PTSD – A Way Out A mindful way to heal

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The see-saw quality of PTSD: Traumas ability to enter our consciousness when he/she feels like it.

PTSD demonstrates separate qualities, a stand alone power source and a tight relationship with our negative emotions.

My image of PTSD is a roller coaster, a big, tall monster of a ride.

In real life my lows are much deeper than the highs.

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The highs are always guarded, not trusting what the world has in store next.

Explanation: In childhood I had no control, no impact on what would happen to me.

Life since childhood carries that harmful unknown, out there, just beyond my visual reach.

Our traumatized mind scours the future incessantly looking to avoid more damage.

Such a waste of time, it happens automatically without directed thought from me.

My behavior has never caused my trauma, so I had no control over the outcome of my PTSD.

My personality was hard wired feeling like this..

When Trauma erupts, ignoring it is quite impossible, so we either avoid it or work to improve it.

This dominates life, I avoided, hiding in my dark garage, the only flaw was bringing my traumatized 🧠 brain with me.

I isolated physically for six months, my trauma filled brain (mind) still dominated life, if I was alone or amongst 30,000.

Back to basics, accept and try to release, exercise to deplete the cortisol or meditate.

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Karina Margit Erdelyi:

We are living in strange times, with much of the world under quarantine for the novel coronavirus—and that’s precisely the kind of stress that may impact future offspring according to some scientists.A growing body of research suggests that trauma (like from extreme stress or starvation among many other things) can be passed from one generation to the next.

Here’s how: Trauma can leave a chemical mark on a person’s genes, which can then be passed down to future generations. This mark doesn’t cause a genetic mutation, but it does alter the mechanism by which the gene is expressed. This alteration is not genetic, but epigenetic. 

We spoke with Dr. Chris Mason, Associate Professor at Weill Cornell Medicine, with appointments at the Tri-Institutional Program in Computational Biology and Medicine between Cornell, Memorial Sloan-Kettering Cancer Center and Rockefeller University, and Director of the Mason Lab. He shared that “epigenetics, in simplified terms, is the study of the biological control mechanisms of DNA—the light switches that turn genes on or off. What does that mean? In essence: epigenetics control how or why your genes are expressed.”

What would have seemed preposterous 20 years ago has become a fast-emerging field of study. Today the idea that a person’s experience could alter their biology, and behavior of their children and grandchildren has gained serious traction. Animal and some smaller human studies have shown that exposure to stressors like immense stress or cold can trigger metabolic changes in subsequent generations—and we may just be living in such a time as we grapple with the mounting COVID-19 crisis.

So, What Exactly Are These Epigenetic Studies?

Differences among groups who had gone through extreme physical and psychological stress, like Holocaust survivors, those who were born to parents who lived through “The Dutch Hunger Winter,” and sons of Confederate prisoner-of-war soldiers in the American Civil War, all make the case the most clearly, but they’re not the whole picture. There has also been a lot of work in the lab focused on this phenomenon, and that work really accelerated after The Human Genome Project (HGP) was completed in 2003. Here’s a look at what scientists have learned from both case studies and experiments.

How Extreme Situations Have Impacted Offspring

Mason shared that the field of epigenetics gained real traction about a decade ago, when scientists published seminal research on the Dutch Hunger Winter, an extended period of famine that took place towards the end of World War II when the Nazis blocked food supplies in October 1944, thrusting much of the Netherlands into famine. When the Dutch were liberated in May 1945, more than 20,000 had died of starvation. Pregnant women were particularly vulnerable; and the famine impacted the unborn children for the rest of their lives.

Scientists found that those who had been in utero during the famine were a few pounds heavier than average. (The thinking goes that the mothers, because they were starving, automatically quieted a gene in their unborn children involved in burning the body’s fuel.) When the children reached middle age, they had higher LDL (“bad”) cholesterol and triglyceride levels. They also suffered higher rates of obesity, diabetes, cardiovascular disease, and schizophrenia. When scientists looked into why, they found that these children carried a specific chemical mark—an epigenetic signature—on one of their genes.

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Dr. Rachel Yehuda, Director of the Traumatic Stress Studies Division at the Icahn School of Medicine at Mount Sinai in New York City, conducted a 2015 study on the children of 40 Holocaust survivors.  She found that they had epigenetic changes to a gene linked to their levels of cortisol, a hormone involved in the stress response. She also found a distinctive pattern of DNA methylation, another epigenetic marker. The study concluded that both parents and unborn children were affected on a genetic level.

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