Yehuda's team studied 32 Holocaust survivors and 22 of their adult children. Both groups showed methylation differences at the same site of the FKBP5 gene, though in opposite directions. A later, larger study found a similar pattern in the children of survivors.
The findings suggest that parental trauma may be associated with measurable biological differences in the next generation. They cannot show that epigenetic changes were directly inherited, or how much reflects pregnancy, family environment, or other factors. Scientists are still investigating.
The Dutch Hunger Winter
Near the end of World War II, the Netherlands suffered a severe famine. About 60 years later, scientists compared people conceived during the famine with their own brothers and sisters. The famine group had slightly lower methylation on a growth-related gene. Same parents, same home, a different storm before birth.
This study is about famine, not psychological trauma. It shows that very early adversity can be associated with lasting epigenetic differences.
Our genes and our experiences interact, and that interaction can leave measurable marks.
What we know, and what we don't yet know
The field has grown beyond small single-gene studies. In 2024, an international team combined data from 23 military and civilian groups, about 5,000 people who had all experienced trauma. They found 11 DNA methylation sites in blood that differed in people with PTSD. A 2024 review of 92 studies concluded that these markers are promising but not yet ready for clinical use.
What the evidence supports
- Trauma and early adversity are associated with differences in DNA methylation.
- Genes and experience interact. Neither one alone tells the whole story.
- Some findings have now been repeated in large, diverse groups.
What we don't yet know
- Cause or effect. Most studies are observational. A methylation pattern linked to PTSD does not prove it caused PTSD.
- Blood versus brain. Most samples come from blood or saliva, which may not reflect what happens in the brain.
- Individual prediction. No epigenetic marker can yet tell one person their risk.
Our biology is not fixed
The genes you were born with stay the same for life. But some epigenetic patterns can change over time, and researchers are studying how those changes relate to stress, recovery, and treatment.
In a small 2013 pilot study, Dr. Yehuda's team followed 16 combat veterans with PTSD through 12 weeks of trauma-focused therapy. In those who improved, methylation of the FKBP5 gene changed along with their symptoms. It was a small study, and larger studies are still limited. We do not yet know whether changes like this help cause recovery, simply reflect it, or differ from person to person. Still, it is a hopeful hint that biology and healing move together. (Yehuda et al., 2013)
What matters most for you today does not depend on epigenetics at all. These approaches are well supported for recovery after trauma:
Evidence-based, trauma-focused therapy, and medication when it is appropriate
Safe, steady relationships and social support
Healthy sleep, regular movement, and nourishing food
Time, a sense of safety, and less ongoing stress
A house damaged by a storm can be repaired. Sometimes it is rebuilt stronger.
One honest note: right now there is no blood or saliva test your clinician can order to measure trauma or predict PTSD. These discoveries are still research. If you see a test like this advertised, ask questions before you pay for it.
Not a flaw. Biology meeting experience.
When I think of my grandmother, my family, and the patients I care for, I no longer see weakness or failure. I see houses that weathered hard storms, each in its own way.
That is why I practice the way I do. I want to understand each person's whole story, including their biology, life experiences, relationships, and the conditions they live in, not just a list of symptoms. And I want every patient to know that how they responded to trauma is not a character flaw. It reflects biology meeting experience, and healing is possible.
If this article stirred up something for you, you are not alone. Talking with a mental health professional can help. If you are in crisis, call or text 988, the Suicide & Crisis Lifeline, available 24/7. For immediate danger, call 911.
This article is for educational purposes only and does not constitute medical advice. Reading it does not establish a provider-patient relationship.